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The Journal of Family Practice is a peer-reviewed and indexed journal that provides its 95,000 family physician readers with timely, practical, and evidence-based information that they can immediately put into practice. Research and applied evidence articles, plus patient-oriented departments like Practice Alert, PURLs, and Clinical Inquiries can be found in print and at jfponline.com. The Web site, which logs an average of 125,000 visitors every month, also offers audiocasts by physician specialists and interactive features like Instant Polls and Photo Rounds Friday—a weekly diagnostic puzzle.
gambling
compulsive behaviors
ammunition
assault rifle
black jack
Boko Haram
bondage
child abuse
cocaine
Daech
drug paraphernalia
explosion
gun
human trafficking
ISIL
ISIS
Islamic caliphate
Islamic state
mixed martial arts
MMA
molestation
national rifle association
NRA
nsfw
pedophile
pedophilia
poker
porn
pornography
psychedelic drug
recreational drug
sex slave rings
slot machine
terrorism
terrorist
Texas hold 'em
UFC
substance abuse
abuseed
abuseer
abusees
abuseing
abusely
abuses
aeolus
aeolused
aeoluser
aeoluses
aeolusing
aeolusly
aeoluss
ahole
aholeed
aholeer
aholees
aholeing
aholely
aholes
alcohol
alcoholed
alcoholer
alcoholes
alcoholing
alcoholly
alcohols
allman
allmaned
allmaner
allmanes
allmaning
allmanly
allmans
alted
altes
alting
altly
alts
analed
analer
anales
analing
anally
analprobe
analprobeed
analprobeer
analprobees
analprobeing
analprobely
analprobes
anals
anilingus
anilingused
anilinguser
anilinguses
anilingusing
anilingusly
anilinguss
anus
anused
anuser
anuses
anusing
anusly
anuss
areola
areolaed
areolaer
areolaes
areolaing
areolaly
areolas
areole
areoleed
areoleer
areolees
areoleing
areolely
areoles
arian
arianed
arianer
arianes
arianing
arianly
arians
aryan
aryaned
aryaner
aryanes
aryaning
aryanly
aryans
asiaed
asiaer
asiaes
asiaing
asialy
asias
ass
ass hole
ass lick
ass licked
ass licker
ass lickes
ass licking
ass lickly
ass licks
assbang
assbanged
assbangeded
assbangeder
assbangedes
assbangeding
assbangedly
assbangeds
assbanger
assbanges
assbanging
assbangly
assbangs
assbangsed
assbangser
assbangses
assbangsing
assbangsly
assbangss
assed
asser
asses
assesed
asseser
asseses
assesing
assesly
assess
assfuck
assfucked
assfucker
assfuckered
assfuckerer
assfuckeres
assfuckering
assfuckerly
assfuckers
assfuckes
assfucking
assfuckly
assfucks
asshat
asshated
asshater
asshates
asshating
asshatly
asshats
assholeed
assholeer
assholees
assholeing
assholely
assholes
assholesed
assholeser
assholeses
assholesing
assholesly
assholess
assing
assly
assmaster
assmastered
assmasterer
assmasteres
assmastering
assmasterly
assmasters
assmunch
assmunched
assmuncher
assmunches
assmunching
assmunchly
assmunchs
asss
asswipe
asswipeed
asswipeer
asswipees
asswipeing
asswipely
asswipes
asswipesed
asswipeser
asswipeses
asswipesing
asswipesly
asswipess
azz
azzed
azzer
azzes
azzing
azzly
azzs
babeed
babeer
babees
babeing
babely
babes
babesed
babeser
babeses
babesing
babesly
babess
ballsac
ballsaced
ballsacer
ballsaces
ballsacing
ballsack
ballsacked
ballsacker
ballsackes
ballsacking
ballsackly
ballsacks
ballsacly
ballsacs
ballsed
ballser
ballses
ballsing
ballsly
ballss
barf
barfed
barfer
barfes
barfing
barfly
barfs
bastard
bastarded
bastarder
bastardes
bastarding
bastardly
bastards
bastardsed
bastardser
bastardses
bastardsing
bastardsly
bastardss
bawdy
bawdyed
bawdyer
bawdyes
bawdying
bawdyly
bawdys
beaner
beanered
beanerer
beaneres
beanering
beanerly
beaners
beardedclam
beardedclamed
beardedclamer
beardedclames
beardedclaming
beardedclamly
beardedclams
beastiality
beastialityed
beastialityer
beastialityes
beastialitying
beastialityly
beastialitys
beatch
beatched
beatcher
beatches
beatching
beatchly
beatchs
beater
beatered
beaterer
beateres
beatering
beaterly
beaters
beered
beerer
beeres
beering
beerly
beeyotch
beeyotched
beeyotcher
beeyotches
beeyotching
beeyotchly
beeyotchs
beotch
beotched
beotcher
beotches
beotching
beotchly
beotchs
biatch
biatched
biatcher
biatches
biatching
biatchly
biatchs
big tits
big titsed
big titser
big titses
big titsing
big titsly
big titss
bigtits
bigtitsed
bigtitser
bigtitses
bigtitsing
bigtitsly
bigtitss
bimbo
bimboed
bimboer
bimboes
bimboing
bimboly
bimbos
bisexualed
bisexualer
bisexuales
bisexualing
bisexually
bisexuals
bitch
bitched
bitcheded
bitcheder
bitchedes
bitcheding
bitchedly
bitcheds
bitcher
bitches
bitchesed
bitcheser
bitcheses
bitchesing
bitchesly
bitchess
bitching
bitchly
bitchs
bitchy
bitchyed
bitchyer
bitchyes
bitchying
bitchyly
bitchys
bleached
bleacher
bleaches
bleaching
bleachly
bleachs
blow job
blow jobed
blow jober
blow jobes
blow jobing
blow jobly
blow jobs
blowed
blower
blowes
blowing
blowjob
blowjobed
blowjober
blowjobes
blowjobing
blowjobly
blowjobs
blowjobsed
blowjobser
blowjobses
blowjobsing
blowjobsly
blowjobss
blowly
blows
boink
boinked
boinker
boinkes
boinking
boinkly
boinks
bollock
bollocked
bollocker
bollockes
bollocking
bollockly
bollocks
bollocksed
bollockser
bollockses
bollocksing
bollocksly
bollockss
bollok
bolloked
bolloker
bollokes
bolloking
bollokly
bolloks
boner
bonered
bonerer
boneres
bonering
bonerly
boners
bonersed
bonerser
bonerses
bonersing
bonersly
bonerss
bong
bonged
bonger
bonges
bonging
bongly
bongs
boob
boobed
boober
boobes
boobies
boobiesed
boobieser
boobieses
boobiesing
boobiesly
boobiess
boobing
boobly
boobs
boobsed
boobser
boobses
boobsing
boobsly
boobss
booby
boobyed
boobyer
boobyes
boobying
boobyly
boobys
booger
boogered
boogerer
boogeres
boogering
boogerly
boogers
bookie
bookieed
bookieer
bookiees
bookieing
bookiely
bookies
bootee
booteeed
booteeer
booteees
booteeing
booteely
bootees
bootie
bootieed
bootieer
bootiees
bootieing
bootiely
booties
booty
bootyed
bootyer
bootyes
bootying
bootyly
bootys
boozeed
boozeer
boozees
boozeing
boozely
boozer
boozered
boozerer
boozeres
boozering
boozerly
boozers
boozes
boozy
boozyed
boozyer
boozyes
boozying
boozyly
boozys
bosomed
bosomer
bosomes
bosoming
bosomly
bosoms
bosomy
bosomyed
bosomyer
bosomyes
bosomying
bosomyly
bosomys
bugger
buggered
buggerer
buggeres
buggering
buggerly
buggers
bukkake
bukkakeed
bukkakeer
bukkakees
bukkakeing
bukkakely
bukkakes
bull shit
bull shited
bull shiter
bull shites
bull shiting
bull shitly
bull shits
bullshit
bullshited
bullshiter
bullshites
bullshiting
bullshitly
bullshits
bullshitsed
bullshitser
bullshitses
bullshitsing
bullshitsly
bullshitss
bullshitted
bullshitteded
bullshitteder
bullshittedes
bullshitteding
bullshittedly
bullshitteds
bullturds
bullturdsed
bullturdser
bullturdses
bullturdsing
bullturdsly
bullturdss
bung
bunged
bunger
bunges
bunging
bungly
bungs
busty
bustyed
bustyer
bustyes
bustying
bustyly
bustys
butt
butt fuck
butt fucked
butt fucker
butt fuckes
butt fucking
butt fuckly
butt fucks
butted
buttes
buttfuck
buttfucked
buttfucker
buttfuckered
buttfuckerer
buttfuckeres
buttfuckering
buttfuckerly
buttfuckers
buttfuckes
buttfucking
buttfuckly
buttfucks
butting
buttly
buttplug
buttpluged
buttpluger
buttpluges
buttpluging
buttplugly
buttplugs
butts
caca
cacaed
cacaer
cacaes
cacaing
cacaly
cacas
cahone
cahoneed
cahoneer
cahonees
cahoneing
cahonely
cahones
cameltoe
cameltoeed
cameltoeer
cameltoees
cameltoeing
cameltoely
cameltoes
carpetmuncher
carpetmunchered
carpetmuncherer
carpetmuncheres
carpetmunchering
carpetmuncherly
carpetmunchers
cawk
cawked
cawker
cawkes
cawking
cawkly
cawks
chinc
chinced
chincer
chinces
chincing
chincly
chincs
chincsed
chincser
chincses
chincsing
chincsly
chincss
chink
chinked
chinker
chinkes
chinking
chinkly
chinks
chode
chodeed
chodeer
chodees
chodeing
chodely
chodes
chodesed
chodeser
chodeses
chodesing
chodesly
chodess
clit
clited
cliter
clites
cliting
clitly
clitoris
clitorised
clitoriser
clitorises
clitorising
clitorisly
clitoriss
clitorus
clitorused
clitoruser
clitoruses
clitorusing
clitorusly
clitoruss
clits
clitsed
clitser
clitses
clitsing
clitsly
clitss
clitty
clittyed
clittyer
clittyes
clittying
clittyly
clittys
cocain
cocaine
cocained
cocaineed
cocaineer
cocainees
cocaineing
cocainely
cocainer
cocaines
cocaining
cocainly
cocains
cock
cock sucker
cock suckered
cock suckerer
cock suckeres
cock suckering
cock suckerly
cock suckers
cockblock
cockblocked
cockblocker
cockblockes
cockblocking
cockblockly
cockblocks
cocked
cocker
cockes
cockholster
cockholstered
cockholsterer
cockholsteres
cockholstering
cockholsterly
cockholsters
cocking
cockknocker
cockknockered
cockknockerer
cockknockeres
cockknockering
cockknockerly
cockknockers
cockly
cocks
cocksed
cockser
cockses
cocksing
cocksly
cocksmoker
cocksmokered
cocksmokerer
cocksmokeres
cocksmokering
cocksmokerly
cocksmokers
cockss
cocksucker
cocksuckered
cocksuckerer
cocksuckeres
cocksuckering
cocksuckerly
cocksuckers
coital
coitaled
coitaler
coitales
coitaling
coitally
coitals
commie
commieed
commieer
commiees
commieing
commiely
commies
condomed
condomer
condomes
condoming
condomly
condoms
coon
cooned
cooner
coones
cooning
coonly
coons
coonsed
coonser
coonses
coonsing
coonsly
coonss
corksucker
corksuckered
corksuckerer
corksuckeres
corksuckering
corksuckerly
corksuckers
cracked
crackwhore
crackwhoreed
crackwhoreer
crackwhorees
crackwhoreing
crackwhorely
crackwhores
crap
craped
craper
crapes
craping
craply
crappy
crappyed
crappyer
crappyes
crappying
crappyly
crappys
cum
cumed
cumer
cumes
cuming
cumly
cummin
cummined
cumminer
cummines
cumming
cumminged
cumminger
cumminges
cumminging
cummingly
cummings
cummining
cumminly
cummins
cums
cumshot
cumshoted
cumshoter
cumshotes
cumshoting
cumshotly
cumshots
cumshotsed
cumshotser
cumshotses
cumshotsing
cumshotsly
cumshotss
cumslut
cumsluted
cumsluter
cumslutes
cumsluting
cumslutly
cumsluts
cumstain
cumstained
cumstainer
cumstaines
cumstaining
cumstainly
cumstains
cunilingus
cunilingused
cunilinguser
cunilinguses
cunilingusing
cunilingusly
cunilinguss
cunnilingus
cunnilingused
cunnilinguser
cunnilinguses
cunnilingusing
cunnilingusly
cunnilinguss
cunny
cunnyed
cunnyer
cunnyes
cunnying
cunnyly
cunnys
cunt
cunted
cunter
cuntes
cuntface
cuntfaceed
cuntfaceer
cuntfacees
cuntfaceing
cuntfacely
cuntfaces
cunthunter
cunthuntered
cunthunterer
cunthunteres
cunthuntering
cunthunterly
cunthunters
cunting
cuntlick
cuntlicked
cuntlicker
cuntlickered
cuntlickerer
cuntlickeres
cuntlickering
cuntlickerly
cuntlickers
cuntlickes
cuntlicking
cuntlickly
cuntlicks
cuntly
cunts
cuntsed
cuntser
cuntses
cuntsing
cuntsly
cuntss
dago
dagoed
dagoer
dagoes
dagoing
dagoly
dagos
dagosed
dagoser
dagoses
dagosing
dagosly
dagoss
dammit
dammited
dammiter
dammites
dammiting
dammitly
dammits
damn
damned
damneded
damneder
damnedes
damneding
damnedly
damneds
damner
damnes
damning
damnit
damnited
damniter
damnites
damniting
damnitly
damnits
damnly
damns
dick
dickbag
dickbaged
dickbager
dickbages
dickbaging
dickbagly
dickbags
dickdipper
dickdippered
dickdipperer
dickdipperes
dickdippering
dickdipperly
dickdippers
dicked
dicker
dickes
dickface
dickfaceed
dickfaceer
dickfacees
dickfaceing
dickfacely
dickfaces
dickflipper
dickflippered
dickflipperer
dickflipperes
dickflippering
dickflipperly
dickflippers
dickhead
dickheaded
dickheader
dickheades
dickheading
dickheadly
dickheads
dickheadsed
dickheadser
dickheadses
dickheadsing
dickheadsly
dickheadss
dicking
dickish
dickished
dickisher
dickishes
dickishing
dickishly
dickishs
dickly
dickripper
dickrippered
dickripperer
dickripperes
dickrippering
dickripperly
dickrippers
dicks
dicksipper
dicksippered
dicksipperer
dicksipperes
dicksippering
dicksipperly
dicksippers
dickweed
dickweeded
dickweeder
dickweedes
dickweeding
dickweedly
dickweeds
dickwhipper
dickwhippered
dickwhipperer
dickwhipperes
dickwhippering
dickwhipperly
dickwhippers
dickzipper
dickzippered
dickzipperer
dickzipperes
dickzippering
dickzipperly
dickzippers
diddle
diddleed
diddleer
diddlees
diddleing
diddlely
diddles
dike
dikeed
dikeer
dikees
dikeing
dikely
dikes
dildo
dildoed
dildoer
dildoes
dildoing
dildoly
dildos
dildosed
dildoser
dildoses
dildosing
dildosly
dildoss
diligaf
diligafed
diligafer
diligafes
diligafing
diligafly
diligafs
dillweed
dillweeded
dillweeder
dillweedes
dillweeding
dillweedly
dillweeds
dimwit
dimwited
dimwiter
dimwites
dimwiting
dimwitly
dimwits
dingle
dingleed
dingleer
dinglees
dingleing
dinglely
dingles
dipship
dipshiped
dipshiper
dipshipes
dipshiping
dipshiply
dipships
dizzyed
dizzyer
dizzyes
dizzying
dizzyly
dizzys
doggiestyleed
doggiestyleer
doggiestylees
doggiestyleing
doggiestylely
doggiestyles
doggystyleed
doggystyleer
doggystylees
doggystyleing
doggystylely
doggystyles
dong
donged
donger
donges
donging
dongly
dongs
doofus
doofused
doofuser
doofuses
doofusing
doofusly
doofuss
doosh
dooshed
doosher
dooshes
dooshing
dooshly
dooshs
dopeyed
dopeyer
dopeyes
dopeying
dopeyly
dopeys
douchebag
douchebaged
douchebager
douchebages
douchebaging
douchebagly
douchebags
douchebagsed
douchebagser
douchebagses
douchebagsing
douchebagsly
douchebagss
doucheed
doucheer
douchees
doucheing
douchely
douches
douchey
doucheyed
doucheyer
doucheyes
doucheying
doucheyly
doucheys
drunk
drunked
drunker
drunkes
drunking
drunkly
drunks
dumass
dumassed
dumasser
dumasses
dumassing
dumassly
dumasss
dumbass
dumbassed
dumbasser
dumbasses
dumbassesed
dumbasseser
dumbasseses
dumbassesing
dumbassesly
dumbassess
dumbassing
dumbassly
dumbasss
dummy
dummyed
dummyer
dummyes
dummying
dummyly
dummys
dyke
dykeed
dykeer
dykees
dykeing
dykely
dykes
dykesed
dykeser
dykeses
dykesing
dykesly
dykess
erotic
eroticed
eroticer
erotices
eroticing
eroticly
erotics
extacy
extacyed
extacyer
extacyes
extacying
extacyly
extacys
extasy
extasyed
extasyer
extasyes
extasying
extasyly
extasys
fack
facked
facker
fackes
facking
fackly
facks
fag
faged
fager
fages
fagg
fagged
faggeded
faggeder
faggedes
faggeding
faggedly
faggeds
fagger
fagges
fagging
faggit
faggited
faggiter
faggites
faggiting
faggitly
faggits
faggly
faggot
faggoted
faggoter
faggotes
faggoting
faggotly
faggots
faggs
faging
fagly
fagot
fagoted
fagoter
fagotes
fagoting
fagotly
fagots
fags
fagsed
fagser
fagses
fagsing
fagsly
fagss
faig
faiged
faiger
faiges
faiging
faigly
faigs
faigt
faigted
faigter
faigtes
faigting
faigtly
faigts
fannybandit
fannybandited
fannybanditer
fannybandites
fannybanditing
fannybanditly
fannybandits
farted
farter
fartes
farting
fartknocker
fartknockered
fartknockerer
fartknockeres
fartknockering
fartknockerly
fartknockers
fartly
farts
felch
felched
felcher
felchered
felcherer
felcheres
felchering
felcherly
felchers
felches
felching
felchinged
felchinger
felchinges
felchinging
felchingly
felchings
felchly
felchs
fellate
fellateed
fellateer
fellatees
fellateing
fellately
fellates
fellatio
fellatioed
fellatioer
fellatioes
fellatioing
fellatioly
fellatios
feltch
feltched
feltcher
feltchered
feltcherer
feltcheres
feltchering
feltcherly
feltchers
feltches
feltching
feltchly
feltchs
feom
feomed
feomer
feomes
feoming
feomly
feoms
fisted
fisteded
fisteder
fistedes
fisteding
fistedly
fisteds
fisting
fistinged
fistinger
fistinges
fistinging
fistingly
fistings
fisty
fistyed
fistyer
fistyes
fistying
fistyly
fistys
floozy
floozyed
floozyer
floozyes
floozying
floozyly
floozys
foad
foaded
foader
foades
foading
foadly
foads
fondleed
fondleer
fondlees
fondleing
fondlely
fondles
foobar
foobared
foobarer
foobares
foobaring
foobarly
foobars
freex
freexed
freexer
freexes
freexing
freexly
freexs
frigg
frigga
friggaed
friggaer
friggaes
friggaing
friggaly
friggas
frigged
frigger
frigges
frigging
friggly
friggs
fubar
fubared
fubarer
fubares
fubaring
fubarly
fubars
fuck
fuckass
fuckassed
fuckasser
fuckasses
fuckassing
fuckassly
fuckasss
fucked
fuckeded
fuckeder
fuckedes
fuckeding
fuckedly
fuckeds
fucker
fuckered
fuckerer
fuckeres
fuckering
fuckerly
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Large, painful mass on neck
The FP diagnosed acne keloidalis nuchae (AKN) based on the large keloidal mass with multiple hairs growing from single follicles. When multiple hairs grow from single follicles, this is called tufted folliculitis and is seen in various types of scarring alopecia.
The FP told the patient that the exact cause of AKN is unclear, but that it can occur in patients with tightly curled hair shafts and those whose posterior hairline is shaved with a razor. (For more on AKN, see last week’s case here.) The FP advised the patient to avoid short haircuts.
As far as treatment was concerned, the FP discussed the 2 best options: intralesional steroids and/or surgery. The major risks of intralesional steroids are pain at the time of injection and hypopigmentation of the skin at the site of injection weeks to months after the injection. Also, there is no guarantee that the steroid injection will work. As for surgery, the FP advised that there would be a significant risk of intraoperative bleeding and postoperative scarring; also, a plastic surgeon would need to be called in.
The patient was not interested in the surgery, and opted for the intralesional steroid injection, instead. The FP explained the risks and benefits of the procedure, got the patient’s written consent, and injected triamcinolone acetonide 10 mg/mL into the mass using a 25-gauge needle. This was difficult to do because the mass was firm. During a follow-up visit a month later, the FP noted that the mass was smaller. At the patient’s request, a second injection was performed. This one involved a stronger concentration: 40 mg/mL triamcinolone.
Photos and text for Photo Rounds Friday courtesy of Richard P. Usatine, MD. This case was adapted from: Mayeaux, EJ. Pseudofolliculitis and acne keloidalis nuchae. In: Usatine R, Smith M, Mayeaux EJ, et al, eds. Color Atlas of Family Medicine. 2nd ed. New York, NY: McGraw-Hill; 2013:665-670.
To learn more about the Color Atlas of Family Medicine, see: www.amazon.com/Color-Family-Medicine-Richard-Usatine/dp/0071769641/
You can now get the second edition of the Color Atlas of Family Medicine as an app by clicking on this link: usatinemedia.com
The FP diagnosed acne keloidalis nuchae (AKN) based on the large keloidal mass with multiple hairs growing from single follicles. When multiple hairs grow from single follicles, this is called tufted folliculitis and is seen in various types of scarring alopecia.
The FP told the patient that the exact cause of AKN is unclear, but that it can occur in patients with tightly curled hair shafts and those whose posterior hairline is shaved with a razor. (For more on AKN, see last week’s case here.) The FP advised the patient to avoid short haircuts.
As far as treatment was concerned, the FP discussed the 2 best options: intralesional steroids and/or surgery. The major risks of intralesional steroids are pain at the time of injection and hypopigmentation of the skin at the site of injection weeks to months after the injection. Also, there is no guarantee that the steroid injection will work. As for surgery, the FP advised that there would be a significant risk of intraoperative bleeding and postoperative scarring; also, a plastic surgeon would need to be called in.
The patient was not interested in the surgery, and opted for the intralesional steroid injection, instead. The FP explained the risks and benefits of the procedure, got the patient’s written consent, and injected triamcinolone acetonide 10 mg/mL into the mass using a 25-gauge needle. This was difficult to do because the mass was firm. During a follow-up visit a month later, the FP noted that the mass was smaller. At the patient’s request, a second injection was performed. This one involved a stronger concentration: 40 mg/mL triamcinolone.
Photos and text for Photo Rounds Friday courtesy of Richard P. Usatine, MD. This case was adapted from: Mayeaux, EJ. Pseudofolliculitis and acne keloidalis nuchae. In: Usatine R, Smith M, Mayeaux EJ, et al, eds. Color Atlas of Family Medicine. 2nd ed. New York, NY: McGraw-Hill; 2013:665-670.
To learn more about the Color Atlas of Family Medicine, see: www.amazon.com/Color-Family-Medicine-Richard-Usatine/dp/0071769641/
You can now get the second edition of the Color Atlas of Family Medicine as an app by clicking on this link: usatinemedia.com
The FP diagnosed acne keloidalis nuchae (AKN) based on the large keloidal mass with multiple hairs growing from single follicles. When multiple hairs grow from single follicles, this is called tufted folliculitis and is seen in various types of scarring alopecia.
The FP told the patient that the exact cause of AKN is unclear, but that it can occur in patients with tightly curled hair shafts and those whose posterior hairline is shaved with a razor. (For more on AKN, see last week’s case here.) The FP advised the patient to avoid short haircuts.
As far as treatment was concerned, the FP discussed the 2 best options: intralesional steroids and/or surgery. The major risks of intralesional steroids are pain at the time of injection and hypopigmentation of the skin at the site of injection weeks to months after the injection. Also, there is no guarantee that the steroid injection will work. As for surgery, the FP advised that there would be a significant risk of intraoperative bleeding and postoperative scarring; also, a plastic surgeon would need to be called in.
The patient was not interested in the surgery, and opted for the intralesional steroid injection, instead. The FP explained the risks and benefits of the procedure, got the patient’s written consent, and injected triamcinolone acetonide 10 mg/mL into the mass using a 25-gauge needle. This was difficult to do because the mass was firm. During a follow-up visit a month later, the FP noted that the mass was smaller. At the patient’s request, a second injection was performed. This one involved a stronger concentration: 40 mg/mL triamcinolone.
Photos and text for Photo Rounds Friday courtesy of Richard P. Usatine, MD. This case was adapted from: Mayeaux, EJ. Pseudofolliculitis and acne keloidalis nuchae. In: Usatine R, Smith M, Mayeaux EJ, et al, eds. Color Atlas of Family Medicine. 2nd ed. New York, NY: McGraw-Hill; 2013:665-670.
To learn more about the Color Atlas of Family Medicine, see: www.amazon.com/Color-Family-Medicine-Richard-Usatine/dp/0071769641/
You can now get the second edition of the Color Atlas of Family Medicine as an app by clicking on this link: usatinemedia.com
Lesions on back of neck
The FP diagnosed acne keloidalis nuchae (AKN), a condition that occurs most often in black men, but can be seen in all ethnic groups. The lesions are often painful and cosmetically disfiguring. The exact cause of AKN is uncertain, but it often develops in areas of pseudofolliculitis or folliculitis. It may be associated with haircuts where the posterior hairline is shaved with a razor and in individuals with tightly curled hair shafts. Other possible etiologies include irritation from shirt collars and a chronic bacterial infection.
Tretinoin cream 0.025% may be useful in patients with a mild case of the disease, but it is rarely helpful in moderate to severe cases. It is first applied nightly for a week, and then reduced to every second or third night. Tretinoin may be used in conjunction with a mid-potency topical corticosteroid that is applied each morning.
In this case, the FP recommended that the patient avoid using a razor on the back of his neck and that he allow his hair to grow a bit longer there. This would minimize the irritation and also cover up some of the visible lesions. The FP also prescribed a 2-week course of doxycycline 100 mg bid and topical tretinoin 0.025% cream in the evening, with triamcinolone 0.1% cream in the morning to help with the itching and inflammation.
The patient returned a month later with fewer symptoms and lesions. The FP explained that there are no curative treatments and that he should stick with the current topical treatments for a bit longer.
Photos and text for Photo Rounds Friday courtesy of Richard P. Usatine, MD. This case was adapted from: Mayeaux, EJ. Pseudofolliculitis and acne keloidalis nuchae. In: Usatine R, Smith M, Mayeaux EJ, et al, eds. Color Atlas of Family Medicine. 2nd ed. New York, NY: McGraw-Hill; 2013:665-670.
To learn more about the Color Atlas of Family Medicine, see: www.amazon.com/Color-Family-Medicine-Richard-Usatine/dp/0071769641/
You can now get the second edition of the Color Atlas of Family Medicine as an app by clicking on this link: usatinemedia.com
The FP diagnosed acne keloidalis nuchae (AKN), a condition that occurs most often in black men, but can be seen in all ethnic groups. The lesions are often painful and cosmetically disfiguring. The exact cause of AKN is uncertain, but it often develops in areas of pseudofolliculitis or folliculitis. It may be associated with haircuts where the posterior hairline is shaved with a razor and in individuals with tightly curled hair shafts. Other possible etiologies include irritation from shirt collars and a chronic bacterial infection.
Tretinoin cream 0.025% may be useful in patients with a mild case of the disease, but it is rarely helpful in moderate to severe cases. It is first applied nightly for a week, and then reduced to every second or third night. Tretinoin may be used in conjunction with a mid-potency topical corticosteroid that is applied each morning.
In this case, the FP recommended that the patient avoid using a razor on the back of his neck and that he allow his hair to grow a bit longer there. This would minimize the irritation and also cover up some of the visible lesions. The FP also prescribed a 2-week course of doxycycline 100 mg bid and topical tretinoin 0.025% cream in the evening, with triamcinolone 0.1% cream in the morning to help with the itching and inflammation.
The patient returned a month later with fewer symptoms and lesions. The FP explained that there are no curative treatments and that he should stick with the current topical treatments for a bit longer.
Photos and text for Photo Rounds Friday courtesy of Richard P. Usatine, MD. This case was adapted from: Mayeaux, EJ. Pseudofolliculitis and acne keloidalis nuchae. In: Usatine R, Smith M, Mayeaux EJ, et al, eds. Color Atlas of Family Medicine. 2nd ed. New York, NY: McGraw-Hill; 2013:665-670.
To learn more about the Color Atlas of Family Medicine, see: www.amazon.com/Color-Family-Medicine-Richard-Usatine/dp/0071769641/
You can now get the second edition of the Color Atlas of Family Medicine as an app by clicking on this link: usatinemedia.com
The FP diagnosed acne keloidalis nuchae (AKN), a condition that occurs most often in black men, but can be seen in all ethnic groups. The lesions are often painful and cosmetically disfiguring. The exact cause of AKN is uncertain, but it often develops in areas of pseudofolliculitis or folliculitis. It may be associated with haircuts where the posterior hairline is shaved with a razor and in individuals with tightly curled hair shafts. Other possible etiologies include irritation from shirt collars and a chronic bacterial infection.
Tretinoin cream 0.025% may be useful in patients with a mild case of the disease, but it is rarely helpful in moderate to severe cases. It is first applied nightly for a week, and then reduced to every second or third night. Tretinoin may be used in conjunction with a mid-potency topical corticosteroid that is applied each morning.
In this case, the FP recommended that the patient avoid using a razor on the back of his neck and that he allow his hair to grow a bit longer there. This would minimize the irritation and also cover up some of the visible lesions. The FP also prescribed a 2-week course of doxycycline 100 mg bid and topical tretinoin 0.025% cream in the evening, with triamcinolone 0.1% cream in the morning to help with the itching and inflammation.
The patient returned a month later with fewer symptoms and lesions. The FP explained that there are no curative treatments and that he should stick with the current topical treatments for a bit longer.
Photos and text for Photo Rounds Friday courtesy of Richard P. Usatine, MD. This case was adapted from: Mayeaux, EJ. Pseudofolliculitis and acne keloidalis nuchae. In: Usatine R, Smith M, Mayeaux EJ, et al, eds. Color Atlas of Family Medicine. 2nd ed. New York, NY: McGraw-Hill; 2013:665-670.
To learn more about the Color Atlas of Family Medicine, see: www.amazon.com/Color-Family-Medicine-Richard-Usatine/dp/0071769641/
You can now get the second edition of the Color Atlas of Family Medicine as an app by clicking on this link: usatinemedia.com
“I feel dizzy, Doctor”
› Refer a patient who reports that his dizziness is accompanied by hearing loss to an otolaryngologist for evaluation. C
› Use the HINTS (Head Impulse, Nystagmus, and Test of Skew) procedure to differentiate central from peripheral vertigo. A
› Use the Dix-Hallpike procedure to diagnose benign paroxysmal positional vertigo. B
Strength of recommendation (SOR)
A Good-quality patient-oriented evidence
B Inconsistent or limited-quality patient-oriented evidence
C Consensus, usual practice, opinion, disease-oriented evidence, case series
With an estimated lifetime prevalence of 17% to 30%,1 dizziness is a relatively common clinical symptom, but the underlying cause can be difficult to diagnose. That’s because patients’ descriptions of dizziness are often imprecise, and this symptom is associated with a wide range of conditions. A careful history and physical examination are key to diagnosis, as is an understanding of the mechanisms of dizziness.
This article covers the range of diagnoses that should be considered when a patient presents with dizziness, and provides insight regarding features of the patient’s history that can better elucidate the specific etiology.
What do patients mean when they say, “I feel dizzy”?
“Dizziness” is a vague term, and patients who report dizziness should be asked to further describe the sensation. Patients may use the word dizziness in an attempt to describe many sensations, including faintness, giddiness, light-headedness, or unsteadiness.2 In 1972, Drachman and Hart proposed a classification system for dizziness that describes 4 categories—presyncope, vertigo, disequilibrium, and atypical (TABLE 1).3 These classifications are still commonly used today, and the discussion that follows describes potential causes of dizziness in each of these 4 categories. A stepwise approach for evaluating a patient who reports dizziness can be found in the ALGORITHM.3-6
Syncopal-related dizziness can have a cardiovascular cause
Presyncope is a feeling of impending loss of consciousness that’s sometimes accompanied by generalized muscle weakness and/or partial vision loss. Taking a careful history regarding the events surrounding the episode should distinguish this type of dizziness, and doing so is essential because most of the underlying pathogenesis involves the cardiovascular system and requires specific interventions.
Dysrhythmias can cause syncope and may or may not be accompanied by a feeling of palpitations. Diagnosis is made by electrocardiogram (EKG) followed by the use of a Holter monitor.
Vasovagal syncope is caused by a sudden slowing of the pulse that’s the result of stimulation of the vagal nerve. It can occur from direct stimulation of the nerve from palpation (or strangulation), or from an intense autonomic discharge, as when people are frightened or confronted with something upsetting (eg, the sight of blood.)
Orthostatic hypotension results from a change in body position in which either autonomic mechanisms cannot maintain venous tone, causing a sudden drop in blood pressure, or in which the heart cannot compensate by speeding up, as when a patient is taking a beta-adrenergic antagonist or has first-degree heart block. It can also result from hypovolemia.
Measuring the patient’s blood pressure in the recumbent, seated, and standing positions can verify the diagnosis if an episode occurred soon before the examination. This kind of dizziness can be treated by instructing the patient to rise slowly, or by making appropriate medication adjustments. If conservative measures fail, medications such as midodrine or droxidopa can be tried.7
Hypoglycemia, hypoxia, or hyperventilation can also precipitate syncopal symptoms. Taking a careful history to assess for the presence of seizure-related features such as tonic/clonic movements or loss of bowel and bladder control can be helpful in distinguishing this form of dizziness.
Vertigo can have a central or peripheral cause
Vertigo is dizziness that is characterized by the sensation of spinning. The presence of vertigo implies disease of the inner ear or central nervous system. The “wiring diagram” of the vestibulo-ocular reflex is fairly straightforward, but sorting out the symptoms that arise from lesions within the system can be a diagnostic challenge. Vertigo has classically been divided into causes that are central (originating in the central nervous system) or peripheral (originating in the peripheral nervous system).
The HINTS (Head Impulse, Nystagmus, and Test of Skew) protocol is a group of 3 tests that can be used to differentiate central from peripheral vertigo (TABLE 2).8,9 To perform the head impulse test, the examiner asks the patient to focus his gaze on a target and then rapidly turns the patient’s head to the side, watching the eyes for any corrective movements.10 When the eyes make a corrective saccade, the test is considered to be positive for a peripheral lesion.
Horizontal nystagmus is assessed by having the patient look in the direction of the fast phase of the nystagmus. If the nystagmus increases in intensity, then the test is considered positive for a peripheral lesion.
Vertigo can have many possible causes
Finally, the “test of skew” is performed by again having the patient fixate on the examiner’s nose. Each eye is tested by being covered, and then uncovered. If the uncovered eye has to move to refocus on the examiner’s nose, then the test is positive for a central lesion. A positive head impulse, positive horizontal nystagmus, and negative test of skew is 100% sensitive and 96% specific for a peripheral lesion.11
Benign paroxysmal positional vertigo (BPPV) is vertigo that is triggered by movement of the head. It occurs when otoconia that are normally embedded in gel in the utricle become dislodged and migrate into the 3 fluid-filled semicircular canals, where they interfere with the normal fluid movement these canals use to sense head motion, causing the inner ear to send false signals to the brain.12
Diagnosis is confirmed by performing the Dix-Hallpike maneuver to elicit nystagmus. The patient is moved from a seated to a supine position with her head turned 45 degrees to the right and held for 30 seconds. For a demonstration of the Dix-Hallpike maneuver, see https://youtu.be/8RYB2QlO1N4. The Dix-Hallpike maneuver is also the first step of a treatment for BBPV known as the Epley maneuver. (See “The Epley maneuver: A procedure for treating BPPV”.13,14)
Benign paroxysmal positional vertigo (BPPV) can be treated with the Epley maneuver. Like the Dix-Hallpike maneuver, the Epley maneuver isolates the posterior semicircular canal of the affected ear. However, it goes a step further to reposition otolithic debris away from the ampulla of the posterior canal, rolling it through the canal and depositing it in the utricle, where it will not stimulate nerve endings and produce symptoms.
For a demonstration of the Epley maneuver, see https://youtu.be/jBzID5nVQjk. A computer-controlled form of the Epley maneuver has been developed and can be as effective as the manual version of this procedure.13
In 38% of patients, BPPV spontaneously resolves. The Epley maneuver can improve this rate to 64% with a single treatment, and one additional maneuver improves the success rate to 83.3%.14 If this procedure doesn’t work the first time, there may be more sediment that didn’t have enough time to settle during the procedure. Therefore, the Epley maneuver can be repeated 3 times a day, and performed on subsequent days as needed.
Labyrinthitis—inflammation of the inner ear that can cause vertigo—is suggested by an acute, non-recurrent episode of dizziness that is often preceded by an upper respiratory infection. If the external canal is extremely painful and/or develops a vesicular rash, the patient might have herpes zoster of the geniculate ganglion (Ramsay Hunt syndrome type 2).
Vertigo can have many possible causes
Vestibular migraine and Meniere’s disease. When a patient who has a history of migraines experiences symptoms of vertigo, vestibular migraine should be suspected, and treatment should focus on migraine therapy rather than vestibular therapy.15
Symptoms of Meniere’s disease and vestibular migraine can overlap.16 The current definition of Meniere’s disease requires ≥2 definitive episodes of vertigo with hearing loss plus tinnitus and/or aural symptoms.17 Thirty percent of vertigo episodes in patients with Meniere's disease can be attributed to BPPV.18
Acoustic neuroma. In addition to vertigo, acoustic neuroma is often associated with gradual hearing loss, tinnitus, and facial numbness (from compression of cranial nerve V preoperatively) or facial weakness (from compression of cranial nerve VII postoperatively). Unilateral hearing loss should prompt evaluation with magnetic resonance imaging.
“Acoustic neuroma” is a misnomer. The lesion arises from the vestibular (not the acoustic) portion of the 8th cranial nerve, and isn’t a neuroma; it is a schwannoma.19 Although it actually arises peripherally within the vestibular canal, it typically expands centrally and compresses other nerves centrally, which can make the clinical diagnosis more challenging if one were using the classical schema of differentiating between peripheral and central causes of vertigo.
Age-related vestibular loss occurs when the aging process causes deterioration of most of the components of the vestibulo-ocular reflex, resulting in dizziness and vertigo. Usually, the cerebral override mechanisms can compensate for the degeneration.
Other causes of vertigo include cerebellar infarction (3% of patients with vertigo),20 sound-induced vertigo (Tullio phenomenon),21 obstructive sleep apnea,22 and systemic sclerosis.23 Diabetes can cause a reduction in vestibular sensitivity that is evidenced by an increased reliance on visual stimuli to resolve vestibulo-visual conflict.24
Disequilibrium
Disequilibrium is predominantly a loss of balance. Patients with disequilibrium have the feeling that they are about to fall, specifically without the sensation of spinning. They may appear to sway, and will reach out for something to support them. Disequilibrium can be a component of vertigo, or it may suggest a more specific diagnosis, such as ataxia, which is a lack of coordination when walking.
Atypical causes of dizziness
“Light-headedness” may have an element of euphoria or may be indistinguishable from the early part of a syncopal episode. Because other causes of light-headedness can be difficult to distinguish from presyncope, it is important to consider syncope in the differential diagnosis.
The differential of light-headedness can also include panic attack, early hyperventilation, and toxin exposure (such as diphenylarsinic acid,25 pregabalin,26 or paint thinner27).
CORRESPONDENCE
Shannon Paul Starr, MD, Louisiana State University Health Sciences Center, 200 W. Esplanade #412, Kenner, LA 70065; sstarr@lsuhsc.edu.
1. Murdin L, Schilder AG. Epidemiology of balance symptoms and disorders in the community: a systematic review. Otol Neurotol. 2015;36:387-392.
2. Stedman TL. Stedman’s medical dictionary, illustrated. 24th ed. Baltimore, Md: William & Wilkins; 1982:419.
3. Drachman DA, Hart CW. An approach to the dizzy patient. Neurology. 1972;22:323-334.
4. Angtuaco EJ, Wippold FJ II, Cornelius RS, et al; Expert Panel on Neurologic Imaging. ACR appropriateness criteria: hearing loss and/or vertigo. 2013. American College of Radiology Web site. Available at: http://www.acr.org/~/media/914834f9cfa74e6c803e8e9c6909cd7e.pdf. Accessed September 3, 2015.
5. Dros J, Maarsingh OR, van der Windt DA, et al. Profiling dizziness in older primary care patients: an empirical study. PLoS One. 2011;6:e16481.
6. Post RE, Dickerson LM. Dizziness: a diagnostic approach. Am Fam Physician. 2010;82:361-369.
7. Biaggioni I. New developments in the management of neurogenic orthostatic hypotension. Curr Cardiol Rep. 2014;16:542.
8. Batuecas-Caletrío Á, Yáñez-González R, Sánchez-Blanco C, et al. [Peripheral vertigo versus central vertigo. Application of the HINTS protocol]. Rev Neurol. 2014;59:349-353.
9. Kattah JC, Talkad AV, Wang DZ, et al. HINTS to diagnose stroke in the acute vestibular syndrome: three-step bedside oculomotor examination more sensitive than early MRI diffusion-weighted imaging. Stroke. 2009;40:3504-3510.
10. Barraclough K, Bronstein A. Vertigo. BMJ. 2009;339:b3493.
11. Newman-Toker DE, Kerber KA, Hsieh YH, et al. HINTS outperforms ABCD2 to screen for stroke in acute continuous vertigo and dizziness. Acad Emerg Med. 2013;20:986-996.
12. Vestibular Disorders Association. Benign Paroxysmal Positional Vertigo. Vestibular Disorders Association Web site. Available at: http://vestibular.org/understanding-vestibular-disorders/types-vestibular-disorders/benign-paroxysmal-positional-vertigo. Accessed September 1, 2015.
13. Shan X, Peng X, Wang E. Efficacy of computer-controlled repositioning procedure for benign paroxysmal positional vertigo. Laryngoscope. 2015;125:715-719.
14. Lee JD, Shim DB, Park HJ, et al. A multicenter randomized double-blind study: comparison of the Epley, Semont, and sham maneuvers for the treatment of posterior canal benign paroxysmal positional vertigo. Audiol Neurootol. 2014;19:336-341.
15. Stolte B, Holle D, Naegel S, et al. Vestibular migraine. Cephalalgia. 2015;35:262-270.
16. Lopez-Escamez JA, Dlugaiczyk J, Jacobs J, et al. Accompanying symptoms overlap during attacks in Menière’s disease and vestibular migraine. Front Neurol. 2014;5:265.
17. Beasley NJ, Jones NS. Menière’s disease: evolution of a definition. J Laryngol Otol. 1996;110:1107-1113.
18. Taura A, Funabiki K, Ohgita H, et al. One-third of vertiginous episodes during the follow-up period are caused by benign paroxysmal positional vertigo in patients with Meniere’s disease. Acta Otolaryngol. 2014;134:1140-1145.
19. Pineda A, Feder BH. Acoustic neuroma: a misnomer. Is Surg. 1967;33:40-43.
20. Seemungal BM. Neuro-otological emergencies. Curr Opin Neurol. 2007;20:32-39.
21. Harrison RV. On the biological plausibility of Wind Turbine Syndrome. Int J Environ Health Res. 2015;25:463-468.
22. Kayabasi S, Iriz A, Cayonu M, et al. Vestibular functions were found to be impaired in patients with moderate-tosevere obstructive sleep apnea. Laryngoscope. 2015;125:1244-1248.
23. Rabelo MB, Corona AP. Auditory and vestibular dysfunctions in systemic sclerosis: literature review. Codas. 2014;26:337-342.
24. Razzak RA, Bagust J, Docherty S, et al. Augmented asymmetrical visual field dependence in asymptomatic diabetics: evidence of subclinical asymmetrical bilateral vestibular dysfunction. J Diabetes Complications. 2015;29:68-72.
25. Ogata T, Nakamura Y, Endo G, et al. [Subjective symptoms and miscarriage after drinking well water exposed to diphenylarsinic acid]. Nihon Koshu Eisei Zasshi. 2014;61:556-564.
26. Qu C, Xie Y, Qin F, et al. Neuropsychiatric symptoms accompanying thrombocytopenia following pregabalin treatment for neuralgia: a case report. Int J Clin Pharm. 2014;36:1138-1140.
27. Rahimi HR, Agin K, Shadnia S, et al. Clinical and biochemical analysis of acute paint thinner intoxication in adults: a retrospective descriptive study. Toxicol Mech Methods. 2015;25:42-47.
› Refer a patient who reports that his dizziness is accompanied by hearing loss to an otolaryngologist for evaluation. C
› Use the HINTS (Head Impulse, Nystagmus, and Test of Skew) procedure to differentiate central from peripheral vertigo. A
› Use the Dix-Hallpike procedure to diagnose benign paroxysmal positional vertigo. B
Strength of recommendation (SOR)
A Good-quality patient-oriented evidence
B Inconsistent or limited-quality patient-oriented evidence
C Consensus, usual practice, opinion, disease-oriented evidence, case series
With an estimated lifetime prevalence of 17% to 30%,1 dizziness is a relatively common clinical symptom, but the underlying cause can be difficult to diagnose. That’s because patients’ descriptions of dizziness are often imprecise, and this symptom is associated with a wide range of conditions. A careful history and physical examination are key to diagnosis, as is an understanding of the mechanisms of dizziness.
This article covers the range of diagnoses that should be considered when a patient presents with dizziness, and provides insight regarding features of the patient’s history that can better elucidate the specific etiology.
What do patients mean when they say, “I feel dizzy”?
“Dizziness” is a vague term, and patients who report dizziness should be asked to further describe the sensation. Patients may use the word dizziness in an attempt to describe many sensations, including faintness, giddiness, light-headedness, or unsteadiness.2 In 1972, Drachman and Hart proposed a classification system for dizziness that describes 4 categories—presyncope, vertigo, disequilibrium, and atypical (TABLE 1).3 These classifications are still commonly used today, and the discussion that follows describes potential causes of dizziness in each of these 4 categories. A stepwise approach for evaluating a patient who reports dizziness can be found in the ALGORITHM.3-6
Syncopal-related dizziness can have a cardiovascular cause
Presyncope is a feeling of impending loss of consciousness that’s sometimes accompanied by generalized muscle weakness and/or partial vision loss. Taking a careful history regarding the events surrounding the episode should distinguish this type of dizziness, and doing so is essential because most of the underlying pathogenesis involves the cardiovascular system and requires specific interventions.
Dysrhythmias can cause syncope and may or may not be accompanied by a feeling of palpitations. Diagnosis is made by electrocardiogram (EKG) followed by the use of a Holter monitor.
Vasovagal syncope is caused by a sudden slowing of the pulse that’s the result of stimulation of the vagal nerve. It can occur from direct stimulation of the nerve from palpation (or strangulation), or from an intense autonomic discharge, as when people are frightened or confronted with something upsetting (eg, the sight of blood.)
Orthostatic hypotension results from a change in body position in which either autonomic mechanisms cannot maintain venous tone, causing a sudden drop in blood pressure, or in which the heart cannot compensate by speeding up, as when a patient is taking a beta-adrenergic antagonist or has first-degree heart block. It can also result from hypovolemia.
Measuring the patient’s blood pressure in the recumbent, seated, and standing positions can verify the diagnosis if an episode occurred soon before the examination. This kind of dizziness can be treated by instructing the patient to rise slowly, or by making appropriate medication adjustments. If conservative measures fail, medications such as midodrine or droxidopa can be tried.7
Hypoglycemia, hypoxia, or hyperventilation can also precipitate syncopal symptoms. Taking a careful history to assess for the presence of seizure-related features such as tonic/clonic movements or loss of bowel and bladder control can be helpful in distinguishing this form of dizziness.
Vertigo can have a central or peripheral cause
Vertigo is dizziness that is characterized by the sensation of spinning. The presence of vertigo implies disease of the inner ear or central nervous system. The “wiring diagram” of the vestibulo-ocular reflex is fairly straightforward, but sorting out the symptoms that arise from lesions within the system can be a diagnostic challenge. Vertigo has classically been divided into causes that are central (originating in the central nervous system) or peripheral (originating in the peripheral nervous system).
The HINTS (Head Impulse, Nystagmus, and Test of Skew) protocol is a group of 3 tests that can be used to differentiate central from peripheral vertigo (TABLE 2).8,9 To perform the head impulse test, the examiner asks the patient to focus his gaze on a target and then rapidly turns the patient’s head to the side, watching the eyes for any corrective movements.10 When the eyes make a corrective saccade, the test is considered to be positive for a peripheral lesion.
Horizontal nystagmus is assessed by having the patient look in the direction of the fast phase of the nystagmus. If the nystagmus increases in intensity, then the test is considered positive for a peripheral lesion.
Vertigo can have many possible causes
Finally, the “test of skew” is performed by again having the patient fixate on the examiner’s nose. Each eye is tested by being covered, and then uncovered. If the uncovered eye has to move to refocus on the examiner’s nose, then the test is positive for a central lesion. A positive head impulse, positive horizontal nystagmus, and negative test of skew is 100% sensitive and 96% specific for a peripheral lesion.11
Benign paroxysmal positional vertigo (BPPV) is vertigo that is triggered by movement of the head. It occurs when otoconia that are normally embedded in gel in the utricle become dislodged and migrate into the 3 fluid-filled semicircular canals, where they interfere with the normal fluid movement these canals use to sense head motion, causing the inner ear to send false signals to the brain.12
Diagnosis is confirmed by performing the Dix-Hallpike maneuver to elicit nystagmus. The patient is moved from a seated to a supine position with her head turned 45 degrees to the right and held for 30 seconds. For a demonstration of the Dix-Hallpike maneuver, see https://youtu.be/8RYB2QlO1N4. The Dix-Hallpike maneuver is also the first step of a treatment for BBPV known as the Epley maneuver. (See “The Epley maneuver: A procedure for treating BPPV”.13,14)
Benign paroxysmal positional vertigo (BPPV) can be treated with the Epley maneuver. Like the Dix-Hallpike maneuver, the Epley maneuver isolates the posterior semicircular canal of the affected ear. However, it goes a step further to reposition otolithic debris away from the ampulla of the posterior canal, rolling it through the canal and depositing it in the utricle, where it will not stimulate nerve endings and produce symptoms.
For a demonstration of the Epley maneuver, see https://youtu.be/jBzID5nVQjk. A computer-controlled form of the Epley maneuver has been developed and can be as effective as the manual version of this procedure.13
In 38% of patients, BPPV spontaneously resolves. The Epley maneuver can improve this rate to 64% with a single treatment, and one additional maneuver improves the success rate to 83.3%.14 If this procedure doesn’t work the first time, there may be more sediment that didn’t have enough time to settle during the procedure. Therefore, the Epley maneuver can be repeated 3 times a day, and performed on subsequent days as needed.
Labyrinthitis—inflammation of the inner ear that can cause vertigo—is suggested by an acute, non-recurrent episode of dizziness that is often preceded by an upper respiratory infection. If the external canal is extremely painful and/or develops a vesicular rash, the patient might have herpes zoster of the geniculate ganglion (Ramsay Hunt syndrome type 2).
Vertigo can have many possible causes
Vestibular migraine and Meniere’s disease. When a patient who has a history of migraines experiences symptoms of vertigo, vestibular migraine should be suspected, and treatment should focus on migraine therapy rather than vestibular therapy.15
Symptoms of Meniere’s disease and vestibular migraine can overlap.16 The current definition of Meniere’s disease requires ≥2 definitive episodes of vertigo with hearing loss plus tinnitus and/or aural symptoms.17 Thirty percent of vertigo episodes in patients with Meniere's disease can be attributed to BPPV.18
Acoustic neuroma. In addition to vertigo, acoustic neuroma is often associated with gradual hearing loss, tinnitus, and facial numbness (from compression of cranial nerve V preoperatively) or facial weakness (from compression of cranial nerve VII postoperatively). Unilateral hearing loss should prompt evaluation with magnetic resonance imaging.
“Acoustic neuroma” is a misnomer. The lesion arises from the vestibular (not the acoustic) portion of the 8th cranial nerve, and isn’t a neuroma; it is a schwannoma.19 Although it actually arises peripherally within the vestibular canal, it typically expands centrally and compresses other nerves centrally, which can make the clinical diagnosis more challenging if one were using the classical schema of differentiating between peripheral and central causes of vertigo.
Age-related vestibular loss occurs when the aging process causes deterioration of most of the components of the vestibulo-ocular reflex, resulting in dizziness and vertigo. Usually, the cerebral override mechanisms can compensate for the degeneration.
Other causes of vertigo include cerebellar infarction (3% of patients with vertigo),20 sound-induced vertigo (Tullio phenomenon),21 obstructive sleep apnea,22 and systemic sclerosis.23 Diabetes can cause a reduction in vestibular sensitivity that is evidenced by an increased reliance on visual stimuli to resolve vestibulo-visual conflict.24
Disequilibrium
Disequilibrium is predominantly a loss of balance. Patients with disequilibrium have the feeling that they are about to fall, specifically without the sensation of spinning. They may appear to sway, and will reach out for something to support them. Disequilibrium can be a component of vertigo, or it may suggest a more specific diagnosis, such as ataxia, which is a lack of coordination when walking.
Atypical causes of dizziness
“Light-headedness” may have an element of euphoria or may be indistinguishable from the early part of a syncopal episode. Because other causes of light-headedness can be difficult to distinguish from presyncope, it is important to consider syncope in the differential diagnosis.
The differential of light-headedness can also include panic attack, early hyperventilation, and toxin exposure (such as diphenylarsinic acid,25 pregabalin,26 or paint thinner27).
CORRESPONDENCE
Shannon Paul Starr, MD, Louisiana State University Health Sciences Center, 200 W. Esplanade #412, Kenner, LA 70065; sstarr@lsuhsc.edu.
› Refer a patient who reports that his dizziness is accompanied by hearing loss to an otolaryngologist for evaluation. C
› Use the HINTS (Head Impulse, Nystagmus, and Test of Skew) procedure to differentiate central from peripheral vertigo. A
› Use the Dix-Hallpike procedure to diagnose benign paroxysmal positional vertigo. B
Strength of recommendation (SOR)
A Good-quality patient-oriented evidence
B Inconsistent or limited-quality patient-oriented evidence
C Consensus, usual practice, opinion, disease-oriented evidence, case series
With an estimated lifetime prevalence of 17% to 30%,1 dizziness is a relatively common clinical symptom, but the underlying cause can be difficult to diagnose. That’s because patients’ descriptions of dizziness are often imprecise, and this symptom is associated with a wide range of conditions. A careful history and physical examination are key to diagnosis, as is an understanding of the mechanisms of dizziness.
This article covers the range of diagnoses that should be considered when a patient presents with dizziness, and provides insight regarding features of the patient’s history that can better elucidate the specific etiology.
What do patients mean when they say, “I feel dizzy”?
“Dizziness” is a vague term, and patients who report dizziness should be asked to further describe the sensation. Patients may use the word dizziness in an attempt to describe many sensations, including faintness, giddiness, light-headedness, or unsteadiness.2 In 1972, Drachman and Hart proposed a classification system for dizziness that describes 4 categories—presyncope, vertigo, disequilibrium, and atypical (TABLE 1).3 These classifications are still commonly used today, and the discussion that follows describes potential causes of dizziness in each of these 4 categories. A stepwise approach for evaluating a patient who reports dizziness can be found in the ALGORITHM.3-6
Syncopal-related dizziness can have a cardiovascular cause
Presyncope is a feeling of impending loss of consciousness that’s sometimes accompanied by generalized muscle weakness and/or partial vision loss. Taking a careful history regarding the events surrounding the episode should distinguish this type of dizziness, and doing so is essential because most of the underlying pathogenesis involves the cardiovascular system and requires specific interventions.
Dysrhythmias can cause syncope and may or may not be accompanied by a feeling of palpitations. Diagnosis is made by electrocardiogram (EKG) followed by the use of a Holter monitor.
Vasovagal syncope is caused by a sudden slowing of the pulse that’s the result of stimulation of the vagal nerve. It can occur from direct stimulation of the nerve from palpation (or strangulation), or from an intense autonomic discharge, as when people are frightened or confronted with something upsetting (eg, the sight of blood.)
Orthostatic hypotension results from a change in body position in which either autonomic mechanisms cannot maintain venous tone, causing a sudden drop in blood pressure, or in which the heart cannot compensate by speeding up, as when a patient is taking a beta-adrenergic antagonist or has first-degree heart block. It can also result from hypovolemia.
Measuring the patient’s blood pressure in the recumbent, seated, and standing positions can verify the diagnosis if an episode occurred soon before the examination. This kind of dizziness can be treated by instructing the patient to rise slowly, or by making appropriate medication adjustments. If conservative measures fail, medications such as midodrine or droxidopa can be tried.7
Hypoglycemia, hypoxia, or hyperventilation can also precipitate syncopal symptoms. Taking a careful history to assess for the presence of seizure-related features such as tonic/clonic movements or loss of bowel and bladder control can be helpful in distinguishing this form of dizziness.
Vertigo can have a central or peripheral cause
Vertigo is dizziness that is characterized by the sensation of spinning. The presence of vertigo implies disease of the inner ear or central nervous system. The “wiring diagram” of the vestibulo-ocular reflex is fairly straightforward, but sorting out the symptoms that arise from lesions within the system can be a diagnostic challenge. Vertigo has classically been divided into causes that are central (originating in the central nervous system) or peripheral (originating in the peripheral nervous system).
The HINTS (Head Impulse, Nystagmus, and Test of Skew) protocol is a group of 3 tests that can be used to differentiate central from peripheral vertigo (TABLE 2).8,9 To perform the head impulse test, the examiner asks the patient to focus his gaze on a target and then rapidly turns the patient’s head to the side, watching the eyes for any corrective movements.10 When the eyes make a corrective saccade, the test is considered to be positive for a peripheral lesion.
Horizontal nystagmus is assessed by having the patient look in the direction of the fast phase of the nystagmus. If the nystagmus increases in intensity, then the test is considered positive for a peripheral lesion.
Vertigo can have many possible causes
Finally, the “test of skew” is performed by again having the patient fixate on the examiner’s nose. Each eye is tested by being covered, and then uncovered. If the uncovered eye has to move to refocus on the examiner’s nose, then the test is positive for a central lesion. A positive head impulse, positive horizontal nystagmus, and negative test of skew is 100% sensitive and 96% specific for a peripheral lesion.11
Benign paroxysmal positional vertigo (BPPV) is vertigo that is triggered by movement of the head. It occurs when otoconia that are normally embedded in gel in the utricle become dislodged and migrate into the 3 fluid-filled semicircular canals, where they interfere with the normal fluid movement these canals use to sense head motion, causing the inner ear to send false signals to the brain.12
Diagnosis is confirmed by performing the Dix-Hallpike maneuver to elicit nystagmus. The patient is moved from a seated to a supine position with her head turned 45 degrees to the right and held for 30 seconds. For a demonstration of the Dix-Hallpike maneuver, see https://youtu.be/8RYB2QlO1N4. The Dix-Hallpike maneuver is also the first step of a treatment for BBPV known as the Epley maneuver. (See “The Epley maneuver: A procedure for treating BPPV”.13,14)
Benign paroxysmal positional vertigo (BPPV) can be treated with the Epley maneuver. Like the Dix-Hallpike maneuver, the Epley maneuver isolates the posterior semicircular canal of the affected ear. However, it goes a step further to reposition otolithic debris away from the ampulla of the posterior canal, rolling it through the canal and depositing it in the utricle, where it will not stimulate nerve endings and produce symptoms.
For a demonstration of the Epley maneuver, see https://youtu.be/jBzID5nVQjk. A computer-controlled form of the Epley maneuver has been developed and can be as effective as the manual version of this procedure.13
In 38% of patients, BPPV spontaneously resolves. The Epley maneuver can improve this rate to 64% with a single treatment, and one additional maneuver improves the success rate to 83.3%.14 If this procedure doesn’t work the first time, there may be more sediment that didn’t have enough time to settle during the procedure. Therefore, the Epley maneuver can be repeated 3 times a day, and performed on subsequent days as needed.
Labyrinthitis—inflammation of the inner ear that can cause vertigo—is suggested by an acute, non-recurrent episode of dizziness that is often preceded by an upper respiratory infection. If the external canal is extremely painful and/or develops a vesicular rash, the patient might have herpes zoster of the geniculate ganglion (Ramsay Hunt syndrome type 2).
Vertigo can have many possible causes
Vestibular migraine and Meniere’s disease. When a patient who has a history of migraines experiences symptoms of vertigo, vestibular migraine should be suspected, and treatment should focus on migraine therapy rather than vestibular therapy.15
Symptoms of Meniere’s disease and vestibular migraine can overlap.16 The current definition of Meniere’s disease requires ≥2 definitive episodes of vertigo with hearing loss plus tinnitus and/or aural symptoms.17 Thirty percent of vertigo episodes in patients with Meniere's disease can be attributed to BPPV.18
Acoustic neuroma. In addition to vertigo, acoustic neuroma is often associated with gradual hearing loss, tinnitus, and facial numbness (from compression of cranial nerve V preoperatively) or facial weakness (from compression of cranial nerve VII postoperatively). Unilateral hearing loss should prompt evaluation with magnetic resonance imaging.
“Acoustic neuroma” is a misnomer. The lesion arises from the vestibular (not the acoustic) portion of the 8th cranial nerve, and isn’t a neuroma; it is a schwannoma.19 Although it actually arises peripherally within the vestibular canal, it typically expands centrally and compresses other nerves centrally, which can make the clinical diagnosis more challenging if one were using the classical schema of differentiating between peripheral and central causes of vertigo.
Age-related vestibular loss occurs when the aging process causes deterioration of most of the components of the vestibulo-ocular reflex, resulting in dizziness and vertigo. Usually, the cerebral override mechanisms can compensate for the degeneration.
Other causes of vertigo include cerebellar infarction (3% of patients with vertigo),20 sound-induced vertigo (Tullio phenomenon),21 obstructive sleep apnea,22 and systemic sclerosis.23 Diabetes can cause a reduction in vestibular sensitivity that is evidenced by an increased reliance on visual stimuli to resolve vestibulo-visual conflict.24
Disequilibrium
Disequilibrium is predominantly a loss of balance. Patients with disequilibrium have the feeling that they are about to fall, specifically without the sensation of spinning. They may appear to sway, and will reach out for something to support them. Disequilibrium can be a component of vertigo, or it may suggest a more specific diagnosis, such as ataxia, which is a lack of coordination when walking.
Atypical causes of dizziness
“Light-headedness” may have an element of euphoria or may be indistinguishable from the early part of a syncopal episode. Because other causes of light-headedness can be difficult to distinguish from presyncope, it is important to consider syncope in the differential diagnosis.
The differential of light-headedness can also include panic attack, early hyperventilation, and toxin exposure (such as diphenylarsinic acid,25 pregabalin,26 or paint thinner27).
CORRESPONDENCE
Shannon Paul Starr, MD, Louisiana State University Health Sciences Center, 200 W. Esplanade #412, Kenner, LA 70065; sstarr@lsuhsc.edu.
1. Murdin L, Schilder AG. Epidemiology of balance symptoms and disorders in the community: a systematic review. Otol Neurotol. 2015;36:387-392.
2. Stedman TL. Stedman’s medical dictionary, illustrated. 24th ed. Baltimore, Md: William & Wilkins; 1982:419.
3. Drachman DA, Hart CW. An approach to the dizzy patient. Neurology. 1972;22:323-334.
4. Angtuaco EJ, Wippold FJ II, Cornelius RS, et al; Expert Panel on Neurologic Imaging. ACR appropriateness criteria: hearing loss and/or vertigo. 2013. American College of Radiology Web site. Available at: http://www.acr.org/~/media/914834f9cfa74e6c803e8e9c6909cd7e.pdf. Accessed September 3, 2015.
5. Dros J, Maarsingh OR, van der Windt DA, et al. Profiling dizziness in older primary care patients: an empirical study. PLoS One. 2011;6:e16481.
6. Post RE, Dickerson LM. Dizziness: a diagnostic approach. Am Fam Physician. 2010;82:361-369.
7. Biaggioni I. New developments in the management of neurogenic orthostatic hypotension. Curr Cardiol Rep. 2014;16:542.
8. Batuecas-Caletrío Á, Yáñez-González R, Sánchez-Blanco C, et al. [Peripheral vertigo versus central vertigo. Application of the HINTS protocol]. Rev Neurol. 2014;59:349-353.
9. Kattah JC, Talkad AV, Wang DZ, et al. HINTS to diagnose stroke in the acute vestibular syndrome: three-step bedside oculomotor examination more sensitive than early MRI diffusion-weighted imaging. Stroke. 2009;40:3504-3510.
10. Barraclough K, Bronstein A. Vertigo. BMJ. 2009;339:b3493.
11. Newman-Toker DE, Kerber KA, Hsieh YH, et al. HINTS outperforms ABCD2 to screen for stroke in acute continuous vertigo and dizziness. Acad Emerg Med. 2013;20:986-996.
12. Vestibular Disorders Association. Benign Paroxysmal Positional Vertigo. Vestibular Disorders Association Web site. Available at: http://vestibular.org/understanding-vestibular-disorders/types-vestibular-disorders/benign-paroxysmal-positional-vertigo. Accessed September 1, 2015.
13. Shan X, Peng X, Wang E. Efficacy of computer-controlled repositioning procedure for benign paroxysmal positional vertigo. Laryngoscope. 2015;125:715-719.
14. Lee JD, Shim DB, Park HJ, et al. A multicenter randomized double-blind study: comparison of the Epley, Semont, and sham maneuvers for the treatment of posterior canal benign paroxysmal positional vertigo. Audiol Neurootol. 2014;19:336-341.
15. Stolte B, Holle D, Naegel S, et al. Vestibular migraine. Cephalalgia. 2015;35:262-270.
16. Lopez-Escamez JA, Dlugaiczyk J, Jacobs J, et al. Accompanying symptoms overlap during attacks in Menière’s disease and vestibular migraine. Front Neurol. 2014;5:265.
17. Beasley NJ, Jones NS. Menière’s disease: evolution of a definition. J Laryngol Otol. 1996;110:1107-1113.
18. Taura A, Funabiki K, Ohgita H, et al. One-third of vertiginous episodes during the follow-up period are caused by benign paroxysmal positional vertigo in patients with Meniere’s disease. Acta Otolaryngol. 2014;134:1140-1145.
19. Pineda A, Feder BH. Acoustic neuroma: a misnomer. Is Surg. 1967;33:40-43.
20. Seemungal BM. Neuro-otological emergencies. Curr Opin Neurol. 2007;20:32-39.
21. Harrison RV. On the biological plausibility of Wind Turbine Syndrome. Int J Environ Health Res. 2015;25:463-468.
22. Kayabasi S, Iriz A, Cayonu M, et al. Vestibular functions were found to be impaired in patients with moderate-tosevere obstructive sleep apnea. Laryngoscope. 2015;125:1244-1248.
23. Rabelo MB, Corona AP. Auditory and vestibular dysfunctions in systemic sclerosis: literature review. Codas. 2014;26:337-342.
24. Razzak RA, Bagust J, Docherty S, et al. Augmented asymmetrical visual field dependence in asymptomatic diabetics: evidence of subclinical asymmetrical bilateral vestibular dysfunction. J Diabetes Complications. 2015;29:68-72.
25. Ogata T, Nakamura Y, Endo G, et al. [Subjective symptoms and miscarriage after drinking well water exposed to diphenylarsinic acid]. Nihon Koshu Eisei Zasshi. 2014;61:556-564.
26. Qu C, Xie Y, Qin F, et al. Neuropsychiatric symptoms accompanying thrombocytopenia following pregabalin treatment for neuralgia: a case report. Int J Clin Pharm. 2014;36:1138-1140.
27. Rahimi HR, Agin K, Shadnia S, et al. Clinical and biochemical analysis of acute paint thinner intoxication in adults: a retrospective descriptive study. Toxicol Mech Methods. 2015;25:42-47.
1. Murdin L, Schilder AG. Epidemiology of balance symptoms and disorders in the community: a systematic review. Otol Neurotol. 2015;36:387-392.
2. Stedman TL. Stedman’s medical dictionary, illustrated. 24th ed. Baltimore, Md: William & Wilkins; 1982:419.
3. Drachman DA, Hart CW. An approach to the dizzy patient. Neurology. 1972;22:323-334.
4. Angtuaco EJ, Wippold FJ II, Cornelius RS, et al; Expert Panel on Neurologic Imaging. ACR appropriateness criteria: hearing loss and/or vertigo. 2013. American College of Radiology Web site. Available at: http://www.acr.org/~/media/914834f9cfa74e6c803e8e9c6909cd7e.pdf. Accessed September 3, 2015.
5. Dros J, Maarsingh OR, van der Windt DA, et al. Profiling dizziness in older primary care patients: an empirical study. PLoS One. 2011;6:e16481.
6. Post RE, Dickerson LM. Dizziness: a diagnostic approach. Am Fam Physician. 2010;82:361-369.
7. Biaggioni I. New developments in the management of neurogenic orthostatic hypotension. Curr Cardiol Rep. 2014;16:542.
8. Batuecas-Caletrío Á, Yáñez-González R, Sánchez-Blanco C, et al. [Peripheral vertigo versus central vertigo. Application of the HINTS protocol]. Rev Neurol. 2014;59:349-353.
9. Kattah JC, Talkad AV, Wang DZ, et al. HINTS to diagnose stroke in the acute vestibular syndrome: three-step bedside oculomotor examination more sensitive than early MRI diffusion-weighted imaging. Stroke. 2009;40:3504-3510.
10. Barraclough K, Bronstein A. Vertigo. BMJ. 2009;339:b3493.
11. Newman-Toker DE, Kerber KA, Hsieh YH, et al. HINTS outperforms ABCD2 to screen for stroke in acute continuous vertigo and dizziness. Acad Emerg Med. 2013;20:986-996.
12. Vestibular Disorders Association. Benign Paroxysmal Positional Vertigo. Vestibular Disorders Association Web site. Available at: http://vestibular.org/understanding-vestibular-disorders/types-vestibular-disorders/benign-paroxysmal-positional-vertigo. Accessed September 1, 2015.
13. Shan X, Peng X, Wang E. Efficacy of computer-controlled repositioning procedure for benign paroxysmal positional vertigo. Laryngoscope. 2015;125:715-719.
14. Lee JD, Shim DB, Park HJ, et al. A multicenter randomized double-blind study: comparison of the Epley, Semont, and sham maneuvers for the treatment of posterior canal benign paroxysmal positional vertigo. Audiol Neurootol. 2014;19:336-341.
15. Stolte B, Holle D, Naegel S, et al. Vestibular migraine. Cephalalgia. 2015;35:262-270.
16. Lopez-Escamez JA, Dlugaiczyk J, Jacobs J, et al. Accompanying symptoms overlap during attacks in Menière’s disease and vestibular migraine. Front Neurol. 2014;5:265.
17. Beasley NJ, Jones NS. Menière’s disease: evolution of a definition. J Laryngol Otol. 1996;110:1107-1113.
18. Taura A, Funabiki K, Ohgita H, et al. One-third of vertiginous episodes during the follow-up period are caused by benign paroxysmal positional vertigo in patients with Meniere’s disease. Acta Otolaryngol. 2014;134:1140-1145.
19. Pineda A, Feder BH. Acoustic neuroma: a misnomer. Is Surg. 1967;33:40-43.
20. Seemungal BM. Neuro-otological emergencies. Curr Opin Neurol. 2007;20:32-39.
21. Harrison RV. On the biological plausibility of Wind Turbine Syndrome. Int J Environ Health Res. 2015;25:463-468.
22. Kayabasi S, Iriz A, Cayonu M, et al. Vestibular functions were found to be impaired in patients with moderate-tosevere obstructive sleep apnea. Laryngoscope. 2015;125:1244-1248.
23. Rabelo MB, Corona AP. Auditory and vestibular dysfunctions in systemic sclerosis: literature review. Codas. 2014;26:337-342.
24. Razzak RA, Bagust J, Docherty S, et al. Augmented asymmetrical visual field dependence in asymptomatic diabetics: evidence of subclinical asymmetrical bilateral vestibular dysfunction. J Diabetes Complications. 2015;29:68-72.
25. Ogata T, Nakamura Y, Endo G, et al. [Subjective symptoms and miscarriage after drinking well water exposed to diphenylarsinic acid]. Nihon Koshu Eisei Zasshi. 2014;61:556-564.
26. Qu C, Xie Y, Qin F, et al. Neuropsychiatric symptoms accompanying thrombocytopenia following pregabalin treatment for neuralgia: a case report. Int J Clin Pharm. 2014;36:1138-1140.
27. Rahimi HR, Agin K, Shadnia S, et al. Clinical and biochemical analysis of acute paint thinner intoxication in adults: a retrospective descriptive study. Toxicol Mech Methods. 2015;25:42-47.
4 ways to mitigate vaccine pain (and one practice to avoid)
Which is better for IBS pain in women—antispasmodics or antidepressants?
It’s unclear which therapy is more effective because the evidence is insufficient. What is known is that tricyclic antidepressants, peppermint oil, and antispasmodics all have been shown superior to placebo for treating abdominal pain in female patients with irritable bowel syndrome (IBS) (strength of recommendation: A, meta-analyses).
Antispasmodics and tricyclics alleviate abdominal pain
A 2011 Cochrane review of 56 randomized controlled trials (RCTs) with 3725 patients compared bulking agents, antispasmodics, or antidepressants with placebo for treating IBS.1 The pooled results from 13 RCTs with 1392 patients (65% female, mean age 45 years) showed that more patients had improved abdominal pain with antispasmodics than placebo over treatment periods varying from 6 days to 6 months (58% vs 46%; relative risk [RR]=1.3; 95% confidence interval [CI], 1.1-1.6; number needed to treat [NNT]=7).
The clinical relevance of the antispasmodic data is limited because the antispasmodics found effective for abdominal pain aren’t available in the United States. The pooled results from 8 RCTs with 517 patients (72% female, mean age 40) demonstrated greater improvement of abdominal pain with tricyclic and selective serotonin reuptake inhibitor antidepressants than placebo over 6 to 12 weeks (54% vs 37%; RR=1.5; 95% CI, 1.1–2.1; NNT=5). However, subgroup analysis found a statistically significant benefit for tricyclic antidepressants (4 trials; N=320; RR=1.3; 95% CI, 1.0-1.6) but no benefit for SSRIs (4 trials; N=197; RR=2.3; 95% CI, 0.79-6.7).
Effective antispasmodics aren’t available in the United States
A 2012 meta-analysis of 23 RCTs with 2585 patients examined the effect of antispasmodic agents, alone or in combination, to treat IBS.2 Pooled results from 13 RCTs with 2394 patients (69% female, ages 16 years or older) favored treatment with antispasmodics over placebo for abdominal pain (odds ratio [OR]=1.5; 95% CI, 1.3-1.8). No difference in adverse events was found between antispasmodics and placebo (9 trials; N=2239; OR=0.74; 95% CI, 0.54-0.98). The antispasmodics found effective for abdominal pain in this meta-analysis aren’t available in the United States.
Peppermint oil helps, but can cause heartburn
A 2013 meta-analysis of 9 RCTs with 726 patients compared various doses of enteric-coated peppermint oil with placebo over a minimum of 2 weeks’ treatment.3 Five RCTs with 357 patients (62% female, 13.4% children) demonstrated improvement of abdominal pain in 57% of patients taking peppermint oil compared with 27% receiving placebo (RR=2.1; 95% CI, 1.6-2.8; NNT=4 at 2 to 8 weeks). No statistically significant heterogeneity was identified among the treatment groups.
Pooled analysis found that peppermint oil patients were more likely than placebo patients to experience an adverse event (7 trials; N=474; 22% vs 13%; RR=1.7; 95% CI, 1.3-2.4), but that the events were generally mild and transient. The most frequently reported adverse event was heartburn.
1. Ruepert L, Quartero AO, de Wit NJ, et al. Bulking agents, antispasmodics, and antidepressants for the treatment of irritable bowel syndrome. Cochrane Database Syst Rev. 2011;(8):CD003460.
2. Martinez-Vasquez MA, Vasquez-Elizondro G, Gonzalez-Gonzalez JA, et al. Effect of antispasmodic agents, alone or in combination, in the treatment of irritable bowel syndrome: systematic review and meta-analysis. Rev Gastroenterol Mexico. 2012;77:82-90.
3. Khanna R, MacDonald JK, Levesque BG. Peppermint oil for the treatment of irritable bowel syndrome: a systematic review and meta-analysis. J Clin Gastroenterol. 2014;48:505-512.
It’s unclear which therapy is more effective because the evidence is insufficient. What is known is that tricyclic antidepressants, peppermint oil, and antispasmodics all have been shown superior to placebo for treating abdominal pain in female patients with irritable bowel syndrome (IBS) (strength of recommendation: A, meta-analyses).
Antispasmodics and tricyclics alleviate abdominal pain
A 2011 Cochrane review of 56 randomized controlled trials (RCTs) with 3725 patients compared bulking agents, antispasmodics, or antidepressants with placebo for treating IBS.1 The pooled results from 13 RCTs with 1392 patients (65% female, mean age 45 years) showed that more patients had improved abdominal pain with antispasmodics than placebo over treatment periods varying from 6 days to 6 months (58% vs 46%; relative risk [RR]=1.3; 95% confidence interval [CI], 1.1-1.6; number needed to treat [NNT]=7).
The clinical relevance of the antispasmodic data is limited because the antispasmodics found effective for abdominal pain aren’t available in the United States. The pooled results from 8 RCTs with 517 patients (72% female, mean age 40) demonstrated greater improvement of abdominal pain with tricyclic and selective serotonin reuptake inhibitor antidepressants than placebo over 6 to 12 weeks (54% vs 37%; RR=1.5; 95% CI, 1.1–2.1; NNT=5). However, subgroup analysis found a statistically significant benefit for tricyclic antidepressants (4 trials; N=320; RR=1.3; 95% CI, 1.0-1.6) but no benefit for SSRIs (4 trials; N=197; RR=2.3; 95% CI, 0.79-6.7).
Effective antispasmodics aren’t available in the United States
A 2012 meta-analysis of 23 RCTs with 2585 patients examined the effect of antispasmodic agents, alone or in combination, to treat IBS.2 Pooled results from 13 RCTs with 2394 patients (69% female, ages 16 years or older) favored treatment with antispasmodics over placebo for abdominal pain (odds ratio [OR]=1.5; 95% CI, 1.3-1.8). No difference in adverse events was found between antispasmodics and placebo (9 trials; N=2239; OR=0.74; 95% CI, 0.54-0.98). The antispasmodics found effective for abdominal pain in this meta-analysis aren’t available in the United States.
Peppermint oil helps, but can cause heartburn
A 2013 meta-analysis of 9 RCTs with 726 patients compared various doses of enteric-coated peppermint oil with placebo over a minimum of 2 weeks’ treatment.3 Five RCTs with 357 patients (62% female, 13.4% children) demonstrated improvement of abdominal pain in 57% of patients taking peppermint oil compared with 27% receiving placebo (RR=2.1; 95% CI, 1.6-2.8; NNT=4 at 2 to 8 weeks). No statistically significant heterogeneity was identified among the treatment groups.
Pooled analysis found that peppermint oil patients were more likely than placebo patients to experience an adverse event (7 trials; N=474; 22% vs 13%; RR=1.7; 95% CI, 1.3-2.4), but that the events were generally mild and transient. The most frequently reported adverse event was heartburn.
It’s unclear which therapy is more effective because the evidence is insufficient. What is known is that tricyclic antidepressants, peppermint oil, and antispasmodics all have been shown superior to placebo for treating abdominal pain in female patients with irritable bowel syndrome (IBS) (strength of recommendation: A, meta-analyses).
Antispasmodics and tricyclics alleviate abdominal pain
A 2011 Cochrane review of 56 randomized controlled trials (RCTs) with 3725 patients compared bulking agents, antispasmodics, or antidepressants with placebo for treating IBS.1 The pooled results from 13 RCTs with 1392 patients (65% female, mean age 45 years) showed that more patients had improved abdominal pain with antispasmodics than placebo over treatment periods varying from 6 days to 6 months (58% vs 46%; relative risk [RR]=1.3; 95% confidence interval [CI], 1.1-1.6; number needed to treat [NNT]=7).
The clinical relevance of the antispasmodic data is limited because the antispasmodics found effective for abdominal pain aren’t available in the United States. The pooled results from 8 RCTs with 517 patients (72% female, mean age 40) demonstrated greater improvement of abdominal pain with tricyclic and selective serotonin reuptake inhibitor antidepressants than placebo over 6 to 12 weeks (54% vs 37%; RR=1.5; 95% CI, 1.1–2.1; NNT=5). However, subgroup analysis found a statistically significant benefit for tricyclic antidepressants (4 trials; N=320; RR=1.3; 95% CI, 1.0-1.6) but no benefit for SSRIs (4 trials; N=197; RR=2.3; 95% CI, 0.79-6.7).
Effective antispasmodics aren’t available in the United States
A 2012 meta-analysis of 23 RCTs with 2585 patients examined the effect of antispasmodic agents, alone or in combination, to treat IBS.2 Pooled results from 13 RCTs with 2394 patients (69% female, ages 16 years or older) favored treatment with antispasmodics over placebo for abdominal pain (odds ratio [OR]=1.5; 95% CI, 1.3-1.8). No difference in adverse events was found between antispasmodics and placebo (9 trials; N=2239; OR=0.74; 95% CI, 0.54-0.98). The antispasmodics found effective for abdominal pain in this meta-analysis aren’t available in the United States.
Peppermint oil helps, but can cause heartburn
A 2013 meta-analysis of 9 RCTs with 726 patients compared various doses of enteric-coated peppermint oil with placebo over a minimum of 2 weeks’ treatment.3 Five RCTs with 357 patients (62% female, 13.4% children) demonstrated improvement of abdominal pain in 57% of patients taking peppermint oil compared with 27% receiving placebo (RR=2.1; 95% CI, 1.6-2.8; NNT=4 at 2 to 8 weeks). No statistically significant heterogeneity was identified among the treatment groups.
Pooled analysis found that peppermint oil patients were more likely than placebo patients to experience an adverse event (7 trials; N=474; 22% vs 13%; RR=1.7; 95% CI, 1.3-2.4), but that the events were generally mild and transient. The most frequently reported adverse event was heartburn.
1. Ruepert L, Quartero AO, de Wit NJ, et al. Bulking agents, antispasmodics, and antidepressants for the treatment of irritable bowel syndrome. Cochrane Database Syst Rev. 2011;(8):CD003460.
2. Martinez-Vasquez MA, Vasquez-Elizondro G, Gonzalez-Gonzalez JA, et al. Effect of antispasmodic agents, alone or in combination, in the treatment of irritable bowel syndrome: systematic review and meta-analysis. Rev Gastroenterol Mexico. 2012;77:82-90.
3. Khanna R, MacDonald JK, Levesque BG. Peppermint oil for the treatment of irritable bowel syndrome: a systematic review and meta-analysis. J Clin Gastroenterol. 2014;48:505-512.
1. Ruepert L, Quartero AO, de Wit NJ, et al. Bulking agents, antispasmodics, and antidepressants for the treatment of irritable bowel syndrome. Cochrane Database Syst Rev. 2011;(8):CD003460.
2. Martinez-Vasquez MA, Vasquez-Elizondro G, Gonzalez-Gonzalez JA, et al. Effect of antispasmodic agents, alone or in combination, in the treatment of irritable bowel syndrome: systematic review and meta-analysis. Rev Gastroenterol Mexico. 2012;77:82-90.
3. Khanna R, MacDonald JK, Levesque BG. Peppermint oil for the treatment of irritable bowel syndrome: a systematic review and meta-analysis. J Clin Gastroenterol. 2014;48:505-512.
Evidence-based answers from the Family Physicians Inquiries Network
Is arthroscopic subacromial decompression effective for shoulder impingement?
It’s impossible to say for certain in the absence of randomized controlled trials. However, in patients whose impingement symptoms don’t improve after 3 to 6 months, arthroscopic subacromial decompression (ASD) is associated with modest (about 10%) long-term improvement in pain and function compared with open acromioplasty or baseline (strength of recommendation [SOR]: B, cohort studies).
Patients older than 57 years may do better with surgery than physical therapy (SOR: B, single cohort study).
EVIDENCE SUMMARY
Six cohort studies found that patients who underwent ASD for subacromial impingement had improved pain and function scores at 4.5 to 12 years after surgery (TABLE1-7). Weaknesses of the overall data set include use of heterogeneous outcome measures across studies, lack of sham surgical controls, and lack of blinding.
ASD improves pain and function slightly more than other treatments
One prospective and one retrospective cohort trial compared ASD with another intervention. In the prospective trial, ASD was associated with a 10% better combined pain and function score than open acromioplasty at 12 years.1 In the retrospective trial, ASD was also associated with a 10% better combined pain and function score than prolonged physical therapy in patients older than 57 years (the median age of study participants) but not patients younger than 57 years.2
Two other studies found improvements in pain and function
Two other prospective cohort studies didn’t use a comparison group but followed changes in standardized shoulder pain and function scores for 5 to 6 years after ASD. In one study, pain decreased 6 points on a 10-point visual analog scale by 6 months postop (P<.001).3 In both studies, a 9% to 10% improvement in function was seen between 6 months and 5 to 6 years after surgery.3,4
A third cohort study that asked patients about overall pain and satisfaction 8 to 11 years after ASD found that most were “very” or “quite” satisfied and half were pain-free.5,6
Rotator cuff tears found less likely with ASD
An anatomic study obtained ultrasounds of patients 13 to 17 years after ASD and compared the findings to rotator cuff ultrasounds of the general population.7 Patients who had ASD were 22% less likely to demonstrate rotator cuff tears at the end of the study (no statistics were reported to measure significance).
RECOMMENDATIONS
Guidelines from the Washington State Department of Labor and Industry state that patients who should undergo isolated subacromial decompression (with or without acromioplasty) need to have documented subacromial impingement syndrome with magnetic resonance imaging evidence of rotator cuff tendonopathy or tear, have undergone 12 weeks of conservative therapy (including at least active assisted range of motion and home-based exercises), and have had a subacromial injection with a local anesthetic that has provided documented relief of pain.8
No current guidelines are available from national or international orthopedic or sports medicine organizations.
1. Odenbring S, Wagner P, Atroshi I. Long-term outcomes of arthroscopic acromioplasty of chronic shoulder impingement syndrome: a prospective cohort study with a minimum of 12 years’ follow-up. Arthroscopy. 2008;24:1092–1098.
2. Biberthaler P, Beirer M, Kirchhoff S, et al. Significant benefit for older patients after arthroscopic subacromial decompression: a long-term follow-up study. Int Orthop. 2013;37:457–462.
3. Lunsjo K, Bengtsson M, Nordqvist A, et al. Patients with shoulder impingement remain satisfied 6 years after arthroscopic subacromial decompression. Acta Orthop. 2011;82:711–713.
4. Dom K, Van Glabbeek F, Van Riet RP, et al. Arthroscopic subacromial decompression for advanced (stage II) impingement syndrome: a study of 52 patients with 5 year follow-up. Acta Orthop Belg. 2003;69:13–17.
5. Klintberg IH, Karlsson J, Svantesson U. Health-related quality of life, patient satisfaction, and physical activity 8–11 years after arthroscopic subacromial decompression. J Shoulder Elbow Surg. 2011;20:598–608.
6. Klintberg IH, Svantesson U, Karlsson J. Long-term patient satisfaction and functional outcome 8-11 years after subacromial decompression. Knee Surg Sports Traumatol Arthrosc. 2010;18:394–403.
7. Bjornsson H, Norlin R, Knutsson A, et al. Fewer rotator cuff tears fifteen years after arthroscopic subacromial decompression. J Shoulder Elbow Surg. 2010;19:111–115.
8. Washington State Department of Labor and Industries. Shoulder Conditions Diagnosis and Treatment Guideline. Available at: http://www.lni.wa.gov/ClaimsIns/Files/OMD/MedTreat/FINALguidelineShoulderConditionsOct242013.pdf. Accessed October 20, 2015.
It’s impossible to say for certain in the absence of randomized controlled trials. However, in patients whose impingement symptoms don’t improve after 3 to 6 months, arthroscopic subacromial decompression (ASD) is associated with modest (about 10%) long-term improvement in pain and function compared with open acromioplasty or baseline (strength of recommendation [SOR]: B, cohort studies).
Patients older than 57 years may do better with surgery than physical therapy (SOR: B, single cohort study).
EVIDENCE SUMMARY
Six cohort studies found that patients who underwent ASD for subacromial impingement had improved pain and function scores at 4.5 to 12 years after surgery (TABLE1-7). Weaknesses of the overall data set include use of heterogeneous outcome measures across studies, lack of sham surgical controls, and lack of blinding.
ASD improves pain and function slightly more than other treatments
One prospective and one retrospective cohort trial compared ASD with another intervention. In the prospective trial, ASD was associated with a 10% better combined pain and function score than open acromioplasty at 12 years.1 In the retrospective trial, ASD was also associated with a 10% better combined pain and function score than prolonged physical therapy in patients older than 57 years (the median age of study participants) but not patients younger than 57 years.2
Two other studies found improvements in pain and function
Two other prospective cohort studies didn’t use a comparison group but followed changes in standardized shoulder pain and function scores for 5 to 6 years after ASD. In one study, pain decreased 6 points on a 10-point visual analog scale by 6 months postop (P<.001).3 In both studies, a 9% to 10% improvement in function was seen between 6 months and 5 to 6 years after surgery.3,4
A third cohort study that asked patients about overall pain and satisfaction 8 to 11 years after ASD found that most were “very” or “quite” satisfied and half were pain-free.5,6
Rotator cuff tears found less likely with ASD
An anatomic study obtained ultrasounds of patients 13 to 17 years after ASD and compared the findings to rotator cuff ultrasounds of the general population.7 Patients who had ASD were 22% less likely to demonstrate rotator cuff tears at the end of the study (no statistics were reported to measure significance).
RECOMMENDATIONS
Guidelines from the Washington State Department of Labor and Industry state that patients who should undergo isolated subacromial decompression (with or without acromioplasty) need to have documented subacromial impingement syndrome with magnetic resonance imaging evidence of rotator cuff tendonopathy or tear, have undergone 12 weeks of conservative therapy (including at least active assisted range of motion and home-based exercises), and have had a subacromial injection with a local anesthetic that has provided documented relief of pain.8
No current guidelines are available from national or international orthopedic or sports medicine organizations.
It’s impossible to say for certain in the absence of randomized controlled trials. However, in patients whose impingement symptoms don’t improve after 3 to 6 months, arthroscopic subacromial decompression (ASD) is associated with modest (about 10%) long-term improvement in pain and function compared with open acromioplasty or baseline (strength of recommendation [SOR]: B, cohort studies).
Patients older than 57 years may do better with surgery than physical therapy (SOR: B, single cohort study).
EVIDENCE SUMMARY
Six cohort studies found that patients who underwent ASD for subacromial impingement had improved pain and function scores at 4.5 to 12 years after surgery (TABLE1-7). Weaknesses of the overall data set include use of heterogeneous outcome measures across studies, lack of sham surgical controls, and lack of blinding.
ASD improves pain and function slightly more than other treatments
One prospective and one retrospective cohort trial compared ASD with another intervention. In the prospective trial, ASD was associated with a 10% better combined pain and function score than open acromioplasty at 12 years.1 In the retrospective trial, ASD was also associated with a 10% better combined pain and function score than prolonged physical therapy in patients older than 57 years (the median age of study participants) but not patients younger than 57 years.2
Two other studies found improvements in pain and function
Two other prospective cohort studies didn’t use a comparison group but followed changes in standardized shoulder pain and function scores for 5 to 6 years after ASD. In one study, pain decreased 6 points on a 10-point visual analog scale by 6 months postop (P<.001).3 In both studies, a 9% to 10% improvement in function was seen between 6 months and 5 to 6 years after surgery.3,4
A third cohort study that asked patients about overall pain and satisfaction 8 to 11 years after ASD found that most were “very” or “quite” satisfied and half were pain-free.5,6
Rotator cuff tears found less likely with ASD
An anatomic study obtained ultrasounds of patients 13 to 17 years after ASD and compared the findings to rotator cuff ultrasounds of the general population.7 Patients who had ASD were 22% less likely to demonstrate rotator cuff tears at the end of the study (no statistics were reported to measure significance).
RECOMMENDATIONS
Guidelines from the Washington State Department of Labor and Industry state that patients who should undergo isolated subacromial decompression (with or without acromioplasty) need to have documented subacromial impingement syndrome with magnetic resonance imaging evidence of rotator cuff tendonopathy or tear, have undergone 12 weeks of conservative therapy (including at least active assisted range of motion and home-based exercises), and have had a subacromial injection with a local anesthetic that has provided documented relief of pain.8
No current guidelines are available from national or international orthopedic or sports medicine organizations.
1. Odenbring S, Wagner P, Atroshi I. Long-term outcomes of arthroscopic acromioplasty of chronic shoulder impingement syndrome: a prospective cohort study with a minimum of 12 years’ follow-up. Arthroscopy. 2008;24:1092–1098.
2. Biberthaler P, Beirer M, Kirchhoff S, et al. Significant benefit for older patients after arthroscopic subacromial decompression: a long-term follow-up study. Int Orthop. 2013;37:457–462.
3. Lunsjo K, Bengtsson M, Nordqvist A, et al. Patients with shoulder impingement remain satisfied 6 years after arthroscopic subacromial decompression. Acta Orthop. 2011;82:711–713.
4. Dom K, Van Glabbeek F, Van Riet RP, et al. Arthroscopic subacromial decompression for advanced (stage II) impingement syndrome: a study of 52 patients with 5 year follow-up. Acta Orthop Belg. 2003;69:13–17.
5. Klintberg IH, Karlsson J, Svantesson U. Health-related quality of life, patient satisfaction, and physical activity 8–11 years after arthroscopic subacromial decompression. J Shoulder Elbow Surg. 2011;20:598–608.
6. Klintberg IH, Svantesson U, Karlsson J. Long-term patient satisfaction and functional outcome 8-11 years after subacromial decompression. Knee Surg Sports Traumatol Arthrosc. 2010;18:394–403.
7. Bjornsson H, Norlin R, Knutsson A, et al. Fewer rotator cuff tears fifteen years after arthroscopic subacromial decompression. J Shoulder Elbow Surg. 2010;19:111–115.
8. Washington State Department of Labor and Industries. Shoulder Conditions Diagnosis and Treatment Guideline. Available at: http://www.lni.wa.gov/ClaimsIns/Files/OMD/MedTreat/FINALguidelineShoulderConditionsOct242013.pdf. Accessed October 20, 2015.
1. Odenbring S, Wagner P, Atroshi I. Long-term outcomes of arthroscopic acromioplasty of chronic shoulder impingement syndrome: a prospective cohort study with a minimum of 12 years’ follow-up. Arthroscopy. 2008;24:1092–1098.
2. Biberthaler P, Beirer M, Kirchhoff S, et al. Significant benefit for older patients after arthroscopic subacromial decompression: a long-term follow-up study. Int Orthop. 2013;37:457–462.
3. Lunsjo K, Bengtsson M, Nordqvist A, et al. Patients with shoulder impingement remain satisfied 6 years after arthroscopic subacromial decompression. Acta Orthop. 2011;82:711–713.
4. Dom K, Van Glabbeek F, Van Riet RP, et al. Arthroscopic subacromial decompression for advanced (stage II) impingement syndrome: a study of 52 patients with 5 year follow-up. Acta Orthop Belg. 2003;69:13–17.
5. Klintberg IH, Karlsson J, Svantesson U. Health-related quality of life, patient satisfaction, and physical activity 8–11 years after arthroscopic subacromial decompression. J Shoulder Elbow Surg. 2011;20:598–608.
6. Klintberg IH, Svantesson U, Karlsson J. Long-term patient satisfaction and functional outcome 8-11 years after subacromial decompression. Knee Surg Sports Traumatol Arthrosc. 2010;18:394–403.
7. Bjornsson H, Norlin R, Knutsson A, et al. Fewer rotator cuff tears fifteen years after arthroscopic subacromial decompression. J Shoulder Elbow Surg. 2010;19:111–115.
8. Washington State Department of Labor and Industries. Shoulder Conditions Diagnosis and Treatment Guideline. Available at: http://www.lni.wa.gov/ClaimsIns/Files/OMD/MedTreat/FINALguidelineShoulderConditionsOct242013.pdf. Accessed October 20, 2015.
Evidence-based answers from the Family Physicians Inquiries Network
EHR use and patient satisfaction: What we learned
ABSTRACT
Purpose Few studies have quantitatively examined the degree to which the use of the computer affects patients’ satisfaction with the clinician and the quality of the visit. We conducted a study to examine this association.
Methods Twenty-three clinicians (21 internal medicine physicians, 2 nurse practitioners) were recruited from 4 Veteran Affairs Medical Center (VAMC) clinics located in San Diego, Calif. Five to 6 patients for most clinicians (one patient each for 2 of the clinicians) were recruited to participate in a study of patient-physician communication. The clinicians’ computer use and the patient-clinician interactions in the exam room were captured in real time via video recordings of the interactions and the computer screen, and through the use of the Morae usability testing software system, which recorded clinician clicks and scrolls on the computer. After the visit, patients were asked to complete a satisfaction survey.
Results The final sample consisted of 126 consultations. Total patient satisfaction (beta=0.014; P=.027) and patient satisfaction with patient-centered communication (beta=0.02; P=.02) were significantly associated with higher clinician “gaze time” at the patient. A higher percentage of gaze time during a visit (controlling for the length of the visit) was significantly associated with greater satisfaction with patient-centered communication (beta=0.628; P=.033).
Conclusions Higher clinician gaze time at the patient predicted greater patient satisfaction. This suggests that clinicians would be well served to refine their multitasking skills so that they communicate in a patient-centered manner while performing necessary computer-related tasks. These findings also have important implications for clinical training with respect to using an electronic health record (EHR) system in ways that do not impede the one-on-one conversation between clinician and patient.
Primary care physicians’ use of electronic health record (EHR) systems has markedly increased in recent years. For example, a 2008 study of more than 1000 randomly selected practicing physicians in Massachusetts found that 33% utilized an EHR.1 Many physicians believe that EHR systems are beneficial to patient care,2 and several studies have supported this perception, showing clear benefits of EHR use. A study of one component of EHR systems—computerized physician order entry (CPOE)—found that CPOEs resulted in a >50% decrease in serious medication errors.3 Other errors have declined with the use of EHR systems, as well; Virapongse et al1 found a trend towards fewer paid malpractice claims against physicians who used an EHR compared to those physicians using paper charting.
EHR systems may also improve efficiency. In a study of a health maintenance organization (HMO) model, initiating an EHR system improved efficiency by decreasing office visits.4 Widespread adoption of EHR systems could save an estimated $81 billion annually through reductions in errors and adverse events, and improved preventive care and chronic disease management.5 In a survey of approximately 300 patients who had been evaluated at a family medicine clinic for hypertension, high blood pressure without hypertension, or hyperlipidemia, 75% indicated that they felt EHRs had a positive impact on their care.6
However, some clinicians are concerned about the possible negative impact of EHR systems on health care. One major concern is that EHR systems might increase physician workload7 and the amount of time spent using a computer during patient visits. A study that examined physician EHR use found that while time spent on certain tasks, such as prescription writing and lab ordering, was reduced, there was an overall increase in time spent on computer tasks related to charting, preventive care, and chronic disease management.8 Baron et al9 also found an increase in time spent using the EHR during each clinic session in one private practice setting.
Physicians are also concerned that EHR systems might interfere with the patient-physician interaction (eg, maintaining eye contact, paying attention to patients’ concerns) by directing the physician’s attention away from the patient and toward the computer.10 In one study, this concern increased after physicians started utilizing a new EHR system.11 Although a survey of inpatients indicated that residents engaged in greater patient-physician communication after an EHR was implemented,12 a separate study conducted in an outpatient setting found physicians spent less time looking at patients after converting from a paper-based system to an EHR system.13
Very few studies have quantitatively examined the association of patient satisfaction with clinician EHR usage. The goal of this study was to examine the correlation of patient satisfaction with actual EHR usage in an ambulatory setting. The data reported in this paper are part of a larger study aimed at understanding EHR use in a VAMC.
METHODS
Study design and sample
The study participants were clinicians in 4 VAMC community clinics located in San Diego, Calif. Twenty-three clinicians (21 general internal medicine physicians and 2 nurse practitioners) were enrolled in the study. Most clinicians identified 5 to 6 patients from their practices to participate in the study (2 participants identified only one patient each). All patients were visiting their clinician for either an acute visit or a follow-up visit.
Although there were slight variations in clinic room size and shape, all rooms were equipped with a compact desk against a wall, a rolling desk chair, a desktop computer with keyboard and mouse, and a second, fixed chair placed diagonal to the physician’s chair. Two rooms had dual monitors. There was a standard examination table in all examination rooms.
The clinicians’ computer use and the patient-clinician interactions in the exam room were captured in real time via video recordings of the interactions and the computer screen. A usability testing software system (Morae) was used to record clinicians’ computer activities, including mouse clicks and scrolls on the computer. The Computerized Patient Records System (CPRS) was the EHR used by all clinicians in this study.
At the end of the visit, patients were asked to complete a satisfaction survey with questions in 3 domains: the physician’s engagement in patient-centered communication, the physician’s clinical skills, and the physician’s interpersonal skills.
Data analysis
Descriptive statistics were used to document patient characteristics, the clinicians’ EHR usage (total number of mouse clicks and scrolls during the visit) and interaction with the patient (gaze time at EHR vs at patient and companion), and to summarize patient satisfaction with the visit. To account for clinician cluster effect, a linear mixed effects model was used to assess the associations between patient satisfaction with the clinician and 2 variables: the amount of clinician time spent viewing or using the computer and the clinician time spent interacting with the patient.
We also assessed the above associations by controlling for visit length. Visit lengths not significant at P<.10 were reported as unadjusted analyses.
All analyses were performed using R statistical software, with a P value of <.05 interpreted as statistically significant.
RESULTS
Satisfaction surveys and video and Morae data were collected for 126 individual patient office visits to the 23 participating physicians and nurses. A majority of the patients who participated in the study were older (mean: 60.5 years; standard deviation [SD]=13.4 years), male as expected in a VA setting (96.8%), Caucasian (65.1%), and had at least some college education (81.7%, TABLE 1).
Patients rated their satisfaction in 3 domains—patient-centered communication, physician clinical skills, and physician interpersonal skills—using a 1 to 5 scale (1=least satisfied, 5=most satisfied). Patients in this study were highly satisfied with their physician or nurse in all 3 domains and overall (TABLE 2), with an average satisfaction score of 4.52 ± 0.51 for patient-centered communication, 4.71 ± 0.56 for physician clinical skills, 4.86 ± 0.32 for physician interpersonal skills, and 4.64 ± 0.38 for total satisfaction.
The physicians and nurses used their EHR system extensively during the visits as delineated by the number of clicks and scrolls on the computer. The average number of clicks and scrolls was 192, with a maximum of 685 clicks and scrolls during one visit. The average visit lasted 30.7 minutes, and on average the clinician spent 12.7 minutes (SD: 8.22 minutes), or an average of about 39.4% of total visit time, viewing or working on the EHR; an average of 10.8 minutes (SD: 5.63 minutes), or an average of about 36.3% of total visit time, was spent interacting with the patient (TABLE 3).
Without adjusting for visit length, patient satisfaction with the clinicians’ patientcentered communication (beta=0.02; P=.02) and total satisfaction (beta=0.014; P=.027) were significantly associated with clinicians’ gaze time at the patient; more clinician gaze time at the patient resulted in greater patient satisfaction (TABLE 4). Adding visit length to the above models had no significant effect (P>.10); therefore, we did not include it in the models.
Patient satisfaction with clinicians’ interpersonal skills was positively associated with gaze time at the patient (beta=0.013, P =.017) without adjusting for visit length. Since the normal assumption of residuals was not plausible based on a normal probability plot, we also assessed the association by dichotomizing the score (5=very satisfied vs <5=not very satisfied) and this significance disappeared. This association was not significant while controlling for visit length.
The percentage of gaze time at the patient (the fraction of patient gaze time over the entire visit) was not significantly associated with patient-centered communication (beta=0.483, P=.12, TABLE 4) when not adjusted for visit length. After adjusting for visit length (P=.052), the association became significant (beta=0.628, P=.033); thus, the higher percentage of time the clinician spent interacting with the patient, the more satisfied the patient was.
DISCUSSION
In this study, patients were highly satisfied with their clinicians despite often high usage of the EHR. Gadd and Penrod11 reported that patients perceived no impact on communication or eye contact with the clinician despite the initiation of an EHR system in 6 large academic medical practices. Another study demonstrated no significant differences in patient satisfaction with their physicians when comparing patients whose physicians used a paper charting system with those who used an EHR system.14
The fact that patients demonstrated high levels of satisfaction with patient-clinician communication even for clinicians with high EHR usage is somewhat surprising. However, Hsu et al15 found patients’ satisfaction with their clinicians’ communication about medical issues and familiarity with them increased 7 months after implementing an EHR system. In a different study that analyzed videotaped interactions between patients and 5 physicians, the patients found it disturbing not knowing what their doctor was doing when he or she worked on the computer, and preferred being able to see the computer screen.16 This study suggests that it’s advisable for clinicians to describe what they are doing when they use the computer, so that patients better understand how this time spent inputting data actually benefits them.
EHRs can be time-consuming. Physicians and nurses in our study interacted with the EHR a great deal during the office visit, as evidenced by the large average number of clicks and scrolls. This finding confirms clinicians’ perceptions of the amount of work the EHR system requires. For example, in a semi-structured interview of physicians regarding their use of a VA EHR system,10 one respondent noted that the reminders in the EHR required hundreds of clicks.
In our study, the average number of clicks and scrolls during the visit was 192, with some clinicians registering hundreds more. In fact, concerns about the time involved in the use of the EHR and about the adequacy of data collection may lead some clinicians who currently don’t have an EHR system to be reluctant to integrate one into their practices.17
Makoul et al18 found that compared with physicians who used a paper chart, physicians who used an EHR system were more active in clarifying information from the patient and encouraging patient questions during visits, although the study found a trend toward less active roles in more patient-centered communication when using an EHR system. This latter finding is similar to the concerns raised in our study.
Clinical and communication skills are factors, too. One study found that compared to patients who were cared for by more experienced physicians, patients seen by residents using EHRs were more likely to feel that the physician spent less time talking with them and examining them; they were also more likely to report that the visit felt less personal.19 Another study found that clinicians with poor baseline communication skills had more difficulties interacting with patients when an EHR system was introduced than those who had better baseline communication skills.20
Training needed to improve communication during EHR use. Research has shown that when used properly and thoughtfully, EHR use can result in greater patient engagement.21 But, as noted above, there are challenges, suggesting a need for training clinicians to more successfully use an EHR system while simultaneously communicating with their patients.
Study limitations. This study was conducted at a single site, using a single EHR system deployed in the VA clinics. We cannot generalize our findings to other sites or types of clinic systems. Other EHR systems may have different functionalities, which may affect the time required to provide the same type of medical care.
In addition, the study involved only 23 physicians and nurses in a single health system. Other clinicians may have patterns different from those we studied, although a wide range of patterns was seen among the participants, as demonstrated by the large variation in the number of clicks and scrolls. Another limitation is that study patients were not randomly selected, but rather referred by the provider, and the visits were not blinded to either the provider or patient. This may cause some selection bias.
In this study of VA clinicians’ EHR use, patients expressed satisfaction with the clinicians’ clinical skills and patient-centered communication when the clinician spent more time and a greater percentage of the visit engaging the patient. EHR systems need to be designed in a clinician-friendly manner that allows for increased time during the interaction for face-to-face communication between the clinician and the patient, and to ease the workload of EHR documentation. In the meantime, clinicians should be trained in how to expedite their use of the EHR during the clinical visit as well as outside of the exam room in order to improve their patients’ satisfaction.
CORRESPONDENCE
Neil J. Farber, MD, University of California, San Diego, 8939 Villa La Jolla Drive, La Jolla, CA 92037; nfarber@ucsd.edu.
1. Virapongse A, Bates DW, Shi P, et al. Electronic health records and malpractice claims in office practice. Arch Intern Med. 2008;168:2362-2367.
2. DesRoches CM, Campbell EG, Rao SR, et al. Electronic health records in ambulatory care—a national survey of physicians. N Engl J Med. 2008;359:50-60.
3. Bates DW, Leape LL, Cullen DJ, et al. Effect of computerized physician order entry and a team intervention on prevention of serious medication errors. JAMA. 1998;280:1311-1316.
4. Chen C, Garrido T, Chock D, et al. The Kaiser Permanente Electronic Health Record: transforming and streamlining modalities of care. Health Aff (Millwood). 2009;28:323-333.
5. Hillestad R, Bigelow J, Bower A, et al. Can electronic medical record systems transform health care? Potential health benefits, savings, and costs. Health Aff (Millwood). 2005;24:1103-1117.
6. Garrison GM, Bernard ME, Rasmussen NH. 21st-century health care: the effect of computer use by physicians on patient satisfaction at a family medicine clinic. Fam Med. 2002;34:362-368.
7. Likourezos A, Chalfin DB, Murphy DG, et al. Physician and nurse satisfaction with an Electronic Medical Record system. J Emerg Med. 2004;27:419-424.
8. Howard J, Clark EC, Friedman A, et al. Electronic health record impact on work burden in small, unaffiliated, community-based primary care practices. J Gen Intern Med. 2013;28:107-113.
9. Baron RJ. What’s keeping us so busy in primary care? A snapshot from one practice. N Engl J Med. 2010;362:1632-1636.
10. Bonner LM, Simons CE, Parker LE, et al. ‘To take care of the patients’: Qualitative analysis of Veterans Health Administration personnel experiences with a clinical informatics system. Implement Sci. 2010;5:63.
11. Gadd CS, Penrod LE. Dichotomy between physicians’ and patients’ attitudes regarding EMR use during outpatient encounters. Proc AMIA Symp. 2000:275-279.
12. Migdal CW, Namavar AA, Mosley VN, et al. Impact of electronic health records on the patient experience in a hospital setting. J Hosp Med. 2014;9:627-633.
13. Asan O, D Smith P, Montague E. More screen time, less face time - implications for EHR design. J Eval Clin Pract. 2014;20:896-901.
14. Legler JD, Oates R. Patients’ reactions to physician use of a computerized medical record system during clinical encounters. J Fam Pract. 1993;37:241-244.
15. Hsu J, Huang J, Fung V, et al. Health information technology and physician-patient interactions: impact of computers on communication during outpatient primary care visits. J Am Med Inform Assoc. 2005;12:474-480.
16. Als AB. The desk-top computer as a magic box: patterns of behaviour connected with the desk-top computer; GPs’ and patients’ perceptions. Fam Pract. 1997;14:17-23.
17. Bates DW. Physicians and ambulatory electronic health records. Health Aff (Millwood). 2005;24:1180-1189.
18. Makoul G, Curry RH, Tang PC. The use of electronic medical records: communication patterns in outpatient encounters. J Am Med Inform Assoc. 2001;8:610-615.
19. Rouf E, Whittle J, Lu N, et al. Computers in the exam room: differences in physician-patient interaction may be due to physician experience. J Gen Intern Med. 2007;22:43-48.
20. Frankel R, Altschuler A, George S, et al. Effects of exam-room computing on clinician-patient communication: a longitudinal qualitative study. J Gen Intern Med. 2005;20:677-682.
21. Asan O, Young HN, Chewning B, et al. How physician electronic health record screen sharing affects patient and doctor nonverbal communication in primary care. Patient Educ Couns. 2015;98:310-316.
ABSTRACT
Purpose Few studies have quantitatively examined the degree to which the use of the computer affects patients’ satisfaction with the clinician and the quality of the visit. We conducted a study to examine this association.
Methods Twenty-three clinicians (21 internal medicine physicians, 2 nurse practitioners) were recruited from 4 Veteran Affairs Medical Center (VAMC) clinics located in San Diego, Calif. Five to 6 patients for most clinicians (one patient each for 2 of the clinicians) were recruited to participate in a study of patient-physician communication. The clinicians’ computer use and the patient-clinician interactions in the exam room were captured in real time via video recordings of the interactions and the computer screen, and through the use of the Morae usability testing software system, which recorded clinician clicks and scrolls on the computer. After the visit, patients were asked to complete a satisfaction survey.
Results The final sample consisted of 126 consultations. Total patient satisfaction (beta=0.014; P=.027) and patient satisfaction with patient-centered communication (beta=0.02; P=.02) were significantly associated with higher clinician “gaze time” at the patient. A higher percentage of gaze time during a visit (controlling for the length of the visit) was significantly associated with greater satisfaction with patient-centered communication (beta=0.628; P=.033).
Conclusions Higher clinician gaze time at the patient predicted greater patient satisfaction. This suggests that clinicians would be well served to refine their multitasking skills so that they communicate in a patient-centered manner while performing necessary computer-related tasks. These findings also have important implications for clinical training with respect to using an electronic health record (EHR) system in ways that do not impede the one-on-one conversation between clinician and patient.
Primary care physicians’ use of electronic health record (EHR) systems has markedly increased in recent years. For example, a 2008 study of more than 1000 randomly selected practicing physicians in Massachusetts found that 33% utilized an EHR.1 Many physicians believe that EHR systems are beneficial to patient care,2 and several studies have supported this perception, showing clear benefits of EHR use. A study of one component of EHR systems—computerized physician order entry (CPOE)—found that CPOEs resulted in a >50% decrease in serious medication errors.3 Other errors have declined with the use of EHR systems, as well; Virapongse et al1 found a trend towards fewer paid malpractice claims against physicians who used an EHR compared to those physicians using paper charting.
EHR systems may also improve efficiency. In a study of a health maintenance organization (HMO) model, initiating an EHR system improved efficiency by decreasing office visits.4 Widespread adoption of EHR systems could save an estimated $81 billion annually through reductions in errors and adverse events, and improved preventive care and chronic disease management.5 In a survey of approximately 300 patients who had been evaluated at a family medicine clinic for hypertension, high blood pressure without hypertension, or hyperlipidemia, 75% indicated that they felt EHRs had a positive impact on their care.6
However, some clinicians are concerned about the possible negative impact of EHR systems on health care. One major concern is that EHR systems might increase physician workload7 and the amount of time spent using a computer during patient visits. A study that examined physician EHR use found that while time spent on certain tasks, such as prescription writing and lab ordering, was reduced, there was an overall increase in time spent on computer tasks related to charting, preventive care, and chronic disease management.8 Baron et al9 also found an increase in time spent using the EHR during each clinic session in one private practice setting.
Physicians are also concerned that EHR systems might interfere with the patient-physician interaction (eg, maintaining eye contact, paying attention to patients’ concerns) by directing the physician’s attention away from the patient and toward the computer.10 In one study, this concern increased after physicians started utilizing a new EHR system.11 Although a survey of inpatients indicated that residents engaged in greater patient-physician communication after an EHR was implemented,12 a separate study conducted in an outpatient setting found physicians spent less time looking at patients after converting from a paper-based system to an EHR system.13
Very few studies have quantitatively examined the association of patient satisfaction with clinician EHR usage. The goal of this study was to examine the correlation of patient satisfaction with actual EHR usage in an ambulatory setting. The data reported in this paper are part of a larger study aimed at understanding EHR use in a VAMC.
METHODS
Study design and sample
The study participants were clinicians in 4 VAMC community clinics located in San Diego, Calif. Twenty-three clinicians (21 general internal medicine physicians and 2 nurse practitioners) were enrolled in the study. Most clinicians identified 5 to 6 patients from their practices to participate in the study (2 participants identified only one patient each). All patients were visiting their clinician for either an acute visit or a follow-up visit.
Although there were slight variations in clinic room size and shape, all rooms were equipped with a compact desk against a wall, a rolling desk chair, a desktop computer with keyboard and mouse, and a second, fixed chair placed diagonal to the physician’s chair. Two rooms had dual monitors. There was a standard examination table in all examination rooms.
The clinicians’ computer use and the patient-clinician interactions in the exam room were captured in real time via video recordings of the interactions and the computer screen. A usability testing software system (Morae) was used to record clinicians’ computer activities, including mouse clicks and scrolls on the computer. The Computerized Patient Records System (CPRS) was the EHR used by all clinicians in this study.
At the end of the visit, patients were asked to complete a satisfaction survey with questions in 3 domains: the physician’s engagement in patient-centered communication, the physician’s clinical skills, and the physician’s interpersonal skills.
Data analysis
Descriptive statistics were used to document patient characteristics, the clinicians’ EHR usage (total number of mouse clicks and scrolls during the visit) and interaction with the patient (gaze time at EHR vs at patient and companion), and to summarize patient satisfaction with the visit. To account for clinician cluster effect, a linear mixed effects model was used to assess the associations between patient satisfaction with the clinician and 2 variables: the amount of clinician time spent viewing or using the computer and the clinician time spent interacting with the patient.
We also assessed the above associations by controlling for visit length. Visit lengths not significant at P<.10 were reported as unadjusted analyses.
All analyses were performed using R statistical software, with a P value of <.05 interpreted as statistically significant.
RESULTS
Satisfaction surveys and video and Morae data were collected for 126 individual patient office visits to the 23 participating physicians and nurses. A majority of the patients who participated in the study were older (mean: 60.5 years; standard deviation [SD]=13.4 years), male as expected in a VA setting (96.8%), Caucasian (65.1%), and had at least some college education (81.7%, TABLE 1).
Patients rated their satisfaction in 3 domains—patient-centered communication, physician clinical skills, and physician interpersonal skills—using a 1 to 5 scale (1=least satisfied, 5=most satisfied). Patients in this study were highly satisfied with their physician or nurse in all 3 domains and overall (TABLE 2), with an average satisfaction score of 4.52 ± 0.51 for patient-centered communication, 4.71 ± 0.56 for physician clinical skills, 4.86 ± 0.32 for physician interpersonal skills, and 4.64 ± 0.38 for total satisfaction.
The physicians and nurses used their EHR system extensively during the visits as delineated by the number of clicks and scrolls on the computer. The average number of clicks and scrolls was 192, with a maximum of 685 clicks and scrolls during one visit. The average visit lasted 30.7 minutes, and on average the clinician spent 12.7 minutes (SD: 8.22 minutes), or an average of about 39.4% of total visit time, viewing or working on the EHR; an average of 10.8 minutes (SD: 5.63 minutes), or an average of about 36.3% of total visit time, was spent interacting with the patient (TABLE 3).
Without adjusting for visit length, patient satisfaction with the clinicians’ patientcentered communication (beta=0.02; P=.02) and total satisfaction (beta=0.014; P=.027) were significantly associated with clinicians’ gaze time at the patient; more clinician gaze time at the patient resulted in greater patient satisfaction (TABLE 4). Adding visit length to the above models had no significant effect (P>.10); therefore, we did not include it in the models.
Patient satisfaction with clinicians’ interpersonal skills was positively associated with gaze time at the patient (beta=0.013, P =.017) without adjusting for visit length. Since the normal assumption of residuals was not plausible based on a normal probability plot, we also assessed the association by dichotomizing the score (5=very satisfied vs <5=not very satisfied) and this significance disappeared. This association was not significant while controlling for visit length.
The percentage of gaze time at the patient (the fraction of patient gaze time over the entire visit) was not significantly associated with patient-centered communication (beta=0.483, P=.12, TABLE 4) when not adjusted for visit length. After adjusting for visit length (P=.052), the association became significant (beta=0.628, P=.033); thus, the higher percentage of time the clinician spent interacting with the patient, the more satisfied the patient was.
DISCUSSION
In this study, patients were highly satisfied with their clinicians despite often high usage of the EHR. Gadd and Penrod11 reported that patients perceived no impact on communication or eye contact with the clinician despite the initiation of an EHR system in 6 large academic medical practices. Another study demonstrated no significant differences in patient satisfaction with their physicians when comparing patients whose physicians used a paper charting system with those who used an EHR system.14
The fact that patients demonstrated high levels of satisfaction with patient-clinician communication even for clinicians with high EHR usage is somewhat surprising. However, Hsu et al15 found patients’ satisfaction with their clinicians’ communication about medical issues and familiarity with them increased 7 months after implementing an EHR system. In a different study that analyzed videotaped interactions between patients and 5 physicians, the patients found it disturbing not knowing what their doctor was doing when he or she worked on the computer, and preferred being able to see the computer screen.16 This study suggests that it’s advisable for clinicians to describe what they are doing when they use the computer, so that patients better understand how this time spent inputting data actually benefits them.
EHRs can be time-consuming. Physicians and nurses in our study interacted with the EHR a great deal during the office visit, as evidenced by the large average number of clicks and scrolls. This finding confirms clinicians’ perceptions of the amount of work the EHR system requires. For example, in a semi-structured interview of physicians regarding their use of a VA EHR system,10 one respondent noted that the reminders in the EHR required hundreds of clicks.
In our study, the average number of clicks and scrolls during the visit was 192, with some clinicians registering hundreds more. In fact, concerns about the time involved in the use of the EHR and about the adequacy of data collection may lead some clinicians who currently don’t have an EHR system to be reluctant to integrate one into their practices.17
Makoul et al18 found that compared with physicians who used a paper chart, physicians who used an EHR system were more active in clarifying information from the patient and encouraging patient questions during visits, although the study found a trend toward less active roles in more patient-centered communication when using an EHR system. This latter finding is similar to the concerns raised in our study.
Clinical and communication skills are factors, too. One study found that compared to patients who were cared for by more experienced physicians, patients seen by residents using EHRs were more likely to feel that the physician spent less time talking with them and examining them; they were also more likely to report that the visit felt less personal.19 Another study found that clinicians with poor baseline communication skills had more difficulties interacting with patients when an EHR system was introduced than those who had better baseline communication skills.20
Training needed to improve communication during EHR use. Research has shown that when used properly and thoughtfully, EHR use can result in greater patient engagement.21 But, as noted above, there are challenges, suggesting a need for training clinicians to more successfully use an EHR system while simultaneously communicating with their patients.
Study limitations. This study was conducted at a single site, using a single EHR system deployed in the VA clinics. We cannot generalize our findings to other sites or types of clinic systems. Other EHR systems may have different functionalities, which may affect the time required to provide the same type of medical care.
In addition, the study involved only 23 physicians and nurses in a single health system. Other clinicians may have patterns different from those we studied, although a wide range of patterns was seen among the participants, as demonstrated by the large variation in the number of clicks and scrolls. Another limitation is that study patients were not randomly selected, but rather referred by the provider, and the visits were not blinded to either the provider or patient. This may cause some selection bias.
In this study of VA clinicians’ EHR use, patients expressed satisfaction with the clinicians’ clinical skills and patient-centered communication when the clinician spent more time and a greater percentage of the visit engaging the patient. EHR systems need to be designed in a clinician-friendly manner that allows for increased time during the interaction for face-to-face communication between the clinician and the patient, and to ease the workload of EHR documentation. In the meantime, clinicians should be trained in how to expedite their use of the EHR during the clinical visit as well as outside of the exam room in order to improve their patients’ satisfaction.
CORRESPONDENCE
Neil J. Farber, MD, University of California, San Diego, 8939 Villa La Jolla Drive, La Jolla, CA 92037; nfarber@ucsd.edu.
ABSTRACT
Purpose Few studies have quantitatively examined the degree to which the use of the computer affects patients’ satisfaction with the clinician and the quality of the visit. We conducted a study to examine this association.
Methods Twenty-three clinicians (21 internal medicine physicians, 2 nurse practitioners) were recruited from 4 Veteran Affairs Medical Center (VAMC) clinics located in San Diego, Calif. Five to 6 patients for most clinicians (one patient each for 2 of the clinicians) were recruited to participate in a study of patient-physician communication. The clinicians’ computer use and the patient-clinician interactions in the exam room were captured in real time via video recordings of the interactions and the computer screen, and through the use of the Morae usability testing software system, which recorded clinician clicks and scrolls on the computer. After the visit, patients were asked to complete a satisfaction survey.
Results The final sample consisted of 126 consultations. Total patient satisfaction (beta=0.014; P=.027) and patient satisfaction with patient-centered communication (beta=0.02; P=.02) were significantly associated with higher clinician “gaze time” at the patient. A higher percentage of gaze time during a visit (controlling for the length of the visit) was significantly associated with greater satisfaction with patient-centered communication (beta=0.628; P=.033).
Conclusions Higher clinician gaze time at the patient predicted greater patient satisfaction. This suggests that clinicians would be well served to refine their multitasking skills so that they communicate in a patient-centered manner while performing necessary computer-related tasks. These findings also have important implications for clinical training with respect to using an electronic health record (EHR) system in ways that do not impede the one-on-one conversation between clinician and patient.
Primary care physicians’ use of electronic health record (EHR) systems has markedly increased in recent years. For example, a 2008 study of more than 1000 randomly selected practicing physicians in Massachusetts found that 33% utilized an EHR.1 Many physicians believe that EHR systems are beneficial to patient care,2 and several studies have supported this perception, showing clear benefits of EHR use. A study of one component of EHR systems—computerized physician order entry (CPOE)—found that CPOEs resulted in a >50% decrease in serious medication errors.3 Other errors have declined with the use of EHR systems, as well; Virapongse et al1 found a trend towards fewer paid malpractice claims against physicians who used an EHR compared to those physicians using paper charting.
EHR systems may also improve efficiency. In a study of a health maintenance organization (HMO) model, initiating an EHR system improved efficiency by decreasing office visits.4 Widespread adoption of EHR systems could save an estimated $81 billion annually through reductions in errors and adverse events, and improved preventive care and chronic disease management.5 In a survey of approximately 300 patients who had been evaluated at a family medicine clinic for hypertension, high blood pressure without hypertension, or hyperlipidemia, 75% indicated that they felt EHRs had a positive impact on their care.6
However, some clinicians are concerned about the possible negative impact of EHR systems on health care. One major concern is that EHR systems might increase physician workload7 and the amount of time spent using a computer during patient visits. A study that examined physician EHR use found that while time spent on certain tasks, such as prescription writing and lab ordering, was reduced, there was an overall increase in time spent on computer tasks related to charting, preventive care, and chronic disease management.8 Baron et al9 also found an increase in time spent using the EHR during each clinic session in one private practice setting.
Physicians are also concerned that EHR systems might interfere with the patient-physician interaction (eg, maintaining eye contact, paying attention to patients’ concerns) by directing the physician’s attention away from the patient and toward the computer.10 In one study, this concern increased after physicians started utilizing a new EHR system.11 Although a survey of inpatients indicated that residents engaged in greater patient-physician communication after an EHR was implemented,12 a separate study conducted in an outpatient setting found physicians spent less time looking at patients after converting from a paper-based system to an EHR system.13
Very few studies have quantitatively examined the association of patient satisfaction with clinician EHR usage. The goal of this study was to examine the correlation of patient satisfaction with actual EHR usage in an ambulatory setting. The data reported in this paper are part of a larger study aimed at understanding EHR use in a VAMC.
METHODS
Study design and sample
The study participants were clinicians in 4 VAMC community clinics located in San Diego, Calif. Twenty-three clinicians (21 general internal medicine physicians and 2 nurse practitioners) were enrolled in the study. Most clinicians identified 5 to 6 patients from their practices to participate in the study (2 participants identified only one patient each). All patients were visiting their clinician for either an acute visit or a follow-up visit.
Although there were slight variations in clinic room size and shape, all rooms were equipped with a compact desk against a wall, a rolling desk chair, a desktop computer with keyboard and mouse, and a second, fixed chair placed diagonal to the physician’s chair. Two rooms had dual monitors. There was a standard examination table in all examination rooms.
The clinicians’ computer use and the patient-clinician interactions in the exam room were captured in real time via video recordings of the interactions and the computer screen. A usability testing software system (Morae) was used to record clinicians’ computer activities, including mouse clicks and scrolls on the computer. The Computerized Patient Records System (CPRS) was the EHR used by all clinicians in this study.
At the end of the visit, patients were asked to complete a satisfaction survey with questions in 3 domains: the physician’s engagement in patient-centered communication, the physician’s clinical skills, and the physician’s interpersonal skills.
Data analysis
Descriptive statistics were used to document patient characteristics, the clinicians’ EHR usage (total number of mouse clicks and scrolls during the visit) and interaction with the patient (gaze time at EHR vs at patient and companion), and to summarize patient satisfaction with the visit. To account for clinician cluster effect, a linear mixed effects model was used to assess the associations between patient satisfaction with the clinician and 2 variables: the amount of clinician time spent viewing or using the computer and the clinician time spent interacting with the patient.
We also assessed the above associations by controlling for visit length. Visit lengths not significant at P<.10 were reported as unadjusted analyses.
All analyses were performed using R statistical software, with a P value of <.05 interpreted as statistically significant.
RESULTS
Satisfaction surveys and video and Morae data were collected for 126 individual patient office visits to the 23 participating physicians and nurses. A majority of the patients who participated in the study were older (mean: 60.5 years; standard deviation [SD]=13.4 years), male as expected in a VA setting (96.8%), Caucasian (65.1%), and had at least some college education (81.7%, TABLE 1).
Patients rated their satisfaction in 3 domains—patient-centered communication, physician clinical skills, and physician interpersonal skills—using a 1 to 5 scale (1=least satisfied, 5=most satisfied). Patients in this study were highly satisfied with their physician or nurse in all 3 domains and overall (TABLE 2), with an average satisfaction score of 4.52 ± 0.51 for patient-centered communication, 4.71 ± 0.56 for physician clinical skills, 4.86 ± 0.32 for physician interpersonal skills, and 4.64 ± 0.38 for total satisfaction.
The physicians and nurses used their EHR system extensively during the visits as delineated by the number of clicks and scrolls on the computer. The average number of clicks and scrolls was 192, with a maximum of 685 clicks and scrolls during one visit. The average visit lasted 30.7 minutes, and on average the clinician spent 12.7 minutes (SD: 8.22 minutes), or an average of about 39.4% of total visit time, viewing or working on the EHR; an average of 10.8 minutes (SD: 5.63 minutes), or an average of about 36.3% of total visit time, was spent interacting with the patient (TABLE 3).
Without adjusting for visit length, patient satisfaction with the clinicians’ patientcentered communication (beta=0.02; P=.02) and total satisfaction (beta=0.014; P=.027) were significantly associated with clinicians’ gaze time at the patient; more clinician gaze time at the patient resulted in greater patient satisfaction (TABLE 4). Adding visit length to the above models had no significant effect (P>.10); therefore, we did not include it in the models.
Patient satisfaction with clinicians’ interpersonal skills was positively associated with gaze time at the patient (beta=0.013, P =.017) without adjusting for visit length. Since the normal assumption of residuals was not plausible based on a normal probability plot, we also assessed the association by dichotomizing the score (5=very satisfied vs <5=not very satisfied) and this significance disappeared. This association was not significant while controlling for visit length.
The percentage of gaze time at the patient (the fraction of patient gaze time over the entire visit) was not significantly associated with patient-centered communication (beta=0.483, P=.12, TABLE 4) when not adjusted for visit length. After adjusting for visit length (P=.052), the association became significant (beta=0.628, P=.033); thus, the higher percentage of time the clinician spent interacting with the patient, the more satisfied the patient was.
DISCUSSION
In this study, patients were highly satisfied with their clinicians despite often high usage of the EHR. Gadd and Penrod11 reported that patients perceived no impact on communication or eye contact with the clinician despite the initiation of an EHR system in 6 large academic medical practices. Another study demonstrated no significant differences in patient satisfaction with their physicians when comparing patients whose physicians used a paper charting system with those who used an EHR system.14
The fact that patients demonstrated high levels of satisfaction with patient-clinician communication even for clinicians with high EHR usage is somewhat surprising. However, Hsu et al15 found patients’ satisfaction with their clinicians’ communication about medical issues and familiarity with them increased 7 months after implementing an EHR system. In a different study that analyzed videotaped interactions between patients and 5 physicians, the patients found it disturbing not knowing what their doctor was doing when he or she worked on the computer, and preferred being able to see the computer screen.16 This study suggests that it’s advisable for clinicians to describe what they are doing when they use the computer, so that patients better understand how this time spent inputting data actually benefits them.
EHRs can be time-consuming. Physicians and nurses in our study interacted with the EHR a great deal during the office visit, as evidenced by the large average number of clicks and scrolls. This finding confirms clinicians’ perceptions of the amount of work the EHR system requires. For example, in a semi-structured interview of physicians regarding their use of a VA EHR system,10 one respondent noted that the reminders in the EHR required hundreds of clicks.
In our study, the average number of clicks and scrolls during the visit was 192, with some clinicians registering hundreds more. In fact, concerns about the time involved in the use of the EHR and about the adequacy of data collection may lead some clinicians who currently don’t have an EHR system to be reluctant to integrate one into their practices.17
Makoul et al18 found that compared with physicians who used a paper chart, physicians who used an EHR system were more active in clarifying information from the patient and encouraging patient questions during visits, although the study found a trend toward less active roles in more patient-centered communication when using an EHR system. This latter finding is similar to the concerns raised in our study.
Clinical and communication skills are factors, too. One study found that compared to patients who were cared for by more experienced physicians, patients seen by residents using EHRs were more likely to feel that the physician spent less time talking with them and examining them; they were also more likely to report that the visit felt less personal.19 Another study found that clinicians with poor baseline communication skills had more difficulties interacting with patients when an EHR system was introduced than those who had better baseline communication skills.20
Training needed to improve communication during EHR use. Research has shown that when used properly and thoughtfully, EHR use can result in greater patient engagement.21 But, as noted above, there are challenges, suggesting a need for training clinicians to more successfully use an EHR system while simultaneously communicating with their patients.
Study limitations. This study was conducted at a single site, using a single EHR system deployed in the VA clinics. We cannot generalize our findings to other sites or types of clinic systems. Other EHR systems may have different functionalities, which may affect the time required to provide the same type of medical care.
In addition, the study involved only 23 physicians and nurses in a single health system. Other clinicians may have patterns different from those we studied, although a wide range of patterns was seen among the participants, as demonstrated by the large variation in the number of clicks and scrolls. Another limitation is that study patients were not randomly selected, but rather referred by the provider, and the visits were not blinded to either the provider or patient. This may cause some selection bias.
In this study of VA clinicians’ EHR use, patients expressed satisfaction with the clinicians’ clinical skills and patient-centered communication when the clinician spent more time and a greater percentage of the visit engaging the patient. EHR systems need to be designed in a clinician-friendly manner that allows for increased time during the interaction for face-to-face communication between the clinician and the patient, and to ease the workload of EHR documentation. In the meantime, clinicians should be trained in how to expedite their use of the EHR during the clinical visit as well as outside of the exam room in order to improve their patients’ satisfaction.
CORRESPONDENCE
Neil J. Farber, MD, University of California, San Diego, 8939 Villa La Jolla Drive, La Jolla, CA 92037; nfarber@ucsd.edu.
1. Virapongse A, Bates DW, Shi P, et al. Electronic health records and malpractice claims in office practice. Arch Intern Med. 2008;168:2362-2367.
2. DesRoches CM, Campbell EG, Rao SR, et al. Electronic health records in ambulatory care—a national survey of physicians. N Engl J Med. 2008;359:50-60.
3. Bates DW, Leape LL, Cullen DJ, et al. Effect of computerized physician order entry and a team intervention on prevention of serious medication errors. JAMA. 1998;280:1311-1316.
4. Chen C, Garrido T, Chock D, et al. The Kaiser Permanente Electronic Health Record: transforming and streamlining modalities of care. Health Aff (Millwood). 2009;28:323-333.
5. Hillestad R, Bigelow J, Bower A, et al. Can electronic medical record systems transform health care? Potential health benefits, savings, and costs. Health Aff (Millwood). 2005;24:1103-1117.
6. Garrison GM, Bernard ME, Rasmussen NH. 21st-century health care: the effect of computer use by physicians on patient satisfaction at a family medicine clinic. Fam Med. 2002;34:362-368.
7. Likourezos A, Chalfin DB, Murphy DG, et al. Physician and nurse satisfaction with an Electronic Medical Record system. J Emerg Med. 2004;27:419-424.
8. Howard J, Clark EC, Friedman A, et al. Electronic health record impact on work burden in small, unaffiliated, community-based primary care practices. J Gen Intern Med. 2013;28:107-113.
9. Baron RJ. What’s keeping us so busy in primary care? A snapshot from one practice. N Engl J Med. 2010;362:1632-1636.
10. Bonner LM, Simons CE, Parker LE, et al. ‘To take care of the patients’: Qualitative analysis of Veterans Health Administration personnel experiences with a clinical informatics system. Implement Sci. 2010;5:63.
11. Gadd CS, Penrod LE. Dichotomy between physicians’ and patients’ attitudes regarding EMR use during outpatient encounters. Proc AMIA Symp. 2000:275-279.
12. Migdal CW, Namavar AA, Mosley VN, et al. Impact of electronic health records on the patient experience in a hospital setting. J Hosp Med. 2014;9:627-633.
13. Asan O, D Smith P, Montague E. More screen time, less face time - implications for EHR design. J Eval Clin Pract. 2014;20:896-901.
14. Legler JD, Oates R. Patients’ reactions to physician use of a computerized medical record system during clinical encounters. J Fam Pract. 1993;37:241-244.
15. Hsu J, Huang J, Fung V, et al. Health information technology and physician-patient interactions: impact of computers on communication during outpatient primary care visits. J Am Med Inform Assoc. 2005;12:474-480.
16. Als AB. The desk-top computer as a magic box: patterns of behaviour connected with the desk-top computer; GPs’ and patients’ perceptions. Fam Pract. 1997;14:17-23.
17. Bates DW. Physicians and ambulatory electronic health records. Health Aff (Millwood). 2005;24:1180-1189.
18. Makoul G, Curry RH, Tang PC. The use of electronic medical records: communication patterns in outpatient encounters. J Am Med Inform Assoc. 2001;8:610-615.
19. Rouf E, Whittle J, Lu N, et al. Computers in the exam room: differences in physician-patient interaction may be due to physician experience. J Gen Intern Med. 2007;22:43-48.
20. Frankel R, Altschuler A, George S, et al. Effects of exam-room computing on clinician-patient communication: a longitudinal qualitative study. J Gen Intern Med. 2005;20:677-682.
21. Asan O, Young HN, Chewning B, et al. How physician electronic health record screen sharing affects patient and doctor nonverbal communication in primary care. Patient Educ Couns. 2015;98:310-316.
1. Virapongse A, Bates DW, Shi P, et al. Electronic health records and malpractice claims in office practice. Arch Intern Med. 2008;168:2362-2367.
2. DesRoches CM, Campbell EG, Rao SR, et al. Electronic health records in ambulatory care—a national survey of physicians. N Engl J Med. 2008;359:50-60.
3. Bates DW, Leape LL, Cullen DJ, et al. Effect of computerized physician order entry and a team intervention on prevention of serious medication errors. JAMA. 1998;280:1311-1316.
4. Chen C, Garrido T, Chock D, et al. The Kaiser Permanente Electronic Health Record: transforming and streamlining modalities of care. Health Aff (Millwood). 2009;28:323-333.
5. Hillestad R, Bigelow J, Bower A, et al. Can electronic medical record systems transform health care? Potential health benefits, savings, and costs. Health Aff (Millwood). 2005;24:1103-1117.
6. Garrison GM, Bernard ME, Rasmussen NH. 21st-century health care: the effect of computer use by physicians on patient satisfaction at a family medicine clinic. Fam Med. 2002;34:362-368.
7. Likourezos A, Chalfin DB, Murphy DG, et al. Physician and nurse satisfaction with an Electronic Medical Record system. J Emerg Med. 2004;27:419-424.
8. Howard J, Clark EC, Friedman A, et al. Electronic health record impact on work burden in small, unaffiliated, community-based primary care practices. J Gen Intern Med. 2013;28:107-113.
9. Baron RJ. What’s keeping us so busy in primary care? A snapshot from one practice. N Engl J Med. 2010;362:1632-1636.
10. Bonner LM, Simons CE, Parker LE, et al. ‘To take care of the patients’: Qualitative analysis of Veterans Health Administration personnel experiences with a clinical informatics system. Implement Sci. 2010;5:63.
11. Gadd CS, Penrod LE. Dichotomy between physicians’ and patients’ attitudes regarding EMR use during outpatient encounters. Proc AMIA Symp. 2000:275-279.
12. Migdal CW, Namavar AA, Mosley VN, et al. Impact of electronic health records on the patient experience in a hospital setting. J Hosp Med. 2014;9:627-633.
13. Asan O, D Smith P, Montague E. More screen time, less face time - implications for EHR design. J Eval Clin Pract. 2014;20:896-901.
14. Legler JD, Oates R. Patients’ reactions to physician use of a computerized medical record system during clinical encounters. J Fam Pract. 1993;37:241-244.
15. Hsu J, Huang J, Fung V, et al. Health information technology and physician-patient interactions: impact of computers on communication during outpatient primary care visits. J Am Med Inform Assoc. 2005;12:474-480.
16. Als AB. The desk-top computer as a magic box: patterns of behaviour connected with the desk-top computer; GPs’ and patients’ perceptions. Fam Pract. 1997;14:17-23.
17. Bates DW. Physicians and ambulatory electronic health records. Health Aff (Millwood). 2005;24:1180-1189.
18. Makoul G, Curry RH, Tang PC. The use of electronic medical records: communication patterns in outpatient encounters. J Am Med Inform Assoc. 2001;8:610-615.
19. Rouf E, Whittle J, Lu N, et al. Computers in the exam room: differences in physician-patient interaction may be due to physician experience. J Gen Intern Med. 2007;22:43-48.
20. Frankel R, Altschuler A, George S, et al. Effects of exam-room computing on clinician-patient communication: a longitudinal qualitative study. J Gen Intern Med. 2005;20:677-682.
21. Asan O, Young HN, Chewning B, et al. How physician electronic health record screen sharing affects patient and doctor nonverbal communication in primary care. Patient Educ Couns. 2015;98:310-316.
Test your skills: Which imaging studies would you order for these neurologic complaints?
› Use clinical decision tools and American College of Radiology Appropriateness Criteria to determine levels of evidence for ordering specific imaging studies. A
› Consider ordering an imaging study when headache is accompanied by a new neurologic symptom. Computed tomography (CT) without contrast is best for patients who are acutely ill. In the non-emergent setting, magnetic resonance imaging (MRI) with contrast is the optimal study. A
› Order structural neuroimaging as part of the initial work-up of suspected dementia. MRI is the test of choice. A
Strength of recommendation (SOR)
A Good-quality patient-oriented evidence
B Inconsistent or limited-quality patient-oriented evidence
C Consensus, usual practice, opinion, disease-oriented evidence, case series
When patients present with neurologic complaints in outpatient primary care practice, 2 key questions often arise: Should brain imaging be ordered, and if so, which study? Careful history-taking and physical exam findings can suggest differential diagnoses and help determine whether imaging studies could identify potential underlying causes. Further considerations in making a decision are the type of information each modality offers, the possible need for contrast media, benefits vs radiation exposure risks, potential contraindications, and cost and local availability. In this article, we present 3 common outpatient scenarios, and in each case we describe the evidence to support clinical decision-making about imaging.
The American College of Radiology (ACR) Appropriateness Criteria Web site (http://www.acr.org/Quality-Safety/Appropriateness-Criteria) provides radiation exposure information, numerical ratings of imaging studies for individual clinical scenarios, evidence tables, and reference tables for each of its recommendations.1 ACR’s recommendations were developed by expert panels of diagnostic radiologists, interventional radiologists, and radiation oncologists, and designed to help physicians order the most appropriate imaging studies based on patients’ clinical conditions.2 We used these criteria to develop an evaluation strategy for each of our clinical scenarios.
CASE 1 › Carrie D is a 45-year-old woman with a history of migraine without aura generally controlled with Excedrin (acetaminophen, aspirin, and caffeine). She arrives at your office with a 2-day history of severe headache over the top of her head and associated tingling sensation over the left side of her face, but with no vision changes, weakness, or slurred speech. She denies any prior history of numbness or tinging with past headaches. She is a business executive and reports that in the last few weeks, her company has been involved in a high-profile merger. On physical exam, her vital signs are within normal limits. She does not appear acutely ill, but on exam she reports diminished sensation to light touch over the left side of her face, left arm, and left leg compared with the right side.
›› What imaging options might you consider?
A prospective review of physicians in an ambulatory family practice setting found that neurologic imaging was typically ordered for patients with headache who were suspected of having a brain tumor or subarachnoid hemorrhage.3 For our patient, who has a history of migraines without aura and whose current severe headache is accompanied by an abnormal sensation on one side of the face, the following questions are relevant: Is this presentation part of her primary headache syndrome or could there be a different cause? If there is a different cause, is it likely to be detected with brain imaging such as computed tomography (CT) or magnetic resonance imaging (MRI)?
Patients with isolated headache and an absence of neurologic symptoms or abnormalities on neurologic exam are unlikely to have a clinically significant intracranial abnormality.4-10 Imaging of the brain is typically not indicated for these patients.2 However, given that this patient does have a positive focal neurologic finding, a CT or MRI is indicated, as findings are more likely to influence management decisions.
The decision to order CT or MRI should be based on how acutely ill the patient is. CT without contrast is an excellent tool to rule out suspected emergent intracranial abnormalities such as an intracranial hemorrhage, hydrocephalus, or a mass.11 In patients presenting with symptoms suggesting acute illness such as carotid or vertebral artery dissection, the most appropriate test would be CT angiography of the head and neck.2
However, the list of less dire causes of headache is vast. Included in this list would be trauma, other vascular disorders such as arteriovenous malformation or temporal arteritis, infection, abnormal intracranial pressure (mass, pseudotumor cerebri, intracranial hypotension), and disorders of the head/face/spine (eg, temporomandibular joint disorder).12
In the non-acute setting where a patient has stable vital signs and is not in acute distress, an MRI with contrast would be the most appropriate test to identify such causes. Avoid contrast only if there is a firm contraindication, such as pregnancy, severely impaired renal function, or known allergy to gadolinium. If history and physical exam findings suggest possible stroke, arrange for MRI and MR angiography with contrast, even if the result of a head CT scan is negative. The ALGORITHM13 offers guidance for choosing imaging studies for headache based on history, physical exam, and laboratory findings.
›› And you order...
…an MRI of the brain with contrast.
Though Ms. D does have a focal neurologic finding in addition to her headache, she does not appear to be acutely ill. Ordering an MRI with contrast is the best first step.
CASE 2 › Anne B is a 72-year-old woman with a history of hypertension, hyperlipidemia, and type 2 diabetes. Her daughter brings her in to see you because she is concerned about Ms. B’s memory. Ms. B’s daughter reports that she has become increasingly forgetful over the past 6 months, often forgetting recent events. At first the forgetfulness was occasional, but now it seems to happen daily and interfere with activities of daily living (ADLs). The week before this visit, Ms. B left a pot heating on the stove because she forgot she had started cooking. She realized what had happened only when her smoke alarm went off. Ms. B’s daughter also thinks her mother may be taking some of her medications incorrectly.
Physical exam and laboratory findings are unremarkable. On the mental status exam, Ms. B has difficulty with registration and recall.
›› What imaging options might you consider?
Ms. B has exhibited progressive memory loss over 6 months and it is now affecting her ADLs. Her symptoms could be secondary to any one of many reversible medical causes, such as adverse medication effects, depression, or vitamin B12 deficiency. If clinical and laboratory evaluations exclude these reversible causes, consider dementia.
With numerous disorders having overlapping symptoms, the diagnosis of degenerative central nervous system (CNS) disease can be extremely tricky. Complicating the issue is the fact that a single patient can have 2 or more concurrent neurodegenerative diseases. Clinical testing is essential in the diagnosis and management of degenerative CNS diseases, but testing sensitivity and specificity are highly variable depending upon the disease.14
Neuroimaging is an important supplement to clinical testing in excluding intracranial abnormalities. There are significant negative consequences of missing reversible causes of memory problems and incorrectly assigning a clinical diagnosis of dementia. Neuroimaging can be subdivided into structural and functional imaging, and structural imaging is the first step in evaluation.15
The American Academy of Neurology recommends the use of structural neuroimaging with CT or MRI in the initial evaluation of patients with dementia to detect such treatable problems as a subdural hematoma, frontal lobe mass, or hydrocephalus.12 Structural imaging may also identify anatomic changes characteristic of degenerative CNS diseases such as Alzheimer’s disease, dementia with Lewy bodies, frontotemporal dementia, vascular dementia, Creutzfeldt-Jakob disease, and Huntington’s disease; however, sensitivities and specificities of testing are low.14
›› And you order...
…an MRI of the brain without contrast.
In Ms. B’s case, structural neuroimaging is indicated as part of the initial work-up of supposed dementia. An MRI without contrast is recommended over CT because it is more sensitive in detecting white matter changes in vascular dementia.16 In cases where an MRI >is unavailable or contraindicated (eg, a patient with a pacemaker), a CT is a reasonable alternative.
CASE 3 › Bob C is a 78-year-old man with a history of chronic obstructive pulmonary disease and hypertension who arrives at your walk-in clinic accompanied by his home health aide a few hours after having tripped and fallen over a rug at home. At baseline, Mr. C is ambulatory and independent in ADLs.
He takes all of his medications, including a daily baby aspirin (81 mg). Mr. C says he did not lose consciousness at the time of the fall and insists he feels fine, but you notice a bruise developing over his right temporal skull.
›› What imaging options might you consider?
With acute head trauma deemed severe enough clinically to warrant imaging, non-contrast CT is the most appropriate initial test to identify possible intracranial hemorrhage.11 The Glasgow Coma Scale (GCS) is the tool most widely used for clinical evaluation17 (TABLE 118). The score is based on an assessment of 3 features: eye response, speech, and movement. Head injury is classified as mild (13-15), moderate (9-12), or severe (≤8). It is universally agreed that patients with moderate or severe head injury should be further evaluated with a head CT.
With mild head injury, recommendations for follow-up are less straightforward. The New Orleans Criteria (NOC) and Canadian CT Head Rule (CCHR) are commonly used in triaging patients with minor head trauma in a cost effective way11 (TABLES 219 and 320). The cost-effectiveness of these assessment tools is still questionable, but both have very high sensitivity for identifying patients who will require neurosurgery intervention.21,22 Although the NOC is slightly more sensitive at identifying patients with nonsurgical clinically significant abnormalities, it has a greatly reduced specificity compared with the CCHR.23-25
›› And you order...
…a non-contrast head CT.
Mr. C presents with a GCS of 15, indicating mild head trauma. However, in elderly patients, especially ones taking anticoagulation medication, even mild trauma can result in clinically significant abnormalities such as a subdural hematoma.1 Although Mr. C’s physical and neurologic exams are not worrisome, both the NOC and CCHR recommend further evaluation with a non-contrast head CT based on his age.
CORRESPONDENCE
Urmi A. Desai, MD, MS, Columbia University Medical Center, 610 West 158th Street, New York, NY 10032; uad2101@columbia.edu.
1. American College of Radiology. Appropriateness criteria. American College of Radiology Web site. Available at: https://acsearch.acr.org/list. Accessed January 4, 2015.
2. American College of Radiology. About the ACR appropriateness criteria. American College of Radiology Web site. Available at: http://www.acr.org/Quality-Safety/Appropriateness-Criteria/About-AC. Accessed July 20, 2015.
3. Becker LA, Green LA, Beaufait D, et al. Use of CT scans for the investigation of headache: a report from ASPN, Part 1. J Fam Pract. 1993;37:129-134.
4. Sandrini G, Friberg L, Jänig W, et al. Neurophysiological tests and neuroimaging procedures in non-acute headache: guidelines and recommendations. Eur J Neurol. 2004;11:217-224.
5. Sempere AP, Porta-Etessam J, Medrano V, et al. Neuroimaging in the evaluation of patients with non-acute headache. Cephalalgia. 2005;25:30-35.
6. Gilbert JW, Johnson KM, Larkin GL, et al. Atraumatic headache in US emergency departments: recent trends in CT/MRI utilisation and factors associated with severe intracranial pathology. Emerg Med J. 2012;29:576-581.
7. Tsushima Y, Endo K. MR imaging in the evaluation of chronic or recurrent headache. Radiology. 2005;235:575-579.
8. Jordan JE, Ramirez GF, Bradley WG, et al. Economic and outcomes assessment of magnetic resonance imaging in the evaluation of headache. J Natl Med Assoc. 2000;92:573-578.
9. Mitchell CS, Osborn RE, Grosskreutz SR. Computed tomography in the headache patient: is routine evaluation really necessary? Headache. 1993;33:82-86.
10. Frishberg BM. The utility of neuroimaging in the evaluation of headache in patients with normal neurologic examinations. Neurology. 1994;44:1191-1197.
11. Osborn AG. Osborn’s Brain: Imaging, Pathology, and Anatomy. Salt Lake City, Utah: Amirsys Publishing; 2013.
12. Silberstein SD. Chronic daily headache. J Am Osteopath Assoc. 2005;105:23S-29S.
13. Douglas AC, Wippold FJ 2nd, Broderick DF, et al. ACR Appropriateness Criteria Headache. J Am Coll Radiol. 2014;11:657-667.
14. Knopman DS, DeKosky ST, Cummings JL, et al. Practice parameter: diagnosis of dementia (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2001;56:1143-1153.
15. Wippold FJ 2nd, Brown DC, Broderick DF, et al. ACR Appropriateness Criteria Dementia and Movement Disorders. J Am Coll Radiol. 2015;12:19-28.
16. Kantarci K, Jack CR Jr. Neuroimaging in Alzheimer disease: an evidence-based review. Neuroimaging Clin N Am. 2003;13:197-209.
17. Teasdale G, Maas A, Lecky F, et al. The Glasgow Coma Scale at 40 years: standing the test of time. Lancet Neurol. 2014;13:844-854.
18. Teasdale G, Jennett B. Assessment of coma and impaired consciousness. A practical scale. Lancet. 1974;2:81-84.
19. Haydel MJ, Preston CA, Mills TJ, et al. Indications for computed tomography in patients with minor head injury. N Engl J Med. 2000;343:100-105.
20. Stiell IG, Wells GA, Vandemheen K, et al. The Canadian CT Head Rule for patients with minor head injury. Lancet. 2001;357:1391-1396.
21. Davis PC, Drayer BP, Anderson RE, et al. Head trauma. American College of Radiology. ACR Appropriateness Criteria. Radiology. 2000;215 Suppl:507-524.
22. Stiell IG, Clement CM, Grimshaw JM, et al. A prospective clusterrandomized trial to implement the Canadian CT Head Rule in emergency departments. CMAJ. 2010;182:1527-1532.
23. Smits M, Dippel DW, Nederkoorn PJ, et al. Minor head injury: CT-based strategies for management—a cost-effectiveness analysis. Radiology. 2010;254:532-540.
24. Stiell IG, Clement CM, Rowe BH, et al. Comparison of the Canadian CT Head Rule and the New Orleans Criteria in patients with minor head injury. JAMA. 2005;294:1511-1518.
25. Smits M, Dippel DW, de Haan GG, et al. External validation of the Canadian CT Head Rule and the New Orleans Criteria for CT scanning in patients with minor head injury. JAMA. 2005;294:1519-1525.
› Use clinical decision tools and American College of Radiology Appropriateness Criteria to determine levels of evidence for ordering specific imaging studies. A
› Consider ordering an imaging study when headache is accompanied by a new neurologic symptom. Computed tomography (CT) without contrast is best for patients who are acutely ill. In the non-emergent setting, magnetic resonance imaging (MRI) with contrast is the optimal study. A
› Order structural neuroimaging as part of the initial work-up of suspected dementia. MRI is the test of choice. A
Strength of recommendation (SOR)
A Good-quality patient-oriented evidence
B Inconsistent or limited-quality patient-oriented evidence
C Consensus, usual practice, opinion, disease-oriented evidence, case series
When patients present with neurologic complaints in outpatient primary care practice, 2 key questions often arise: Should brain imaging be ordered, and if so, which study? Careful history-taking and physical exam findings can suggest differential diagnoses and help determine whether imaging studies could identify potential underlying causes. Further considerations in making a decision are the type of information each modality offers, the possible need for contrast media, benefits vs radiation exposure risks, potential contraindications, and cost and local availability. In this article, we present 3 common outpatient scenarios, and in each case we describe the evidence to support clinical decision-making about imaging.
The American College of Radiology (ACR) Appropriateness Criteria Web site (http://www.acr.org/Quality-Safety/Appropriateness-Criteria) provides radiation exposure information, numerical ratings of imaging studies for individual clinical scenarios, evidence tables, and reference tables for each of its recommendations.1 ACR’s recommendations were developed by expert panels of diagnostic radiologists, interventional radiologists, and radiation oncologists, and designed to help physicians order the most appropriate imaging studies based on patients’ clinical conditions.2 We used these criteria to develop an evaluation strategy for each of our clinical scenarios.
CASE 1 › Carrie D is a 45-year-old woman with a history of migraine without aura generally controlled with Excedrin (acetaminophen, aspirin, and caffeine). She arrives at your office with a 2-day history of severe headache over the top of her head and associated tingling sensation over the left side of her face, but with no vision changes, weakness, or slurred speech. She denies any prior history of numbness or tinging with past headaches. She is a business executive and reports that in the last few weeks, her company has been involved in a high-profile merger. On physical exam, her vital signs are within normal limits. She does not appear acutely ill, but on exam she reports diminished sensation to light touch over the left side of her face, left arm, and left leg compared with the right side.
›› What imaging options might you consider?
A prospective review of physicians in an ambulatory family practice setting found that neurologic imaging was typically ordered for patients with headache who were suspected of having a brain tumor or subarachnoid hemorrhage.3 For our patient, who has a history of migraines without aura and whose current severe headache is accompanied by an abnormal sensation on one side of the face, the following questions are relevant: Is this presentation part of her primary headache syndrome or could there be a different cause? If there is a different cause, is it likely to be detected with brain imaging such as computed tomography (CT) or magnetic resonance imaging (MRI)?
Patients with isolated headache and an absence of neurologic symptoms or abnormalities on neurologic exam are unlikely to have a clinically significant intracranial abnormality.4-10 Imaging of the brain is typically not indicated for these patients.2 However, given that this patient does have a positive focal neurologic finding, a CT or MRI is indicated, as findings are more likely to influence management decisions.
The decision to order CT or MRI should be based on how acutely ill the patient is. CT without contrast is an excellent tool to rule out suspected emergent intracranial abnormalities such as an intracranial hemorrhage, hydrocephalus, or a mass.11 In patients presenting with symptoms suggesting acute illness such as carotid or vertebral artery dissection, the most appropriate test would be CT angiography of the head and neck.2
However, the list of less dire causes of headache is vast. Included in this list would be trauma, other vascular disorders such as arteriovenous malformation or temporal arteritis, infection, abnormal intracranial pressure (mass, pseudotumor cerebri, intracranial hypotension), and disorders of the head/face/spine (eg, temporomandibular joint disorder).12
In the non-acute setting where a patient has stable vital signs and is not in acute distress, an MRI with contrast would be the most appropriate test to identify such causes. Avoid contrast only if there is a firm contraindication, such as pregnancy, severely impaired renal function, or known allergy to gadolinium. If history and physical exam findings suggest possible stroke, arrange for MRI and MR angiography with contrast, even if the result of a head CT scan is negative. The ALGORITHM13 offers guidance for choosing imaging studies for headache based on history, physical exam, and laboratory findings.
›› And you order...
…an MRI of the brain with contrast.
Though Ms. D does have a focal neurologic finding in addition to her headache, she does not appear to be acutely ill. Ordering an MRI with contrast is the best first step.
CASE 2 › Anne B is a 72-year-old woman with a history of hypertension, hyperlipidemia, and type 2 diabetes. Her daughter brings her in to see you because she is concerned about Ms. B’s memory. Ms. B’s daughter reports that she has become increasingly forgetful over the past 6 months, often forgetting recent events. At first the forgetfulness was occasional, but now it seems to happen daily and interfere with activities of daily living (ADLs). The week before this visit, Ms. B left a pot heating on the stove because she forgot she had started cooking. She realized what had happened only when her smoke alarm went off. Ms. B’s daughter also thinks her mother may be taking some of her medications incorrectly.
Physical exam and laboratory findings are unremarkable. On the mental status exam, Ms. B has difficulty with registration and recall.
›› What imaging options might you consider?
Ms. B has exhibited progressive memory loss over 6 months and it is now affecting her ADLs. Her symptoms could be secondary to any one of many reversible medical causes, such as adverse medication effects, depression, or vitamin B12 deficiency. If clinical and laboratory evaluations exclude these reversible causes, consider dementia.
With numerous disorders having overlapping symptoms, the diagnosis of degenerative central nervous system (CNS) disease can be extremely tricky. Complicating the issue is the fact that a single patient can have 2 or more concurrent neurodegenerative diseases. Clinical testing is essential in the diagnosis and management of degenerative CNS diseases, but testing sensitivity and specificity are highly variable depending upon the disease.14
Neuroimaging is an important supplement to clinical testing in excluding intracranial abnormalities. There are significant negative consequences of missing reversible causes of memory problems and incorrectly assigning a clinical diagnosis of dementia. Neuroimaging can be subdivided into structural and functional imaging, and structural imaging is the first step in evaluation.15
The American Academy of Neurology recommends the use of structural neuroimaging with CT or MRI in the initial evaluation of patients with dementia to detect such treatable problems as a subdural hematoma, frontal lobe mass, or hydrocephalus.12 Structural imaging may also identify anatomic changes characteristic of degenerative CNS diseases such as Alzheimer’s disease, dementia with Lewy bodies, frontotemporal dementia, vascular dementia, Creutzfeldt-Jakob disease, and Huntington’s disease; however, sensitivities and specificities of testing are low.14
›› And you order...
…an MRI of the brain without contrast.
In Ms. B’s case, structural neuroimaging is indicated as part of the initial work-up of supposed dementia. An MRI without contrast is recommended over CT because it is more sensitive in detecting white matter changes in vascular dementia.16 In cases where an MRI >is unavailable or contraindicated (eg, a patient with a pacemaker), a CT is a reasonable alternative.
CASE 3 › Bob C is a 78-year-old man with a history of chronic obstructive pulmonary disease and hypertension who arrives at your walk-in clinic accompanied by his home health aide a few hours after having tripped and fallen over a rug at home. At baseline, Mr. C is ambulatory and independent in ADLs.
He takes all of his medications, including a daily baby aspirin (81 mg). Mr. C says he did not lose consciousness at the time of the fall and insists he feels fine, but you notice a bruise developing over his right temporal skull.
›› What imaging options might you consider?
With acute head trauma deemed severe enough clinically to warrant imaging, non-contrast CT is the most appropriate initial test to identify possible intracranial hemorrhage.11 The Glasgow Coma Scale (GCS) is the tool most widely used for clinical evaluation17 (TABLE 118). The score is based on an assessment of 3 features: eye response, speech, and movement. Head injury is classified as mild (13-15), moderate (9-12), or severe (≤8). It is universally agreed that patients with moderate or severe head injury should be further evaluated with a head CT.
With mild head injury, recommendations for follow-up are less straightforward. The New Orleans Criteria (NOC) and Canadian CT Head Rule (CCHR) are commonly used in triaging patients with minor head trauma in a cost effective way11 (TABLES 219 and 320). The cost-effectiveness of these assessment tools is still questionable, but both have very high sensitivity for identifying patients who will require neurosurgery intervention.21,22 Although the NOC is slightly more sensitive at identifying patients with nonsurgical clinically significant abnormalities, it has a greatly reduced specificity compared with the CCHR.23-25
›› And you order...
…a non-contrast head CT.
Mr. C presents with a GCS of 15, indicating mild head trauma. However, in elderly patients, especially ones taking anticoagulation medication, even mild trauma can result in clinically significant abnormalities such as a subdural hematoma.1 Although Mr. C’s physical and neurologic exams are not worrisome, both the NOC and CCHR recommend further evaluation with a non-contrast head CT based on his age.
CORRESPONDENCE
Urmi A. Desai, MD, MS, Columbia University Medical Center, 610 West 158th Street, New York, NY 10032; uad2101@columbia.edu.
› Use clinical decision tools and American College of Radiology Appropriateness Criteria to determine levels of evidence for ordering specific imaging studies. A
› Consider ordering an imaging study when headache is accompanied by a new neurologic symptom. Computed tomography (CT) without contrast is best for patients who are acutely ill. In the non-emergent setting, magnetic resonance imaging (MRI) with contrast is the optimal study. A
› Order structural neuroimaging as part of the initial work-up of suspected dementia. MRI is the test of choice. A
Strength of recommendation (SOR)
A Good-quality patient-oriented evidence
B Inconsistent or limited-quality patient-oriented evidence
C Consensus, usual practice, opinion, disease-oriented evidence, case series
When patients present with neurologic complaints in outpatient primary care practice, 2 key questions often arise: Should brain imaging be ordered, and if so, which study? Careful history-taking and physical exam findings can suggest differential diagnoses and help determine whether imaging studies could identify potential underlying causes. Further considerations in making a decision are the type of information each modality offers, the possible need for contrast media, benefits vs radiation exposure risks, potential contraindications, and cost and local availability. In this article, we present 3 common outpatient scenarios, and in each case we describe the evidence to support clinical decision-making about imaging.
The American College of Radiology (ACR) Appropriateness Criteria Web site (http://www.acr.org/Quality-Safety/Appropriateness-Criteria) provides radiation exposure information, numerical ratings of imaging studies for individual clinical scenarios, evidence tables, and reference tables for each of its recommendations.1 ACR’s recommendations were developed by expert panels of diagnostic radiologists, interventional radiologists, and radiation oncologists, and designed to help physicians order the most appropriate imaging studies based on patients’ clinical conditions.2 We used these criteria to develop an evaluation strategy for each of our clinical scenarios.
CASE 1 › Carrie D is a 45-year-old woman with a history of migraine without aura generally controlled with Excedrin (acetaminophen, aspirin, and caffeine). She arrives at your office with a 2-day history of severe headache over the top of her head and associated tingling sensation over the left side of her face, but with no vision changes, weakness, or slurred speech. She denies any prior history of numbness or tinging with past headaches. She is a business executive and reports that in the last few weeks, her company has been involved in a high-profile merger. On physical exam, her vital signs are within normal limits. She does not appear acutely ill, but on exam she reports diminished sensation to light touch over the left side of her face, left arm, and left leg compared with the right side.
›› What imaging options might you consider?
A prospective review of physicians in an ambulatory family practice setting found that neurologic imaging was typically ordered for patients with headache who were suspected of having a brain tumor or subarachnoid hemorrhage.3 For our patient, who has a history of migraines without aura and whose current severe headache is accompanied by an abnormal sensation on one side of the face, the following questions are relevant: Is this presentation part of her primary headache syndrome or could there be a different cause? If there is a different cause, is it likely to be detected with brain imaging such as computed tomography (CT) or magnetic resonance imaging (MRI)?
Patients with isolated headache and an absence of neurologic symptoms or abnormalities on neurologic exam are unlikely to have a clinically significant intracranial abnormality.4-10 Imaging of the brain is typically not indicated for these patients.2 However, given that this patient does have a positive focal neurologic finding, a CT or MRI is indicated, as findings are more likely to influence management decisions.
The decision to order CT or MRI should be based on how acutely ill the patient is. CT without contrast is an excellent tool to rule out suspected emergent intracranial abnormalities such as an intracranial hemorrhage, hydrocephalus, or a mass.11 In patients presenting with symptoms suggesting acute illness such as carotid or vertebral artery dissection, the most appropriate test would be CT angiography of the head and neck.2
However, the list of less dire causes of headache is vast. Included in this list would be trauma, other vascular disorders such as arteriovenous malformation or temporal arteritis, infection, abnormal intracranial pressure (mass, pseudotumor cerebri, intracranial hypotension), and disorders of the head/face/spine (eg, temporomandibular joint disorder).12
In the non-acute setting where a patient has stable vital signs and is not in acute distress, an MRI with contrast would be the most appropriate test to identify such causes. Avoid contrast only if there is a firm contraindication, such as pregnancy, severely impaired renal function, or known allergy to gadolinium. If history and physical exam findings suggest possible stroke, arrange for MRI and MR angiography with contrast, even if the result of a head CT scan is negative. The ALGORITHM13 offers guidance for choosing imaging studies for headache based on history, physical exam, and laboratory findings.
›› And you order...
…an MRI of the brain with contrast.
Though Ms. D does have a focal neurologic finding in addition to her headache, she does not appear to be acutely ill. Ordering an MRI with contrast is the best first step.
CASE 2 › Anne B is a 72-year-old woman with a history of hypertension, hyperlipidemia, and type 2 diabetes. Her daughter brings her in to see you because she is concerned about Ms. B’s memory. Ms. B’s daughter reports that she has become increasingly forgetful over the past 6 months, often forgetting recent events. At first the forgetfulness was occasional, but now it seems to happen daily and interfere with activities of daily living (ADLs). The week before this visit, Ms. B left a pot heating on the stove because she forgot she had started cooking. She realized what had happened only when her smoke alarm went off. Ms. B’s daughter also thinks her mother may be taking some of her medications incorrectly.
Physical exam and laboratory findings are unremarkable. On the mental status exam, Ms. B has difficulty with registration and recall.
›› What imaging options might you consider?
Ms. B has exhibited progressive memory loss over 6 months and it is now affecting her ADLs. Her symptoms could be secondary to any one of many reversible medical causes, such as adverse medication effects, depression, or vitamin B12 deficiency. If clinical and laboratory evaluations exclude these reversible causes, consider dementia.
With numerous disorders having overlapping symptoms, the diagnosis of degenerative central nervous system (CNS) disease can be extremely tricky. Complicating the issue is the fact that a single patient can have 2 or more concurrent neurodegenerative diseases. Clinical testing is essential in the diagnosis and management of degenerative CNS diseases, but testing sensitivity and specificity are highly variable depending upon the disease.14
Neuroimaging is an important supplement to clinical testing in excluding intracranial abnormalities. There are significant negative consequences of missing reversible causes of memory problems and incorrectly assigning a clinical diagnosis of dementia. Neuroimaging can be subdivided into structural and functional imaging, and structural imaging is the first step in evaluation.15
The American Academy of Neurology recommends the use of structural neuroimaging with CT or MRI in the initial evaluation of patients with dementia to detect such treatable problems as a subdural hematoma, frontal lobe mass, or hydrocephalus.12 Structural imaging may also identify anatomic changes characteristic of degenerative CNS diseases such as Alzheimer’s disease, dementia with Lewy bodies, frontotemporal dementia, vascular dementia, Creutzfeldt-Jakob disease, and Huntington’s disease; however, sensitivities and specificities of testing are low.14
›› And you order...
…an MRI of the brain without contrast.
In Ms. B’s case, structural neuroimaging is indicated as part of the initial work-up of supposed dementia. An MRI without contrast is recommended over CT because it is more sensitive in detecting white matter changes in vascular dementia.16 In cases where an MRI >is unavailable or contraindicated (eg, a patient with a pacemaker), a CT is a reasonable alternative.
CASE 3 › Bob C is a 78-year-old man with a history of chronic obstructive pulmonary disease and hypertension who arrives at your walk-in clinic accompanied by his home health aide a few hours after having tripped and fallen over a rug at home. At baseline, Mr. C is ambulatory and independent in ADLs.
He takes all of his medications, including a daily baby aspirin (81 mg). Mr. C says he did not lose consciousness at the time of the fall and insists he feels fine, but you notice a bruise developing over his right temporal skull.
›› What imaging options might you consider?
With acute head trauma deemed severe enough clinically to warrant imaging, non-contrast CT is the most appropriate initial test to identify possible intracranial hemorrhage.11 The Glasgow Coma Scale (GCS) is the tool most widely used for clinical evaluation17 (TABLE 118). The score is based on an assessment of 3 features: eye response, speech, and movement. Head injury is classified as mild (13-15), moderate (9-12), or severe (≤8). It is universally agreed that patients with moderate or severe head injury should be further evaluated with a head CT.
With mild head injury, recommendations for follow-up are less straightforward. The New Orleans Criteria (NOC) and Canadian CT Head Rule (CCHR) are commonly used in triaging patients with minor head trauma in a cost effective way11 (TABLES 219 and 320). The cost-effectiveness of these assessment tools is still questionable, but both have very high sensitivity for identifying patients who will require neurosurgery intervention.21,22 Although the NOC is slightly more sensitive at identifying patients with nonsurgical clinically significant abnormalities, it has a greatly reduced specificity compared with the CCHR.23-25
›› And you order...
…a non-contrast head CT.
Mr. C presents with a GCS of 15, indicating mild head trauma. However, in elderly patients, especially ones taking anticoagulation medication, even mild trauma can result in clinically significant abnormalities such as a subdural hematoma.1 Although Mr. C’s physical and neurologic exams are not worrisome, both the NOC and CCHR recommend further evaluation with a non-contrast head CT based on his age.
CORRESPONDENCE
Urmi A. Desai, MD, MS, Columbia University Medical Center, 610 West 158th Street, New York, NY 10032; uad2101@columbia.edu.
1. American College of Radiology. Appropriateness criteria. American College of Radiology Web site. Available at: https://acsearch.acr.org/list. Accessed January 4, 2015.
2. American College of Radiology. About the ACR appropriateness criteria. American College of Radiology Web site. Available at: http://www.acr.org/Quality-Safety/Appropriateness-Criteria/About-AC. Accessed July 20, 2015.
3. Becker LA, Green LA, Beaufait D, et al. Use of CT scans for the investigation of headache: a report from ASPN, Part 1. J Fam Pract. 1993;37:129-134.
4. Sandrini G, Friberg L, Jänig W, et al. Neurophysiological tests and neuroimaging procedures in non-acute headache: guidelines and recommendations. Eur J Neurol. 2004;11:217-224.
5. Sempere AP, Porta-Etessam J, Medrano V, et al. Neuroimaging in the evaluation of patients with non-acute headache. Cephalalgia. 2005;25:30-35.
6. Gilbert JW, Johnson KM, Larkin GL, et al. Atraumatic headache in US emergency departments: recent trends in CT/MRI utilisation and factors associated with severe intracranial pathology. Emerg Med J. 2012;29:576-581.
7. Tsushima Y, Endo K. MR imaging in the evaluation of chronic or recurrent headache. Radiology. 2005;235:575-579.
8. Jordan JE, Ramirez GF, Bradley WG, et al. Economic and outcomes assessment of magnetic resonance imaging in the evaluation of headache. J Natl Med Assoc. 2000;92:573-578.
9. Mitchell CS, Osborn RE, Grosskreutz SR. Computed tomography in the headache patient: is routine evaluation really necessary? Headache. 1993;33:82-86.
10. Frishberg BM. The utility of neuroimaging in the evaluation of headache in patients with normal neurologic examinations. Neurology. 1994;44:1191-1197.
11. Osborn AG. Osborn’s Brain: Imaging, Pathology, and Anatomy. Salt Lake City, Utah: Amirsys Publishing; 2013.
12. Silberstein SD. Chronic daily headache. J Am Osteopath Assoc. 2005;105:23S-29S.
13. Douglas AC, Wippold FJ 2nd, Broderick DF, et al. ACR Appropriateness Criteria Headache. J Am Coll Radiol. 2014;11:657-667.
14. Knopman DS, DeKosky ST, Cummings JL, et al. Practice parameter: diagnosis of dementia (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2001;56:1143-1153.
15. Wippold FJ 2nd, Brown DC, Broderick DF, et al. ACR Appropriateness Criteria Dementia and Movement Disorders. J Am Coll Radiol. 2015;12:19-28.
16. Kantarci K, Jack CR Jr. Neuroimaging in Alzheimer disease: an evidence-based review. Neuroimaging Clin N Am. 2003;13:197-209.
17. Teasdale G, Maas A, Lecky F, et al. The Glasgow Coma Scale at 40 years: standing the test of time. Lancet Neurol. 2014;13:844-854.
18. Teasdale G, Jennett B. Assessment of coma and impaired consciousness. A practical scale. Lancet. 1974;2:81-84.
19. Haydel MJ, Preston CA, Mills TJ, et al. Indications for computed tomography in patients with minor head injury. N Engl J Med. 2000;343:100-105.
20. Stiell IG, Wells GA, Vandemheen K, et al. The Canadian CT Head Rule for patients with minor head injury. Lancet. 2001;357:1391-1396.
21. Davis PC, Drayer BP, Anderson RE, et al. Head trauma. American College of Radiology. ACR Appropriateness Criteria. Radiology. 2000;215 Suppl:507-524.
22. Stiell IG, Clement CM, Grimshaw JM, et al. A prospective clusterrandomized trial to implement the Canadian CT Head Rule in emergency departments. CMAJ. 2010;182:1527-1532.
23. Smits M, Dippel DW, Nederkoorn PJ, et al. Minor head injury: CT-based strategies for management—a cost-effectiveness analysis. Radiology. 2010;254:532-540.
24. Stiell IG, Clement CM, Rowe BH, et al. Comparison of the Canadian CT Head Rule and the New Orleans Criteria in patients with minor head injury. JAMA. 2005;294:1511-1518.
25. Smits M, Dippel DW, de Haan GG, et al. External validation of the Canadian CT Head Rule and the New Orleans Criteria for CT scanning in patients with minor head injury. JAMA. 2005;294:1519-1525.
1. American College of Radiology. Appropriateness criteria. American College of Radiology Web site. Available at: https://acsearch.acr.org/list. Accessed January 4, 2015.
2. American College of Radiology. About the ACR appropriateness criteria. American College of Radiology Web site. Available at: http://www.acr.org/Quality-Safety/Appropriateness-Criteria/About-AC. Accessed July 20, 2015.
3. Becker LA, Green LA, Beaufait D, et al. Use of CT scans for the investigation of headache: a report from ASPN, Part 1. J Fam Pract. 1993;37:129-134.
4. Sandrini G, Friberg L, Jänig W, et al. Neurophysiological tests and neuroimaging procedures in non-acute headache: guidelines and recommendations. Eur J Neurol. 2004;11:217-224.
5. Sempere AP, Porta-Etessam J, Medrano V, et al. Neuroimaging in the evaluation of patients with non-acute headache. Cephalalgia. 2005;25:30-35.
6. Gilbert JW, Johnson KM, Larkin GL, et al. Atraumatic headache in US emergency departments: recent trends in CT/MRI utilisation and factors associated with severe intracranial pathology. Emerg Med J. 2012;29:576-581.
7. Tsushima Y, Endo K. MR imaging in the evaluation of chronic or recurrent headache. Radiology. 2005;235:575-579.
8. Jordan JE, Ramirez GF, Bradley WG, et al. Economic and outcomes assessment of magnetic resonance imaging in the evaluation of headache. J Natl Med Assoc. 2000;92:573-578.
9. Mitchell CS, Osborn RE, Grosskreutz SR. Computed tomography in the headache patient: is routine evaluation really necessary? Headache. 1993;33:82-86.
10. Frishberg BM. The utility of neuroimaging in the evaluation of headache in patients with normal neurologic examinations. Neurology. 1994;44:1191-1197.
11. Osborn AG. Osborn’s Brain: Imaging, Pathology, and Anatomy. Salt Lake City, Utah: Amirsys Publishing; 2013.
12. Silberstein SD. Chronic daily headache. J Am Osteopath Assoc. 2005;105:23S-29S.
13. Douglas AC, Wippold FJ 2nd, Broderick DF, et al. ACR Appropriateness Criteria Headache. J Am Coll Radiol. 2014;11:657-667.
14. Knopman DS, DeKosky ST, Cummings JL, et al. Practice parameter: diagnosis of dementia (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2001;56:1143-1153.
15. Wippold FJ 2nd, Brown DC, Broderick DF, et al. ACR Appropriateness Criteria Dementia and Movement Disorders. J Am Coll Radiol. 2015;12:19-28.
16. Kantarci K, Jack CR Jr. Neuroimaging in Alzheimer disease: an evidence-based review. Neuroimaging Clin N Am. 2003;13:197-209.
17. Teasdale G, Maas A, Lecky F, et al. The Glasgow Coma Scale at 40 years: standing the test of time. Lancet Neurol. 2014;13:844-854.
18. Teasdale G, Jennett B. Assessment of coma and impaired consciousness. A practical scale. Lancet. 1974;2:81-84.
19. Haydel MJ, Preston CA, Mills TJ, et al. Indications for computed tomography in patients with minor head injury. N Engl J Med. 2000;343:100-105.
20. Stiell IG, Wells GA, Vandemheen K, et al. The Canadian CT Head Rule for patients with minor head injury. Lancet. 2001;357:1391-1396.
21. Davis PC, Drayer BP, Anderson RE, et al. Head trauma. American College of Radiology. ACR Appropriateness Criteria. Radiology. 2000;215 Suppl:507-524.
22. Stiell IG, Clement CM, Grimshaw JM, et al. A prospective clusterrandomized trial to implement the Canadian CT Head Rule in emergency departments. CMAJ. 2010;182:1527-1532.
23. Smits M, Dippel DW, Nederkoorn PJ, et al. Minor head injury: CT-based strategies for management—a cost-effectiveness analysis. Radiology. 2010;254:532-540.
24. Stiell IG, Clement CM, Rowe BH, et al. Comparison of the Canadian CT Head Rule and the New Orleans Criteria in patients with minor head injury. JAMA. 2005;294:1511-1518.
25. Smits M, Dippel DW, de Haan GG, et al. External validation of the Canadian CT Head Rule and the New Orleans Criteria for CT scanning in patients with minor head injury. JAMA. 2005;294:1519-1525.
Fever • eschars on right leg and groin • inguinal lymphadenopathy • Dx?
THE CASE
A 76-year-old man with a history of coronary artery disease presented with a fever, headache, and malaise one week after returning from a big game hunting trip in South Africa. Five days after his return, he noticed lesions on his right leg that eventually scabbed over. He sought care at his local emergency department and with his primary care physician, and completed an empiric trial of azithromycin. His symptoms, however, persisted and he was referred to our institution for evaluation and treatment.
On exam, he had a temperature of 100.5° F, inguinal lymphadenopathy, and 2 eschars: a 1.5 cm one on his right groin and an identical one on the medial aspect of the right popliteal fossa (FIGURE 1).
THE DIAGNOSIS
Laboratory studies showed a white blood cell count of 3000/mcL, hemoglobin of 14.1 g/dL, and platelet count of 142,000/mcL; peripheral blood smear was normal. Blood and urine cultures showed no growth. A malaria smear and antibodies for Lyme disease, dengue fever, Chikungunya virus, and Q fever were also negative. A biopsy of the eschar demonstrated epidermal and dermal necrosis consistent with infectious vasculitis caused by rickettsial disease (FIGURE 2). A polymerase chain reaction (PCR) for the spotted fever group (R rickettsii, R akari, and R conorii) and typhus fever group of rickettsial agents (R typhi and R prowazekii) were negative. However, a PCR was positive for R africae, confirming the diagnosis of African tick-bite fever (ATBF).
DISCUSSION
Two common reasons patients returning from international travel seek medical attention are fever and rash.1 Initial assessment should include a detailed travel history of urban and rural exposures and any possible exposure to ticks or fleas. The time course of symptoms is important because some tropical infections can have long incubation periods.2
Rickettsial diseases are the most common febrile illness in patients returning from international travel.1 ATBF caused by R africae is the most common rickettsiosis among returning travelers1 and may be the most widespread of all spotted fever group rickettsiae that are known to be pathogenic to humans.3R africae is endemic to South Africa. The risk of contracting R africae is 4 to 5 times higher than the risk of contracting malaria in South Africa.1
R africae is transmitted through cattle and game ticks (Amblyomma species),1-7 and tends to cause mild illness with rare progression to complicated disease.3 The risk of infection is particularly high from November to April,7 and our patient had traveled during April.
Most patients with ATBF present with fever, headache, and malaise, and 50% develop a variable rash.1,2 Local lymphadenopathy often develops, and marked neck stiffness can occur.2 An eschar is present in 95% of cases.2 The finding of an eschar is often indicative of rickettsial infection; however, not all rickettsioses show eschars, and the absence of an eschar does not exclude rickettsial infection.1
ATBF is usually benign and self-limiting, and no fatalities have been reported.2,4,8 Complications such as peripheral nerve involvement, encephalitis, and myocarditis are rare.5,8 Since rickettsial diseases may be more severe in elderly patients with underlying diseases, empiric treatment with inpatient monitoring is justifiable.5
Don’t wait for lab confirmation to begin antibiotics
Laboratory findings in a patient with ATBF include pancytopenia, elevated serum C-reactive protein, and abnormal liver function tests.2,4 A blood PCR detects R africae,1,3 and if a rash or eschar is present, a biopsy can confirm the diagnosis.1 However, confirming the diagnosis is difficult if seroconversion has not occurred and PCR is not readily available.1 Also, antibodies may not be detected in patients who have a mild case of ATBF or those who are immunocompromised.5
If you suspect your patient has ATBF, don’t wait for laboratory confirmation; instead, initiate empiric treatment with doxycycline 100 mg bid twice daily for 5 to 7 days.1,2,4
Preventive measures include repellant lotions, clothing, and gear
Since there are no vaccines or prophylactic treatments for ATBF, counsel travelers on preventive measures.9 Instruct patients who plan to visit an endemic area such as sub-Saharan Africa or the West Indies to wear long-sleeved shirts, long pants, and hats. Individuals should also tuck their shirts into their pants and their pants into socks, as well as wear closed-toe shoes. When possible, it’s advisable to avoid woody and brushy areas.
Over-the-counter repellant lotions that contain ≥20% DEET are effective at preventing tick bites for several hours after an application, but should be reapplied as directed.9 These lotions should be applied after sunscreen. Advise patients that they can purchase clothing and gear that have been treated with the pesticide permethrin, or they can treat clothing and gear themselves. Explain, however, that permethrin should not be applied directly to skin.
Finally, instruct travelers to perform daily tick inspections and shower or bathe as soon as possible after returning from the outdoors.9 Educate patients on the proper technique for tick removal, which is described on the Centers for Disease Control and Prevention’s Web site at http://www.cdc.gov/ticks/removing_a_tick.html.
Our patient completed a 2-week course of doxycycline 100 mg bid. His symptoms and laboratory abnormalities completely resolved.
THE TAKEAWAY
ATBF is the most common rickettsiosis among patients returning from international travel. Because patients may present with several nonspecific symptoms, maintain a high index of suspicion for rickettsial infection among patients returning from sub-Saharan Africa or the West Indies. Though the disease usually can be successfully managed in the outpatient setting with doxycycline, elderly patients or those with comorbid conditions may require inpatient care. Educate patients who plan to travel to an endemic area about measures they can take to prevent exposure to ticks and subsequent infection.
1. Neumayr A, Hatz C, Blum J. Not to be missed! Differential diagnoses of common dermatological problems in returning travellers. Travel Med Infect Dis. 2013;11:337-349.
2. Yates J, Smith P. Fever and rash. Medicine. 2014;42:96-99.
3. Jensenius M, Fournier PE, Kelly P, et al. African tick bite fever. Lancet Infect Dis. 2003;3:557-564.
4. Frean J, Blumberg L, Ogunbanjo GA. Tick bite fever in South Africa. S Afr Fam Pract. 2008;50:33-35.
5. Roch N, Epaulard O, Pelloux I, et al. African tick bite fever in elderly patients: 8 cases in French tourists returning from South Africa. Clin Infect Dis. 2008;47:e28-e35.
6. Caruso G, Zasio C, Guzzo F, et al. Outbreak of African tick-bite fever in six Italian tourists returning from South Africa. Eur J Clin Microbiol Infect Dis. 2002;21:133-136.
7. Tsai YS, Wu YH, Kao PT, et al. African tick bite fever. J Formos Med Assoc. 2008;107:73-76.
8. Jensenius M, Fournier PE, Fladby T, et al. Sub-acute neuropathy in patients with African tick bite fever. Scand J Infect Dis. 2006;38:114-118.
9. Centers for Disease Control and Prevention. African tick-bite fever. Centers for Disease Control and Prevention Web site. Available at: http://wwwnc.cdc.gov/travel/diseases/african-tick-bite-fever. Accessed September 24, 2015.
THE CASE
A 76-year-old man with a history of coronary artery disease presented with a fever, headache, and malaise one week after returning from a big game hunting trip in South Africa. Five days after his return, he noticed lesions on his right leg that eventually scabbed over. He sought care at his local emergency department and with his primary care physician, and completed an empiric trial of azithromycin. His symptoms, however, persisted and he was referred to our institution for evaluation and treatment.
On exam, he had a temperature of 100.5° F, inguinal lymphadenopathy, and 2 eschars: a 1.5 cm one on his right groin and an identical one on the medial aspect of the right popliteal fossa (FIGURE 1).
THE DIAGNOSIS
Laboratory studies showed a white blood cell count of 3000/mcL, hemoglobin of 14.1 g/dL, and platelet count of 142,000/mcL; peripheral blood smear was normal. Blood and urine cultures showed no growth. A malaria smear and antibodies for Lyme disease, dengue fever, Chikungunya virus, and Q fever were also negative. A biopsy of the eschar demonstrated epidermal and dermal necrosis consistent with infectious vasculitis caused by rickettsial disease (FIGURE 2). A polymerase chain reaction (PCR) for the spotted fever group (R rickettsii, R akari, and R conorii) and typhus fever group of rickettsial agents (R typhi and R prowazekii) were negative. However, a PCR was positive for R africae, confirming the diagnosis of African tick-bite fever (ATBF).
DISCUSSION
Two common reasons patients returning from international travel seek medical attention are fever and rash.1 Initial assessment should include a detailed travel history of urban and rural exposures and any possible exposure to ticks or fleas. The time course of symptoms is important because some tropical infections can have long incubation periods.2
Rickettsial diseases are the most common febrile illness in patients returning from international travel.1 ATBF caused by R africae is the most common rickettsiosis among returning travelers1 and may be the most widespread of all spotted fever group rickettsiae that are known to be pathogenic to humans.3R africae is endemic to South Africa. The risk of contracting R africae is 4 to 5 times higher than the risk of contracting malaria in South Africa.1
R africae is transmitted through cattle and game ticks (Amblyomma species),1-7 and tends to cause mild illness with rare progression to complicated disease.3 The risk of infection is particularly high from November to April,7 and our patient had traveled during April.
Most patients with ATBF present with fever, headache, and malaise, and 50% develop a variable rash.1,2 Local lymphadenopathy often develops, and marked neck stiffness can occur.2 An eschar is present in 95% of cases.2 The finding of an eschar is often indicative of rickettsial infection; however, not all rickettsioses show eschars, and the absence of an eschar does not exclude rickettsial infection.1
ATBF is usually benign and self-limiting, and no fatalities have been reported.2,4,8 Complications such as peripheral nerve involvement, encephalitis, and myocarditis are rare.5,8 Since rickettsial diseases may be more severe in elderly patients with underlying diseases, empiric treatment with inpatient monitoring is justifiable.5
Don’t wait for lab confirmation to begin antibiotics
Laboratory findings in a patient with ATBF include pancytopenia, elevated serum C-reactive protein, and abnormal liver function tests.2,4 A blood PCR detects R africae,1,3 and if a rash or eschar is present, a biopsy can confirm the diagnosis.1 However, confirming the diagnosis is difficult if seroconversion has not occurred and PCR is not readily available.1 Also, antibodies may not be detected in patients who have a mild case of ATBF or those who are immunocompromised.5
If you suspect your patient has ATBF, don’t wait for laboratory confirmation; instead, initiate empiric treatment with doxycycline 100 mg bid twice daily for 5 to 7 days.1,2,4
Preventive measures include repellant lotions, clothing, and gear
Since there are no vaccines or prophylactic treatments for ATBF, counsel travelers on preventive measures.9 Instruct patients who plan to visit an endemic area such as sub-Saharan Africa or the West Indies to wear long-sleeved shirts, long pants, and hats. Individuals should also tuck their shirts into their pants and their pants into socks, as well as wear closed-toe shoes. When possible, it’s advisable to avoid woody and brushy areas.
Over-the-counter repellant lotions that contain ≥20% DEET are effective at preventing tick bites for several hours after an application, but should be reapplied as directed.9 These lotions should be applied after sunscreen. Advise patients that they can purchase clothing and gear that have been treated with the pesticide permethrin, or they can treat clothing and gear themselves. Explain, however, that permethrin should not be applied directly to skin.
Finally, instruct travelers to perform daily tick inspections and shower or bathe as soon as possible after returning from the outdoors.9 Educate patients on the proper technique for tick removal, which is described on the Centers for Disease Control and Prevention’s Web site at http://www.cdc.gov/ticks/removing_a_tick.html.
Our patient completed a 2-week course of doxycycline 100 mg bid. His symptoms and laboratory abnormalities completely resolved.
THE TAKEAWAY
ATBF is the most common rickettsiosis among patients returning from international travel. Because patients may present with several nonspecific symptoms, maintain a high index of suspicion for rickettsial infection among patients returning from sub-Saharan Africa or the West Indies. Though the disease usually can be successfully managed in the outpatient setting with doxycycline, elderly patients or those with comorbid conditions may require inpatient care. Educate patients who plan to travel to an endemic area about measures they can take to prevent exposure to ticks and subsequent infection.
THE CASE
A 76-year-old man with a history of coronary artery disease presented with a fever, headache, and malaise one week after returning from a big game hunting trip in South Africa. Five days after his return, he noticed lesions on his right leg that eventually scabbed over. He sought care at his local emergency department and with his primary care physician, and completed an empiric trial of azithromycin. His symptoms, however, persisted and he was referred to our institution for evaluation and treatment.
On exam, he had a temperature of 100.5° F, inguinal lymphadenopathy, and 2 eschars: a 1.5 cm one on his right groin and an identical one on the medial aspect of the right popliteal fossa (FIGURE 1).
THE DIAGNOSIS
Laboratory studies showed a white blood cell count of 3000/mcL, hemoglobin of 14.1 g/dL, and platelet count of 142,000/mcL; peripheral blood smear was normal. Blood and urine cultures showed no growth. A malaria smear and antibodies for Lyme disease, dengue fever, Chikungunya virus, and Q fever were also negative. A biopsy of the eschar demonstrated epidermal and dermal necrosis consistent with infectious vasculitis caused by rickettsial disease (FIGURE 2). A polymerase chain reaction (PCR) for the spotted fever group (R rickettsii, R akari, and R conorii) and typhus fever group of rickettsial agents (R typhi and R prowazekii) were negative. However, a PCR was positive for R africae, confirming the diagnosis of African tick-bite fever (ATBF).
DISCUSSION
Two common reasons patients returning from international travel seek medical attention are fever and rash.1 Initial assessment should include a detailed travel history of urban and rural exposures and any possible exposure to ticks or fleas. The time course of symptoms is important because some tropical infections can have long incubation periods.2
Rickettsial diseases are the most common febrile illness in patients returning from international travel.1 ATBF caused by R africae is the most common rickettsiosis among returning travelers1 and may be the most widespread of all spotted fever group rickettsiae that are known to be pathogenic to humans.3R africae is endemic to South Africa. The risk of contracting R africae is 4 to 5 times higher than the risk of contracting malaria in South Africa.1
R africae is transmitted through cattle and game ticks (Amblyomma species),1-7 and tends to cause mild illness with rare progression to complicated disease.3 The risk of infection is particularly high from November to April,7 and our patient had traveled during April.
Most patients with ATBF present with fever, headache, and malaise, and 50% develop a variable rash.1,2 Local lymphadenopathy often develops, and marked neck stiffness can occur.2 An eschar is present in 95% of cases.2 The finding of an eschar is often indicative of rickettsial infection; however, not all rickettsioses show eschars, and the absence of an eschar does not exclude rickettsial infection.1
ATBF is usually benign and self-limiting, and no fatalities have been reported.2,4,8 Complications such as peripheral nerve involvement, encephalitis, and myocarditis are rare.5,8 Since rickettsial diseases may be more severe in elderly patients with underlying diseases, empiric treatment with inpatient monitoring is justifiable.5
Don’t wait for lab confirmation to begin antibiotics
Laboratory findings in a patient with ATBF include pancytopenia, elevated serum C-reactive protein, and abnormal liver function tests.2,4 A blood PCR detects R africae,1,3 and if a rash or eschar is present, a biopsy can confirm the diagnosis.1 However, confirming the diagnosis is difficult if seroconversion has not occurred and PCR is not readily available.1 Also, antibodies may not be detected in patients who have a mild case of ATBF or those who are immunocompromised.5
If you suspect your patient has ATBF, don’t wait for laboratory confirmation; instead, initiate empiric treatment with doxycycline 100 mg bid twice daily for 5 to 7 days.1,2,4
Preventive measures include repellant lotions, clothing, and gear
Since there are no vaccines or prophylactic treatments for ATBF, counsel travelers on preventive measures.9 Instruct patients who plan to visit an endemic area such as sub-Saharan Africa or the West Indies to wear long-sleeved shirts, long pants, and hats. Individuals should also tuck their shirts into their pants and their pants into socks, as well as wear closed-toe shoes. When possible, it’s advisable to avoid woody and brushy areas.
Over-the-counter repellant lotions that contain ≥20% DEET are effective at preventing tick bites for several hours after an application, but should be reapplied as directed.9 These lotions should be applied after sunscreen. Advise patients that they can purchase clothing and gear that have been treated with the pesticide permethrin, or they can treat clothing and gear themselves. Explain, however, that permethrin should not be applied directly to skin.
Finally, instruct travelers to perform daily tick inspections and shower or bathe as soon as possible after returning from the outdoors.9 Educate patients on the proper technique for tick removal, which is described on the Centers for Disease Control and Prevention’s Web site at http://www.cdc.gov/ticks/removing_a_tick.html.
Our patient completed a 2-week course of doxycycline 100 mg bid. His symptoms and laboratory abnormalities completely resolved.
THE TAKEAWAY
ATBF is the most common rickettsiosis among patients returning from international travel. Because patients may present with several nonspecific symptoms, maintain a high index of suspicion for rickettsial infection among patients returning from sub-Saharan Africa or the West Indies. Though the disease usually can be successfully managed in the outpatient setting with doxycycline, elderly patients or those with comorbid conditions may require inpatient care. Educate patients who plan to travel to an endemic area about measures they can take to prevent exposure to ticks and subsequent infection.
1. Neumayr A, Hatz C, Blum J. Not to be missed! Differential diagnoses of common dermatological problems in returning travellers. Travel Med Infect Dis. 2013;11:337-349.
2. Yates J, Smith P. Fever and rash. Medicine. 2014;42:96-99.
3. Jensenius M, Fournier PE, Kelly P, et al. African tick bite fever. Lancet Infect Dis. 2003;3:557-564.
4. Frean J, Blumberg L, Ogunbanjo GA. Tick bite fever in South Africa. S Afr Fam Pract. 2008;50:33-35.
5. Roch N, Epaulard O, Pelloux I, et al. African tick bite fever in elderly patients: 8 cases in French tourists returning from South Africa. Clin Infect Dis. 2008;47:e28-e35.
6. Caruso G, Zasio C, Guzzo F, et al. Outbreak of African tick-bite fever in six Italian tourists returning from South Africa. Eur J Clin Microbiol Infect Dis. 2002;21:133-136.
7. Tsai YS, Wu YH, Kao PT, et al. African tick bite fever. J Formos Med Assoc. 2008;107:73-76.
8. Jensenius M, Fournier PE, Fladby T, et al. Sub-acute neuropathy in patients with African tick bite fever. Scand J Infect Dis. 2006;38:114-118.
9. Centers for Disease Control and Prevention. African tick-bite fever. Centers for Disease Control and Prevention Web site. Available at: http://wwwnc.cdc.gov/travel/diseases/african-tick-bite-fever. Accessed September 24, 2015.
1. Neumayr A, Hatz C, Blum J. Not to be missed! Differential diagnoses of common dermatological problems in returning travellers. Travel Med Infect Dis. 2013;11:337-349.
2. Yates J, Smith P. Fever and rash. Medicine. 2014;42:96-99.
3. Jensenius M, Fournier PE, Kelly P, et al. African tick bite fever. Lancet Infect Dis. 2003;3:557-564.
4. Frean J, Blumberg L, Ogunbanjo GA. Tick bite fever in South Africa. S Afr Fam Pract. 2008;50:33-35.
5. Roch N, Epaulard O, Pelloux I, et al. African tick bite fever in elderly patients: 8 cases in French tourists returning from South Africa. Clin Infect Dis. 2008;47:e28-e35.
6. Caruso G, Zasio C, Guzzo F, et al. Outbreak of African tick-bite fever in six Italian tourists returning from South Africa. Eur J Clin Microbiol Infect Dis. 2002;21:133-136.
7. Tsai YS, Wu YH, Kao PT, et al. African tick bite fever. J Formos Med Assoc. 2008;107:73-76.
8. Jensenius M, Fournier PE, Fladby T, et al. Sub-acute neuropathy in patients with African tick bite fever. Scand J Infect Dis. 2006;38:114-118.
9. Centers for Disease Control and Prevention. African tick-bite fever. Centers for Disease Control and Prevention Web site. Available at: http://wwwnc.cdc.gov/travel/diseases/african-tick-bite-fever. Accessed September 24, 2015.
Was this CT with contrast unnecessary—and harmful? ... Patient dies after being prescribed opioids right after detoxification
Was this CT with contrast unnecessary—and harmful?
A 52-YEAR-OLD WOMAN presented to the emergency department (ED) with leg pain and vaginal bleeding. The ED physicians ordered a computed tomography (CT) scan with contrast. Following the administration of the contrast dye, the patient’s blood pressure spiked and a brain aneurysm ruptured. The patient immediately underwent cranial surgery and recovered well. However, she still suffers from paralysis, cognitive issues, and weakness in her left arm and leg. She has been unable to return to her job.
PLAINTIFF’S CLAIM The doctors ran several unnecessary tests, including the CT scan, which caused her to have an allergic reaction.
THE DEFENSE The CT scan was necessary to rule out a stomach abscess, and the ruptured aneurysm was caused by her medical condition and not the dye.
VERDICT $3.62 million New Jersey verdict.
COMMENT Here is a sober reminder that doing more tests does not protect one from litigation. We are not told enough in this short report to know if there was a legitimate indication for a CT scan, but the large award suggests there was not. The Choosing Wisely campaign (http://www.choosingwisely.org), which has a goal of “advancing a national dialogue on avoiding wasteful or unnecessary medical tests, treatments and procedures,” is not just about saving money—it is about practicing medicine appropriately.
Patient dies after being prescribed opioids right after detoxification
A 52-YEAR-OLD WOMAN had been going to the same physician for 17 years. While she was under his care, she had been prescribed various narcotics, benzodiazepines, and barbiturates, and she had become addicted to them. The patient suffered a fall at home that was allegedly caused by an overdose of these medications. During a 3-week hospitalization after her fall, the woman went through a detoxification protocol to ease her dependence on the drugs. During her next appointment with her physician, he prescribed alprazolam and morphine sulfate daily. A week later, the woman died, allegedly due to an overdose of the alprazolam and morphine sulfate.
PLAINTIFF’S CLAIM The defendant’s failure to investigate the reason for the decedent’s hospitalization violated the standard of care. If the physician had inquired about his patient’s recent hospitalization, he would have been told about her detoxification, and wouldn’t have prescribed her any potentially addictive drugs.
THE DEFENSE The physician admitted that if he had known about his patient’s detoxification, he would not have prescribed her any medication. However, the doctor in charge of overseeing the detoxification told the patient not to see the defendant again, and not to take any prescriptions from him.
VERDICT $156,853 Illinois verdict.
COMMENT There is good reason to be wary of prescribing strong opioids and benzodiazepines for chronic pain in primary care practice. With the sharp increase in overdose deaths from opioids and the marginal evidence, at best, that supports the use of opioids for chronic, nonmalignant pain, such patients should—in my opinion—be managed directly in a pain/addiction program, or in close collaboration with one.
State Boards of Medicine are becoming appropriately stringent about opioids, so don’t risk losing your medical license or being sued. Use narcotic-use contracts, random drug testing, and co-management, and check your state narcotic prescribing database regularly if you treat chronic pain patients.
Was this CT with contrast unnecessary—and harmful?
A 52-YEAR-OLD WOMAN presented to the emergency department (ED) with leg pain and vaginal bleeding. The ED physicians ordered a computed tomography (CT) scan with contrast. Following the administration of the contrast dye, the patient’s blood pressure spiked and a brain aneurysm ruptured. The patient immediately underwent cranial surgery and recovered well. However, she still suffers from paralysis, cognitive issues, and weakness in her left arm and leg. She has been unable to return to her job.
PLAINTIFF’S CLAIM The doctors ran several unnecessary tests, including the CT scan, which caused her to have an allergic reaction.
THE DEFENSE The CT scan was necessary to rule out a stomach abscess, and the ruptured aneurysm was caused by her medical condition and not the dye.
VERDICT $3.62 million New Jersey verdict.
COMMENT Here is a sober reminder that doing more tests does not protect one from litigation. We are not told enough in this short report to know if there was a legitimate indication for a CT scan, but the large award suggests there was not. The Choosing Wisely campaign (http://www.choosingwisely.org), which has a goal of “advancing a national dialogue on avoiding wasteful or unnecessary medical tests, treatments and procedures,” is not just about saving money—it is about practicing medicine appropriately.
Patient dies after being prescribed opioids right after detoxification
A 52-YEAR-OLD WOMAN had been going to the same physician for 17 years. While she was under his care, she had been prescribed various narcotics, benzodiazepines, and barbiturates, and she had become addicted to them. The patient suffered a fall at home that was allegedly caused by an overdose of these medications. During a 3-week hospitalization after her fall, the woman went through a detoxification protocol to ease her dependence on the drugs. During her next appointment with her physician, he prescribed alprazolam and morphine sulfate daily. A week later, the woman died, allegedly due to an overdose of the alprazolam and morphine sulfate.
PLAINTIFF’S CLAIM The defendant’s failure to investigate the reason for the decedent’s hospitalization violated the standard of care. If the physician had inquired about his patient’s recent hospitalization, he would have been told about her detoxification, and wouldn’t have prescribed her any potentially addictive drugs.
THE DEFENSE The physician admitted that if he had known about his patient’s detoxification, he would not have prescribed her any medication. However, the doctor in charge of overseeing the detoxification told the patient not to see the defendant again, and not to take any prescriptions from him.
VERDICT $156,853 Illinois verdict.
COMMENT There is good reason to be wary of prescribing strong opioids and benzodiazepines for chronic pain in primary care practice. With the sharp increase in overdose deaths from opioids and the marginal evidence, at best, that supports the use of opioids for chronic, nonmalignant pain, such patients should—in my opinion—be managed directly in a pain/addiction program, or in close collaboration with one.
State Boards of Medicine are becoming appropriately stringent about opioids, so don’t risk losing your medical license or being sued. Use narcotic-use contracts, random drug testing, and co-management, and check your state narcotic prescribing database regularly if you treat chronic pain patients.
Was this CT with contrast unnecessary—and harmful?
A 52-YEAR-OLD WOMAN presented to the emergency department (ED) with leg pain and vaginal bleeding. The ED physicians ordered a computed tomography (CT) scan with contrast. Following the administration of the contrast dye, the patient’s blood pressure spiked and a brain aneurysm ruptured. The patient immediately underwent cranial surgery and recovered well. However, she still suffers from paralysis, cognitive issues, and weakness in her left arm and leg. She has been unable to return to her job.
PLAINTIFF’S CLAIM The doctors ran several unnecessary tests, including the CT scan, which caused her to have an allergic reaction.
THE DEFENSE The CT scan was necessary to rule out a stomach abscess, and the ruptured aneurysm was caused by her medical condition and not the dye.
VERDICT $3.62 million New Jersey verdict.
COMMENT Here is a sober reminder that doing more tests does not protect one from litigation. We are not told enough in this short report to know if there was a legitimate indication for a CT scan, but the large award suggests there was not. The Choosing Wisely campaign (http://www.choosingwisely.org), which has a goal of “advancing a national dialogue on avoiding wasteful or unnecessary medical tests, treatments and procedures,” is not just about saving money—it is about practicing medicine appropriately.
Patient dies after being prescribed opioids right after detoxification
A 52-YEAR-OLD WOMAN had been going to the same physician for 17 years. While she was under his care, she had been prescribed various narcotics, benzodiazepines, and barbiturates, and she had become addicted to them. The patient suffered a fall at home that was allegedly caused by an overdose of these medications. During a 3-week hospitalization after her fall, the woman went through a detoxification protocol to ease her dependence on the drugs. During her next appointment with her physician, he prescribed alprazolam and morphine sulfate daily. A week later, the woman died, allegedly due to an overdose of the alprazolam and morphine sulfate.
PLAINTIFF’S CLAIM The defendant’s failure to investigate the reason for the decedent’s hospitalization violated the standard of care. If the physician had inquired about his patient’s recent hospitalization, he would have been told about her detoxification, and wouldn’t have prescribed her any potentially addictive drugs.
THE DEFENSE The physician admitted that if he had known about his patient’s detoxification, he would not have prescribed her any medication. However, the doctor in charge of overseeing the detoxification told the patient not to see the defendant again, and not to take any prescriptions from him.
VERDICT $156,853 Illinois verdict.
COMMENT There is good reason to be wary of prescribing strong opioids and benzodiazepines for chronic pain in primary care practice. With the sharp increase in overdose deaths from opioids and the marginal evidence, at best, that supports the use of opioids for chronic, nonmalignant pain, such patients should—in my opinion—be managed directly in a pain/addiction program, or in close collaboration with one.
State Boards of Medicine are becoming appropriately stringent about opioids, so don’t risk losing your medical license or being sued. Use narcotic-use contracts, random drug testing, and co-management, and check your state narcotic prescribing database regularly if you treat chronic pain patients.