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Adding an extra 18 months of warfarin therapy to the standard 6 months of anticoagulation delays the recurrence of venous thrombosis in patients who have a first episode of unprovoked pulmonary embolism – but the risk of recurrence resumes as soon as the warfarin is discontinued, according to a report published online July 7 in JAMA.
“Our results suggest that patients such as those who participated in our study require long-term secondary prophylaxis measures. Whether these should include systematic treatment with vitamin K antagonists, new anticoagulants, or aspirin, or be tailored according to patient risk factors (including elevated D-dimer levels) needs further investigation,” said Dr. Francis Couturaud of the department of internal medicine and chest diseases, University of Brest (France) Hospital, and his associates (JAMA 2015;314:31-40).
Adults with a first episode of unprovoked VT are at much greater risk of recurrence when the standard 6 months of anticoagulation runs out, compared with those whose VT is provoked by a known, transient risk factor such as lengthy surgery, trauma with immobilization of the lower limbs, or bed rest extending longer than 72 hours.
Some experts have advocated extending anticoagulation further in such patients; but whether this is actually beneficial remains uncertain, the investigators said, because most studies have not pursued follow-up beyond the end of treatment.
The researchers performed a multicenter, double-blind trial in which 371 consecutive patients with a first episode of unprovoked PE completed 6 months of anticoagulation and then were randomly assigned to a further 18 months on either warfarin or matching placebo.
During this 18-month treatment period, the primary outcome – a composite of recurrent VT (including PE) and major bleeding – occurred in 3.3% of the warfarin group and 13.5% of the placebo group. That significant difference translated to a 78% reduction in favor of warfarin (hazard ratio, 0.22), Dr. Couturaud and his associates said.
However, after the treatment period ended, the composite outcome occurred in 17.7% of the warfarin group and 10.3% of the placebo group. Thus, the risk of recurrence returned to its normal high level once warfarin was discontinued, the study authors noted.
The study was supported by the Programme Hospitalier de Recherche Clinique (the French Department of Health) and the University Hospital of Brest (France). Dr. Couturaud reported receiving research grants, honoraria, and travel pay from Actelion, AstraZeneca, Bayer, Daiichi Sankyo, Intermune, Leo Pharma, and Pfizer, and his associates reported ties to numerous industry sources.
Related Information
- Computed tomographic pulmonary angiography (CTPA) may be useful in the diagnosis of suspected PE, wrote Dr. Gregoire Le Gal and co-authors from the University of Ottawa. Alternately, a V/Q scan may be performed. The complete accompanying article on diagnostic testing methods for suspected pulmonary embolism can be found here.
- The recently approved anticoagulant edoxaban is similar to warfarin in its ability to treat acute VTE, according to a report published in the Medical Letter on Drugs and Therapeutics in the same issue. However, further study is needed to evaluate its safety and efficacy compared with dabigatran, rivaroxaban, and apixaban, the three other oral anticoagulant drugs currently FDA-approved for acute VTE.
- A meta-analysis of 3,716 patients with VTE found that long-term treatment with Vitamin K antagonists was associated with lower rates of thromboembolic events (relative risk = 0.20) and higher rates of bleeding complications (RR = 3.44), compared with short-term therapy, Dr. Saskia Middeldorp and Dr. Barbara A. Hutten of the University of Amsterdam reported in the same issue. There was no difference in mortality between the two groups.
- Currently, recommended treatment duration for PE can range from three months to lifelong treatment, wrote Dr. Jill Jin in a clinical synopsis for patients published with the study.
- Read the full article and listen to the related podcast: http://jama.jamanetwork.com/article.aspx?doi=10.1001/jama.2015.7046
Madhu Rajaraman contributed to this report.
Adding an extra 18 months of warfarin therapy to the standard 6 months of anticoagulation delays the recurrence of venous thrombosis in patients who have a first episode of unprovoked pulmonary embolism – but the risk of recurrence resumes as soon as the warfarin is discontinued, according to a report published online July 7 in JAMA.
“Our results suggest that patients such as those who participated in our study require long-term secondary prophylaxis measures. Whether these should include systematic treatment with vitamin K antagonists, new anticoagulants, or aspirin, or be tailored according to patient risk factors (including elevated D-dimer levels) needs further investigation,” said Dr. Francis Couturaud of the department of internal medicine and chest diseases, University of Brest (France) Hospital, and his associates (JAMA 2015;314:31-40).
Adults with a first episode of unprovoked VT are at much greater risk of recurrence when the standard 6 months of anticoagulation runs out, compared with those whose VT is provoked by a known, transient risk factor such as lengthy surgery, trauma with immobilization of the lower limbs, or bed rest extending longer than 72 hours.
Some experts have advocated extending anticoagulation further in such patients; but whether this is actually beneficial remains uncertain, the investigators said, because most studies have not pursued follow-up beyond the end of treatment.
The researchers performed a multicenter, double-blind trial in which 371 consecutive patients with a first episode of unprovoked PE completed 6 months of anticoagulation and then were randomly assigned to a further 18 months on either warfarin or matching placebo.
During this 18-month treatment period, the primary outcome – a composite of recurrent VT (including PE) and major bleeding – occurred in 3.3% of the warfarin group and 13.5% of the placebo group. That significant difference translated to a 78% reduction in favor of warfarin (hazard ratio, 0.22), Dr. Couturaud and his associates said.
However, after the treatment period ended, the composite outcome occurred in 17.7% of the warfarin group and 10.3% of the placebo group. Thus, the risk of recurrence returned to its normal high level once warfarin was discontinued, the study authors noted.
The study was supported by the Programme Hospitalier de Recherche Clinique (the French Department of Health) and the University Hospital of Brest (France). Dr. Couturaud reported receiving research grants, honoraria, and travel pay from Actelion, AstraZeneca, Bayer, Daiichi Sankyo, Intermune, Leo Pharma, and Pfizer, and his associates reported ties to numerous industry sources.
Related Information
- Computed tomographic pulmonary angiography (CTPA) may be useful in the diagnosis of suspected PE, wrote Dr. Gregoire Le Gal and co-authors from the University of Ottawa. Alternately, a V/Q scan may be performed. The complete accompanying article on diagnostic testing methods for suspected pulmonary embolism can be found here.
- The recently approved anticoagulant edoxaban is similar to warfarin in its ability to treat acute VTE, according to a report published in the Medical Letter on Drugs and Therapeutics in the same issue. However, further study is needed to evaluate its safety and efficacy compared with dabigatran, rivaroxaban, and apixaban, the three other oral anticoagulant drugs currently FDA-approved for acute VTE.
- A meta-analysis of 3,716 patients with VTE found that long-term treatment with Vitamin K antagonists was associated with lower rates of thromboembolic events (relative risk = 0.20) and higher rates of bleeding complications (RR = 3.44), compared with short-term therapy, Dr. Saskia Middeldorp and Dr. Barbara A. Hutten of the University of Amsterdam reported in the same issue. There was no difference in mortality between the two groups.
- Currently, recommended treatment duration for PE can range from three months to lifelong treatment, wrote Dr. Jill Jin in a clinical synopsis for patients published with the study.
- Read the full article and listen to the related podcast: http://jama.jamanetwork.com/article.aspx?doi=10.1001/jama.2015.7046
Madhu Rajaraman contributed to this report.
Adding an extra 18 months of warfarin therapy to the standard 6 months of anticoagulation delays the recurrence of venous thrombosis in patients who have a first episode of unprovoked pulmonary embolism – but the risk of recurrence resumes as soon as the warfarin is discontinued, according to a report published online July 7 in JAMA.
“Our results suggest that patients such as those who participated in our study require long-term secondary prophylaxis measures. Whether these should include systematic treatment with vitamin K antagonists, new anticoagulants, or aspirin, or be tailored according to patient risk factors (including elevated D-dimer levels) needs further investigation,” said Dr. Francis Couturaud of the department of internal medicine and chest diseases, University of Brest (France) Hospital, and his associates (JAMA 2015;314:31-40).
Adults with a first episode of unprovoked VT are at much greater risk of recurrence when the standard 6 months of anticoagulation runs out, compared with those whose VT is provoked by a known, transient risk factor such as lengthy surgery, trauma with immobilization of the lower limbs, or bed rest extending longer than 72 hours.
Some experts have advocated extending anticoagulation further in such patients; but whether this is actually beneficial remains uncertain, the investigators said, because most studies have not pursued follow-up beyond the end of treatment.
The researchers performed a multicenter, double-blind trial in which 371 consecutive patients with a first episode of unprovoked PE completed 6 months of anticoagulation and then were randomly assigned to a further 18 months on either warfarin or matching placebo.
During this 18-month treatment period, the primary outcome – a composite of recurrent VT (including PE) and major bleeding – occurred in 3.3% of the warfarin group and 13.5% of the placebo group. That significant difference translated to a 78% reduction in favor of warfarin (hazard ratio, 0.22), Dr. Couturaud and his associates said.
However, after the treatment period ended, the composite outcome occurred in 17.7% of the warfarin group and 10.3% of the placebo group. Thus, the risk of recurrence returned to its normal high level once warfarin was discontinued, the study authors noted.
The study was supported by the Programme Hospitalier de Recherche Clinique (the French Department of Health) and the University Hospital of Brest (France). Dr. Couturaud reported receiving research grants, honoraria, and travel pay from Actelion, AstraZeneca, Bayer, Daiichi Sankyo, Intermune, Leo Pharma, and Pfizer, and his associates reported ties to numerous industry sources.
Related Information
- Computed tomographic pulmonary angiography (CTPA) may be useful in the diagnosis of suspected PE, wrote Dr. Gregoire Le Gal and co-authors from the University of Ottawa. Alternately, a V/Q scan may be performed. The complete accompanying article on diagnostic testing methods for suspected pulmonary embolism can be found here.
- The recently approved anticoagulant edoxaban is similar to warfarin in its ability to treat acute VTE, according to a report published in the Medical Letter on Drugs and Therapeutics in the same issue. However, further study is needed to evaluate its safety and efficacy compared with dabigatran, rivaroxaban, and apixaban, the three other oral anticoagulant drugs currently FDA-approved for acute VTE.
- A meta-analysis of 3,716 patients with VTE found that long-term treatment with Vitamin K antagonists was associated with lower rates of thromboembolic events (relative risk = 0.20) and higher rates of bleeding complications (RR = 3.44), compared with short-term therapy, Dr. Saskia Middeldorp and Dr. Barbara A. Hutten of the University of Amsterdam reported in the same issue. There was no difference in mortality between the two groups.
- Currently, recommended treatment duration for PE can range from three months to lifelong treatment, wrote Dr. Jill Jin in a clinical synopsis for patients published with the study.
- Read the full article and listen to the related podcast: http://jama.jamanetwork.com/article.aspx?doi=10.1001/jama.2015.7046
Madhu Rajaraman contributed to this report.
FROM JAMA
Key clinical point: Eighteen additional months of warfarin therapy delays the recurrence of unprovoked pulmonary embolism.
Major finding: During treatment, the primary outcome – a composite of recurrent venous thromboembolism and major bleeding – occurred in 3.3% of the warfarin group and 13.5% of the placebo group, a significant difference that translated to a 78% reduction in favor of warfarin (hazard ratio, 0.22).
Data source: A multicenter, randomized, double-blind, placebo-controlled clinical trial involving 371 patients followed for a mean of 41 months.
Disclosures: This study was supported by the Programme Hospitalier de Recherche Clinique (the French Department of Health) and the University Hospital of Brest (France). Dr. Couturaud reported receiving research grants, honoraria, and travel pay from Actelion, AstraZeneca, Bayer, Daiichi Sankyo, Intermune, Leo Pharma, and Pfizer, and his associates reported ties to numerous industry sources.