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Long-term risk of recurrence after discontinuing anticoagulants for a first unprovoked venous thromboembolism: protocol for a systematic review and meta-analysis.

Identifieur interne : 000583 ( PubMed/Corpus ); précédent : 000582; suivant : 000584

Long-term risk of recurrence after discontinuing anticoagulants for a first unprovoked venous thromboembolism: protocol for a systematic review and meta-analysis.

Auteurs : Faizan Khan ; Alvi Rahman ; Marc Carrier ; Clive Kearon ; Sam Schulman ; Francis Couturaud ; Paolo Prandoni ; Sabine Eichinger ; Cecilia Becattini ; Giancarlo Agnelli ; Harry R. Büller ; Timothy A. Brighton ; Gualtiero Palareti ; Laurent Pinede ; Elham Sabri ; Brian Hutton ; George A. Wells ; Marc A. Rodger

Source :

RBID : pubmed:28939565

Abstract

For patients with a first unprovoked venous thromboembolism (VTE), the optimal duration of anticoagulation is a crucial clinical dilemma which has yet to be resolved. The decision to stop anticoagulant therapy (AT) after the initial 3-6 months or to continue AT indefinitely, is primarily governed by the long-term risk of recurrence when treatment is discontinued. This risk however, is not well established, hindering decision making.

DOI: 10.1136/bmjopen-2017-016950
PubMed: 28939565

Links to Exploration step

pubmed:28939565

Le document en format XML

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<nlm:affiliation>Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands.</nlm:affiliation>
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<name sortKey="Brighton, Timothy A" sort="Brighton, Timothy A" uniqKey="Brighton T" first="Timothy A" last="Brighton">Timothy A. Brighton</name>
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<nlm:affiliation>Department of Haematology, Prince of Wales Hospital, Sydney, Australia.</nlm:affiliation>
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<name sortKey="Palareti, Gualtiero" sort="Palareti, Gualtiero" uniqKey="Palareti G" first="Gualtiero" last="Palareti">Gualtiero Palareti</name>
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<name sortKey="Pinede, Laurent" sort="Pinede, Laurent" uniqKey="Pinede L" first="Laurent" last="Pinede">Laurent Pinede</name>
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<name sortKey="Hutton, Brian" sort="Hutton, Brian" uniqKey="Hutton B" first="Brian" last="Hutton">Brian Hutton</name>
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<name sortKey="Wells, George A" sort="Wells, George A" uniqKey="Wells G" first="George A" last="Wells">George A. Wells</name>
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<front>
<div type="abstract" xml:lang="en">For patients with a first unprovoked venous thromboembolism (VTE), the optimal duration of anticoagulation is a crucial clinical dilemma which has yet to be resolved. The decision to stop anticoagulant therapy (AT) after the initial 3-6 months or to continue AT indefinitely, is primarily governed by the long-term risk of recurrence when treatment is discontinued. This risk however, is not well established, hindering decision making.</div>
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<DateCreated>
<Year>2017</Year>
<Month>09</Month>
<Day>23</Day>
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<Year>2017</Year>
<Month>10</Month>
<Day>11</Day>
</DateRevised>
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<Volume>7</Volume>
<Issue>9</Issue>
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<Month>Sep</Month>
<Day>21</Day>
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<ArticleTitle>Long-term risk of recurrence after discontinuing anticoagulants for a first unprovoked venous thromboembolism: protocol for a systematic review and meta-analysis.</ArticleTitle>
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<AbstractText Label="INTRODUCTION" NlmCategory="BACKGROUND">For patients with a first unprovoked venous thromboembolism (VTE), the optimal duration of anticoagulation is a crucial clinical dilemma which has yet to be resolved. The decision to stop anticoagulant therapy (AT) after the initial 3-6 months or to continue AT indefinitely, is primarily governed by the long-term risk of recurrence when treatment is discontinued. This risk however, is not well established, hindering decision making.</AbstractText>
<AbstractText Label="METHODS AND ANALYSIS" NlmCategory="UNASSIGNED">We will conduct a systematic review and a meta-analysis of studies involving patients diagnosed with a first, symptomatic unprovoked VTE or VTE provoked by minor transient risk factors, who have completed at least 3 months of initial AT; and who were followed-up for standardised time intervals of 1, 2, 5, 10 and 20 years (±3 months) after stopping AT. We will search (from inception to January 2017) MEDLINE, Embase and the Cochrane library for randomised controlled trials and prospective observational studies. Two reviewers will conduct all screening and data collection independently. The primary outcome of the rate of recurrent VTE at the standardised time intervals will be calculated for each study from the total number of recurrent events and the corresponding number of patient-years of follow-up. We will use a random-effects model to pool study results and report a weighted estimate of the absolute rate of recurrent VTE (events per 100 patient-years) over standardised time intervals of 1, 2, 5, 10 and 20 years after discontinuing anticoagulants.</AbstractText>
<AbstractText Label="ETHICS AND DISSEMINATION" NlmCategory="UNASSIGNED">Ethical approval is not applicable for this study. Findings from this study will be disseminated through peer-reviewed journal publication as well as relevant national and international conference presentations.</AbstractText>
<AbstractText Label="PROSPERO REGISTRATION NUMBER" NlmCategory="UNASSIGNED">CRD42017056309.</AbstractText>
<CopyrightInformation>© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.</CopyrightInformation>
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</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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<Initials>M</Initials>
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<Affiliation>Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Ottawa Blood Disease Centre, The Ottawa Hospital, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
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<LastName>Becattini</LastName>
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<Affiliation>Internal and Cardiovascular Medicine, Stroke Unit, University of Perugia, Perugia, Italy.</Affiliation>
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<LastName>Agnelli</LastName>
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</AffiliationInfo>
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<LastName>Büller</LastName>
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<Affiliation>Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
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<LastName>Brighton</LastName>
<ForeName>Timothy A</ForeName>
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<Affiliation>Department of Haematology, Prince of Wales Hospital, Sydney, Australia.</Affiliation>
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<ForeName>Gualtiero</ForeName>
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<Affiliation>University of Bologna, Bologna, Italy.</Affiliation>
</AffiliationInfo>
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<LastName>Pinede</LastName>
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<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Department of Internal Medicine, Infirmerie Protestante, Lyon, France.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sabri</LastName>
<ForeName>Elham</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hutton</LastName>
<ForeName>Brian</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.</Affiliation>
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<LastName>Wells</LastName>
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<Initials>GA</Initials>
<AffiliationInfo>
<Affiliation>Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Cardiovascular Research Methods Centre, University of Ottawa Heart Institute, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
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<ForeName>Marc A</ForeName>
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<AffiliationInfo>
<Affiliation>Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Ottawa Blood Disease Centre, The Ottawa Hospital, Ottawa, Ontario, Canada.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<CollectiveName>MARVELOUS Collaborators</CollectiveName>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">anticaogulants</Keyword>
<Keyword MajorTopicYN="N">recurrence</Keyword>
<Keyword MajorTopicYN="N">venous thrombosis</Keyword>
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<CoiStatement>Competing interests: MC reports receiving research support form Leo Pharma and BMS, and honoraria from Pfizer, Bayer, BMS, and Sanofi, outside the submitted work. SS reports receiving honoraria from Boehringer Ingelheim, Bayer HealthCare, Daiichi Sankyo and Sanofi, and research support from Boehringer Ingelheim, Baxter and Octapharma, outside the submitted work. FC reports having received research grant support from Pfizer, honoraria for board memberships or symposia from Bayer and AstraZeneca, and travel support from Bayer, Daiichi Sankyo, Leo Pharma, Intermune, and Actelion, outside the submitted work. PP reports receiving consultancy and lectures fees from Bayer Pharma, Sanofi, Daiichi-Sankyo and Pfizer, outside the submitted work. CB reports receiving lectures fees from Bayer HealthCare, Bristol Meyer Squibb and Boehringer Ingelheim, outside the submitted work. GA reports personal fees from Bristol-Myers-Squibb, Pfizer, Bayer Healthcare, Boehringer Ingelheim, and Daiichi Sankyo, outside the submitted work. HRB reports receiving research support and consultancy fees from Sanofi-aventis, Bayer HealthCare, Bristol-Myers Squibb, Daiichi-Sankyo, GlaxoSmithKline, Pfizer, Roche, Isis, Thrombogenics, and Boehringer Ingelheim, outside the submitted work. TAB reports receiving personal fees from Bayer, Bayer Australia, Novo Nordisk, and Glaxo Smith Klein, outside the submitted work. GP reports Advisory Board for Alfa-Wassermann, Daiichi-Sankyo, Pfizer and Roche, and speaker fees from Werfen, outside the submitted work. BH reports receiving honoraria from Cornerstone Research Group for provision of methodologic advice related to systematic reviews and meta-analysis. MAR reports receiving research support from Biomerieux, outside of the submitted work. All other authors (FK, AR, CK, SE, LP, ES and GAW) declare that they have no relevant competing interests.</CoiStatement>
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