Dual antiplatelet therapy following percutaneous coronary intervention: protocol for a systematic review
IntroductionDual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is ongoing debate about the optimal duration, especially in specific patient groups. In the proposed systematic review, we intend to assess the opt...
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Published in | BMJ open Vol. 9; no. 6; p. e022271 |
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Abstract | IntroductionDual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is ongoing debate about the optimal duration, especially in specific patient groups. In the proposed systematic review, we intend to assess the optimal duration of DAPT following PCI with stenting, with a focus on clinically relevant patient subgroups.Methods and analysisWe will perform a comprehensive search of the published literature for randomised controlled trials (RCTs) assessing the benefits and harms of extended DAPT (>12 months) compared with short-term DAPT (6–12 months) following PCI with stenting (bare metal or drug eluting). ClinicalTrials.gov and ICTRP will also be searched to identify ongoing and completed clinical trials. Two independent reviewers will select studies for inclusion, and the risk of bias will be assessed by use of Cochrane’s Risk of Bias tool. The primary outcome of interest is death (all-cause, cardiovascular, non-cardiovascular). Secondary outcomes are bleeding (major, minor, gastrointestinal), urgent target vessel revascularisation, major adverse cardiovascular events, myocardial infarction, stroke and stent thrombosis. Subgroup data will be sought for patients with prior myocardial infarction, acute coronary syndrome at presentation and diabetes, and based on smoking status and age group. Data will be analysed by random-effects meta-analysis, and separate analyses will be performed for patient subgroups. Bayesian network meta-analysis will be performed to investigate the effect of individual P2Y12 inhibitors at different DAPT durations longer than 6 months.Ethics and disseminationThis review will provide a comprehensive overview of the available evidence of the benefits and harms associated with extending DAPT beyond 12 months following PCI with stenting and the effects on clinically important subgroups. The results of this review will inform clinical and policy decisions regarding the optimal treatment duration of DAPT following PCI with stenting.Systematic review registrationPROSPERO no. CRD42018082587 |
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AbstractList | Dual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is ongoing debate about the optimal duration, especially in specific patient groups. In the proposed systematic review, we intend to assess the optimal duration of DAPT following PCI with stenting, with a focus on clinically relevant patient subgroups.
We will perform a comprehensive search of the published literature for randomised controlled trials (RCTs) assessing the benefits and harms of extended DAPT (>12 months) compared with short-term DAPT (6-12 months) following PCI with stenting (bare metal or drug eluting). ClinicalTrials.gov and ICTRP will also be searched to identify ongoing and completed clinical trials. Two independent reviewers will select studies for inclusion, and the risk of bias will be assessed by use of Cochrane's Risk of Bias tool. The primary outcome of interest is death (all-cause, cardiovascular, non-cardiovascular). Secondary outcomes are bleeding (major, minor, gastrointestinal), urgent target vessel revascularisation, major adverse cardiovascular events, myocardial infarction, stroke and stent thrombosis. Subgroup data will be sought for patients with prior myocardial infarction, acute coronary syndrome at presentation and diabetes, and based on smoking status and age group. Data will be analysed by random-effects meta-analysis, and separate analyses will be performed for patient subgroups. Bayesian network meta-analysis will be performed to investigate the effect of individual P2Y12 inhibitors at different DAPT durations longer than 6 months.
This review will provide a comprehensive overview of the available evidence of the benefits and harms associated with extending DAPT beyond 12 months following PCI with stenting and the effects on clinically important subgroups. The results of this review will inform clinical and policy decisions regarding the optimal treatment duration of DAPT following PCI with stenting.
PROSPERO no. CRD42018082587. IntroductionDual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is ongoing debate about the optimal duration, especially in specific patient groups. In the proposed systematic review, we intend to assess the optimal duration of DAPT following PCI with stenting, with a focus on clinically relevant patient subgroups.Methods and analysisWe will perform a comprehensive search of the published literature for randomised controlled trials (RCTs) assessing the benefits and harms of extended DAPT (>12 months) compared with short-term DAPT (6–12 months) following PCI with stenting (bare metal or drug eluting). ClinicalTrials.gov and ICTRP will also be searched to identify ongoing and completed clinical trials. Two independent reviewers will select studies for inclusion, and the risk of bias will be assessed by use of Cochrane’s Risk of Bias tool. The primary outcome of interest is death (all-cause, cardiovascular, non-cardiovascular). Secondary outcomes are bleeding (major, minor, gastrointestinal), urgent target vessel revascularisation, major adverse cardiovascular events, myocardial infarction, stroke and stent thrombosis. Subgroup data will be sought for patients with prior myocardial infarction, acute coronary syndrome at presentation and diabetes, and based on smoking status and age group. Data will be analysed by random-effects meta-analysis, and separate analyses will be performed for patient subgroups. Bayesian network meta-analysis will be performed to investigate the effect of individual P2Y12 inhibitors at different DAPT durations longer than 6 months.Ethics and disseminationThis review will provide a comprehensive overview of the available evidence of the benefits and harms associated with extending DAPT beyond 12 months following PCI with stenting and the effects on clinically important subgroups. The results of this review will inform clinical and policy decisions regarding the optimal treatment duration of DAPT following PCI with stenting.Systematic review registrationPROSPERO no. CRD42018082587 Dual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is ongoing debate about the optimal duration, especially in specific patient groups. In the proposed systematic review, we intend to assess the optimal duration of DAPT following PCI with stenting, with a focus on clinically relevant patient subgroups.INTRODUCTIONDual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is ongoing debate about the optimal duration, especially in specific patient groups. In the proposed systematic review, we intend to assess the optimal duration of DAPT following PCI with stenting, with a focus on clinically relevant patient subgroups.We will perform a comprehensive search of the published literature for randomised controlled trials (RCTs) assessing the benefits and harms of extended DAPT (>12 months) compared with short-term DAPT (6-12 months) following PCI with stenting (bare metal or drug eluting). ClinicalTrials.gov and ICTRP will also be searched to identify ongoing and completed clinical trials. Two independent reviewers will select studies for inclusion, and the risk of bias will be assessed by use of Cochrane's Risk of Bias tool. The primary outcome of interest is death (all-cause, cardiovascular, non-cardiovascular). Secondary outcomes are bleeding (major, minor, gastrointestinal), urgent target vessel revascularisation, major adverse cardiovascular events, myocardial infarction, stroke and stent thrombosis. Subgroup data will be sought for patients with prior myocardial infarction, acute coronary syndrome at presentation and diabetes, and based on smoking status and age group. Data will be analysed by random-effects meta-analysis, and separate analyses will be performed for patient subgroups. Bayesian network meta-analysis will be performed to investigate the effect of individual P2Y12 inhibitors at different DAPT durations longer than 6 months.METHODS AND ANALYSISWe will perform a comprehensive search of the published literature for randomised controlled trials (RCTs) assessing the benefits and harms of extended DAPT (>12 months) compared with short-term DAPT (6-12 months) following PCI with stenting (bare metal or drug eluting). ClinicalTrials.gov and ICTRP will also be searched to identify ongoing and completed clinical trials. Two independent reviewers will select studies for inclusion, and the risk of bias will be assessed by use of Cochrane's Risk of Bias tool. The primary outcome of interest is death (all-cause, cardiovascular, non-cardiovascular). Secondary outcomes are bleeding (major, minor, gastrointestinal), urgent target vessel revascularisation, major adverse cardiovascular events, myocardial infarction, stroke and stent thrombosis. Subgroup data will be sought for patients with prior myocardial infarction, acute coronary syndrome at presentation and diabetes, and based on smoking status and age group. Data will be analysed by random-effects meta-analysis, and separate analyses will be performed for patient subgroups. Bayesian network meta-analysis will be performed to investigate the effect of individual P2Y12 inhibitors at different DAPT durations longer than 6 months.This review will provide a comprehensive overview of the available evidence of the benefits and harms associated with extending DAPT beyond 12 months following PCI with stenting and the effects on clinically important subgroups. The results of this review will inform clinical and policy decisions regarding the optimal treatment duration of DAPT following PCI with stenting.ETHICS AND DISSEMINATIONThis review will provide a comprehensive overview of the available evidence of the benefits and harms associated with extending DAPT beyond 12 months following PCI with stenting and the effects on clinically important subgroups. The results of this review will inform clinical and policy decisions regarding the optimal treatment duration of DAPT following PCI with stenting.PROSPERO no. CRD42018082587.SYSTEMATIC REVIEW REGISTRATIONPROSPERO no. CRD42018082587. |
Author | Bai, Zemin So, Derek Y F Skidmore, Becky Elliott, Jesse Boucher, Michel Wells, George A Kelly, Shannon E |
AuthorAffiliation | 3 Independent Information Specialist , Ottawa , Ontario , Canada 1 Cardiovascular Research Methods Centre , University of Ottawa Heart Institute , Ottawa , Ontario , Canada 4 Program and Policy Development , Canadian Agency for Drugs and Technologies in Health (CADTH) , Ottawa , Ontario , Canada 5 University of Ottawa Heart Institute , Ottawa , Ontario , Canada 2 School of Epidemiology and Public Health , University of Ottawa , Ottawa , Ontario , Canada |
AuthorAffiliation_xml | – name: 4 Program and Policy Development , Canadian Agency for Drugs and Technologies in Health (CADTH) , Ottawa , Ontario , Canada – name: 2 School of Epidemiology and Public Health , University of Ottawa , Ottawa , Ontario , Canada – name: 1 Cardiovascular Research Methods Centre , University of Ottawa Heart Institute , Ottawa , Ontario , Canada – name: 3 Independent Information Specialist , Ottawa , Ontario , Canada – name: 5 University of Ottawa Heart Institute , Ottawa , Ontario , Canada |
Author_xml | – sequence: 1 givenname: Jesse orcidid: 0000-0002-2501-1641 surname: Elliott fullname: Elliott, Jesse email: gawells@ottawaheart.ca organization: School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada – sequence: 2 givenname: Shannon E surname: Kelly fullname: Kelly, Shannon E email: gawells@ottawaheart.ca organization: School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada – sequence: 3 givenname: Zemin surname: Bai fullname: Bai, Zemin email: gawells@ottawaheart.ca organization: Cardiovascular Research Methods Centre, University of Ottawa Heart Institute, Ottawa, Ontario, Canada – sequence: 4 givenname: Becky surname: Skidmore fullname: Skidmore, Becky email: gawells@ottawaheart.ca organization: Independent Information Specialist, Ottawa, Ontario, Canada – sequence: 5 givenname: Michel surname: Boucher fullname: Boucher, Michel email: gawells@ottawaheart.ca organization: Program and Policy Development, Canadian Agency for Drugs and Technologies in Health (CADTH), Ottawa, Ontario, Canada – sequence: 6 givenname: Derek Y F surname: So fullname: So, Derek Y F email: gawells@ottawaheart.ca organization: University of Ottawa Heart Institute, Ottawa, Ontario, Canada – sequence: 7 givenname: George A surname: Wells fullname: Wells, George A email: gawells@ottawaheart.ca organization: School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada |
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Cites_doi | 10.1016/j.amjcard.2017.03.011 10.1016/j.ijcard.2016.06.070 10.1093/eurheartj/ehu278 10.1016/j.ctrsc.2015.08.003 10.1186/2046-4053-4-1 10.1016/S0140-6736(15)60263-X 10.1371/journal.pmed.1000097 10.1177/0272989X12455847 10.1016/j.amjcard.2016.03.005 10.1093/eurheartj/ehx419 10.1136/bmj.h1618 10.1177/0003319715586500 10.1016/j.cjca.2013.07.001 10.1038/srep13204 10.1097/MJT.0000000000000307 10.1007/s00392-015-0860-1 10.1002/9780470712184 |
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Snippet | IntroductionDual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is... Dual antiplatelet therapy (DAPT) is routinely given to patients after percutaneous coronary intervention (PCI) with stenting; however, there is ongoing debate... |
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SubjectTerms | Acute Coronary Syndrome - prevention & control Acute coronary syndromes Angioplasty Cardiovascular disease Cardiovascular Medicine Clinical decision making Decision making Drug administration Drug therapy Dual Anti-Platelet Therapy - methods Evidence-based medicine Heart attacks Humans Intervention Meta-analysis Myocardial Infarction - prevention & control Patients Percutaneous Coronary Intervention Platelet Aggregation Inhibitors - therapeutic use Research Design Stents Systematic review Systematic Reviews as Topic Thrombosis Thrombosis - prevention & control |
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Title | Dual antiplatelet therapy following percutaneous coronary intervention: protocol for a systematic review |
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