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A prospective, randomized, open-label trial of 6-month versus 12-month dual antiplatelet therapy after drug-eluting stent implantation in ST-elevation myocardial infarction: Rationale and design of the "DAPT-STEMI trial"

Kedhi, E. (författare)
Fabris, E. (författare)
van der Ent, M. (författare)
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Kennedy, M. W. (författare)
Buszman, P. (författare)
von Birgelen, C. (författare)
Cook, S. (författare)
Wedel, Hans (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin,Institute of Medicine
Zijlstra, F. (författare)
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 (creator_code:org_t)
Elsevier BV, 2017
2017
Engelska.
Ingår i: American Heart Journal. - : Elsevier BV. - 0002-8703. ; 188, s. 11-17
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background The optimal duration of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention with second-generation drug eluting stents (DESs) is unclear. Because prolonged DAPT is associated with higher bleeding risk and health care costs, establishing optimal DAPT duration is of paramount importance. No other randomized controlled trials have evaluated the safety of shorter DAPT duration in ST-elevation myocardial infarction (STEMI) patients treated with second generation DESs and latest P2Y12 platelet receptor inhibitors. Hypothesis Six months of DAPT after Resolute Integrity stent implantation in STEMI patients is not inferior to 12 months of DAPT in clinical outcomes. Study design The Dual Antiplatelet Therapy After Drug-Eluting Stent Implantation In ST-elevation Myocardial Infarction (DAPT-STEMI) trial is a randomized, multicenter, international, open-label trial designed to examine the safety (noninferiority) of 6-month DAPT after Resolute Integrity stent implantation in STEMI patients compared with 12-month DAPT. Event-free patients on DAPT at 6month will be randomized (1:1 fashion) between single (aspirin only) versus DAPT for an additional 6 months and followed until 2 years after primary percutaneous coronary intervention. The primary end point is a patient-oriented composite endpoint of all-cause mortality, any myocardial infarction, any revascularization, stroke, and major bleeding (net adverse clinical events [NACE]) at 18 months after randomization. To achieve a power of 85% for a noninferiority limit of 1.66, a total of 1100 enrolled patients are required. Summary The DAPT-STEMI trial aims to assess in STEMI patients treated with second-generation DESs whether discontinuation of DAPT after 6 months of event-free survival is noninferior to routine 12-month DAPT.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

percutaneous coronary intervention
college-of-cardiology
non-inferiority trial
cardiovascular angiography
network metaanalysis
clopidogrel therapy
atrial-fibrillation
segment elevation
heart-association
american-college
Cardiovascular System & Cardiology

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