Key result
Longer-duration DAPT after DES placement decreased myocardial infarction risk (RR 0.73; 95% CI 0.58-0.92) but increased mortality (RR 1.19) and major bleeding (RR 1.63) versus shorter-duration DAPT.
Why the study?
Does longer-duration DAPT reduce myocardial infarction or mortality compared to shorter-duration DAPT in adults after drug-eluting stent placement?
Meta-Analysis (n=29,531)
Does longer-duration DAPT reduce myocardial infarction or mortality compared to shorter-duration DAPT in adults after drug-eluting stent placement?
Effect estimate: RR 0.73 (95% CI 0.58 to 0.92)
Extended DAPT after DES placement reduces myocardial infarctions but increases mortality and major bleeding, highlighting the need for individualized treatment decisions based on patient risk profiles.
Favors shorter DAPT after DES to minimize mortality and bleeding; confirms net trade-offs in Level 1 evidence.
BACKGROUND: The appropriate duration of dual-antiplatelet therapy (DAPT) after drug-eluting stent (DES) placement remains controversial. PURPOSE: To summarize data on clinical outcomes with longer- versus shorter-duration DAPT after DES placement in adults with coronary artery disease. DATA SOURCES: Ovid MEDLINE and EMBASE, 1996 to 27 March 2015, and manual screening of references. STUDY SELECTION: Randomized, controlled trials comparing longer- versus shorter-duration DAPT after DES placement. DATA EXTRACTION: Two reviewers screened potentially eligible articles; extracted data on populations, interventions, and outcomes; assessed risk of bias; and used the Grading of Recommendations Assessment, Development and Evaluation guidelines to rate overall confidence in effect estimates. DATA SYNTHESIS: Among 1010 articles identified, 9 trials including 29,531 patients were eligible; data were complete for 28,808 patients. Moderate-quality evidence showed that longer-duration DAPT decreased risk for myocardial infarction (risk ratio [RR], 0.73 [95% CI, 0.58 to 0.92]) and increased mortality (RR, 1.19 [CI, 1.04 to 1.36]). High-quality evidence showed that DAPT increased risk for major bleeding (RR, 1.63 [CI, 1.34 to 1.99]). LIMITATION: Confidence in estimates were decreased owing to imprecision for most outcomes (particularly myocardial infarction), risk of bias from limited blinding in 7 of 9 studies, indirectness due to variability in use of first- and second-generation stents, and off-protocol use of DAPT in some studies. CONCLUSION: Extended DAPT is associated with approximately 8 fewer myocardial infarctions per 1000 treated patients per year but 6 more major bleeding events than shorter-duration DAPT. Because absolute effects are very small and closely balanced, decisions regarding the duration of DAPT therapy must take into account patients' values and preference. PRIMARY FUNDING SOURCE: None.
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Spencer et al. (2015) conducted a meta-analysis in Coronary artery disease (n=29,531). Longer-duration dual-antiplatelet therapy vs. Shorter-duration dual-antiplatelet therapy was evaluated on Myocardial infarction (RR 0.73, 95% CI 0.58 to 0.92). Longer-duration DAPT after DES placement decreased myocardial infarction risk (RR 0.73; 95% CI 0.58-0.92) but increased mortality (RR 1.19) and major bleeding (RR 1.63) versus shorter-duration DAPT.
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