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January 23, 2015European Heart Journal431 citationsOpen Access

ISAR-SAFE: a randomized, double-blind, placebo-controlled trial of 6 vs. 12 months of clopidogrel therapy after drug-eluting stenting

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SSStefanie SchüpkeRBRobert A. ByrneJBJurriën M. ten Berg

Structured PICO

Does 6 months of clopidogrel therapy compared to 12 months provide non-inferior clinical outcomes in patients undergoing drug-eluting stent implantation?

P
Population
4,000 patients who underwent drug-eluting stent (DES) implantation and were receiving aspirin and clopidogrel at 6 months post-implantation
I
Intervention
6 months of clopidogrel therapy (randomized to a 6-month period of placebo starting at 6 months post-DES)
C
Comparator
12 months of clopidogrel therapy (randomized to an additional 6-month period of clopidogrel starting at 6 months post-DES)
O
Outcome
Composite of death, myocardial infarction, stent thrombosis, stroke, and thrombolysis in myocardial infarction major bleeding at 9 months after randomizationcomposite

Six months of clopidogrel therapy was non-inferior to 12 months after DES implantation, though the trial was limited by premature termination and low event rates.

Limitations

  • Premature termination owing to slow recruitment
  • Lower than expected event rates

Abstract

BACKGROUND: In patients receiving aspirin, the optimal duration of clopidogrel therapy after drug-eluting stent (DES) implantation remains unclear. METHODS: This multicentre, randomized, double-blind, placebo-controlled trial tested the hypothesis that in patients undergoing DES implantation, 6 months of clopidogrel is non-inferior to 12 months in terms of clinical outcomes. At 6 months after DES implantation, patients on clopidogrel were randomly assigned to either a 6-month period of placebo or an additional 6-month period of clopidogrel. The primary endpoint was the composite of death, myocardial infarction, stent thrombosis, stroke, and thrombolysis in myocardial infarction major bleeding at 9 months after randomization. RESULTS: Owing to slow recruitment and low event rates, the trial was stopped prematurely after enrolment of 4005 of 6000 planned patients. Of 4000 patients included in the final analysis, 1997 received 6 months of clopidogrel and 2003 received 12 months. The primary endpoint occurred in 29 patients (1.5%) assigned to 6 months of clopidogrel and 32 patients (1.6%) assigned to 12 months, observed difference -0.1%, upper limit of one-sided 95% confidence interval (CI) 0.5%, limit of non-inferiority 2%, Pfor noninferiority <0.001. Stent thrombosis was observed in five patients (0.3%) assigned to 6 months of clopidogrel and three patients (0.2%) assigned to 12 months; hazard ratio (HR) 1.66, 95% CI: 0.40-6.96, P = 0.49. Thrombolysis in myocardial infarction major bleeding was observed in 4 patients (0.2%) assigned to 6 months clopidogrel and 5 patients (0.3%) assigned to 12 months; HR 0.80, 95% CI: 0.21-2.98, P = 0.74. CONCLUSIONS: In the present trial, characterized by low event rates, we did not observe a significant difference in net clinical outcome between 6 and 12 months of clopidogrel therapy after DES implantation. However, the results of the trial must be considered in view of its premature termination and lower than expected event rates. The trial is registered with ClinicalTrials.gov, Identifier: NCT00661206.

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Cite This Study

Schüpke et al. (2015) studied this question.

synapsesocial.com/papers/6a7d16f31ec2a9317b425093https://doi.org/10.1093/eurheartj/ehu523
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