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Meta-Analysis
. 2008 Jan 26;336(7637):195-8.
doi: 10.1136/bmj.39430.529549.BE. Epub 2008 Jan 17.

Aspirin "resistance" and risk of cardiovascular morbidity: systematic review and meta-analysis

Affiliations
Meta-Analysis

Aspirin "resistance" and risk of cardiovascular morbidity: systematic review and meta-analysis

George Krasopoulos et al. BMJ. .

Abstract

Objective: To determine if there is a relation between aspirin "resistance" and clinical outcomes in patients with cardiovascular disease.

Design: Systematic review and meta-analysis.

Data source: Electronic literature search without language restrictions of four databases and hand search of bibliographies for other relevant articles.

Review methods: Inclusion criteria included a test for platelet responsiveness and clinical outcomes. Aspirin resistance was assessed, using a variety of platelet function assays.

Results: 20 studies totalling 2930 patients with cardiovascular disease were identified. Most studies used aspirin regimens, ranging from 75-325 mg daily, and six studies included adjunct antiplatelet therapy. Compliance was confirmed directly in 14 studies and by telephone or interviews in three. Information was insufficient to assess compliance in three studies. Overall, 810 patients (28%) were classified as aspirin resistant. A cardiovascular related event occurred in 41% of patients (odds ratio 3.85, 95% confidence interval 3.08 to 4.80), death in 5.7% (5.99, 2.28 to 15.72), and an acute coronary syndrome in 39.4% (4.06, 2.96 to 5.56). Aspirin resistant patients did not benefit from other antiplatelet treatment.

Conclusion: Patients who are resistant to aspirin are at a greater risk of clinically important cardiovascular morbidity long term than patients who are sensitive to aspirin.

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Conflict of interest statement

Competing interests: None declared.

Figures

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Fig 1 Flow of papers through review process
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Fig 2 Risk of any cardiovascular event in aspirin resistant patients
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Fig 3 Risks of any cardiovascular event in aspirin resistant and aspirin sensitive patients treated with aspirin alone, and aspirin and clopidogrel (with or without an inhibitor of platelet glycoprotein IIb/IIIa)
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Fig 4 Dose related effect of aspirin on cardiovascular outcome
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Fig 5 Funnel plot for detection of possible publication bias

Comment in

References

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