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Clinical implications of clopidogrel non-response in cardiovascular patients: a systematic review and meta-analysis.
Combescure, C; Fontana, P; Mallouk, N; Berdague, P; Labruyere, C; Barazer, I; Gris, J C; Laporte, S; Fabbro-Peray, P; Reny, J L.
  • Combescure C; Division of Clinical Epidemiology, Geneva University Hospital, Geneva, Switzerland.
J Thromb Haemost ; 8(5): 923-33, 2010 May.
Article en En | MEDLINE | ID: mdl-20156305
ABSTRACT
UNLABELLED BSUMMARY

BACKGROUND:

Previous studies have shown an important risk of cardiovascular events in patients with clopidogrel biological non-response, and data have shown considerable, unexplored heterogeneity.

OBJECTIVES:

To evaluate the magnitude of cardiovascular risk associated with clopidogrel non-response and to explore heterogeneity.

METHODS:

This was a systematic review and meta-analysis of prospective studies of patients treated with clopidogrel for symptomatic atherothrombosis, evaluated by light transmission aggregometry with ADP and monitored prospectively for clinical ischemic events.

RESULTS:

Fifteen studies were included, totaling 3960 patients, of whom 25% were considered to be clopidogrel non-responders. The global relative risk (RR) for recurrent ischemic events in clopidogrel non-responders was 3.5 [95% confidence interval (CI) 2.4-5.2, P < 0.0001]. The results of the different studies were heterogeneous (Cochran P = 0.01 and I(2) = 52%). The most recent studies yielded lower RRs [global RR = 2.9 (95% CI 2.3-3.8) after 2007, and global RR = 6.6 (95% CI 3.7-11.9) before 2007, P = 0.01]. Heterogeneity was present in the group of studies in which more than 10% of patients took glycoprotein (GP)IIb-IIIa inhibitors [Cochran P = 0.003 and I(2) = 70%; RR = 3.8 (95% CI 2.9-5.1)] and was absent in the other studies [Cochran P = 0.88 and I(2) = 0; RR = 2.5 (95% CI 1.7-3.6)]. The RR was significantly higher in studies using higher ADP maximal aggregation cut-offs (> 65%) for clopidogrel non-response than in studies using lower cut-offs [RR = 5.8 (95% CI 3.2-10.3) and RR = 2.9 (95% CI 2.2-3.7), respectively, P = 0.03].

CONCLUSIONS:

The risk of ischemic events associated with clopidogrel non-response is now more precisely defined. The risk is heterogeneous across studies, possibly because of an interaction with GPIIb-IIIa inhibitors and the use of different cut-offs to identify non-responders.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ticlopidina / Inhibidores de Agregación Plaquetaria / Enfermedades Cardiovasculares Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2010 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Ticlopidina / Inhibidores de Agregación Plaquetaria / Enfermedades Cardiovasculares Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Año: 2010 Tipo del documento: Article