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Systematic review and Plenary paper

Clinical importance of thrombocytopenia in patients with acute coronary syndromes: a systematic review and meta-analysis

, , , &
Pages 817-827
Received 31 Aug 2018
Accepted 13 Sep 2018
Published online: 22 Oct 2018

Abstract

Thrombocytopenia (TP) is common in hospitalized patients. In the context of acute coronary syndromes (ACS), TP has been linked to adverse clinical outcomes. We present a systematic review and meta-analysis of the evidence on the clinical importance of preexisting and in-hospital acquired TP in the context of ACS. Specifically, we address (a) the prevalence and associated factors with TP in the context of ACS; and (b) the association between TP and all-cause mortality, major adverse cardiovascular events (MACEs), and major bleeding. We conducted systematic literature searches in MEDLINE and Web of Science. For the meta-analysis, we fit linear mixed models with a random study-specific intercept for the aggregate outcomes. A total of 16 studies and 190 915 patients were included in this study. Of these patients, 8.8% ± 1.2% presented with preexisting TP while 5.8% ± 1.0% developed TP after hospital admission. Preexisting TP was not statistically significantly associated with adverse outcomes. Acquired TP was associated with greater risk of all-cause mortality (risk difference [RD]: 4.3%; 95% confidence interval [CI]: 2–6%; p = 0.04), MACE (RD: 8.5%; 95% CI: 1–16.0%; p = 0.037), and major bleeding (RD: 11.9%; 95% CI: 5–19%; p = 0.005). In conclusion, TP is a prevalent condition in patients admitted for an ACS and identifies a high-risk patient population more likely to experience ischemic and bleeding complications, as well as higher mortality.

Acknowledgments

This work was funded by a grant from the Faculty of Pharmacy, Université de Montréal. V.D. was supported by an internal award from the Faculty of Medicine, Université de Montréal. M.E.S. is a Canadian Institutes of Health Research (CIHR) New Investigator. E.M.J. is supported by research grants from the Fonds de Recherche du Québec en santé (FRQS), the Canadian Institutes for Health Research (CIHR), the Canada Foundation for Innovation (CFI), the AGE-WELL Network of Centres of Excellence (NCE), and by the Fondation de l’Institut de Cardiologie de Montréal. M.L. is supported by research grants from the Fonds de Recherche du Québec en santé (FRQS), the Canadian Institutes for Health Research (CIHR), the Canada Foundation for Innovation (CFI), Diabetes Quebec, and by the Fondation de l’Institut de Cardiologie de Montréal.

Disclosure Statement

V.D., M.E.S., and G.R. have no relationship with industry to disclose. E.M.J. holds research grants from AstraZeneca. M.L. has received in-kind and financial support for investigator-initiated grants from Roche Diagnostics, Aggredyne, and LEO Pharma.

Additional information

Funding

This work was supported by the Université de Montréal.

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