American Journal of Cardiology
Volume 103, Issue 2 , Pages 175-180, 15 January 2009

Thrombocytopenia in Patients With an Acute Coronary Syndrome (from the Global Registry of Acute Coronary Events [GRACE])

  • Joel M. Gore, MD

      Affiliations

    • University of Massachusetts Medical School, Worcester, Massachusetts
    • Corresponding Author InformationCorresponding author: Tel: 508-856-3871; fax: 508-856-4571
  • ,
  • Frederick A. Spencer, MD

      Affiliations

    • McMaster University, Hamilton, Ontario, Canada
  • ,
  • Enrique P. Gurfinkel, MD

      Affiliations

    • ICYCC Favaloro Foundation, Buenos Aires, Argentina
  • ,
  • José López-Sendón, MD

      Affiliations

    • Hospital Universitario LePaz, Madrid, Spain
  • ,
  • Ph. Gabriel Steg, MD

      Affiliations

    • INSERM U-698 and Université Paris VII Hôpital Bichat-Claude Bernard, AP-HP, Paris, France
  • ,
  • Christopher B. Granger, MD

      Affiliations

    • Duke University Medical Center, Durham, North Carolina
  • ,
  • Gordon FitzGerald, PhD

      Affiliations

    • University of Massachusetts Medical School, Worcester, Massachusetts
  • ,
  • Giancarlo Agnelli, MD

      Affiliations

    • Department of Internal and Cardiovascular Medicine, University of Perugia, Perugia, Italy
  • ,
  • GRACE Investigators

Received 11 July 2008; received in revised form 22 August 2008; accepted 22 August 2008. published online 13 November 2008.

The incidence of thrombocytopenia after hospital admission, patient and treatment characteristics, and outcomes in patients enrolled in the prospective multinational GRACE were examined. Heparin (unfractionated or low molecular weight) and glycoprotein IIb/IIIa-inhibition can be associated with immune-mediated thrombocytopenia of clinical importance. The prevalence of thrombocytopenia in patients with acute coronary syndromes (ACSs) in general and specifically related to these therapies and associated outcomes have been studied little outside of clinical trials. Patients with an ACS were stratified into 4 groups of those with heparin-induced thrombocytopenia (HIT), those with glycoprotein IIb/IIIa-associated thrombocytopenia (GAT), those with other thrombocytopenia (not diagnosed as HIT or associated with glycoprotein inhibitors), and those with no thrombocytopenia. From June 2000 to September 2007, a total of 52,647 patients with an ACS and information for platelet count were enrolled in GRACE. Of these, 152 (0.3%) were reported to develop HIT, 324 (0.6%) developed GAT, and 368 (0.7%) developed other thrombocytopenia. Patients with HIT, GAT, or other thrombocytopenia were significantly more likely to die in the hospital versus those without these diseases (adjusted odds ratio [OR] 1.94, 95% confidence interval [CI] 1.07 to 3.53; adjusted OR 3.45, 95% CI 2.35 to 5.05; and adjusted OR 2.83, 95% CI 1.97 to 4.06, respectively). They were also more likely to experience major bleeding, (re)infarction, or stroke. In conclusion, in this large multinational registry, 1.6% of patients with ACS were reported to develop thrombocytopenia, with only 0.3% being HIT. Regardless of whether patients had clinically recognized HIT, GAT, or other thrombocytopenia, all 3 groups had significantly higher rates of major bleeding, recurrent infarction, stroke, and death.

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 The Global Registry of Acute Coronary Events (GRACE) is supported by an unrestricted educational grant from Sanofi-Aventis, Paris, France, to the Center for Outcomes Research, University of Massachusetts Medical School, Worcester, Massachusetts. Dr. Gore was supported by Sanofi-Aventis. Dr. Gurfinkel was supported by research/other grants from Sanofi-Aventis, Eli Lilly, Pasteur, and Schering; is on the Speakers' Bureau of Bristol-Myers Squibb; and a Consultant/Advisory Board member of the TIMI Group and Sanofi-Aventis. Dr. López-Sendón was supported by research grants from the TIMI Group, Sanofi-Aventis, Servier, BMS, and Amgem; received honoraria from Servier, Novartis, and Pfizer; and is a Consultant/Advisory Board member for Servier, Medtronic, Lilly, and CVT. Dr. Steg was supported by a research grant from Sanofi-Aventis; is on the Speakers Bureau for Boehringer Ingelheim, Bristol-Myers Squibb, GlaxoSmithKline, Merck Sharp & Dohme, Novartis, Nycomed, Sanofi-Aventis, Sankyo, Servier, and ZLB-Behring; and is a Consultant/Advisory Board member of AstraZeneca, Bristol-Myers Squibb, GlaxoSmithKline, Merck Sharp & Dohme, Pfizer, Sanofi-Aventis, Servier, and Takeda. Dr. Granger was supported by Alexion, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, deCODE Genetics, Genentech, GlaxoSmithKline, Novartis, Proctor & Gamble, Sanofi-Aventis, The Medicines Company, INO Therapeutics, and Medicure. Giancarlo Agnelli was supported by Sanofi-Aventis.

PII: S0002-9149(08)01515-4

doi:10.1016/j.amjcard.2008.08.055

American Journal of Cardiology
Volume 103, Issue 2 , Pages 175-180, 15 January 2009