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Prior antiplatelet therapy and outcome following intracerebral hemorrhage: A systematic review

  • B. B. Thompson
  • , Y. Béjot
  • , V. Caso
  • , J. Castillo
  • , H. Christensen
  • , M. L. Flaherty
  • , C. Foerch
  • , K. Ghandehari
  • , M. Giroud
  • , S. M. Greenberg
  • , H. Hallevi
  • , J. C. Hemphill
  • , P. Heuschmann
  • , S. Juvela
  • , K. Kimura
  • , P. K. Myint
  • , Y. Nagakane
  • , H. Naritomi
  • , S. Passero
  • , M. R. Rodríguez-Yáñez
  • J. Roquer, J. Rosand, N. S. Rost, P. Saloheimo, V. Salomaa, J. Sivenius, T. Sorimachi, M. Togha, K. Toyoda, W. Turaj, K. N. Vemmos, C. D.A. Wolfe, D. Woo, E. E. Smith
  • Brown University
  • Department of Neurology and Stroke Registry of Dijon
  • University Hospital of Perugia
  • Complejo Hospitalario Universitario de Santiago
  • University of Copenhagen
  • University of Cincinnati
  • Goethe University Frankfurt
  • Mashhad University of Medical Sciences
  • Institut de veille sanitaire
  • Massachusetts General Hospital
  • Tel Aviv Sourasky Medical Center
  • University of California at San Francisco
  • King's College London
  • Charité – Universitätsmedizin Berlin
  • University of Turku
  • Kawasaki Medical School
  • University of East Anglia
  • National Cerebral and Cardiovascular Center
  • University of Siena
  • Hospital del Mar
  • University of Oulu
  • Hospital District of Helsinki and Uusimaa
  • National Institute for Health and Welfare
  • University of Eastern Finland
  • Niigata University
  • Tehran University of Medical Sciences
  • Jagiellonian University Medical College
  • National and Kapodistrian University of Athens
  • Guy's and St Thomas' NHS Foundation Trust
  • University of Calgary

Research output: Contribution to journalReview articlepeer-review

169 Scopus citations

Abstract

Objectives:: Antiplatelet therapy (APT) promotes bleeding; therefore, APT might worsen outcome in patients with intracerebral hemorrhage (ICH). We performed a systematic review and meta-analysis to address the hypothesis that pre-ICH APT use is associated with mortality and poor functional outcome following Ich. Methods:: The Medline and Embase databases were searched in February 2008 using relevant key words, limited to human studies in the English language. Cohort studies of consecutive patients with ICH reporting mortality or functional outcome according to pre-ICH APT use were identified. Of 2,873 studies screened, 10 were judged to meet inclusion criteria by consensus of 2 authors. Additionally, we solicited unpublished data from all authors of cohort studies with >100 patients published within the last 10 years, and received data from 15 more studies. Univariate and multivariable-adjusted odds ratios (ORs) for mortality and poor functional outcome were abstracted as available and pooled using a random effects model. Results:: We obtained mortality data from 25 cohorts (15 unpublished) and functional outcome data from 21 cohorts (14 unpublished). Pre-ICH APT users had increased mortality in both univariate (OR 1.41, 95% confidence interval [CI] 1.21 to 1.64) and multivariable-adjusted (OR 1.27, 95% CI 1.10 to 1.47) pooled analyses. By contrast, the pooled OR for poor functional outcome was no longer significant when using multivariable-adjusted estimates (univariate OR 1.29, 95% CI 1.09 to 1.53; multivariable-adjusted OR 1.10, 95% CI 0.93 to 1.29). Conclusions:: In cohort studies, APT use at the time of ICH compared to no APT use was independently associated with increased mortality but not with poor functional outcome.

Original languageEnglish
Pages (from-to)1333-1342
Number of pages10
JournalNeurology
Volume75
Issue number15
DOIs
StatePublished - Oct 12 2010

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