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Clinical study| Volume 62, P188-194, April 2019

Outcomes of intraparenchymal hemorrhage after direct oral anticoagulant or vitamin K antagonist therapy: A systematic review and meta-analysis

  • Aislyn C. DiRisio
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Icahn School of Medicine at Mount Sinai, New York, NY, USA
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  • Maya Harary
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
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  • Ivo S. Muskens
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Department of Neurosurgery, Brain Center Rudolf Magnus University Medical Center Utrecht, Utrecht, the Netherlands
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  • Ismaeel Yunusa
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Department of Pharmaceutical Business and Administrative Sciences, School of Pharmacy, MCPHS University, Boston, MA, USA
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  • William B. Gormley
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
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  • Linda S. Aglio
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
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  • Timothy R. Smith
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
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  • Jean M. Connors
    Affiliations
    Division of Hematology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA
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  • Author Footnotes
    1 Co-senior author.
    Rania A. Mekary
    Footnotes
    1 Co-senior author.
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Department of Pharmaceutical Business and Administrative Sciences, School of Pharmacy, MCPHS University, Boston, MA, USA
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  • Author Footnotes
    1 Co-senior author.
    Marike L.D. Broekman
    Correspondence
    Corresponding author at: Department of Neurosurgery, Haaglanden Medical Center, The Hague, The Netherlands.
    Footnotes
    1 Co-senior author.
    Affiliations
    Computational Neuroscience Outcomes Center, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, USA

    Department of Neurosurgery, Brain Center Rudolf Magnus University Medical Center Utrecht, Utrecht, the Netherlands

    Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA
    Search for articles by this author
  • Author Footnotes
    1 Co-senior author.
Published:November 21, 2018DOI:https://doi.org/10.1016/j.jocn.2018.11.032

      Highlights

      • Intraparenchymal hemorrhage (IPH) is a feared complication of oral anticoagulation.
      • DOAC-IPH was not associated with increased mortality or hematoma expansion compared to VKA-IPH.
      • DOAC-IPH may be associated with a smaller hematoma volume as compared to VKA-IPH.

      Abstract

      Direct Oral Anticoagulants (DOAC) are increasingly used as an alternative to vitamin-K antagonists (VKA) for anticoagulation and have shown lower rates of intracranial hemorrhage; however, there is disagreement in the literature over the outcomes of the intraparenchymal hemorrhages (IPH) associated with DOACs, and clinical concern regarding the lack of standardized reversal strategies for DOACs. Thus, the aim of this meta-analysis was to compare mortality, hematoma volume, and risk of hematoma expansion in patients who developed an IPH on DOACs versus VKA. A systematic review of the literature was conducted in accordance with the PRISMA guidelines. Studies were selected that reported on mortality, hematoma expansion, and hematoma volume in DOAC-associated IPH. Pooled risk ratios (RR) were calculated for mortality and hematoma expansion and pooled mean difference (MD) was calculated for hematoma volume (ml) using random-effect models. 15 studies reporting on 1238 patients were included in the systematic review. Eleven of these compared DOAC-IPH to VKA-IPH and were pooled quantitatively. DOAC-IPH was not associated with increased mortality risk (RR: 0.95, 95%-CI: 0.72 –1.27) or increased hematoma expansion risk (RR: 0.92; 95%-CI: 0.75–1.12) compared to VKA-IPH. The hematoma volume of DOAC- IPH was statistically significantly smaller than VKA-IPH (MD: −12.14 ml; 95%-CI: −15.38; −8.89). In conclusion, DOAC-IPH was not associated with increased mortality or hematoma expansion compared to VKA-IPH and may be associated with a smaller hematoma volume.

      Keywords

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