Research and Practice in Thrombosis and Haemostasis (Dec 2021)

Randomized trials of therapeutic heparin for COVID‐19: A meta‐analysis

  • Michelle Sholzberg,
  • Bruno R. daCosta,
  • Grace H. Tang,
  • Hassan Rahhal,
  • Musaad AlHamzah,
  • Lisa Baumann Kreuziger,
  • Fionnuala Ní Áinle,
  • Mozah Obaid Almarshoodi,
  • Paula D. James,
  • David Lillicrap,
  • Marc Carrier,
  • Andrew Beckett,
  • Michael Fralick,
  • Saskia Middeldorp,
  • Agnes Y. Y. Lee,
  • Kevin E. Thorpe,
  • Elnara Márcia Negri,
  • Mary Cushman,
  • Peter Jüni,
  • the RAPID Trial Investigators

DOI
https://doi.org/10.1002/rth2.12638
Journal volume & issue
Vol. 5, no. 8
pp. n/a – n/a

Abstract

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Abstract Background Pulmonary endothelial injury and microcirculatory thromboses likely contribute to hypoxemic respiratory failure, the most common cause of death, in patients with COVID‐19. Randomized controlled trials (RCTs) suggest differences in the effect of therapeutic heparin between moderately and severely ill patients with COVID‐19. We did a systematic review and meta‐analysis of RCTs to determine the effects of therapeutic heparin in hospitalized patients with COVID‐19. Methods We searched PubMed, Embase, Web of Science, medRxiv, and medical conference proceedings for RCTs comparing therapeutic heparin with usual care, excluding trials that used oral anticoagulation or intermediate doses of heparin in the experimental arm. Mantel‐Haenszel fixed‐effect meta‐analysis was used to combine odds ratios (ORs). Results and Conclusions There were 3 RCTs that compared therapeutic heparin to lower doses of heparin in 2854 moderately ill ward patients, and 3 RCTs in 1191 severely ill patients receiving critical care. In moderately ill patients, there was a nonsignificant reduction in all‐cause death (OR, 0.76; 95% CI, 0.57‐1.02), but significant reductions in the composite of death or invasive mechanical ventilation (OR, 0.77; 95% CI, 0.60 0.98), and death or any thrombotic event (OR, 0.58; 95% CI, 0.45‐0.77). Organ support‐free days alive (OR, 1.29; 95% CI, 1.07‐1.57) were significantly increased with therapeutic heparin. There was a nonsignificant increase in major bleeding. In severely ill patients, there was no evidence for benefit of therapeutic heparin, with significant treatment‐by‐subgroup interactions with illness severity for all‐cause death (P = .034). In conclusion, therapeutic heparin is beneficial in moderately ill patients but not in severely ill patients hospitalized with COVID‐19.

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