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. 2020 Oct 2;2020(10):CD013739. doi: 10.1002/14651858.CD013739

Liu 2020.

Study characteristics
Methods
  • Study design: retrospective cohort

  • Type of publication: preprint

  • Setting and dates: ICU (intervention); hospital ward (comparator), 8 February 2020‐3 April 2020

  • Country: China

  • Language: English

  • Number of centres: 1

  • Trial registration number: NR

Participants
  • Number of participants: 154 allocated (intervention = 61; comparator = 93)

  • Age: 72.41 ± 10.4 years (mean ± SD) in intervention group, 70.1 ± 11.01 years (mean ± SD) in comparator group

  • Gender: 94 (61%) male

  • Comorbidities: NR

  • Confounding factors: prior anticoagulation (NR), surgery (NR), cancer (NR), antiplatelet use (NR), history of VTE (NR)

  • Type of ventilator support: NR


Inclusion criteria
  • COVID‐19 confirmed by a PCR test


Exclusion criteria
  • NR

Interventions
  • Intervention of interest: with anticoagulation (heparin). Type and dose were not described

  • Comparator: without anticoagulation

  • Concomitant therapy: possible use of tocilizumab, but the proportion of participants was not described

  • Duration of follow‐up: NR

Outcomes There is no differentiation between primary and secondary outcomes.
  • Mortality

  • Laboratorial parameters (blood routine characteristics, coagulation parameters)

  • Thrombocytopenia

Notes
  • Sponsor/funding: grants 2016CB02400 and 2017YFC1201103 from the National Major Research and Development Program of China. The study authors declare that "The founder of this study did not contributed to data collection, analysis, and interpretation, and the manuscript preparation."

  • COIs: all study authors declare no competing interests