Study characteristics |
Methods |
Study design: retrospective cohort
Type of publication: peer‐reviewed journal publication
Setting and dates: hospital, 1 January 2020‐13 February 2020
Country: China
Language: English
Number of centres: 1
Trial registration number: NR
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Participants |
Number of participants: 449 allocated (intervention = 99; comparator = 350)
Age: 65.1 ± 12.0 years (mean ± SD)
Gender: 268 (60%) male
Comorbidities: hypertension (39.4%), diabetes (20.7%), heart diseases (9.1%)
Confounding factors: prior anticoagulation (NR), surgery (NR), cancer (NR), antiplatelet use (NR), history of VTE (NR)
Type of ventilator support: NR
Inclusion criteria
Exclusion criteria
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Interventions |
-
Intervention of interest: anticoagulation for ≥ 7 days
UFH (10,000‐15,000 IU/d) in 5 participants, or
LMWH (40‐60 mg enoxaparin/d) in 94 participants
Comparator: no anticoagulants
Concomitant therapy: all participants received antiviral
Duration of follow‐up: 28 days after ICU admission
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Outcomes |
There is no differentiation between primary and secondary outcomes.
Mortality
Coagulation parameters
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Notes |
Sponsor/funding: National Mega Project on Major Infectious Disease Prevention of China, Grant/Award Number: 2017ZX10103005‐007
COIs: the study authors declare that they have no conflicts of interest.
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