Table 1.
Baseline characteristics of included studies
Characteristics | Klok et al. | Cui et al. | Chen et al. | Tang et al. | Wang et al. | Helms et al. |
---|---|---|---|---|---|---|
Sample size | 184 | 81 | 25 | 449 | 1026 | 150 |
Study design | Multi-center, retrospective study | Single-center retrospective study | Single-center, retrospective study | Retrospective analysis | Multi-center, retrospective study | Multi-center, prospective cohort |
Study population | Severely ill COVID-19 patients admitted to the ICU | Severely ill COVID-19 patients admitted to the ICU | Hospitalized COVID-19 patients who underwent CTPA | Hospitalized, severely ill COVID-19 patients | Hospitalized COVID-19 patients | Severely ill, admitted to ICU |
Age in years (mean) | 64 | 60 | Not reported | 65.1 ± 12.0 | 42 for Padua score < 4 and 52 for score of ≥ 4 | 63 (median) |
Male sex (%) | 139 (76%) | 37 (46%) | Not reported | 268 (60%) | Not reported | 122 (81.3) |
Prophylaxis for VTE |
All patients received at least standard doses of thromboprophylaxis Prophylaxis options: LMWH nadroparin 2850 IU/day > 100 kg = LMWH nadroparin 5700 IU/day Therapeutic anticoagulation: 17 (9.2%) on admission |
None | 20 pts. treated with LMWH 0.6 mg/kg every 12 h | • 94/99 patients received LMWH (40–60 mg/day) for 7 days or longer | 10 (7%) of 140 patients for whom anticoagulation data were available had received anticoagulant drugs during hospitalization (nine received heparin and one received rivaroxaban) |
Low molecular weight heparin 4000 UI/day or if contra-indicated, unfractionated heparin at 5–8 U/kg/h 105 (70%) prophylactic dosing 45 (30%) therapeutic dosing |