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. 2022 Jul 9;31:101949. doi: 10.1016/j.jcot.2022.101949

Table 4.

Subgroup analysis of VTE and other adverse events by prophylaxis type for ISS>15.

Patients (N) VTE Prophylaxis Agent
P-value
UH (%) LMWH (%)



Outcome
VTE (PE or DVT) 53 18 (18.8) 35 (7.4) 0.0017
PE 20 8 (8.3) 12 (2.6) 0.012
DVT 41 13 (13.5) 28 (6) 0.016
ARDS 19 2 (2.1) 17 (3.6) 0.755
Cardiac arrest 8 3 (3.1) 5 (1.1) 0.141
MI 2 1 (1) 1 (0.2) 0.314
Stroke/CVA 3 0 (0) 3 (0.6) 1.000
Unplanned Intubation 17 4 (4.2) 13 (2.8) 0.509
Bleed Event 0 0 (0) 0 (0) 1.000
Any complication 90 26 (27.1) 64 (13.6) 0.0021
Death 7 4 (4.2) 3 (0.6) 0.0181



Hospital Length of Stay (Days) 0.026
1 to 4 39 3 (3.1) 36 (7.7)
5 to 9 193 25 (26) 168 (35.7)
10 or greater 333 68 (70.8) 265 (56.4)



ICU length of stay (Days) 0.067
1 to 4 154 21 (21.9) 133 (28.3)
5 to 9 116 22 (22.9) 94 (20)
10 or greater 150 36 (37.5) 114 (24.3)

†Significant P-values are defined as <0.05/12 = 0.0041 after Bonferroni correction and are presented in bold.

ISS: Injury Severity Scale, VTE: venous thromboembolism, UH: unfractionated heparin, LMWH: low molecular weight heparin, DVT: deep vein thrombosis, PE: pulmonary embolism, ARDS: acute respiratory distress syndrome, MI: myocardial infarction, CVA: cerebrovascular accident.