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. 2022 Dec 21;7(12):792–799. doi: 10.1530/EOR-22-0053

Table 2.

Summary of characteristics of included studies.

Reference Patients, n Gender (M:F) Mean age History of VTE Follow-up Surgery Treatment Mobilization after surgery (days) Outcome
(17) 70 24:46 52.2 None At POD 14 and POD 30 THA Aspirin 100 mg bid: 34 patients (5 weeks);
Rivaroxaban 10 mg qd: 36 patients (5 weeks)
POD1 (walk with crutch assisted) Evaluation with lower limb USG, 3 patients in both groups with distal DVT.
(18) 329 223:106 47 15 For 90 days Trauma1 Aspirin 81 mg bid: 165 patients*;
Enoxaparin 30 mg bid : 164 patients*
Not stated 90 days event-free in 99 patients in the aspirin group (59.9%) and 98 patients in the LMWH group (59.4%); No significant statistic difference within both group
(19) 3424 1637:1787 62.8 81 For 90 days THA and TKA Aspirin : 81 mg qd: Hip : 902 patients (30 days), Knee : 805 patients (9 days);
Rivaroxaban : 10 mg qd: Hip :902 patients (30 days);
Rivaroxaban : 10 mg qd : 815 patients (9 days)
Not stated VTE occurred in 11 patients (0.64%) among aspirin group and 12 patients (0.70%) in rivaroxaban group (P < 0.001 for noninferiority and P = 0.84 for superiority).
(20) 120 9:111 64.4 None For 6 weeks TKA Aspirin 100 mg qd : 60 patients (14 days);
LMWH 5000 U/day, POD 1-5, continued with Rivaroxaban 10 mg qd (POD 6 -14)
POD1 (active-passive motion, walking with crane) DVT in 10 patients (16.7%) when using Aspirin and 11 patients (18.3%) when using LMWH and rivaroxaban but no significant difference (P = 0.500)
(21) 324 80:244 64 None For 4 weeks TKA Aspirin 100 mg qd : 110 patients (14 days);
Rivaroxaban 10 mg qd : 102 patients (14 days); LMWH 4000 U qd : 112 patients (14 days)
POD 2 (walking with walking aids under the guidance of caregivers) Incidence of DVT higher in Aspirin group versus Rivaroxaban (18 (16.36%) vs 3 (2.94%),P = 0.017)); No significant difference in DVT incidence with Aspirin compared to s.c. LMWH (14 (12.50%) vs 18 (16.36%), P = 0.831).
(22) 778 444:334 57.8 13 For 90 days THA Aspirin 81 mg qd : 380 patients (28 days);
Dalteparin 5000 U qd : 398 patients (28 days)
Not stated Venous thromboembolism was found in 5 of 398 patients among Dalteparin group and 1 of 380 patients among Aspirin group.
Aspirin was found to be significantly non-inferior (P < 0.001) but not superior (P = 0.22) to Dalteparin.
(23) 900 328:572 63.8 Not stated For 12 months TKA Aspirin 325 mg bid: 194 patients (4 weeks);
Enoxaparin 40mg qd SC (2 weeks) + Aspirin 325 mg bid (2 weeks): 706 patients
POD 1 Symptomatic DVT occurs in 4 patients (2.1%) within the aspirin group and 15 (2.1%) within the LMWH group (P = 0.957).
(24) 275 99:176 68.9 None For 4–-6weeks TKA Aspirin 325 mg bid + CCD: 129 (4 weeks);
Enoxaparin 30mg bid (until discharge), 40mg qd (3 weeks)+ CCD : 135
Not stated. The incidence of DVT for Aspirin (18/129) and Enoxaparin (17/135) was without significant difference (P = 0.34).

1Extremity fracture proximal to the carpals or metatarsal, and hip or acetabular fracture;

*Duration depends on hospital guideline.

CCD, calf compression device; THA, total hip arthroplasty; TKA, total knee arthroplasty,