Key result
Intermediate-dose tinzaparin shows no benefit over low-dose enoxaparin for thrombosis or bleeding.
Why the study?
Acutely ill hospitalized patients have a high thrombosis risk even post-discharge, but the safest and most effective thromboprophylaxis strategy remains under debate.
Does intermediate-dose tinzaparin prevent thrombotic events without increasing bleeding compared to low-dose enoxaparin in hospitalized internal medicine patients with a PADUA score ≥ 4?
Observational (n=346)
No
Does intermediate-dose tinzaparin prevent thrombotic events without increasing bleeding compared to low-dose enoxaparin in hospitalized internal medicine patients with a PADUA score ≥ 4?
In high-risk hospitalized medical patients, intermediate-dose tinzaparin and low-dose enoxaparin demonstrated similar rates of thrombotic and bleeding events, though the study was underpowered to detect small differences.
Background/Objectives: Acutely ill patients in hospital are at high risk for thrombosis, even post-discharge. However, the safest and most effective strategy for thromboprophylaxis in such patients is still under debate. Our aim was to compare the subcutaneous use of low-dose prophylactic enoxaparin versus intermediate-dose tinzaparin. Methods: Patients in an internal medicine clinic of a tertiary hospital in Athens, Greece, with increased risk for thrombosis (PADUA score ≥ 4) received either intermediate-dose tinzaparin (8000 anti-Xa units) or 40 mg enoxaparin as thromboprophylaxis. Efficacy and adverse effects were evaluated and compared up to 14 days post-discharge. Results: A total of 251 patients who received tinzaparin were compared with 95 patients under enoxaparin thromboprophylaxis. No statistically significant difference was found in the number of bleeding and/or clinically evident thrombotic events between the two groups [6 versus 14 bleeding (p = 0.2603) events and 0 versus 1 venous thrombotic event (p = 0.999) in the enoxaparin and tinzaparin groups, respectively]. Moreover, no difference was found in length of stay [enoxaparin: 10 days (95%CI: 9–12 days); tinzaparin: 8 days (95%CI: 8–10 days, HR = 1.18, 95%CI: 0.91–1.54, p = 0.2] or mortality [11 deaths with enoxaparin (11.58%, 95%CI: 6.59–19.55%) and 50 deaths with tinzaparin (19.92%, 95%CI: 15.45–25.30%, OR: 1.9, 95%CI: 0.94–3.83, p = 0.069)]. The use of thromboprophylaxis for two weeks post-discharge did not result in any bleeding or clinically evident thrombotic events in either group. Conclusions: In our cohort, the use of intermediate-dose tinzaparin was similar to the use of low-dose enoxaparin for patients with a high PADUA score in terms of thrombotic and/or bleeding events.
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Kaklamanos et al. (2026) conducted an observational in Acute medical illness with high risk for venous thromboembolism (n=346). Intermediate-dose tinzaparin vs. Low-dose enoxaparin (40 mg) was evaluated on Bleeding events (p=0.2603). Intermediate-dose tinzaparin showed no statistically significant difference compared to low-dose enoxaparin in the incidence of bleeding (14 vs 6 events, p=0.2603) or clinically evident thrombotic events (1 vs 0 events, p=0.999) in high-risk hospitalized internal medicine patients.
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