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Apixaban versus enoxaparin to prevent venous thromboembolism in post-operative patients with gynecologic cancers at an urban academic medical center. | LitMetric

AI Article Synopsis

  • A clinical trial found that using apixaban for post-operative venous thromboembolism (VTE) prevention in gynecologic oncology patients is as safe and effective as enoxaparin (LMWH) at a single urban academic center.
  • A retrospective study analyzed 215 patients who had exploratory laparotomies, comparing outcomes for those discharged with apixaban to those discharged with enoxaparin.
  • Results showed similar VTE rates in both groups (3.33% for apixaban vs. 4.61% for enoxaparin) and lower major bleeding events with apixaban (1.31% vs. 3.08%), indicating that apixaban is a safe alternative for

Article Abstract

Objective: A recent clinical trial demonstrated that the use of apixaban was safe and equal to enoxaparin (LMWH) in post-operative gynecologic oncology patients. This study aimed to determine if these findings are applicable in a diverse patient population at a single site urban academic medical center.

Methods: This was a retrospective cohort study of patients who underwent an exploratory laparotomy for confirmed or presumed gynecologic cancer from the years 2017-2023 at a single-site urban academic medical center. Venous thromboembolism (VTE) prophylaxis with LMWH was standard practice at our institution up until January 2021 after which apixaban became standard for post-operative prophylaxis in our division. Baseline demographic and clinical characteristics of patients receiving apixaban post-operatively were compared to the population previously receiving enoxaparin. The primary outcome was a VTE event within 90 days of surgery. Secondary outcomes included major and minor bleeding events.

Results: Two hundred fifteen patients met inclusion criteria, of which 65 were discharged on enoxaparin and 150 were discharged on apixaban. Baseline characteristics in terms of age, race/ethnicity and BMI found no significant difference between the two groups. Rates of any VTE event within 90 days of surgery were similar for apixaban and LMWH (3.33 % vs. 4.61 %, p = 0.6). Secondary outcomes demonstrated that the rate of a major bleeding event in apixaban group was 1.31 % and LMWH group was 3.08 %, (. Minor bleeding events in the apixaban group were comparable to the LMWH group (10.60 % vs 10.16 %, p = 0.5.

Conclusions: In this real world, urban setting, for women undergoing laparotomy for gynecologic cancer, apixaban as post-operative VTE prophylaxis showed no increase in VTE events and appeared safe with no increase in bleeding events compared to LMWH. This study adds to the literature demonstrating that apixaban is safe and effective for VTE prophylaxis in our gynecologic oncology patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11532814PMC
http://dx.doi.org/10.1016/j.gore.2024.101535DOI Listing

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