# Aspirin vs. enoxaparin for thromboprophylaxis after total hip arthroplasty, total knee arthroplasty, or hip fracture surgery—a systematic review and meta-analysis

**Authors:** Abuduwupuer Haibier, Mailidan Maimaitiniyazi, Hang Lin, Wei Liu, Wencui Li

PMC · DOI: 10.3389/fmed.2026.1790739 · Frontiers in Medicine · 2026-02-23

## TL;DR

This study compares aspirin and enoxaparin for preventing blood clots after major orthopedic surgeries and finds aspirin is equally effective but safer in reducing bleeding risks.

## Contribution

The study provides a systematic review and meta-analysis comparing aspirin and enoxaparin for thromboprophylaxis in orthopedic surgery patients.

## Key findings

- Aspirin and enoxaparin are similarly effective in preventing pulmonary embolism and deep vein thrombosis.
- Aspirin significantly reduces the risk of major and minor bleeding compared to enoxaparin.
- No significant differences were found in wound complications or mortality between the two groups.

## Abstract

To systematically evaluate the efficacy and safety of aspirin vs. enoxaparin for the prevention of venous thromboembolism (VTE) following major orthopedic surgeries.

We systematically searched PubMed, the Cochrane Library, Embase, China National Knowledge Infrastructure (CNKI), Wanfang, and CQVIP (VIP) databases from their inception until August 2025 for randomized controlled trials (RCTs) and cohort studies comparing aspirin with enoxaparin for thromboprophylaxis in patients undergoing major orthopedic surgeries (total hip/knee arthroplasty, hip fracture surgery). Two researchers independently performed literature screening, data extraction, and risk-of-bias assessment for the included studies. A meta-analysis was conducted using Review Manager (RevMan) version 5.3 software.

A total of studies involving 126,367 patients (43,441 in the aspirin group and 82,926 in the enoxaparin group) were included. Regarding efficacy, the initial meta-analysis showed no significant difference in the incidence of pulmonary embolism (PE; odds ratio [OR] = 1.14, 95% CI: 0.66–1.95) or deep vein thrombosis (DVT; primary analysis: Test for overall effect: Z = 0.43, p = 0.67). However, sensitivity analyses after removing key contributors to heterogeneity revealed that the incidence of DVT was significantly lower in the enoxaparin group (OR = 0.78, 95% CI: 0.64–0.96, p = 0.02), while the incidence of PE was significantly higher in the aspirin group (sensitivity analysis: Test for overall effect: Z = 2.30, p = 0.02). Regarding safety, the risks of both major bleeding (OR = 0.60, 95% CI: 0.40–0.89, p = 0.01) and minor bleeding (OR = 0.57, 95% CI: 0.49–0.66, p < 0.00001) were significantly lower in the aspirin group. No statistically significant differences were found between the two groups in terms of wound complications, 90-day all-cause mortality (primary analysis: OR = 0.81, 95% CI: 0.37–1.78, p = 0.60), or readmission rates.

For patients undergoing major orthopedic surgery, aspirin is comparable to enoxaparin in preventing the primary efficacy outcomes of VTE (pulmonary embolism and deep vein thrombosis) but demonstrates a significant advantage in reducing the risk of minor bleeding. Aspirin represents an effective and safer prophylactic option, particularly for patients with higher bleeding risk profiles.

## Linked entities

- **Chemicals:** aspirin (PubChem CID 2244)
- **Diseases:** venous thromboembolism (MONDO:0005399), pulmonary embolism (MONDO:0005279)

## Full-text entities

- **Genes:** COX1 (cytochrome c oxidase subunit I) [NCBI Gene 4512] {aka COI, MTCO1}, F10 (coagulation factor X) [NCBI Gene 2159] {aka FX, FXA}, PTGS1 (prostaglandin-endoperoxide synthase 1) [NCBI Gene 5742] {aka COX1, COX3, PCOX1, PES-1, PGG/HS, PGHS-1}
- **Diseases:** renal impairment (MESH:D007674), organ (MESH:D000092124), DVT (OMIM:612862), hip fracture (MESH:D006620), VTE (MESH:D054556), thrombosis (MESH:D013927), DVT (MESH:D020246), infection (MESH:D007239), thrombophilia (MESH:D019851), function (MESH:D003291), obesity (MESH:D009765), bleeding (MESH:D006470), PE (MESH:D011655), fractures (MESH:D050723), hematoma (MESH:D006406), complications (MESH:D008107), HL (MESH:C538324), wound complications (MESH:D014947), ecchymosis (MESH:D004438), splenic rupture (MESH:D013161), cancer (MESH:D009369), impairment of (MESH:D060825)
- **Chemicals:** LMWH (MESH:D006495), heparin (MESH:D006493), enoxaparinn (-), dabigatran (MESH:D000069604), TXA2 (MESH:D013928), ASA (MESH:D001241), Enoxaparin (MESH:D017984)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12926655/full.md

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926655/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926655/full.md

---
Source: https://tomesphere.com/paper/PMC12926655