# The impact of antithrombin III supplementation on prognosis during extracorporeal membrane oxygenation: a systematic review and meta-analysis

**Authors:** Ya-Ting Zeng, Yi-Nan Liu, Zi-Han Chen, Qiang Chen, Kai-Peng Sun

PMC · DOI: 10.1080/07853890.2025.2542439 · 2025-08-04

## TL;DR

This study finds that adding antithrombin III during ECMO treatment does not improve patient outcomes and may even increase risks in some cases.

## Contribution

The study provides a systematic review and meta-analysis of antithrombin III's effects in ECMO patients, revealing no mortality benefit and potential risks.

## Key findings

- Antithrombin III supplementation did not reduce mortality in ECMO patients.
- It showed no significant benefit in reducing bleeding or thrombosis events.
- In cardiac ECMO patients, it was linked to increased mortality but reduced thromboembolism risk.

## Abstract

To systematically evaluate the impact of antithrombin III (AT III) supplementation on the prognosis of patients undergoing extracorporeal membrane oxygenation (ECMO).

A comprehensive literature search was conducted in PubMed, Web of Science, Embase, and the Cochrane Library for studies assessing the effects of AT III supplementation on ECMO patient outcomes. The risk of bias was assessed using the Cochrane Risk of Bias and The Newcastle-Ottawa Scale.

A total of six studies involving 18,641 ECMO-treated patients were included. The meta-analysis showed that AT III supplementation did not reduce mortality in ECMO patients (RR = 1.17, 95% CI: 0.85–1.60, p = 0.34) and had no significant benefit in reducing bleeding events (RR = 1.04, 95% CI: 0.90–1.21, p = 0.56) or thrombosis (RR = 1.29, 95% CI: 0.81–2.05, p = 0.29). Subgroup analysis revealed that in cardiac ECMO patients, AT III supplementation was associated with an increased mortality but a reduced risk of thromboembolism. Conversely, in other ECMO support types, AT III supplementation was linked to a higher incidence of thromboembolism, with adult patients also showing an increased thromboembolism rate. No statistically significant differences were observed in other subgroup analyses.

Overall, AT III supplementation does not reduce in-hospital mortality, bleeding, or thrombotic complications in ECMO patients and may even pose risks in certain populations. Therefore, routine AT III supplementation in ECMO patients may be not currently recommended.

## Linked entities

- **Proteins:** SERPINC1 (serpin family C member 1)

## Full-text entities

- **Genes:** F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, SERPINC1 (serpin family C member 1) [NCBI Gene 462] {aka AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2}, F10 (coagulation factor X) [NCBI Gene 2159] {aka FX, FXA}
- **Diseases:** Critically ill (MESH:D016638), disseminated intravascular coagulation (MESH:D004211), sepsis (MESH:D018805), respiratory and cardiac failure (MESH:D012131), acquired (MESH:D003638), AT deficiency (MESH:D020152), acidosis (MESH:D000138), ECMO (MESH:D000860), Bleeding (MESH:D006470), thrombosis (MESH:D013927), thromboembolism (MESH:D013923)
- **Chemicals:** Heparin (MESH:D006493)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12322988/full.md

---
Source: https://tomesphere.com/paper/PMC12322988