# Peripheral Versus Central Cannulation for Venoarterial Extracorporeal Membrane Oxygenation (VA-ECMO): A Meta-Analysis of Bleeding and Vascular Complications

**Authors:** Giorgi Chilingarashvili, Giorgi Maisuradze, Aimal Shah, Franco Campoli, Laura Knittig, Avilash Mondal, Vakhtang Robakidze, Tuy Nguyen, Vien Truong

PMC · DOI: 10.7759/cureus.101271 · Cureus · 2026-01-11

## TL;DR

Peripheral ECMO cannulation reduces bleeding risk but increases limb ischemia risk compared to central cannulation, with no significant differences in other complications.

## Contribution

This study provides a meta-analysis comparing peripheral and central VA-ECMO cannulation strategies, highlighting their respective risks for bleeding and limb ischemia.

## Key findings

- Peripheral cannulation is associated with a 45% lower risk of major bleeding compared to central cannulation.
- Peripheral cannulation increases the risk of limb ischemia by 43% compared to central cannulation.
- No significant differences were found in infection, renal replacement therapy, or cerebrovascular accidents between the two cannulation methods.

## Abstract

Extracorporeal membrane oxygenation (ECMO) is increasingly utilized in refractory cardiogenic shock, though the optimal cannulation strategy remains debated, due to divergent vascular and bleeding complications. Peripheral (femoral) access offers ease of deployment but may increase limb ischemia risk, while central (aortic/right atrial) cannulation improves antegrade flow, but carries a higher surgical bleeding burden. We performed a meta-analysis to compare outcomes between peripheral and central cannulation, focusing on major complications, including bleeding, limb ischemia, infection, renal replacement therapy (RRT), and cerebrovascular accidents (CVAs).

We systematically searched MEDLINE, Scopus, and Cochrane CENTRAL from inception through February 2025, excluding overlapping registry-based analyses. The DerSimonian-Laird effects model was applied to compute pooled odds ratios (ORs) with 95% confidence intervals (CIs). Publication bias was assessed using a visual funnel plot and the Egger's and Begg's tests. A leave-one-out sensitivity analysis was conducted to evaluate the robustness of the findings. All analyses were conducted in R statistical software (v4.3.2, R Foundation for Statistical Computing, Vienna, Austria), using the meta, metafor, and dmetar packages.

Fifteen studies were included (N = 2,913). Patients receiving peripheral ECMO were slightly younger (54.8 ± 14.3 vs. 57.0 ± 13.7 years) and more often male (72% vs. 64%). Peripheral cannulation was associated with a lower risk of major bleeding (risk ratio (RR) 0.55, 95% CI 0.43-0.70), but a higher risk of limb ischemia (RR 1.43, 95% CI 1.17-1.75). No significant differences were observed for infection (RR 0.88, 95% CI 0.39-2.01), RRT (RR 1.17, 95% CI 0.66-2.08), or CVA (RR 1.19, 95% CI 0.78-1.83). Sensitivity analyses, using a leave-one-out approach, confirmed the robustness of the findings, yielding nearly identical pooled estimates and indicating that no single study disproportionately influenced the results.

Peripheral venoarterial ECMO (VA-ECMO) cannulation is associated with a significantly lower risk of bleeding, but a higher risk of limb ischemia, compared with central access, with no significant differences observed in infection, RRT, or CVAs. Therefore, the choice between peripheral and central access should be individualized, based on patient-specific risk profiles, particularly balancing bleeding risk against ischemic risk.

## Linked entities

- **Diseases:** cardiogenic shock (MONDO:0800175)

## Full-text entities

- **Diseases:** Bleeding (MESH:D006470), infection (MESH:D007239), CVAs (MESH:D020521), cardiogenic shock (MESH:D012770), ischemic (MESH:D002545), Vascular Complications (MESH:D003925), limb ischemia (MESH:D007511)
- **Chemicals:** VA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12887600/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12887600/full.md

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Source: https://tomesphere.com/paper/PMC12887600