Multisite veno venous extracorporeal support in children below 5 kg, experience from a referral center
- Journal
- Journal of pediatric surgery (Q1)
- Published
- 13 October 2026
- Study design
- Cohort / observational study
- Evidence level
- Level 4, Very Low (CEBM 4)
- Authors
- Erik Hervieux, Julie Starck, Garance Martin, Cyril Guillier, Sébastien Faraj, Pauline Leroux, et al.
- PMID
- 42869276
- DOI
- 10.1016/j.jpedsurg.2026.163538
Why clinicians should know about it
- Picked for Neonatology (paper of the day, 17 October 2026): Multisite VV ECMO in infants <5 kg
Abstract
INTRODUCTION: Refractory respiratory failure is one of the leading indications for extracorporeal membrane oxygenation (ECMO) in neonates and children. Despite strong arguments supporting the use of veno-venous ECMO (VV ECMO), the international ELSO registry still reports a higher rate of veno-arterial ECMO (VA ECMO) in such situations. We report our experience with multisite V-V ECMO in children weighing less than 5 kg. METHODS: We conducted a single-center retrospective study from January 2017 to December 2025. All patients weighing less than 5 kg who underwent multisite VV ECMO were included in the analysis. RESULTS: During the study period, 52 patients weighing less than 5 kg underwent VV ECMO. Among these, 43 (83 %) received multisite VV ECMO. The median weight was 3.5 kg (2.9 - 4.3) and 12 patients (28 %) weighed less than 3 kg. Seventeen (39 %) patients were initially supported with VA ECMO and subsequently converted to VV ECMO. Percutaneous cannulation was performed using 21 femoral cannulas (48 %) and 17 jugular cannulas (39%). All vascular complications occurred during percutaneous femoral cannulation. Median blood flows on days 1, 3 and 7 were 106 ml/kg/min (92 - 117), 105 ml/kg/min (94 - 116) and 101 ml/kg/min (93 - 118), respectively. The median duration of ECMO support was 12 days (6 - 17). Twenty-six (60%) patients were successfully weaned from ECMO, and 25 were alive 6 months after ECMO support. CONCLUSION: Multisite VV ECMO is an effective cannulation strategy in children weighing less than 5 kg with refractory respiratory failure.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.