Alternative venous access sites for dual-lumen extracorporeal membrane oxygenation cannulation

Author:

Schoeberl Armin-Kai12ORCID,Staudacher Dawid3ORCID,Kawashima Mitsuaki4ORCID,Fischer Courtney4,Cypel Marcelo4ORCID,Buchtele Nina5ORCID,Staudinger Thomas5ORCID,Aigner Clemens1ORCID,Hoetzenecker Konrad1ORCID,Schweiger Thomas1ORCID

Affiliation:

1. Department of Thoracic Surgery, Medical University of Vienna , Vienna, Austria

2. Department of Cardiothoracic and Vascular Surgery, Kepler University Hospital, Medical Faculty Johannes Kepler University Linz , Linz, Austria

3. Department of Intensive Care Medicine, University of Freiburg , Freiburg, Germany

4. Department of Thoracic Surgery, University of Toronto , Toronto, ON, Canada

5. Department of Medicine I, Intensive Care Unit, Medical University of Vienna , Vienna, Austria

Abstract

Abstract OBJECTIVES Dual-lumen cannulas for veno-venous (VV) extracorporeal membrane oxygenation (ECMO) support are typically inserted in the right internal jugular vein (RIJV); however, some scenarios can make this venous route inaccessible. This multicentre case series aims to evaluate if single-site cannulation using an alternative venous access is safe and feasible in patients with an inaccessible RIJV. METHODS We performed a multi-institutional retrospective analysis including high-volume ECMO centres with substantial experience in dual-lumen cannulation (DLC) (defined as >10 DLC per year). Three centres [Freiburg (Germany), Toronto (Canada) and Vienna (Austria)] agreed to share their data, including baseline characteristics, technical ECMO and cannulation data as well as complications related to ECMO cannulation and outcome. RESULTS A total of 20 patients received alternative DLC for respiratory failure. Cannula insertion sites included the left internal jugular vein (n = 5), the right (n = 7) or left (n = 3) subclavian vein and the right (n = 4) or left (n = 1) femoral vein. The median cannula size was 26 (19–28) French. The median initial target ECMO flow was 2.9 (1.8–3.1) l/min and corresponded with used cannula size and estimated cardiac output. No procedural complications were reported during cannulation and median ECMO runtime was 15 (9–22) days. Ten patients were successfully bridged to lung transplantation (n = 5) or lung recovery (n = 5). Ten patients died during or after ECMO support. CONCLUSIONS Alternative venous access sites for single-site dual-lumen catheters are a safe and feasible option to provide veno-venous ECMO support to patients with inaccessible RIJV.

Publisher

Oxford University Press (OUP)

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