Venovenous extracorporeal membrane oxygenation during high-risk airway interventions

Author:

Stokes John W1ORCID,Katsis James M23ORCID,Gannon Whitney D4,Rice Todd W4ORCID,Lentz Robert J14ORCID,Rickman Otis B14ORCID,Avasarala Sameer K4,Benson Clayne5,Bacchetta Matthew167ORCID,Maldonado Fabien14ORCID

Affiliation:

1. Department of Thoracic Surgery, Vanderbilt University Medical Center, Nashville, TN, USA

2. Department of Pulmonary and Critical Care Medicine, Rush University Medical Center, Chicago, IL, USA

3. Department of Cardiovascular and Thoracic Surgery, Rush University, Medical Center, Chicago, IL, USA

4. Department of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center, Nashville, TN, USA

5. Department of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN, USA

6. Department of Cardiac Surgery, Vanderbilt University Medical Center, Nashville, TN, USA

7. Department of Biomedical Engineering, Vanderbilt University Medical Center, Nashville, TN, USA

Abstract

Abstract OBJECTIVES Practice patterns for the use of extracorporeal membrane oxygenation (ECMO) during high-risk airway interventions vary, and data are limited. We aim to characterize our recent experience using ECMO for procedural support during whole-lung lavage (WLL) and high-risk bronchoscopy for central airway obstruction (CAO). METHODS We performed a retrospective cohort study of adults who received ECMO during WLL and high-risk bronchoscopy from 1 July 2018 to 30 March 2020. Our primary end point was successful completion of the intervention. Secondary end points included ECMO-associated complications and hospital survival. RESULTS Eight patients received venovenous ECMO for respiratory support during 9 interventions; 3 WLLs for pulmonary alveolar proteinosis were performed in 2 patients, and 6 patients underwent 6 bronchoscopic interventions for CAO. We initiated ECMO prior to the intervention in 8 cases and during the intervention in 1 case for respiratory decompensation. All 9 interventions were successfully completed. Median ECMO duration was 17.8 h (interquartile range, 15.9–26.6) for the pulmonary alveolar proteinosis group and 1.9 h (interquartile range, 1.4–8.1) for the CAO group. There was 1 cannula-associated deep vein thrombosis; there were no other ECMO complications. Seven patients (87.5%) and 4 (50.0%) patients survived to discharge and 1 year postintervention, respectively. CONCLUSIONS Use of venovenous ECMO to facilitate high-risk airway interventions is safe and feasible. Planned preprocedural ECMO initiation may prevent avoidable respiratory emergencies and extend therapeutic airway interventions to patients otherwise considered too high-risk to treat. Guidelines are needed to inform the utilization of ECMO during high-risk bronchoscopy and other airway interventions.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine,Surgery

Reference29 articles.

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