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Updated: Jan 21, 2026

Veno-Venous Extracorporeal Membrane Oxygenation in a Mouse
Published on: October 24, 2018
Conversion From Venovenous to Venoarterial Extracorporeal Membrane Oxygenation Is Associated With Increased Mortality
Mark L Kovler1, Alejandro V Garcia1, Ross M Beckman1
1Johns Hopkins Hospital Division of Pediatric General Surgery, Baltimore, Maryland.
Insights
Converting pediatric patients from venovenous (VV) to venoarterial (VA) extracorporeal membrane oxygenation (ECMO) increases mortality risk. This highlights potential issues in initial mode selection for respiratory and circulatory support.
Area of Science:
- Pediatric critical care medicine
- Cardiopulmonary support technologies
- Extracorporeal membrane oxygenation (ECMO)
Background:
- Increasing use of venovenous (VV) extracorporeal membrane oxygenation (ECMO) for pediatric respiratory disease.
- A subset of patients require conversion to venoarterial (VA) ECMO for circulatory support.
- VV-to-VA conversion is associated with higher mortality rates.
Purpose of the Study:
- To describe pediatric patients requiring VV-to-VA ECMO conversion.
- To highlight the increased mortality associated with this conversion.
- To identify potential factors influencing the need for conversion.
Main Methods:
- Extracted data from the Extracorporeal Life Support Organization (ELSO) registry.
- Analyzed demographic and disease-specific data for 1382 patients.
- Compared survival rates of converted patients with age-matched unconverted ECMO runs.
- Calculated relative risk (RR) of death using chi-squared tests.
Main Results:
- Overall hospital survival for neonates converted to VA ECMO was 60% (RR 1.23) compared to unconverted runs (83% VV, 64% VA).
- Survival for older children converted to VA ECMO was 46% (RR 1.16) compared to unconverted runs (66% VV, 51% VA).
- VV-to-VA conversion was statistically associated with increased mortality in both neonates and older children.
Conclusions:
- VV-to-VA conversion in pediatric patients is linked to significantly increased mortality.
- The need for conversion may indicate under-recognition of disease severity or inappropriate initial ECMO mode selection.
- Further research is crucial to identify predictors of VV ECMO failure and optimize initial support strategies.
Background:
There is an increasing national trend toward initial venovenous (VV) extracorporeal membrane oxygenation (ECMO) for infants and children with respiratory disease; however, some proportion of patients initiated on VV ECMO will ultimately require conversion to venoarterial (VA) support for circulatory augmentation. The purpose of this work is to describe patients who required conversion from VV to VA ECMO and to highlight the increased mortality in this population.
Materials And Methods:
Demographic and disease-specific data on children who underwent VV-to-VA ECMO conversion were extracted from the Extracorporeal Life Support Organization registry. Survival comparisons to age-matched patients undergoing unconverted ECMO runs were made using the 2016 Extracorporeal Life Support Organization International Summary report. The relative risk (RR) of death associated with VV-to-VA conversion was calculated, and statistical analysis of survival was performed using a chi-squared test with P < 0.05 for significance.
Results:
This study cohort consisted of 1382 patients who required VV-to-VA conversion. The overall hospital survival rate for neonates requiring conversion was 60%, compared with 83% for unconverted VV runs and 64% for unconverted VA runs (RR 1.23; 95% confidence interval, 1.14-1.34). Similarly, the survival of older children requiring conversion was 46% compared with 66% and 51%, respectively (RR 1.16; 95% confidence interval, 1.06-1.27).
Conclusions:
VV-to-VA conversion does occur and is associated with increased mortality. The need for conversion from VV to VA ECMO may represent an early failure to recognize physiologic parameters or disease severity that would be better managed with initial VA support. Further research is needed to pinpoint the cause of increased mortality and to identify predictors of VV failure to optimize initial mode selection.
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