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Impact of CRRT in Patients with PARDS Treated with VV-ECMO
Sébastien Redant1,2, Océane Barbance1,2, Ashita Tolwani3
1Departments of Intensive Care, Brugmann University Hospital, 1020 Brussels, Belgium.
Insights
Adding continuous renal replacement therapy (CRRT) to extracorporeal membrane oxygenation (ECMO) for pediatric acute respiratory distress syndrome (PARDS) increases blood product use but does not affect mortality rates in critically ill children.
Area of Science:
- Pediatric critical care medicine
- Nephrology
- Cardiopulmonary support
Background:
- Pediatric acute respiratory distress syndrome (PARDS) has high mortality, often linked to fluid overload.
- Extracorporeal membrane oxygenation (ECMO) is a life-support measure for severe PARDS but can exacerbate fluid overload and lead to acute kidney injury (AKI).
Purpose of the Study:
- To investigate the association between continuous renal replacement therapy (CRRT) and mortality in pediatric patients with PARDS undergoing ECMO.
- To evaluate the impact of CRRT on morbidity and resource utilization in this patient population.
Main Methods:
- Retrospective 7-year study of pediatric patients with PARDS requiring ECMO.
- Comparison of patients who received CRRT versus those who did not.
- Analysis of severity of illness scores, blood product administration, and outcomes including mortality and morbidity.
Main Results:
- No significant difference in overall mortality between groups.
- CRRT was associated with increased use of blood products and noradrenaline.
- No significant impact on ECMO duration or length of pediatric intensive care unit (PICU) stay.
Conclusions:
- The addition of CRRT to ECMO in pediatric patients with PARDS is not associated with increased mortality.
- CRRT use in this setting correlates with higher consumption of blood products.
Abstract:
The high mortality of pediatric acute respiratory distress syndrome (PARDS) is partly related to fluid overload. Extracorporeal membrane oxygenation (ECMO) is used to treat pediatric patients with severe PARDS, but can result in acute kidney injury (AKI) and worsening fluid overload. The objective of this study was to determine whether the addition of CRRT to ECMO in patients with PARDS is associated with increased mortality.
Methods:
We conducted a retrospective 7-year study of patients with PARDS requiring ECMO and divided them into those requiring CRRT and those not requiring CRRT. We calculated severity of illness scores, the amount of blood products administered to both groups, and determined the impact of CRRT on mortality and morbidity.
Results:
We found no significant difference in severity of illness scores except the vasoactive inotropic score (VIS, 45 ± 71 vs. 139 ± 251, p = 0.042), which was significantly elevated during the initiation and the first three days of ECMO. CRRT was associated with an increase in the use of blood products and noradrenaline (p < 0.01) without changing ECMO duration, length of PICU stay or mortality.
Conclusion:
The addition of CRRT to ECMO is associated with a greater consumption of blood products but no increase in mortality.
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