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Updated: May 4, 2026

Insertion, Maintenance, and Removal of the Percutaneous Dual Lumen Cannula Right Ventricular Assist Device
Published on: July 20, 2022
Right ventricular dysfunction in children supported with pulsatile ventricular assist devices
Ann Karimova1, Charissa R Pockett2, Nagore Lasuen1
1Cardiothoracic Unit, Great Ormond Street Hospital for Children, London, United Kingdom.
Insights
Right ventricular dysfunction (RVD) affects 42% of pediatric ventricular assist device (VAD) recipients, with preoperative extracorporeal support and elevated urea being key risk factors for biventricular assist (BiVAD). Management of RVD in these children requires further study.
Area of Science:
- Pediatric cardiology
- Cardiovascular surgery
- Biomedical engineering
Background:
- Right ventricular dysfunction (RVD) is a significant concern in pediatric patients requiring ventricular assist devices (VADs).
- Understanding the incidence, risk factors, and outcomes of RVD is crucial for improving patient management.
- Previous studies have not fully elucidated the preoperative characteristics associated with RVD in this population.
Purpose of the Study:
- To determine the incidence and severity of RVD in pediatric VAD recipients.
- To identify preoperative factors predicting RVD development.
- To assess the impact of RVD on outcomes, including survival and postoperative morbidity.
Main Methods:
- A retrospective analysis of pediatric patients bridged to transplantation with VADs between 2004 and 2011.
- RVD was defined by specific criteria including central venous pressure, inotropic support, inhaled nitric oxide duration, or requirement for biventricular assist (BiVAD).
- Preoperative variables were analyzed to identify associations with RVD and BiVAD requirement.
Main Results:
- Of 57 pediatric VAD recipients, 42% (24 patients) developed RVD.
- Younger age, prior extracorporeal mechanical support, and elevated urea, creatinine, and bilirubin levels were associated with RVD.
- Elevated urea and extracorporeal mechanical support were significant risk factors for requiring BiVAD.
Conclusions:
- RVD occurs in approximately 40% of pediatric VAD recipients, impacting peri-implantation morbidity and bridging outcomes.
- Preoperative extracorporeal membrane oxygenation and elevated urea are identified risk factors for BiVAD.
- Further research into the management of RVD in pediatric VAD patients is warranted.
Objectives:
To describe the incidence and severity of right ventricular dysfunction (RVD) in pediatric ventricular assist device (VAD) recipients and to identify the preoperative characteristics associated with RVD and their effect on outcomes.
Methods:
Children bridged to transplantation from 2004 to 2011 were included. RVD was defined as the use of a left VAD (LVAD) with an elevated central venous pressure of >16 mm Hg with inotropic therapy and/or inhaled nitric oxide for >96 hours or biventricular assist (BiVAD).
Results:
A total of 57 children (median age, 2.97 years; range 35 days to 15.8 years) were supported. Of the 57, 43 (75%) had an LVAD, and of those, 10 developed RVD. The remaining 14 (25%) required BiVAD. Thus, RVD occurred in 24 of 57 patients (42%). Preoperative variables such as younger age (P = .01), use of extracorporeal mechanical support (P = .006), and elevated urea (P = .03), creatinine (P = .02), and bilirubin (P = .001) were associated with RVD. Multiple logistic regression analysis indicated that elevated urea and extracorporeal mechanical support (odds ratio, 26.4; 95% confidence interval, 2.3-307.3; and odds ratio, 27.8; 95% confidence interval, 2.5-312.3, respectively) were risk factors for BiVAD. The patients who developed RVD on LVAD had a complicated postoperative course but excellent survival (100%), comparable to those with preserved right ventricular function (91%). The survival for those requiring BiVAD was reduced (71%).
Conclusions:
RVD occurred in approximately 40% of pediatric VAD recipients and affects their peri-implantation morbidity and bridging outcomes. Preoperative extracorporeal membrane oxygenation and elevated urea were risk factors for BiVAD. Additional studies of the management of RVD in children after VAD implantation are warranted.
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