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Updated: Aug 19, 2026

Stem Cell Transplantation in an in vitro Simulated Ischemia/Reperfusion Model
Published on: November 5, 2011
Extracorporeal membrane oxygenation after stem cell transplant: clinical decision-making in the absence of evidence
Rachel K Wolfson1, Madelyn D Kahana, James B Nachman
1Sections of Critical Care, University of Chicago, IL, USA.
Insights
Innovative therapies like extracorporeal membrane oxygenation (ECMO) can be ethically considered for critically ill children lacking supporting data. This case highlights the importance of informed consent and data collection for advancing pediatric critical care.
Area of Science:
- Pediatric Critical Care Medicine
- Bioethics
- Oncology
Background:
- Ethical considerations for innovative therapies in critically ill children with limited supporting data are complex.
- Autologous peripheral blood stem cell transplant (APBSCT) is a complex procedure with potential complications.
Observation:
- A 13-year-old patient with stage III neuroblastoma, sepsis, and hemodynamic instability post-APBSCT received extracorporeal membrane oxygenation (ECMO) support.
- The patient survived to discharge after a 6-day ECMO course, despite a lack of data supporting ECMO use in neutropenic oncology patients post-transplant.
Findings:
- Clinical features suggested the patient was a reasonable ECMO candidate, justifying its use despite limited evidence.
- Informed consent was obtained from the family, and rigorous data collection was emphasized.
Implications:
- It is ethical to consider innovative therapies in critically ill children when patient characteristics suggest potential success, even without strong evidence.
- This case underscores the need for clear entry criteria, treatment protocols, and hypothesis-driven data collection for unproven therapies in pediatric critical care.
- The fluid boundaries between standard therapy, innovative therapy, and research necessitate careful ethical consideration and robust data gathering.
Objective:
To discuss the ethical dilemmas that arise in considering innovative therapies for critically ill children when there is little data to support their use.
Design:
Case report of a 13-yr-old patient after autologous peripheral blood stem cell transplant for stage III neuroblastoma with sepsis and hemodynamic instability who survived to discharge after a 6-day course of extracorporeal membrane oxygenation (ECMO) support. The case serves as a source of discussion of the following: the use of available data in deciding to proceed with an unproved therapy, the approach to conversations to obtain informed consent, and the need for institutional oversight and hypothesis-driven data collection to advance pediatric critical care.
Setting:
Pediatric intensive care unit at a university hospital.
Patient:
One adolescent with stage III neuroblastoma.
Results:
Despite a lack of data to support the use of ECMO in a neutropenic oncology patient after autologous peripheral blood stem cell transplant, our patient had clinical features that suggested he was a reasonable ECMO candidate. His family gave informed consent to use ECMO and he survived. It is ethical to consider and use innovative therapies when patient characteristics are suggestive that the therapy may be successful even in the absence of evidence. This requires physicians' attention to the best interest of the patient and should occur in the setting of informed consent and rigorous data collection.
Conclusions:
The boundaries among standard therapy, innovative therapy, and research can be quite fluid. This case illustrates the ethical imperative to consider therapies that may be appropriate for a critically ill child even without evidence predictive of success, to have entry criteria and treatment protocols for such therapies, and to collect data from such experiences to advance the standard of care.
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