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Updated: Jul 20, 2026

Isolation Method for Long-Term and Short-Term Hematopoietic Stem Cells
Published on: May 19, 2023
To stop or not to stop: how much support should be provided to mechanically ventilated pediatric bone marrow and stem
1Pediatric Blood and Marrow Transplant Division, Duke University Medical Center, 2400 Pratt Street, Suite 1400, Durham, NC 27705, USA. paul.martin@duke.edu
Insights
Pediatric stem cell transplant (SCT) patients needing intensive care have survival rates of 15-36%. Lack of improvement by week two in the pediatric intensive care unit (PICU) indicates poor prognosis, suggesting withdrawal of life support.
Area of Science:
- Pediatric critical care medicine
- Hematopoietic stem cell transplantation (HSCT) outcomes
Background:
- Existing studies on intensive care for pediatric SCT patients are retrospective and single-institution, limiting generalizability.
- Survival rates for pediatric SCT patients requiring intensive care range from 15% to 36%.
Purpose of the Study:
- To analyze the clinical relevance of intensive care support for pediatric SCT patients.
- To identify adverse risk factors and prognostic indicators for survival in this population.
Main Methods:
- Review of existing retrospective, single-institution reports on pediatric SCT patients requiring intensive care.
- Analysis of survival rates and adverse risk factors, including multi-organ system failure (MSOF).
Main Results:
- Pediatric SCT patients in intensive care have a survival rate of 15-36%, which is significant given overall post-transplant survival rates.
- Adverse risk factors vary by institution due to differences in patient populations and protocols.
- Multi-organ system failure (MSOF) is a consistent predictor of poor survival.
- Lack of significant improvement by the second week of pediatric intensive care unit (PICU) care is associated with a low likelihood of survival.
Conclusions:
- Intensive care support for pediatric SCT patients can be beneficial, with survival rates not necessarily dismal.
- Prognosis is poor for patients not showing objective improvement within two weeks of PICU admission.
- Withdrawal of life support should be considered in cases of prolonged critical care without improvement.
- Further prospective, multi-institutional studies are needed to evaluate specific interventions and establish reliable predictive models.
Abstract:
Every publication to date reporting the outcome of intensive care support for pediatric SCT patients must be viewed with caution because all are single-institution, retrospective reports. Nevertheless, some of the conclusions made by these investigators appear to be clinically relevant. First, an SCT patient who requires intensive care support does not automatically have a dismal chance of survival. Survival rates in recent reports range from 15% to 36%, which is reasonable when the overall post-transplant survival rate for non-ICU patients may be only 50%. Second, adverse risk factors differ from center to center, likely due to the wide variation in patient populations, donor source, and transplant preparation regimens. Third, MSOF is a consistent adverse risk factor for survival. An additional conclusion that can be drawn from the data presented in this article is that patients who do not show significant, objective improvement by the second week of PICU care are unlikely to survive. The limitation or withdrawal of life-sustaining medical support should be recommended to the patient, the patient's family, and the patient's doctors. Although there are no predictive models that are 100% reliable for these clinical situations, in the author's experience, most families and physicians view critical care support beyond 2 weeks, in the absence of clinical improvement, as futile care. It is clear that better data are needed in the form of prospective, multi-institutional studies that include the therapeutic efficacy of interventions such as high-frequency oscillatory ventilation, continuous venovenous hemodialysis, early use of noninvasive ventilation (ie, noninvasive positive pressure ventilation), the use of biologic agents to decrease inflammation, the impact of new antifungal medications, and lung-protective ventilation with permissive hypercapnia. Of these potential therapies, the author is aware of only one multi-institutional study involving continuous venovenous hemodialysis at this time.
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