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Research Consenting Practices in Critically Ill Children: A Scoping Review
Sarah B Kandil1, Madhuradhar Chegondi2, Melissa C Funaro3
1Department of Pediatrics, Critical Care Medicine, Yale University School of Medicine, New Haven, Connecticut.
Improving clinical trial enrollment for critically ill children requires addressing consent barriers. Strategies like deferred consent and multicenter designs show promise for better participation in pediatric critical care research.
Area of Science:
- Pediatric Critical Care Medicine
- Clinical Trial Methodology
- Bioethics
Background:
- Enrollment in clinical trials for critically ill children faces significant hurdles, including surrogate decision-making, time constraints, and caregiver burden.
- Effective clinical research is vital for advancing medical care for critically ill pediatric populations.
Conclusions:
- While direct research on improving consent in pediatric critical care trials is limited, identified facilitators and successful enrollment strategies should be integrated.
- Implementing alternative consent models and multicenter approaches may enhance participation in critical care research involving children.
- Addressing identified barriers and leveraging facilitators are crucial for optimizing clinical trial enrollment in this vulnerable population.
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