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Pupillomotor Dysfunction and Outcomes After Decompressive Craniectomy in Pediatric Patients.
Martin Petkov1, Aurelia Peraud1, Ohad Sharon1
1Department of Neurosurgery, University of Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany.
Journal of Clinical Medicine
|February 27, 2026
Summary
Pediatric decompressive craniectomy (DC) shows pupillomotor dysfunction linked to early death, but survivors can achieve good long-term recovery. Early intervention is key, as children show significant neurological recovery potential.
Area of Science:
- Pediatric Neurosurgery
- Critical Care Medicine
- Neurological Surgery
Background:
- Decompressive craniectomy (DC) is vital for refractory intracranial pressure (ICP).
- Pediatric outcomes post-DC, particularly pupillomotor dysfunction, are understudied.
- Anisocoria's significance in pediatric DC warrants further investigation.
Purpose of the Study:
- To evaluate the clinical relevance of pupillomotor dysfunction in pediatric patients undergoing DC.
- To assess the association between pupillomotor dysfunction and outcomes in pediatric DC.
- To explore long-term functional recovery in pediatric DC survivors.
Main Methods:
- Retrospective review of 25 pediatric patients undergoing DC (2004-2024).
- Data collected: demographics, etiology, surgical details, neurological status (GCS, pupillary status), and midline shift.
- Functional outcomes assessed using pediatric Glasgow Outcome Scale Extended (pGOS-E) over 4 years.
Main Results:
- Traumatic brain injury was the leading cause (16/25).
- Pupillomotor dysfunction occurred in 15/25 patients, associated with increased in-hospital mortality (p=0.02).
- Survivors with initial dysfunction showed moderate disability (median pGOS-E=6 at 12 months).
Conclusions:
- Pediatric pupillomotor dysfunction predicts higher early mortality but not necessarily poor long-term outcomes.
- Children demonstrate substantial neurological recovery potential post-DC, even with severe initial findings.
- Timely surgical intervention should be considered despite initial clinical severity.
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