Evidence map›Paper›PMID 42686840›Full record

ArticlePediatric research2026

Factors associated with ventriculoperitoneal shunt conversion and intraparenchymal hemorrhage following ventriculosubgaleal shunt for post-hemorrhagic ventricular dilatation.

Vanessa Krohn, Emilie Groulx-Boivin, Christine Saint-Martin, Raed Abuazzah, Marc Beltempo, Roy Dudley, Jarred Garfinkle

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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Vanessa KrohnDivision of Neonatology, Department of Pediatrics, McGill University, Montreal Children's Hospital, Montreal, QC, Canada.ORCID http://orcid.org/0009-0005-8699-3238
Emilie Groulx-BoivinDepartments of Pediatrics and Neurology and Neurosurgery, McGill University, Montreal Children's Hospital, Montreal, QC, Canada.
Christine Saint-MartinDepartment of Diagnostic Radiology, McGill University, Montreal Children's Hospital, Montreal, QC, Canada.
Raed AbuazzahDepartment of Diagnostic Radiology, McGill University, Montreal Children's Hospital, Montreal, QC, Canada.
Marc BeltempoDivision of Neonatology, Department of Pediatrics, McGill University, Montreal Children's Hospital, Montreal, QC, Canada.
Roy Dudley *Division of Neurosurgery, Department of Pediatric Surgery, McGill University, Montreal Children's Hospital, Montreal, QC, Canada.
Jarred Garfinkle *Division of Neonatology, Department of Pediatrics, McGill University, Montreal Children's Hospital, Montreal, QC, Canada. jarred.garfinkle@mcgill.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPost-hemorrhagic ventricular dilatation (PHVD) is often managed with temporizing measures like ventriculosubgaleal shunts (VSGS). We aimed to identify factors associated with (1) ventriculoperitoneal shunt (VPS) conversion and (2) intraparenchymal hemorrhage (IPH) following VSGS.

methodsRetrospective cohort study of infants born ≤34 gestational age (GA) with PHVD managed with VSGS between 2012-2024. Clinical and imaging characteristics were compared between infants with and without VPS conversion and between infants with and without post-VSGS IPH.

resultsForty-two infants received VSGS. Compared to neonates without VPS (n = 7), those who received a VPS (n = 35) had lower GA at birth (mean 27.5 weeks [SD3.0] vs. 30.1 weeks [2.0], p = 0.029) and larger ventricular size ipsilateral to the catheter immediately after intervention (median ventricular index [mm above p97] 1.3 mm vs. -1.7 mm, p = 0.048, and median anterior horn width 6.5 mm vs. 3.7 mm, p = 0.022). IPH occurred in 9/42 (21%) infants following VSGS and no risk factors were identified.

conclusionGreater GA and smaller post-VSGS ventricular size were associated with lower rates of VPS conversion. Post-VSGS IPH was common, but the absence of associated factors suggests a heterogenous pathophysiology. Future work should focus on refining temporizing strategies to reduce VPS dependence and characterize the spectrum and pathogenesis of post-VSGS IPH. IMPACT: Greater gestational age at birth and smaller post-VSGS shunt ventricular size were associated with a lower likelihood of ventriculoperitoneal shunt conversion Post-VSGS intraparenchymal hemorrhage was common and exhibited topographic and morphologic heterogeneity. No risk factors for post-VSGS intraparenchymal hemorrhage were identified. The findings underscore the need to refine temporizing strategies in post-hemorrhagic ventricular dilatation to reduce ventriculoperitoneal shunt dependency and complications.

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