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Adult outcome of pediatric hydrocephalus
Matthieu Vinchon1, Marc Baroncini, Isabelle Delestret
1Department of Pediatric Neurosurgery, Hôpital Roger Salengro, Lille University Hospital, CHRU de Lille, Lille Cedex, France. matthieu.vinchon@chru-lille.fr
Insights
Pediatric hydrocephalus patients require lifelong care, with many experiencing long-term motor and cognitive issues. Adult outcomes highlight the need for organized transition to adult neurosurgery services.
Area of Science:
- Neurosurgery
- Pediatric Neurology
- Long-term Patient Outcomes
Background:
- Pediatric hydrocephalus management has advanced, but adult outcomes remain under-documented.
- Understanding the long-term healthcare needs of adults treated for childhood hydrocephalus is crucial for care planning.
- This study reviews long-term data from a pediatric hydrocephalus cohort followed into adulthood.
Purpose of the Study:
- To determine the long-term healthcare profile and outcomes of individuals treated for hydrocephalus in childhood.
- To identify the need for lifelong follow-up and organized transition to adult neurosurgical care.
Main Methods:
- Retrospective review of a pediatric hydrocephalus database from a single institution covering a large population.
- Inclusion criteria: patients treated for hydrocephalus before age 18 and followed up past age 20.
- Data analysis included shunt revision rates, weaning from shunts, mortality, and long-term neurological sequels.
Main Results:
- Of 456 patients followed for a mean of 24.2 years, 17.8% required shunt operations after age 20.
- Significant long-term sequels included motor (46.5%) and cognitive (47.6%) deficits; only 18% had no sequels.
- Adult employment and schooling were limited, with 54.5% having IQ ≥80 but only 41.4% normal schooling and 33.7% competitive employment.
Conclusions:
- Individuals treated for hydrocephalus in childhood necessitate lifelong neurosurgical follow-up.
- While late mortality is low, morbidity is substantial, with a significant proportion requiring adult shunt surgeries.
- Organized transition protocols from pediatric to adult neurosurgery are essential for this vulnerable patient group.
Introduction:
The outlook of pediatric hydrocephalus has spectacularly improved over the past decades; however, the adult outcome is still poorly documented. Determining the healthcare profile of these patients is important in order to organize the management of this growing population. We decided to review our pediatric hydrocephalus database for pediatric patients treated for hydrocephalus and followed up into adulthood.
Methods:
Our institution has a virtual monopoly for pediatric hydrocephalus, serving a four-million-plus population; the transition to adult care is also managed in the same institution. We retrospectively reviewed patients younger than 18 treated for hydrocephalus since 1980 and followed up beyond the age of 20.
Results:
We reviewed 456 patients, with a mean initial age of 55.6 months, and followed up for a mean of 24.2 years. In 81 patients (17.8%), the last shunt operation occurred after 20 years; 22 of these (4.9% of the total) having never been revised earlier. Sixteen patients (3.5%) could be weaned of their shunt. Thirteen patients died in adult age, 5 of these dying of shunt-related causes. The most prominent sequels were motor (46.5%) and cognitive (47.6%); only 82 patients (18.0%) had no sequel at all. Intelligence quotient values were ≥80 in 54.5% of tested patients; however, schooling was normal in only 41.4%, and only 33.7% was employed in the competitive labor market.
Conclusion:
Adults treated for hydrocephalus in childhood require a life-long follow-up. Late mortality is low but not null, morbidity is high, and many patients require shunt surgery during adulthood. The transition from child to adult neurosurgery needs to be organized for these vulnerable patients.
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