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ArticleNeurosurgical review2026

Pediatric hydrocephalus in Nigeria: a scoping review of management, treatment outcomes, and challenges.

Chidera Stanley Anthony, Nwamaka Chidera Bob-Ume, Ikponmwosa Jude Ogieuhi, Victor Oluwatomiwa Ajekiigbe, Victor Olamiposi Olaiya, Oluchukwu Vivian Igwebuike, Kingsley Chidi Anachuna, Faith Temiloluwa Adetayo, Chimaobi Nwevo, Olufemi Akinmeji and 3 more

Abstract readScoping Review
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In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Chidera Stanley AnthonyUniversity of Calabar, Calabar, Nigeria.
Nwamaka Chidera Bob-UmeAll Saints University College of Medicine, St. Vincent and the Grenadines, Kingstown, Saint Vincent And The Grenadines.
Ikponmwosa Jude OgieuhiNorthwestern Medicine McHenry Hospital, McHenry, 60050, IL, USA. jude.ogieuhi@gmail.com.
Victor Oluwatomiwa AjekiigbeLadoke Akintola University of Technology, Ogbomosho, Nigeria.
Victor Olamiposi OlaiyaIzhvesk State Medical Academy, Izhvesk, Russia.
Oluchukwu Vivian IgwebuikeUniversity of Nigeria, Nsukka, Nigeria.
Kingsley Chidi AnachunaUniversity of Calabar, Calabar, Nigeria.
Faith Temiloluwa AdetayoBabcock University Teaching Hospital, Ilishan-Remo, Ogun, Nigeria.
Chimaobi NwevoNYCHHC/South Brooklyn Health, New York City, 10001, NY, USA.
Olufemi AkinmejiOlabisi Onabanjo University, Ago-Iwoye, Ogun, Nigeria.
Temilade Patience AdejumoLadoke Akintola University of Technology, Ogbomosho, Nigeria.
Kenechukwu Clinton AgudosiTorrens University, Brisbane, Australia.
Azeezat Olajumoke AdekanmbiLadoke Akintola University of Technology, Ogbomosho, Nigeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric hydrocephalus continues to pose a significant neurosurgical challenge in Nigeria driven by delayed diagnosis, barriers to treatment, and loss to long-term follow-up. Systemic, infrastructural, and socioeconomic limitations in hydrocephalus care persist across sub-Saharan Africa (SSA) despite major advances globally. This scoping review maps the current landscape of pediatric hydrocephalus in Nigeria, with emphasis on management trends, treatment outcomes, and context-specific challenges. We searched PubMed, Scopus, Web of Science, African Journals Online (AJOL), Nigerian Journal Online (NJOL), as well as grey literature, for studies published within the past 15 years. Eligible studies reported causes, management approaches, treatment outcomes, or barriers to care. Data were synthesized thematically in narrative form. Ten hospital-based studies (n = 1,127) conducted at tertiary institutions and spanning multiple geopolitical zones in Nigeria were included. All were cohort studies (eight retrospective and two prospective) and reported a male predominance. Congenital hydrocephalus, most commonly attributed to aqueductal stenosis and Chiari II malformations, was more common in infants and young children (40-90% across studies), while post-infectious causes were more common in older children. Ventriculoperitoneal (VP) shunting was the predominant treatment modality, while endoscopic third ventriculostomy (ETV) was used in a few centers. Shunt infections were the most common complication, with rates ranging from 11% to 28%. Late presentation was reported with presentation ages ranging between 1 and 12 months of age. High out-of-pocket expenses, limited access to advanced imaging, lack of trained neurosurgeons, and sociocultural barriers to timely care were among the challenges encountered. Pediatric hydrocephalus in Nigeria is characterized by delayed presentation, limited treatment options, and geographical disparities in care. Although ETV is gaining popularity as a treatment modality, VP shunting remains the standard of care. To improve outcomes, neurosurgical services should be decentralized, community-level awareness enhanced, insurance coverage expanded, and national guidelines for hydrocephalus management established.

Indexed as

HydrocephalusChildHumansInfantMaleNigeriaTreatment OutcomeVentriculoperitoneal ShuntVentriculostomyEndoscopic third ventriculostomyNeurosurgeryNigeriaPediatric hydrocephalusScoping reviewVentriculoperitoneal shunt

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.