# Ventriculoperitoneal shunt distal dysfunction due to peritoneal malabsorption: etiologies and management strategies—An institutional review

**Authors:** Muhammad Ateya, Mehmet Saim Kazan, Ahmet Özak, Zafer Erdoğan

PMC · DOI: 10.1007/s10143-026-04176-2 · Neurosurgical Review · 2026-02-23

## TL;DR

This study examines why some ventriculoperitoneal shunts in children with hydrocephalus fail due to peritoneal malabsorption and identifies risk factors and treatment outcomes.

## Contribution

The study identifies new risk factors for peritoneal malabsorption in VP shunts and evaluates management strategies in pediatric patients.

## Key findings

- Peritoneal malabsorption in VP shunts is significantly associated with prior abdominal surgery, axial deformity, and multiple previous shunt revisions.
- Management of peritoneal malabsorption achieved peritoneal salvage in 7 of 10 patients, but often required multiple interventions.
- Patients with peritoneal malabsorption had significantly longer hospital stays and variable success rates with treatment.

## Abstract

This study aims to investigate the etiology, risk factors, and management outcomes of peritoneal malabsorption, including pseudocysts and non-hepatic ascites, as a complication of ventriculoperitoneal (VP) shunting in pediatric hydrocephalus patients, with a focus on identifying predictors of distal dysfunction and evaluating therapeutic strategies. A retrospective review was conducted on 81 unique pediatric patients (≤ 18 years) undergoing 113 VP shunt revision episodes at Akdeniz University Hospital (2019–2023). Variables included age, sex, catheter site, hydrocephalus type, revision history, axial deformity severity, and abdominal surgery history. Peritoneal malabsorption occurred in 10 patients (11 revision episodes; 10 pseudocysts and 1 non-hepatic ascites), were analyzed for risk factors and management outcomes, with a minimum 9-month follow-up using ultrasonography and CT scans. Peritoneal malabsorption occurred in 10 patients (11 revision episodes), with statistically significant risk factors including history of multiple previous revisions (OR 8.02, 95% CI 1.86–34.63, p = 0.002), prior peritoneal-breaching abdominal surgery (OR 11.81, 95% CI 2.73–51.04, p = 0.001), and axial deformity (OR 4.07, 95% CI 1.03–16.03, p = 0.034; 2.77-fold increase per severity grade, p = 0.027). Prior abdominal surgery was present in 60% of malabsorption patients vs. 11.3% without, including even minor procedures (e.g., PEG placement, appendectomy, inguinal hernia repair). Management achieved peritoneal salvage in 7 of 10 patients; 5 episodes required only one procedure, while 6 episodes involved multiple interventions, with 3 ultimately needing ventriculoatrial shunt conversion. This small single-center series identifies prior abdominal surgery, axial deformity, and history of multiple previous revisions as factors associated with peritoneal malabsorption in VP shunts, suggesting mechanical and inflammatory contributions. Management remains challenging, with variable success rates and significantly prolonged hospitalization. These findings highlight the need for preoperative risk assessment and larger studies to refine therapeutic strategies.

## Linked entities

- **Diseases:** hydrocephalus (MONDO:0001150)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** Inguinal hernia (MESH:D006552), sacral agenesis (MESH:C537221), inflammation (MESH:D007249), arachnoid cyst (MESH:D016080), circulatory dysfunction (MESH:D012769), subdural hygroma (MESH:D013353), trauma (MESH:D014947), fibrosis (MESH:D005355), pneumoperitoneum (MESH:D011027), meningomyelocele (MESH:D008591), anasarca (MESH:D004487), vasculopathy (MESH:D000090122), lumbar kyphosis (MESH:C566002), irritation (MESH:D001523), malignancy (MESH:D009369), kyphosis (MESH:D007738), intraventricular hemorrhage (MESH:D000074042), ventriculoatrial shunt (MESH:C562451), spinal deformities (MESH:D013122), acute hydrocephalus (MESH:D000208), adhesions (MESH:D000267), CSF malabsorption (MESH:D008286), pseudocyst (MESH:D010192), portal hypertension (MESH:D006975), scoliosis (MESH:D012600), ascites (MESH:D001201), infection (MESH:D007239), Peritoneal malabsorption (MESH:D010538), intestinal obstruction (MESH:D007415), hepatic disease (MESH:D056486), kyphoscoliosis (MESH:C565711), deformity (MESH:D009140), NEC (MESH:D020345), Abdominal pseudocyst (MESH:D000007), porencephalic cyst (MESH:D003560), Axial deformity (MESH:C537791), Congenital hydrocephalus (MESH:D006849), oncologic (MESH:D000072716), Reabsorption (OMIM:109660)
- **Chemicals:** PEG (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926232/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926232/full.md

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Source: https://tomesphere.com/paper/PMC12926232