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Updated: Aug 22, 2026

Neuronavigation and Laparoscopy Guided Ventriculoperitoneal Shunt Insertion for the Treatment of Hydrocephalus
Published on: October 14, 2022
Distal catheter obstruction from non-infectious cause in ventriculo-peritoneal shunted children
1Department of Paediatric Surgery, University Children's Hospital, Uppsala, Sweden. Kai.Arnell@kirurgi.uu.se
Insights
Hydrocephalic children may experience shunt malfunction due to a non-infectious peritoneal reaction causing abdominal pseudocysts. Ventriculo-atrial shunting can be a successful alternative when peritoneal shunts fail.
Area of Science:
- Pediatric Neurosurgery
- Medical Device Complications
Background:
- Ventriculo-peritoneal shunting is standard for pediatric hydrocephalus.
- Non-infectious peritoneal reactions can cause shunt malfunction.
Purpose of the Study:
- Investigate shunt malfunction in hydrocephalic children.
- Identify causes and outcomes of distal catheter complications.
Main Methods:
- Retrospective analysis of eight hydrocephalic children with shunt malfunction.
- Clinical evaluation, CSF analysis, blood tests, and surgical interventions.
- Laparotomy for peritoneal assessment and shunt revision.
Main Results:
- Seven children developed abdominal pseudocysts; one had CSF accumulation.
- Peritoneal reaction was hyperemic and edematous; no infection detected initially.
- Ventriculo-atrial shunting was successful in most cases after VP shunt failure.
Conclusions:
- Transient, non-infectious peritoneal reactions can cause shunt malfunction and pseudocysts.
- Ventriculo-atrial shunting is a viable alternative for refractory cases.
- Peritoneal catheter replacement is possible if infection is absent.
Abstract:
In hydrocephalic children, ventriculo-peritoneal shunting is the preferred treatment with few complications. However, an obviously non-infectious peritoneal reaction to the cerebrospinal fluid (CSF) may occasionally lead to shunt malfunction. In eight hydrocephalic children, shunt malfunction with distal catheter complication was found with abdominal pseudocyst formation in seven cases and accumulation of the CSF in one. All children had a normal CSF cell count and glucose concentration, and white cell count, and C-reactive protein in peripheral blood were normal. No CSF infection could be detected despite prolonged aerobic and anaerobic cultures. After initial externalisation of the shunt and subsequent routine administration of antibiotics because infection initially was suspected, ventriculo-peritoneal shunting was attempted one to three times with identical failure before successful conversion to a ventriculo-atrial system. At laparotomy the peritoneum and intestinal serosa were hyperaemic and oedematous in all patients, five of whom also had pseudocysts and two of whom also had intra-abdominal adhesions. Four children had a revision 6-24 years after the ventriculo-atrial conversion due to short atrial catheter with distal obstruction. In three of them, the distal catheter was successfully replaced into the peritoneal cavity. The fourth child, however, developed an infectious abdominal pseudocyst with adhesions due to a then undetected Propionibacterium acnes infection. After externalisation and antibiotics, a new ventriculo-atrial shunt was inserted. At follow-up between 5 months to nearly 6 years later, the three children with peritoneal catheters did not show any signs of shunt malfunction or abdominal problems. Thus hydrocephalic children may develop shunt malfunction with distal catheter obstruction due to a still unexplained, transient, non-infectious peritoneal reaction leading to abdominal pseudocyst formation or accumulation of CSF. In some children, however, it may later be possible to replace the distal catheter into the peritoneal cavity, if no infection is involved.
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