VP shunts

Cite this article as:
Angharad Griffiths. VP shunts, Don't Forget the Bubbles, 2020. Available at:

Rhiannon is a 2 year old with spina bifida who had a VP shunt inserted during the first month.  It was revised because of a “blockage” at 18 months.  She has not been herself for the last 24hours; more lethargic than usual- especially this morning when she woke up where she also felt hot.  She vomited in the car on the way to the Emergency Department.  She has had previous urinary tract infections.

Rhiannon was afebrile on presentation in ED.  In triage, she was observed as being awake and drinking from a bottle but wasn’t perturbed by having her observations taken or finger-prick glucose.  Overall she was a little quiet in the ED and her mum was concerned that this was absolutely different from her baseline.  Her urine microscopy was not concerning.  She had a mild neutrophilia and a normal CRP.  Subcutaneous examination of her shunt, from her skull to the right clavicle was normal.  She vomited once in the ED.


This is a common presentation and one that can be challenging to manage. Missing a shunt problem can have catastrophic consequences. This post will take you through some pearls and pitfalls of managing children with VP shunts presenting to the ED.


What is a VP shunt?

A ventriculoperitoneal (VP) shunt is a medical device used to drain fluid via a pressure gradient, away from the brain for conditions of excessive cerebrospinal fluid (CSF).  The intention is to shunt fluid away and avoid excessive pressure on the brain.  It is one of the commonest performed neurosurgical procedures and is the treatment of choice for the vast majority of patients with hydrocephalus.


Shunts drain according to the differential pressure gradient between the ventricle and the tip of the distal catheter.  The ventricular end of the catheter is inserted through a burr hole in the right parietooccipital region and the valve often sits behind the right ear.  The distal portion is subcutaneously tunneled down into the abdomen where it’s positioned inside the peritoneal cavity.

The diagnosis of raised intracranial pressure in children with VP shunts is challenging.  The symptoms are non-specific and the commonest causes often benign.  Rhiannon could easily have a simple viral illness or her symptoms could be associated with rising intracranial pressure. Missing a shunt malfunction in these patients can be catastrophic.


Physiology of CSF circulation and drainage

  • CSF  is produced at a rate of approximately 20ml/h in children and adults. In normal circumstances, in a normal adult, CSF is recycled three times a day. The normal adult volumes of CSF (approximately 150mls) are reached by age 5.  The volume in a neonate can be estimated at  2ml/kg.
  • Around 50% of CSF is created by the choroid plexus of the lateral, third and fourth ventricles.  The rest of the CSF arises from the extracellular fluid of the brain.  CSF travels out of the foramen of Lushka and foramen of Magendie (at the level of the fourth ventricle), and heads through to the subarachnoid spaces, along the spinal cord to the cerebral hemispheres.  Over the cerebral hemispheres, the CSF is reabsorbed by arachnoid villi and then into the venous sinuses which drain into the jugular (internal) veins.
  • Intracranial pressure (ICP) rises when CSF production exceeds absorption.
  • Hydrocephalus is the consequence of the excessive accumulation of CSF. This could be from disruptions in formation, flow or absorption.
  • As hydrocephalus worsens and intracranial pressure increases, the temporal and frontal horns dilate, sometimes asymmetrically; and there’s elevation of the corpus callosum and stretching of white matter tracts.


Lateral = Lushka — Median = Magendie


Shunting CSF is an effective way to avoid the neurological damage that ensues if the build-up of CSF is left untreated.

Three shunts types are mainly used to shunt CSF: Ventriculoperitoneal (VP), ventriculopleural (VPL), and ventriculoatrial (VA). By far, the commonest are VP shunts.


Reasons for shunt placement

There is a myriad of reasons as to why a VP shunt should be placed.  They can be categorized into congenital or acquired causes.


Having a VP shunt in itself is a cause for concern for patients and caregivers.  Common areas for concern in paediatric patients include:

  • Flying and travel: there is no evidence that flying is dangerous but patients have concern over access to neurosurgical help should they need it. Shunt alert cards displaying the type of shunt are available.  The need for augmented travel insurance is also an area of concern.
  • Sports: Contact sports such as boxing are contra-indicated, and the US paediatric neurosurgeons named wrestling and football (soccer) as the commonest sports with adverse events.  Neurosurgeons in the UK are advising that football and rugby wearing a skullcap are acceptable.  You can still go scuba diving.
  • Future employment: in the UK, the Royal Air Force, Royal Navy and Police Force are the only services that preclude entry.
  • Programmable shunts and magnets: Background magnetic fields of household objects such as microwaves etc are safe as are walk-through metal detectors.  Post MRI check is advised with some programmable shunts but all are MRI safe.  The iPad2 has a strong magnetic field and can re-program some shunt valves, thus important to keep them at safe distances.
  • Shunt length: reassurance that placing sufficient length inside the abdomen will suffice and allow for growth.
  • Weight: Obesity is a risk factor for failure of VP shunts and dislodgement.


Shunt related complications

Failure rates are quoted as 30-40% at 1 year and 50% at 2 years in the paediatric cohort. A patient can expect to have 2-3 shunt revisions over the course of 20 years and the median time to shunt failure is just 1 and a half years. Paediatric revisions are more commonplace than adult revisions.


Risk factors for shunt failure include:

  • Younger patients (<6months), particularly neonates
  • Complex comorbidities, for example, cardiac, myelomeningocele, IVH’s, tumour and post-meningitic hydrocephalus, spinal dysraphism, and congenital hydrocephalus
  • Prior shunt failure and short time intervals between revisions
  • Male sex
  • Low socioeconomic status


Causes of shunt failure

Obstruction, blockage or occlusion

The commonest cause of shunt malfunction is proximal occlusion. There’s no clear data on whether programmable or non-programmable shunts are less likely to occlude.

It’s hypothesized that on insertion, the lumen can be obstructed with brain parenchyma from the cerebral cortex before reaching the ventricle, or choroid plexus when inserted near to the foramen of Monroe. It can also be occluded with blood following choroid plexus haemorrhage along with other cellular matter such as macrophages, giant cells, connective tissue, fibrin networks, debris, neoplastic cells.

Distal catheter blockage tends to occur later and when it occurs, it should raise the suspicion for an intra-abdominal pseudocyst or adhesions which may affect future peritoneal catheter placements.

Shunt infection

Shunt infection is the second most common reason for malfunction. The data is mixed, particularly as some older papers use data from before the time of antibiotic-impregnated catheters, skewing the data. Risk factors include young age (including neonates), post-op CSF leak, previous shunt infections, and the presence of a gastrostomy tube.

The vast majority of shunt infections are acute.  Far fewer late-onset infections have been reported. They can be attributed, mostly, to peritonitis, abdominal pseudocyst, bowel perforation, and haematogenous inoculation.

Shunt infection is associated with an increased risk of seizure disorder, decreased intellectual performance, and a two-fold increase in long term mortality. Re-infection occurs in one-quarter of children.

The proportion of shunt infections falls off rapidly after the first several months following implantation. The vast majority occur during the first 6 months. Children will present with signs of shunt failure, as well as systemic infection.  Fever is common and if we were to sample CSF (which is not often done in the ED), the presence of >10% neutrophils in the ventricular fluid is highly specific and sensitive of infection.

The commonest organisms are skin flora, including Staphylococcus epidermidis, Staph. aureus and gram-negative rods.  Infections with Staph. aureus and epidermidis are associated with an earlier onset as they are skin commensals. Infections with Staph. aureus are associated with a significantly increased likelihood of subsequent shunt infection.

Shunt fracture

This is often a late complication and almost always occurs along the distal portion between the valve and peritoneum.  With age, fibrous tissue becomes calcified and does not slide freely within the subcutaneous tissue then the tubing can crack.  This is more likely to happen in the neck where most movement occurs.

Tension can also form along areas of calcification causing tethering and stretching as the child grows.  It is important to note that early shunt fracture can occur and this could be a consequence of trauma to the tubing during surgery.

CSF can still drain resulting in an insidious duration of symptoms, clouding and confusing the diagnostic process.

Shunt series radiographs should always be sought in this cohort, though frequently fractures and disconnections are incidental findings during surveillance exams.

VP shunt fracture. Reused with permission from Education and Practice, Archives of Disease of Childhood


Shunt disconnections

Catheters are generally multi-component and hubbed together so disconnections can occur soon after surgery. The disconnection impedes the flow of CSF and it may still leak.  The onset of these symptoms may be slow.  Disconnections can happen at either the proximal or distal aspect of the valve.

Case courtesy of Dr Adam Eid Ramsey, Radiopaedia.org. From the case rID: 71794


Abdominal pseudocyst

This is a rare complication of VP shunts and is usually a late complication occurring years after initial placement. A pseudocysts is a fluid-filled sac that collects at the distal tip of the catheter.  It is thought that they form because of inflammation or due to abdominal adhesions.  It can present with abdominal pain or distention with, or without, a palpable abdominal mass.  Neurological symptoms occur when there is elevated ICP.

Shunt migration

The proximal or distal catheter tip may migrate.  With growth, the proximal catheter can withdraw from the ventricle (extremely rare), or the distal catheter can shift away from the peritoneum.  The distal tubing can become tethered and cause traction on some of the components causing a disconnection.  Distal migration occurs as the child grows.



It is possible that a VP shunt can over-drain as well and ‘under-drain’.  With rapid over-drainage, the dura can be stressed and subdural haematomas and/or extra-axial fluid collections can form.

A slit ventricular syndrome occurs when gravitational forces exert a siphoning effect on the ventricles.  This effect is generally amplified by pressure.


Clinical presentation of shunt malfunction

Children with a blocked shunt can present with a myriad of symptoms including:

  • headache
  • nausea
  • vomiting
  • fever
  • irritability
  • abnormal level of consciousness

Infants and older children may present differently.


  • difficulty feeding
  • bulging fontanelle

Older children may present more specifically with

  • Nausea, somnolence, lethargy, cognitive difficulties, or eye pain.


Predictably, fever is commoner in children with shunt infections. Those with shunts because of myelomeningoceles may present with symptoms such as:-

  • weakness,
  • difficulty walking
  • bowel/bladder dysfunction
  • lower cranial nerve palsies.

Children present with these symptoms all the time to the ED. They are clearly not specific to a shunt problem.  As a consequence, diagnosing shunt malfunction on clinical grounds alone is incredibly difficult. Patients with shunt fracture or disconnection can present with a slow onset of symptoms.  They may have pain/tenderness localized to the area of fracture/disconnection or an area of calcification of an area of fluctuant swelling.


Diagnosis, evaluation, and imaging

The diagnosis of a shunt malfunction requires a combination of CT, shunt series radiographs, and occasionally (though seldom in the ED), CSF sampling.

A CT is likely to show an increase in ventricular size and occasionally, periventricular lucency representing oedema.  There may be increasing ventricular size on cross-sectional imaging but up to 15% will have “such profound alterations on brain compliance that their ventricles will not enlarge in the face of shunt failure and increased ICP”.  Ventricular size doesn’t appear to reach a plateau until approximately 14months after placement of the shunt (regardless of type implanted).

A lumbar puncture (LP) may demonstrate increased opening pressures, but not always.  It is also used for evidence of infection.  This not performed commonly in the ED in the context of possible shunt malfunction.

Shunt series (SS) radiographs are used to check the overall course of the catheter, looking for disconnection or disruption.  The series will not show obstructions, only damage to the catheter. It can rarely demonstrate complications such as a CSF pseudocyst (abnormal separation of bowel loops near the catheter tip) but shouldn’t be relied upon for this.

The number of radiographs needed varies according to the size of the child.  It is usually 3-4 radiographs, including two views of the skull and the continuous trajectory of the shunt tubing down the neck, chest, and then looping into the abdomen.

If a series is performed after the scan, theoretically a 2 view skull radiographs can be eliminated, provided that the chest x-ray includes the base of the neck. Unnecessary radiation may then be avoided.

The use of ultrasound is an area of ongoing research and has been largely unvalidated in children with VP shunts.


No clear cause for Rhiannon’s symptoms was found following a thorough examination.  A CT was performed because of concern over shunt failure. Her ventricles were noted to be slightly larger than a CT performed previously.  Shunt series radiographs showed continuous, non-kinked tubing.  She was admitted under the care of the Neurosurgeons and her shunt was revised.  No physical reason for shunt obstruction was found.


Selected references

Mansson PK, Johansson S, Ziebell M, Juhler M. Forty years of shunt surgery at Rigshospitalet, Denmark: A retrospective study comparing past and present rates and causes of revision and infection. BMJ Open. 2017;7(1).

Berry JG, Hall MA, Ph D. A multi-institutional 5 year analysis of Initial and multiple ventricular shunt revisions in children. Neurosurgery. 2008;62(2):445–54.

Pople IK. Hydrocephalus and shunts: What the neurologist should know. Neurol Pract. 2002;73(1).

Paff M, Alexandru-Abrams D, Muhonen M, Loudon W. Ventriculoperitoneal shunt complications: A review. Interdiscip Neurosurg Adv Tech Case Manag. 2018;13(June 2017):66–70.

Gonzalez DO, Mahida JB, Asti L, Ambeba EJ, Kenney B, Governale L, et al. Predictors of Ventriculoperitoneal Shunt Failure in Children Undergoing Initial Placement or Revision. Pediatr Neurosurg. 2016;52(1):6–12.

Wu Y. V Entriculoperitoneal S Hunt C Omplications in C Alifornia : 1990 To 2000. 2007;61(3):557–63.

Brinker T, Stopa E, Morrison J, Klinge P. A new look at cerebrospinal fluid circulation. Fluids Barriers CNS. 2014;11(1):1–16.

Rochette A, Malenfant Rancourt MP, Sola C, Prodhomme O, Saguintaah M, Schaub R, et al. Cerebrospinal fluid volume in neonates undergoing spinal anaesthesia: A descriptive magnetic resonance imaging study. Br J Anaesth [Internet]. 2016;117(2):214–9. Available from: https://dx.doi.org/10.1093/bja/aew185

Desai KR, Babb JS, Amodio JB. The utility of the plain radiograph “shunt series” in the evaluation of suspected ventriculoperitoneal shunt failure in pediatric patients. Pediatr Radiol. 2007;37(5):452–6.

Stone JJ, Walker CT, Jacobson M, Phillips V, Silberstein HJ. Revision rate of pediatric ventriculoperitoneal shunts after 15 years: Clinical article. J Neurosurg Pediatr. 2013;11(1):15–9.

Brian W. Hanak et al. Cerebrospinal fluid shunting compliations in children. Pediatr Neur. 2017;52(6):381–400.

Hanak BW, Ross EF, Harris CA, Browd SR, Shain W. Toward a better understanding of the cellular basis for cerebrospinal fluid shunt obstruction: Report on the construction of a bank of explanted hydrocephalus devices. J Neurosurg Pediatr. 2016;18(2):213–23.

Khan F, Shamim MS, Rehman A, Bari ME. Analysis of factors affecting ventriculoperitoneal shunt survival in pediatric patients. Child’s Nerv Syst. 2013;29(5):791–802.

Shastin D, Zaben M, Leach P. Life with a cerebrospinal fluid (CSF) shunt. BMJ [Internet]. 2016;355(October):1–5. Available from: https://dx.doi.org/doi:10.1136/bmj.i5209

Simon TD, Butler J, Whitlock KB, Browd SR, Holubkov R, Kestle JRW, et al. Risk factors for first cerebrospinal fluid shunt infection: Findings from a multi-center prospective cohort study. J Pediatr [Internet]. 2014;164(6):1462-1468.e2. Available from: https://dx.doi.org/10.1016/j.jpeds.2014.02.013

Buster BE, Bonney PA, Cheema AA, Glenn CA, Conner AK, Safavi-Abbasi S, et al. Proximal ventricular shunt malfunctions in children: Factors associated with failure. J Clin Neurosci [Internet]. 2016;24:94–8. Available from: https://dx.doi.org/10.1016/j.jocn.2015.08.024

Mcgirt MJ, Zaas A, Fuchs HE, George TM, Kaye K, Sexton DJ. Factors Infecton for Pediatrc and Venticulopertoneal of Shunlt Predictors Infectous Patiogens. 2014;36(7):858–62.

Mcclinton D, Carraccio C, Englander R. Predictors of ventriculoperitoneal shunt pathology. Pediatr Infect Dis J. 2001;20(6):593–7.

Erol FS, Ozturk S, Akgun B, Kaplan M. Ventriculoperitoneal shunt malfunction caused by fractures and disconnections over 10 years of follow-up. Child’s Nerv Syst. 2017;33(3):475–81.

Dabdoub CB, Dabdoub CF, Chavez M, Villarroel J, Ferrufino JL, Coimbra A, et al. Abdominal cerebrospinal fluid pseudocyst: A comparative analysis between children and adults. Child’s Nerv Syst. 2014;30(4):579–89.

Boyle TP, Kimia AA, Nigrovic LE. Validating a clinical prediction rule for ventricular shunt malfunction. Pediatr Emerg Care. 2018;34(11):751–6.

Tuli S, O’Hayon B, Drake J, Clarke M, Kestle J. Change in ventricular size and effect of ventricular catheter placement in pediatric patients with shunted hydrocephalus. Neurosurgery. 1999;45(6):1329–35.

DeFlorio RM, Shah CC. Techniques that decrease or eliminate ionizing radiation for evaluation of ventricular shunts in children with hydrocephalus. Semin Ultrasound, CT MRI [Internet]. 2014;35(4):365–73. Available from: https://dx.doi.org/10.1053/j.sult.2014.05.002

Smyth MD, Narayan P, Tubbs RS, Leonard JR, Park TS, Loukas M, et al. Cumulative diagnostic radiation exposure in children with ventriculoperitoneal shunts: A review. Child’s Nerv Syst. 2008;24(4):493–7.

Ventriculoperitoneal shunts

Cite this article as:
Ben Lawton. Ventriculoperitoneal shunts, Don't Forget the Bubbles, 2013. Available at:

An 8 yr old boy presents after three vomits at home.  He has a background of spastic diplegic cerebral palsy and has a ventriculo-peritoneal (VP) shunt.  He is usually ambulatory and attends a mainstream school.

What goes wrong with VP shunts? How can we assess them for failure or infection?

The Bottom Line

  • Infection and mechanical failure are common complications of VP shunts
  • Fever and new (<six months old) shunts are big risk factors for shunt infection
  • Children with a shunt that has been present for >six months, along with the absence of fever, vomiting, and headache, are unlikely to have a shunt complication as the cause of their presentation
  • Children with a VP shunt and symptoms or signs that may represent raised ICP need consideration of a non-contrast CT head
  • Shunt series is fairly low yield but indicated if you have reason to suspect shunt fracture
  • Children with a VP shunt remain susceptible to all the usual diseases of childhood
  • There is data to support the use of the PECARN head injury rule, but not the other widely used minor head injury rules, in children with VP shunts 


What is a VP shunt?

Ventriculoperitoneal shunts are the most commonly used method of diverting CSF flow for the treatment of hydrocephalus from any cause. The shunt system consists of a proximal catheter that sits in the lateral ventricle, a one-way valve to prevent the backflow of CSF, and a distal catheter that sits in the peritoneal cavity. Programmable valves are available where the rate of CSF flow can be adjusted with a magnet. Shunts can alternatively drain into the atria or pleural space but these are much less common. They do not correct the underlying problem but do prevent complications of raised intracranial pressure when there is an obstruction to the flow of CSF.


Labeled shunt



What complications can VP shunts develop?

VP shunts are prone to failure and infection. Failure may result from mechanical obstruction, over-drainage, or loculation of the ventricular system. Abdominal problems such as bowel perforation can occur and rarely shunts have been known to migrate to the bladder or scrotal sac.


How can I tell if this child’s shunt is infected?

Infections are much more common in recently sited shunts, with 90% of infections occurring in the first six months post-insertion. Symptoms such as erythema along the shunt tract, meningism, or peritonism strongly suggest that the shunt is infected but are rarely present. Fever is usual but not universal, while lethargy, headache, and irritability are common. If these factors, in the context of the child’s other symptoms and exam findings, leave you suspicious of an infected shunt a neurosurgeon should tap it. The most frequently identified bugs are Staph. epidermidis and Staph. aureus, which can generate biofilms making antibiotic treatment very difficult.


How can I tell if this child’s shunt is failing?

Clinical features of shunt failure are those of raised intracranial pressure. Persistent headache, lethargy, vomiting, changes in the neurological exam, or visual function may all be identified. A plain X-ray shunt series includes views of the skull, neck, thorax, and abdomen allowing the integrity of the shunt system to be assessed. the shunt series is rarely helpful but indicated of you are considering a fractured shunt in the differential. A non-contrast CT may identify migration of the proximal tip of the intra-ventricular catheter or secondary features of increased ICP such as ventriculomegaly. CTs are most useful when compared with previous scans but remember you can have raised ICP and a normal CT. It is also worth considering the total radiation dose received by kids with shunts when CT is used liberally.


How will I recognize over drainage?

Symptoms (usually headaches) that are exaggerated by sitting/standing and improved with lying down. Occasionally the drainage can be so rapid it can lead to tearing of the bridging veins of the dura and a subdural haematoma.





Further History

On further assessment, this child was afebrile, reported two episodes of diarrhoea, and revealed that his sister was suffering similar symptoms. It was 2 years since his most recent shunt revision, he denied having a headache and his neurological examination was consistent with that previously recorded in the chart. He was given ondansetron and, after successfully completing a trial of oral fluid, was discharged.

The same patient returned 2 hours later having sustained a minor head injury. He was GCS 15 and met the PECARN low-risk criteria. The medical student had read the sub-group analysis of the PECARN data, which showed similar rates of clinically important traumatic brain injuries after minor blunt head trauma in children with and without VP shunts. The consultant reviewed this data and was happy to apply the PECARN rule to this patient and discharged him with appropriate head injury advice and without a CT.


Selected references

Fleisher and Ludwig. Textbook of Pediatric Emergency Medicine, 6th Edition Ch126

Piatt and Garton (2008) Clinical diagnosis of ventriculoperitoneal shunt failure among children with hydrocephalus. Pediatr Emerg Care 24(4);201-210

Nigrovic et al (2013) The Prevalence of Traumatic Brain Injuries After Minor Blunt Head Trauma in Children With Ventricular Shunts

Ann Emerg Med 61(4);389-93

Tapping VP shunts – Pediatric EM Morsels