Cerebral shunts are commonly used to treat hydrocephalus, the swelling of the brain due to excess buildup of cerebrospinal fluid (CSF). If left unchecked, the cerebrospinal fluid can build up leading to an increase in intracranial pressure (ICP) which can lead to intracranial hematoma, cerebral edema, crushed brain tissue or herniation. The cerebral shunt can be used to alleviate or prevent these problems in patients who suffer from hydrocephalus or other related diseases. Shunts can come in a variety of forms but most of them consist of a valve housing connected to a catheter, the end of which is usually placed in the peritoneal cavity. The main differences between shunts are usually in the materials used to construct them, the types of valve (if any) used, and whether the valve is programmable or not.
A diagram of a typical brain shunt
Types of valves
|Delta||Designed to prevent overdrainage. Remains closed until ICP reaches a predetermined level. Leaves shunted ventricle larger than the non-shunted ventricles.|
|Medium pressure cylindrical||Can lead to uneven drainage of ventricles.|
|Nulsen and Spitz||Contains two ball-valve units connected with a spring. Does not have an adjustable pressure setting. First mass-produced valve used to treat hydrocephalus in 1956.|
|Spitz-Holter||Uses slits in silicone to avoid mechanical failure.|
|Anti-siphon||Prevents over drainage by preventing the siphon effect. The device closes when the pressure within the valve becomes negative relative to the ambient pressure. Prevents overdrainage that might occur when a patient sits, stands or rapidly changes posture.|
|Sigma||The Sigma valve operates on a flow-control mechanism as opposed to the pressure-control system of other valves. The device can regulate CSF flow changes without being programmed or surgically changed. The first iteration was introduced in 1987. Valve operated in three stages to prevent over and under drainage.|
The location of the shunt is determined by the neurosurgeon based on the type and location of the blockage causing hydrocephalus. All brain ventricles are candidates for shunting. The catheter is most commonly placed in the abdomen but other locations include the heart and lungs. Shunts can often be named after the route used by the neurosurgeon. The distal end of the catheter can be located in just about any tissue with enough epithelial cells to absorb the incoming CSF. Below are some common routing plans for cerebral shunts.
|Route||Location of Fluid Drain|
|Ventriculo-peritoneal shunt (VP shunt)||Peritoneal cavity|
|Ventriculo-atrial shunt (VA shunt)||Right atrium of the heart|
|Ventriculo-pleural shunt (VPL shunt)||Pleural cavity|
|Ventriculo-cisternal shunt (VC shunt)||Cisterna magna|
|Ventriculo-subgaleal shunt (SG shunt)||Subgaleal space|
|Lumbar-peritoneal shunt (LP shunt)||Peritoneal cavity|
A subgaleal shunt is usually a temporary measure used in infants who are too small or premature to tolerate other shunt types. The surgeon forms a pocket beneath the epicranial aponeurosis (the subgaleal space) and allows CSF to drain from the ventricles, creating a fluid-filled swelling on the baby's scalp. These shunts are normally converted to VP or other shunt types once the infant is big enough.
Surgical wound healing for a ventriculo-peritoneal shunt (VP shunt)
There are a number of complications associated with shunt placement. Many of these complications occur during childhood and cease once the patient has reached adulthood. Many of the complications seen in patients require immediate shunt revision (the replacement or reprogramming of the already existing shunt). The common symptoms often resemble the new onset of hydrocephalus such as headaches, nausea, vomiting, double-vision, and an alteration of consciousness. Furthermore, in the pediatric population, the shunt failure rate 2 years after implantation has been estimated to be as high as 50%.
Infection is a common complication that normally affects pediatric patients because they have not yet built up immunities to a number of different diseases. Normally, the incidence of infection decreases as the patient grows older and the body gains immunity to various infectious agents. Shunt infection is a common problem and can occur in up to 27% of patients with a shunt. Infection can lead to long term cognitive defects, neurological problems, and in some cases death. Common microbial agents for shunt infection include Staphylococcus epidermidis, Staphylococcus aureus, and Candida albicans. Further factors leading to shunt infection include shunt insertion at a young age (<6 months old) and the type of hydrocephalus being treated. There is no strong correlation between infection and shunt type. The symptoms of a shunt infection are very similar to the symptoms seen in hydrocephalus but can also include fever and elevated white blood cell counts.
Treatment of shunt infections
Treatment of a CSF shunt infection generally includes removal of the shunt and placement of a temporary ventricular reservoir until the infection is resolved. There are four main methods of treating ventriculoperitoneal (VP) shunt infections: (1) antibiotics; (2) removal of infected shunt with immediate replacement; (3) externalization of shunt with eventual replacement; (4) removal of infected shunt with external ventricular drain (EVD) placement and eventual shunt re-insertion. The last method is best with over 95% success rate.
Medical treatment of shunt infection
Initial empiric therapy for CSF shunt infection should include broad coverage that includes gram-negative aerobic bacilli including pseudomonas and gram-positive organisms including Staph aureus and coagulase negative staphylococcus, such as a combination of ceftazidime and vancomycin. Some clinicians add either parenteral or intrathecal aminoglycosides to provide enhanced pseudomonas coverage, although the efficacy of this is not clear at this time. Meropenem and aztreonam are additional options that are effective against gram-negative bacterial infections.
Surgical treatment of shunt infection
To evaluate the benefit of surgical shunt removal or externalization followed by removal, Wong et al. compared two groups: one with medical treatment alone and another with medical and surgical treatment simultaneously. 28 patients suffering from infection after ventriculoperitoneal shunt implantation over an 8-year period in their neurosurgical center were studied. 17 of these patients were treated with shunt removal or externalization followed by removal in addition to IV antibiotics while the other 11 were treated with IV antibiotics only. The group receiving both surgical shunt removal and antibiotics showed lower mortality – 19% versus 42% (p = 0.231). Despite the fact that these results are not statistically significant, Wong et al. suggest managing VP shunt infections via both surgical and medical treatment.
An analysis of 17 studies published over the past 30 years regarding children with CSF shunt infections revealed that treating with both shunt removal and antibiotics successfully treated 88% of 244 infections, while antibiotic therapy alone successfully treated the CSF shunt infection in only 33% of 230 infections.
While typical surgical methods of handling VP shunt infections involve removal and reimplantation of the shunt, different types of operations have used with success in select patients. Steinbok et al. treated a case of recurrent VP shunt infections in an eczematous patient with a ventriculosubgaleal shunt for two months till the eczema healed completely. This type of shunt allowed them to avoid the area of diseased skin that acted as the source of infection. Jones et al. have treated 4 patients with non-communicating hydrocephalus that suffered VP shunt infections with shunt removal and third ventriculostomy. These patients were cured of the infection and have not required shunt re-insertion, thus showing the effectiveness of this procedure in these types of patients.
Another leading cause of shunt failure is the blockage of the shunt at either the proximal or distal end. At the proximal end the shunt valve can become blocked due to the buildup of excess protein in the CSF. The extra protein will collect at the point of drainage and slowly clog the valve. The shunt can also become blocked at the distal end if the shunt is pulled out of the abdominal cavity (in the case of VP shunts), or from similar protein buildup. Other causes of blockage are overdrainage and slit ventricle syndrome.
Over drainage occurs when a shunt has not been adequately designed for the particular patient. Overdrainage can lead to a number of different complications some of which are highlighted below.
Usually one of two types of overdrainage can occur. First when the CSF drains too rapidly, a condition known as extra-axial fluid collection can occur. In this condition the brain collapses on itself resulting in the collection of CSF or blood around the brain. This can cause severe brain damage by compressing the brain. Furthermore, a subdural hematoma may develop. Extra-axial fluid collection can be treated in three different ways depending on the severity of the condition. Usually the shunt will be replaced or reprogrammed to release less CSF and the fluid collected around the brain will be drained. The second condition known as slit ventricle syndrome occurs when CSF slowly overdrains, over several years. More information on slit ventricle syndrome appears below.
Chiari I malformation
Recent studies have shown that over drainage of CSF due to shunting can lead to acquired Chiari I Malformation. It was previously thought that Chiari I Malformation was a result of a congenital defect but new studies have shown that overdrainage of Cysto-peritoneal shunts used to treat arachnoid cysts can lead to the development of posterior fossa overcrowding and tonsillar herniation, the latter of which is the classic definition of Chiari Malformation I. Common symptoms include major headaches, hearing loss, fatigue, muscle weakness and loss of cerebellum function.
Slit ventricle syndrome
Slit ventricle syndrome is an uncommon disorder associated with shunted patients, but results in a large number of shunt revisions. The condition usually occurs several years after shunt implantation. The most common symptoms are similar to normal shunt malfunction, but there are several key differences. First the symptoms are often cyclical and will appear and then subside several times over a lifetime. Second, the symptoms can be alleviated by lying prone. In the case of shunt malfunction neither time nor postural position will affect the symptoms.
The condition is often thought to occur during a period where overdrainage and brain growth occur simultaneously. In this case the brain fills the intraventricular space, leaving the ventricles collapsed. Furthermore, the compliance of the brain will decrease, which prevents the ventricles from enlarging, thus reducing the chance for curing the syndrome. The collapsed ventricles can also block the shunt valve, leading to obstruction. Since the effects of slit ventricle syndrome are irreversible, constant care in managing the condition is needed.
An intraventricular hemorrhage can occur at any time during or after a shunt insertion or revision. Intraparenchymal hemorrhages that are multi-focal in nature have also been described in the pediatric population following ventriculoperitoneal shunting. The hemorrhage can cause an impairment in shunt function which can lead to severe neurological deficiencies. Studies have shown that intraventricular hemorrhage can occur in nearly 31% of shunt revisions.
Conditions requiring shunting
Below is a short list of known complications that can lead to hydrocephalus requiring shunting.
|Congenital hydrocephalus||A wide range of genetic abnormalities that could lead to hydrocephalus at birth.||0.04-0.08%|
|Tumor||A number of different tumors can lead to CSF blockage if they are located in certain areas. Some of these areas include the lateral or third ventricles, the posterior fossa, and intraspinal tumors. The tumors may be malignant or benign.||Unknown|
|Post-haemorrhagic hydrocephalus||Bleeding into the ventricles of the brain, especially in infancy, can lead to blockage of CSF drainage and cause hydrocephalus.|
|Spina bifida||Specifically spina bifida myelomeningocele can cause the development of hydrocephalus because the cerebellum will block the flow of CSF in a development of Chiari Malformation II.||.125%|
|Congenital aqueductal stenosis||A genetic disorder which can cause deformations of the nervous system. The defect is commonly associated with mental retardation, abducted thumbs and spastic paraplegia.||.003%|
|Craniosynostosis||Craniosynostosis occurs when the sutures of the skull close too early. The result of multiple sutures fusing before the brain stops growing is an increase in ICP leading to hydrocephalus.||0.05%|
|Post-meningitic hydrocephalus||The inflammation and scarring caused by meningitis can inhibit CSF absorption.|
|Dandy-Walker syndrome||Patients usually present with a cystic deformity of the fourth ventricle, hypoplasia of the cerebellar vermis, and an enlarged posterior fossa. The condition is a genetically heritable disease.||0.003%|
|Arachnoid cyst||A defect caused when CSF forms a collection that is trapped in the arachnoid membranes. The resulting cyst can then block the normal flow of CSF from the brain resulting in hydrocephalus as well as other defects. The most common locations for an arachnoid cyst are the middle fossa and the posterior fossa. The most common symptoms are nausea and vertigo.||0.05%|
|Idiopathic intracranial hypertension||A rare neurological disorder affecting approximately 1 in 100,000 people, most of whom are women of child bearing age. IIH results in a raised intracranial pressure and can lead to permanent loss of vision.|
Though there have been many cases of patients reaching "shunt independence", there is no common accord in which doctors can agree in which a patient might survive without a shunt. Another problem with shunt removal is that it is very difficult to discern when a patient might be shunt independent without very specific conditions. Overall shunt removal is a rare but not unheard of procedure.
- Hlatky, Roman; Valadka, Alex B.; Robertson, Claudia S. (2003). "Intracranial hypertension and cerebral ischemia after severe traumatic brain injury". Neurosurgical Focus. 14 (4): e2. doi:10.3171/foc.2003.14.4.2. PMID 15679301.
- Bradley, William G.; Bahl, Gautam; Alksne, John F. (2006). "Idiopathic normal pressure hydrocephalus may be a 'Two Hit' disease: Benign external hydrocephalus in infancy followed by deep white matter ischemia in late adulthood". Journal of Magnetic Resonance Imaging. 24 (4): 747–55. doi:10.1002/jmri.20684. PMID 16958056.
- Jain, Harsh; Natarajan, Kal; Sgouros, Spyros (2005). "Influence of the shunt type in the difference in reduction of volume between the two lateral ventricles in shunted hydrocephalic children". Child's Nervous System. 21 (7): 552–8. doi:10.1007/s00381-004-1096-y. PMID 15682319.
- (2008). http://www.medtronic.com/neurosurgery/valves.html Archived 2010-03-24 at the Wayback Machine, Retrieved November 30, 2009
- Boockvar, John A.; Loudon, William; Sutton, Leslie N. (2001). "Development of the Spitz—Holter valve in Philadelphia". Journal of Neurosurgery. 95 (1): 145–7. doi:10.3171/jns.2001.95.1.0145. PMID 11453388.
- Anti-Siphon Device; Integra Neurosciences; Label 2002
- http://www.integra-ls.com/products/?product=47 Archived 2010-03-26 at the Wayback Machine, Retrieved November 30, 2009
- Interview with Dr. Gary R. Gropper; Piedmont Neurosurgery; October 15, 2009
- Rizvi, Syed Ali A.; Wood, Martin (2010). "Ventriculosubgaleal Shunting for Post-Haemorrhagic Hydrocephalus in Premature Neonates". Pediatric Neurosurgery. 46 (5): 335–9. doi:10.1159/000320135. PMID 21346395.
- Drake, J. M.; Kestle, J. R. W.; Tuli, S. (2000). "CSF shunts 50 years on - past, present and future". Child's Nervous System. 16 (10–11): 800–4. doi:10.1007/s003810000351. PMID 11151733.
- Enger, P. Ø.; Svendsen, F.; Wester, K. (2003). "CSF shunt infections in children: experiences from a population-based study". Acta Neurochirurgica. 145 (4): 243–8, discussion 248. doi:10.1007/s00701-002-1068-5. PMID 12748883.
- Brook, Itzhak (2002). "Meningitis and shunt infection caused by anaerobic bacteria in children". Pediatric Neurology. 26 (2): 99–105. doi:10.1016/S0887-8994(01)00330-7. PMID 11897473.
- Shah, Samir S.; Smith, Michael J.; Zaoutis, Theoklis E. (2005). "Device-related Infections in Children". Pediatric Clinics of North America. 52 (4): 1189–208, x. doi:10.1016/j.pcl.2005.05.003. PMID 16009263.
- James, H E; Walsh, J W; Wilson, H D; Connor, J D; Bean, J R; Tibbs, P A (1980). "Prospective randomized study of therapy in cerebrospinal fluid shunt infection". Neurosurgery. 7 (5): 459–63. doi:10.1097/00006123-198011000-00006. PMID 7003434.
- Steinbok, Paul; Cochrane, D. Douglas (1994). "Ventriculosubgaleal shunt in the management of recurrent ventriculoperitoneal shunt infection". Child's Nervous System. 10 (8): 536–9. doi:10.1007/BF00335079. PMID 7882378.
- Morris, Andrew; Low, Donald E. (1999). "Nosocomial bacterial meningitis, including central nervous system shunt infections". Infectious Disease Clinics of North America. 13 (3): 735–50. doi:10.1016/s0891-5520(05)70103-3. PMID 10470564.
- Wong, George Kwok Chu; Wong, Sin Man; Poon, Wai Sang (2011). "Ventriculoperitoneal shunt infection: intravenous antibiotics, shunt removal and more aggressive treatment?". ANZ Journal of Surgery. 81 (4): 307. doi:10.1111/j.1445-2197.2011.05690.x. PMID 21418491.
- Schreffler, Rachel T.; Schreffler, Andrew J.; Wittler, Robert R. (2002). "Treatment of cerebrospinal fluid shunt infections: a decision analysis". The Pediatric Infectious Disease Journal. 21 (7): 632–6. doi:10.1097/00006454-200207000-00006. PMID 12237594.
- Jones, R. F.C.; Stening, W. A.; Kwok, B. C.T.; Sands, T. M. (1993). "Third Ventriculostomy for Shunt Infections in Children". Neurosurgery. 32 (5): 855–9, discussion 860. doi:10.1227/00006123-199305000-00024. PMID 8492866.
- Browd, Samuel R.; Gottfried, Oren N.; Ragel, Brian T.; Kestle, John R.W. (2006). "Failure of Cerebrospinal Fluid Shunts: Part II: Overdrainage, Loculation, and Abdominal Complications". Pediatric Neurology. 34 (3): 171–6. doi:10.1016/j.pediatrneurol.2005.05.021. PMID 16504785.
- Martínez-Lage, Juan F.; Ruíz-Espejo, Antonio M.; Almagro, María-José; Alfaro, Raúl; Felipe-Murcia, Matías; López López-Guerrero, A. (2009). "CSF overdrainage in shunted intracranial arachnoid cysts: a series and review". Child's Nervous System. 25 (9): 1061–9. doi:10.1007/s00381-009-0910-y. PMID 19452154.
- Gkolemis, C; Zogopoulos, P; Kokkalis, P; Stamatopoulos, G; Syrmos, N; and Paleologos, T.S. (2014) "Management of multiple, late onset complications in a 33-year-old female, with a ventriculoperitoneal shunt and crohn's disease," Pakistan Journal of Neurological Sciences (PJNS): Vol. 9: Iss. 3, Article 10.
- Oushy, Soliman; Parker, Jonathon J.; Campbell, Kristen; Palmer, Claire; Wilkinson, Corbett; Stence, Nicholas V.; Handler, Michael H.; Mirsky, David M. (November 2017). "Frontal and occipital horn ratio is associated with multifocal intraparenchymal hemorrhages in neonatal shunted hydrocephalus". Journal of Neurosurgery. Pediatrics. 20 (5): 432–438. doi:10.3171/2017.6.PEDS16481. ISSN 1933-0715. PMID 28885094.
- Brownlee, Richard D.; Dold, Oliver N.R.; Myles, Terence (1995). "Intraventricular Hemorrhage Complicating Ventricular Catheter Revision: Incidence and Effect on Shunt Survival". Pediatric Neurosurgery. 22 (6): 315–20. doi:10.1159/000120922. PMID 7577666.
- Schrander-Stumpel, C.; Fryns, J. -P. (1998). "Congenital hydrocephalus: Nosology and guidelines for clinical approach and genetic counselling". European Journal of Pediatrics. 157 (5): 355–62. doi:10.1007/s004310050830. PMID 9625330.
- Zuccaro, Graciela; Sosa, Fidel; Cuccia, Vicente; Lubieniecky, Fabiana; Monges, Jorge (1999). "Lateral ventricle tumors in children: a series of 54 cases". Child's Nervous System. 15 (11–12): 774–85. doi:10.1007/s003810050470. PMID 10603022.
- MedlinePlus Encyclopedia Myelomeningocele
- Tal, Y.; Freigang, B.; Dunn, H. G.; Durity, F. A.; Moyes, P. D. (1980). "Dandy-Walker Syndrome: Analysis of 21 Cases". Developmental Medicine & Child Neurology. 22 (2): 189–201. doi:10.1111/j.1469-8749.1980.tb04327.x. PMID 7380119.
- Imaging in Dandy-Walker Malformation at eMedicine
- Samii, Madjid; Carvalho, Gustavo A; Schuhmann, Martin U; Matthies, Cordula (1999). "Arachnoid cysts of the posterior fossa". Surgical Neurology. 51 (4): 376–82. doi:10.1016/S0090-3019(98)00095-0. PMID 10199290.
- Iannelli, A.; Rea, G.; Di Rocco, C. (2005). "CSF shunt removal in children with hydrocephalus". Acta Neurochirurgica. 147 (5): 503–7, discussion 507. doi:10.1007/s00701-005-0494-6. PMID 15838593.
|Wikimedia Commons has media related to Cerebral shunt.|