Shunt-related headaches: the slit ventricle syndromes

PurposeThe purpose of this work is to review the pathophysiology and treatment of severe headache disorders in patients having a shunt for hydrocephalus.Materials and methodsThe literature on the management of the slit ventricle syndrome is reviewed as well as an assessment of personal experiences over a 30-year period in the management of severe headache disorders in shunted patients.ResultsIf the slit ventricle syndrome is defined as severe, life-modifying headaches in patients with shunts and normal or smaller than normal ventricles with ventricular shunts for the treatment of hydrocephalus, there are five different pathophysiologies that are involved in the process. These pathologies are defined by intracranial pressure measurement as severe intracranial hypotension analogous to spinal headaches, intermittent obstruction of the ventricular catheter, intracranial hypertension with small ventricles and a failed shunt (normal volume hydrocephalus), intracranial hypertension with a working shunt (cephalocranial hypertension), and shunt-related migraine. The treatment of these conditions and identifying patients with each condition are facilitated by attempting to remove the shunt.ConclusionsFollowing the analysis of attempts to remove shunts, there are three possible outcomes. In about a quarter of patients, the shunt can be removed without having to be replaced. This is most common in patients treated in infancy for post-hemorrhagic hydrocephalus or patients shunted early after or before brain tumor surgery. Another half of patients have increased intracranial pressure and enlarged ventricles. In these patients, there is an 80% success rate for endoscopic third ventriculostomy. Finally, the most severe form of the slit ventricle syndrome involves intracranial hypertension without ventriculomegaly, which is managed optimally by shunt strategies that emphasize drainage of the cortical subarachnoid space such as lumbo-peritoneal shunts or shunts that include cisterna magna catheters.

[1]  H. Rekate,et al.  Ventricular shunt removal: the ultimate treatment of the slit ventricle syndrome. , 1998, Journal of neurosurgery.

[2]  M. Walker,et al.  Diagnosis and treatment of the slit ventricle syndrome. , 1993, Neurosurgery clinics of North America.

[3]  H. Rekate,et al.  Treatment of refractory intracranial hypertension in a spina bifida patient by a concurrent ventricular and cisterna magna-to-peritoneal shunt , 2005, Child's Nervous System.

[4]  H. Rekate,et al.  Lumboperitoneal Shunts in Children , 2002, Pediatric Neurosurgery.

[5]  F. Nulsen,et al.  Treatment of hydrocephalus by direct shunt from ventricle to jugular vain. , 1951, Surgical forum.

[6]  J. Drake,et al.  Death from chronic tonsillar herniation in a patient with lumboperitoneal shunt and Crouzon's disease. , 1992, British journal of neurosurgery.

[7]  A. Borit Communicating Hydrocephalus Causing Aqueductal Stenosis , 1976 .

[8]  A. Chutorian,et al.  Increased intraventricular pressure without ventriculomegaly in children with shunts: "normal volume" hydrocephalus. , 1979, Neurosurgery.

[9]  H. Rekate,et al.  Elevated intracranial venous pressure as a universal mechanism in pseudotumor cerebri of varying etiologies , 1996, Neurology.

[10]  D. Becker,et al.  Control of hydrocephalus by valve-regulated shunt. , 1967, Journal of neurosurgery.

[11]  J. Fuh,et al.  Chronic daily headache in adolescents , 2006, Neurology.

[12]  H. Portnoy,et al.  Anti-siphon and reversible occlusion valves for shunting in hydrocephalus and preventing post-shunt subdural hematomas. , 1973, Journal of neurosurgery.

[13]  E. Hendrick,et al.  Subtemporal decompression for the slit-ventricle syndrome after shunting in hydrocephalic children. , 1979, Child's brain.

[14]  R. Hayward,et al.  Aetiology of herniation of the hindbrain in craniosynostosis. An investigation incorporating intracranial pressure monitoring and magnetic resonance imaging. , 1997, Pediatric neurosurgery.

[15]  A. Borti Communicating hydrocephalus causing aqueductal stenosis. , 1976, Neuropadiatrie.

[16]  H. Rekate Classification of slit-ventricle syndromes using intracranial pressure monitoring. , 1993, Pediatric neurosurgery.

[17]  H. Rekate,et al.  Reexpansion of previously collapsed ventricles: the slit ventricle syndrome. , 1982, Journal of neurosurgery.

[18]  H. Rekate,et al.  Severe intracranial hypertension in slit ventricle syndrome managed using a cisterna magna-ventricle-peritoneum shunt. , 2006, Journal of neurosurgery.

[19]  F. Epstein,et al.  Subtemporal craniectomy for recurrent shunt obstruction secondary to small ventricles. , 1974, Journal of neurosurgery.

[20]  A. Olivi,et al.  Slit-ventricle syndrome: review of 15 cases. , 1987, Pediatric neuroscience.

[21]  E. Tyler-Kabara,et al.  Slit-ventricle Syndrome Secondary to Shunt-induced Suture Ossification , 2001, Neurosurgery.

[22]  H. Rekate Adults with Hydrocephalus Treated in Infancy and Childhood , 2002 .

[23]  C. Rocco,et al.  Acquired Chiari type I malformation managed by supratentorial cranial enlargement , 2003, Child's Nervous System.

[24]  Spitz Eb,et al.  Treatment of hydrocephalus by direct shunt from ventricle to jugular vain. , 1951 .

[25]  D. Chapman,et al.  Population‐Based U.S. Study of Severe Headaches in Adults: Psychological Distress and Comorbidities , 2006, Headache.

[26]  H. Rekate,et al.  Establishing the Diagnosis of Shunt Independence , 1982 .

[27]  S. Kunze,et al.  New Valves - New Dangers? 22 Valves (38 Probes) Designed in the 'Nineties in Ultralong-Term Tests (365 Days) , 1999, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.