Long-term shunt dependency rates in patients treated for IIH with CSF diversion have not been established. We therefore present our experience with 5 children shunted for IIH during the years 1984–2000 with very long-time follow-up. Three out of these patients have experienced late or very late episodes of severe shunt failure during the second or third decade after initial shunt treatment. They were all boys and may not be representative for IIH patients as a whole. Three of them appear, however, to be permanently shunt dependent, indicating that long-term shunt-dependency in children treated for IIH with CSF diversion may be more common than previously expected.
- idiopathic intracranial hypertension (IIH)
- CSF diversion
- shunt dependency
In 1937 Walter Dandy published a series of 22 patients treated surgically for intracranial hyper-tension without a tumor . Among his cases treated with subtemporal decompression during a period of 10 years, there were 3 children. Later on, this condition with papilledema, headache and visual disturbances was called benign intracranial hypertension, and many of them could be managed favorably by medical treatment . In more severe cases, it soon became clear that this obscure disease is not always that benign . In severe cases the term malignant pseudotumor was introduced . Later on the term Idiopathic Intracranial Hypertension (IIH) was introduced .
Neurosurgical treatment with CSF diversion has been performed in severe cases where the response to medical treatment has been unsatisfactory, or as primary treatment in patients with severe visual affection [6, 7]. Unlike the situation for hydrocephalic children treated with CSF shunts who for the most become shunt dependent, clinical results on long term shunt dependency in IIH are unavailable.
Modified Dandy criteria:
1.1 Diagnostic work-up
Idiopathic intracranial hypertension is a diagnosis where other causes I leading to increased intracranial pressure have been excluded by CT or MRI, including unobstructed venous outflow. Normal CSF composition rules out infection. The diagnosic procedure of intracranial hypertension itself is usually performed by a simple lumbar puncture. This gives CSF for analysis, and fluid may spurt out in cases of severe IIH. When the Intracranial pressure (ICP) is measured via the lumbar route, the patient is posisioned flat with the puncture site in equal hight as the IIIrd ventricle. The needle seize should not be very thin (G19), to obtain a presice manometric pressure reading. Loss of fluid should be avoided, since the pressure falls rapidly unless ICP is very high. Pathological elevated ICP is above 25 cm H2O (15–20 in children). ICP is,however, influenced by a number of factors that may give misleading results when ICP is evaluated by the lumbar route.
Firstly, the patient should be cooperative and relaxed. Furthermore ICP is highly influenced by changes in PaCO2. If the patient is anxious and hyperventilate, ICP will fall rapidly. The pressure recording can also be performed by the use of standard fluid pressure transduces and may be combined by other diagnostic work-up, such as lumbar infusion tests. In children, these diagnostic procedures must be undertaken during general anesthesia and normocapnia.
When patients with severe headache but without papilledema or visual affection, are given a IIH diagnosis, correct evaluation of the CSF hydrodynamic situation is pertinent. If CSF pressure is observed under unstable conditions or is influenced rapid changes in the central venous pressure, misinterpretations may take place. Queckensteds test (venous compression in the neck) demonstrates this effect on the CSF pressure, and was previously used to exclude a spinal block. Lumbar infusion tests can be used to explore the need for therapeutic CSF diversion, and of course demonstrate that an indwelling shunt is patent (LP-shunt or VP-shunt). A simple lumbar puncture will of course also be helpful to exclude severe shunt failure, as well as shunt infection.
It should be pointed out that the lumbar puncture itself will give an opportunity to explore the possibilities for a good result in IHH patients. After puncture with a 19G cannula, CSF will leak during the following three weeks, especially in true IIH patients with increased CSF pressure. This is why some individuals without IIH, will experience post-puncture headache due to intracranial hypotension. The beneficial effect of LP and CSF removal on severe headache and visual affection, is often temporary and repeated punctures or shunt implantation will be needed.
All children (0–19 years old) who underwent a shunt implantation for IIH during the years 1980–2000 in our institution were identified from the surgical protocols. Ethical approval was obtained from the medical ethics committee of Norway, the Regional Committee of Medicine and Heath.
We present our experience with these pediatric patients shunted for IIH during the years 1984 to 2000; and therefore have long-term follow-up.
Five pediatric patients aged 0–19 years presented with clinical signs and symptoms of increased ICP.
They had small ventricles, no venous outflow obstruction, high opening pressure on LP and normal CSF composition.
They were all males, four were in the first decade (age: 1,3,4,5 and 18 years). All had bilateral papilledema, headache and visual disturbances in spite of medical treatment (Acetazolamide, corticiosteroids, furosemide). They all had normal weight for age. The results are summarized in Table 1.
|Patient number Age/sex||Year||Shunt procedure||Number of shunt proce-dures||Follow-up|
|1 M 18||1984||LP||3||36||Yes||Headache, visual loss, papilledema|
|2003||LP(rev)||Headache, blurred vision|
|2 M 4||1988||CA||32||No||Papilledema, VIth n. palsy, visual loss|
|3 M 3||1989||CP||3||31||Yes||Papilledema, visual loss|
|2006||LP||Headache, vomiting, High CSF pessure|
|4 M 5||1991||CP||5||29||Yes||Hedache, papilledema, ataxia, blurred vision, unstable level of consciousness|
|2004||VP||Headache, vomit, diplopia,papilledema|
|2006||LP||Episodes of vislual loss, high ICP|
|2009||Remove P-kat||Abdominal disability|
|5 M 1||2000||LP||1||18||?||Blilat. VIth nerve palsy, papilledema|
3.1 Case 1
In 2013 another episode of clinical shunt failure took place, and the symptoms again responded favorably after implantation of a VP shunt. Today, with 36 years follow-up, he is in full-time work as a diary worker.
3.2 Case 2
3.3 Case 3
Due to the dramatic clinical symptoms with complete visual loss, corticosteroid treatment was implemented and an acute shunt procedure was performed during the same general anesthesia. A proximal catheter was introduced into cisterna Magna and connected to a low pressure Holter valve with diversion to the peritoneal cavity.
His vision gradually reappeared within days, and after one week there was normal vision and pupillary reactivity to light. Some ataxia and clumsy motor function persisted for weeks, but after 6 months his clinical condition was quite normal. During the first two years of treatment he experienced a few episodes with headache, ataxia and diplopia (VIth nerve paresis) which resolved spontaneously within a couple of days or after pumping on the Holter valve. At the age of 5 years (1991) he demonstrated episodes of overdrainage in the upright position, which subsided after implementation of an ASD (anti-syphon-device) distal to the valve.
Thereafter his clinical condition was uneventful for many years. During his university studies (in 2006), he became acutely ill with signs of increased ICP (headache and vomiting). There was no choked discs, but lumbar puncture revealed markedly increase CSF pressure level (50 cm H2O) and no signs of infection. Once more MRI was normal (Figure 1). After a shunt revision (LP-shunt), his clinical condition normalized within a few days. In 2009, he experienced shunt failure once more, again followed by rapidly improvement after shunt revision. Thereafter he has been working full time, and has been clinically quite well for another 11 years.
This case with a very rewarding clinical result indicate that this 35 year-old man in excellent condition most likely is permanently shunt dependent.
3.4 Case 4
3.5 Case 5
Clinical series of patient with IIH are heterogenous with respect to age, sex and the severity of disease. When Dandy presented his series of 22 cases in 1937, he gave an individual and detailed overview of clinical history, symptoms and signs of his patients . They illustrate the severity of the problems these patients were faced with when they sought neurosurgical treatment 80–90 years ago. One of 3 children in Dandys` series was:
4.1 Dandy’s case 12
4.1.1. Historical perspective on IIH management
Patients with extreme presentations in terms of visual disturbancies and headache underwent subtemporal decompression procedures in small volumes during the following decades. Although positive clinical responses were obtained in shortly after decompression in many of them, the procedures were dangerous and serial lumbar punctures had to be performed to achieve more long lasting relief from the decompression. When lumbo-peritoneal shunting was introduced in the treatment of hydrocephalus in the 1950ies, it was therefor natural to explore this treatment also in severe cases of pseudotumor. When other CSF diversion procedures for HC were established in the 1960ies (VA-shunts) , and later on VP-shunts , they were also found applicable in treatment of iIH.
Although shunt procedures are generally effective in relieving the CSF pressure in IIH, these CSF procedures have a substantial number of complications. When medical treatment for IIH became available (Diamox, Furosemide etc), non-surgical treatment would be preferred by many, since shunt failure, shunt infection and shunt dependency could therefore be omitted.
During the 1980ies and 1990ies, the number of patients with IIH increased rapidly, especially among people with severely increased body mass index, with a clear female dominance .
In some of these patients bariatric surgery has been introduced to reduce the weight problem and may also solve the IIH or alt least reduce the need for CSF diversion procedures . It also seems that morbid overweight increases the problems with CSF diversion to the peritoneal cavity.
Several studies have compared lumboperitoneal shunts versus ventriculoperitoneal shunts in the treatment of IIH . Both types of CSF are highly effective in the acute stage, but there are more revisions during the following years in patients treated with LP-shunts . McGirt and coworkers furthermore underscore that while CSF diversion is effective in the acute stage, several patients experience that headaches returns. The found that this happens more often in patients without papilledema and long-standing symptoms before shunt treatment.
In early years LP shunts were considered applicable since it was technically easy to achieve CSF from the lumbar CSF reservoir, compared to get ventricular access in patients with small or slit ventricles.
In recent decades modern imaging (MR,CT) and stereotactic placement of ventricular catheters have resulted in ventriculo-peritoneal CSF shunting as the most used procedure, at least in adults. In patients with severe overweight, distal end problems with abdominal complaints is common.
Pediatric IIH is a rare disease  and pediatric cases are often presented in series of institutional IIH patients of all ages, where females of reproductive age dominate. Another problem is that clinically IIH covers a wide spectrum of symptoms and signs. When patients without papilledema or frank visual affection are included, non-surgical management is preferred and may lead to satisfactory outcomes. Long-term follow-up of IIH-children treated conservatively (with papilledema) has demonstrated that some are left with visual defects . In recent years focus has been directed to the small group of IIH patients where troublesome headaches are not the main threat, but visual affection. If treatment over time is not efficient in reducing papilledema and visual affection, permanent reduction in visual acuity, visual field defects and even blindness may take place [16, 17].
This was the case in our Case 1, where serial lumbar taps gave excellent symptomatic relief of headache for 3 weeks, but during the fourth week the symptoms built up. When a LP-shunt eventually was implanted after 6 months, his visual acuity was reduced by 50%, and only improved slightly during the subsequent year. He obviously should have been shunted earlier. The visual threat also have a strong time component, implying that when visual deterioration is rapid or abrupt, surgical intervention is imminent (CSF-diversion or optical nerve sheath fenestration). Progression of visual affection over weeks have been considered a strong indication for surgery, with the prospect of avoiding further visual affection. Our Case 3, demonstrates that frank blindness can be treated successfully with restoration of vision, but this raises the question of emergency surgery in such rare cases. A number of publications point to this problem when patients with IIH are faced in emergency departments [6, 18,–20]. These rare, but very important experiences are in accord with the eminent and detailed clinical observations made by Walter Dandy 80 years ago.
Thus, neurosurgical treatment by CSF diversion is well established in IIH patients with severe visual affection as well as in cases with unsatisfactory response to medical treatment . When the clinical result is good over years, as in our patient 5, it is difficult to know if the shunt is still functioning or the underlying condition has normalized spontaneously .
However, our five cases with very long-term follow up (20–36 years) demonstrate episodes of shunt failure in three of them, up to 29 years after initial shunt treatment. All together 7 episodes of shunt failure requiring shunt revision were observed. Only one of these distinct shunt failures took place during the first decade after implantation (after 3 years, disconnection). The others occurred from 13 to 29 years after implantation. All the shunt failures were restricted to 3 out of the 5 patients, and all of these 3 experienced repeated delayed shunt failures (in the second or third decade after initial treatment). There are few pediatric series with shunt treated IIH children reported. Niotakis and coworker report on 7 cases who underwent lumbar CSF shunt surgery. There was 2 acute procedures due to severe visual affection, but 3 patients presented with severe headache without papilledema. All patients had shunt revisions, due to symptoms of overdrainage or obstruction. An adult series from Dublin  reported low failure rates both in LP-shunts (11%) and VP shunts (14%), nevertheless revision rates were 60% in LP shunts and 30% in VP shunts. Bjørnson and coworkers report a lower revision rate (11%) in VP-shunted IIH adults. The follow-up periods in these studies are restricted, and late shunt failures have not been reported in adults (beyond 7 years).
Since IIH has been considered a benign and perhaps self restoring condition, this might explain the lack of long-term follow-up studies. Good long-term results can therefore both be explained by a no-longer existing CSF diversion demand andsome of the well functioning shunted patients may in fact have functioning shunt. This question has not been addressed, but very late shunt failure has not been reported. Many revisions in reported in IIH shunted individuals, describe other problems than shunt failure (obstruction or hypofunction); i.e. overdrainage, shunt infection or unstable diversion.
Shunt implantation in children with severe IIH raises the question of making these children permanently shunt dependent . While some authors have addressed this question, no cases with late or very late shunt failure has been reported, until our case 3, published in 2017 . Four of our pediatric cases have been published previously , and our case 1 was not included since his age of 18 did not fit with the series (reviewers opinion).
This case with 30 years follow-up, indicate that individuals shunted for IIH can be persistently dependent on their shunt, and may experience acute shunt failure even after many years of treatment. We also consider our patient 1, with shunt failures 19 and 29 years after initial treatment to be permanently shunt dependent. Also patient 4 with shunt failure after 15 years is most likely in the need for life-long shunt treatment.
The last two patients tell a different story. Patient 2 had a good clinical response to shunt treatment in 24 years and thereafter experienced progressive symptoms from overdrainage. His shunt was therefore removed under ICP observation for 4 days, and he responded well. After 3 years further follow-up, we consider him shunt independent.
Our small group of shunt treated IIH children is peculiar since they are all boys, compared to the well known female dominance in IIH patients as a whole. It is, however, also known that females do not outnumber males in the first decade in IIH treated children . In a report from a large pediatric emergency unit, children with papilledema and visual affection diagnosed with IIH, were twice as common in boys compared with girls in the first decade of life, while the opposite was found in the second decade . It is unclear if our small study group is representative for all pediatric IIH patients and for the large group of adult IIH patients, many with high body mass index (BMI).
Clinical studies describing adult IIH cohorts illustrate the female dominance, often up to 90 per cent.
Comparison of treatment strategies as well as results is troublesome because inclusion criteria may vary. In the United States a rapidly rising incidence of cerebrospinal fluid shunting procedures for idiopathic intracranial hypertension was described for the years 1988–2002 . The increase seemed to correlate with the rapid rise in morbid obesity. The increase was 320% for the population as a whole, but only 38% for males, and 52% for pediatric cases (<13 yrs., both sexes).
Bariatric surgery is considered to be beneficial for overweight IIH patients, and may reduce the need for shunt treatment. Bariatric surgery has been used as primary treatment as well as additional surgical procedure in IIH patients after CSF shunt procedures. The are a number of reports on multiple shunt procedures in such patients. In a group of 6 patients where bariatric surgery was performed in shunted IIH individuals, the shunt was externalized and clamped. Due to severe overdrainage symptoms, shunt removal was planned, but the shunt had to be acutely reestablished due to unexpected and clear shunt dependency .
This points to another problem, namely that evaluation of shunt function in IIH patients can be difficult. When headache is the dominating clinical problem, differentiation between high-pressure symptoms (shunt failure), visual affection; and low-pressure symptoms (over drainage) may be challenging. It is easy when overdrainage-symptoms in terms of headache and dizziness are rapidly reversed in recumbent position, but if the CSF drainage is unstable the clinical picture may include both. In such situations ICP-monitoring or use of lumbar or ventricular infusion tests may be helpful [27, 30], and additional shunt revisions and increased risk of shunt infection can be reduced.
Although the report from Roth and coworkers  presented 6 aldults that were unexpectedly shunt dependent, it is remarkable that long-term shunt dependency has not been a topic. Since benign intracranial hypertension has been considered a self-solving condition, long lasting shunt dependency may therefore have been unexpected, but perhaps also overlooked. In research on shunt patency in hydrocephalic patients, the term
The proportion of patients still having their initial shunt unrevised was anticipated to represent individuals with persistent shunt dependency, but harboring still functioning shunts.
In our long-term follow-up of children shunted for hydrocephalus I the 1960is and 1980 we have found shunt dependency rates of about 90% [2, 11]. That is why ETV is now a preferred treatment when feasible in primary management of hydrocephalus. The other 10% are for sure not shunt dependent, since their shunt has been explanted, in some of them in combination with an ETV procedure. The correct description would therefore be that up to 90% still are or can be more or less shunt dependent.
The shunt dependency rates for pediatric IIH treated with CSF diversion are actually not known, and long-term follow-up reports are scarce. Our limited experience, however, indicate that permanent shunt dependency may be more common than previously expected. In adults this topic has hardly been addressed.
Conflict of interest
|IIH||idiopathic intracranial hypertension|