Background

Cerebrospinal fluid (CSF) shunting is the standard treatment of hydrocephalus [1,2,3]. Ventriculo-peritoneal shunt (VP) is the mainstay for CSF diversion [4,5,6]. However, despite the progress in management and the advances in shunt hardware design, malfunction rates continue to be disappointingly high [7, 8]. CSF shunt malfunction is a potential life-threatening condition if goes unrecognized and thus it requires instantaneous diagnosis and prompt management [9, 10].

Unenhanced CT has been used for the evaluation of CSF shunts in the emergency setting [8, 10,11,12]. Rapid MRI brain protocols using single-shot fast T2 sequences have been employed for shunt assessment without risk of sedation or radiation exposure. Both CT and rapid MRI protocols have been focusing mainly on demonstration of ventricular system dilatation, visualization of ventricular configuration, transependymal CSF permeation, and catheter localization. However, visualization of the catheter lumen remained problematic [13,14,15].

Newly developed high-resolution heavily T2-weighted volumetric sequences (e.g., three-dimensional driven equilibrium 3D-DRIVE) have been recently added to the MR protocol for imaging of hydrocephalus [16,17,18]. The high-resolution sequences are superior to conventional MR protocol in the assessment of subarachnoid space and demonstration of thin obstructive membranes [17, 18].

Correct recognition of shunt failure is challenging. Moreover, the exact malfunctioning shunt part is difficult to identify. To the best of our knowledge, there is no consensus imaging approach for standardizing the evaluation of CSF shunts [8, 19, 20]. Moreover, the importance of 3D-DRIVE in shunt assessment was investigated in only one study [3], and the significance of phase contrast (PC) MR sequence in the evaluation of CSF shunts was discussed in a few papers in the literature [11, 21]. In addition, the value of MRI in the assessment of the abdominal end of the shunt was not thoroughly investigated. Our aim is to study the utility of different MR pulse sequences in evaluating the cranial and abdominal ends of CSF shunts in order to identify the potential cause of shunt failure and its impact on patient management.

Methods

After ethical committee approval, a prospective cohort study was conducted at our institution. The patients included in the study were either referred for routine follow-up or having symptoms suggestive of subacute or chronic shunt malfunction. The latter group included patients with headache, decline in their visual abilities or eye motility, unsteady gait, mood changes, decreased school performance, psychomotor retardation, new onset or increased frequency of seizures, vomiting, abdominal pain or increased abdominal girth, swelling, or CSF leakage along the shunt track. Younger infants could present with increasing occipitofrontal circumference, bulging fontanelle, poor feeding, somnolence, or decreased activity. Patients with rapidly decreasing conscious level, apneic spells, bradycardia, or pupillary alterations were excluded from the study, as these signs indicate brain herniation and require emergent management [22]. As we aimed to assess the abdominal end of the shunt, patients with ventriculoatrial and ventriculopleural shunts were also excluded. Finally, 25 patients were enrolled in the study. An informed consent was provided by the patients or their guardians.

All patients were subjected to history taking and full neurological examination at presentation. After the acquisition of images, patients were followed, and surgical details were documented if they underwent surgery. At surgery, shunts were visually inspected and tested for patency of the proximal and distal catheter ends via reservoir injection and detection of distal runoff, respectively. Patients were further categorized based on the location of the shunt malfunction (as having abnormalities related to the cranial end, abdominal end, or both).

Abdomino-pelvic ultrasound

Abdomino-pelvic ultrasound scan was performed on all patients in the supine position using both linear and convex ultrasound transducers (7.5–11 MHz and 2.5–7.5 MHz, respectively, GE LOGIQ P9 ultrasound machine, USA) by the same radiologist (7 years of experience) who later participated in the MRI imaging analysis. All abdominal quadrants were scanned. The abdominal end of the shunt was traced, and the related fluid was assessed (either free, localized, or absent).

MRI examination

Pediatric patients younger than 5 years of age were sedated prior to the MRI scan using chloral hydrate (100 mg/ml); the dose was calculated according to body weight (100 mg/kg, maximum dose for infants ≤ 1 year 1 gm/dose and for pediatric > 1 year 2 gm/dose) according to our Radiology and Anaesthesia departments’ guidelines.

All patients were scanned in a supine position by using a 3 T machine (Achieva dStream, Philips medical system, Eindhoven, The Netherlands) using an eight-channel SENSE head coil (SENSE acceleration factor of 16) for brain scan and appropriate Torso coil (SENSE acceleration factor of 32) for the acquisition of abdominal images.

For assessment of the cranial end of the shunt, high-resolution 3D-DRIVE was acquired in the coronal plane. Other conventional brain sequences (diffusion-weighted imaging (DWI), fluid attenuation inversion recovery (FLAIR), T1-WI, T2-WI, and susceptibility-weighted imaging (SWI) in axial planes) were also obtained. ECG-gated quantitative PC sequence was acquired perpendicular to the long axis of the shunt catheter at the suboccipital region distal to its valve, the location where it was settled and unaffected by breath movement. A circular region of interest (ROI) was adjusted over the inner diameter of the shunt in the resultant axial re-phased image by the same radiologist (7 years of experience), and then QF processing software was applied to estimate CSF flow curve and velocity parameters (Fig. 1). For assessment of the abdominal end of the shunt, abdomino-pelvic T2 spectral presaturation with inversion recovery (T2 SPIR) was acquired in axial, coronal, and sagittal planes. (Detailed MRI sequences’ parameters are listed in Table 1.)

Fig. 1
figure 1

(A, reconstructed 3D-DRIVE in sagittal plane) ECG-gated quantitative PC was acquired perpendicular to the long axis of the shunt catheter at the suboccipital region distal to its valve. B A ROI was drawn over the inner diameter of the shunt tube in axial re-phased image. C CSF flow curve and velocity parameters were calculated by CSF-QF software

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Table 1 Detailed MRI sequences’ parameters
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Image analysis

MRI images were analyzed by two radiologists having 7 and 20 years of experience. The utility of each pulse sequence was assessed according to its ability to precisely locate the cranial portion of the shunt, visualization of its lumen, as well as evaluating the ventricular system, periventricular white matter and the presence of collections or blood products. The shunt reservoir and valve were also assessed regarding the presence of related collection or catheter disconnection. The shunt catheter was considered patent if it had fluid signal within its lumen, whereas the presence of intraluminal low T2 signal intensity could suggest luminal occlusion [3]. Abdominal sequences were assessed according to their ability to localize the abdominal end of the shunt and assess the related fluid collections.

Statistical analysis

In patients with multiple inserted shunts, the findings of the most recently inserted shunt were used in statistical analysis. The importance of each sequence was determined by its ability to detect additional information that other sequences did not provide, or whether it provided clinically valuable data when compared to other sequences.

The relation between ventricular catheter location and its proximity to the surrounding structures with its luminal patency was studied and statistically tested using the Fisher’s exact test.

The catheter luminal flow distal to the valve was quantitatively analyzed on the quantitative PC sequence. The estimated results (flux and mean velocity values) for patent shunts were statistically compared to those with complications. Asymptomatic patients and patients with suspected shunt malfunction were compared regarding the presence of dilated ventricles and abnormal periventricular white matter signal intensity. Patients who underwent surgery and those who underwent conservative management were compared regarding the presence of shunt-related abnormalities as well with the estimation of the positive and negative likelihood ratios.

Results

Twenty-five patients (18 males, 7 females, median age 2.5 years, IQR 0.75–15) were enrolled in the study. There were eight asymptomatic patients who were referred for routine follow-up, and 17 patients (having 21 shunts) who experienced symptoms suggestive of shunt malfunction. Three patients had more than one inserted shunt. Finally, there were 28 VP shunts and single ventriculo-gallbladder (VGB) shunt; all had first-generation type valves (fixed differential pressure valves with no related motion or metallic artifacts). An average of 15 min was required for the sedation of children under the age of 5 prior to the MRI scan.

3D-DRIVE (in coronal plane supplemented by axial, sagittal, and various obliquities reformations) was able to precisely assess the cranial portion of all evaluated shunts regarding their location, integrity, luminal patency, and periventricular white matter signal alteration (Fig. 2). In addition, ventricular system and extra-axial spaces anatomical details were well demonstrated in all patients. Although axial FLAIR and T2-WI were able to assess the ventricular size and periventricular white matter signal intensity, they failed to precisely demonstrate the catheter lumen. In addition, ventricular loculations were demonstrated similarly on T2-WI and 3D-DRIVE in four patients; however, the fine internal ventricular septae related to the shunt were only perceived in 3D-DRIVE in three patients (p < 0.001) (Fig. 3).

Fig. 2
figure 2

Reconstructed 3D-DRIVE in axial oblique plane (A) and coronal oblique plane (B) demonstrates luminal CSF signal throughout a patent cranial portion of shunt

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Fig. 3
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A 2-month-old boy presented with fever and poor feeding. A, B Reconstructed 3D-DRIVE in axial and sagittal oblique planes, respectively, shows multiple fine ventricular septae surrounding proximal catheter that shows intraluminal faint low signal, which may represent intraluminal extension of these septae along with luminal debris. C Axial T2-WI for the same patient does not show any intraventricular septae or shunt catheter lumen

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Extra-axial hematoma was detected in four patients. Determination of signal intensity on T1-WI, and T2-WI, or 3D-DRIVE was valuable in the determination of the age of the subdural collection (Fig. 4). Three patients had a subacute hematoma and one had a chronic collection. Variable diffusion restriction was seen only in two patients. SWI demonstrated old hemosiderin foci (in 14 patients). Both DWI and SWI were found to have less considerable clinical value in terms of patients’ management.

Fig. 4
figure 4

A 7-month-old boy was referred for routine follow-up. Left parieto-occipital early subacute subdural hematoma that displays similar hypointense signal in both 3D-DRIVE and T2-WI and hyperintense signal in T1-WI, related foci of blooming artifact in SWI (D, E magnitude and phase images, respectively) with no related diffusion restriction (not shown). The proximal catheter and reservoir of the shunt are patent, both demonstrating luminal CSF signal (seen in A)

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Abdomino-pelvic T2 SPIR was able to evaluate the abdominal end of the shunt in all patients and to detect related complications (either loculated intraperitoneal collection (CSF pseudocyst), extraperitoneal migration, CSF ascites, or absent intraperitoneal fluid). However, only two planes could be sufficient for three-dimensional assessment for cases with the loculated collection. The findings of abdomino-pelvic MRI scan were in excellent agreement with ultrasound findings (Cohen’s Kappa 0.9). However, compared to ultrasound, MRI was unable to detect a small gallbladder wall defect in the only patient with a VGB shunt who developed CSF pseudocyst (Fig. 5).

Fig. 5
figure 5

A 2-year-old boy with ventriculo-gallbladder shunt presented with increasing abdominal girth. A Coronal abdomino-pelvic T2 SPIR and B corresponding ultrasound show a large abdomino-pelvic loculated fluid (CSF pseudocyst) with gallbladder mural defect (arrow) demonstrated in ultrasound image

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The luminal patency of the shunt proximal catheter was found to be correlated with the exact location of its terminal portion and the nature of the surrounding structures (p: 0.002). An altered intraluminal signal was demonstrated in 8 shunts; all were located either in close proximity to the choroid plexus, or surrounded by intraventricular septae. And, of the seventeen totally patent proximal catheters, eleven were found to be freely located within the lateral ventricle away from the choroid plexus.

Quantitative PC sequence was evaluated in only 19 shunts: patent shunts (8), cranial end complications (7), and abdominal end complications (5), the remaining shunts were excluded from the analysis due to motion artifact. The flux and mean velocity of patent shunts were found to be 0.03 ml/s and 0.3 cm/s, respectively. All shunts with cranial end complications had weak flux and lower mean velocity values (0.008 ml/s and 0.16 cm/sec, respectively), except for one patient who had a CSF collection surrounding shunt reservoir, she had accelerated flow (flux: 0.1 ml/sec, mean velocity: 2.2 cm/sec). Shunts with abdominal end complications had relatively higher flux and mean velocity values (0.057 ml/sec and 1.1 cm/sec, respectively). However, there was no statistically significant difference regarding flux and velocity values between patients with complicated shunts and those with patent shunts (p: 0.5 and 0.3, respectively).

Detailed MRI findings for patients are summarized in Tables 2 and 3. Among asymptomatic patients, total luminal patency of the cranial portions of the shunts was demonstrated in all but one patient. Abdominal sequences revealed minimal free intraperitoneal fluid in all but one patient (Patient 8; Table 2); his MRI showed appreciable amount of free intraperitoneal fluid (CSF ascites) (Fig. 6).

Table 2 Clinical and MRI findings of asymptomatic patients
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Table 3 Clinical and MRI findings of symptomatic patients
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Fig. 6
figure 6

A 6-month-old boy was referred for routine follow-up. A, B Abdomino-pelvic T2 SPIR in coronal and axial planes, respectively, shows large volume of free ascites (CSF ascites). The cranial portion of this shunt is patent (not shown). This patient experienced increasing occipitofrontal circumference during regular follow-up visits (1.5 months after imaging), and he underwent an alternative CSF diversion (VA shunt insertion)

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Despite clinical suspicion of shunt malfunction, total luminal patency of the cranial portions of the shunts was demonstrated in four shunts, with related minimal free intraperitoneal fluid around their abdominal ends (Patients 1–4; Table 3). However, shunt malfunction attributed to cranial end complications was demonstrated in eight symptomatic patients (Patients 5–12; Table 3) in the form of intraluminal faint or dark signal signifying luminal occlusion (Fig. 3, 7), catheter disconnection from the reservoir/valve (Fig. 8), extraventricular course of the proximal catheter (Fig. 9), isolated fluid collection surrounding shunt reservoir (Fig. 10), or slit ventricle with possible overshunting. Shunt malfunction attributed to abdominal end complications was demonstrated in three patients (Patients 15–17; Table 3). Two patients were found to have loculated intraperitoneal fluid collections (CSF pseudocysts) (Fig. 5), while the abdominal scans of the third patient did not show the expected minimal free intraperitoneal fluid. Combined cranial and abdominal end complications were demonstrated in two other patients (Patients 13, 14; Table 3).

Fig. 7
figure 7

Reconstructed 3D-DRIVE in axial oblique planes. A A 15-year-old male patient presented with unsteady gait and convergent squint, B A 24-year-old male patient presented with headache and attacks of vomiting. Both show proximal catheter intraluminal dark signal occluding segment where side holes are located, closely adjacent to left lateral ventricular choroid plexus (could suggest choroid plexus ingrowth). In addition to transependymal permeation and adhesion between proximal catheter terminal part and related ventricular ependymal lining (arrow) in (B)

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Fig. 8
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A 27-year-old male patient presented with headache and blurring of vision. Reconstructed 3D-DRIVE for the same patient who had 3 shunts, (A, B) in axial plane, showing collapsed reservoir (circle) with separated its proximal catheter (black arrow), (C) in coronal oblique, showing separated distal catheter from its valve with related fluid (white arrow); he had another right frontal shunt (non-complicated, not shown)

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Fig. 9
figure 9

Reconstructed 3D-DRIVE in coronal oblique planes, A A 9-month-old asymptomatic boy, yet the clinical examination of his shunt showed poor filling of the reservoir, shows extraventricular migration of the proximal catheter. B A 36-year-old female patient presented with fluctuating conscious level, shows embedded proximal catheter (terminal 2 cm) within septum pellucidum and shows intraluminal dark signal

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Fig. 10
figure 10

A 9-month-old girl presented with scalp swelling. A Reconstructed 3D-DRIVE in coronal oblique plane shows fluid collection surrounding shunt reservoir near skull burr hole; the proximal catheter and reservoir are seen patent with no evidence of disconnection. Turbulent CSF flow-related artifact is noted within the ventricular system and fluid collection as well (appreciated in FLAIR sequence, not shown). B CSF flow curve shows high flow rate values (flux: 0.1 ml/sec)

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Among patients having cranial end-related complications (11 patients, two of them had additional abdominal end complications), eight underwent surgery. The remaining three patients underwent conservative management despite the apparent shunt complication (Patient 7; Table 2 and Patients 9, 12; Table 3); two of them could be independent of the occluded shunt, as one had no obstructing lesions at the time of the MRI scan and the other had metastatic brain lesions on treatment. The third patient had overshunting. However, among the ten patients with no shunt-related abnormalities, only one patient (Patient 1; Table 3) underwent surgery (as additional shunt was inserted in an entrapped CSF pocket) (p < 0.001), positive likelihood and negative likelihood ratios = 7.27, 0.3, respectively, sensitivity = 0.7, specificity = 0.9). All patients with abdominal end-related complications (4 patients) underwent shunt revision (p < 0.001). There is no significant difference between patients who underwent surgery and those with conservative management, or symptomatic and asymptomatic patients in terms of the prevalence of ventricular dilatation or white matter signal abnormality (p: 0.6 and 0.3, respectively).

Discussion

The diagnosis of CFS shunt malfunction could be clinically challenging [2, 20]. Moreover, there is no standardized diagnostic imaging protocol to evaluate CSF shunts [8, 20]. We aimed to demonstrate the value of different MR pulse sequences in evaluating both the cranial and abdominal ends of CSF shunts in order to guide patient management. Guided by the patients’ clinical scenarios and presenting symptoms, each institution determines its imaging protocol in accordance with its available resources [15].

Fast MRI brain sequences (single-shot T2 sequences, e.g., HASTE) could be adopted in the setting of acute patient presentation [13,14,15]. Alternatively, low-dose pediatric unenhanced CT protocols could be used if MRI is not available [15]. CT and fast MRI sequences depend on the assessment of the ventricular size and configuration, localization of the shunt, and detection of periventricular white matter signal alteration [15]. However, shunt may fail without ventricular dilatation [23, 24] and, white matter signal alteration could be not only secondary to transependymal CSF permeation but also due to defective myelination [18]. Moreover, our results did not reveal any statistically significant difference between symptomatic and asymptomatic patients regarding the presence of ventricular dilatation or periventricular white matter signal alteration. This could decrease the reliability of both signs, and hence CT and rapid MRI sequences, in the diagnosis of shunt malfunction.

The most frequent cause of shunt malfunction is shunt catheter blockage, which may be caused by debris or blood clots early postoperatively, or secondary to choroid plexus ingrowth in long-term shunts [12, 25]. Additionally, intraventricular adhesions/septae, which can develop as a complication of neonatal meningitis or intraventricular hemorrhage, can surround and embed ventricular catheters resulting in shunt malfunction [26]. Both CT and fast MRI sequences have low sensitivity in the assessment of the shunt catheter lumen. Our study revealed that PHILIPS-developed 3D-DRIVE sequence had significant advantages over other sequences. Similar sequences were developed by GE and Siemens manufacturers (Fat Imaging Employing Steady-State Acquisition FIESTA, Constructive Interference In Steady State CISS, respectively). 3D-DRIVE can clearly demonstrate the ventricular catheter lumen as previously documented [3]; in addition, fine intraventricular adhesions/septae and its relation to the catheter were adequately visualized [3, 17]. We have found that the location of the proximal catheters' terminal part and its relation to the surrounding structures, especially choroid plexus, significantly affect the proximal catheter patency and could indicate the cause of obstruction as previously documented [27, 28].

T2-WI and FLAIR sequences did not add additional diagnostic information other than those found in the 3D-DRIVE sequence. In addition, they failed to demonstrate the shunt catheter lumen and the fine intraventricular septations related to the shunt. T1-WI was found to be of value in aging determination of the hematomas in combination with T2-based DRIVE [29]. DWI and SWI could be considered as non-essential sequences in the setting of suspected shunt malfunction, despite their known role in the standard neuroimaging protocol.

It was reported that enhanced sequences following intravenous contrast administration could be added to distinguish choroid plexus ingrowth from other causes of luminal occlusion, as fatal intraventricular hemorrhage may occur during attempts to remove these retained ventricular catheters [3, 30, 31]. Nevertheless, contrast-enhanced sequences were not added to our protocol. Contrast injection is time-consuming. In addition, it might be contraindicated in some circumstances or for some individuals with renal impairment. Moreover, any ventricular catheters that revealed luminal blockage should be handled properly, taking the risk of hemorrhage into account [26, 31]. However, when shunt-related infections are clinically suspected, contrast could be used to demonstrate abnormal enhancement pattern of leptomeningeal and ventricular ependymal lining that are typical with meningitis and ventriculitis, respectively [12, 32].

Shunt catheter fractures or disconnection accounts for 4.5–13.6% of shunt failure [33]. Catheter disconnection usually occurs in the neck as it is the most mobile part of the body [33, 34]. DRIVE sequence with its three-dimensional capabilities was able to demonstrate catheter disconnection either proximal or distal catheter from reservoir or valve, respectively. Catheter fractures along the subcutaneous tunneled distal catheter could be diagnosed by radiographic shunt series [35, 36]. However, the diagnostic yield and sensitivity of the radiographic shunt series are very low; it can detect the cause of malfunction in less than 10% of pediatric patients and even fewer adult shunts [3, 35, 36]. It was documented that patients with suspected shunt malfunction should proceed with more reliable images, and the use of shunt series should be restricted to patients with clinical suspicion of mechanical cause of shunt malfunction, and non-diagnostic other tests [35, 36]. None of our patients required radiographic shunt series for their diagnosis.

Few reports have described the role of cross-sectional imaging in identifying shunt malfunction attributed to abdominal end complications [2, 12, 32, 37, 38]. In our dataset, MRI showed excellent agreement with ultrasound and operative findings, making MRI a good one-stop destination for assessment of patients with suspected shunt malfunction. The presence of minimal free fluid within the peritoneal cavity could be considered an indicator of healthy peritoneal membrane [39]. The presence of CSF collections or absence of peritoneal fluid despite patent cranial end are signs of abdominal end-related complications [2, 40]. The latter finding could be explained by omental plugging within the side holes of the shunt. Tiny omental projections insinuate through the catheter side holes causing luminal blockage. It has an estimated incidence between 7 and 18% [11, 40]. On the contrary, sterile CSF ascites is considered a rare abdominal complication of the VP shunt that can occur secondary to defective peritoneal CSF absorptive capacity or secondary to choroid plexus CSF overproduction, and in this instance, it is necessary to use an alternative CSF diverting technique (such as a ventriculoatrial or VGB approach) or choroid plexus cauterization, respectively [41, 42]. Other causes of abdominal end complications include extraperitoneal catheter migration that was documented in obese patients with raised intraabdominal pressure that can impair CSF drainage or lead to catheter migration [2, 43,44,45].

Failure of adequate control of hydrocephalus implies shunt failure which is clinically indicated by shunt removal, revision, or replacement [33]. Shunt malfunction was confirmed at surgery in all operated patients. Apart from three patients, all patients with cranial and/or abdominal end complications underwent surgery (either shunt revision or an additional shunt was inserted, which confirms shunt failure). All apart from one patient with no catheter-related abnormality underwent conservative management. MRI results were found to have a high diagnostic performance for the assessment of patients with suspected shunt malfunction.

Quantitative PC assessment of patent shunts showed sluggish flux and low mean velocity values, as the patients were scanned while supine, where the hydrostatic pressure difference between the abdominal cavity and the ventricular system is almost zero. This could be explained by the normalized intracranial pressure and subsequent lack of driving force for CSF flow inside the shunt system [46].

Prior studies revealed low-velocity values in malfunctioned shunts, irrespective of the site and type of shunt malfunction [11, 21]. However, we have found that quantitative PC assessment varied depending on the location and type of shunt-related complication. Shunts with proximal catheter intraluminal signal alteration and those with overshunting were found to have sluggish flux and lower mean velocity values. The perceived sluggish flow in occluded shunts could be explained by partial rather than total occlusion of shunt side holes. It was documented that, CSF can flow within a normal range of flow rates even while the ICP is dangerously elevated due to the buildup of CSF and the ensuing increase in ICP [46,47,48]. In the setting of shunt fracture or disconnection, CSF flow could be dependent on the presence of fibrous tract at the site of the shunt discontinuity [48]. On the contrary, the patent shunt with CSF collection surrounding the reservoir and those with abdominal end-related complications were found to have relatively higher flux and mean velocity values than those with patent shunts. Similarly, brisk CSF flow was found during CSF shunt scintigraphy, which could be indicative of valve malfunction or complications in the drainage compartment or distal catheter. [48]. Although PC assessment did not show statistically significant differences between patients with complicated and patent shunts, the analyzed findings could give insights into CSF dynamics through CSF shunts in patients with different causes of shunt malfunction.

The limitations of our study included a relatively small sample size and a small number of asymptomatic patients with patent shunts. Different commercial shunt types were not taken into consideration. Also, this detailed MRI protocol for shunt assessment could be unsuitable for patients with signs of acute shunt malfunction and possible brainstem herniation in whom timely management is of utmost importance. However, it was found to be clinically relevant in a substantial number of symptomatic patients having subacute or chronic symptoms.

Conclusions

MRI could be a one-stop destination for CSF shunt assessment in patients with suspected non-acute shunt malfunction; 3D-DRIVE and T1-WI of the brain, together with T2 SPIR of the abdomen and pelvis, were found to be essential sequences for evaluation of the cranial and abdominal ends of the CSF shunts, respectively. These sequences were found to have clinical relevance in terms of accurately locating the exact site and possible cause of shunt-related complications.