Neurosurgery 98:1206–1220, 2026
This systematic review and meta-analysis evaluates diagnostic performance of noninvasive and minimally invasive tests (X-ray shunt series, CT, MRI, nuclear scintigraphy, thermal flow) for cerebrospinal fluid shunt failure in pediatric and adult patients, synthesizing 33 studies and 8,077 patients. Pooled accuracy was 82%, sensitivity 67%, and specificity 88%, with X-ray series showing lower sensitivity but higher specificity compared with CT.
The analysis highlights substantial study bias—especially in patient selection and reference standards—and concludes no existing test is adequate as a standalone diagnostic for shunt failure, underscoring the need to optimize diagnostic pathways, reduce harm, and develop improved point-of-care functional tests.
Objective Assess diagnostic performance of noninvasive/minimally invasive tests (X-ray shunt series, CT, MRI, nuclear scintigraphy, thermal flow evaluation) for suspected CSF shunt failure in pediatric and adult patients.
Methods Systematic review/meta-analysis (PROSPERO CRD42024596142) including patients with permanent CSF shunts who underwent the above index tests; performance (accuracy, sensitivity, specificity) modeled via meta-regression incorporating test type, age group, follow-up timeframe, and shunt type.
Evidence base PubMed search (Oct 22, 2024) screened 465 articles; 33 studies included, totaling 8077 patients.
Pooled performance Overall pooled accuracy 82%, sensitivity 67%, specificity 88% across included tests.
Key comparative finding (sensitivity) X-ray shunt series had significantly lower sensitivity than CT (OR 0.106, 95% CI 0.056–0.201; overall effect of test type on sensitivity P = .013).
Key comparative finding (specificity) No overall effect of test type on specificity (P = .192), but X-ray shunt series showed higher specificity than CT in subgroup analysis (OR 4.04, 95% CI 1.938–8.424).
Covariates No significant effects of age group, follow-up timeframe, or shunt type on accuracy, sensitivity, or specificity.
Conclusion/limitations No test performed well enough to serve as a standalone diagnostic for shunt failure; evidence limited by high risk of bias, especially in the reference standard domain for most studies.



















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