Cerebrospinal fluid shunting for idiopathic normal pressure hydrocephalus: a comprehensive meta‑analysis with trial sequential analysis of randomized controlled trials
- Journal
- Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (Q1)
- Published
- 2 October 2026
- Study design
- Systematic review / meta-analysis of RCTs
- Evidence level
- Level 1, High (CEBM 1a)
- Authors
- Mohammed Altaha, Ayat Jassim Al Eid, Hoor Hussain Aloraidh, Zahraa Aqeel Alshakhs, Alanoud Salah Almukhaylid, Fatimah Sami Albatih, et al.
- PMID
- 42825924
- DOI
- 10.1007/s10072-026-09424-3
Why clinicians should know about it
- Picked for Dermatology (top studies of the week, 4 October 2026): High-quality evidence in a top journal
- Picked for Epidemiology (top studies of the week, 4 October 2026): Meta‑analysis of RCTs (clinical trial focus)
- Picked for Neurology (clinical) (top studies of the week, 4 October 2026): CSF shunting meta‑analysis for idiopathic normal pressure hydrocephalus
Abstract
BACKGROUND: Idiopathic normal pressure hydrocephalus (iNPH) is a potentially reversible neurocognitive disorder causing severe functional decline in the elderly. Cerebrospinal fluid (CSF) shunting aims to relieve ventricular stress and restore perfusion; however, high-quality placebo-controlled evidence has historically been limited. METHODS: This PRISMA-compliant systematic review and meta-analysis (PROSPERO: CRD420261372290) evaluated adults aged 60 years or older with iNPH. We included randomized controlled trials (RCTs) comparing immediate active CSF shunting against placebo or no shunting. The primary outcome was the change in gait speed using standardized timed assessments. Data were pooled using a restricted maximum-likelihood random-effects model, supplemented by Trial Sequential Analysis (TSA) and GRADE assessment to control for random error. RESULTS: Four RCTs comprising 224 patients were included. Shunting significantly improved the primary outcome of gait velocity (SMD 0.73, 95% CI 0.45 to 1.01; P < 0.0001). Significant secondary improvements were observed in qualitative gait function (SMD 0.81, P = 0.007), functional independence (OR 3.92, P < 0.0001), continuous modified Rankin Scale reduction (MD - 0.73, P < 0.0001), Mini-Mental State Examination or Montreal Cognitive Assessment scores (SMD 0.37, P = 0.009), and Symbol Digit Test performance (SMD 0.47, P = 0.002). TSA confirmed conclusive evidence for functional disability reduction before reaching the required information size. Shunting increased the incidence of positional headaches (OR 5.62, 95% CI 1.16 to 27.18). The pooled estimate for subdural hematoma was imprecise and did not reach statistical significance (OR 4.07, 95% CI 0.62 to 26.94) and should not be interpreted as evidence of an absence of risk given the small number of events. No significant difference was observed for ischemic stroke (OR 0.64, 95% CI 0.18 to 2.33), also based on few events. CONCLUSION: Cerebrospinal fluid shunting appears to provide meaningful clinical benefit in patients with idiopathic normal pressure hydrocephalus, particularly through improvement in gait velocity and functional independence. However, the evidence suggests a more limited or uncertain effect on cognitive and urinary symptoms. Importantly, the available randomized evidence is too imprecise to rule out an increase in major complications such as surgically treated subdural hematoma; positional headaches were significantly more frequent with shunting, and the largest included trial independently reported a significant excess of subdural bleeding. These safety signals warrant careful discussion with patients considering shunt surgery. These findings support shunting as an effective therapeutic option for appropriately selected patients with iNPH, while emphasizing the need for careful patient selection, standardized outcome assessment, and further high-quality, large-scale trials with longer follow-up.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.