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DOI 10.1056/nejmoa2503109

Медицинская библиотека · The New England journal of medicine · 2025

A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus.

Luciano Mark G, Williams Michael A, Hamilton Mark G, Katzen Heather L, Dasher Nickolas A, Moghekar Abhay, Hua Jun, Malm Jan, Eklund Anders, Alpert Abel Naomi, Raslan Ahmed M, Elder Benjamin D, Savage Jesse J, Barrow Daniel L, Shahlaie Kiarash, Jensen Hailey, Zwimpfer Thomas J, Wollett Jessica, Hanley Daniel F, Holubkov Richard, PENS Trial Investigators and the Adult Hydrocephalus Clinical Research Network

СтатьяРандомизированное исследованиеМногоцентровое исследованиеПеревод в очереди

Аннотация

BACKGROUND

Idiopathic normal-pressure hydrocephalus is a neurologic disorder characterized by impaired gait, balance, cognition, and bladder control in older adults. The disorder is treated with shunt surgery, but the effectiveness of shunting is unclear.

METHODS

We conducted a double-blind, randomized, placebo-controlled trial involving participants selected for shunt surgery on the basis of gait-velocity improvement with cerebrospinal fluid (CSF) drainage. Participants were randomly assigned to an open-shunt valve setting (opening pressure, 110 mm of water) or a placebo valve setting (opening pressure, >400 mm of water) of a noninvasively adjustable shunt. The primary outcome was the change in gait velocity 3 months after surgery. Secondary outcomes were the change at 3 months in the Tinetti scale total score (range, 0 to 28; lower scores indicate worse gait and balance), Montreal Cognitive Assessment (MoCA) score (range, 0 to 30; lower scores indicate worse cognition), and Overactive Bladder Questionnaire score (range, 0 to 100; higher scores indicate worse urinary incontinence).

RESULTS

A total of 99 participants underwent randomization and received the assigned intervention. At 3 months, gait velocity had increased in the open-shunt group (mean [±SD] change, 0.23±0.23 m per second; assessed in 49 participants) and was unchanged in the placebo group (mean change, 0.03±0.23 m per second; assessed in 49 participants), resulting in a treatment difference of 0.21 m per second (95% confidence interval, 0.12 to 0.31; P<0.001). A significantly greater improvement in the open-shunt group than the placebo group was seen for the Tinetti scale score (mean change, 2.9 points vs. 0.5 points; P = 0.003) but not the MoCA score (1.3 points vs. 0.3 points) or the Overactive Bladder Questionnaire score (-3.3 points vs. -1.5 points). The results regarding adverse events were mixed, with more participants in the placebo group reporting falls (46% vs. 24%), an equal percentage having cerebral bleeding (2% in both groups), and more participants in the open-shunt group having subdural bleeding (12% vs. 2%) and positional headaches (59% vs. 28%).

CONCLUSIONS

Among participants with idiopathic normal-pressure hydrocephalus who had a response to temporary CSF drainage, shunting resulted in significant improvements at 3 months in gait velocity and a measure of gait and balance but not in measures of cognition or incontinence. (Funded by the National Institute of Neurological Disorders and Stroke and the Trial Innovation Network; PENS ClinicalTrials.gov number, NCT05081128.).

Для цитирования: Luciano Mark G, Williams Michael A, Hamilton Mark G, Katzen Heather L, Dasher Nickolas A, Moghekar Abhay, Hua Jun, Malm Jan, Eklund Anders, Alpert Abel Naomi, Raslan Ahmed M, Elder Benjamin D, Savage Jesse J, Barrow Daniel L, Shahlaie Kiarash, Jensen Hailey, Zwimpfer Thomas J, Wollett Jessica, Hanley Daniel F, Holubkov Richard, PENS Trial Investigators and the Adult Hydrocephalus Clinical Research Network. A Randomized Trial of Shunting for Idiopathic Normal-Pressure Hydrocephalus.. The New England journal of medicine. 2025. DOI: 10.1056/nejmoa2503109.

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