Dutch Normal-Pressure Hydrocephalus Study: randomized comparison of low- and medium-pressure shunts

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  • 1 Departments of Neurology and Neurosurgery, Westeinde Hospital, The Hague, The Netherlands; Department of Neurosurgery, University Hospital, Rotterdam, The Netherlands; Department of Neurosurgery, Free University Hospital, Amsterdam, The Netherlands; Departments of Neurosurgery and Pediatric Neurology, University Hospital, Utrecht, The Netherlands; and Department of Medical Statistics, University Hospital, Leiden, The Netherlands
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Object. The goal of this prospective study was to compare outcome after placement of a low- or medium-pressure shunt in patients with normal-pressure hydrocephalus (NPH).

Methods. Ninety-six patients with NPH were randomized to receive a low-pressure ventriculoperitoneal shunt (LPV; 40 ± 10 mm H2O) or medium high—pressure ventriculoperitoneal shunt (MPV; 100 ± 10 mm H2O). The patients' gait disturbance and dementia were quantified by applying an NPH scale, and their level of disability was evaluated by using the modified Rankin scale (mRS). Patients were examined prior to and 1, 3, 6, 9, and 12 months after surgery. Primary outcome measures were determined by differences between preoperative and last NPH scale scores and mRS grades. The LPV and MPV shunt groups were compared by calculating both the differences between mean improvements and the proportions of patients showing improvement.

Intention-to-treat analysis of mRS grades yielded a mean improvement of 1.27 ± 1.41 for patients with LPV shunts and 0.68 ± 1.58 for patients with MPV shunts (p = 0.06). Improvement was found in 74% of patients with LPV shunts and in 53% of patients with MPV shunts (p = 0.06) and a marked-to-excellent improvement in 45% of patients with LPV shunts and 28% of patients with MPV shunts (p = 0.12). All outcome measures indicated trends in favor of the LPV shunt group, with only the dementia scale reaching significance. After exclusion of serious events and deaths unrelated to NPH, efficacy analysis showed the advantage of LPV shunts to be diminished. Reduction in ventricular size was also significantly greater for patients in the LPV shunt group (p = 0.009). Subdural effusions occurred in 71% of patients with an LPV shunt and in 34% with an MPV shunt; however, their influence on patient outcome was limited.

Conclusions. Outcome was better for patients who had an LPV shunt than for those with an MPV shunt, although most differences were not statistically significant. The authors advise that patients with NPH be treated with an LPV shunt.

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Contributor Notes

Current address for Dr. Boon: University Hospital, Rotterdam, The Netherlands.Address reprint requests to: Joseph T. J. Tans, M.D., Department of Neurology, Westeinde Hospital, Lijnbaan 32, Post Box 432, 2501 CK, The Hague, The Netherlands.
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