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Lumbar drain trial outcomes of normal pressure hydrocephalus: a single-center experience of 254 patients.
El Ahmadieh, Tarek Y; Wu, Eva M; Kafka, Benjamin; Caruso, James P; Neeley, Om J; Plitt, Aaron; Aoun, Salah G; Olson, Daiwai M; Ruchinskas, Robert A; Cullum, C Munro; Barnett, Samuel; Welch, Babu G; Batjer, H Hunt; White, Jonathan A.
Afiliação
  • El Ahmadieh TY; 1Department of Neurological Surgery.
  • Wu EM; 2School of Medicine, and.
  • Kafka B; 1Department of Neurological Surgery.
  • Caruso JP; 1Department of Neurological Surgery.
  • Neeley OJ; 1Department of Neurological Surgery.
  • Plitt A; 1Department of Neurological Surgery.
  • Aoun SG; 1Department of Neurological Surgery.
  • Olson DM; 1Department of Neurological Surgery.
  • Ruchinskas RA; 3Department of Neurology & Neurotherapeutics, Zale Lipshy Hospital; and.
  • Cullum CM; 3Department of Neurology & Neurotherapeutics, Zale Lipshy Hospital; and.
  • Barnett S; 4Department of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas.
  • Welch BG; 1Department of Neurological Surgery.
  • Batjer HH; 3Department of Neurology & Neurotherapeutics, Zale Lipshy Hospital; and.
  • White JA; 4Department of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas.
J Neurosurg ; 132(1): 306-312, 2019 01 04.
Article em En | MEDLINE | ID: mdl-30611143
ABSTRACT

OBJECTIVE:

A short-term lumbar drain (LD) trial is commonly used to assess the response of normal pressure hydrocephalus (NPH) patients to CSF diversion. However, it remains unknown whether the predictors of passing an LD trial match the predictors of improvement after ventriculoperitoneal shunting. The aim of this study was to examine outcomes, complication rates, and associations between predictors and outcomes after an LD trial in patients with NPH.

METHODS:

The authors retrospectively reviewed the records of 254 patients with probable NPH who underwent an LD trial between March 2008 and September 2017. Multivariate regression models were constructed to examine predictors of passing the LD trial. Complications associated with the LD trial procedure were recorded.

RESULTS:

The mean patient age was 77 years and 56.7% were male. The mean durations of gait disturbance, cognitive decline, and urinary incontinence were 29 months, 32 months, and 28 months, respectively. Of the 254 patients, 30% and 16% reported objective and subjective improvement after the LD trial, respectively. Complications included a sheared LD catheter, meningitis, lumbar epidural abscess, CSF leak at insertion site, transient lower extremity numbness, slurred speech, refractory headaches, and hyponatremia. Multivariate analyses using MAX-R revealed that a prior history of stroke predicted worse outcomes, while disproportionate subarachnoid spaces (uneven enlargement of supratentorial spaces) predicted better outcomes after the LD trial (r2 = 0.12, p < 0.05).

CONCLUSIONS:

The LD trial is generally safe and well tolerated. The best predictors of passing the LD trial include a negative history of stroke and having disproportionate subarachnoid spaces.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Drenagem / Hidrocefalia de Pressão Normal Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: J Neurosurg Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Drenagem / Hidrocefalia de Pressão Normal Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Revista: J Neurosurg Ano de publicação: 2019 Tipo de documento: Article