Publication

Delayed cerebral ischemia predicts neurocognitive impairment following aneurysmal subarachnoid hemorrhage

Journal Paper/Review - May 15, 2014

Units
PubMed
Doi

Citation
Stienen M, Smoll N, Weisshaupt R, Fandino J, Hildebrandt G, Studerusgermann A, Schatlo B. Delayed cerebral ischemia predicts neurocognitive impairment following aneurysmal subarachnoid hemorrhage. World Neurosurg 2014; 82:e599-605.
Type
Journal Paper/Review (English)
Journal
World Neurosurg 2014; 82
Publication Date
May 15, 2014
Issn Print
1878-8750
Pages
e599-605
Brief description/objective

BACKGROUND
Prior studies have shown that the incidence of neuropsychological deficits (NPDs) after aneurysmal subarachnoid hemorrhage (aSAH) is high despite excellent outcome according to neurologic grading scales. Delayed cerebral ischemia (DCI) occurs in 30% of patients after aSAH and significantly contributes to the mortality and morbidity of aSAH. We tested the hypothesis that DCI is associated with neuropsychological outcome.

METHODS
Files of patients treated between January 2009 and August 2012 at 2 neurovascular centers were reviewed. Neuropsychological outcome was assessed in a face-to-face-interview of 2-2.5 hours' duration and graded as no (regular), minimal, moderate, or severe deficit according to normative population data by an experienced, independent neuropsychologist. The test battery was applied with consideration of the patients' individual premorbid level of workload and social activities and accounted for the following cognitive domains: memory, attention, executive function, visual and spatial perception, language and calculation, and behavior.

RESULTS
Of 226 patients treated at 2 centers, 187 were discharged alive. Full neuropsychological outcome assessment was available in 92 patients. DCI developed in 28 (30.4%) patients; 24 of these patients (85.7%) showed moderate to severe NPD. From a univariate perspective, patients with DCI were 6.38 times as likely to experience moderate to severe NPD after aSAH as patients without DCI (odds ratio [OR]; 95% confidence interval [CI], 1.98-20.50; P = 0.002), which remained statistically significant after correction for admission World Federation of Neurological Surgeons Grading System and Fisher scores, patient age, hydrocephalus, and further potential confounders (OR, 4.9; 95% CI, 1.26-19.58; P = 0.022). Of all factors analyzed, DCI was the strongest predictor of NPD in the multivariate analysis, followed by chronic hydrocephalus (OR, 4.85; 95% CI, 1.26-18.63; P = 0.022) and patient age ≥ 50 years (OR, 4.06; 95% CI, 1.39-11.92; P = 0.001).

CONCLUSIONS
Patients with evidence of DCI during their hospital course have a 5-fold increased risk of experiencing moderate to severe NPD compared with patients who do not develop DCI after aSAH. Secondary events occurring during acute hospitalization (DCI, hydrocephalus) may be more important to the overall neuropsychological outcome than hemorrhage (Fisher) and clinical severity (World Federation of Neurological Surgeons Grading System) scores at admission.