Abstract
Labovitz DL, Allen Hauser W, Sacco RL
Neurology 2001;57:200–206
Background
Early seizure (ES) has been reported in 2 to 6% of strokes and is a predictor of recurrent seizures. Acute stroke has been reported to cause 22% of all cases of status epilepticus (SE) in adults. The determinants of ES and SE after stroke, however, are not well understood.
Methods
An incidence study was conducted to identify all cases of first stroke in adult residents of northern Manhattan. Cases of ES and SE within 7 days of stroke were identified through medical record review. Statistical analyses were performed by using univariate and multivariate logistic regression models.
Results
The cohort consisted of 904 patients; ES occurred in 37 (4.1%). The frequency of ES by stroke subtype and location was deep infarct in two (0.6%) of 356, lobar infarct in 20 (5.9%) of 341, deep intracerebral hemorrhage (ICH) in four (4.0%) of 101, lobar ICH in seven (14.3%) of 49, and subarachnoid hemorrhage in four (8.0%) of 50. SE occurred in 10 (1.1%) patients, representing 27.0% of patients with ES. Diabetes, hypertension, current smoking, alcohol use, age, gender, and race/ethnicity were not significant determinants of ES. In a subgroup of patients who had a National Institutes of Health (NIH) stroke scale (NIHSS) score recorded, NIHSS score was not an independent predictor of ES in multivariate analysis. After accounting for stroke severity, ES was not a predictor of 30-day case fatality.
Conclusions
Lesion location and stroke subtype are strong determinants of ES risk, even after adjusting for stroke severity. ES does not predict 30-day mortality. SE occurs in more than one fourth of patients with ES.
Commentary
The study is the first to consider simultaneously the effect of stroke subtype [intracerebral hemorrhage (ICH),subarachnoid hemorrhage (SAH),or infarct and location (lobar vs. deep)] to determine odds ratios for developing ES. In multivariate analysis, lobar ICH, SAH, and infarction all had significantly increased risk of ES compared with deep infarction. Together these two parameters had a higher predictive value for ES than did stroke severity as measured by the National Institutes of Health Stroke Scale (NIHSS) score, which was available for 60% of the patients.
Thirty-day case fatality rate (CFR) was 14.7% overall, and was much higher in patients with SE (30% CFR) or ES (37.8% CFR). The relations between variables contributing to this increased mortality are complex. Whereas ES predicted increased 30-day CFR in a multivariate analysis including stroke subtype and location, addition of the NIHSS score to the model confounded this association.
This methodologically sound study demonstrates that stratification by stroke subtype and location simultaneously is essential in assessing risk of ES after acute stroke. It raises interesting theoretical questions regarding the different mechanisms that lead to ES and late seizures. Deeper understanding of the complex interaction of risk factors for these conditions may lead to future searches for reduction in the development of epilepsy and mortality in these patients.
