Status Epilepticus Associated With Subtentorial Posterior Fossa Lesions

BACKGROUND Nonconvulsive status epilepticus (SE) is a frequent complication in critically ill patients in the intensive care unit. While seizures have been reported in association with subtentorial posterior fossa lesions, the frequency of occurrence of SE among these patients is not known. OBJECTIV...

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Published inArchives of neurology (Chicago) Vol. 66; no. 12; pp. 1500 - 1504
Main Authors Grill, Marie F, Treiman, David M, Maganti, Rama K
Format Journal Article
LanguageEnglish
Published Chicago, IL American Medical Association 01.12.2009
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Summary:BACKGROUND Nonconvulsive status epilepticus (SE) is a frequent complication in critically ill patients in the intensive care unit. While seizures have been reported in association with subtentorial posterior fossa lesions, the frequency of occurrence of SE among these patients is not known. OBJECTIVES To examine prevalence, clinical features, potential risk factors, and outcome of SE among patients presenting with subtentorial posterior fossa lesions. DESIGN Retrospective review of our hospital database was conducted to identify patients with posterior fossa lesions complicated by SE over 1 year between April 1, 2007, and May 1, 2008. SETTING Tertiary care setting. PATIENTS Patients with subtentorial posterior fossa lesions admitted to the hospital for neurological or neurosurgical care. MAIN OUTCOME MEASURES Prevalence of SE, potential risk factors, and eventual neurological outcome. RESULTS Over 1 year, 13 of 501 patients (2.6%) admitted to the hospital with posterior fossa lesions had SE. Some patients had risk factors for SE such as sepsis, use of particular drugs, or intracranial bleeding, while others had no other clear identifiable cause. CONCLUSIONS Status epilepticus can be a potential complication in patients with posterior fossa cranial lesions and can be seen in up to 2.6% of such patients. Most have unfavorable outcome.Arch Neurol. 2009;66(12):1500-1504-->
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ISSN:0003-9942
2168-6149
1538-3687
2168-6157
DOI:10.1001/archneurol.2009.275