Abstract
Status epilepticus (SE) and its subsequent sequelae have been described and documented since the seventh century, B.C. Despite this, it remains a significant medical and public health problem. According to a prospective, population-based study in Richmond, Virginia, a projected 126,000–195,000 cases of SE will occur in the United States each year with 22,000–42,000 resulting in death (1). A retrospective, population-based study in Rochester, Minnesota, showed an age-adjusted incidence of 18.3/100,000, with the greatest incidence in children under 1 yr of age and adults over 60 yr of age (2). The studies mentioned above report that a majority of patients (54%) presenting with SE had no prior history of epilepsy (1,2) and only 18% of unprovoked SE occurred in patients with known epilepsy. There has been an increase in the incidence of SE in patients between 1975 and 1984 (22.4/1000 population) compared to 1965 and 1974 (13.9/1000) (1,2). The majority of this increase is attributable to an increasing incidence in the elderly suffering SE secondary to anoxic encephalopathy, neurologic complications of medical illness, and other severe neurologic insults. Management of these patients poses unique challenges, and we can expect to treat an increasing number of these patients as the population ages and medical technology for the failing organ systems improves. Treatments, whether medical or surgical, carry multiple complication profiles. Other chapters in this book have dealt with specific medical illnesses and their propensity to precipitate seizures.
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Smith, M.C., Del Signore, M. (2002). Status Epilepticus in the Critically Ill. In: Delanty, N. (eds) Seizures. Current Clinical Neurology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-094-0_20
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DOI: https://doi.org/10.1007/978-1-59259-094-0_20
Publisher Name: Humana Press, Totowa, NJ
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