A Comparison of Four Treatments for Generalized Convulsive Status Epilepticus
David M. Treiman, M.D., Patti D. Meyers, M.P.A., Nancy Y. Walton, Ph.D., Joseph F. Collins, Sc.D., Cindy Colling, R.Ph., M.S., A. James Rowan, M.D., Adrian Handforth, M.D., Edward Faught, M.D., Vincent P. Calabrese, M.D., Basim M. Uthman, M.D., R. Eugene Ramsay, M.D., Meenal B. Mamdani, M.D., Pratap Yagnik, M.D., John C. Jones, M.D., Elizabeth Barry, M.D., Jane G. Boggs, M.D., Andres M. Kanner, M.D., for The Veterans Affairs Status Epilepticus Cooperative Study Group
Background and Methods Although generalized convulsive statusepilepticus is a life-threatening emergency, the best initialdrug treatment is uncertain. We conducted a five-year randomized,double-blind, multicenter trial of four intravenous regimens:diazepam (0.15 mg per kilogram of body weight) followed by phenytoin(18 mg per kilogram), lorazepam (0.1 mg per kilogram), phenobarbital(15 mg per kilogram), and phenytoin (18 mg per kilogram). Patientswere classified as having either overt generalized status epilepticus(defined as easily visible generalized convulsions) or subtlestatus epilepticus (indicated by coma and ictal discharges onthe electroencephalogram, with or without subtle convulsivemovements such as rhythmic muscle twitches or tonic eye deviation).Treatment was considered successful when all motor and electroencephalographicseizure activity ceased within 20 minutes after the beginningof the drug infusion and there was no return of seizure activityduring the next 40 minutes. Analyses were performed with dataon only the 518 patients with verified generalized convulsivestatus epilepticus as well as with data on all 570 patientswho were enrolled.
Results Three hundred eighty-four patients had a verified diagnosisof overt generalized convulsive status epilepticus. In thisgroup, lorazepam was successful in 64.9 percent of those assignedto receive it, phenobarbital in 58.2 percent, diazepam and phenytoinin 55.8 percent, and phenytoin in 43.6 percent (P=0.02 for theoverall comparison among the four groups). Lorazepam was significantlysuperior to phenytoin in a pairwise comparison (P=0.002). Amongthe 134 patients with a verified diagnosis of subtle generalizedconvulsive status epilepticus, no significant differences amongthe treatments were detected (range of success rates, 7.7 to24.2 percent). In an intention-to-treat analysis, the differencesamong treatment groups were not significant, either among thepatients with overt status epilepticus (P=0.12) or among thosewith subtle status epilepticus (P=0.91). There were no differencesamong the treatments with respect to recurrence during the 12-hourstudy period, the incidence of adverse reactions, or the outcomeat 30 days.
Conclusions As initial intravenous treatment for overt generalizedconvulsive status epilepticus, lorazepam is more effective thanphenytoin. Although lorazepam is no more efficacious than phenobarbitalor diazepam and phenytoin, it is easier to use.
Source Information
From the Neurology Services of the Veterans Affairs Medical Centers in West Los Angeles, Calif. (D.M.T., P.D.M., N.Y.W., A.H.), Bronx, N.Y. (A.J.R.), Birmingham, Ala. (E.F.), Richmond, Va. (V.P.C.), Gainesville, Fla. (B.M.U.), and Miami (R.E.R.), and the Hines Veterans Affairs Medical Center, Chicago (M.B.M.); the Departments of Neurology of the University of California at Los Angeles School of Medicine, Los Angeles (D.M.T., N.Y.W.), Mount Sinai College of Medicine, New York (A.J.R.), the University of Alabama School of Medicine, Birmingham (E.F.), the Medical College of Virginia, Richmond (V.P.C.), the University of Florida School of Medicine, Gainesville (B.M.U.), the University of Miami School of Medicine, Miami (R.E.R.), and the Loyola University School of Medicine, Chicago (M.B.M.); the Veterans Affairs Cooperative Studies Program Coordinating Center, Perry Point, Md. (J.F.C.); and the Veterans Affairs Cooperative Studies Program Clinical Research Pharmacy Coordinating Center, Albuquerque, N.M. (C.C.). Other authors were Pratap Yagnik, M.D. (Neurology Service, Veterans Affairs Medical Center, and Department of Neurology, Medical College of Pennsylvania both in Philadelphia); John C. Jones, M.D. (Neurology Service, Veterans Affairs Medical Center, and Department of Neurology, University of Wisconsin School of Medicine both in Madison); Elizabeth Barry, M.D. (Neurology Service, Veterans Affairs Medical Center, and Department of Neurology, University of Maryland School of Medicine both in Baltimore); Jane G. Boggs, M.D. (Neurology Service, Veterans Affairs Medical Center, and Department of Neurology, Medical College of Virginia both in Richmond); and Andres M. Kanner, M.D. (Neurology Service, Veterans Affairs Medical Center, and Department of Neurology, University of Wisconsin School of Medicine both in Madison).
Address reprint requests to Dr. Treiman at the Department of Neurology, University of Medicine and Dentistry of New JerseyRobert Wood Johnson Medical School, 97 Paterson St., New Brunswick, NJ 08901-0019.
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