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Randomized Controlled Trial
. 2019 Nov 28;381(22):2103-2113.
doi: 10.1056/NEJMoa1905795.

Randomized Trial of Three Anticonvulsant Medications for Status Epilepticus

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Free PMC article
Randomized Controlled Trial

Randomized Trial of Three Anticonvulsant Medications for Status Epilepticus

Jaideep Kapur et al. N Engl J Med. .
Free PMC article

Abstract

Background: The choice of drugs for patients with status epilepticus that is refractory to treatment with benzodiazepines has not been thoroughly studied.

Methods: In a randomized, blinded, adaptive trial, we compared the efficacy and safety of three intravenous anticonvulsive agents - levetiracetam, fosphenytoin, and valproate - in children and adults with convulsive status epilepticus that was unresponsive to treatment with benzodiazepines. The primary outcome was absence of clinically evident seizures and improvement in the level of consciousness by 60 minutes after the start of drug infusion, without additional anticonvulsant medication. The posterior probabilities that each drug was the most or least effective were calculated. Safety outcomes included life-threatening hypotension or cardiac arrhythmia, endotracheal intubation, seizure recurrence, and death.

Results: A total of 384 patients were enrolled and randomly assigned to receive levetiracetam (145 patients), fosphenytoin (118), or valproate (121). Reenrollment of patients with a second episode of status epilepticus accounted for 16 additional instances of randomization. In accordance with a prespecified stopping rule for futility of finding one drug to be superior or inferior, a planned interim analysis led to the trial being stopped. Of the enrolled patients, 10% were determined to have had psychogenic seizures. The primary outcome of cessation of status epilepticus and improvement in the level of consciousness at 60 minutes occurred in 68 patients assigned to levetiracetam (47%; 95% credible interval, 39 to 55), 53 patients assigned to fosphenytoin (45%; 95% credible interval, 36 to 54), and 56 patients assigned to valproate (46%; 95% credible interval, 38 to 55). The posterior probability that each drug was the most effective was 0.41, 0.24, and 0.35, respectively. Numerically more episodes of hypotension and intubation occurred in the fosphenytoin group and more deaths occurred in the levetiracetam group than in the other groups, but these differences were not significant.

Conclusions: In the context of benzodiazepine-refractory convulsive status epilepticus, the anticonvulsant drugs levetiracetam, fosphenytoin, and valproate each led to seizure cessation and improved alertness by 60 minutes in approximately half the patients, and the three drugs were associated with similar incidences of adverse events. (Funded by the National Institute of Neurological Disorders and Stroke; ESETT ClinicalTrials.gov number, NCT01960075.).

Figures

Figure 1.
Figure 1.. Randomization, Group Assignments, and Analyses.
The safety analysis included all enrollments (including patients who enrolled more than once). The intention-to-treat analysis included all unique patients but did not include repeat enrollments of the same patient. The per-protocol analysis excluded repeat enrollments, enrollments in which there were eligibility deviations, and enrollments in which patients did not receive the assigned drug dose.
Figure 2.
Figure 2.. Posterior Probabilities of Success According to Treatment Group for the Primary Outcome of Cessation of Status Epilepticus at 60 Minutes.
The relative posterior probabilities of treatment success with regard to the primary outcome for each drug are shown. The percentage of patients with treatment success was 47% (95% credible interval, 39 to 55) in the levetiracetam group, 45% (95% credible interval, 36 to 54) in the fosphenytoin group, and 46% (95% credible interval, 38 to 55) in the valproate group.

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