Abstract
Greater than two million Americans suffer from epilepsy, and 10 % of the population has at least one convulsion in their lifetime. Phenytoin has been commercially available in the United States since 1938 and had been a first-step anticonvulsant for all types of epilepsy, with the exception of absence seizures. In conjunction with benzodiazepines, phenytoin is efficacious in the acute treatment of status epilepticus [1] and has been used prophylactically after head injury [2]. Phenytoin was used as a class 1B antidysrhythmic agent, particularly in the setting of digoxin toxicity, but it no longer is considered a first-line agent for that indication.
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Grading System for Levels of Evidence Supporting Recommendations in Critical Care Toxicology, 2nd Edition
Grading System for Levels of Evidence Supporting Recommendations in Critical Care Toxicology, 2nd Edition
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Evidence obtained from at least one properly randomized controlled trial.
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Evidence obtained from well-designed controlled trials without randomization.
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Evidence obtained from well-designed cohort or case–control analytic studies, preferably from more than one center or research group.
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Evidence obtained from multiple time series with or without the intervention. Dramatic results in uncontrolled experiments (such as the results of the introduction of penicillin treatment in the 1940s) could also be regarded as this type of evidence.
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Opinions of respected authorities, based on clinical experience, descriptive studies and case reports, or reports of expert committees.
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LoVecchio, F. (2016). Hydantoins: Phenytoin and Fosphenytoin. In: Brent, J., Burkhart, K., Dargan, P., Hatten, B., Megarbane, B., Palmer, R. (eds) Critical Care Toxicology. Springer, Cham. https://doi.org/10.1007/978-3-319-20790-2_24-1
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