Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome

A 20-year-old woman with Dravet syndrome and multiple prior episodes of status epilepticus presented to our hospital in November 2018 in super-refractory status epilepticus. After 5 weeks of unsuccessful continuous treatment with anesthetics, including pentobarbital and ketamine, we sought and were...

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Main Authors: David Millett, Suzanne Pach
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Epilepsy & Behavior Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2589986421000356
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spelling doaj-0381bb308e1249858612154465f943892021-06-15T04:15:10ZengElsevierEpilepsy & Behavior Reports2589-98642021-01-0116100461Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndromeDavid Millett0Suzanne Pach1Corresponding author at: Hoag Memorial Hospital Presbyterian, One Hoag Drive, Newport Beach, CA 92658-6100, USA.; Hoag Memorial Hospital Presbyterian, Newport Beach, CA, USAHoag Memorial Hospital Presbyterian, Newport Beach, CA, USAA 20-year-old woman with Dravet syndrome and multiple prior episodes of status epilepticus presented to our hospital in November 2018 in super-refractory status epilepticus. After 5 weeks of unsuccessful continuous treatment with anesthetics, including pentobarbital and ketamine, we sought and were granted an emergency approval by the United States Food and Drug Administration to administer fenfluramine, an investigational new drug, to this patient. One week of treatment with fenfluramine at 0.4 mg/kg/day was ineffective. The dose of fenfluramine was titrated to 0.7 mg/kg/day, and after 1 week, electrographic seizures ceased. One week later, the patient was seizure-free and off all anesthetic agents. Add-on treatment with fenfluramine was continued with no further episodes of status epilepticus and >90% reduction in tonic-clonic seizures. This case report illustrates the potential for fenfluramine to prevent reoccurrence of status epilepticus and to manage super-refractory status epilepticus in patients with Dravet syndrome.http://www.sciencedirect.com/science/article/pii/S2589986421000356Dravet syndromeFenfluramineNeurocognitive responseSuper-refractory status epilepticus
collection DOAJ
language English
format Article
sources DOAJ
author David Millett
Suzanne Pach
spellingShingle David Millett
Suzanne Pach
Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome
Epilepsy & Behavior Reports
Dravet syndrome
Fenfluramine
Neurocognitive response
Super-refractory status epilepticus
author_facet David Millett
Suzanne Pach
author_sort David Millett
title Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome
title_short Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome
title_full Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome
title_fullStr Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome
title_full_unstemmed Fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with Dravet syndrome
title_sort fenfluramine in the successful treatment of super-refractory status epilepticus in a patient with dravet syndrome
publisher Elsevier
series Epilepsy & Behavior Reports
issn 2589-9864
publishDate 2021-01-01
description A 20-year-old woman with Dravet syndrome and multiple prior episodes of status epilepticus presented to our hospital in November 2018 in super-refractory status epilepticus. After 5 weeks of unsuccessful continuous treatment with anesthetics, including pentobarbital and ketamine, we sought and were granted an emergency approval by the United States Food and Drug Administration to administer fenfluramine, an investigational new drug, to this patient. One week of treatment with fenfluramine at 0.4 mg/kg/day was ineffective. The dose of fenfluramine was titrated to 0.7 mg/kg/day, and after 1 week, electrographic seizures ceased. One week later, the patient was seizure-free and off all anesthetic agents. Add-on treatment with fenfluramine was continued with no further episodes of status epilepticus and >90% reduction in tonic-clonic seizures. This case report illustrates the potential for fenfluramine to prevent reoccurrence of status epilepticus and to manage super-refractory status epilepticus in patients with Dravet syndrome.
topic Dravet syndrome
Fenfluramine
Neurocognitive response
Super-refractory status epilepticus
url http://www.sciencedirect.com/science/article/pii/S2589986421000356
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AT suzannepach fenfluramineinthesuccessfultreatmentofsuperrefractorystatusepilepticusinapatientwithdravetsyndrome
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