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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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 |
work_keys_str_mv |
AT davidmillett fenfluramineinthesuccessfultreatmentofsuperrefractorystatusepilepticusinapatientwithdravetsyndrome AT suzannepach fenfluramineinthesuccessfultreatmentofsuperrefractorystatusepilepticusinapatientwithdravetsyndrome |
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1721377512595914752 |