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Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient

BACKGROUND: A ketogenic diet (KD) may have a role in treating patients in super-refractory status epilepticus (SRSE). Sodium-glucose cotransporter 2 (SGLT2) inhibitors have a risk of ketoacidosis that could facilitate induction of KD. CASE SUMMARY: A 42-year-old with a history of drug resistant epil...

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Detalles Bibliográficos
Autores principales: Blunck, Joseph R., Newman, Joseph W., Fields, Ronald K., Croom, John E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068319/
https://www.ncbi.nlm.nih.gov/pubmed/30073144
http://dx.doi.org/10.1016/j.ebcr.2018.05.002
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author Blunck, Joseph R.
Newman, Joseph W.
Fields, Ronald K.
Croom, John E.
author_facet Blunck, Joseph R.
Newman, Joseph W.
Fields, Ronald K.
Croom, John E.
author_sort Blunck, Joseph R.
collection PubMed
description BACKGROUND: A ketogenic diet (KD) may have a role in treating patients in super-refractory status epilepticus (SRSE). Sodium-glucose cotransporter 2 (SGLT2) inhibitors have a risk of ketoacidosis that could facilitate induction of KD. CASE SUMMARY: A 42-year-old with a history of drug resistant epilepsy developed SRSE requiring several pharmacological interventions during her hospital course including the initiation of KD that failed. SGLT2 inhibitor therapy was initiated in a successful attempt to augment ketone production. CONCLUSION: SGLT2 inhibitors may have a therapeutic value in SRSE patients who cannot achieve ketosis with KD alone.
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spelling pubmed-60683192018-08-02 Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient Blunck, Joseph R. Newman, Joseph W. Fields, Ronald K. Croom, John E. Epilepsy Behav Case Rep Article BACKGROUND: A ketogenic diet (KD) may have a role in treating patients in super-refractory status epilepticus (SRSE). Sodium-glucose cotransporter 2 (SGLT2) inhibitors have a risk of ketoacidosis that could facilitate induction of KD. CASE SUMMARY: A 42-year-old with a history of drug resistant epilepsy developed SRSE requiring several pharmacological interventions during her hospital course including the initiation of KD that failed. SGLT2 inhibitor therapy was initiated in a successful attempt to augment ketone production. CONCLUSION: SGLT2 inhibitors may have a therapeutic value in SRSE patients who cannot achieve ketosis with KD alone. Elsevier 2018-06-20 /pmc/articles/PMC6068319/ /pubmed/30073144 http://dx.doi.org/10.1016/j.ebcr.2018.05.002 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Blunck, Joseph R.
Newman, Joseph W.
Fields, Ronald K.
Croom, John E.
Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient
title Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient
title_full Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient
title_fullStr Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient
title_full_unstemmed Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient
title_short Therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient
title_sort therapeutic augmentation of ketogenic diet with a sodium-glucose cotransporter 2 inhibitor in a super-refractory status epilepticus patient
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068319/
https://www.ncbi.nlm.nih.gov/pubmed/30073144
http://dx.doi.org/10.1016/j.ebcr.2018.05.002
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