Efficacy of long-term adrenocorticotropic hormone therapy for West syndrome: A retrospective multicenter case series.

Nationwide survey West syndrome adrenocorticotropic hormone long‐term treatment retrospective case series

Journal

Epilepsia open
ISSN: 2470-9239
Titre abrégé: Epilepsia Open
Pays: United States
ID NLM: 101692036

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 10 06 2020
revised: 09 04 2021
entrez: 7 6 2021
pubmed: 8 6 2021
medline: 19 3 2022
Statut: epublish

Résumé

Long-term adrenocorticotropic therapy (LT-ACTH), which consisted of 2-4 weeks of daily injections of adrenocorticotropic hormone (ACTH) and subsequent months of weekly injections, was tried for relapsed West syndrome (WS) or other intractable epilepsies in small case reports. Our aim was to explore the efficacy of LT-ACTH for preventing WS relapse, as well as the prevalence of its adverse events. This is a retrospective, nationwide, multicenter case series of patients with WS who underwent LT-ACTH. Clinical information of the patients and protocol of LT-ACTH were collected from participating institutes in this study. We defined clinical response to ACTH as achievement of hypsarrhythmia and epileptic spasms resolution. Patients who responded to daily ACTH injections were identified and assessed whether they experienced WS relapse during/after the weekly ACTH injection period. The outcome was measured by the nonrelapse rate at 24 months after daily ACTH injections using the Kaplan-Meier method. Clinical information of 16 children with WS was analyzed. The median age at LT-ACTH initiation was 14.5 months (range: 7-68 months). Thirteen (81%) patients had previously undergone conventional ACTH treatment. The LT-ACTH regimens comprised a median of 16 days of daily injections (range: 11-28 days) and 10 months of weekly injections (range: 3-22 months). Seven patients experienced WS relapse during/after subsequent weekly ACTH period, and the nonrelapse rate at 24 months after daily injections was estimated at 60.6% (95% confidence interval: 32.3%-80.0%). Height stagnation, hypertension, and irritability were observed; lethal adverse events were not reported. Our study firstly explored the efficacy of LT-ACTH for preventing WS relapse. LT-ACTH might be a treatment option for patients with relapsed or intractable WS; however, we note that our study is limited by its small sample size and the lack of an appropriate control group.

Identifiants

pubmed: 34095686
doi: 10.1002/epi4.12497
pii: EPI412497
pmc: PMC8166796
doi:

Substances chimiques

Adrenocorticotropic Hormone 9002-60-2

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

402-412

Informations de copyright

© 2021 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

Déclaration de conflit d'intérêts

None of the authors has any conflict of interest to disclose. We confirm that we have read the Journal's position on issues regarding ethical publication and affirm that this report is consistent with those guidelines.

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Auteurs

Shimpei Baba (S)

Department of Child Neurology Comprehensive Epilepsy Center Seirei Hamamatsu General Hospital Hamamatsu Japan.

Tohru Okanishi (T)

Department of Child Neurology Comprehensive Epilepsy Center Seirei Hamamatsu General Hospital Hamamatsu Japan.

Yoichiro Homma (Y)

General Internal Medicine Seirei Hamamatsu General Hospital Hamamatsu Japan.

Takeshi Yoshida (T)

Department of Pediatrics Kyoto University Graduate School of Medicine Kyoto Japan.

Tomohide Goto (T)

Department of Neurology Kanagawa Children's Medical Center Yokohama Japan.

Tatsuya Fukasawa (T)

Department of Pediatrics Anjo Kosei Hospital Anjo Japan.

Satoru Kobayashi (S)

Department of Pediatrics Nagoya City West Medical Center Nagoya Japan.

Atsushi Kamei (A)

Department of Pediatrics Iwate Medical University School of Medicine Shiwa Japan.

Yuji Fujii (Y)

Department of Pediatrics Hiroshima City Funairi Citizens Hospital Hiroshima Japan.

Naomi Hino-Fukuyo (N)

Department of Pediatrics Tohoku Medical and Pharmaceutical University Sendai Japan.

Keitaro Yamada (K)

Department of Pediatric Neurology Aichi Developmental Disability Center Central Hospital Kasugai Japan.

Atsuro Daida (A)

Department of Pediatrics St. Luke's International Hospital Tokyo Japan.

Hisashi Kawawaki (H)

Department of Pediatric Neurology Osaka City General Hospital Osaka Japan.

Hideki Hoshino (H)

Department of Pediatrics Teikyo University School of Medicine Tokyo Japan.

Hitoshi Sejima (H)

Department of Pediatrics Matsue Red-Cross Hospital Matsue Japan.

Yusuke Ishida (Y)

Department of Pediatrics Kobe University Graduate School of Medicine Kobe Japan.

Tetsuya Okazaki (T)

Division of Child Neurology Department of Brain and Neurosciences School of Medicine Tottori University Faculty of Medicine Yonago Japan.

Takehiko Inui (T)

Department of Pediatric Neurology Miyagi Children's Hospital Miyagi Japan.

Sotaro Kanai (S)

Department of Child Neurology Comprehensive Epilepsy Center Seirei Hamamatsu General Hospital Hamamatsu Japan.

Hirotaka Motoi (H)

Department of Child Neurology Comprehensive Epilepsy Center Seirei Hamamatsu General Hospital Hamamatsu Japan.

Shinji Itamura (S)

Department of Child Neurology Comprehensive Epilepsy Center Seirei Hamamatsu General Hospital Hamamatsu Japan.

Mitsuyo Nishimura (M)

Division of Clinical Laboratory Seirei Hamamatsu General Hospital Hamamatsu Japan.

Hideo Enoki (H)

Department of Child Neurology Comprehensive Epilepsy Center Seirei Hamamatsu General Hospital Hamamatsu Japan.

Ayataka Fujimoto (A)

Epilepsy and Surgery Comprehensive Epilepsy Center Seirei Hamamatsu General Hospital Hamamatsu Japan.

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