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Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity

BACKGROUND: Spinal muscular atrophy (SMA) is a genetic disease characterized by degeneration of the spinal cord, resulting in progressive muscle atrophy. Recently, nusinersen has been approved for treating SMA, which should be administered intrathecally. CASE PRESENTATION: Patient 1 was a 36-year-ol...

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Autores principales: Nakao, Sayo, Yamada, Shinichi, Tsuda, Katsuya, Yokomizo, Taishi, Sato, Teruyuki, Tanoue, Shuichi, Hiraki, Teruyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171013/
https://www.ncbi.nlm.nih.gov/pubmed/32314319
http://dx.doi.org/10.1186/s40981-020-00334-7
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author Nakao, Sayo
Yamada, Shinichi
Tsuda, Katsuya
Yokomizo, Taishi
Sato, Teruyuki
Tanoue, Shuichi
Hiraki, Teruyuki
author_facet Nakao, Sayo
Yamada, Shinichi
Tsuda, Katsuya
Yokomizo, Taishi
Sato, Teruyuki
Tanoue, Shuichi
Hiraki, Teruyuki
author_sort Nakao, Sayo
collection PubMed
description BACKGROUND: Spinal muscular atrophy (SMA) is a genetic disease characterized by degeneration of the spinal cord, resulting in progressive muscle atrophy. Recently, nusinersen has been approved for treating SMA, which should be administered intrathecally. CASE PRESENTATION: Patient 1 was a 36-year-old woman with SMA type 2. Patients 2 and 3 were 10- and 17-year-old girls with SMA type 1. In patients 1 and 2, the needle was inserted into the spinal column, but outflow of cerebrospinal fluid was unable to be confirmed. CT revealed that the dural sac terminated at the L5 level in patients 1 and 3 and at the L5/S1 level in patient 2. CONCLUSIONS: Patients with SMA often present with high-grade scoliosis, making intrathecal administration difficult. In addition, the dural sac may terminate at a level higher than normal. To ensure intrathecal administration, the level of dural sac termination must be confirmed by CT before puncture.
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spelling pubmed-71710132020-04-23 Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity Nakao, Sayo Yamada, Shinichi Tsuda, Katsuya Yokomizo, Taishi Sato, Teruyuki Tanoue, Shuichi Hiraki, Teruyuki JA Clin Rep Case Report BACKGROUND: Spinal muscular atrophy (SMA) is a genetic disease characterized by degeneration of the spinal cord, resulting in progressive muscle atrophy. Recently, nusinersen has been approved for treating SMA, which should be administered intrathecally. CASE PRESENTATION: Patient 1 was a 36-year-old woman with SMA type 2. Patients 2 and 3 were 10- and 17-year-old girls with SMA type 1. In patients 1 and 2, the needle was inserted into the spinal column, but outflow of cerebrospinal fluid was unable to be confirmed. CT revealed that the dural sac terminated at the L5 level in patients 1 and 3 and at the L5/S1 level in patient 2. CONCLUSIONS: Patients with SMA often present with high-grade scoliosis, making intrathecal administration difficult. In addition, the dural sac may terminate at a level higher than normal. To ensure intrathecal administration, the level of dural sac termination must be confirmed by CT before puncture. Springer Berlin Heidelberg 2020-04-20 /pmc/articles/PMC7171013/ /pubmed/32314319 http://dx.doi.org/10.1186/s40981-020-00334-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Case Report
Nakao, Sayo
Yamada, Shinichi
Tsuda, Katsuya
Yokomizo, Taishi
Sato, Teruyuki
Tanoue, Shuichi
Hiraki, Teruyuki
Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
title Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
title_full Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
title_fullStr Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
title_full_unstemmed Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
title_short Intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
title_sort intrathecal administration of nusinersen for spinal muscular atrophy: report of three cases with severe spinal deformity
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7171013/
https://www.ncbi.nlm.nih.gov/pubmed/32314319
http://dx.doi.org/10.1186/s40981-020-00334-7
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