doi: 10.1016/j.ejpn.2021.02.009.
Online ahead of print.
Affiliations
Affiliations
- 1 Neuromuscular Unit, Neuropediatric Department, Institut de Recerca Pediàtrica Hospital Sant Joan de Déu, Barcelona, Spain; Center for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Spain. Electronic address: [email protected].
- 2 Department of Radiology, Hospital Sant Joan de Déu, Barcelona, Spain.
- 3 Department of Anesthesiology, Hospital Sant Joan de Déu, Barcelona, Spain.
- 4 Neuromuscular Unit, Neuropediatric Department, Institut de Recerca Pediàtrica Hospital Sant Joan de Déu, Barcelona, Spain; Center for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Spain.
- 5 Department of Statistics, Fundació Sant Joan de Déu, Barcelona, Spain.
- 6 Department of Rehabilitation, Hospital Sant Joan de Déu, Barcelona, Spain.
- 7 Global Health Institute Barcelona (ISGlobal), Barcelona, Spain; Department of Experimental and Health Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiology and Public Health (CIBERESP), Madrid, Spain.
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Laura Carrera-García et al.
Eur J Paediatr Neurol.
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doi: 10.1016/j.ejpn.2021.02.009.
Online ahead of print.
Authors
Affiliations
- 1 Neuromuscular Unit, Neuropediatric Department, Institut de Recerca Pediàtrica Hospital Sant Joan de Déu, Barcelona, Spain; Center for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Spain. Electronic address: [email protected].
- 2 Department of Radiology, Hospital Sant Joan de Déu, Barcelona, Spain.
- 3 Department of Anesthesiology, Hospital Sant Joan de Déu, Barcelona, Spain.
- 4 Neuromuscular Unit, Neuropediatric Department, Institut de Recerca Pediàtrica Hospital Sant Joan de Déu, Barcelona, Spain; Center for the Biomedical Research on Rare Diseases (CIBERER), ISCIII, Spain.
- 5 Department of Statistics, Fundació Sant Joan de Déu, Barcelona, Spain.
- 6 Department of Rehabilitation, Hospital Sant Joan de Déu, Barcelona, Spain.
- 7 Global Health Institute Barcelona (ISGlobal), Barcelona, Spain; Department of Experimental and Health Sciences, Universitat Pompeu Fabra (UPF), Barcelona, Spain; CIBER Epidemiology and Public Health (CIBERESP), Madrid, Spain.
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Abstract
The approval of nusinersen for the treatment of spinal muscular atrophy (SMA) has significantly changed the natural history of the disease. Nevertheless, scoliosis secondary to axial muscle weakness occurs at some point in most of patients with SMA and a conventional posterior interlaminar approach for intrathecal administration of nusinersen can be particularly challenging to perform in patients with severe scoliosis and/or previous spine fusion surgeries. We developed a protocol for the administration of nusinersen in pediatric patients, which includes a decision-tree algorithm that categorizes patients according to the estimated technical difficulty for the intrathecal administration. Complex spine patients were defined as those with a Cobb angle greater than 50° and/or a history of spinal surgery, while the rest of patients were considered non-complex. Nusinersen was successfully administered through a conventional non-CT-guided lumbar puncture in all 14 non-complex spine patients (110 out of 110 procedures; 100%). The feasibility of the intrathecal injection in the 15 complex spine patients was assessed by 3D CT. Administration was considered unfeasible in 7 out of these 15 patients according to imaging. In the 8 complex spine patients in whom the administration was considered feasible, conventional non-CT-guided lumbar punctures were successful only in 19 out of 53 procedures (36%). The remaining 34 procedures (64%) were guided by CT scan, all successful. Our work demonstrates that a cut-off point of 50° in Cobb angle and history of spinal surgery can reliably be used to anticipate the need for CT guidance in nusinersen administration.
Keywords:
Computer tomography; Intrathecal administration; Nusinersen; Scoliosis; Spinal muscular atrophy; Spondylodesis.
Copyright © 2021. Published by Elsevier Ltd.
Conflict of interest statement
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article. CO has received funding from AveXis as speaker in sponsored educational activities. DNdB has received funding from AveXis and Biogen as speaker in sponsored educational activities. AN has received funding as a speaker in sponsored symposium and educational activities or a member of advisory boards for SMA studies for AveXis, Biogen, Ionis Pharmaceuticals, Novartis, Roche Pharmaceuticals and Scholar Rock. AN is the principal investigator for ongoing Avexis, Ionis Pharmaceuticals/Biogen, Roche and Scholar Rock clinical trials. Research support from FundAME has been received.
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