Intrathecal Injections in Children With Spinal Muscular Atrophy

Author:

Haché Manon1,Swoboda Kathryn J.2,Sethna Navil3,Farrow-Gillespie Alan4,Khandji Alexander5,Xia Shuting6,Bishop Kathie M.6

Affiliation:

1. Division of Pediatric Anesthesia, Columbia University Medical Center, New York, NY, USA

2. Department of Neurology, Massachusetts General Hospital, Boston, MA, USA

3. Department of Anesthesiology, Perioperative and Pain Medicine, Boston Children’s Hospital, Boston, MA, USA

4. Department of Anesthesiology and Pain Management, University of Texas Southwestern Medical School, Dallas, TX, USA

5. Department of Radiology, Columbia University, New York, NY, USA

6. Ionis Pharmaceuticals, Inc., Carlsbad, CA, USA

Abstract

Nusinersen (ISIS-SMNRx or ISIS 396443) is an antisense oligonucleotide drug administered intrathecally to treat spinal muscular atrophy. We summarize lumbar puncture experience in children with spinal muscular atrophy during a phase 1 open-label study of nusinersen and its extension. During the studies, 73 lumbar punctures were performed in 28 patients 2 to 14 years of age with type 2/3 spinal muscular atrophy. No complications occurred in 50 (68%) lumbar punctures; in 23 (32%) procedures, adverse events were attributed to lumbar puncture. Most common adverse events were headache (n = 9), back pain (n = 9), and post–lumbar puncture syndrome (n = 8). In a subgroup analysis, adverse events were more frequent in older children, children with type 3 spinal muscular atrophy, and with a 21- or 22-gauge needle compared to a 24-gauge needle or smaller. Lumbar punctures were successfully performed in children with spinal muscular atrophy; lumbar puncture–related adverse event frequency was similar to that previously reported in children.

Publisher

SAGE Publications

Subject

Clinical Neurology,Pediatrics, Perinatology, and Child Health

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