Intrathecal nusinersen treatment after ventriculo-peritoneal shunt placement: A case report focusing on the neurofilament light chain in cerebrospinal fluid
Autor: | Kozue Shiomi, Harutsugu Tatebe, Takahiko Tokuda, Takenori Tozawa, Tomohiro Chiyonobu, Hisahide Nishio, Takashi Kasai |
---|---|
Rok vydání: | 2020 |
Předmět: |
medicine.medical_specialty
business.industry General Medicine Spinal muscular atrophy medicine.disease Surgery Hydrocephalus Shunt (medical) 03 medical and health sciences 0302 clinical medicine Cerebrospinal fluid Developmental Neuroscience Pediatrics Perinatology and Child Health medicine Nusinersen Neurology (clinical) Implant business Adverse effect Meningitis 030217 neurology & neurosurgery |
Zdroj: | Brain and Development. 42:311-314 |
ISSN: | 0387-7604 |
DOI: | 10.1016/j.braindev.2019.12.006 |
Popis: | Background In July 2018, a rare and serious adverse effect (AE), namely, communicating hydrocephalus unrelated to meningitis or bleeding, was reported in relation to five patients treated with nusinersen for spinal muscular atrophy (SMA). Some patients were managed using a ventriculo-peritoneal shunt (VPS) implant and continued to receive nusinersen treatment. However, there is limited information concerning the effectiveness and safety of nusinersen treatment for patients with a VPS. Case report A female patient exhibited general hypotonia soon after birth and was diagnosed, using genetic analysis, with spinal muscular atrophy. She required permanent invasive ventilation from 2 months of age. She developed a progressive hydrocephalus and underwent placement of a VPS in infancy. Treatment with nusinersen was initiated when she was 7 years old. The neurofilament light-chain (NfL) concentration in the cerebrospinal fluid (CSF) decreased over time with nusinersen treatment. Twelve months have passed since the start of nusinersen treatment and no AEs have been observed. Conclusion Nusinersen treatment may be effective and safe, even after placement of a VPS. NfL levels in the CSF could be valuable markers of disease activity/treatment response even in advanced stages of SMA. |
Databáze: | OpenAIRE |
Externí odkaz: |