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Surgical Management of Hirayama Disease (Monomelic Amyotrophy): Systematic Review and Meta-Analysis of Patient-Level Data.
Pennington, Zach; Lakomkin, Nikita; Michalopoulos, Giorgos D; Mikula, Anthony L; Ahn, Edward S; Bydon, Mohamad; Clarke, Michelle J; Elder, Benjamin D; Fogelson, Jeremy L.
Afiliación
  • Pennington Z; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA. Electronic address: pennington.zachary@mayo.edu.
  • Lakomkin N; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Michalopoulos GD; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Mikula AL; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Ahn ES; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Bydon M; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Clarke MJ; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Elder BD; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Fogelson JL; Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota, USA.
World Neurosurg ; 172: e278-e290, 2023 Apr.
Article en En | MEDLINE | ID: mdl-36623725
ABSTRACT

BACKGROUND:

Hirayama disease or juvenile-onset monomelic amyotrophy is a clinical syndrome that disproportionately affects young males. Standard of care revolves around conservative management, but some patients experience disease progression that may benefit from surgical intervention.

METHODS:

Using Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, a systematic review of previous reports of surgical treatment for Hirayama disease was performed. Studies were included if they provided individual patient-level data, described the clinical presentation and surgical intervention, and reported neurological improvement at last follow-up. Comparison between those who improved and those with stable symptoms at last follow-up was performed. Decision-tree analysis was used to identify the best predictors of neurological improvement by last follow-up.

RESULTS:

Of 624 unique articles, 30 were included in the qualitative review and 23 in the meta-analysis. Among the 70 patients in the meta-analysis, mean age was 21.2 ± 6.3 years, 91% were male, and mean symptom duration at presentation was 43.3 ± 61.8 months. Fifty-nine patients (84.3%) had improvement in their neurological symptoms by last follow-up. Univariable analysis showed the only significant predictor of improvement in neurological symptoms by last follow-up was the use of stabilization-alone versus decompression with or without stabilization. Baseline clinical symptoms nor radiographic features predicted outcome. Decision-tree analysis showed surgical strategy (stabilization-alone vs. decompression ± stabilization), age (<20 vs. ≥20), and surgical approach (anterior-only vs. posterior-only or anterior-posterior) predicted a higher likelihood of neurological improvement by last follow-up.

CONCLUSIONS:

Nearly 85% of patients experienced improvement in neurological symptoms. Improvement was best for those who underwent stabilization-alone, and decision-tree analysis suggested that the likelihood of improvement was also superior for patients under 20 years of age and those treated with an anterior versus posterior or staged approach.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Imagen por Resonancia Magnética / Atrofias Musculares Espinales de la Infancia Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Idioma: En Revista: World Neurosurg Asunto de la revista: NEUROCIRURGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Imagen por Resonancia Magnética / Atrofias Musculares Espinales de la Infancia Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research / Systematic_reviews Idioma: En Revista: World Neurosurg Asunto de la revista: NEUROCIRURGIA Año: 2023 Tipo del documento: Article