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Use of the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND) in X-Linked Myotubular Myopathy: Content Validity and Psychometric Performance.
Duong, Tina; Harding, Gale; Mannix, Sally; Abel, Cristina; Phillips, Dawn; Alfano, Lindsay N; Bönnemann, Carsten G; Lilien, Charlotte; Lowes, Linda P; Servais, Laurent; Warken-Madelung, Birgit; Nieto Bergman, Susie; James, Emma S; Noursalehi, Mojtaba; Prasad, Suyash; Rico, Salvador; Bilder, Deborah A.
Afiliação
  • Duong T; Stanford University, Palo Alto, CA, USA.
  • Harding G; Evidera, Bethesda, MD, USA.
  • Mannix S; Evidera, Bethesda, MD, USA.
  • Abel C; Evidera, Bethesda, MD, USA.
  • Phillips D; Evidera, Bethesda, MD, USA.
  • Alfano LN; Nationwide Children's Hospital, Columbus, OH, USA.
  • Bönnemann CG; National Institute of Neurological Disorders and Stroke, Bethesda, MD, USA.
  • Lilien C; MDUK Oxford Neuromuscular Centre, Oxford, United Kingdom.
  • Lowes LP; Institut I-Motion, Institut de Myologie, Paris, France.
  • Servais L; Nationwide Children's Hospital, Columbus, OH, USA.
  • Warken-Madelung B; MDUK Oxford Neuromuscular Centre, Oxford, United Kingdom.
  • Nieto Bergman S; Institut I-Motion, Institut de Myologie, Paris, France.
  • James ES; University Hospital Liège & University of La Citadelle, Liège, Belgium.
  • Noursalehi M; Haunersches Children's Hospital of the University of Munich, Munich, Germany.
  • Prasad S; Audentes Therapeutics, an Astellas Company, San Francisco, CA, USA.
  • Rico S; Encoded Therapeutics, South San Francisco, CA, USA formerly at Audentes Therapeutics, an Astellas Company, San Francisco, CA, USA.
  • Bilder DA; Audentes Therapeutics, an Astellas Company, San Francisco, CA, USA.
J Neuromuscul Dis ; 8(1): 63-77, 2021.
Article em En | MEDLINE | ID: mdl-32925083
ABSTRACT
X-linked myotubular myopathy (XLMTM) is a life-threatening, congenital myopathy characterized by extreme hypotonia, weakness, delayed motor milestones, and respiratory failure, often resulting in pediatric mortality. This study evaluated the content validity and psychometric performance of the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders as a measure of neuromuscular functioning in children with X-linked myotubular myopathy. This study was conducted in two phases. Phase I assessed the content validity of the measure for use in an XLMTM pediatric population through literature review, clinical expert interviews, caregiver interviews, and a modified-Delphi panel among clinicians. Phase II assessed psychometric performance based on the INCEPTUS observational clinical study and the ASPIRO interventional gene therapy study, including tests of reliability (internal consistency, test-retest, and interrater), validity (construct and criterion), and responsiveness based on observational and interventional clinical trial data analyses. Data established construct validity and reliability of the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders among XLMTM patients before administration of resamirigene bilparvovec, and sensitivity to study drug administration as evidenced by the significant post-administration response in ASPIRO. Findings support the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders as an appropriate neuromuscular functioning assessment in a pediatric X-linked myotubular myopathy patient population.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Psicometria / Índice de Gravidade de Doença / Avaliação de Resultados em Cuidados de Saúde / Miopatias Congênitas Estruturais Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Psicometria / Índice de Gravidade de Doença / Avaliação de Resultados em Cuidados de Saúde / Miopatias Congênitas Estruturais Idioma: En Ano de publicação: 2021 Tipo de documento: Article