Validation of the parent‐proxy version of the pediatric Charcot‐Marie‐Tooth disease quality of life instrument for children aged 0–7 years

Author:

Wu Tong Tong1,Finkel Richard S.2,Siskind Carly E.3,Feely Shawna M. E.4,Burns Joshua56,Reilly Mary M.7,Muntoni Francesco78,Milev Evelin78,Estilow Timothy9,Shy Michael E.4ORCID,Ramchandren Sindhu101112ORCID,

Affiliation:

1. Department of Biostatistics and Computational Biology University of Rochester Rochester New York USA

2. Center for Experimental Neurotherapeutics St. Jude Children's Research Hospital Memphis Tennessee USA

3. Department of Neurology Stanford University Stanford California USA

4. Department of Neurology University of Iowa Hospitals and Clinics Iowa City Iowa USA

5. Faculty of Medicine and Health University of Sydney School of Health Sciences Sydney New South Wales Australia

6. Pediatric Gait Analysis Service of New South Wales, Sydney Children's Hospitals Network Sydney New South Wales Australia

7. Centre for Neuromuscular Diseases UCL Queen Square Institute of Neurology London UK

8. Dubowitz Neuromuscular Centre NIHR Great Ormond Street Hospital Biomedical Research Centre, UCL Great Ormond Street Institute of Child Health and Great Ormond Street Hospital London UK

9. Division of Neurology, Department of Pediatrics Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

10. Department of Neurology University of Michigan Ann Arbor Michigan USA

11. Department of Neurology Wayne State University Detroit Michigan USA

12. The Janssen Pharmaceutical Companies of Johnson & Johnson Titusville New Jersey USA

Abstract

AbstractObjectiveTo evaluate the parent‐proxy version of the pediatric Charcot Marie Tooth specific quality of life (pCMT‐QOL) outcome instrument for children aged 7 or younger with CMT. We have previously developed and validated the direct‐report pCMT‐QOL for children aged 8–18 years and a parent proxy version of the instrument for children 8–18 years old. There is currently no CMT‐QOL outcome measure for children aged 0–7 years old.MethodsTesting was conducted in parents or caregivers of children aged 0–7 years old with CMT evaluated at participating INC sites from the USA, United Kingdom, and Australia. The development of the instrument was iterative, involving identification of relevant domains, item pool generation, prospective pilot testing and clinical assessments, structured focus group interviews, and psychometric testing. The parent‐proxy instrument was validated rigorously by examining previously identified domains and undergoing psychometric tests for children aged 0–7.ResultsThe parent‐proxy pCMT‐QOL working versions were administered to 128 parents/caregivers of children aged 0–7 years old between 2010 and 2016. The resulting data underwent rigorous psychometric analysis, including factor analysis, internal consistency, and convergent validity, and longitudinal analysis to develop the final parent‐proxy version of the pCMT‐QOL outcome measure for children aged 0–7 years old.ConclusionsThe parent‐proxy version of the pCMT‐QOL outcome measure, known as the pCMT‐QOL (0–7 years parent‐proxy) is a valid and sensitive proxy measure of health‐related QOL for children aged 0–7 years with CMT.

Funder

Muscular Dystrophy Association

National Institutes of Health

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

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