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

被引:2
|
作者
Wu, Tong Tong [1 ]
Finkel, Richard [2 ]
Siskind, Carly E. [3 ]
Feely, Shawna M. E. [4 ]
Burns, Joshua [5 ,6 ]
Reilly, Mary M. [7 ]
Muntoni, Francesco [7 ,8 ,9 ]
Milev, Evelin [7 ,8 ,9 ]
Estilow, Timothy [10 ]
Shy, Michael E. [4 ]
Ramchandren, Sindhu [11 ,12 ,13 ]
机构
[1] Univ Rochester, Dept Biostat & Computat Biol, Rochester, NY USA
[2] St Jude Childrens Res Hosp, Ctr Expt Neurotherapeut, Memphis, TN USA
[3] Stanford Univ, Dept Neurol, Stanford, CA USA
[4] Univ Iowa Hosp & Clin, Dept Neurol, Iowa City, IA USA
[5] Univ Sydney, Fac Med & Hlth, Sch Hlth Sci, Sydney, NSW, Australia
[6] Sydney Childrens Hosp Network, Pediat Gait Anal Serv New South Wales, Sydney, NSW, Australia
[7] UCL Queen Sq Inst Neurol, Ctr Neuromuscular Dis, London, England
[8] NIHR Great Ormond St Hosp Biomed Res Ctr, UCL Great Ormond St Inst Child Hlth, Dubowitz Neuromuscular Ctr, London, England
[9] Great Ormond St Hosp Sick Children, London, England
[10] Childrens Hosp Philadelphia, Dept Pediat, Div Neurol, Philadelphia, PA USA
[11] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[12] Wayne State Univ, Dept Neurol, Detroit, MI USA
[13] Johnson & Johnson, Janssen Pharmaceut Co, Titusville, NJ USA
基金
美国国家卫生研究院;
关键词
Inherited Neuropathy Consortium; HEALTH QUESTIONNAIRE; RELIABILITY; VALIDITY;
D O I
10.1111/jns.12557
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveTo 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.
引用
收藏
页码:382 / 389
页数:8
相关论文
共 19 条
  • [1] Validation of the parent-proxy pediatric Charcot-Marie-Tooth disease quality of life outcome measure
    Wu, Tong Tong
    Finkel, Richard S. S.
    Siskind, Carly E. E.
    Feely, Shawna M. E.
    Burns, Joshua
    Reilly, Mary M. M.
    Muntoni, Francesco
    Estilow, Timothy
    Shy, Michael E. E.
    Ramchandren, Sindhu
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2023, 28 (02) : 237 - 251
  • [2] Validation of the Italian version of the Charcot-Marie-Tooth disease Pediatric Scale
    Zuccarino, Riccardo
    Prada, Valeria
    Moroni, Isabella
    Pagliano, Emanuela
    Foscan, Maria
    Robbiano, Giulia
    Pisciotta, Chiara
    Cornett, Kayla
    Shy, Rosemary
    Schenone, Angelo
    Pareyson, Davide
    Shy, Michael
    Burns, Joshua
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2020, 25 (02) : 138 - 142
  • [3] Quality of Life in Children With Charcot-Marie-Tooth Disease
    Burns, Joshua
    Ryan, Monique M.
    Ouvrier, Robert A.
    JOURNAL OF CHILD NEUROLOGY, 2010, 25 (03) : 343 - 347
  • [4] Development and Validation of the Pediatric Charcot-Marie-Tooth Disease Quality of Life Outcome Measure
    Ramchandren, Sindhu
    Wu, Tong Tong
    Finkel, Richard S.
    Siskind, Carly E.
    Feely, Shawna M. E.
    Burns, Joshua
    Reilly, Mary M.
    Ot, Timothy Estilow
    Shy, Michael E.
    ANNALS OF NEUROLOGY, 2021, 89 (02) : 369 - 379
  • [5] Validation of the Spanish version of the Charcot-Marie-Tooth disease Pediatric Scale (CMTPedS)
    Pitarch-Castellano, Inmaculada
    Argente-Escrig, Herminia
    Frasquet, Marina
    Damia-Vidal, Maria
    Canet-Barrera, Alberto
    Sevilla, Teresa
    Burns, Johua
    REVISTA DE NEUROLOGIA, 2022, 74 (03) : 78 - 82
  • [6] Impact of Charcot-Marie-Tooth disease on quality of life in children
    Burns, J.
    Ryan, M. M.
    Ouvrier, R. A.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2007, 12 : 13 - 13
  • [7] Development and construct validation of a parent-proxy quality of life instrument in children with bronchopulmonary dysplasia aged 4–8 years old
    Lysbert Meijer-Schaap
    Anthony E. J. Dubois
    Boudewijn J. Kollen
    Jet Tijmens-van der Hulst
    Bertine M. J. Flokstra-de Blok
    Elianne J. L. E. Vrijlandt
    Quality of Life Research, 2019, 28 : 523 - 533
  • [8] Assessment of disability and quality of life in children with Charcot-Marie-Tooth disease
    Moroni, I
    Pagliano, M.
    Milani, M.
    Perletti, C.
    Taroni, F.
    Uziel, G.
    Pareyson, D.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2007, 12 (02) : 164 - 164
  • [9] Parent-proxy pediatric CMT quality of life outcome measure: Validation of the Italian version
    Danti, Federica Rachele
    Pagliano, Emanuela
    Pareyson, Davide
    Foscan, Maria
    Marchi, Alessia
    Feoli, Alessia
    Bruschi, Fabio
    Piscosquito, Giuseppe
    Shy, Micheal E.
    Ramchandren, Sindhu
    Moroni, Isabella
    Wu, Tong Tong
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2024, 29 (01) : 107 - 110
  • [10] Development and construct validation of a parent-proxy quality of life instrument in children with bronchopulmonary dysplasia aged 4-8years old
    Meijer-Schaap, Lysbert
    Dubois, Anthony E. J.
    Kollen, Boudewijn J.
    Tijmens-van der Hulst, Jet
    Flokstra-de Blok, Bertine M. J.
    Vrijlandt, Elianne J. L. E.
    QUALITY OF LIFE RESEARCH, 2019, 28 (02) : 523 - 533