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Development and validation of a short version of the quality of life-DSD questionnaire for parents of young children with conditions affecting sex development.
Ali, Salma R; Gardner, Melissa; Xin, Yiqiao; O'Toole, Stuart; Flett, Martyn; Lee, Boma; Steven, Mairi; Sandberg, David E; Ahmed, S Faisal.
Afiliação
  • Ali SR; Developmental Endocrinology Research Group, Royal Hospital for Children, University of Glasgow, Glasgow, UK.
  • Gardner M; Office for Rare Conditions, University of Glasgow, Glasgow, UK.
  • Xin Y; Susan B Meister Child Health Evaluation and Research Center, Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
  • O'Toole S; Health Economics and Health Technology Assessment, Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
  • Flett M; Department of Paediatric Surgery, Royal Hospital for Children, Glasgow, UK.
  • Lee B; Department of Paediatric Surgery, Royal Hospital for Children, Glasgow, UK.
  • Steven M; Department of Paediatric Surgery, Royal Hospital for Children, Glasgow, UK.
  • Sandberg DE; Department of Paediatric Surgery, Royal Hospital for Children, Glasgow, UK.
  • Ahmed SF; Susan B Meister Child Health Evaluation and Research Center, Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Endocr Connect ; 13(11)2024 Oct 01.
Article em En | MEDLINE | ID: mdl-39255500
ABSTRACT

Background:

There is a paucity of information on health-related quality of life (HRQoL) outcomes in parents and children with conditions affecting sex development. The objective of this study was to develop short forms of HRQoL questionnaires which consist of a 63-item and 25-item parent self-report (PSR) and parent proxy-report (PPR), respectively, optimizing use in routine clinical settings.

Methods:

Short questionnaires were developed following exploratory factor analysis using raw data from 132 parents. Long and short PSRs were completed by 24 parents of children with conditions affecting sex development, with a median age of 3.6 years (range 0.1, 6.6); 21 (88%) were boys, and 11 (46%) had proximal hypospadias. A subset of 19 parents completed both long and short PPRs.

Results:

Item selection, based on factor loadings of >0.8 and expert consultation, produced short PSRs and PPRs containing 16 and 7 items, respectively. There was no statistically significant difference in 11 out of 12 (92%) scales on the PSR and 4 out of 5 (80%) scales on the PPR when comparing short and long questionnaire scores. The short and long questionnaires took <1 min and 5 min to complete, respectively. Eighteen parents (75%) reported that the time taken to complete the short questionnaires was acceptable; 10 (42%) preferred short questionnaires. Ten (42%) versus 6 (25%) stated a preference for completing the short versus long questionnaires.

Conclusion:

The short versions were largely representative of the long questionnaires and are acceptable for evaluating psychosocial distress in young children and their caregivers. Further psychometric validation of the short forms is warranted.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article