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Health State Utility Values in Children and Adolescents with Disabilities: A Systematic Review
Lucy Kanya1, Nana Anokye2, Ahmad Hecham Alani1
1Department of Health Policy, London School of Economics and Political Science, London, United Kingdom.
Objectives:
To (1) provide a comprehensive summary of the methods used to obtain health state utility values (HSUVs) from children and adolescents with disabilities (CAD), (2) describe the administration and psychometric properties of these methods in children and adolescents with disabilities, and (3) report summary statistics for HSUVs obtained from each method.
Study Design:
English-language studies from MEDLINE (via PubMed), PsychInfo, Scopus, CINAHL Plus, EconLit, and Embase were searched from inception to November 2024. Two reviewers independently screened titles, abstracts, and full texts. Studies were included if they used direct or indirect methods to measure HSUVs, reported utilities and/or psychometric properties of these measures, and involved CAD aged 0-19 years. Two reviewers independently extracted study details including sample descriptors, instruments used, and summary statistics. Studies quality was assessed using a novel tool derived from 3 validated checklists.
Results:
Of the 3541 screened articles, 31 met inclusion criteria. Only 2 studies used direct methods, such as time trade-off, visual analog scale, and standard gamble, whereas 29 employed generic measures (eg, EuroQol 5 Dimensions, Health Utilities Index 3) with diverse preference elicitation methods. Excessive dependence on proxy respondents was noted, and psychometric properties of generic measures were mixed.
Conclusions:
Inconsistent HSUVs reporting and limited data availability are common. Reported HSUV summary statistics may be inaccurate if methodologies are unsuitable for the population. This review emphasizes the need for validated instruments to assess HSUVs in CAD.
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