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Client Service Receipt Inventory as a standardised tool for measurement of socio-economic costs in the rare genetic disease population (CSRI-Ra).
Chung, Claudia C Y; Fung, Jasmine L F; Lui, Adrian C Y; Chan, Marcus C Y; Ng, Yvette N C; Wong, Wilfred H S; Lee, So Lun; Knapp, Martin; Chung, Brian H Y.
Afiliação
  • Chung CCY; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Fung JLF; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Lui ACY; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Chan MCY; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Ng YNC; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Wong WHS; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Lee SL; Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, 1/F New Clinical Building, 102 Pokfulam Road, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Knapp M; The Duchess of Kent Children's Hospital, Pok Fu Lam, Hong Kong Special Administrative Region, China.
  • Chung BHY; Care Policy and Evaluation Centre, Health and Social Care Policy, Department of Health Policy, London School of Economics and Political Science, Houghton Street, London, WC2A 2AE, UK. M.Knapp@lse.ac.uk.
Sci Rep ; 11(1): 23837, 2021 12 13.
Article em En | MEDLINE | ID: mdl-34903789
ABSTRACT
The measurement of costs is fundamental in healthcare decision-making, but it is often challenging. In particular, standardised methods have not been developed in the rare genetic disease population. A reliable and valid tool is critical for research to be locally meaningful yet internationally comparable. Herein, we sought to develop, contextualise, translate, and validate the Client Service Receipt Inventory for the RAre disease population (CSRI-Ra) to be used in cost-of-illness studies and economic evaluations for healthcare planning. Through expert panel discussions and focus group meetings involving 17 rare disease patients, carers, and healthcare and social care professionals from Hong Kong, we have developed the CSRI-Ra. Rounds of forward and backward translations were performed by bilingual researchers, and face validity and semantic equivalence were achieved through interviews and telephone communications with focus group participants and an additional of 13 healthcare professional and university students. Intra-class correlation coefficient (ICC) was used to assess criterion validity between CSRI-Ra and electronic patient record in a sample of 94 rare disease patients and carers, with overall ICC being 0.69 (95% CI 0.56-0.78), indicating moderate to good agreement. Following rounds of revision in the development, contextualisation, translation, and validation stages, the CSRI-Ra is ready for use in empirical research. The CSRI-Ra provides a sufficiently standardised yet adaptable method for collecting socio-economic data related to rare genetic diseases. This is important for near-term and long-term monitoring of the resource consequences of rare diseases, and it provides a tool for use in economic evaluations in the future, thereby helping to inform planning for efficient and effective healthcare. Adaptation of the CSRI-Ra to other populations would facilitate international research.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Custos e Análise de Custo / Doenças Raras / Honorários Médicos / Serviços de Saúde / Doenças Genéticas Inatas Tipo de estudo: Health_economic_evaluation / Prognostic_studies / Qualitative_research Aspecto: Determinantes_sociais_saude / Patient_preference Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Custos e Análise de Custo / Doenças Raras / Honorários Médicos / Serviços de Saúde / Doenças Genéticas Inatas Tipo de estudo: Health_economic_evaluation / Prognostic_studies / Qualitative_research Aspecto: Determinantes_sociais_saude / Patient_preference Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China