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Preferences for Neurodevelopmental Follow-Up Care for Children: A Discrete Choice Experiment

Author

Listed:
  • Pakhi Sharma

    (Queensland University of Technology)

  • Sanjeewa Kularatna

    (Queensland University of Technology
    Health Services and Systems Research, Duke-NUS Medical School)

  • Bridget Abell

    (Queensland University of Technology)

  • Steven M. McPhail

    (Queensland University of Technology
    Metro South Health)

  • Sameera Senanayake

    (Queensland University of Technology
    Health Services and Systems Research, Duke-NUS Medical School)

Abstract

Introduction Identifying and addressing neurodevelopmental delays in children can be challenging for families and the healthcare system. Delays in accessing services and early interventions are common. The design and delivery of these services, and associated outcomes for children, may be improved if service provision aligns with families’ needs and preferences for receiving care. The aim of this study is to identify families’ preferences for neurodevelopmental follow-up care for children using an established methodology. Methods We used a discrete choice experiment (DCE) to elicit families’ preferences. We collected data from families and caregivers of children with neurodevelopmental needs. The DCE process included four stages. In stage 1, we identified attributes and levels to be included in the DCE using literature review, interviews, and expert advice. The finalised attributes were location, mode of follow-up, out-of-pocket cost per visit, mental health counselling for parents, receiving educational information, managing appointments, and waiting time. In stage 2, we generated choice tasks that contained two alternatives and a ‘neither’ option for respondents to choose from, using a Bayesian d-efficient design. These choice tasks were compiled in a survey that also included demographic questions. We conducted pre- and pilot tests to ensure the functionality of the survey and obtain priors. In stage 3, the DCE survey was administered online. We received 301 responses. In stage 4, the analysis was conducted using a latent class model. Additionally, we estimated the relative importance of attributes and performed a scenario analysis. Results Two latent classes were observed. More families with full-time employees, higher incomes, postgraduate degrees, and those living in metropolitan areas were in class 1 compared with class 2. Class 1 families preferred accessing local public health clinics, face-to-face follow-up, paying AUD100 to AUD500, mental health support, group educational activities, health service-initiated appointments, and waiting

Suggested Citation

  • Pakhi Sharma & Sanjeewa Kularatna & Bridget Abell & Steven M. McPhail & Sameera Senanayake, 2024. "Preferences for Neurodevelopmental Follow-Up Care for Children: A Discrete Choice Experiment," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 17(6), pages 645-662, November.
  • Handle: RePEc:spr:patien:v:17:y:2024:i:6:d:10.1007_s40271-024-00717-3
    DOI: 10.1007/s40271-024-00717-3
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    References listed on IDEAS

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    1. Sanjeewa Kularatna & Michelle Allen & Ruvini M. Hettiarachchi & Fiona Crawford-Williams & Sameera Senanayake & David Brain & Nicolas H. Hart & Bogda Koczwara & Carolyn Ee & Raymond J. Chan, 2023. "Cancer Survivor Preferences for Models of Breast Cancer Follow-Up Care: Selecting Attributes for Inclusion in a Discrete Choice Experiment," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 16(4), pages 371-383, July.
    2. Juan Marcos Gonzalez, 2019. "A Guide to Measuring and Interpreting Attribute Importance," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 12(3), pages 287-295, June.
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