A multidisciplinary approach to the clinical management of Prader-Willi syndrome

Jessica Duis1, Pieter J van Wattum2,3, Ann Scheimann4

  • 1Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.

Insights

Multidisciplinary clinics improve care for Prader-Willi syndrome (PWS), a rare neuroendocrine disorder. Establishing Centers of Excellence fosters collaboration and advances research for better patient outcomes.

Area of Science:

  • Neuroendocrinology
  • Genetics
  • Rare Diseases

Background:

  • Prader-Willi syndrome (PWS) is a rare neuroendocrine disorder affecting 1/15,000-1/30,000 individuals.
  • Unmet medical needs in PWS highlight the importance of multidisciplinary care approaches.
  • Collaboration between academic centers, medical homes, industry, and parent organizations is crucial.

Purpose of the Study:

  • To define the role and structure of multidisciplinary clinics for Prader-Willi syndrome (PWS) care.
  • To propose the development of "Centers of Excellence" for PWS.
  • To address the lack of evidence-based management approaches and gaps in care.

Main Methods:

  • Interviews were conducted with medical professionals, scientists, managed care experts, parents, and individuals with PWS from July 1 to December 1, 2016.
  • Literature review was performed to support the findings.
  • Consensus data from interviews were analyzed by specialty.

Main Results:

  • Multidisciplinary clinics facilitate comprehensive, patient-centered care for individuals with PWS and their families.
  • Consensus data defined unique aspects of PWS care, research, and management.
  • The concept of a "Center of Excellence" for PWS was defined beyond the multidisciplinary clinic model.

Conclusions:

  • Multidisciplinary clinics promote collaboration, evidence-based standards of care, and knowledge advancement through research, including RCTs.
  • These clinics serve as a resource for the community, support global telemedicine, and inform translational research.
  • Addressing knowledge gaps in PWS management is essential for improving patient outcomes, reducing caregiver burden, and advancing therapies.
Abstract

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