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A multidisciplinary approach to the clinical management of Prader-Willi syndrome.
Duis, Jessica; van Wattum, Pieter J; Scheimann, Ann; Salehi, Parisa; Brokamp, Elly; Fairbrother, Laura; Childers, Anna; Shelton, Althea Robinson; Bingham, Nathan C; Shoemaker, Ashley H; Miller, Jennifer L.
Afiliação
  • Duis J; Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • van Wattum PJ; Department of Psychiatry, Child Study Center, Yale School of Medicine, New Haven, Connecticut.
  • Scheimann A; Clifford Beers Clinic, New Haven, Connecticut.
  • Salehi P; Pediatric Gastroenterology, Johns Hopkins Children's Center, Baltimore, Maryland.
  • Brokamp E; Division of Endocrinology and Diabetes, Seattle Children's, University of Washington, Seattle, Washington.
  • Fairbrother L; Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Childers A; Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Shelton AR; Division of Medical Genetics and Genomic Medicine, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Bingham NC; Neuro-Sleep Division, Department of Neurology, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Shoemaker AH; Division of Pediatric Endocrinology, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Miller JL; Division of Pediatric Endocrinology, Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, Tennessee.
Mol Genet Genomic Med ; 7(3): e514, 2019 03.
Article em En | MEDLINE | ID: mdl-30697974
ABSTRACT

BACKGROUND:

Prader-Willi syndrome (PWS) is a complex neuroendocrine disorder affecting approximately 1/15,000-1/30,000 people. Unmet medical needs of individuals with PWS make it a rare disease that models the importance of multidisciplinary approaches to care with collaboration between academic centers, medical homes, industry, and parent organizations. Multidisciplinary clinics support comprehensive, patient-centered care for individuals with complex genetic disorders and their families. Value comes from improved communication and focuses on quality family-centered care.

METHODS:

Interviews with medical professionals, scientists, managed care experts, parents, and individuals with PWS were conducted from July 1 to December 1, 2016. Review of the literature was used to provide support.

RESULTS:

Data are presented based on consensus from these interviews by specialty focusing on unique aspects of care, research, and management. We have also defined the Center of Excellence beyond the multidisciplinary clinic.

CONCLUSION:

Establishment of clinics motivates collaboration to provide evidence-based new standards of care, increases the knowledge base including through randomized controlled trials, and offers an additional resource for the community. They have a role in global telemedicine, including to rural areas with few resources, and create opportunities for clinical work to inform basic and translational research. As a care team, we are currently charged with understanding the molecular basis of PWS beyond the known genetic cause; developing appropriate clinical outcome measures and biomarkers; bringing new therapies to change the natural history of disease; improving daily patient struggles, access to care, and caregiver burden; and decreasing healthcare load. Based on experience to date with a PWS multidisciplinary clinic, we propose a design for this approach and emphasize the development of "Centers of Excellence." We highlight the dearth of evidence for management approaches creating huge gaps in care practices as a means to illustrate the importance of the collaborative environment and translational approaches.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Gerenciamento Clínico / Comunicação Interdisciplinar Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Gerenciamento Clínico / Comunicação Interdisciplinar Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies / Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article