Initiating an undiagnosed diseases program in the Western Australian public health system

نویسندگان

  • Gareth Baynam
  • Stephanie Broley
  • Alicia Bauskis
  • Nicholas Pachter
  • Fiona McKenzie
  • Sharron Townshend
  • Jennie Slee
  • Cathy Kiraly-Borri
  • Anand Vasudevan
  • Anne Hawkins
  • Lyn Schofield
  • Petra Helmholz
  • Richard Palmer
  • Stefanie Kung
  • Caroline E. Walker
  • Caron Molster
  • Barry Lewis
  • Kym Mina
  • John Beilby
  • Gargi Pathak
  • Cathryn Poulton
  • Tudor Groza
  • Andreas Zankl
  • Tony Roscioli
  • Marcel E. Dinger
  • John S. Mattick
  • William Gahl
  • Stephen Groft
  • Cynthia Tifft
  • Domenica Taruscio
  • Paul Lasko
  • Kenjiro Kosaki
  • Helene Wilhelm
  • Bela Melegh
  • Jonathan Carapetis
  • Sayanta Jana
  • Gervase Chaney
  • Allison Johns
  • Peter Wynn Owen
  • Frank Daly
  • Tarun Weeramanthri
  • Hugh Dawkins
  • Jack Goldblatt
چکیده

BACKGROUND New approaches are required to address the needs of complex undiagnosed diseases patients. These approaches include clinical genomic diagnostic pipelines, utilizing intra- and multi-disciplinary platforms, as well as specialty-specific genomic clinics. Both are advancing diagnostic rates. However, complementary cross-disciplinary approaches are also critical to address those patients with multisystem disorders who traverse the bounds of multiple specialties and remain undiagnosed despite existing intra-specialty and genomic-focused approaches. The diagnostic possibilities of undiagnosed diseases include genetic and non-genetic conditions. The focus on genetic diseases addresses some of these disorders, however a cross-disciplinary approach is needed that also simultaneously addresses other disorder types. Herein, we describe the initiation and summary outcomes of a public health system approach for complex undiagnosed patients - the Undiagnosed Diseases Program-Western Australia (UDP-WA). RESULTS Briefly the UDP-WA is: i) one of a complementary suite of approaches that is being delivered within health service, and with community engagement, to address the needs of those with severe undiagnosed diseases; ii) delivered within a public health system to support equitable access to health care, including for those from remote and regional areas; iii) providing diagnoses and improved patient care; iv) delivering a platform for in-service and real time genomic and phenomic education for clinicians that traverses a diverse range of specialties; v) retaining and recapturing clinical expertise; vi) supporting the education of junior and more senior medical staff; vii) designed to integrate with clinical translational research; and viii) is supporting greater connectedness for patients, families and medical staff. CONCLUSION The UDP-WA has been initiated in the public health system to complement existing clinical genomic approaches; it has been targeted to those with a specific diagnostic need, and initiated by redirecting existing clinical and financial resources. The UDP-WA supports the provision of equitable and sustainable diagnostics and simultaneously supports capacity building in clinical care and translational research, for those with undiagnosed, typically rare, conditions.

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عنوان ژورنال:

دوره 12  شماره 

صفحات  -

تاریخ انتشار 2017