Learning to make a difference for chILD: Value creation through network collaboration and team science

Author:

McKnight Lauren1ORCID,Schultz André23ORCID,Vidic Nada1ORCID,Palmer Elizabeth E.14ORCID,Jaffe Adam15ORCID

Affiliation:

1. Discipline of Paediatrics and Child Health, School of Clinical Medicine UNSW Sydney Kensington New South Wales Australia

2. Telethon Kids Institute University of Western Australia Perth Western Australia Australia

3. Department of Respiratory and Sleep Medicine Perth Children's Hospital Perth Western Australia Australia

4. Centre for Clinical Genetics Sydney Children's Hospital Randwick New South Wales Australia

5. Respiratory Department Sydney Children's Hospital Randwick New South Wales Australia

Abstract

AbstractAddressing the recognized challenges and inequalities in providing high quality healthcare for rare diseases such as children's interstitial lung disease (chILD) requires collaboration across institutional, geographical, discipline, and system boundaries. The Children's Interstitial Lung Disease Respiratory Network of Australia and New Zealand (chILDRANZ) is an example of a clinical network that brings together multidisciplinary health professionals for collaboration, peer learning, and advocacy with the goal of improving the diagnosis and management of this group of rare and ultra‐rare conditions. This narrative review explores the multifaceted benefits arising from social learning spaces within rare disease clinical networks by applying the value creation framework. The operation of the chILDRANZ network is used as an example across the framework to highlight how value is generated, realized, and transferred within such collaborative clinical and research networks. The community of practice formed in the chILDRANZ multidisciplinary meetings provides a strong example of social learning that engages with the uncertainty inherent in rare disease diagnosis and management and pays attention to generate new knowledge and best practice to make a difference for children and families living with chILD. This review underscores international calls for further investment in, and support of, collaborative clinical networks and virtual centers of excellence for rare disease.

Funder

National Health and Medical Research Council

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

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