Hostname: page-component-8448b6f56d-tj2md Total loading time: 0 Render date: 2024-04-19T19:24:04.571Z Has data issue: false hasContentIssue false
  • English
  • Français

Involvement of patients and parents in research undertaken by the Australian and New Zealand Fontan Registry

Published online by Cambridge University Press:  17 August 2017

Yves d’Udekem ,
Victoria Forsdick  and
Karin du Plessis
Yves d’Udekem*
Affiliation:
Cardiac Surgery Department, Royal Children’s Hospital, Melbourne, Victoria, Australia Department of Pediatrics, Faculty of Medicine, The University of Melbourne, Melbourne, Victoria, Australia Murdoch Children’s Research Institute, Melbourne, Victoria, Australia
Victoria Forsdick
Affiliation:
Royal Children’s Hospital, Melbourne, Victoria, Australia Australian and New Zealand Fontan Registry Steering Committee Patient Representative, Victoria, Australia
Karin du Plessis
Affiliation:
Murdoch Children’s Research Institute, Melbourne, Victoria, Australia
*
Correspondence to: Prof. Y. d’Udekem, The Royal Children’s Hospital, Melbourne, 3 West Clinical Offices, 50 Flemington Road, Parkville, Victoria, 3052, Australia. Tel: +613 9345 5200; Fax: +61 3 9345 6001; E-mail: yves.dudekem@rch.org.au
Get access Rights & Permissions [Opens in a new window]

Abstract

Research that is closely connected with the population it is studying and in which the translational value to healthcare is high is a laudable goal, but it is not often achieved. The Australian and New Zealand Fontan Registry has developed a model for involving patients and parents of children with a Fontan circulation in its research. The model involves consumer participation in the overarching Steering Committee, and has set in place multiple channels of communication allowing the early dissemination of research findings before peer-reviewing, and consumer feedback at all levels of the research. Our focus was not only to provide information but also to give a voice to this community and include them as researchers. These communication channels are a part of a larger network involving the practitioner community, support groups, funding agencies, and health authorities. This close connection with the target research population has multiple benefits: safeguarding the project; controlling and adjusting both the messages conveyed and the investigations; building a community; raising new ideas for research; increasing our research participation rate; increasing the weight of our endeavours; and, above all, increasing our own satisfaction in our research undertakings. In conclusion, the interactions with patients and their families within Australia and New Zealand provide one potential model for the involvement of patients and parents that may result in research that is more relevant, focussed, and practically applicable in a healthcare setting.

Keywords

CHDFontanconsumer involvement in research
Type
Original Article
Information
Cardiology in the Young , Volume 28 , Issue 4 , April 2018 , pp. 517 - 521
Check for updates
Copyright
© Cambridge University Press 2017 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Coulter, A, Dunn, N. After Bristol: putting patients at the centre. Commentary: Patient centred care: timely, but is it practical? BMJ 2002; 324: 648–651.CrossRefGoogle Scholar
2. Kitson, A, Marshall, A, Bassett, K, Zeitz, K. What are the core elements of patient-centred care? A narrative review and synthesis of the literature from health policy, medicine and nursing. J Adv Nurs 2013; 69: 4–15.CrossRefGoogle Scholar
3. Australian Commission on Safety and Quality in Health Care. Australian Commission on Safety and Quality in Health Care Annual Report 2015–16. Sydney, 2016.Google Scholar
4. Iyengar, AJ, Winlaw, DS, Galati, JC, et al. The Australia and New Zealand Fontan Registry: description and initial results from the first population-based Fontan registry. Intern Med J 2014; 44: 148–155.CrossRefGoogle ScholarPubMed
5. Stevens, DP, Marshall, BC. A decade of healthcare improvement in cystic fibrosis: lessons for other chronic diseases. BMJ Qual Saf 2014; 23 (Suppl 1): i1–i2.CrossRefGoogle ScholarPubMed
6. Siracusa, CM, Weiland, JL, Acton, JD, et al. The impact of transforming healthcare delivery on cystic fibrosis outcomes: a decade of quality improvement at Cincinnati Children’s Hospital. BMJ Qual Saf 2014; 23 (Suppl 1): i56–i63.CrossRefGoogle ScholarPubMed
7. Lambert, E, d’Udekem, Y, Cheung, M, et al. Sympathetic and vascular dysfunction in adult patients with Fontan circulation. Int J Cardiol 2013; 167: 1333–1338.CrossRefGoogle ScholarPubMed
8. Pickering, RM, Kunkel, D, Fitton, C, Ashburn, A, Jenkinson, D. In-hospital recruitment to observational studies of stroke. Int J Rehabil Res 2010; 33: 56–63.CrossRefGoogle ScholarPubMed