Abstract
Abstract
Background
Patient participation in decision-making has become a hallmark of responsive healthcare systems. Cancer networks in many countries have committed to involving people living with and beyond cancer (PLC) at multiple levels. However, PLC participation in network governance remains highly variable for reasons that are poorly understood. This study aims to share lessons learned regarding mechanisms that enable PLC participation in cancer network governance.
Methods
This multiple case study, using a qualitative approach in a natural setting, was conducted over six years in three local cancer networks within the larger national cancer network in Quebec (Canada), where PLC participation is prescribed by the Cancer Directorate. Data were collected from multiple sources, including individual and focus group interviews (n = 89) with policymakers, managers, clinicians and PLC involved in national and local cancer governance committees. These data were triangulated and iteratively analysed according to a framework based on functions of collaborative governance in the network context.
Results
We identify three main mechanisms that enable PLC participation in cancer network governance: (1) consistent emphasis on patient-centred care as a network objective; (2) flexibility, time and support to translate mandated PLC representation into meaningful participation; and (3) recognition of the distinct knowledge of PLC in decision-making. The shared vision of person-centred care facilitates PLC participation. The quality of participation improves through changes in how committee meetings are conducted, and through the establishment of a national committee where PLC can pool their experience, develop skills and establish a common voice on priority issues. PLC knowledge is especially valued around particular challenges such as designing integrated care trajectories and overcoming barriers to accessing care. These three mechanisms interact to enable PLC participation in governance and are activated to varying extents in each local network.
Conclusions
This study reveals that mandating PLC representation on governance structures is a powerful context element enabling participation, but that it also delineates which governance functions are open to influence from PLC participation. While the activation of mechanisms is context dependent, the insights from this study in Quebec are transferable to cancer networks in other jurisdictions seeking to embed PLC participation in decision-making.
Funder
Fonds de Recherche du Québec - Santé
Publisher
Springer Science and Business Media LLC
Reference58 articles.
1. Evans JM, Matheson G, Buchman S, MacKinnon M, Meertens E, Ross J, Johal H. Integrating cancer care beyond the hospital and across the cancer pathway: a patient-centred approach. Healthc Q. 2015;17 Spec No:28–32.
2. Fashoyin-Aje LA, Martinez KA, Dy SM. New patient-centered care standards from the commission on cancer: opportunities and challenges. J Support Oncol. 2012;10(3):107–11.
3. Haward RA. The Calman–Hine report: a personal retrospective on the UK’s first comprehensive policy on cancer services. Lancet Oncol. 2006;74(6):336–46.
4. McConigley R, Platt V, Holloway K, Smith J. Developing a sustainable model of rural cancer care: the Western Australian Cancer Network project. AJRH. 2011;19(6):324–8.
5. Halabi IOS, Voz B, Gillain B, Durieux N, Odero N, Baumann A, Ziegler M, Gagnayre O, Guillaume R, Bragard M, Scholtes I, Voz B, Gillain B, Durieux N, Odero N, Baumann A, Ziegler M, Gagnayre O, Guillaume R. M et al: “Patient participation” and related concepts: a scoping review on their dimensional composition. Patient Educ Couns. 2020;103(1):5–14.
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献