Affiliation:
1. European Haemophilia Consortium , Brussels , Belgium
Abstract
Abstract
Introduction
Patient agency refers to the abilities and capabilities of patients to act, contribute, influence and make decisions about their healthcare. It depends on both the willingness of patients to participate and the constraints imposed by healthcare providers, services and systems. To determine the factors affecting patient agency, especially for patients with chronic, rare diseases such as haemophilia requiring lifelong care, it is important to consider the patterns, structures, and mental models that define the ecosystem that patients are a part of, irrespective of their level of engagement.
Identifying key challenges
At the first workshop of the EHC Think Tank Workstream on Patient Agency in December 2021, participants identified five key themes for in-depth discussion relevant to patient agency: the concept of shared decision-making (SDM), patient empowerment, the spectrum of engagement, cultural change and health literacy. The Iceberg Model was used to unpack challenges by identifying composite factors on four levels: events, patterns, structures and mental models.
Summary
Across the five themes, four common perceived challenges stand out: uneven relationships between patients and healthcare professionals, services and systems; paternalism and hierarchical cultures; failure to recognise problems; conservatism and resistance to change. Despite some progress towards patient empowerment, a ‘glass ceiling’ prevents patients from driving transformation and taking leadership roles in strategy, policymaking and governance. Patient engagement is fluid and those who could benefit most are least likely to engage. Health literacy is perceived as the problem of the patient, not the system, and patients rather than healthcare providers are typically expected to adapt. Preliminary suggestions for addressing these challenges include behavioural communication training for patients and healthcare professionals, a learning system for empowered patient and family care, and a level playing field for stakeholders to interact equally, leading to mutual acceptance and respect.
Reference45 articles.
1. Nunes F, Andersen T, Fitzpatrick G. The agency of patients and carers in medical care and self-care technologies for interacting with doctors. Health Informatics J 2019; 25(2): 330–349. doi: 10.1177/1460458217712054.
2. Ocloo J, Goodrich J, Tanaka H, et al. The importance of power, context and agency in improving patient experience through a patient and family centred care approach. Health Res Policy Syst 2020; 18(1): 10. doi: 10.1186/s12961-019-0487-1.
3. Goodman M. Systems thinking: what, why, when, where and how? The Systems Thinker. Available from https://thesystemsthinker.com/systems-thinking-what-why-when-where-and-how/ (accessed 17 February 2022).
4. Salzburg Global Seminar. Salzburg statement on shared decision making. BMJ 2011; 342:d1745. doi: 10.1136/bmj.d1745.
5. Coulter A, Härter M, Moumjid-Ferdjaoui N, Perestelo-Perez L, van der Weijden T. European Experience with Shared Decision Making. 2015. halshs-01247699. Available from https://halshs.archives-ouvertes.fr/halshs-01247699/document (accessed 24 January 2022).
Cited by
6 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