Health democracy in Europe: Cancer patient organization participation in health policy

10Citations
Citations of this article
68Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

Background: Patient organization participation in health policy decision making is an understudied area of inquiry. A handful of qualitative studies have suggested that the growing number of patient organizations in Europe and their increasing involvement in policy issues do not result in high political effectiveness. However, existing research is largely country-specific. Objective: To examine the degree and impact of cancer patient organization (CPO) participation in health policy decision making in EU-28 and to identify their correlates. Methods: A total of 1266 members of CPOs participated in this study, recruited from a diversity of sources. CPO participation in health policy was assessed with the Health Democracy Index, a previously developed instrument measuring the degree and impact of patient organization participation in various realms of health policy. Additional questions collected information about participants' and the CPO's characteristics. Data were gleaned in the form of an online self-reported instrument. Results: The highest degree of CPO participation was observed with respect to hospital boards, reforms in health policy and ethics committees for clinical trials. On the contrary, the lowest was discerned with regard to panels in other important health-related organizations and in the Ministry of Health. The reverse pattern of results was observed concerning the Impact subscale. As regards the correlates of CPO participation, legislation bore the strongest association with the Degree subscale, while organizational factors emerged as the most important variables with regard to the Impact subscale. Conclusions: Research findings indicate that a high degree of CPO participation does not necessarily ensure a high impact. Efforts to promote high and effective CPO participation should be geared towards the establishment of a health-care law based on patient rights as well as to the formation of coalitions among CPOs and the provision of training to its members.

References Powered by Scopus

Global patterns of cancer incidence and mortality rates and trends

2294Citations
N/AReaders
Get full text

Effectiveness of strategies for informing, educating, and involving patients

767Citations
N/AReaders
Get full text

Patient empowerment, patient participation and patient-centeredness in hospital care: A concept analysis based on a literature review

645Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Oncology nursing workforce: challenges, solutions, and future strategies

88Citations
N/AReaders
Get full text

Cancer patients' organisation participation in heath policy decision-making: A snapshot/cluster analysis of the EU-28 countries

5Citations
N/AReaders
Get full text

Nursing Leaders as Visionaries and Enablers of Action

4Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Souliotis, K., Peppou, L. E., Agapidaki, E., Tzavara, C., Debiais, D., Hasurdjiev, S., & Sarkozy, F. (2018). Health democracy in Europe: Cancer patient organization participation in health policy. Health Expectations, 21(2), 474–484. https://doi.org/10.1111/hex.12638

Readers over time

‘17‘18‘19‘20‘21‘22‘23‘24‘2505101520

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 25

64%

Researcher 7

18%

Professor / Associate Prof. 4

10%

Lecturer / Post doc 3

8%

Readers' Discipline

Tooltip

Medicine and Dentistry 11

32%

Nursing and Health Professions 10

29%

Social Sciences 8

24%

Psychology 5

15%

Save time finding and organizing research with Mendeley

Sign up for free
0