The Dimensions of Tokenism in Patient and Family Engagement: A Concept Analysis of the Literature

被引:24
作者
Majid, Umair [1 ,2 ]
机构
[1] Univ Toronto, Inst Hlth Policy Management & Evaluat, Toronto, ON, Canada
[2] Univ Hlth Network, Clin Decis Making & Hlth Care, 13th Floor,100 Elizabeth St West, Toronto, ON, Canada
来源
JOURNAL OF PATIENT EXPERIENCE | 2020年 / 7卷 / 06期
关键词
patient engagement; tokenism; meaningful engagement; patient perspectives; narratives; concept analysis; content analysis; qualitative methods; qualitative evidence synthesis; PUBLIC INVOLVEMENT; CARE; SERVICES; PEOPLE;
D O I
10.1177/2374373520925268
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Patient engagement (PE) has become embedded in discussions about health service planning and quality improvement, and the goal has been to find ways to observe the potential beneficial outcomes associated with PE. Patients and health care professionals use various terms to depict PE, for example, partnership and collaboration. Similarly, tokenism is consistently used to describe PE that has gone wrong. There is a lack of clarity, however, on the meanings and implications of tokenism on PE activities. The objective of this concept analysis was to examine the peer-reviewed and gray literature that has discussed tokenism to identify how we currently understand and use the concept. This review discusses 4 dimensions of tokenism: unequal power, limited impact, ulterior motives, and opposite of meaningful PE. These dimensions explicate the different components, meanings, and implications of tokenism in PE practice. The findings of this review emphasize how tokenism is primarily perceived as negative by supporters of PE, but this attribution depends on patients' preferences for engagement. In addition, this review compares the dimensions of tokenism with the levels of engagement in the International Association of the Public Participation spectrum. This review suggests that there are 2 gradations of tokenism; while tokenism represents unequal power relationships in favor of health care professionals, this may lead to either limited or no meaningful change or change that is primarily aligned with the personal and professional goals of clinicians, managers, and decision-makers.
引用
收藏
页码:1610 / 1620
页数:11
相关论文
共 36 条
  • [1] LADDER OF CITIZEN PARTICIPATION
    ARNSTEIN, SR
    [J]. JOURNAL OF THE AMERICAN INSTITUTE OF PLANNERS, 1969, 35 (04): : 216 - 224
  • [2] Participatory Organizational Change in Community-Based Health and Human Services: From Tokenism to Political Engagement
    Bess, Kimberly D.
    Prilleltensky, Isaac
    Perkins, Douglas D.
    Collins, Leslie V.
    [J]. AMERICAN JOURNAL OF COMMUNITY PSYCHOLOGY, 2009, 43 (1-2) : 134 - 148
  • [3] Engaging patients to improve quality of care: a systematic review
    Bombard, Yvonne
    Baker, G. Ross
    Orlando, Elaina
    Fancott, Carol
    Bhatia, Pooja
    Casalino, Selina
    Onate, Kanecy
    Denis, Jean-Louis
    Pomey, Marie-Pascale
    [J]. IMPLEMENTATION SCIENCE, 2018, 13
  • [4] Culture and Process Change as a Priority for Patient Engagement in Medicines Development
    Boutin, Marc
    Dewulf, Lode
    Hoos, Anton
    Geissler, Jan
    Todaro, Veronica
    Schneider, Roslyn F.
    Garzya, Vincenzo
    Garvey, Andrew
    Robinson, Paul
    Saffer, Tonya
    Krug, Sarah
    Sargeant, Ify
    [J]. THERAPEUTIC INNOVATION & REGULATORY SCIENCE, 2017, 51 (01) : 29 - 38
  • [5] A Systematic Review of the Impact of Patient and Public Involvement on Service Users, Researchers and Communities
    Brett, Jo
    Staniszewska, Sophie
    Mockford, Carole
    Herron-Marx, Sandra
    Hughes, John
    Tysall, Colin
    Suleman, Rashida
    [J]. PATIENT-PATIENT CENTERED OUTCOMES RESEARCH, 2014, 7 (04) : 387 - 395
  • [6] Buckley Jenny, 2004, Prof Nurse, V19, P499
  • [7] 'Practical' resources to support patient and family engagement in healthcare decisions: a scoping review
    Burns, Katharina Kovacs
    Bellows, Mandy
    Eigenseher, Carol
    Gallivan, Jennifer
    [J]. BMC HEALTH SERVICES RESEARCH, 2014, 14
  • [8] Breaking the Glass Ceiling: Increasing the Meaningful Involvement of Women Living With HIV/AIDS (MIWA) in the Design and Delivery of HIV/AIDS Services
    Carter, Allison
    Greene, Saara
    Nicholson, Valerie
    O'Brien, Nadia
    Sanchez, Margarite
    De Pokomandy, Alexandra
    Loutfy, Mona
    Kaida, Angela
    [J]. HEALTH CARE FOR WOMEN INTERNATIONAL, 2015, 36 (08) : 936 - 964
  • [9] Cavanagh S., 1997, NURSE RES, V4, P5, DOI DOI 10.7748/NR.4.3.5.S2
  • [10] Beyond tokenistic involvement of older people in research - a framework for future development and understanding
    Dewar, BJ
    [J]. JOURNAL OF CLINICAL NURSING, 2005, 14 (3A) : 48 - 53