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Published in: Journal of Bioethical Inquiry 2/2019

01-06-2019 | Original Research

Exploring Ethical Issues Related to Patient Engagement in Healthcare: Patient, Clinician and Researcher’s Perspectives

Authors: Marjorie Montreuil, Joé T. Martineau, Eric Racine

Published in: Journal of Bioethical Inquiry | Issue 2/2019

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Abstract

Patient engagement in healthcare is increasingly discussed in the literature, and initiatives engaging patients in quality improvement activities, organizational design, governance, and research are becoming more and more common and have even become mandatory for certain health institutions. Here we discuss a number of ethical challenges raised by this engagement from patients from the perspectives of research, organizational/quality improvement practices, and patient experiences, while offering preliminary recommendations as to how to address them. We identified three broad categories of ethical issues that intersect between the different types of patient engagement: (1) establishing a shared vision about goals of patient engagement and respective roles; (2) the process and method of engaging with patients; and (3) practical aspects of patient engagement. To explain these issues, we build from our personal, professional, and academic experiences, as well as traditions such as pragmatism and hermeneutics that stress the importance of participation, empowerment, and engagement.  Patient engagement can be highly valuable at numerous levels, but particular attention should be paid to the process of engaging with patients and related ethical issues. Some lessons from the literature on the ethics of participatory research can be translated to organizational and quality improvement practices.
Literature
go back to reference Banks, S., A. Armstrong, K. Carter, et al. 2013. Everyday ethics in community-based participatory research. Contemporary Social Science 8(3): 263–277.CrossRef Banks, S., A. Armstrong, K. Carter, et al. 2013. Everyday ethics in community-based participatory research. Contemporary Social Science 8(3): 263–277.CrossRef
go back to reference Barello, S., G. Graffigna, and E. Vegni. 2012. Patient engagement as an emerging challenge for healthcare services: Mapping the literature. Nursing Research and Practice Nursing Research and Practice 2012(2): 1–7. Barello, S., G. Graffigna, and E. Vegni. 2012. Patient engagement as an emerging challenge for healthcare services: Mapping the literature. Nursing Research and Practice Nursing Research and Practice 2012(2): 1–7.
go back to reference Bradbury-Jones, C., and J. Taylor. 2015. Engaging with children as co-researchers: Challenges, counter-challenges and solutions. International Journal of Social Research Methodology 18(2): 161–173.CrossRef Bradbury-Jones, C., and J. Taylor. 2015. Engaging with children as co-researchers: Challenges, counter-challenges and solutions. International Journal of Social Research Methodology 18(2): 161–173.CrossRef
go back to reference Buchanan, D.R., F.G. Miller, and N. Wallerstein. 2007. Ethical issues in community-based participatory research: Balancing rigorous research with community participation in community intervention studies. Progress in Community Health Partnerships: Research, Education, and Action 1(2): 153–60.CrossRef Buchanan, D.R., F.G. Miller, and N. Wallerstein. 2007. Ethical issues in community-based participatory research: Balancing rigorous research with community participation in community intervention studies. Progress in Community Health Partnerships: Research, Education, and Action 1(2): 153–60.CrossRef
go back to reference Bush, P.L., P. Pluye, C. Loignon, et al. 2017. Organizational participatory research: A systematic mixed studies review exposing its extra benefits and the key factors associated with them. Implementation Science 12(1): 119.CrossRefPubMed Bush, P.L., P. Pluye, C. Loignon, et al. 2017. Organizational participatory research: A systematic mixed studies review exposing its extra benefits and the key factors associated with them. Implementation Science 12(1): 119.CrossRefPubMed
go back to reference Canadian Institutes of Health Research (CIHR). 2014. Strategy for patient-oriented research: Patient engagement framework. Ottawa: Canada. Canadian Institutes of Health Research (CIHR). 2014. Strategy for patient-oriented research: Patient engagement framework. Ottawa: Canada.
go back to reference Cargo, M., and S.L. Mercer. 2008. The value and challenges of participatory research: Strengthening its practice. Annual Review of Public Health 29: 325–350.CrossRef Cargo, M., and S.L. Mercer. 2008. The value and challenges of participatory research: Strengthening its practice. Annual Review of Public Health 29: 325–350.CrossRef
go back to reference Carman, K.L., P. Dardess, M. Maurer, et al. 2013. Patient and family engagement: A framework for understanding the elements and developing interventions and policies. Health Affairs 32(2): 223–231.CrossRef Carman, K.L., P. Dardess, M. Maurer, et al. 2013. Patient and family engagement: A framework for understanding the elements and developing interventions and policies. Health Affairs 32(2): 223–231.CrossRef
go back to reference Carroll, S., G. Embuldeniya, J. Abelson, M. McGillion, A. Berkesse, and J. Healey. 2017. Questioning patient engagement: Research scientists’ perceptions of the challenges of patient engagement in a cardiovascular research network. PPA Patient Preference and Adherence 11: 1573–1583.CrossRefPubMed Carroll, S., G. Embuldeniya, J. Abelson, M. McGillion, A. Berkesse, and J. Healey. 2017. Questioning patient engagement: Research scientists’ perceptions of the challenges of patient engagement in a cardiovascular research network. PPA Patient Preference and Adherence 11: 1573–1583.CrossRefPubMed
go back to reference Doria, N., B. Condran, L. Boulos, et al. 2018. Sharpening the focus: Differentiating between focus groups for patient engagement vs. qualitative research. Research Involvement and Engagement 4(1): 19.CrossRefPubMedPubMedCentral Doria, N., B. Condran, L. Boulos, et al. 2018. Sharpening the focus: Differentiating between focus groups for patient engagement vs. qualitative research. Research Involvement and Engagement 4(1): 19.CrossRefPubMedPubMedCentral
go back to reference Dunston, R., A. Lee, D. Boud, P. Brodie, and M. Chiarella. 2009. Co-production and health system reform–from re-imagining to re-making. Australian Journal of Public Administration 68(1): 39–52.CrossRef Dunston, R., A. Lee, D. Boud, P. Brodie, and M. Chiarella. 2009. Co-production and health system reform–from re-imagining to re-making. Australian Journal of Public Administration 68(1): 39–52.CrossRef
go back to reference Gouinlock, J. 1978. Dewey’s theory of moral deliberation. Ethics 88(1977–1978): 218–228.CrossRef Gouinlock, J. 1978. Dewey’s theory of moral deliberation. Ethics 88(1977–1978): 218–228.CrossRef
go back to reference Gouinlock, J. (ed). 2002. The moral writings of John Dewey, Great Books in Philosophy. Amherst, NY: Prometheus Books. Gouinlock, J. (ed). 2002. The moral writings of John Dewey, Great Books in Philosophy. Amherst, NY: Prometheus Books.
go back to reference Green, L.W. 2008. Making research relevant: If it is an evidence-based practice, where’s the practice-based evidence? Family practice 25(S1): i20–i24.CrossRefPubMed Green, L.W. 2008. Making research relevant: If it is an evidence-based practice, where’s the practice-based evidence? Family practice 25(S1): i20–i24.CrossRefPubMed
go back to reference Green, L.W., Royal Society of Canada, and BC Consortium for Health Promotion Research. 1995. Study of participatory research in health promotion: Review and recommendations for the development of participatory research in health promotion in Canada. Royal Society of Canada. Green, L.W., Royal Society of Canada, and BC Consortium for Health Promotion Research. 1995. Study of participatory research in health promotion: Review and recommendations for the development of participatory research in health promotion in Canada. Royal Society of Canada.
go back to reference Hagan, T.L., K. Schmidt, G.R. Ackison, M. Murphy, and J.R. Jones. 2017. Not the last word: Dissemination strategies for patient-centred research in nursing. Journal of Research in Nursing 22(5): 388–402.CrossRefPubMed Hagan, T.L., K. Schmidt, G.R. Ackison, M. Murphy, and J.R. Jones. 2017. Not the last word: Dissemination strategies for patient-centred research in nursing. Journal of Research in Nursing 22(5): 388–402.CrossRefPubMed
go back to reference Hahn, D.L., A.E. Hoffmann, M. Felzien, J.W. LeMaster, J. Xu, and L.J. Fagnan. 2017. Tokenism in patient engagement. Family practice 34(3): 290–295.PubMed Hahn, D.L., A.E. Hoffmann, M. Felzien, J.W. LeMaster, J. Xu, and L.J. Fagnan. 2017. Tokenism in patient engagement. Family practice 34(3): 290–295.PubMed
go back to reference Higgins, T., E. Larson, and R. Schnall. 2017. Unraveling the meaning of patient engagement: A concept analysis. Patient Education and Counseling 100(1): 30–36.CrossRefPubMed Higgins, T., E. Larson, and R. Schnall. 2017. Unraveling the meaning of patient engagement: A concept analysis. Patient Education and Counseling 100(1): 30–36.CrossRefPubMed
go back to reference International Committee of Medical Journal Editors. 2016. Recommendations for the conduct, reporting, editing, and publication of scholarly work in medical journals. www.icmje.org/recommendations. Accessed January 16, 2019. International Committee of Medical Journal Editors. 2016. Recommendations for the conduct, reporting, editing, and publication of scholarly work in medical journals. www.​icmje.​org/​recommendations. Accessed January 16, 2019.
go back to reference Ives, J., S. Damery, and S. Redwod. 2013. PPI, paradoxes and Plato: Who’s sailing the ship? Journal of Medical Ethics 39(3): 181–185.CrossRefPubMed Ives, J., S. Damery, and S. Redwod. 2013. PPI, paradoxes and Plato: Who’s sailing the ship? Journal of Medical Ethics 39(3): 181–185.CrossRefPubMed
go back to reference Jagosh, J., A.C. Macaulay, P. Pluye et al. 2012. Uncovering the benefits of participatory research: Implications of a realist review for health research and practice. The Milbank Quarterly 90(2): 311–346.CrossRefPubMedPubMedCentral Jagosh, J., A.C. Macaulay, P. Pluye et al. 2012. Uncovering the benefits of participatory research: Implications of a realist review for health research and practice. The Milbank Quarterly 90(2): 311–346.CrossRefPubMedPubMedCentral
go back to reference Johnson, K.E., T.M. Mroz, M. Abraham, et al. 2016. Promoting patient and family partnerships in ambulatory care improvement: A narrative review and focus group findings. Advances in Therapy 33(8): 1417–1439.CrossRefPubMedPubMedCentral Johnson, K.E., T.M. Mroz, M. Abraham, et al. 2016. Promoting patient and family partnerships in ambulatory care improvement: A narrative review and focus group findings. Advances in Therapy 33(8): 1417–1439.CrossRefPubMedPubMedCentral
go back to reference Kaner, S. 2014. Facilitator’s guide to participatory decision-making. San Francisco, CA: John Wiley & Sons. Kaner, S. 2014. Facilitator’s guide to participatory decision-making. San Francisco, CA: John Wiley & Sons.
go back to reference Kelly, G., S-Y. Wang, G. Lucas, L. Fraenkel, and C.P. Gross. 2017. Facilitating meaningful engagement on community advisory committees in patient-centered outcome research. Progress in Community Health Partnerships: Research, Education, and Action 11(3): 243–251.CrossRef Kelly, G., S-Y. Wang, G. Lucas, L. Fraenkel, and C.P. Gross. 2017. Facilitating meaningful engagement on community advisory committees in patient-centered outcome research. Progress in Community Health Partnerships: Research, Education, and Action 11(3): 243–251.CrossRef
go back to reference Määttä, S., K. Lützén, and S. Öresland. 2017. Contract theories and partnership in health care. A philosophical inquiry to the philosophy of John Rawls and Seyla Benhabib. NUP Nursing Philosophy 18(3): e12164.CrossRef Määttä, S., K. Lützén, and S. Öresland. 2017. Contract theories and partnership in health care. A philosophical inquiry to the philosophy of John Rawls and Seyla Benhabib. NUP Nursing Philosophy 18(3): e12164.CrossRef
go back to reference Maguire, K., and N. Britten. 2017. “How can anybody be representative for those kind of people?” Forms of patient representation in health research, and why it is always contestable. Social Science & Medicine 183: 62–69.CrossRef Maguire, K., and N. Britten. 2017. “How can anybody be representative for those kind of people?” Forms of patient representation in health research, and why it is always contestable. Social Science & Medicine 183: 62–69.CrossRef
go back to reference Marlett, N., S. Shklarov, D. Marshall, M. Santana, and T. Wasylak. 2015. Building new relationships in research: A model of patient engagement research. Quality of Life Research 24(5): 1057–1067.CrossRefPubMed Marlett, N., S. Shklarov, D. Marshall, M. Santana, and T. Wasylak. 2015. Building new relationships in research: A model of patient engagement research. Quality of Life Research 24(5): 1057–1067.CrossRefPubMed
go back to reference Mikesell, L., E. Bromley, and D. Khodyakov. 2013. Ethical community-engaged research: A literature review. American Journal of Public Health 103(12): 7.CrossRef Mikesell, L., E. Bromley, and D. Khodyakov. 2013. Ethical community-engaged research: A literature review. American Journal of Public Health 103(12): 7.CrossRef
go back to reference Minkler, M. 2016. Ethical challenges for the “outside” researcher in community-based participatory research. Health Education & Behavior 31(6): 684–697.CrossRef Minkler, M. 2016. Ethical challenges for the “outside” researcher in community-based participatory research. Health Education & Behavior 31(6): 684–697.CrossRef
go back to reference Minkler, M., P. Fadem, M. Perry, K. Blum, L. Moore, and J. Rogers. 2002. Ethical dilemmas in participatory action research: A case study from the disability community. Health Education & Behavior 29(1): 14–29.CrossRef Minkler, M., P. Fadem, M. Perry, K. Blum, L. Moore, and J. Rogers. 2002. Ethical dilemmas in participatory action research: A case study from the disability community. Health Education & Behavior 29(1): 14–29.CrossRef
go back to reference Montreuil, M., and F.A. Carnevale. 2018. Participatory hermeneutic ethnography: A methodological framework for health ethics research with children. Qualitative Health Research 28(7): 1135–1144.CrossRefPubMed Montreuil, M., and F.A. Carnevale. 2018. Participatory hermeneutic ethnography: A methodological framework for health ethics research with children. Qualitative Health Research 28(7): 1135–1144.CrossRefPubMed
go back to reference Montreuil, M., C. Thibeault, L. McHarg, and F.A. Carnevale. 2018. Children’s moral experiences of crisis management in a child mental health setting. International Journal of Mental Health Nursing 27(5): 1440–1448.CrossRefPubMed Montreuil, M., C. Thibeault, L. McHarg, and F.A. Carnevale. 2018. Children’s moral experiences of crisis management in a child mental health setting. International Journal of Mental Health Nursing 27(5): 1440–1448.CrossRefPubMed
go back to reference Parry, D., J. Salsberg, and A.C. Macaulay. 2009. A guide to researcher and knowledge-user collaboration in health research. Canadian Institutes of Health Research (CIHR). Parry, D., J. Salsberg, and A.C. Macaulay. 2009. A guide to researcher and knowledge-user collaboration in health research. Canadian Institutes of Health Research (CIHR).
go back to reference Pomey, M.P., L. Flora, P. Karazivan, et al. 2015. Le “Montreal model”: Enjeux du partenariat relationnel entre patients et professionnels de la santé [The “Montreal model”: Challenges of the partnership relationship between patients and health professionals]. Sante publique 27(1): 41–50.CrossRef Pomey, M.P., L. Flora, P. Karazivan, et al. 2015. Le “Montreal model”: Enjeux du partenariat relationnel entre patients et professionnels de la santé [The “Montreal model”: Challenges of the partnership relationship between patients and health professionals]. Sante publique 27(1): 41–50.CrossRef
go back to reference Pomey, M.P., D.P. Ghadiri, P. Karazivan, N. Fernandez, and N. Clavel. 2015. Patients as partners: A qualitative study of patients’ engagement in their health care. PloS One 10(4): e0122499.CrossRefPubMedPubMedCentral Pomey, M.P., D.P. Ghadiri, P. Karazivan, N. Fernandez, and N. Clavel. 2015. Patients as partners: A qualitative study of patients’ engagement in their health care. PloS One 10(4): e0122499.CrossRefPubMedPubMedCentral
go back to reference Pomey, M-P., H. Hihat, M. Khalifa, P. Lebel, A. Néron, and V. Dumez. 2015. Patient partnership in quality improvement of healthcare services: Patients’ inputs and challenges faced. Patient Experience Journal 2(1): 29–42.CrossRef Pomey, M-P., H. Hihat, M. Khalifa, P. Lebel, A. Néron, and V. Dumez. 2015. Patient partnership in quality improvement of healthcare services: Patients’ inputs and challenges faced. Patient Experience Journal 2(1): 29–42.CrossRef
go back to reference Racine, E., E. Bell, B. Farlow, et al. 2017. The “ouR-HOPE” approach for ethics and communication about neonatal neurological injury. Developmental Medicine & Child Neurology 59(2): 125–135.CrossRef Racine, E., E. Bell, B. Farlow, et al. 2017. The “ouR-HOPE” approach for ethics and communication about neonatal neurological injury. Developmental Medicine & Child Neurology 59(2): 125–135.CrossRef
go back to reference Renedo, A., and C. Marston. 2011. Healthcare professionals’ representations of “patient and public involvement” and creation of “public participant” identities: Implications for the development of inclusive and bottom-up community participation initiatives. Journal of Community & Applied Social Psychology 21(3): 268–280.CrossRef Renedo, A., and C. Marston. 2011. Healthcare professionals’ representations of “patient and public involvement” and creation of “public participant” identities: Implications for the development of inclusive and bottom-up community participation initiatives. Journal of Community & Applied Social Psychology 21(3): 268–280.CrossRef
go back to reference Smith, E., F. Ross, S. Donovan, et al. 2008. Service user involvement in nursing, midwifery and health visiting research: A review of evidence and practice. International Journal of Nursing Studies 45(2): 298–315.CrossRefPubMed Smith, E., F. Ross, S. Donovan, et al. 2008. Service user involvement in nursing, midwifery and health visiting research: A review of evidence and practice. International Journal of Nursing Studies 45(2): 298–315.CrossRefPubMed
go back to reference Stolper, M., B. Molewijk, and G. Widdershoven. 2015. Learning by doing. Training health care professionals to become facilitator of moral case deliberation. HEC forum. Stolper, M., B. Molewijk, and G. Widdershoven. 2015. Learning by doing. Training health care professionals to become facilitator of moral case deliberation. HEC forum.
go back to reference Taylor, C. 1971. Interpretation and the sciences of man. The Review of Metaphysics, 3–51. Taylor, C. 1971. Interpretation and the sciences of man. The Review of Metaphysics, 3–51.
go back to reference ----. 2004. Modern social imaginaries. Durham: Duke University Press. ----. 2004. Modern social imaginaries. Durham: Duke University Press.
go back to reference Tri-Council Policy Statement 2 (TCPS2). 2014. Ethical conduct for research involving humans. Ottawa: Government of Canada. Tri-Council Policy Statement 2 (TCPS2). 2014. Ethical conduct for research involving humans. Ottawa: Government of Canada.
go back to reference Veatch, R. 1988. The patient as partner: A theory of human experimentation ethics. Journal of Religious Ethics 16(1): 190. Veatch, R. 1988. The patient as partner: A theory of human experimentation ethics. Journal of Religious Ethics 16(1): 190.
go back to reference Wallerstein, N., and B. Duran. 2017. The theoretical, historical and practice roots of CBPR. In Community based participatory research for health: Advancing social and health equity, edited by N. Wallerstein, B. Duran, J.G. Oetzel, and M. Minkler, 17–30. San Francisco, CA: John Wiley & Sons, Inc. Wallerstein, N., and B. Duran. 2017. The theoretical, historical and practice roots of CBPR. In Community based participatory research for health: Advancing social and health equity, edited by N. Wallerstein, B. Duran, J.G. Oetzel, and M. Minkler, 17–30. San Francisco, CA: John Wiley & Sons, Inc.
go back to reference Widdershoven, G., T. Abma, and B. Molewijk. 2009. Empirical ethics as dialogical practice. Bioethics 23(4): 236–248.CrossRefPubMed Widdershoven, G., T. Abma, and B. Molewijk. 2009. Empirical ethics as dialogical practice. Bioethics 23(4): 236–248.CrossRefPubMed
go back to reference Wilson, E., A. Kenny, and V. Dickson-Swift. 2018. Ethical challenges in community-based participatory research: A scoping review. Qualitative Health Research 28(2): 189–199.CrossRefPubMed Wilson, E., A. Kenny, and V. Dickson-Swift. 2018. Ethical challenges in community-based participatory research: A scoping review. Qualitative Health Research 28(2): 189–199.CrossRefPubMed
Metadata
Title
Exploring Ethical Issues Related to Patient Engagement in Healthcare: Patient, Clinician and Researcher’s Perspectives
Authors
Marjorie Montreuil
Joé T. Martineau
Eric Racine
Publication date
01-06-2019
Publisher
Springer Singapore
Published in
Journal of Bioethical Inquiry / Issue 2/2019
Print ISSN: 1176-7529
Electronic ISSN: 1872-4353
DOI
https://doi.org/10.1007/s11673-019-09904-6

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