From rhetoric to reality: including patient voices in supportive cancer care planning.

作者: Sara K. Tedford Gold , Julia Abelson , Cathy A. Charles

DOI: 10.1111/J.1369-7625.2005.00334.X

关键词:

摘要: Objective  To explore the extent and manner of patient participation in planning regional supportive care networks throughout province Ontario. We consider disconnect between rhetoric reality involvement network co-ordination. Context  In 1997, Province Ontario, Canada, established a new, regionalized cancer system. By transferring responsibility to level networks, architects new provincial system hoped broaden decision making enhance responsiveness decisions communities. Research approach  Through qualitative, multiple case study approach we evaluated processes involving patients development. In-depth, semi-structured interviews document analysis were complemented by observations meetings, council meetings. Results  The development three regions reveal significant gap intentions involve health their actual involvement. This can be explained by: (i) lack clear direction regarding these networks; (ii) dominance centres activities; and, (iii) emergence competing priorities. Discussion  These trends expose complexity notion public how it is embedded social political contexts. failed attempt at efforts result benign neglect intents contexts which meant occur.

参考文章(27)
THEODORE R. MARMOR, JAMES A. MORONE, Representing Consumer Interests: Imbalanced Markets, Health Planning, and the HSAs Milbank Quarterly. ,vol. 83, pp. 125- 165 ,(1980) , 10.1111/J.1468-0009.2005.00431.X
ROB KRUEGER, SETH TULER, THOMAS WEBLER, What Is a Good Public Participation Process? Five Perspectives from the Public Environmental Management. ,vol. 27, pp. 435- 450 ,(2001) , 10.1007/S002670010160
Kevin Brazil, Tim Whelan, Mary Ann O’Brien, Jonathan Sussman, Nancy Pyette, Daryl Bainbridge, Towards improving the co-ordination of supportive cancer care services in the community Health Policy. ,vol. 70, pp. 125- 131 ,(2004) , 10.1016/J.HEALTHPOL.2004.02.007
Christopher Clough, Involving patients and the public in the NHS Clinical Medicine. ,vol. 3, pp. 551- 554 ,(2003) , 10.7861/CLINMEDICINE.3-6-551
Damien Contandriopoulos, A sociological perspective on public participation in health care. Social Science & Medicine. ,vol. 58, pp. 321- 330 ,(2004) , 10.1016/S0277-9536(03)00164-3
Jacques Godbout, Is consumer control possible in health care services? The Quebec case. International Journal of Health Services. ,vol. 11, pp. 151- 167 ,(1981) , 10.2190/3FA2-182B-PELY-BQB1
Rachel Jewkes, Anne Murcott, Community representatives: Representing the “community”? Social Science & Medicine. ,vol. 46, pp. 843- 858 ,(1998) , 10.1016/S0277-9536(97)00209-8
Sherry R. Arnstein, A Ladder of Citizen Participation Journal of The American Planning Association. ,vol. 35, pp. 216- 224 ,(1969) , 10.1080/01944366908977225