Speaking up for ourselves: The evolution of consumer advocacy in health care

International Journal of Technology Assessment in Health Care

Volumn 14, Issue 1, 1998, Pages 3-23

  Bastian, Hilda ^a  

^a Consum Netwk Cochrane C ^*

Author keywords

[No Author keywords available]

Indexed keywords

CONSUMER; EVOLUTION; HEALTH CARE; PHILOSOPHY; REVIEW;

EID: 0031934531     PISSN: 02664623     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0266462300010485     Document Type: Review

References (20)

1. Agency for Health Care Policy and Research. Using clinical practice guidelines to evaluate quality of care, vol. 1: Issues. Washington, DC: U.S. Department of Health and Human Services, Public Health Service, 1995.
2. Albany Consulting Group. Integrating consumer views about quality in general practice. A report commissioned by Consumers' Health Forum and the Commonwealth Department of Human Services and Health. Canberra: Commonwealth of Australia, 1996.
3. Anspach, R. R. From stigma to identity politics: Political activism among the physically disabled and former mental patients. Social Science and Medicine, 1979, 13A, 765-73.
4. Australian Consumers' Association and Combined Pensioners' Association NSW. 'Too much of a good thing' - A study of older consumers and their medications. Sydney: Australian Consumers' Association, 1988.
5. Bailey, M. E. Community-based organizations and CDC as partners in HIV education and prevention. Public Health Reports, 1991, 106, 702-08.
6. Baldry, E. The development of the health consumer movement and its effect on value changes and health policy in Australia. Unpublished Ph.D. thesis. Sydney: School of Health Services Management, The University of New South Wales, 1992.
7. Bastian, H. Consumer involvement in ethics committees - A postcard from the trenches. Health Forum, 1992, 24, 11-12.
8. Bastian, H. The power of sharing knowledge: Consumer participation in the Cochrane Collaboration. Oxford: UK Cochrane Centre, 1994.
9. Bastian, H. Missing links: Some thoughts on consumers and health outcomes. Health Outcomes (Australian Institute of Health and Welfare), 1995, 5, 3-4.
10. Bastian, H. Raising the standard: Practice guidelines and consumer participation. International Journal for Quality in Health Care, 1996, 8, 485-90.
11. Bastian, H. Workshops for consumers. Australasian Cochrane Centre News, 1996, 2, 5.
12. Bastian, H (ed.). The Consumer Network Newsletter. Adelaide: Australasian Cochrane Centre, 1996.
13. Bastian, H. Review of deaths after planned home births: Update. Homebirth Australia Newsletter, 1996, 45, 24-25.
14. Bell, D. Celebrating success 1988 to 1995: A history of the Marion-Brighton-Glenelg Health and Social Welfare Council. Adelaide: Marion-Brighton-Glenelg Health and Social Welfare Council, 1995.
15. Beresford, P. Researching citizen-involvement: A collaborative or colonising enterprise? In M. Barnes & G. Wistow (eds.). Researching user involvement. Leeds: The Nuffield Institute for Health Services Studies, University of Leeds, undated, 16-32.
16. Bergman, A. B. The 'discovery' of sudden infant death syndrome: Lessons in the practice of political medicine. Seattle: University of Washington Press, 1986.
17. Bichmann, W., Rifkin, S. B., & Shrestha, M. Towards the measurement of community participation. World Health Forum, 1989, 10, 467-72.
18. Blaxter, M. Consumer issues within the NHS. In Consumers and research in the NHS: An R&D contribution to consumer involvement in the NHS. Leeds: Department of Health, 1995.
19. Boston Women's Book Collective. Our bodies, ourselves. New York: Simon and Schuster, 1971.
20. Bowling, A., Jacobson, B., & Southgate, L. Explorations in consultation of the public and health professionals on priority setting in an inner London health district. Social Science and Medicine, 1993, 37, 851-57.