Publication Cover
AIDS Care
Psychological and Socio-medical Aspects of AIDS/HIV
Volume 6, 1994 - Issue 3
33
Views
27
CrossRef citations to date
0
Altmetric
Original Articles

Whose health is it? Views about decision-making and information-seeking from people with HIV infection and their professional carers

, , , , , & show all
Pages 349-356 | Published online: 25 Sep 2007

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (2)

Anna Scheyett, Mimi Kim, Jeffrey Swanson, Marvin Swartz, Eric Elbogen, Richard Van Dorn & Joelle Ferron. (2009) Autonomy and the Use of Directive Intervention in the Treatment of Individuals with Serious Mental Illnesses: A Survey of Social Work Practitioners. Social Work in Mental Health 7:4, pages 283-306.
Read now
Eric Mykhalovskiy & Liza McCoy. (2002) Troubling ruling discourses of health: Using institutional ethnography in community-based research. Critical Public Health 12:1, pages 17-37.
Read now

Articles from other publishers (25)

Jeffrey I. Campbell, Nir Eyal, Angella Musiimenta, Bridget Burns, Sylvia Natukunda, Nicholas Musinguzi & Jessica E. Haberer. (2018) Ugandan Study Participants Experience Electronic Monitoring of Antiretroviral Therapy Adherence as Welcomed Pressure to Adhere. AIDS and Behavior 22:10, pages 3363-3372.
Crossref
Brian Skehan & Maryann Davis. (2017) Aligning Mental Health Treatments with the Developmental Stage and Needs of Late Adolescents and Young Adults. Child and Adolescent Psychiatric Clinics of North America 26:2, pages 177-190.
Crossref
June Koo Lee, Bhumsuk Keam, Ah Reum An, Tae Min Kim, Se-Hoon Lee, Dong-Wan Kim & Dae Seog Heo. (2012) Surrogate decision-making in Korean patients with advanced cancer: a longitudinal study. Supportive Care in Cancer 21:1, pages 183-190.
Crossref
Wolfgang Strube & Florian Steger. (2012) Patient autonomy and informed consent?individual preferences of senior study participants in GermanyPatientenautonomie und informierte Einwilligung ? Individuelle Pr?ferenzen von Seniorenstudierenden in Deutschland. Wiener klinische Wochenschrift 124:11-12, pages 384-390.
Crossref
Betty Chewning, Carma L. Bylund, Bupendra Shah, Neeraj K. Arora, Jennifer A. Gueguen & Gregory Makoul. (2012) Patient preferences for shared decisions: A systematic review. Patient Education and Counseling 86:1, pages 9-18.
Crossref
Kelli Stajduhar, Laura Funk, Eva Jakobsson & Joakim Öhlén. (2010) A critical analysis of health promotion and ‘empowerment’ in the context of palliative family care-giving. Nursing Inquiry 17:3, pages 221-230.
Crossref
Rashmi Kumar, P. Todd Korthuis, Somnath Saha, Geetanjali Chander, Victoria Sharp, Jonathon Cohn, Richard Moore & Mary Catherine Beach. (2010) Decision-Making Role Preferences Among Patients with HIV: Associations with Patient and Provider Characteristics and Communication Behaviors. Journal of General Internal Medicine 25:6, pages 517-523.
Crossref
Rebecca L. Volpe. (2010) Patients’ Expressed and Unexpressed Needs for Information for Informed Consent. The Journal of Clinical Ethics 21:1, pages 45-57.
Crossref
E Michiels, R DeschepperJ Bilsen, F Mortier & L Deliens. (2009) Information disclosure to terminally ill patients and their relatives: self-reported practice of Belgian clinical specialists and general practitioners. Palliative Medicine 23:4, pages 345-353.
Crossref
Jennifer M. Knopf, Richard W. Hornung, Gail B. Slap, Robert F. DeVellis & Maria T. Britto. (2008) Views of treatment decision making from adolescents with chronic illnesses and their parents: a pilot study. Health Expectations 11:4, pages 343-354.
Crossref
Sydney Morss Dy. (2007) Instruments for Evaluating Shared Medical Decision Making. Medical Care Research and Review 64:6, pages 623-649.
Crossref
Rachel E. Davis, Rosamond Jacklin, Nick Sevdalis & Charles A. Vincent. (2007) Patient involvement in patient safety: what factors influence patient participation and engagement?. Health Expectations 10:3, pages 259-267.
Crossref
Rebecca Say, Madeleine Murtagh & Richard Thomson. (2006) Patients’ preference for involvement in medical decision making: A narrative review. Patient Education and Counseling 60:2, pages 102-114.
Crossref
Wendy Levinson, Audiey Kao, Alma Kuby & Ronald A. Thisted. (2005) Not all patients want to participate in decision making. Journal of General Internal Medicine 20:6, pages 531-535.
Crossref
Robert M. KaplanDominick L. Frosch. (2005) Decision Making in Medicine and Health Care. Annual Review of Clinical Psychology 1:1, pages 525-556.
Crossref
Heather M Davey, Jacqueline Lim, Phyllis N Butow, Alexandra L Barratt & Sally Redman. (2004) Women's preferences for and views on decision-making for diagnostic tests. Social Science & Medicine 58:9, pages 1699-1707.
Crossref
Heather M. Davey, Alexandra L. Barratt, Elizabeth Davey, Phyllis N. Butow, Sally Redman, Nehmat Houssami & Glenn P. Salkeld. (2002) Medical tests: women's reported and preferred decision‐making roles and preferences for information on benefits, side‐effects and false results. Health Expectations 5:4, pages 330-340.
Crossref
Eduardo Bruera, Jie S. Willey, J. Lynn Palmer & Marguerite Rosales. (2002) Treatment decisions for breast carcinoma. Cancer 94:7, pages 2076-2080.
Crossref
Barbara K Redman & Sara T Fry. (2016) Nurses’ Ethical Conflicts: what is really known about them?. Nursing Ethics 7:4, pages 360-366.
Crossref
Hilda Bastian. (2000) Allies or enemies? Evidence‐based medicine and consumer choice. Medical Journal of Australia 172:1, pages 5-6.
Crossref
Nicola Robinson. (2002) People with HIV/AIDS: who cares?. Journal of Advanced Nursing 28:4, pages 771-778.
Crossref
Hilda Bastian. (2009) Speaking Up for Ourselves: The Evolution of Consumer Advocacy in Health Care . International Journal of Technology Assessment in Health Care 14:1, pages 3-23.
Crossref
A. Kessel & Michael J. Crawford. (1997) Openness with patients: a categorical imperative to correct an imbalance. Science and Engineering Ethics 3:3, pages 297-304.
Crossref
Helen Schietinger & Elaine M. Daniels. (1996) WHAT NURSES NEED TO KNOW. Nursing Clinics of North America 31:1, pages 137-152.
Crossref
Phuong Nguyen. (2017) Immersing the Lay Self into Medication Reasoning: A Theory of Parental Health Behavior in the Context of Asian Developing Countries. SSRN Electronic Journal.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.