Do Health Care Relationships Affect the Quality of Life of Persons with HIV/AIDS?

2.50
Hdl Handle:
http://hdl.handle.net/10755/149188
Type:
Presentation
Title:
Do Health Care Relationships Affect the Quality of Life of Persons with HIV/AIDS?
Abstract:
Do Health Care Relationships Affect the Quality of Life of Persons with HIV/AIDS?
Conference Sponsor:Sigma Theta Tau International
Conference Year:2003
Author:Anderson, Elizabeth H., PhD, APRN, BC
P.I. Institution Name:University of Connecticut
Title:Assistant Professor
Co-Authors:Margaret Hull Spencer, MS, APRN, BC; Seja-Joyce Fishman, MS, APRN, BC
Objective: Persons with HIV/AIDS experience nausea/vomiting with prescribed medications. Ability to follow regimens and not have nausea/vomiting can impact quality of life. How relationships with health care workers influence quality of life in persons with HIV/AIDS is not known. Research question: Do health care relationships effect quality of life in persons with HIV/AIDS over and above self-efficacy and nausea/ vomiting? Design: Longitudinal correlational. Sample/setting: Convenience sample of 43 men and 27 women, mean age 43.1 (SD = 8.7), and CD4 count of 214.5 (SD = 231.9) were interviewed. Ethnic/racial backgrounds: Hispanic (43%), Black (41%), and Caucasian (16%). Majority had less than high school education (54.3%), yearly income
Repository Posting Date:
26-Oct-2011
Date of Publication:
17-Oct-2011
Sponsors:
Sigma Theta Tau International

Full metadata record

DC FieldValue Language
dc.typePresentationen_GB
dc.titleDo Health Care Relationships Affect the Quality of Life of Persons with HIV/AIDS?en_GB
dc.identifier.urihttp://hdl.handle.net/10755/149188-
dc.description.abstract<table><tr><td colspan="2" class="item-title">Do Health Care Relationships Affect the Quality of Life of Persons with HIV/AIDS?</td></tr><tr class="item-sponsor"><td class="label">Conference Sponsor:</td><td class="value">Sigma Theta Tau International</td></tr><tr class="item-year"><td class="label">Conference Year:</td><td class="value">2003</td></tr><tr class="item-author"><td class="label">Author:</td><td class="value">Anderson, Elizabeth H., PhD, APRN, BC</td></tr><tr class="item-institute"><td class="label">P.I. Institution Name:</td><td class="value">University of Connecticut</td></tr><tr class="item-author-title"><td class="label">Title:</td><td class="value">Assistant Professor</td></tr><tr class="item-email"><td class="label">Email:</td><td class="value">eandersoncsj@snet.net</td></tr><tr class="item-co-authors"><td class="label">Co-Authors:</td><td class="value">Margaret Hull Spencer, MS, APRN, BC; Seja-Joyce Fishman, MS, APRN, BC</td></tr><tr><td colspan="2" class="item-abstract">Objective: Persons with HIV/AIDS experience nausea/vomiting with prescribed medications. Ability to follow regimens and not have nausea/vomiting can impact quality of life. How relationships with health care workers influence quality of life in persons with HIV/AIDS is not known. Research question: Do health care relationships effect quality of life in persons with HIV/AIDS over and above self-efficacy and nausea/ vomiting? Design: Longitudinal correlational. Sample/setting: Convenience sample of 43 men and 27 women, mean age 43.1 (SD = 8.7), and CD4 count of 214.5 (SD = 231.9) were interviewed. Ethnic/racial backgrounds: Hispanic (43%), Black (41%), and Caucasian (16%). Majority had less than high school education (54.3%), yearly income</td></tr></table>en_GB
dc.date.available2011-10-26T09:57:42Z-
dc.date.issued2011-10-17en_GB
dc.date.accessioned2011-10-26T09:57:42Z-
dc.description.sponsorshipSigma Theta Tau Internationalen_GB
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