Abstract
Purpose
The purpose of this secondary analysis was to test Ferrans et al.’s (J Nurs Scholarsh 37(4):336–342, 2005) revised model of health-related quality of life (HRQoL) (2005) modified from the Wilson and Cleary (J Am Med Assoc 273(1):59–65, 1995) model on women living with HIV. The primary aim was to test this model, examining the relations among the five central components (biological function, symptoms, functional status, general health perceptions, and HRQoL). The secondary aim was to explore the individual (age, children, race, marital status, education) and environmental (HIV-related stigma, social support) characteristics that may impact the main components of the model.
Methods
This study employed a cross-sectional correlational design using baseline data from 178 women living with HIV/AIDS who participated in one of the two independent randomized controlled trials designed to enhance HIV medication adherence. Path analysis using structural equation modeling was used to examine the hypothesized multivariate relations proposed in the revised Wilson and Cleary (J Am Med Assoc 273(1):59–65, 1995) model of HRQoL.
Results
While the revised model did not fit, exploratory post hoc modified models with a path from depressive symptoms to overall general health had an adequate model fit. Women with lower depressive symptoms (r = −.457, p < .01), lower HIV-related stigma (r = −.462, p < .01), higher social support (r = .413, p < .01), higher physical functioning (r = .350, p < .01), and higher general health perceptions (r = .537, p < .01) had higher overall HRQoL.
Conclusions
The results of this study have the potential to assist healthcare professionals in improving HRQoL for women living with HIV/AIDS.
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References
UNAIDS. (2016). UNAIDS global statistics 2015 fact sheet. Retrieved from http://www.unaids.org/sites/default/files/media_asset/UNAIDS_FactSheet_en.pdf
Deeks, S. G., Lewin, S. R., & Havlir, D. V. (2013). The end of AIDS: HIV infection as a chronic disease. Lancet, 382(9903), 1525–1533.
Chêne, G., et al. (2016). Cohort profile: Collaboration of Observational HIV Epidemiological Research Europe (COHERE) in EuroCoord. International Journal of Epidemiology. doi:10.1093/ije/dyw211.
Hickner, J. (2014). Shifting our focus to HIV as a chronic disease. The Journal of Family Practice, 63(7), 355.
World Health Organization. (2015). Draft global health sector strategy on HIV, 2016–2021. Retrieved from http://apps.who.int/gb/ebwha/pdf_files/WHA69/A69_31-en.pdf?ua=1
Lazarus, J. V., Safreed-Harmon, K., Barton, S. E., Costagliola, D., Dedes, N., Del Amo Valero, J., et al. (2016). Beyond viral suppression of HIV—The new quality of life frontier. BMC Medicine, 14(1), 94. doi:10.1186/s12916-016-0640-4.
Degroote, S., Vogelaers, D., & Vandijck, D. M. (2014). What determines health-related quality of life among people living with HIV: An updated review of the literature. Archives of Public Health, 72(1), 40. doi:10.1186/2049-3258-72-40.
Vigneshwaran, E., Padmanabhareddy, Y., Devanna, N., & Alvarez-Uria, G. (2013). Gender differences in health related quality of life of people living with HIV/AIDS in the era of highly active antiretroviral therapy. North American Journal of Medical Sciences, 5(2), 102–107. doi:10.4103/1947-2714.107526.
Mrus, J. M., Williams, P. L., Tsevat, J., Cohn, S. E., & Wu, A. W. (2005). Gender differences in health-related quality of life in patients with HIV/AIDS. Quality of Life Research, 14(2), 479–491. doi:10.1007/s11136-004-4693-z.
Eller, L. S., & Mahat, G. (2007). Predictors of life satisfaction in HIV-positive Nepali women. Journal of the Association of Nurses in AIDS Care, 18(5), 17–26. doi:10.1016/j.jana.2007.07.002.
Andrinopoulos, K., Clum, G., Murphy, D. A., Harper, G., Perez, L., Xu, J., et al. (2011). Health related quality of life and psychosocial correlates among HIV-infected adolescent and young adult women in the US. AIDS Education and Prevention, 23(4), 367–381. doi:10.1521/aeap.2011.23.4.367.
Vyavaharkar, M., Moneyham, L., Murdaugh, C., & Tavakoli, A. (2012). Factors associated with quality of life among rural women with HIV disease. AIDS and Behavior, 16(2), 295–303. doi:10.1007/s10461-011-9917-y.
Baran, R., Mulcahy, F., Krznaric, I., d’Arminio Monforte, A., Samarina, A., Xi, H., et al. (2014). Reduced HIV symptoms and improved health-related quality of life correlate with better access to care for HIV-1 infected women: The ELLA study. Journal of the International AIDS Society, 17(4(Suppl 3)), 1. doi:10.7448/IAS.17.4.19616.
Holtz, C., Sowell, R., Van Brackle, L., Velasquez, G., & Hernandez-Alonso, V. (2014). A quantitative study of factors influencing quality of life in rural Mexican women diagnosed with HIV. The Journal of the Association of Nurses in AIDS Care, 25(6), 555–567. doi:10.1016/j.jana.2014.03.002.
Mutabazi-Mwesigire, D., Katamba, A., Martin, F., Seeley, J., & Wu, A. W. (2015). Factors that affect quality of life among people living with HIV attending an urban clinic in Uganda: A cohort study: E0126810. PLoS ONE. doi:10.1371/journal.pone.0126810.
Feinberg, J., Saag, M., Squires, K., Currier, J., Ryan, R., Coate, B., et al. (2011). Health-related quality of life in the gender, race, and clinical experience trial. AIDS Research and Treatment, 2011, 349165–349168. doi:10.1155/2011/349165.
Ruiz-Pérez, I. R., Olry de Labry Lima, A., del Castillo, L. S., Bano, J. R., Ruz, M. L., & del Arco Jimenez, A. (2009). No differences in quality of life between men and women undergoing HIV antiretroviral treatment. Impact of demographic, clinical and psychosocial factors. AIDS Care, 21(8), 943–952. doi:10.1080/09540120802612840.
Reis, R. K., Santos, C. B., & Gir, E. (2012). Quality of life among Brazilian women living with HIV/AIDS. AIDS Care, 24(5), 626–634. doi:10.1080/09540121.2011.630345.
Lorenz, K. A., Cunningham, W. E., Spritzer, K. L., & Hays, R. D. (2006). Changes in symptoms and health-related quality of life in a nationally representative sample of adults in treatment for HIV. Quality of Life Research, 15(6), 951–958. doi:10.1007/s11136-005-6010-x.
Phaladze, N. A., Human, S., Dlamini, S. B., Hulela, E. B., Hadebe, I. M., Sukati, N. A., et al. (2005). Quality of life and the concept of “living well” with HIV/AIDS in sub-Saharan Africa. Journal of Nursing Scholarship, 37(2), 120–126.
Wilson, I. B., & Cleary, P. D. (1995). Linking clinical variables with health-related quality of life. The Journal of the American Medical Association, 273(1), 59–65.
Ferrans, C. E., Zerwic, J. J., Wilbur, J. E., & Larson, J. L. (2005). Conceptual model of health-related quality of life. Journal of Nursing Scholarship, 37(4), 336–342. doi:10.1111/j.1547-5069.2005.00058.x.
Beck, A. T., Steer, R. A., Ball, R., & Ranieri, W. (1996). Comparison of Beck depression inventories-IA and -II in psychiatric outpatients. Journal of Personality Assessment, 67(3), 588–597. doi:10.1207/s15327752jpa6703_13.
Wu, A. W., Rubin, H. R., Mathews, W. C., Ware, J. E., Jr., Brysk, L. T., Hardy, W. D., et al. (1991). A health status questionnaire using 30 items from the medical outcomes study: Preliminary validation in persons with early HIV infection. Medical Care, 29, 786–798.
Berger, B., Ferrans, C. E., & Lashley, F. R. (2001). Measuring stigma in people with HIV: Psychometric assessment of the HIV Stigma Scale. Research in Nursing and Health, 24(6), 518–529.
Loutfy, M. R., Logie, C. H., Zhang, Y., Blitz, S. L., Margolese, S. L., Tharao, W. E., et al. (2012). Gender and ethnicity differences in HIV-related stigma experienced by people living with HIV in Ontario, Canada. PLoS ONE, 7(12), e48168. doi:10.1371/journal.pone.0048168.
Cohen, S., & Syme, S. L. (1985). Social support and health. Orlando, FL: Academic Press.
Kline, R. B. (2011). Principles and practice of structural equation modeling. New York: Guilford Press.
Muthén, L. K., & Muthén, B. O. (1998–2012). Mplus user’s guide, 7th ed. Los Angeles: Muthén & Muthén.
Sousa, K. H., & Kwok, O. (2006). Putting Wilson and Cleary to the test: Analysis of a HRQOL conceptual model using structural equation modeling. Quality of Life Research, 15(4), 725–737. doi:10.1007/s11136-005-3975-4.
Goodkin, K., Shapshak, P., Asthana, D., Zheng, W., Concha, M., Wilkie, F. L., et al. (2004). Older age and plasma viral load in HIV-1 infection. AIDS, 18 Suppl 1(Supplement 1), S87–S98. doi:10.1097/00002030-200401001-00013.
Mekuria, L. A., Sprangers, M. A. G., Prins, J. M., Yalew, A. W., & Nieuwkerk, P. T. (2015). Health-related quality of life of HIV-infected adults receiving combination antiretroviral therapy in Addis Ababa. AIDS Care, 27(8), 934.
Cowdery, J. E., & Pesa, J. A. (2002). Assessing quality of life in women living with HIV infection. AIDS Care, 14(2), 235–245. doi:10.1080/09540120220104730.
Tran, B. X., Ohinmaa, A., Nguyen, L. T., Nguyen, T. A., & Nguyen, T. H. (2011). Determinants of health-related quality of life in adults living with HIV in Vietnam. AIDS Care, 23(10), 1236–1245. doi:10.1080/09540121.2011.555749.
Basavaraj, K. H., Navya, M. A., & Rashmi, R. (2010). Quality of life in HIV/AIDS. Indian Journal of Sexually Transmitted Diseases and AIDS, 31(2), 75–80. doi:10.4103/0253-7184.74971.
Bengtson, A. M., Pence, B. W., O’Donnell, J., Thielman, N., Heine, A., Zinski, A., et al. (2015). Improvements in depression and changes in quality of life among HIV-infected adults. AIDS Care, 27(1), 47–53. doi:10.1080/09540121.2014.946386.
Zimpel, R. R., & Fleck, M. P. (2014). Depression as a major impact on the quality of life of HIV-positive Brazilians. Psychology, Health and Medicine, 19(1), 47–58. doi:10.1080/13548506.2013.772302.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. For this type of study, formal consent is not required.
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Alsayed, N.S., Sereika, S.M., Albrecht, S.A. et al. Testing a model of health-related quality of life in women living with HIV infection. Qual Life Res 26, 655–663 (2017). https://doi.org/10.1007/s11136-016-1482-4
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DOI: https://doi.org/10.1007/s11136-016-1482-4