Health related quality of life and psychosocial correlates among HIV-infected adolescent and young adult women in the US

AIDS Education and Prevention

Volumn 23, Issue 4, 2011, Pages 367-381

  Andrinopoulos, Katherine ^a   Clum, Gretchen ^a   Murphy, Debra A ^b   Harper, Gary ^c   Perez, Lori ^d   Xu, Jiahong ^d   Cunningham, Shayna ^e   Ellen, Jonathan M ^f  

^a TULANE UNIVERSITY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c DEPAUL UNIVERSITY   (United States)

^d WESTAT   (United States)

^e Sociometrics Corporation   (United States)

^f JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ANXIETY; ARTICLE; CD4 LYMPHOCYTE COUNT; CONTROLLED STUDY; CORRELATION ANALYSIS; DEPRESSION; FEMALE; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS INFECTED PATIENT; HUMAN IMMUNODEFICIENCY VIRUS INFECTION; LIFE SATISFACTION; LINEAR REGRESSION ANALYSIS; MAJOR CLINICAL STUDY; MULTIPLE LINEAR REGRESSION ANALYSIS; PSYCHOSOCIAL CARE; QUALITY OF LIFE; SOCIAL SUPPORT; STATISTICAL SIGNIFICANCE; STIGMA; UNITED STATES; VIRUS LOAD; WELLBEING;

ADAPTATION, PHYSIOLOGICAL; ADOLESCENT; ANXIETY; ATTITUDE TO HEALTH; CD4 LYMPHOCYTE COUNT; DEPRESSION; FEMALE; HEALTH STATUS; HIV INFECTIONS; HUMANS; QUALITY OF LIFE; QUESTIONNAIRES; REGRESSION ANALYSIS; SOCIAL STIGMA; SOCIAL SUPPORT; UNITED STATES; VIRAL LOAD; YOUNG ADULT;

EID: 80052047231     PISSN: 08999546     EISSN: None     Source Type: Journal    
DOI: 10.1521/aeap.2011.23.4.367     Document Type: Article

References (45)

1. Aaronson, N.K., Meyerowitz B.E., Bard M., Bloom J.R., Fawzy F.I,. Feldstein M et al. (1991). Quality of life research in oncology. Past achievements and future priorities. Cancer, 67, 839-843.
2. Berger, B.E., 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, 518-529.
3. Buseh, A. Kelber, S., Stevens, P., & Park, C. (2008). Relationship of Symptoms, Perceived Health, and Stigma With Quality of Life Among Urban HIV-Infected African American Men. Public Health Nursing, 25(5), 409-419.
4. Carrico, A.W., Antoni, M.H., Duran, R.E., Ironson, G., Penedo, F., Fletcher, M.A., Kimas, N., Schneiderman, N. (2006). Reductions in depressed mood and denial coping during cognitive behavioral stress management with HIV-Positive gay men treated with HAART. Annals of Behavioral Medicine, Vol. 31(2): 155-164.
5. Centers for Disease Control and Prevention. (2007a). HIV/AIDS Surveillance Report, 19. Retrieved January 28, 2009, from http://cdc.gov/hiv/topics/surveillance/resources/reports
6. Centers for Disease Control and Prevention. (2007b). HIV prevalence among selected populations: Youth populations. Retrieved January 29, 2009 from http://cdc.gov/hib/topics/teting/resources/reportshiv_prevalence
7. Chin, J., Botsko, M., Behar, E., & Finkelstein, R. (2009). More than ancillary: HIV social services, intermediate outcomes and quality of life. AIDS Care, 21(10), 1289-1297.
8. Chung, L., Pan, A., & Hsiung, P. (2009). Quality of life for patients with major depression in Taiwan: A model-based study of predictive factors. Psychiatry Research, 168, 153-162.
9. Clayson, D., Wild, D., Quarterman, P., Duprat-Lomon, I., Kubin, M., & Coons, S. (2006). A comparative review of the health-related quality-of-life measures for use in HIV/ AIDS clinical trials. Pharamcoeconomics, 24 (8), 751-765.
10. Corrigan, P. (2004). How stigma interferes with mental health care. American Psychology, 59, 614-625.
11. Croog, S.H., & Levine, S. (1989). Quality of life and health care interventions. In H.E. Freeman & S. Levine (Eds.), Handbook of Medical sociology. (4th ed. pp. 508-528). New Jersey: Prentice Hall.
12. Department of Health and Human Services Panel on Antiretorviral Guidelines for Adults and Adolescents. (2008). Guidelines for the use of Antiretroviral agents in HIV-1 infected adults and adolescents. Retrieved January1, 2010, from http://www.aidsinfo.nih.gov/ContentFiles/AdultAdolescentGL.pdf
13. Evers, A.W.M., Kraaimaat, F.W., van Lankveld, W., Jongen, P.J.H., Jacobs, J.W.G., & Bijlsma, J.W.J. (2002). Beyond unfavorable thinking: The illness cognition questionnaire for chronic diseases. Journal of Consulting and Clinical Psychology, 69, 1026-1036.
14. Garrison, C.Z., Addy, C.L., Jackson, K.L., McKeown, R.E., & Waller, J.L (1991). The CESD as a screen for depression and other psychiatric disorders in adolescents. Journal of the American Academy of Child and Adolescent Psychiatry, 30, 636-641.
15. Garvie, P., Lawford, J., Banet, M., & West, R. (2009). Quality of life measurement in paediatric and adolescent populations with HIV: a review of the literature. Child: Care, Health and Development, 35(4), 440-453.
16. Gortmaker, S.L., Lenderking, W.R., Clark, C., Lee, S., Glenn Fowler, M., Oleske, J.M. et al. (1998). Development and use of a pedi atric quality of life questionnaire in AIDS clinical trials: reliability and validity of the general health assessment in children. In D. Droter (Ed.). Measuring health-related quality of life in children and adolescents: Implications for research and practice (pp. 219-235). Mahwah, NJ: Erlbaum.
17. Greeff, M., Uys, L., Wantland, D., Makoae, L., Chirwa, M., Dlamini, P., et al. (2009). Percieved HIV stigma and life satisfaction among persons living with HIV infection n five African countries: A longitudinal study. International Journal of Nursing Studies. DOI: 10.1016/j.ijnurstu.2009.09.008.
18. Jacobson, A.M., de Groot, M., & Samson, J.A. (1994). The evaluation of two measures of quality of life in patients with type I and type II diabetes. Diabetes Care, 17, 267-274.
19. Jacobson, A.M., & Fried, K. (1998). Conceptual issues in developing quality of life assessments for children: Illustrations from studies of insulin-dependent diabetes mellitus. In D. Drotar (Ed.), Measuring Health-related Quality of Life in Children and Adolescents: Implications for research and practice (pp. 131-150). Mahwah, NJ: Erlbaum.
20. Larios, S., Davis, J., Gallo, L., Heinrich, J., & Talavera, G. (2009). Concerns about stigma, social support and quality of life in lowincome HIV-positive Hispanics. Ethnicity & Disease. Vol. 19: 65-70.
21. Lenderking, W.R., Testa, M.A., Katzenstein, D., & Hammer, S. (1997). Measuring quality of life in early HIV disease: The modular approach. Quality of Life Research, 6, 515-530.
22. Liu, C., Ostrow, D., Detels, R., Hu, S., Johnson, L., Kingsley, L., et al. (2006). Impacts of HIV infection and HAART use on quality of life. Quality of Life Research, 15, 941-949.
23. Murphy, D.A., Belzer, M., Durako, S.J., Sarr, M., Wilson, C.M., & Muenz, L.R. (2005). Longitudinal antiretroviral adherence among HIV-infected adolescents. Archives of Pediatrics, 159, 764-770.
24. Orban, L., Stein, R., Koenig, L., Conner, L.C., Rexhouse, E.L., Lewis, J.V., et al (2010). Coping strategies of adolescents living with HIV: Disease-specific stressors and responses. AIDS Care. DOI: 10.1080/09540120903193724.
25. Patel, R., Kassaye, S., Gore-Felton, C., Wyshak, G., Kadizrange, G., Woelk, G., et al. (2009). Quality of life, psychosocial health, and antiretroviral therapy among HIV-positive women in Zimbabwe. AIDS Care, 21(12), 1517-1527.
26. Pearson, C.R., Micek, M.A., Pfeiffer, J., Montoya, P., Matediane, E., Jonasse, T., et al. (2009). One year after ART initiation: psychosocial factors associated with stigma among Mozambicans. AIDS and Behavior, Vol. 13(6): 1189-1196.
27. Radloff, L.S. (1977). The CES-D Scale: A selfreport depression scale for research in the general population. Applied Psychological Measurement,1, 385-401.
28. Rao, D., Hahn, E., Cella, D., & Hernandez, L. (2007). The health related quality of life outcomes of English and Spanish Speaking persons living with HIV/AIDS from the continental United States and Puerto Rico. AIDS Patient Care and STDs, 21(5), 339-346.
29. Reynolds, NR, Neidig, AW, Wu, AL, Gifford, AL, & Holmes, WC (2006). Balancing disfigurement and fear of disease progression: Patient perceptions of HIV body fat redistribution. AIDS Care, 18, 663-673.
30. Russell, D., Cutrona, C.E., Rose, J., Yurko, K. (1984). Social and emotional loneliness: An examination of Weiss's typology of loneliness. Journal of Personality and Social Psychology, Vol. 46: 1313-1321.
31. Sherbourne, C.D., Hays, R.D., Fleishman, J.A., Vitiello, B., Magruder, K.M., Bing, E.G., et al. (2000). Impact of psychiatric conditions on health-related quality of life in persons with HIV infection. American Journal of Psychiatry, 157, 248-254.
32. Smith, K.W., Avis, N.E., & Assmann, S.F. (1999). Distinguishing between quality of life and health status in quality of life research. Quality of Life Research, 8(5), 447-459.
33. Smith, R., Rossetto, K., & Peterson, B. 2008. A meta analysis of disclosure of one's HIV positive status, stigma and social support. AIDS Care, 20(10), 1266-1275.
34. Solomon, S., Batavia, A., Venkatesh, K., Brown, L., Verma, P., Cecelia, A., et al. (2009). A Longitudinal quality-of-life study of HIV infected persons in South India: The case for comprehensive clinical care and support services. AIDS Education and Prevention, 21(2), 104-112.
35. Sowell, R.L., Seals, B.F., Moneyham, L., Demi, A., Cohen, L., & Brake, S. (1999). Quality of life in HIV-infected women in the southeastern United States. AIDS Care, 9, 501-512.
36. Spitzer, W.O. (1987). State of science 1986: Quality of life and functional status as target variables for research. Journal of Chronic Diseases, 40, 465-471.
37. Staring, A.B.P., Ven der Gaag, M., Van den Berge, M., Duivenvoorden, H.J., & Mulder, C.L. (2009). Stigma moderates the associations of insight with depressed mood, low self-esteem, and low quality of life in patients with schizophrenia. Schizophrenia Research, 115(2-3), 363-369.
38. Subramanian, T., Gupte, M.D., Dorairaj, V.S., Preiannan, V., & Mathai, A.K. (2009). Psychosocial impact and quality of life of people living with HIV/AIDS in South India. AIDS Care, 21(4). 473-481.
39. Tate, D., Paul, R.H., Flanigan, T.P., Tashima, K., Nash, J., Adair, C., et al., (2003). The impact of apathy and depression on quality of life in patients infected with HIV. AIDS Patient Care and STDs, 17, 115-120.
40. Thomas, B.E., REhman, F., Suryanarayanan, D., Josephine, K., Dilip, M., Dorairaj, V.S., et al. (2005). How stigmatizing is stigma in the life of people living with HIV: A study on the HIV positive individuals from Chennai, South India. AIDS Care, 17(7), 795-801.
41. Wilson, I.B., & Cleary, P.D. (1995). Linking clinical variables with health-related quality of life. A conceptual model of patient outcomes. Journal of the American Medical Association, 273, 59-65.
42. Wingood, G., DiClemente, R.J., Harrington, K., & Davies, S. (2002). Body image and African American females' sexual health. Journal of Women's Health and Gender Based Medicine, 11, 433-439.
43. World Health Organization. (1946). Preamble to the Constitution of the World Health Organization as adopted by the International Health Conference. New York.
44. Wu, D., Munoz, M., Espiritu, B., Zeladita, J., Sanchez, E., Cllacna, M., et al. (2008). Burden of Depression Among Impoverished HIV Positive Women in Peru. Epidemiology and Social Science, 48(4), 500-504.
45. Yadav, S. (2010). Perceived social support, hope, and quality of life of persons living with HIV/AIDS: a case study from Nepal. Quality of Life Research, Vol. 19 (2): 157-166.