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Negotiating Control of HIV: A Qualitative Analysis of HIV-Positive Latino MSM in North Carolina

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Abstract

The majority of HIV disease management happens outside of clinical encounters. As such, understanding how HIV fits into the lives of patients is key to improving HIV outcomes. The concept of control is a vital part of the social context within which health is managed. This qualitative study explores how a sample of Latino men who have sex with men living with HIV in North Carolina (n = 16) conceptualize and negotiate control in the context of living with HIV. We found that participants use a range of strategies to exert control over their lives including: understanding their infection, engaging with health care, and developing relationships with health professionals. By considering how individuals make sense of their HIV diagnosis and integrate it into their lives, HIV providers can direct efforts at strategic points of control decision-making and advanced clinicians can prioritize issues to address during clinical encounters.

Resumen

Mayormente el manejo de la enfermedad de HIV sucede fuera de los encuentros clínicos. Como tal, entender como es la vida de los pacientes con HIV es fundamental para mejorar los resultados de VIH. Conceptualmente el control es una parte clave del contexto social dentro del cual se maneja el cuidado de la salud. Este estudio cualitativo explora cómo una muestra de hombres latinos que tienen sexo con hombres y viven con VIH en Norte Carolina (n = 16) conceptualizan y negocian control en el contexto de la vida con VIH. Encontramos que los participantes usan un rango de estrategias para mantener el control sobre sus vidas incluyendo: entender su infección, vincularse al sistema de salud, y desarrollar relaciones con los profesionales de salud. Considerando como cada individuo entiende su diagnóstico de HIV e integra este a sus vidas, los proveedores pueden dirigir sus esfuerzos estratégicamente a los momentos claves cuando los pacientes toman decisiones relacionadas al control de su condición y priorizar los temas que se deben tratar en los encuentros clínicos.

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References

  1. Derose KP, Escarce JJ, Lurie N. Immigrants and health care: sources of vulnerability. Health Aff. 2007;26(5):1258–68.

    Article  Google Scholar 

  2. National HIV/AIDS Strategy. Washington, DC; 2010. https://www.whitehouse.gov/sites/default/files/uploads/NHAS.pdf.

  3. Centers for Disease Control and Prevention. HIV surveillance report, 2014. Vol. 26; 2014 http://www.cdc.gov/hiv/library/reports/surveillance/. Accessed 12 Jan 2017.

  4. Foucault M. Power/knowledge: selected interviews and other writings, 1972–1977. In: Gordon C, editor. New York: Vintage; 1980.

  5. Freire P. Pedagogy of the oppressed. New York: Continuum International Publishing Group; 1970.

    Google Scholar 

  6. Greenaway KH, Haslam SA, Cruwys T, Branscombe NR, Ysseldyk R, Heldreth C. From, “we” to “me”: group identification enhances perceived personal control with consequences for health and well-being. J Pers Soc Psychol. 2015;109(1):53–74.

    Article  Google Scholar 

  7. Grob A. perceived control and subjective well-being across nations and across the life span. In: Diener E, Suh EM, editors. Culture and subjective well-being. Cambridge: MIT Press; 2000. p. 319–39.

    Google Scholar 

  8. Wallston KA, Wallston BS, Smith S, Dobbins CJ. Perceived control and health. Curr Psychol Res Rev. 1987;6(1):5–25.

    Article  Google Scholar 

  9. Gabay G. Perceived control over health, communication and patient-physician trust. Patient Educ Couns. 2015;98(12):1550–7. https://doi.org/10.1016/j.pec.2015.06.019.

    Article  Google Scholar 

  10. Wallston BS, Wallston KA. Locus of control and health: a Review of the literature. Health Educ Monogr. 1978;6:107–17.

    Article  CAS  Google Scholar 

  11. Simoni JM, Ng MT. Abuse, health locus of control, and perceived health among HIV-positive women. Health Psychol. 2002;21(1):89–93.

    Article  Google Scholar 

  12. Spalding AD. Racial Minorities and other high-risk groups with HIV and AIDS at increased risk for psychological adjustment problems in association with health locus of control orientation. Soc Work Health Care. 1995;21(3):81–114.

    Article  CAS  Google Scholar 

  13. Wallerstein NB, Duran B. Using community-based participatory research to address health disparities. Health Promot Pract. 2006;7(3):312–23. https://doi.org/10.1177/1524839906289376.

    Article  PubMed  Google Scholar 

  14. Foucault M. The history of sexuality volume 1: an introduction. New York: Vintage; 1978.

    Google Scholar 

  15. Smith K. Fostering regimes of truth: understanding and reflecting on the freedom school way. Pedagog Cult Soc. 2010;18(2):191–209.

    Article  Google Scholar 

  16. Wallerstein NB, Yen IH, Syme SL. Integration of social epidemiology and community-engaged interventions to improve health equity. Am J Public Health. 2011;101(5):822–30.

    Article  Google Scholar 

  17. Arreola S, Santos GM, Beck J, Sundararaj M, Wilson PA, Hebert P, et al. Sexual stigma, criminalization, investment, and access to HIV services among men who have sex with men worldwide. AIDS Behav. 2014;19:227–34.

    Article  Google Scholar 

  18. Viruell-Fuentes EA, Miranda PY, Abdulrahim S. More than culture: structural racism, intersectionality theory, and immigrant health. Soc Sci Med. 2012;75(12):2099–106. https://doi.org/10.1016/j.socscimed.2011.12.037.

    Article  PubMed  Google Scholar 

  19. Department of Health and Human Services. Guidelines for the use of antiretroviral agents in HIV-1-infected adults and adolescents; 2016. http://aidsinfo.nih.gov/guidelines. Accessed from 24 Feb 2017.

  20. Beach MC, Price EG, Gary TL, Robinson KA, Gozu A, Palacio A, et al. Cultural competence: a systematic review of health care provider educational interventions. Med Care. 2005;43(4):356–73.

    Article  Google Scholar 

  21. Chariyeva Z, Golin CE, Earp JA, Maman S, Suchindran C, Zimmer C. The role of self-efficacy and motivation to explain the effect of motivational interviewing time on changes in risky sexual behavior among people living with HIV: a mediation analysis HHS public access. AIDS Behav. 2013;17(2):813–23.

    Article  Google Scholar 

  22. Parsons JT, Rosof E, Punzalan JC, Di Maria L. Integration of motivational interviewing and cognitive behavioral therapy to improve HIV medication adherence and reduce substance use among HIV-positive men and women: results of a pilot project. AIDS Patient Care STDS. 2005;19(1):31–9.

    Article  Google Scholar 

  23. Pappas G, Yujiang J, Seiler N, Malcarney M-B, Horton K, Shaikh I, et al. Perspectives on the role of patient-centered medical homes in HIV care. Am J Public Health. 2014;104(7):49–53. https://doi.org/10.2105/AJPH.2014.302022.

    Article  Google Scholar 

  24. Spiegel HML, Futterman DC. Adolescents and HIV: prevention and clinical care. Curr HIV/AIDS Rep. 2009;6:100–7.

    Article  Google Scholar 

  25. Abraído-Lanza AF, Echeverría SE, Flórez KR. Latino immigrants, acculturation, and health: promising new directions in research. Annu Rev Public Health. 2016;37(1):219–36.

    Article  Google Scholar 

  26. Rao JK, Anderson LA, Inui TS, Frankel RM. Communication interventions make a difference in conversations between physicians and patients: a systematic review of the evidence. Med Care. 2007;45(4):340–9.

    Article  Google Scholar 

  27. Martin ML, Heron SL, Moreno-Walton L, Jones AW, editors. Diversity and inclusion in quality patient care. New York: Springer; 2015.

    Google Scholar 

  28. Institute Of Medicine. Unequal treatment: confronting racial and ethnic disparities in health care. In: Smedley BD, Stith AY, Nelson AR, editors. Washington, DC: National Academies Press; 2003. http://www.nap.edu/catalog/12875.

  29. VargasBustamante A, Fang H, Rizzo JA, Ortega AN, Bustamante AV, Rizzo JA, et al. Understanding observed and unobserved health care access and utilization disparities among U.S. Latino adults. Med Care Res Rev. 2009;66(5):561–77.

    Article  Google Scholar 

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Acknowledgements

This study was funded by Health Resources and Services Administration (HRSA), Grant # 1 H97HA26505-01-00.

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Correspondence to Yesenia Merino.

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All authors declare that they have no conflicts of interest.

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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.

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Merino, Y., Barrington, C., Villa-Torres, L. et al. Negotiating Control of HIV: A Qualitative Analysis of HIV-Positive Latino MSM in North Carolina. AIDS Behav 22, 4048–4056 (2018). https://doi.org/10.1007/s10461-018-2228-9

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  • DOI: https://doi.org/10.1007/s10461-018-2228-9

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