Late entry to HIV care among latinos compared with non-latinos in a southeastern US cohort

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Abstract

Background: Late diagnosis of human immunodeficiency virus (HIV) infection remains common despite advances in therapy and prognosis. The southeastern United States is a rapidly growing Latino settlement area where ethnic disparities may contribute to late presentation to care. Methods: We assessed demographic and clinical factors between racial/ethnic groups at the time of HIV care initiation in the University of North Carolina Center for AIDS Research Clinical Cohort. We identified independent predictors of late presentation, defined as a CD4 + T lymphocyte (CD4) count, 350 cells/mm 3 or an AIDS-defining event (ADE), using log-linear binomial regression. Results: During the period 1999-2009, 853 patients initiated HIV care, of whom 11% were Latino, 28% were white, and 61% were black. Median initial CD4 counts were lower for Latino patients (186 cells/mm 3) than white patients (292 cells/mm 3; P = .006) and black patients (302 cells/mm 3; P = .02). Latino persons were more likely to be late presenters than white or black persons (76% vs 58%; P < .001) and accounted for 86%, 75%, and 50% of all presenting cases of active tuberculosis, histoplasmosis, and toxoplasmosis, respectively. Latino ethnicity, older age, male sex, and earlier entry year were independently associated with late presentation (P < .05 for all). In multivariable analyses, Latino persons were 1.29 times more likely to present to care late than white or black persons (95% confidence interval, 1.15-1.45). Conclusions: Latinos are more likely to initiate HIV care later in the course of illness than are black and white persons and account for a majority of several ADEs. Strategies to improve earlier HIV testing among Latinos in new settlement areas are needed. © The Author 2011.

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Dennis, A. M., Napravnik, S., Seña, A. C., & Eron, J. J. (2011). Late entry to HIV care among latinos compared with non-latinos in a southeastern US cohort. Clinical Infectious Diseases, 53(5), 480–487. https://doi.org/10.1093/cid/cir434

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