Sex, Race, and HIV Risk Disparities in Discontinuity of HIV Care After Antiretroviral Therapy Initiation in the United States and Canada

被引:51
作者
Rebeiro, Peter F. [1 ]
Abraham, Alison G. [2 ]
Horberg, Michael A. [3 ]
Althoff, Keri N. [2 ]
Yehia, Baligh R. [4 ]
Buchacz, Kate [5 ]
Lau, Bryan M. [2 ]
Sterling, Timothy R. [1 ]
Gange, Stephen J. [2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Med, Div Infect Dis, 1161 21st Ave South,A-2200 Med Ctr North, Nashville, TN 37212 USA
[2] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[3] Kaiser Permanente Midatlantic States, Midatlantic Permanente Res Inst, Rockville, MD USA
[4] Univ Penn, Dept Med, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Ctr Dis Control & Prevent, Div HIV AIDS Prevent, Atlanta, GA USA
基金
美国医疗保健研究与质量局; 美国国家卫生研究院; 加拿大健康研究院;
关键词
discontinuity; injection drug use; NA-ACCORD; racial; retention; sex; disparity; DEPARTMENT-OF-HEALTH; INFECTED PERSONS; CLINICAL COHORT; MISSED VISITS; AIDS RESEARCH; FOLLOW-UP; RETENTION; SURVIVAL; GENDER; PHYSICIANS;
D O I
10.1089/apc.2016.0178
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Disruption of continuous retention in care (discontinuity) is associated with HIV disease progression. We examined sex, race, and HIV risk disparities in discontinuity after antiretroviral therapy (ART) initiation among patients in North America. Adults (>= 18 years of age) initiating ART from 2000 to 2010 were included. Discontinuity was defined as first disruption of continuous retention (>= 2 visits separated by > 90 days in the calendar year). Relative hazard ratio (HR) and times from ART initiation until discontinuity by race, sex, and HIV risk were assessed by modeling of the cumulative incidence function (CIF) in the presence of the competing risk of death. Models were adjusted for cohort site, baseline age, and CD4(+) cell count within 1 year before ART initiation; nadir CD4(+) cell count after ART, but before a study event, was assessed as a mediator. Among 17,171 adults initiating ART, median follow-up time was 3.97 years, and 49% were observed to have >= 1 discontinuity of care. In adjusted regression models, the hazard of discontinuity for patients was lower for females versus males [HR: 0.84; 95% confidence interval (CI): 0.79-0.89] and higher for blacks versus non-blacks (HR: 1.17; 95% CI: 1.12-1.23) and persons with injection drug use (IDU) versus non-IDU risk (HR: 1.33; 95% CI: 1.25-1.41). Sex, racial, and HIV risk differences in clinical retention exist, even accounting for access to care and known competing risks for discontinuity. These results point to vulnerable populations at greatest risk for discontinuity in need of improved outreach to prevent disruptions of HIV care.
引用
收藏
页码:129 / 144
页数:16
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