Viral Load Status Before Switching to Dolutegravir-Containing Antiretroviral Therapy and Associations With Human Immunodeficiency Virus Treatment Outcomes in Sub-Saharan Africa

被引:11
作者
Romo, Matthew L. [1 ,2 ]
Edwards, Jessie K. [3 ]
Semeere, Aggrey S. [4 ]
Musick, Beverly S. [5 ]
Urassa, Mark [6 ]
Odhiambo, Francesca [7 ]
Diero, Lameck [8 ]
Kasozi, Charles [9 ]
Murenzi, Gad [10 ]
Lelo, Patricia [11 ]
Wyka, Katarzyna [1 ,2 ]
Kelvin, Elizabeth A. [1 ,2 ]
Sohn, Annette H. [12 ]
Wools-Kaloustian, Kara K. [13 ]
Nash, Denis [1 ,2 ]
机构
[1] CUNY, Grad Sch Publ Hlth & Hlth Policy, Dept Epidemiol & Biostat, New York, NY 10021 USA
[2] CUNY, Grad Sch Publ Hlth & Hlth Policy, Inst Implementat Sci Populat Hlth, New York, NY 10021 USA
[3] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27515 USA
[4] Makerere Univ, Infect Dis Inst, Kampala, Uganda
[5] Indiana Univ Sch Med, Dept Biostat & Hlth Data Sci, Indianapolis, IN 46202 USA
[6] Natl Inst Med Res, Mwanza, Tanzania
[7] Kenya Govt Med Res Ctr, Ctr Microbiol Res, Nairobi, Kenya
[8] Moi Univ, Coll Hlth Sci, Sch Med, Eldoret, Kenya
[9] Masaka Reg Referral Hosp, Masaka, Uganda
[10] Rwanda Mil Hosp, Kigali, Rwanda
[11] Kalembelembe Pediat Hosp, Kinshasa, DEM REP CONGO
[12] AmfAR Fdn AIDS Res, TREAT Asia, Bangkok, Thailand
[13] Indiana Univ Sch Med, Dept Med, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
antiretroviral agents; clinical decision-making; HIV integrase inhibitors; viral load; prognosis; ADVANCED HIV DISEASE; LOW-LEVEL VIREMIA; DRUG-RESISTANCE; VIROLOGICAL FAILURE; RETENTION; TENOFOVIR; PROGRAMS;
D O I
10.1093/cid/ciab1006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients who switched to dolutegravir with a viral load >= 1000 copies/mL or without a recent test had worse subsequent outcomes than those known to be suppressed. These findings have implications for clinical care and surveillance as dolutegravir is implemented. Background Dolutegravir is being rolled out globally as part of preferred antiretroviral therapy (ART) regimens, including among treatment-experienced patients. The role of viral load (VL) testing before switching patients already on ART to a dolutegravir-containing regimen is less clear in real-world settings. Methods We included patients from the International epidemiology Databases to Evaluate AIDS consortium who switched from a nevirapine- or efavirenz-containing regimen to one with dolutegravir. We used multivariable cause-specific hazards regression to estimate the association of the most recent VL test in the 12 months before switching with subsequent outcomes. Results We included 36 393 patients at 37 sites in 5 countries (Democratic Republic of the Congo, Kenya, Rwanda, Tanzania, Uganda) who switched to dolutegravir from July 2017 through February 2020, with a median follow-up of approximately 11 months. Compared with those who switched with a VL <200 copies/mL, patients without a recent VL test or with a preswitch VL >= 1000 copies/mL had significantly increased hazards of an incident VL >= 1000 copies/mL (adjusted hazard ratio [aHR], 2.89; 95% confidence interval [CI], 1.99-4.19 and aHR, 6.60; 95% CI, 4.36-9.99, respectively) and pulmonary tuberculosis or a World Health Organization clinical stage 4 event (aHR, 4.78; 95% CI, 2.77-8.24 and aHR, 13.97; 95% CI, 6.62-29.50, respectively). Conclusions A VL test before switching to dolutegravir may help identify patients who need additional clinical monitoring and/or adherence support. Further surveillance of patients who switched to dolutegravir with an unknown or unsuppressed VL is needed.
引用
收藏
页码:630 / 637
页数:8
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