Detection of HIV Virologic Failure and Switch to Second-Line Therapy: A Systematic Review and Meta-analysis of Data From Sub-Saharan Africa

Author:

Bernabé Kerlly J1,Siedner Mark2345,Tsai Alexander C45,Marconi Vincent C678,Murphy Richard A910

Affiliation:

1. Department of Tropical Medicine, Tulane University School of Public Health and Tropical Medicine, New Orleans, Louisiana, USA

2. Africa Health Research Institute, KwaZulu-Natal, South Africa

3. Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, Massachusetts, USA

4. Harvard Medical School, Boston, Massachusetts, USA

5. Center for Global Health, Massachusetts General Hospital, Boston, Massachusetts, USA

6. Emory University School of Medicine and Rollins School of Public Health, Atlanta, Georgia, USA

7. Emory University Vaccine Center, Atlanta, Georgia, USA

8. Atlanta Veterans Affairs Medical Center, Decatur, Georgia, USA

9. Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA

10. Veterans Affairs Medical Center, White River Junction, Vermont, USA

Abstract

Abstract Background The late recognition of virologic failure (VF) places persons with HIV in Sub-Saharan Africa at risk for HIV transmission, disease progression, and death. We conducted a systematic review and meta-analysis to determine if the recognition and response to VF in the region has improved. Methods We searched for studies reporting CD4 count at confirmed VF or at switch to second-line antiretroviral therapy (ART). Using a random-effects metaregression model, we analyzed temporal trends in CD4 count at VF—or at second-line ART switch—over time. We also explored temporal trends in delay between VF and switch to second-line ART. Results We identified 26 studies enrolling patients with VF and 10 enrolling patients at second-line ART switch. For studies that enrolled patients at VF, pooled mean CD4 cell count at failure was 187 cells/mm3 (95% CI, 111 to 263). There was no significant change in CD4 count at confirmed failure over time (+4 cells/year; 95% CI, –7 to 15). Among studies that enrolled patients at second-line switch, the pooled mean CD4 count was 108 cells/mm3 (95% CI, 63 to 154). CD4 count at switch increased slightly over time (+10 CD4 cells/year; 95% CI, 2 to 19). During the same period, the mean delay between confirmation of VF and switch was 530 days, with no significant decline over time (–14 days/year; 95% CI, –58 to 52). Conclusions VF in Africa remains an event recognized late in HIV infection, a problem compounded by ongoing delays between VF and second-line switch.

Funder

UCLA-Clinical and Translational Research Institute

Emory Center for AIDS Research

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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