Publication

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

Downloadable Content

Persistent URL
Last modified
  • 05/20/2025
Type of Material
Authors
    Kerlly J Bernabe, Tulane UniversityMark Siedner, Africa Health Research Institute, KwaZulu-NatalAlexander C Tsai, Harvard Medical SchoolVincent Marconi, Emory UniversityRichard A Murphy, Geisel School of Medicine at Dartmouth
Language
  • English
Date
  • 2022-05-01
Publisher
  • OXFORD UNIV PRESS INC
Publication Version
Copyright Statement
  • © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 9
Issue
  • 5
Start Page
  • ofac121
End Page
  • ofac121
Grant/Funding Information
  • This research was supported by the UCLA-Clinical and Translational Research Institute (UCLA-CTSI) at Lundquist/Harbor-UCLA and from the Emory Center for AIDS Research (P30 AI050409).
Supplemental Material (URL)
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.
Author Notes
  • Richard A. Murphy, MD, MPH, VA Medical Center, 295 N. Main St, White River Junction, VT 05009. Email: ramurphy@gmail.com
Keywords
Research Categories
  • Health Sciences, Public Health

Tools

Relations

In Collection:

Items