Abstract

BackgroundIn the era of anti-retroviral therapy (ART), the plasma HIV viral load (VL) is an important primary indicator for monitoring the HIV treatment response. To optimize the clinical management of HIV/AIDS patients, we investigated VL high-risk events related to virological failure (VF) and further explored the preventive factors of VL high-risk events.MethodsThe data were derived from China’s HIV/AIDS Comprehensive Response Information Management System. HIV infected patients who initiated or received ART in Guangxi between 2003 and 2019 were included. The contributions of VL after 6 months of ART to VF and AIDS-related death were analysed by Kaplan-Meier curves, log-rank tests and Cox regression analyses. Both descriptive analyses and bivariate logistic regression were employed to further explore the preventive factors related to VL high-risk events of VF.ResultsThe cumulative rates of VF in the high low-level viremia group (high LLV) (χ2 = 18.45; P < 0.001) and non-suppressed group (χ2 = 82.99; P < 0.001) were significantly higher than those in the viral suppression (VS) group. Therefore, the VL high-risk events of VF was defined as highest VL > 200 copies/ml after 6 months of ART. Compared with the VS group, the adjusted hazard risk was 7.221 (95% CI: 2.668; 19.547) in the high LLV group and 8.351 (95% CI: 4.253; 16.398) in the non-suppressed group. Compared with single patients, married or cohabiting (AOR = 0.591; 95% CI: 0.408, 0.856) and divorced or separated (AOR = 0.425, 95% CI: 0.207, 0.873) patients were negatively associated with VL high-risk events. So were patients acquired HIV homosexually (AOR = 0.572; 95% CI: 0.335, 0.978). However, patients who had ART modification were 1.728 times (95% CI: 1.093, 2.732) more likely to have VL high-risk events, and patients who used cotrimoxazole during ART were 1.843 times (95% CI: 1.271, 2.672) more likely to have VL high-risk events.ConclusionsA VL greater than 200 copies/ml is a VL high-risk event for VF. Intervention measurements should be adopted to optimize the surveillance of ART in patients who are single or widowed, who have ART modification, and who use cotrimoxazole during ART.

Highlights

  • In the era of anti-retroviral therapy (ART), the plasma Human immunodeficiency virus (HIV) viral load (VL) is an important primary indicator for monitoring the HIV treatment response

  • To optimize the clinical management of HIV/acquired immunodeficiency syndrome (AIDS) patients, we investigated the risk events related to virological failure (VF) and AIDS-related death based on the data of patients who initiated or received ART in Guangxi between 2003 and 2019 exported from China’s HIV/AIDS Comprehensive Response Information Management System (CRIM S)

  • After 6 months of ART, VF and AIDS-related death were set as the outcome indicators when following HIV patients

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Summary

Introduction

In the era of anti-retroviral therapy (ART), the plasma HIV viral load (VL) is an important primary indicator for monitoring the HIV treatment response. Human immunodeficiency virus (HIV) infection and acquired immunodeficiency syndrome (AIDS) are threats to public health worldwide. The World Health Organization (WHO) estimated that 38 million individuals worldwide were living with HIV by the end of 2019 [1], and nearly 1.7 million of them were new HIV infections [2]. Antiretroviral therapy (ART) is applied to treat HIV-1 infection and improve the life expectancy of HIV/ AIDS patients. To mark the roadmap to the elimination of the AIDS epidemic as a public health threat by 2030 [3], the Joint United Nations Programme on HIV and AIDS (UNAIDS) set the global targets to have 90% of all HIVinfected individuals being diagnosed, 90% of those diagnosed being on ART and 90% of those on ART achieving viral suppression by 2020 (90–90-90 goal). At the beginning of 2021, the 90–90-90 goal has fallen short

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