Prevalence and predictors of persistent low-level HIV viraemia: a retrospective cohort study among people receiving dolutegravir-based antiretroviral therapy in Southern Nigeria.

IF 3.8 Q2 INFECTIOUS DISEASES Therapeutic Advances in Infectious Disease Pub Date : 2024-04-02 eCollection Date: 2024-01-01 DOI:10.1177/20499361241242240
Ogheneuzuazo Onwah, Esther Nwanja, Uduak Akpan, Otoyo Toyo, Chiagozie Nwangeneh, Babatunde Oyawola, Augustine Idemudia, Kolawole Olatunbosun, Onyeka Igboelina, Dolapo Ogundehin, Ezekiel James, Okezie Onyedinachi, Adeoye Adegboye, Andy Eyo
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Abstract

Background: Persistent low-level viraemia (PLLV) is a risk factor for virologic failure among people receiving antiretroviral therapy (ART).

Objectives: We assessed the prevalence and predictors of PLLV among individuals receiving Dolutegravir-based ART in southern Nigeria.

Design: This retrospective cohort study used routine program data from electronic medical records of persons receiving Dolutegravir-based first-line ART in 154 PEPFAR/USAID-supported health facilities in Akwa Ibom and Cross Rivers states, Nigeria.

Methods: Clients on first-line Dolutegravir-based ART ⩾6 months, who had a viral load result in the 12 months preceding October 2021 (baseline), and a second viral load result by September 2022 were included. Persons with low-level viraemia (LLV) (viral load 51-999 copies/ml) received additional adherence support. The outcome analysed was PLLV (two consecutive LLV results). Indices were summarized using descriptive statistics, and predictors of PLLV were determined using multivariate logistic regression.

Results: In total, 141,208 persons on ART were included, of which 63.3% (n = 89,944) were females. The median age was 36 [29-44] years, median ART duration was 19 [11-42] months. At the end of the study, 10.5% (14,759/141,208) had initial LLV, 90.1% (13,304/14,759) of which attained undetectable viral load (⩽50 copies/ml), and 1.1% (163/14,759) transitioned to virologic failure (⩾1000 copies/ml) by the end of the study. PLLV prevalence was 0.9% (1292/141,208). Increasing ART duration [adjusted odds ratio (aOR) = 1.0; 95% confidence interval (CI): 1.005-1.008; p < 0.001] and viral suppression (<1000 copies/ml) before initial LLV (aOR = 1.7; 95% CI: 1.50-2.00; p < 0.001) were positively associated with PLLV, while receipt of tuberculosis preventive therapy reduced the likelihood of PLLV (aOR = 0.3; 95% CI: 0.10-0.94; p = 0.039).

Conclusion: PLLV was uncommon among individuals receiving dolutegravir-based ART and was associated with longer ART duration, prior viral suppression, and non-receipt of tuberculosis preventive therapy. This strengthens recommendations for continuous adherence support and comprehensive health services with ART, to prevent treatment failure.

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持续低水平 HIV 病毒血症的流行率和预测因素:对尼日利亚南部接受基于多鲁特韦的抗逆转录病毒疗法人群的回顾性队列研究。
背景:持续低水平病毒血症(PLLV)是接受抗逆转录病毒疗法(ART)者出现病毒学失败的风险因素:持续低水平病毒血症(PLLV)是导致接受抗逆转录病毒疗法(ART)的患者出现病毒学失败的一个风险因素:我们评估了尼日利亚南部接受基于多罗替拉韦的抗逆转录病毒疗法的患者中 PLLV 的流行率和预测因素:这项回顾性队列研究使用了尼日利亚阿夸伊博姆州和克罗斯里弗斯州 154 家由 PEPFAR/USAID 支持的医疗机构中接受多鲁特韦一线抗逆转录病毒治疗者电子病历中的常规项目数据:方法:纳入接受基于多罗替拉韦的一线抗逆转录病毒疗法 ⩾6 个月的客户,这些客户在 2021 年 10 月(基线)之前的 12 个月中有病毒载量结果,并在 2022 年 9 月之前有第二次病毒载量结果。低水平病毒血症(LLV)患者(病毒载量为 51-999 拷贝/毫升)将获得额外的依从性支持。分析结果为 PLLV(连续两次 LLV 结果)。采用描述性统计对各项指标进行总结,并采用多变量逻辑回归法确定 PLLV 的预测因素:总共纳入了 141 208 名接受抗逆转录病毒疗法的患者,其中 63.3% (n = 89 944)为女性。年龄中位数为 36 [29-44] 岁,抗逆转录病毒疗法持续时间中位数为 19 [11-42] 个月。研究结束时,10.5%(14,759/141,208)的患者出现初始 LLV,其中 90.1%(13,304/14,759)的患者达到检测不到的病毒载量(⩽50 copies/ml),1.1%(163/14,759)的患者在研究结束时转为病毒学失败(⩾1000 copies/ml)。PLLV 感染率为 0.9% (1292/141208)。抗逆转录病毒疗法持续时间的延长[调整后的几率比(aOR)=1.0;95% 置信区间(CI):1.005-1.008;P P = 0.039]:PLLV在接受多罗替拉韦抗病毒治疗的患者中并不常见,它与抗病毒治疗持续时间较长、之前的病毒抑制以及未接受结核病预防治疗有关。这加强了对持续坚持抗逆转录病毒疗法的支持和全面医疗服务的建议,以防止治疗失败。
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来源期刊
CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
9 weeks
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