Desmonde Sophie, Dame Joycelyn, Malateste Karen, David Agatha, Amorissani-Folquet Madeleine, N'Gbeche Sylvie, Sylla Mariam, Takassi Elom, Eboua François Tanoh, Kouakou Kouadio, Bagnan Tossa Lehila, Yonaba Caroline, Leroy Valeriane
CERPOP, Toulouse, France
Korle Bu Teaching Hospital, Accra, Ghana.
BMJ Glob Health. 2025 Jan 14;10(1):e016512. doi: 10.1136/bmjgh-2024-016512.
We describe the 24-month incidence of Dolutegravir (DTG)-containing antiretroviral treatment (ART) initiation since its introduction in 2019 in West Africa.
We included all patients aged 0-24 years on ART from nine clinics in Côte d'Ivoire (n=4), Ghana, Nigeria, Mali, Benin, and Burkina Faso. Baseline varied by clinic and was defined as date of first DTG prescription; patients were followed up until database closure/death/loss to follow-up (LTFU, no visit ≥7 months), whichever came first. We computed the cumulative incidence function for DTG initiation; associated factors were explored in a shared frailty model, accounting for clinic heterogeneity.
Since 2019, 3350 patients were included; 47.2% were female; 78.9% had been on ART ≥12 months. Median baseline age was 12.5 years (IQR 8.4-15.8). Median follow-up was 14 months (IQR 7-22). The overall cumulative incidence of DTG initiation reached 22.7% (95% CI 21.3 to 24.2) and 56.4% (95% CI 54.4 to 58.4) at 12 and 24 months, respectively. In univariate analyses, those aged <5 years and female were overall less likely to switch. Adjusted on ART line and available viral load (VL) at baseline, females aged >10 years were less likely to initiate DTG compared with males of the same age (adjusted HR among 10-14 years: 0.62, 95% CI 0.54 to 0.72; among ≥15 years: 0.43, 95% CI 0.36 to 0.50), as were those with detectable VL (>50 copies/mL) compared with those in viral suppression (aHR 0.86, 95% CI 0.77 to 0.97) and those on PIs compared with those on non-nucleoside reverse-transcriptase inhibitors (aHR after 12 months of roll-out: 0.75, 95% CI 0.65 to 0.86).
Paediatric DTG uptake was incomplete and unequitable in west African settings: DTG use was least likely in children <5 years, females ≥10 years and those with detectable VL. Maintained monitoring and support of treatment practices is required to better ensure universal and equal uptake.
我们描述了自2019年多替拉韦(DTG)在西非引入以来,含DTG的抗逆转录病毒治疗(ART)开始的24个月发生率。
我们纳入了来自科特迪瓦(4个诊所)、加纳、尼日利亚、马里、贝宁和布基纳法索9个诊所的所有接受ART治疗的0至24岁患者。各诊所的基线情况有所不同,定义为首次开具DTG处方的日期;对患者进行随访,直至数据库关闭/死亡/失访(失访定义为无就诊时间≥7个月),以先发生者为准。我们计算了DTG起始的累积发生率函数;在一个共享脆弱模型中探索相关因素,同时考虑诊所的异质性。
自2019年以来,共纳入3350例患者;47.2%为女性;78.9%接受ART治疗≥12个月。基线年龄中位数为12.5岁(四分位间距8.4 - 15.8)。中位随访时间为14个月(四分位间距7 - 22)。DTG起始的总体累积发生率在12个月和24个月时分别达到22.7%(95%置信区间21.3至24.2)和56.4%(95%置信区间54.4至58.4)。在单因素分析中,年龄<5岁的患者和女性总体上转换治疗的可能性较小。在根据ART治疗线和基线时可用病毒载量(VL)进行调整后,10岁以上女性与同年龄男性相比,开始使用DTG的可能性较小(10 - 14岁调整后风险比:0.62,95%置信区间0.54至0.72;≥15岁:0.43,95%置信区间0.36至0.50),病毒载量可检测(>50拷贝/mL)的患者与病毒抑制的患者相比也是如此(调整后风险比0.86,95%置信区间0.77至0.97),使用蛋白酶抑制剂(PI)的患者与使用非核苷类逆转录酶抑制剂的患者相比也是如此(推广12个月后的调整后风险比:0.75,95%置信区间0.65至0.86)。
在西非地区,儿科DTG的使用情况并不完整且存在不公平现象:5岁以下儿童、10岁及以上女性以及病毒载量可检测的患者使用DTG的可能性最小。需要持续监测和支持治疗实践,以更好地确保普遍和平等的使用。