Moshi L S, Okuma J, Luoga E, Kalinjuma A V, Mollel G J, Sigalla G, Wilson L, Dotto E, Glass T, Vanobberghen F, Weisser M
Ifakara Health Institute, Ifakara, Tanzania.
St. Francis Regional Referral Hospital, Ifakara, Tanzania.
HIV Med. 2025 May;26(5):800-812. doi: 10.1111/hiv.70015. Epub 2025 Mar 25.
To assess trends of severe HIV disease (SHD) and mortality/loss to follow-up (LTFU) among children living with HIV in rural Tanzania.
Among children aged 0-14 years living with HIV enrolled in the prospective Kilombero & Ulanga Antiretroviral Cohort in January 2005-December 2023, we determined WHO-defined SHD prevalences at enrolment, mortality/LTFU incidence during follow-up using Kaplan-Meier methods, and associated factors using regression models.
At enrolment, among 1089 children [567 (52%) males, 587 (54%) aged <5 years and 530 (49%) with a HIV WHO stage III/IV], 112/332 (34%) had CD4 cell count <200 cells/μL among those aged 5-14 years. In children aged 5-14 years, SHD was diagnosed in 265/502 (53%) with a prevalence of 35-94% declining after 2013. Among children aged <5 years, 374/587 (64%) had SHD with no change over time. Male gender [adjusted odds ratio = 1.45; 95% confidence interval: 1.10-1.90], age <5 years versus older (1.64; 1.13-2.37), hospitalization versus outpatients (6.72; 3.35-13.5), antiretroviral treatment (ART) start within 30 days versus later (2.18; 1.52-3.13), and enrolment during 2013-2016 versus before (2.29; 1.54-3.41) were associated with SHD. After a median follow-up of 3.3 years [interquartile ratio: 0.8-7.8], 130 (12%) children died and 359 (35%) were LTFU. Predictors of mortality/LTFU were SHD [adjusted hazard ratio (aHR) = 1.54; 95% CI: 1.26-1.89], age <5 years versus older (1.28; 1.01-1.66), hospitalization versus outpatients (1.93; 1.42-2.63), living ≥50 km versus ≤1 km away (1.72; 1.37-2.16) and delayed ART initiation versus within 30 days (3.40; 2.70-4,27), while enrolment 2017-2023 versus before (0.51; 0.37-0.70) was protective.
The persisting high prevalence of paediatric SHD and high mortality/LTFU underscores the need for early diagnosis and care.
评估坦桑尼亚农村地区感染艾滋病毒儿童的严重艾滋病毒疾病(SHD)趋势以及死亡率/失访率(LTFU)。
在2005年1月至2023年12月纳入前瞻性基洛梅罗和乌朗加抗逆转录病毒队列的0至14岁感染艾滋病毒儿童中,我们使用Kaplan-Meier方法确定入组时世卫组织定义的SHD患病率、随访期间的死亡率/LTFU发病率,并使用回归模型确定相关因素。
入组时,在1089名儿童中[567名(52%)为男性,587名(54%)年龄<5岁,530名(49%)处于艾滋病毒世卫组织III/IV期],5至14岁儿童中有112/332名(34%)的CD4细胞计数<200个/μL。在5至14岁儿童中,265/502名(53%)被诊断为SHD,2013年后患病率从35%降至94%。在年龄<5岁的儿童中,374/587名(64%)患有SHD,随时间无变化。男性[调整后的优势比=1.45;95%置信区间:1.10-1.90]、年龄<5岁与年龄较大者相比(1.64;1.13-2.37)、住院与门诊相比(6.72;3.35-13.5)、抗逆转录病毒治疗(ART)在30天内开始与之后开始相比(2.18;1.52-3.13)以及2013-2016年期间入组与之前相比(2.29;1.54-3.41)与SHD相关。在中位随访3.3年[四分位间距:0.8-7.8]后,130名(12%)儿童死亡,359名(35%)失访。死亡率/LTFU的预测因素为SHD[调整后的风险比(aHR)=1.54;95%置信区间:1.26-1.89]、年龄<5岁与年龄较大者相比(1.28;1.01-1.66)、住院与门诊相比(1.93;1.42-2.63)、居住距离≥50公里与≤1公里相比(1.72;1.37-2.16)以及ART启动延迟与30天内相比(3.40;2.70-4.27),而2017-2023年期间入组与之前相比(0.51;0.37-0.70)具有保护作用。
儿科SHD持续高患病率以及高死亡率/LTFU凸显了早期诊断和治疗的必要性。