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首页> 外文期刊>Frontiers in Pediatrics >24-Month Clinical, Immuno-Virological Outcomes, and HIV Status Disclosure in Adolescents Living With Perinatally-Acquired HIV in the IeDEA-COHADO Cohort in Togo and C?te d'Ivoire, 2015–2017
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24-Month Clinical, Immuno-Virological Outcomes, and HIV Status Disclosure in Adolescents Living With Perinatally-Acquired HIV in the IeDEA-COHADO Cohort in Togo and C?te d'Ivoire, 2015–2017

机译:在Togo和C的IEDEA-Cohado Cohort占用艾滋病病毒期间的青少年24个月的临床,免疫病毒学结果和艾滋病毒状态披露,2015-2017

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Background: Adolescents living with perinatally-acquired HIV (APHIV) face challenges including HIV serostatus disclosure. We assessed their 24-month outcomes in relation to the disclosure of their own HIV serostatus. Methods: Nested within the International epidemiologic Database to Evaluate AIDS pediatric West African prospective cohort (IeDEA pWADA), the COHADO cohort included antiretroviral (ART)-treated APHIV aged 10–19 years, enrolled in HIV care before the age of 10 years, in Abidjan (C?te d'Ivoire) and Lomé (Togo) in 2015. We measured the HIV serostatus disclosure at baseline and after 24 months and analyzed its association with a favorable combined 24-month outcome using logistic regression. The 24-month combined clinical immuno-virological outcome was defined as unfavorable when either death, loss to follow-up, progression to WHO-AIDS stage, a decrease of CD4 count 10% compared to baseline, or a detectable viral load (VL 50 copies/mL) occurred at 24 months. Results: Overall, 209 APHIV were included (51.6% = Abidjan, 54.5% = females). At inclusion, the median CD4 cell count was 521/mm 3 [IQR (281–757)]; 29.6% had a VL measurement, of whom, 3.2% were virologically suppressed. APHIV were younger in Lomé {median age: 12 years [interquartile range (IQR): 11–15]} compared to Abidjan [14 years (IQR: 12–15, p = 0.01)]. Full HIV-disclosure increased from 41.6% at inclusion to 74.1% after 24 months. After 24 months of follow-up, six (2.9%) died, eight (3.8%) were lost to follow-up, and four (1.9%) were transferred out. Overall, 73.7% did not progress to the WHO-AIDS stage, and 62.7% had a CD4 count above (±10%) of the baseline value (48.6% in Abidjan vs. 69.0% in Lomé, p 2 years compared to those who had not been disclosed to [aOR = 0.21, 95% CI (0.05–0.84), p = 0.03]. Conclusions: The frequency of HIV-disclosure improved over time and differed across countries but remained low among West African APHIV. Overall, the 24-month outcomes were poor. Disclosure before the study was a marker of a poor 24-month outcome in Lomé. Context-specific responses are urgently needed to improve adolescent care and reach the UNAIDS 90% target of virological success.
机译:背景:与易患艾滋病毒(APHIV)的青少年面临挑战,包括HIV Serostatus披露。我们在披露自己的HIV Serostatus披露中评估了24个月的成果。方法:嵌套在国际流行病学数据库中,以评估艾滋病儿科西非前瞻性队列(IEDEA PWADA),Cohado Cohort包括抗逆转录病毒(ART)-Treated Aphiv,年龄10-19岁,在10岁之前注册艾滋病毒护理,进入2015年Abidjan(C?Te D'Ivoire)和Lomé(多哥)。我们在基线和24个月后测量了HIV Serostatus披露,并使用Logistic回归分析了其与合适的24个月结果的关联。 24个月的联合临床免疫病毒学结果被定义为死亡,随访的丧失,对WHO-AIDS阶段的进展,CD4计数降低,与基线相比,或可检测的病毒载荷( VL& 50份/ ml)发生在24个月。结果:总体而言,包括209个APHIV(51.6%= Abidjan,54.5%=女)。在夹杂物时,中值CD4细胞计数为521 / mm 3 [IQR(281-757)]; 29.6%有VL测量,其中3.2%是病毒学抑制的。 APHIV在Lomé{中位数年龄:12年[四分位数范围(IQR):11-15]}与Abidjan相比[14年(IQR:12-15,P = 0.01)]。完全艾滋病毒披露在24个月后纳入量增加至74.1%。后续24个月后,六次(2.9%)死亡,八(3.8%)损失了随访,四次(1.9%)转移出来。总体而言,73.7%没有进入WHO艾滋病阶段,62.7%的基线值的CD4计数(±10%)(±10%)基线值(阿比扬的48.6%在Lomé,P 2岁时,与那些人相比,P 2岁尚未公开给[AOR = 0.21,95%CI(0.05-0.84),p = 0.03]。结论:艾滋病毒披露的频率随着时间的推移而改善,不同的国家差别,但在西非APHIV中仍然很低。总体而言, 24个月的成果很差。在研究之前披露是Lomé缺乏24个月成果的标志。迫切需要改善青少年护理,达到艾滋病规划署90%的病毒学成功目标。

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