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科特迪瓦阿比让抗逆转录病毒治疗试点项目的病毒学和免疫学结果及项目挑战

Virologic and immunologic outcomes and programmatic challenges of an antiretroviral treatment pilot project in Abidjan, Côte d'Ivoire.

作者信息

Djomand Gaston, Roels Thierry, Ellerbrock Tedd, Hanson Debra, Diomande Fabien, Monga Bondo, Maurice Chantal, Nkengasong John, Konan-Koko Regina, Kadio Auguste, Wiktor Stefan, Lackritz Eve, Saba Joseph, Chorba Terence

机构信息

Projet RETRO-CI, Abidjan, Côte d'Ivoire.

出版信息

AIDS. 2003 Jul;17 Suppl 3:S5-15. doi: 10.1097/00002030-200317003-00002.

Abstract

BACKGROUND

In Côbte d'Ivoire, a pilot project was developed by UNAIDS and the Ministry of Health to improve access to AIDS care, including antiretroviral therapy, for adults and children infected with HIV. This evaluation of the project is the first to provide results of a large number of HIV-infected patients receiving antiretroviral therapy in West Africa.

METHODS

We evaluated records of persons who presented for care from August 1998 to August 2000 at six accredited centers in Abidjan. Patients were treated with two nucleoside reverse transcriptase inhibitors (2NRTI) or highly active antiretroviral therapy (HAART).

RESULTS

Of 2878 patients who were screened, 2351 (83%) were HIV-infected and eligible (CD4 T lymphocyte count < 500 x 10(6) cells/l or plasma HIV-RNA level > 10 000 copies/ml) for antiretroviral therapy. Of those who were eligible, 81% were symptomatic, 63% had a CD4 cell count < 200 x 10(6) cells/l, 12% had previously taken antiretroviral drugs, and 56% returned to the clinic for follow-up. Of the patients screened, 768 (27%) were started on antiretroviral therapy, including 450 on HAART, 296 on 2NRTI, and 22 on other regimens. We analyzed data from 480 HIV-1-infected adults, who were naive to therapy, were prescribed HAART or 2NRTI, and had at least one clinic visit after starting therapy. In an intent-to-treat analysis of patients who received HAART, the estimated plasma HIV-1 RNA level was approximately 1.9 log10 copies/ml (80-fold) lower, while estimated CD4 cell count was > 100 x 10(6) cells/l higher than baseline values, after 1 year of therapy. Approximately 25% of adults on 2NRTI and 50% of those on HAART had < 200 copies/ml, after 1 year of therapy. The probability of an adverse event occurring within 6 months after starting therapy was 0.20. The probability of survival for at least 1 year was 0.84 (95% confidence interval, 0.80-0.89).

CONCLUSION

After starting antiretroviral therapy, these HIV-1-infected patients in West Africa had similar virologic and immunologic outcomes, probability of an adverse event, and estimated survival, as patients enrolled in clinical trials in the USA and Europe. However, only one-third of eligible patients received therapy, highlighting the importance of providing adequate education and support for initiating and adhering to therapy in this and similar programmes.

摘要

背景

在科特迪瓦,联合国艾滋病规划署(UNAIDS)和卫生部开展了一个试点项目,旨在改善感染HIV的成人和儿童获得艾滋病护理的机会,包括抗逆转录病毒疗法。该项目评估首次提供了大量在西非接受抗逆转录病毒疗法的HIV感染患者的结果。

方法

我们评估了1998年8月至2000年8月在阿比让六个经认可的中心就诊的患者记录。患者接受两种核苷类逆转录酶抑制剂(2NRTI)或高效抗逆转录病毒疗法(HAART)治疗。

结果

在2878名接受筛查的患者中,2351名(83%)感染了HIV且符合抗逆转录病毒疗法的条件(CD4 T淋巴细胞计数<500×10⁶细胞/升或血浆HIV-RNA水平>10000拷贝/毫升)。在符合条件的患者中,81%有症状,63%的CD4细胞计数<200×10⁶细胞/升,12%曾服用过抗逆转录病毒药物,56%返回诊所进行随访。在接受筛查的患者中,768名(27%)开始接受抗逆转录病毒疗法,其中450名接受HAART,296名接受2NRTI,22名接受其他治疗方案。我们分析了480名未接受过治疗、被处方HAART或2NRTI且开始治疗后至少有一次门诊就诊的HIV-1感染成人的数据。在对接受HAART的患者进行的意向性分析中,治疗1年后,估计血浆HIV-1 RNA水平比基线值低约1.9 log₁₀拷贝/毫升(80倍),而估计CD4细胞计数比基线值高>100×10⁶细胞/升。治疗1年后,接受2NRTI的成人中约25%以及接受HAART的成人中约50%的血浆HIV-1 RNA水平<200拷贝/毫升。开始治疗后6个月内发生不良事件的概率为0.20。至少存活1年的概率为0.84(95%置信区间,0.80 - 0.89)。

结论

在开始抗逆转录病毒疗法后,这些西非的HIV-1感染患者在病毒学和免疫学结果、不良事件概率以及估计生存率方面与在美国和欧洲参加临床试验的患者相似。然而,只有三分之一的符合条件的患者接受了治疗,这突出了在该项目及类似项目中提供充分教育和支持以启动和坚持治疗的重要性。

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