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乌干达感染艾滋病毒儿童中,出生时暴露于和未暴露于单剂量奈韦拉平的儿童对抗逆转录病毒疗法的反应。

Response to antiretroviral therapy in HIV-infected Ugandan children exposed and not exposed to single-dose nevirapine at birth.

作者信息

Musoke Philippa M, Barlow-Mosha Linda, Bagenda Danstan, Mudiope Peter, Mubiru Michael, Ajuna Patrick, Tumwine James K, Fowler Mary Glenn

机构信息

Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.

出版信息

J Acquir Immune Defic Syndr. 2009 Dec;52(5):560-8. doi: 10.1097/qai.0b013e3181b93a5a.

DOI:10.1097/qai.0b013e3181b93a5a
PMID:19950430
Abstract

OBJECTIVE

To compare the response to a nevirapine (NVP)-based highly active antiretroviral therapy (HAART) in HIV-infected Ugandan children, exposed and nonexposed to single-dose NVP (sd NVP) at birth.

METHODS

HIV-infected study children were initiated on stavudine/lamivudine/NVP as a fixed dose combination. CD4 cell percent and HIV-1 RNA were documented at baseline, 12, 24, 36, and 48 weeks post-initiation of HAART.

RESULTS

Ninety-two children were enrolled in the study, 44 in the sd NVP-exposed and 48 in the nonexposed cohort. The median age at enrollment was 1.7 years [interquartile range (IQR) 1.2-2.4] and 7.8 years (IQR 5.9-9.2) in the sd NVP-exposed and nonexposed cohorts,respectively (P < 0.001). At baseline and week 48 post-HAART, the median CD4 cell percentages were 14% and 33% for the NVP-exposed group and 8% and 22.5% in the nonexposed group (P < 0.0001). The median (IQR) viral load at baseline was 650,568 (359,979-2,086,613) RNA copies/mL and 239,027 (105,904-494,813) RNA copies/mL in the NVP-exposed and nonexposed cohorts, respectively. After 48 weeks of HAART, 76% of the NVP-exposed and 80% of the nonexposed children had a median viral load of < 400 copies/mL (P = 0.74).

CONCLUSIONS

Both HIV-infected Ugandan older infants and children that were exposed and not exposed to sd NVP at birth had favorable treatment outcomes on NVP-containing HAART.

摘要

目的

比较在乌干达感染HIV的儿童中,出生时暴露于和未暴露于单剂量奈韦拉平(sd NVP)的儿童对基于奈韦拉平(NVP)的高效抗逆转录病毒疗法(HAART)的反应。

方法

感染HIV的研究儿童开始使用司他夫定/拉米夫定/NVP固定剂量组合治疗。在HAART开始后的基线、12周、24周、36周和48周记录CD4细胞百分比和HIV-1 RNA。

结果

92名儿童参与了该研究,44名暴露于sd NVP,48名未暴露。暴露组和未暴露组入组时的中位年龄分别为1.7岁[四分位间距(IQR)1.2 - 2.4]和7.8岁(IQR 5.9 - 9.2)(P < 0.001)。在基线和HAART后48周,暴露于NVP组的中位CD4细胞百分比分别为14%和33%,未暴露组为8%和22.5%(P < 0.0001)。暴露组和未暴露组基线时的中位(IQR)病毒载量分别为650,568(359,979 - 2,086,613)RNA拷贝/毫升和239,027(105,904 - 494,813)RNA拷贝/毫升。HAART 48周后,76%暴露于NVP的儿童和80%未暴露的儿童中位病毒载量< 400拷贝/毫升(P = 0.74)。

结论

出生时暴露和未暴露于sd NVP的乌干达感染HIV的大龄婴儿和儿童在含NVP的HAART治疗中均有良好的治疗效果。

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