平均红细胞体积作为hiv感染成人齐多夫定治疗依从性的标志

The Open AIDS Journal Pub Date : 2012-01-01 Epub Date: 2012-05-31 DOI:10.2174/1874613601206010045
Joseph O Mugisha, Katherine Donegan, Sarah Fidler, Gita Ramjee, Andrew Hodson, David T Dunn, Kholoud Porter, Pontiano Kaleebu
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引用次数: 0

摘要

目的:评估平均红细胞体积(MCV)在检测azt治疗依从性方面是否有用。设计:随机对照试验中的观察性研究。方法:我们合并了来自SPARTAC的两个治疗组的数据,这是一项关于原发性HIV感染的短期cART的随机对照试验,将参与者分类为应答者(HIV- rna减少≥1 log(10)或达到结果:在该分析的119名参与者中,73名(61%)是女性,其中71名是非洲随机分配的。在cART启动后的第4周和第12周,分别有98例(88%)和84例(85%)被分类为应答者。MCV在第4周平均增加3%和1%,14%。结论:在可能无法获得HIV RNA的低收入国家,12周的MCV测量可能有助于监测含azt方案的依从性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mean Corpuscular Volume as a Marker for Adherence to Zidovudine-Containing Therapy in HIV-Infected Adults.

Mean Corpuscular Volume as a Marker for Adherence to Zidovudine-Containing Therapy in HIV-Infected Adults.

Mean Corpuscular Volume as a Marker for Adherence to Zidovudine-Containing Therapy in HIV-Infected Adults.

Mean Corpuscular Volume as a Marker for Adherence to Zidovudine-Containing Therapy in HIV-Infected Adults.

Objectives: To assess whether mean corpuscular volume (MCV) is useful in detecting non-adherence to AZTcontaining therapy.

Design: Observational study within randomised controlled trial.

Methods: We combined data from two treatment arms in SPARTAC, an RCT of short-course cART in primary HIV infection, classifying participants as responders (HIV-RNA decrease ≥1 log(10) or reaching <400copies/ml) or nonresponders following cART initiation. We assessed the sensitivity and specificity of using different percentage increases in MCV for accurately differentiating between responders and non-responders. We further examined changes in MCV levels up to 24 weeks after protocol-indicated cART cessation.

Results: Of 119 participants included in this analysis, 73 (61%) were women, 71 of whom were randomised in Africa. Ninety-eight (88%) and 84 (85%) were classified as responders at 4 and 12 weeks respectively following cART initiation. MCV increased by a mean 3% and 1% at week 4, and 14% and <1% at 12 weeks for responders and non-responders. A 2% MCV increase at 4 weeks had 62% sensitivity and specificity for identifying virological response. At 12 weeks, an 8% increase had 89% sensitivity and specificity. In responders, MCV remained lower for individuals in African compared to non-African sites throughout and rose from 85 vs 90 fL at cART start to 96 vs 103 fL at 12 weeks post-initiation then fell to 88 vs 93 fL and 86 vs 89 fL at 12 and 48 weeks post-cessation.

Conclusion: In low-income countries, where HIV RNA may be unavailable, 12-weekly MCV measurements may be useful in monitoring adherence to AZT-containing regimens.

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