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瘙痒性丘疹性皮疹对抗逆转录病毒治疗的反应能否用作监测病毒学结果的临床参数?

Can response of a pruritic papular eruption to antiretroviral therapy be used as a clinical parameter to monitor virological outcome?

作者信息

Castelnuovo Barbara, Byakwaga Hellen, Menten Joris, Schaefer Petra, Kamya Moses, Colebunders Robert

机构信息

Infectious Diseases Institute, Kampala, Uganda.

出版信息

AIDS. 2008 Jan 11;22(2):269-73. doi: 10.1097/QAD.0b013e3282f313a9.

Abstract

BACKGROUND

A pruritic papular eruption (PPE) is a common skin manifestation observed in 12-46% of persons with HIV infection living in tropical countries.

OBJECTIVE

To determine whether PPE responds to HAART and whether monitoring PPE severity could be used as a clinical marker to predict virological outcome in resource-limited settings where viral load testing is not available.

METHODS

The study enrolled 53 patients with PPE for at least 1 month before starting a first-line HAART regimen as part of a prospective study. CD4 cell count and viral load were measured at enrolment and every 3 months. A scoring system was developed to evaluate the PPE severity by asking two questions. Over the last month how itchy has your skin been? Over the last month how has itching interfered with your sleep?

RESULTS

Median CD4 cell count was 15 cells/mul and median viral load 268 663 copies/ml. All patients initiated a regimen containing a nonnucleoside reverse transcriptase inhibitor. Mean PPE score declined from 3.9 at enrolment to 0.1 at 24 months. In 37 (86%) of the 43 patients with at least 6 months of follow-up data, the PPE disappeared and never returned. Patients with viral load > 400 copies/ml at months 9 and/or 12 had significantly higher PPE scores at months 9 to 12 than the patients with < 400 copies/ml.

CONCLUSIONS

In most patients, PPE disappears during HAART and PPE severity scores were higher in patients whose first-line HAART failed to control plasma viral load.

摘要

背景

瘙痒性丘疹疹(PPE)是一种常见的皮肤表现,在生活于热带国家的12% - 46%的HIV感染者中可见。

目的

确定PPE对高效抗逆转录病毒治疗(HAART)是否有反应,以及在无法进行病毒载量检测的资源有限环境中,监测PPE严重程度是否可作为预测病毒学结果的临床指标。

方法

作为一项前瞻性研究的一部分,该研究纳入了53例在开始一线HAART方案前患有PPE至少1个月的患者。在入组时及每3个月测量CD4细胞计数和病毒载量。通过询问两个问题开发了一个评分系统来评估PPE的严重程度。在过去一个月里你的皮肤有多痒?在过去一个月里瘙痒对你的睡眠有何影响?

结果

CD4细胞计数中位数为15个/微升,病毒载量中位数为268663拷贝/毫升。所有患者均开始使用包含非核苷类逆转录酶抑制剂的方案。PPE平均评分从入组时的3.9降至24个月时的0.1。在43例至少有6个月随访数据的患者中,37例(86%)的PPE消失且未再出现。在第9个月和/或第12个月病毒载量>400拷贝/毫升的患者在第9至12个月的PPE评分显著高于病毒载量<400拷贝/毫升的患者。

结论

在大多数患者中,PPE在HAART期间消失,且一线HAART未能控制血浆病毒载量的患者的PPE严重程度评分更高。

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