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接受洛匹那韦/利托那韦抗逆转录病毒疗法的HIV感染患者,尽管服药依从率低于95%,仍能实现较高的病毒学抑制率。

HIV-infected patients receiving lopinavir/ritonavir-based antiretroviral therapy achieve high rates of virologic suppression despite adherence rates less than 95%.

作者信息

Shuter Jonathan, Sarlo Julie A, Kanmaz Tina J, Rode Richard A, Zingman Barry S

机构信息

AIDS Center and Division of Infectious Diseases, Montefiore Medical Center, Bronx, NY 10467, USA.

出版信息

J Acquir Immune Defic Syndr. 2007 May 1;45(1):4-8. doi: 10.1097/QAI.0b013e318050d8c2.

Abstract

BACKGROUND

The observation that extremely high levels of medication adherence are required to achieve complete virologic suppression is based largely on studies of treatment-experienced patients receiving HIV protease inhibitor (PI)-based therapy without ritonavir boosting. This study aims to define the level of adherence needed to achieve virologic suppression in patients receiving boosted PI-based highly active antiretroviral therapy (HAART) with lopinavir/ritonavir.

METHODS

HIV-infected adults receiving a regimen containing lopinavir/ritonavir were recruited into a prospective, observational study of the relation between adherence to lopinavir/ritonavir and virologic outcomes. Adherence was measured using the Medication Event Monitoring System (MEMS; Aardex, Union City, CA). HIV-1 viral load (VL) was measured at week 24.

RESULTS

The final study population contained 64 subjects. Eighty percent had AIDS, 97% received lopinavir/ritonavir before enrollment, and most had more than 7 years of HAART experience. Mean adherence overall was 73%. Eighty percent and 59% achieved a VL <400 copies/mL and a VL <75 copies/mL, respectively. Mean adherence was 75% in those achieving a VL <75 copies/mL. High rates of virologic suppression were observed in all adherence quartiles, including the lowest quartile (range of adherence: 23.5%-53.3%).

CONCLUSIONS

Moderate levels of adherence can lead to virologic suppression in most patients taking lopinavir/ritonavir-based HAART.

摘要

背景

实现完全病毒学抑制需要极高的药物依从性这一观点,很大程度上基于对接受未使用利托那韦增效的基于HIV蛋白酶抑制剂(PI)治疗的有治疗经验患者的研究。本研究旨在确定在接受基于洛匹那韦/利托那韦的增效PI高效抗逆转录病毒疗法(HAART)的患者中实现病毒学抑制所需的依从性水平。

方法

招募接受含洛匹那韦/利托那韦方案治疗的HIV感染成人,进行一项关于洛匹那韦/利托那韦依从性与病毒学结果关系的前瞻性观察性研究。使用药物事件监测系统(MEMS;Aardex,加利福尼亚州联合市)测量依从性。在第24周测量HIV-1病毒载量(VL)。

结果

最终研究人群包含64名受试者。80%患有艾滋病,97%在入组前接受过洛匹那韦/利托那韦治疗,且大多数有超过7年的HAART治疗经验。总体平均依从性为73%。分别有80%和59%的患者实现病毒载量<400拷贝/mL和病毒载量<75拷贝/mL。在病毒载量<75拷贝/mL的患者中,平均依从性为75%。在所有依从性四分位数中均观察到高病毒学抑制率,包括最低四分位数(依从性范围:23.5%-53.3%)。

结论

对于大多数接受基于洛匹那韦/利托那韦的HAART治疗的患者,中等水平的依从性可导致病毒学抑制。

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