School of Pharmacy, University of Maryland, Baltimore, MD, USA.
Ann Pharmacother. 2011 Mar;45(3):372-9. doi: 10.1345/aph.1P587. Epub 2011 Mar 8.
To determine the adherence levels needed for HIV virologic suppression with newer antiretroviral (ARV) medications, including darunavir, etravirine, and raltegravir.
Literature searches of PubMed, MEDLINE (1950-October 2010), and Google Scholar were performed using the following key words in multiple combinations: antiretroviral, HIV, AIDS, adherence, darunavir, raltegravir, and etravirine. A review of the bibliographies of retrieved articles was performed to identify additional references.
All articles in English were identified from the data sources and evaluated. Studies that did not state names of medications or drug classes studied were excluded.
There are differing levels of adherence needed to maintain virologic suppression, depending on the ARV class used. The adherence level needed for unboosted protease inhibitors (PIs) has been established as greater than 95%, but recent studies have shown that greater than 80% adherence to boosted PIs may be sufficient. Nonnucleoside reverse transcriptase inhibitors (NNRTIs) could require lower adherence rates than boosted PIs; however, study results are varied and NNRTIs carry a potential for developing resistance with nonadherence. Studies assessing the adherence needed for raltegravir have yet to be performed.
Studies have shown differing levels of adherence needed among ARV classes of medications. With the advent of boosted PIs and potent medications, the amount of adherence needed has dropped since the 1990s. Although the current data are useful, there are discrepancies in the results due to the methods of adherence measurement. Knowing what adherence levels are needed is valuable in helping to determine the optimal ARV regimen for patients, given their adherence barriers. This knowledge can also help determine which patients require in-depth adherence counseling. Further research with a reliable method of measuring adherence is essential to determine adherence levels needed for newer ARV medications, including darunavir, etravirine, and raltegravir.
确定新型抗逆转录病毒(ARV)药物,包括达芦那韦、依曲韦林和雷特格韦,实现 HIV 病毒学抑制所需的依从水平。
通过对 PubMed、MEDLINE(1950 年至 2010 年 10 月)和 Google Scholar 的文献检索,使用了以下关键词的多种组合:抗逆转录病毒、HIV、艾滋病、依从性、达芦那韦、雷特格韦和依曲韦林。对检索到的文章的参考文献进行了回顾,以确定其他参考资料。
从资料来源中确定并评估了所有英文文章。排除了未说明所研究药物名称或药物类别的研究。
维持病毒学抑制所需的依从水平因所使用的 ARV 类别而异。未增强型蛋白酶抑制剂(PI)的依从水平已确定为大于 95%,但最近的研究表明,增强型 PI 的依从水平大于 80%可能就足够了。非核苷类逆转录酶抑制剂(NNRTI)可能需要低于增强型 PI 的依从率;然而,研究结果各不相同,NNRTI 不依从可能会导致耐药性。尚未进行评估雷特格韦所需依从水平的研究。
研究表明,ARV 类药物之间需要不同水平的依从性。自 20 世纪 90 年代以来,随着增强型 PI 和强效药物的出现,所需的依从水平已经下降。尽管目前的数据很有用,但由于依从性测量方法的差异,结果存在差异。了解需要达到何种依从水平对于确定患者的最佳 ARV 治疗方案非常有价值,因为这涉及到他们的依从性障碍。这种知识还可以帮助确定哪些患者需要深入的依从性咨询。需要进行进一步的研究,采用可靠的方法来测量依从性,以确定新型 ARV 药物(包括达芦那韦、依曲韦林和雷特格韦)所需的依从水平。