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Subtherapeutic Antiretroviral Plasma Concentrations in Routine Clinical Outpatient HIV Care.

机译:常规临床门诊HIV护理中的亚治疗性抗逆转录病毒血浆浓度。

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The objective of this study was to evaluate plasma concentrations of nonnucleoside reverse transcriptase inhibitors (NNRTIs) and protease inhibitors (PIs) within several dosing schemes in a cohort of HIV-infected patients in routine clinical practice and to find possible explanations for subtherapeutic plasma concentrations. Patients were included if a PI or NNRTI was part of their antiretroviral regimen, at least one plasma concentration was obtained, and a complete medication overview from community pharmacy records was available. The study period was from January 1998 to September 2001. Each plasma concentration was related to median plasma concentrations of a pharmacokinetic reference curve, yielding a concentration ratio (CR). A cutoff CR was defined for each antiretroviral drug per specific regimen, discriminating between >/=therapeutic and subtherapeutic concentrations. For the patients with subtherapeutic concentrations, it was sorted out whether drug interactions, adverse events and self-reported symptoms, or nonadherence could be the cause of the lower than expected plasma concentration. Ninety-seven HIV-infected patients fulfilled the criteria. During the defined period, 1145 plasma concentrations were available (median, 11; interquartile range, 8-14). Three hundred fourteen (27.4%) plasma concentrations were classified subtherapeutic. Drug interactions (2; 0.6%), adverse events and self-reported symptoms (67; 21.3%), and nonadherence (14; 4.5%) could only partly explain the subtherapeutic drug levels. Consequently, a large number of the subtherapeutic plasma concentrations (73.6%) remained inexplicable. A high number of subtherapeutic plasma concentrations were observed. No clear causes were found; thus, corrective measures will be difficult to employ. Therefore, therapeutic drug monitoring (TDM) must maintain its crucial place in routine clinical care to be able to identify patients who need extra attention so that therapeutic plasma concentrations are achieved.
机译:这项研究的目的是评估在常规临床实践中一组HIV感染患者的几种给药方案中非核苷类逆转录酶抑制剂(NNRTIs)和蛋白酶抑制剂(PIs)的血浆浓度,并寻找亚治疗性血浆浓度的可能解释。如果PI或NNRTI是其抗逆转录病毒治疗方案的一部分,则至少包括一个血浆浓度,并且可以从社区药房记录中获得完整的药物概述。研究期为1998年1月至2001年9月。每种血浆浓度均与药代动力学参考曲线的中位数血浆浓度相关,得出浓度比(CR)。按照特定方案为每种抗逆转录病毒药物定义了临界值CR,以区分治疗浓度和/或亚治疗浓度。对于具有亚治疗浓度的患者,对是否发生药物相互作用,不良事件和自我报告的症状或不依从的原因进行了归类,以找出低于预期的血浆浓度的原因。有97名HIV感染患者符合标准。在规定的时间段内,血浆浓度为1145(中位数为11;四分位间距为8-14)。 134种(27.4%)血浆浓度被分类为亚治疗。药物相互作用(2; 0.6%),不良事件和自我报告的症状(67; 21.3%)和不依从性(14; 4.5%)只能部分解释亚治疗药物水平。因此,大量的亚治疗血浆浓度(73.6%)仍然无法解释。观察到大量的亚治疗血浆浓度。找不到明确的原因;因此,纠正措施将难以采用。因此,治疗药物监测(TDM)必须在常规临床护理中保持其至关重要的地位,以便能够识别需要额外注意的患者,以达到治疗性血浆浓度。

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