Droste Jacqueline A H, Koopmans Peter P, Hekster Yechiel A, Burger David M
Department of Clinical Pharmacy, University Medical Centre, Nijmegen, The Netherlands.
Ther Drug Monit. 2005 Aug;27(4):412-6. doi: 10.1097/01.ftd.0000162521.16060.13.
The third round of the International Interlaboratory Quality Control Program for Therapeutic Drug Monitoring in HIV infection (QC-program) consisted of the analysis not only of plasma samples but also of patient cases. The case was composed of different topics related to the therapeutic drug monitoring of antiretroviral drugs. The participants were asked to give recommendations concerning dose adjustments, changes to the regimen, and drug-drug interactions to observe whether the expert recommendations were comparable. Of the 30 participants of the QC-program, 16 returned their comments and recommendations with regard to the patient case. The drug level was easy to judge: approximately 90% were able to correctly do so. Almost half of the recommendations (44%) given were satisfactory. Levels of knowledge regarding HIV treatment appeared to be variable among the respondents and for this reason were partly incomparable.
第三届HIV感染治疗药物监测国际实验室间质量控制项目(质量控制项目)不仅包括对血浆样本的分析,还包括对患者病例的分析。病例由与抗逆转录病毒药物治疗药物监测相关的不同主题组成。参与者被要求给出关于剂量调整、治疗方案变更和药物相互作用的建议,以观察专家建议是否具有可比性。在质量控制项目的30名参与者中,16人就患者病例返回了他们的意见和建议。药物水平易于判断:约90%的人能够正确判断。给出的建议中几乎一半(44%)是令人满意的。受访者对HIV治疗的知识水平似乎参差不齐,因此部分无法进行比较。