Department of Clinical Pharmacy, University Medical Center Utrecht, Utrecht, the Netherlands; and.
Department of Intensive Care, Gelderse Vallei Hospital, Ede, the Netherlands.
Ther Drug Monit. 2020 Jun;42(3):381-391. doi: 10.1097/FTD.0000000000000755.
Studies comparing the clinical outcomes between vancomycin intermittent infusion (InI) and continuous infusion (CoI) treated patients are generally underpowered. Moreover, due to large differences in the design and efficacy end points in these studies, a meta-analysis of the currently available data is not feasible. Therefore, this systematic review aimed to compare the exposure variability and target attainment with vancomycin during InI and CoI.
A literature search was performed, and clinical studies reporting on vancomycin-treated populations were selected. After exclusion of reviews, case reports, and articles not published in the English language, 505 articles were screened for reported data on vancomycin serum concentrations. A total of 34 studies were included in the review. Relative standard deviations reported in the included studies were assessed, and vancomycin serum concentration variability and target attainment were compared between vancomycin InI and CoI.
The variability in serum concentrations was significantly larger for InI than for CoI (relative standard deviations 46.5% and 32.1%, respectively; P = 0.001). Notably, variability appeared to be independent of the study population or design. Studies directly comparing target attainment between both modes of administration denoted higher and faster target attainment with CoI in all instances.
In conclusion, CoI was associated with lower variabilities in the serum concentration and favorable target attainment rates compared with InI. These findings are important because vancomycin exposure is considered a major predictor of the patients' clinical outcomes. However, the role of lower serum concentration variability and higher target attainment rates in achieving better clinical outcomes needs to be evaluated in patients treated with vancomycin CoI compared with InI.
比较万古霉素间歇性输注(InI)和连续输注(CoI)治疗患者临床结局的研究通常效力不足。此外,由于这些研究在设计和疗效终点方面存在很大差异,因此目前无法对现有数据进行荟萃分析。因此,本系统评价旨在比较 InI 和 CoI 期间万古霉素的暴露变异性和目标达成率。
进行了文献检索,并选择了报告万古霉素治疗人群的临床研究。排除综述、病例报告和非英文发表的文章后,对报告万古霉素血清浓度数据的 505 篇文章进行了筛选。共有 34 项研究纳入本综述。评估了纳入研究中报告的相对标准偏差,并比较了万古霉素 InI 和 CoI 之间的血清浓度变异性和目标达成率。
InI 的血清浓度变异性明显大于 CoI(相对标准偏差分别为 46.5%和 32.1%;P=0.001)。值得注意的是,变异性似乎与研究人群或设计无关。直接比较两种给药方式目标达成率的研究均表示 CoI 可更快更高地达到目标。
总之,与 InI 相比,CoI 可降低血清浓度的变异性并提高目标达成率。这些发现很重要,因为万古霉素暴露被认为是患者临床结局的主要预测因素。然而,在接受万古霉素 CoI 治疗的患者中,与 InI 相比,较低的血清浓度变异性和较高的目标达成率是否能实现更好的临床结局,需要进一步评估。