Department of Critical Care Medicine, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium,
Intensive Care Med. 2014 Mar;40(3):380-7. doi: 10.1007/s00134-013-3187-2. Epub 2013 Dec 20.
There is variability in the pharmacokinetics (PK) of antibiotics (AB) in critically ill patients. Therapeutic drug monitoring (TDM) could overcome this variability and increase PK target attainment. The objective of this study was to analyse the effect of a dose-adaption strategy based on daily TDM on target attainment.
This was a prospective, partially blinded, and randomised controlled trial in patients with normal kidney function treated with meropenem (MEM) or piperacillin/tazobactam (PTZ). The intervention group underwent daily TDM, with dose adjustment when necessary. The predefined PK/pharmacodynamic (PK/PD) target was 100% fT>4MIC [percentage of time during a dosing interval that the free (f) drug concentration exceeded 4 times the MIC]. The control group received conventional treatment. The primary endpoint was the proportion of patients that reached 100% fT>4MIC and 100 % fT>MIC at 72 h.
Forty-one patients (median age 56 years) were included in the study. Pneumonia was the primary infectious diagnosis. At baseline, 100% fT>4MIC was achieved in 21% of the PTZ patients and in none of the MEM patients; 100% fT>MIC was achieved in 71% of the PTZ patients and 46 % of the MEM patients. Of the patients in the intervention group, 76 % needed dose adaptation, and five required an additional increase. At 72 h, target attainment rates for 100% fT>4MIC and 100% fT>MIC were higher in the intervention group: 58 vs. 16%, p = 0.007 and 95 vs. 68%, p = 0.045, respectively.
Among critically ill patients with normal kidney function, a strategy of dose adaptation based on daily TDM led to an increase in PK/PD target attainment compared to conventional dosing.
抗生素(AB)在危重症患者中的药代动力学(PK)存在变异性。治疗药物监测(TDM)可以克服这种变异性并提高 PK 目标的达成率。本研究的目的是分析基于每日 TDM 的剂量调整策略对目标达成的影响。
这是一项在肾功能正常的接受美罗培南(MEM)或哌拉西林/他唑巴坦(PTZ)治疗的患者中进行的前瞻性、部分盲法、随机对照试验。干预组进行每日 TDM,并在必要时进行剂量调整。预设的 PK/药效学(PK/PD)目标是 100% fT>4MIC[在一个给药间隔内游离(f)药物浓度超过 MIC 的 4 倍的时间百分比]。对照组接受常规治疗。主要终点是达到 100% fT>4MIC 和 100% fT>MIC 的患者比例在 72 小时。
41 例患者(中位年龄 56 岁)纳入研究。肺炎是主要的感染诊断。在基线时,PTZ 患者中有 100% fT>4MIC 的比例为 21%,而 MEM 患者中没有;PTZ 患者中有 100% fT>MIC 的比例为 71%,MEM 患者中有 46%。干预组中有 76%的患者需要剂量调整,有 5 名患者需要额外增加剂量。在 72 小时时,干预组的 100% fT>4MIC 和 100% fT>MIC 的目标达成率更高:58% vs. 16%,p=0.007 和 95% vs. 68%,p=0.045。
在肾功能正常的危重症患者中,与常规剂量相比,基于每日 TDM 的剂量调整策略可提高 PK/PD 目标的达成率。