Jang Soo-Min, Shaw Alex R, Mueller Bruce A
Department of Pharmacy Practice, Loma Linda University School of Pharmacy, Loma Linda, CA 92350, USA.
Medical Strategist, Ironwood Pharmaceuticals, Boston, MA 02110, USA.
Antibiotics (Basel). 2021 Nov 12;10(11):1390. doi: 10.3390/antibiotics10111390.
(1) Purpose of this study: To determine whether patient weight influences the probability of target attainment (PTA) over 72 h of initial therapy with beta-lactam (cefepime, ceftazidime, piperacillin/tazobactam) and carbapenem (imipenem, ertapenem, meropenem) antibiotics in the critical care setting. This is the first paper to address the question of whether patient size affects antibiotic PTA in the ICU. (2) Methods: We performed a post hoc analysis of Monte Carlo simulations conducted in virtual critically ill patients receiving antibiotics and continuous renal replacement therapy. The PTA was calculated for each antibiotic on the following pharmacodynamic (PD) targets: (a) were above the target organism's minimum inhibitory concentration (≥%fT≥1×MIC), (b) were above four times the MIC (≥%fT≥4×MIC), and (c) were always above the MIC (≥100%fT≥MIC) for the first 72 h of antibiotic therapy. The PTA was analyzed in patient weight quartiles [Q1 (lightest)-Q4 (heaviest)]. Optimal doses were defined as the lowest dose achieving ≥90% PTA. (3) Results: The PTA for fT≥1×MIC led to similarly high rates regardless of weight quartiles. Yet, patient weight influenced the PTA for higher PD targets (100%fT≥MIC and fT≥4×MIC) with commonly used beta-lactams and carbapenems. Reaching the optimal PTA was more difficult with a PD target of 100%fT≥MIC compared to fT≥4×MIC. (4) Conclusions: The Monte Carlo simulations showed patients in lower weight quartiles tended to achieve higher antibiotic pharmacodynamic target attainment compared to heavier patients.
(1) 本研究目的:确定在重症监护环境中,患者体重是否会影响使用β-内酰胺类抗生素(头孢吡肟、头孢他啶、哌拉西林/他唑巴坦)和碳青霉烯类抗生素(亚胺培南、厄他培南、美罗培南)进行初始治疗72小时内达到目标值的概率(PTA)。这是第一篇探讨患者体型是否会影响重症监护病房抗生素PTA问题的论文。(2) 方法:我们对接受抗生素和持续肾脏替代治疗的虚拟重症患者进行的蒙特卡洛模拟进行了事后分析。针对以下药效学(PD)目标计算每种抗生素的PTA:(a) 高于目标微生物的最低抑菌浓度(≥%fT≥1×MIC),(b) 高于最低抑菌浓度的四倍(≥%fT≥4×MIC),以及 (c) 在抗生素治疗的前72小时始终高于最低抑菌浓度(≥100%fT≥MIC)。在患者体重四分位数[Q1(最轻)-Q4(最重)]中分析PTA。最佳剂量定义为达到≥90%PTA的最低剂量。(3) 结果:无论体重四分位数如何,fT≥1×MIC的PTA导致的发生率都同样高。然而,患者体重影响了常用β-内酰胺类抗生素和碳青霉烯类抗生素对于更高PD目标(100%fT≥MIC和fT≥4×MIC)的PTA。与fT≥4×MIC相比,达到100%fT≥MIC的PD目标更难实现最佳PTA。(4) 结论:蒙特卡洛模拟显示,与体重较重的患者相比,体重四分位数较低的患者往往能达到更高的抗生素药效学目标值。