Gatti Milo, Tedeschi Sara, Trapani Filippo, Ramirez Stefania, Mancini Rita, Giannella Maddalena, Viale Pierluigi, Pea Federico
Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, 40138 Bologna, Italy.
Clinical Pharmacology Unit, Department for Integrated Infectious Risk Management, IRCCS Azienda Ospedaliero-Universitaria di Bologna, 40138 Bologna, Italy.
Antibiotics (Basel). 2022 Aug 1;11(8):1037. doi: 10.3390/antibiotics11081037.
(1) Objective: To describe the usefulness of a real-time therapeutic drug monitoring (TDM)-based strategy for optimizing pharmacokinetic/pharmacodynamic (PK/PD) target attainment of continuous infusion (CI) ampicillin-based regimens in a case series of patients affected by suspected or documented enterococcal bloodstream infections (BSIs) and/or infective endocarditis (IE). (2) Methods: Patients treated with CI ampicillin-based regimens for documented or suspected enterococcal BSI/IE who underwent real-time therapeutic drug monitoring (TDM)-based expert clinical pharmacological advice (ECPA) between June 2021 and May 2022 were retrospectively assessed. Ampicillin concentrations were determined at steady state, and the free fraction (fCss) was calculated according to a plasma protein binding of 20%. The fCss/MIC ratio was selected as the PD parameter for ampicillin efficacy and was defined as optimal for values between 4 and 8. The requirement for TDM-guided ampicillin dosing adjustments was assessed. (3) Results: Data for 12 patients with documented (n = 10) or suspected (n = 2) enterococcal infections (7 with BSIs and 5 with IE) were retrieved. The ampicillin PK/PD target was optimal over time in all of the 10 documented infections. None of the enterococcal BSIs persisted. Following the first real-time TDM-based ECPA, ampicillin dosage was decreased by >50% in 11 out of 12 patients (91.7%). (4) Conclusions: CI may be helpful in attaining aggressive ampicillin PK/PD targets in patients affected by enterococcal BSIs and/or IE. Administration of CI ampicillin after loading coupled with real-time TDM-based ECPA could be a valuable strategy for managing enterococcal infections.
(1)目的:在一系列疑似或确诊为肠球菌血流感染(BSIs)和/或感染性心内膜炎(IE)的患者中,描述基于实时治疗药物监测(TDM)的策略对优化基于氨苄西林持续输注(CI)方案的药代动力学/药效学(PK/PD)目标达成情况的作用。(2)方法:回顾性评估2021年6月至2022年5月期间接受基于CI氨苄西林方案治疗确诊或疑似肠球菌BSI/IE且接受基于实时治疗药物监测(TDM)的专家临床药理学建议(ECPA)的患者。在稳态时测定氨苄西林浓度,并根据20%的血浆蛋白结合率计算游离分数(fCss)。选择fCss/MIC比值作为氨苄西林疗效的PD参数,定义为4至8之间的值为最佳。评估TDM指导下调整氨苄西林剂量的必要性。(3)结果:检索到12例确诊(n = 10)或疑似(n = 2)肠球菌感染患者的数据(7例BSIs和5例IE)。在所有10例确诊感染中,氨苄西林的PK/PD目标随时间推移是最佳的。没有肠球菌BSIs持续存在。在首次基于实时TDM的ECPA后,12例患者中有11例(91.7%)氨苄西林剂量降低>50%。(4)结论:CI可能有助于在受肠球菌BSIs和/或IE影响的患者中实现积极的氨苄西林PK/PD目标。负荷剂量后给予CI氨苄西林并结合基于实时TDM的ECPA可能是管理肠球菌感染的一种有价值的策略。