Zieck Saskia E, de Vroom Suzanne L, Mulder Frouke Ph, van Twillert Gitte, Mathôt Ron A A, Geerlings Suzanne E, van Hest Reinier M
Department of Pharmacy and Clinical Pharmacology, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
Department of Hospital Pharmacy, Division of Clinical Pharmacology, Noordwest Ziekenhuisgroep, Location Alkmaar, Wilhelminalaan 12, 1815 JF Alkmaar, The Netherlands.
Antibiotics (Basel). 2023 Feb 25;12(3):469. doi: 10.3390/antibiotics12030469.
No prospective evidence exists on the pharmacokinetic/pharmacodynamic (PK/PD) target attainment of ceftazidime in adult patients on general wards. We aimed to investigate whether the PK/PD target of ceftazidime (50% T > MIC) is attained in adult patients on general wards with adequate and impaired renal function receiving regular and guideline-recommended reduced doses of ceftazidime. In this observational, prospective, bicenter cohort study, adult patients admitted to a general ward receiving ceftazidime as part of standard care were included. Three blood samples per patient within 72 h after start of treatment were collected. Data were analyzed with nonlinear mixed effects modeling. The primary endpoint was target attainment of 50% T > MIC during the first 24 h of treatment (50% T > MIC). Forty patients were included from whom 121 blood samples were obtained. All 25/25 patients with adequate renal function, 9/10 patients with moderately impaired renal function (eGFR 30-50 mL/min/1.73 m) and 5/5 patients with severe impaired renal function (eGFR < 30 mL/min/1.73 m) attained 50% T > MIC when applying the clinical breakpoint MIC for of 8 mg/L. The one patient not attaining the PK/PD target did not differ in any of the collected patients' characteristics, except that this patient was the oldest in the study population. However, age was not statistically significantly associated with clearance or volume of distribution in the population pharmacokinetic model and, therefore, not likely the cause for this patient not attaining the PK/PD target. Our results suggest ≥90% probability of the PK/PD target attainment of ceftazidime in patients on general wards with adequate and impaired renal function receiving regular and guideline-recommended reduced doses of ceftazidime for treatment of infections with and all bacteria with lower MIC-values.
对于普通病房成年患者中头孢他啶的药代动力学/药效学(PK/PD)达标情况,目前尚无前瞻性证据。我们旨在调查,在接受常规且符合指南推荐的减量剂量头孢他啶治疗的、肾功能正常及受损的普通病房成年患者中,头孢他啶的PK/PD目标(50%T>MIC)是否能够实现。在这项观察性、前瞻性、双中心队列研究中,纳入了入住普通病房并接受头孢他啶作为标准治疗一部分的成年患者。在治疗开始后72小时内,为每位患者采集三份血样。采用非线性混合效应模型分析数据。主要终点是治疗的前24小时内达到50%T>MIC的目标(50%T>MIC)。纳入了40名患者,共采集到121份血样。当应用8mg/L的临床折点MIC时,所有25/25名肾功能正常的患者、9/10名中度肾功能受损(估算肾小球滤过率[eGFR]为30 - 50mL/min/1.73m²)的患者以及5/5名重度肾功能受损(eGFR<30mL/min/1.73m²)的患者均达到了50%T>MIC。未达到PK/PD目标的那名患者,在收集的任何患者特征方面均无差异,只是该患者是研究人群中年龄最大的。然而,在群体药代动力学模型中,年龄与清除率或分布容积并无统计学显著关联,因此,不太可能是该患者未达到PK/PD目标的原因。我们的结果表明,对于接受常规且符合指南推荐的减量剂量头孢他啶治疗感染的、肾功能正常及受损的普通病房患者,以及所有MIC值较低的细菌感染患者,头孢他啶达到PK/PD目标的概率≥90%。