危重患者头孢呋辛的人群药代动力学及优化剂量。

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Jaap W A Mouton, Julian D Machiels, Arthur M A Pistorius, Rob Ter Heine, Tim Frenzel, Nynke G L Jager, Jeroen A Schouten, Paddy K C Janssen, Rob E Aarnoutse, Roger J Brüggemann
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引用次数: 0

摘要

头孢呋辛是第二代头孢菌素,广泛应用于重症监护病房(ICU)。ICU患者在患者间药代动力学(PK)方面具有很高的变异性,但这种变异性的程度尚不清楚。我们对ICU患者进行了一项观察性PK研究。本研究的目的是了解头孢呋辛的PK,并调查目前临床应用的给药方案的目标实现情况。为了确定最合适的方案,计算了不同最低抑制浓度(MIC)和估计肾小球滤过率(egfr)的非结合药物最低抑制浓度以上时间(%fT > MIC)。20例患者平均年龄66岁,饮食改变肾病(MDRD)(未以BSA为指标)为90 [60-117.5]mL/min。以eGFR为协变量的双室模型最适合数据。对于eGFR为60 mL/min的典型个体,在EUCAST断点为8 mg/L的情况下,1500 mg q8h灌注剂量的目标实现概率(PTA)为43%。对于eGFR高达120 mL/min的典型个体,连续使用4.5 g/天获得100% PTA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Population pharmacokinetics and optimized dosing of cefuroxime in critically ill patients.

Cefuroxime is a second-generation cephalosporin widely used in the intensive care unit (ICU). ICU patients have high variability in interpatient pharmacokinetics (PK), but the extent of this variation is unclear. We performed an observational PK study in ICU patients. The objective of this study was to gain knowledge on the PK of cefuroxime and investigate target attainment of currently clinically applied dosing regimens. To identify the most suitable regimen the time above the minimal inhibitory concentration of the unbound drug (%fT > MIC) was calculated for different minimal inhibitory concentrations (MICs) and estimated Glomerular Filtration rates (eGFRs). Twenty patients were included with an average age of 66 years and modification of diet in renal disease (MDRD) (not indexed by BSA) of 90 [60-117.5] mL/min. A two-compartment model best fitted the data, with eGFR as a covariate. Probability of target attainment (PTA) was 43% for a 1500-mg q8h bolus dosage for the EUCAST break point of 8 mg/L for a typical individual with a eGFR of 60 mL/min. Dosing continuously using 4.5 g/day obtained 100% PTA for a typical individual with a eGFR up to 120 mL/min.

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来源期刊
CiteScore
6.30
自引率
8.80%
发文量
419
审稿时长
1 months
期刊介绍: Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.
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