Recommended Antibiotic Dosage Regimens in Critically Ill Patients with Augmented Renal Clearance: A Systematic Review

加药 医学 抗生素 病危 药代动力学 药效学 重症监护医学 人口 肾功能 药理学 内科学 生物 微生物学 环境卫生
作者
Catarina Mendes Silva,João Pedro Baptista,I. Santos,Paulo Martins
出处
期刊:International Journal of Antimicrobial Agents [Elsevier]
卷期号:59 (5): 106569-106569 被引量:12
标识
DOI:10.1016/j.ijantimicag.2022.106569
摘要

Augmented renal clearance (ARC) is common in critically ill patients and may lead to subtherapeutic levels of antibiotics, thus influencing clinical outcomes and emergence of multidrug-resistant bacteria. The aim of this systematic review was to search the literature for recommendations concerning dosage adjustment for antibiotics administered to critically ill patients with ARC.A search of three electronic databases (Pubmed, Embase and Cochrane) was conducted from inception until the end of March 2021, using terms related to: 1) pharmacokinetics/pharmacodynamics (PK/PD), 2) antibiotic, 3) ARC and 4) critically ill. Two reviewers searched for relevant data and included studies suggesting specific doses for critically ill patients with ARC.Forty-seven studies met the inclusion criteria. Dosage recommendations were found for 18 antibiotics. Differences were found in population characteristics, ARC definition, creatinine clearance (CLCR) determination method, PK methodology and definition of PK/PD targets. Cut-off values for CLCR ranged 120-240 mL/min; the most frequently employed method to define CLCR was Cockcroft-Gault estimation; and 83% of studies used population PK models to predict dosing regimens. All antibiotics, except three, needed upward dosing and/or infusion modality adjustments to reach PK/PD targets.Despite the lack of high-quality studies and high heterogeneity, incremental dosing adjustment of antibiotics was frequently needed for critically ill patients with ARC to achieve the desired PK/PD targets. More research is needed to enlarge the number of antibiotics with recommendations for ARC and to validate current suggestions based on mathematical models in a clinical scenario.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
13秒前
niu52107完成签到,获得积分10
13秒前
chen完成签到,获得积分10
14秒前
一叶知秋完成签到,获得积分10
14秒前
yan完成签到 ,获得积分10
17秒前
Silieze完成签到,获得积分10
17秒前
lojong完成签到,获得积分10
17秒前
dengcl-jack完成签到,获得积分10
17秒前
852应助ABCofMEDICIBE采纳,获得10
18秒前
xiaoxiaoliang完成签到,获得积分10
24秒前
兮以城空完成签到,获得积分10
29秒前
英俊的铭应助科研通管家采纳,获得10
30秒前
SOLOMON应助科研通管家采纳,获得20
30秒前
科目三应助科研通管家采纳,获得10
30秒前
李爱国应助科研通管家采纳,获得10
30秒前
香蕉觅云应助科研通管家采纳,获得10
30秒前
华仔应助科研通管家采纳,获得10
30秒前
小马甲应助科研通管家采纳,获得10
30秒前
Akim应助科研通管家采纳,获得10
30秒前
无花果应助科研通管家采纳,获得10
30秒前
ding应助科研通管家采纳,获得10
30秒前
SOLOMON应助科研通管家采纳,获得20
30秒前
Imp发布了新的文献求助10
31秒前
华仔应助刘金凤采纳,获得10
31秒前
slin_sjtu完成签到,获得积分10
33秒前
36秒前
角鸮完成签到,获得积分10
37秒前
研友_VZG7GZ应助Y0采纳,获得10
39秒前
大学士发布了新的文献求助10
40秒前
兰晋彤发布了新的文献求助10
40秒前
Nancy应助wang采纳,获得10
41秒前
热心白凝完成签到 ,获得积分10
43秒前
脑洞疼应助sjl采纳,获得10
46秒前
调皮雨灵完成签到 ,获得积分10
47秒前
夕荀完成签到,获得积分10
47秒前
50秒前
50秒前
丘比特应助兰晋彤采纳,获得10
51秒前
小蘑菇应助兰晋彤采纳,获得10
51秒前
Ryan完成签到,获得积分10
52秒前
高分求助中
Formgebungs- und Stabilisierungsparameter für das Konstruktionsverfahren der FiDU-Freien Innendruckumformung von Blech 1000
The Illustrated History of Gymnastics 800
The Bourse of Babylon : market quotations in the astronomical diaries of Babylonia 680
Division and square root. Digit-recurrence algorithms and implementations 500
The role of a multidrug-resistance gene (lemdrl) in conferring vinblastine resistance in Leishmania enriettii 330
Elgar Encyclopedia of Consumer Behavior 300
機能營養學前瞻(3 Ed.) 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2510322
求助须知:如何正确求助?哪些是违规求助? 2159917
关于积分的说明 5530065
捐赠科研通 1880171
什么是DOI,文献DOI怎么找? 935659
版权声明 564215
科研通“疑难数据库(出版商)”最低求助积分说明 499574