A Systematic Review of the Definitions, Determinants, and Clinical Outcomes of Antimicrobial De-escalation in the Intensive Care Unit

被引:125
|
作者
Tabah, Alexis [1 ,2 ]
Cotta, Menino Osbert [1 ,2 ,3 ]
Garnacho-Montero, Jose [7 ]
Schouten, Jeroen [8 ]
Roberts, Jason A. [1 ,2 ,3 ]
Lipman, Jeffrey [1 ,2 ,4 ]
Tacey, Mark [5 ,6 ]
Timsit, Jean-Francois [9 ,10 ]
Leone, Marc [11 ]
Zahar, Jean Ralph [12 ]
De Waele, Jan J. [13 ]
机构
[1] Univ Queensland, Royal Brisbane & Womens Hosp, Intens Care Unit, Brisbane, Qld, Australia
[2] Univ Queensland, Burns Trauma & Crit Care Res Ctr, Brisbane, Qld, Australia
[3] Univ Queensland, Sch Pharm, Brisbane, Qld, Australia
[4] Queensland Univ Technol, Fac Hlth, Brisbane, Qld 4001, Australia
[5] Univ Melbourne, Melbourne EpiCtr, Royal Melbourne Hosp, Melbourne, Vic 3010, Australia
[6] Univ Melbourne, Dept Med, Melbourne, Vic 3010, Australia
[7] Hosp Univ Virgen Macarena, Unidad Clin Cuidados Intens, Inst Biomed Sevilla, Seville, Spain
[8] Canisius Wilhelmina Hosp, Dept Intens Care, Nijmegen, Netherlands
[9] Univ Paris Diderot, Sorbonne Paris Cite, INSERM, Hop Bichat,AP HP Reanimat Med & Malad Infect, Paris, France
[10] Univ Paris Diderot, Sorbonne Paris Cite, INSERM, UMR 1137,IAME Team 5,DeSCID Decis Sci Infect Dis, Paris, France
[11] Aix Marseille Univ, Hop Nord, Serv Anesthesie & Reanimat, AP HM, Marseille, France
[12] Univ Angers, CHU Angers, Unite Prevent & Lutte Infect Nosocomiales, Angers, France
[13] Ghent Univ Hosp, Dept Crit Care Med, Ghent, Belgium
基金
英国医学研究理事会;
关键词
de-escalation; stewardship; streamlining; resistance; ANTIBIOTIC-THERAPY; SEVERE SEPSIS; PNEUMONIA; IMPACT;
D O I
10.1093/cid/civ1199
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antimicrobial de-escalation (ADE) is a strategy to reduce the spectrum of antimicrobials and aims to prevent the emergence of bacterial resistance. We present a systematic review describing the definitions, determinants and outcomes associated with ADE. We included 2 randomized controlled trials and 12 cohort studies. There was considerable variability in the definition of ADE. It was more frequently performed in patients with broad-spectrum and/or appropriate antimicrobial therapy (P=.05 to .002), when more agents were used (P=.002), and in the absence of multidrug-resistant pathogens (P<.05). Where investigated, lower or improving severity scores were consistently associated with ADE (P=.04 to <.001). The pooled effect of ADE on mortality is protective (relative risk, 0.68; 95% confidence interval,.52-.88). Because the determinants of ADE are markers of clinical improvement and/or of lower risk of treatment failure this effect on mortality cannot be retained as evidence. None of the studies were designed to investigate the effect of ADE on antimicrobial resistance.
引用
收藏
页码:1009 / 1017
页数:9
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