β-内酰胺抗菌素暴露与碳青霉烯耐药铜绿假单胞菌感染的关系:累积荟萃分析

Prity Rani Deshwal, Muskan Aggarwal, Nalla Surender Reddy, Raisa Fathima, Pramil Tiwari
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引用次数: 0

摘要

背景碳青霉烯类药物对严重的铜绿假单胞菌医院感染有效。因此,耐碳青霉烯假单胞菌是严重的公共卫生威胁。了解耐药铜绿假单胞菌感染中不适当暴露于不同抗菌素的风险有助于阐明在CRPA感染易感患者中使用抗菌素的有效方法。目的探讨β-内酰胺类抗菌药物暴露与对照组患者CRPA感染的关系。方法使用MEDLINE/PubMed和OVID/Embase数据库检索报告抗菌药物暴露为CRPA感染危险因素的病例对照和英语队列研究。使用随机效应和固定效应模型计算合并优势比(OR),并使用累积荟萃分析方法的森林图来更好地显示合并优势比随更新证据积累的变化情况。结果共纳入24项研究,7039名受试者进行累积荟萃分析。CRPA感染的发生与β -内酰胺类抗菌剂碳青霉烯类的暴露呈正相关(OR = 7.60, 95% CI: 3.95 ~ 14.62, P <0.0001)、亚胺培酮(OR = 9.81, 95% CI: 5.56 ~ 17.33)、氨苄西林(OR = 1.86, 95% CI: 1.14 ~ 2.41)、哌拉西林(OR = 2.82, 95% CI: 1.46 ~ 2.43)、青霉素(OR = 1.42, 95% CI: 0.90 ~ 2.24)、头孢菌素(OR = 1.88, 95% CI: 1.46 ~ 2.43)和β内酰胺酶抑制剂(OR = 1.96, 95% CI: 1.44 ~ 2.67)。此外,暴露于其他抗菌药物如喹诺酮(OR = 2.35, 95% CI: 1.78至3.10)、环丙沙星(OR = 2.35, 95% CI: 1.66至3.95)、氨基糖苷(OR = 2.17, 95% CI: 1.60至2.95)、阿米卡星(OR = 3.11, 95% CI: 2.10至4.61)、糖肽(OR = 3.02, 95% CI: 1.92至4.75)和万古霉素(OR = 3.26, 95% CI: 1.48至7.18)也被发现与CRPA感染的发生正相关。结论各种β-内酰胺暴露与耐碳青霉烯类铜绿假单胞菌感染的发生密切相关。这些发现为在耐药铜绿假单胞菌感染患者中使用β-内酰胺类抗菌剂提供了更积极的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of β-lactam antimicrobial's exposure with carbapenem-resistant Pseudomonas aeruginosa infection: a cumulative meta-analysis

Background

Carbapenems are effective against severe Pseudomonas aeruginosa nosocomial infections. Therefore, carbapenem-resistant Pseudomonas aeruginosa is a serious public health threat. An understanding of the risk of inappropriate exposure to different antimicrobials in resistant Pseudomonas aeruginosa infection could help in elucidating the effective approach towards using antimicrobials in vulnerable patients with CRPA infection.

Object

To investigate the association between exposure of β-lactam antimicrobials and CRPA infection relative to control patients.

Methods

The MEDLINE/PubMed and OVID/Embase databases were used to search case-control and cohort studies in English language which reported antimicrobial exposure as risk factors for CRPA infection. The pooled odds ratios (OR) were calculated using a random-effect and fixed-effect model, and forest plots from a cumulative meta-analysis method were used to better show how pooled OR changed as updated evidence accumulated.

Results

A total of 24 studies comprising 7 039 participants were included for cumulative meta-analysis. A positive correlation was found between development of CRPA infection and exposure of beta-lactam antimicrobials: carbapenems (OR = 7.60, 95% CI: 3.95 to 14.62, P < 0.0001), imipenem (OR = 9.81, 95% CI: 5.56 to 17.33), ampicillin (OR = 1.86, 95% CI: 1.14 to 2.41), piperacillin (OR = 2.82, 95% CI: 1.46 to 2.43), penicillins (OR = 1.42, 95% CI: 0.90 to 2.24), cephalosporins (OR = 1.88, 95% CI: 1.46 to 2.43) and β lactamase inhibitors (OR = 1.96, 95% CI: 1.44 to 2.67). Further, exposure of other antimicrobial agents like quinolone (OR = 2.35, 95% CI: 1.78 to 3.10), ciprofloxacin (OR = 2.35, 95% CI: 1.66 to 3.95), aminoglycoside (OR = 2.17, 95% CI: 1.60 to 2.95), amikacin (OR = 3.11, 95% CI: 2.10 to 4.61), glycopeptides (OR = 3.02, 95% CI: 1.92 to 4.75) and vancomycin (OR = 3.26, 95% CI: 1.48 to 7.18), were also found to be positively associated with development of CRPA infection.

Conclusions

Exposure of all kinds of β-lactams is significantly associated with development of carbapenem-resistant Pseudomonas aeruginosa infection. These findings provide an impetus to take a more active approach while using β-lactam antimicrobials in patients with resistant Pseudomonas aeruginosa infections.

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Global health journal (Amsterdam, Netherlands)
Global health journal (Amsterdam, Netherlands) Public Health and Health Policy
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