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基于分离住院日的药敏试验预测铜绿假单胞菌对目标抗菌药物敏感性的能力。

Ability of an antibiogram to predict Pseudomonas aeruginosa susceptibility to targeted antimicrobials based on hospital day of isolation.

机构信息

Duke University, School of Medicine, Durham, North Carolina 27710, USA.

出版信息

Infect Control Hosp Epidemiol. 2012 Jun;33(6):589-93. doi: 10.1086/665721. Epub 2012 Apr 13.

Abstract

OBJECTIVE

To determine the utility of an antibiogram in predicting the susceptibility of Pseudomonas aeruginosa isolates to targeted antimicrobial agents based on the day of hospitalization the specimen was collected.

DESIGN

Single-center retrospective cohort study.

SETTING

A 750-bed tertiary care medical center.

PATIENTS AND METHODS

Isolates from consecutive patients with at least 1 clinical culture positive for P. aeruginosa from January 1, 2000, to June 30, 2007, were included. A study antibiogram was created by determining the overall percentages of P. aeruginosa isolates susceptible to amikacin, ceftazidime, ciprofloxacin, gentamicin, imipenem-cilastin, piperacillin-tazobactam, and tobramycin during the study period. Individual logistic regression models were created to determine the day of infection after which the study antibiogram no longer predicted susceptibility to each antibiotic.

RESULTS

A total of 3,393 isolates were included. The antibiogram became unreliable as a predictor of susceptibility to ceftazidime, imipenem-cilastin, piperacillin-tazobactam, and tobramycin after day 10 and ciprofloxacin after day 15 but longer for gentamicin (day 21) and amikacin (day 28). Time to unreliability of the antibiogram varied for antibiotics based on location of isolation. For example, the time to unreliability of the antibiogram for ceftazidime was 5 days (95% confidence interval [CI], <1-8) in the intensive care unit (ICU) and 12 days (95% CI, 7-21) in non-ICU hospital wards (P = .003).

CONCLUSIONS

The ability of the antibiogram to predict susceptibility of P. aeruginosa decreases as duration of hospitalization increases.

摘要

目的

根据标本采集当天的住院日期,确定抗生素药敏谱在预测铜绿假单胞菌分离株对目标抗菌药物敏感性方面的作用。

设计

单中心回顾性队列研究。

地点

一家拥有 750 张床位的三级保健医疗中心。

患者和方法

连续收集 2000 年 1 月 1 日至 2007 年 6 月 30 日至少有 1 例临床培养为铜绿假单胞菌阳性的患者的标本。通过确定研究期间铜绿假单胞菌分离株对阿米卡星、头孢他啶、环丙沙星、庆大霉素、亚胺培南-西司他丁、哌拉西林-他唑巴坦和妥布霉素的总体敏感率,制定了研究抗生素药敏谱。建立个体逻辑回归模型,以确定在感染后第几天,研究抗生素药敏谱不再预测每种抗生素的敏感性。

结果

共纳入 3393 株分离株。抗生素药敏谱对头孢他啶、亚胺培南-西司他丁、哌拉西林-他唑巴坦和妥布霉素的预测敏感性在第 10 天以后、环丙沙星在第 15 天以后变得不可靠,但对庆大霉素(第 21 天)和阿米卡星(第 28 天)的不可靠时间更长。抗生素药敏谱不可靠的时间因分离部位而异。例如,头孢他啶在重症监护病房(ICU)的不可靠时间为 5 天(95%置信区间,<1-8),而非 ICU 病房的不可靠时间为 12 天(95%置信区间,7-21)(P =.003)。

结论

随着住院时间的延长,抗生素药敏谱预测铜绿假单胞菌敏感性的能力下降。

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