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危重症成人耐头孢曲松革兰氏阴性杆菌首次培养阳性时间。

Time to First Culture Positivity for Gram-Negative Rods Resistant to Ceftriaxone in Critically Ill Adults.

机构信息

Department of Internal Medicine, 12328Vanderbilt University Medical Center, Nashville, TN, USA.

Division of Allergy, Pulmonary, and Critical Care Medicine, 12328Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

J Intensive Care Med. 2021 Jan;36(1):51-57. doi: 10.1177/0885066620963903. Epub 2020 Oct 5.

Abstract

BACKGROUND

The optimal timing for the de-escalation of broad-spectrum antibiotics with activity against and resistant Gram-negative rods (GNRs) in critically ill adults remains unknown.

RESEARCH QUESTION

We tested the hypothesis that cultures will identify GNRs that ultimately demonstrate resistance to ceftriaxone within 48 hours, potentially allowing safe de-escalation at this time point.

STUDY DESIGN AND METHODS

We conducted a secondary analysis of data from the Isotonic Solutions and Major Adverse Renal Events Trial: a pragmatic, cluster-randomized, multiple-crossover trial comparing balanced crystalloids versus saline for intravenous fluid administration in 15,802 critically ill adults at 5 intensive care units (ICUs) at Vanderbilt University Medical Center in Nashville, TN, USA. The primary endpoint was the time-to-positivity of respiratory and blood cultures that ultimately demonstrated growth of GNRs resistant to ceftriaxone. Multivariable logistic regression modeling was used to examine risk factors for the growth of cultures after 48 hours.

RESULTS

A total of 524 respiratory cultures had growth of GNRs, of which 284 (54.2%) had resistance to ceftriaxone. A total of 376 blood cultures grew GNRs, of which 70 (18.6%) had resistance to ceftriaxone. At 48 hours, 87% of respiratory cultures and 85% of blood cultures that ultimately grew GNRs resistant to ceftriaxone had demonstrated growth. Age, gender, predicted risk of inpatient mortality and prior use of antibiotics did not predict the growth of cultures after 48 hours.

INTERPRETATION

Among a cohort of critically ill adults, 13% of respiratory cultures and 15% of blood cultures that ultimately grew GNRs resistant to ceftriaxone did not demonstrate growth until at least 48 hours after collection. Further work is needed to determine the ideal time for critically ill adults to de-escalate from broad-spectrum antibiotics targeting and extended-spectrum β-lactamase-producing gram-negative pathogens.

摘要

背景

在危重症成人中,针对 和耐药革兰阴性杆菌(GNR)的广谱抗生素降阶梯治疗的最佳时机仍不清楚。

研究问题

我们检验了以下假设,即在 48 小时内,培养物将鉴定出最终对头孢曲松耐药的 GNR,从而有可能在此时间点进行安全降阶梯治疗。

研究设计和方法

我们对来自 Isotonic Solutions 和 Major Adverse Renal Events 试验的数据进行了二次分析:这是一项实用的、集群随机、多次交叉试验,比较了平衡晶体液与生理盐水在田纳西州纳什维尔范德比尔特大学医学中心的 5 个重症监护病房(ICU)中对 15802 名危重症成人进行静脉输液。主要终点是最终生长出对头孢曲松耐药的 GNR 的呼吸道和血液培养物的阳性时间。多变量逻辑回归模型用于检查 48 小时后培养物生长的危险因素。

结果

共有 524 份呼吸道培养物生长出 GNR,其中 284 份(54.2%)对头孢曲松耐药。共有 376 份血培养物生长出 GNR,其中 70 份(18.6%)对头孢曲松耐药。在 48 小时时,87%的最终生长出对头孢曲松耐药的 GNR 的呼吸道培养物和 85%的血液培养物已经生长。年龄、性别、住院死亡率的预测风险和抗生素的先前使用并不能预测 48 小时后的培养物生长。

解释

在一组危重症成人中,13%的最终生长出对头孢曲松耐药的 GNR 的呼吸道培养物和 15%的血液培养物直到采集后至少 48 小时才显示出生长。需要进一步研究来确定危重症成人从针对 和产超广谱β-内酰胺酶革兰氏阴性病原体的广谱抗生素降阶梯治疗的最佳时机。

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