[翻译]SARS-CoV-2感染对危重患者头孢他啶-阿维巴坦使用的影响。

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Fátima Mayo Olveira, José Manuel Caro Teller, María Dolores Canales Siguero, Sara Ortiz Pérez, María Del Carmen Jiménez León, José Miguel Ferrari Piquero
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引用次数: 0

摘要

目的:本研究的目的是分析重症监护病房(ICU)在SARS-CoV-2大流行期间头孢他啶-阿维巴坦的抗生素政策可能发生的变化,以确定开始抗菌治疗后28 天的患者死亡率,并描述最常定菌于危重患者的微生物。材料和方法:观察性、单中心、队列研究,纳入2020年3月至2021年9月在ICU接受头孢他啶-阿维巴坦治疗的患者。收集了人口统计学(年龄、性别)、微生物学(定殖、血液培养中分离的微生物)、药物治疗(使用头孢他啶-阿维巴坦治疗的持续时间、与头孢他啶-阿维巴坦协同使用的抗菌剂)和临床(死亡率、住院时间和合并症)变量。作为相关的合并症,我们确定了研究中有多少患者患有糖尿病(DM)、慢性肾脏疾病(CKD)、慢性阻塞性肺疾病(COPD)或肥胖。结果:共纳入89例患者,男性占85.39%。49例患者感染Sars-CoV-2。SARS-CoV-2感染患者中位住院时间为46 d (RIQ = 58 ~ 27),未感染患者中位住院时间为34 d (RIQ = 51 ~ 24)。患者ceftazidime-avibactam治疗平均8 天(RIQ =常规 ),被7 天(RIQ =本季 )COVID-19积极患者和11 天(RIQ = 14:6)COVID-19 -患者(p > 0.05)。41.57% (n = 37)的患者开始经验性治疗头孢他啶-阿维巴坦。SARS-CoV-2感染患者的经验起始率为43%,未感染患者为40%,根据SARS-CoV-2诊断状态的经验起始率差异无统计学意义(p > 0.05)。共有43.8% (n = 39)的患者被多药耐药(MDR)细菌定植。在定植患者的微生物方面,最常见的是肺炎克雷伯菌,占患者的66.6% (n = 26例)。总死亡率为41.6%,SARS-CoV-2感染患者与非感染患者的死亡率差异无统计学意义(分别为42.9%和40%;p > 0.05)。结论:SARS-CoV-2大流行未导致危重患者头孢他啶-阿维巴坦使用标准的改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Translated article] Influence of SARS-CoV-2 infection on the use of ceftazidime-avibactam in the critical patient.

Objective: The objective of the study was to analyse possible changes in antibiotic policy with ceftazidime-avibactam during the SARS-CoV-2 pandemic in an Intensive Care Unit (ICU) to determine patient mortality 28 days after initiation of antimicrobial therapy and to describe the microorganisms that most frequently colonise critically ill patients.

Material and method: Observational, single-centre, cohort study that included patients on treatment with ceftazidime-avibactam in ICU between March 2020 and September 2021. Demographic (age, sex), microbiological (colonisation, microorganisms isolated in blood cultures), pharmacotherapeutic (duration of treatment with ceftazidime-avibactam, antimicrobials used in synergy with ceftazidime-avibactam) and clinical (mortality, length of hospital stay and comorbidities) variables were collected. As associated comorbidities, we identified how many of the patients included in the study had diabetes mellitus (DM), chronic kidney disease (CKD), chronic obstructive pulmonary disease (COPD) or obesity.

Results: Eighty-nine patients were included, 85.39% of whom were male. Forty-nine patients were infected with Sars-CoV-2. Median ICU stay was 46 days (RIQ = 58-27) in SARS-CoV-2 infected and 34 days (RIQ = 51-24) in non-infected patients. Patients were on ceftazidime-avibactam treatment for a median of 8 days (RIQ = 13-4), being 7 days (RIQ = 11-2) in COVID-19 positive patients and 11 days (RIQ = 14-6) in COVID-19 negative patients (p > 0.05). Empirical treatment with ceftazidime-avibactam was started empirically in 41.57% (n = 37) of the patients. The percentage of empiric initiations in SARS-CoV-2 infected patients was 43% and in non-infected patients 40%, with no statistically significant difference between empiric initiation according to SARS-CoV-2 diagnostic status (p > 0.05). A total of 43.8% (n = 39) of the patients were colonised by a multidrug-resistant (MDR) bacterium. Regarding on the microorganisms that colonised patients had, the most frequent was Klebsiella pneumoniae, present in 66.6% of patients (n = 26 patients). Overall mortality was 41.6%, with no statistically significant differences between SARS-CoV-2 infected and non-infected patients (42.9% and 40%, respectively; p > 0.05).

Conclusion: The SARS-CoV-2 pandemic did not lead to a change in the criteria for the use of ceftazidime-avibactam in the critically ill patient.

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来源期刊
FARMACIA HOSPITALARIA
FARMACIA HOSPITALARIA PHARMACOLOGY & PHARMACY-
CiteScore
1.90
自引率
21.40%
发文量
46
审稿时长
37 days
期刊介绍: Una gran revista para acceder a los mejores artículos originales y revisiones de la farmacoterapia actual. Además, es Órgano de expresión científica de la Sociedad Española de Farmacia Hospitalaria, y está indexada en Index Medicus/Medline, EMBASE/Excerpta Médica, Alert, Internacional Pharmaceutical Abstracts y SCOPUS.
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