嗜麦芽血单胞菌发病率与全身使用抗生素之间的相关性:匈牙利一项为期 10 年的回顾性观察研究。

European journal of microbiology & immunology Pub Date : 2024-03-05 Print Date: 2024-05-14 DOI:10.1556/1886.2024.00022
Márió Gajdács, Mária Matuz, Benkő Ria, Zoltán Pető, Edit Hajdú
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引用次数: 0

摘要

碳青霉烯类抗生素的广泛使用可能会导致医院环境中嗜麦芽血单胞菌(SM)的选择压力。我们的研究旨在评估全身使用抗生素与嗜麦芽糖单胞菌发病率之间可能存在的关联。2010年1月1日至2019年12月31日期间,我们在匈牙利一家三级甲等医院开展了一项回顾性观察研究。SM和对三甲双氨-磺胺甲噁唑(SXT)耐药的SM的发病密度以1000个患者日为标准,而全身抗生素的使用则以每100个患者日的定义日剂量(DDDs)表示。SM感染的平均发病密度为0.42/1000个患者日;11.08%的SM对SXT耐药,SXT耐药SM的平均发病密度为0.047/1000个患者日。从 2010 年到 2019 年,可乐定、糖肽类药物和碳青霉烯类药物的消耗率分别增加了 258.82%、278.94% 和 372.72%。与碳青霉烯类(r:0.8759;P < 0.001 和 r:0.8968;P < 0.001)、SXT(r:0.7552;P = 0.011和r: 0.7004; P = 0.024),以及糖肽(r: 0.7542; P = 0.012和r: 0.8138; P < 0.001)分别与SM和SXT耐药SM的发病密度/1000患者日有关。实施机构碳青霉烯类节约策略对于保护这些救命药物至关重要,并可能影响临床环境中感染的微生物谱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation between Stenotrophomonas maltophilia incidence and systemic antibiotic use: A 10-year retrospective, observational study in Hungary.

Extensive use of carbapenems may lead to selection pressure for Stenotrophomonas maltophilia (SM) in hospital environments. The aim of our study was to assess the possible association between systemic antibiotic use and the incidence of SM. A retrospective, observational study was carried out in a tertiary-care hospital in Hungary, between January 1st 2010 and December 31st 2019. Incidence-density for SM and SM resistant to trimethoprim-sulfamethoxazole (SXT) was standardized for 1000 patient-days, while systemic antibiotic use was expressed as defined daily doses (DDDs) per 100 patient-days. Mean incidence density for SM infections was 0.42/1000 patient-days; 11.08% were were resistant to SXT, the mean incidence density for SXT-resistant SM was 0.047/1000 patient-days. Consumption rate for colistin, glycopeptides and carbapenems increased by 258.82, 278.94 and 372.72% from 2010 to 2019, respectively. Strong and significant positive correlations were observed with the consumption of carbapenems (r: 0.8759; P < 0.001 and r: 0.8968; P < 0.001), SXT (r: 0.7552; P = 0.011 and r: 0.7004; P = 0.024), and glycopeptides (r: 0.7542; P = 0.012 and r: 0.8138; P < 0.001) with SM and SXT-resistant SM incidence-density/1000 patient-days, respectively. Implementation of institutional carbapenem-sparing strategies are critical in preserving these life-saving drugs, and may affect the microbial spectrum of infections in clinical settings.

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