Gajdács Márió, Matuz Mária, Ria Benkő, Pető Zoltán, Hajdú Edit
1Department of Oral Biology and Experimental Dental Research, Faculty of Dentistry, University of Szeged, 6720 Szeged, Tisza Lajos krt. 64-66., Hungary.
2Central Pharmacy Department, Albert Szent-Györgyi Medical Center, University of Szeged, 6725 Szeged, Semmelweis utca 6., Hungary.
Eur J Microbiol Immunol (Bp). 2024 Mar 5;14(2):185-194. doi: 10.1556/1886.2024.00022. Print 2024 May 14.
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.
在医院环境中广泛使用碳青霉烯类药物可能会导致嗜麦芽窄食单胞菌(SM)面临选择压力。我们研究的目的是评估全身使用抗生素与SM感染发生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,在匈牙利一家三级护理医院开展了一项回顾性观察研究。将SM以及对甲氧苄啶-磺胺甲恶唑(SXT)耐药的SM的发病密度标准化为每1000个患者日,而全身使用抗生素的情况则表示为每100个患者日的限定日剂量(DDD)。SM感染的平均发病密度为0.42/1000个患者日;11.08%对SXT耐药,对SXT耐药的SM的平均发病密度为0.047/1000个患者日。从2010年到2019年,黏菌素、糖肽类和碳青霉烯类药物的消耗率分别增加了258.82%、278.94%和372.72%。观察到碳青霉烯类药物的消耗量与SM(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)以及糖肽类药物的消耗量与每1000个患者日的SM和对SXT耐药的SM发病密度之间分别存在强且显著的正相关。实施机构性碳青霉烯类药物节约策略对于保存这些救命药物至关重要,并且可能会影响临床环境中感染的微生物谱。