Multidrug-resistant Gram-negative bacteria rate and risk factors in the neonatal intensive care unit: A single-center ten-year experience

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
H. Cakmak, Dilek Yekenkurul, Zehra Şengün, Selvi Yener, P. Duran, F. Davran, K. Kocabay
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引用次数: 0

Abstract

Background: Multidrug resistance (MDR) in gram-negative neonatal infections is difficult to manage, and the risk factors differ among different studies. We aim to investigate the demographics, mortality, MDR status of gram-negative isolates, and risk factors for MDR gram-negative infections. Material-Methods: We conducted a retrospective single-center study about MDR gram-negative infections in neonates between January 2012-January 2022 at Duzce University Hospital in Turkey. This study evaluates neonates with MDR gram-negative infections' risk factors and clinical features. All analyses were performed using IBM SPSS V23. Univariate analyses and multivariate logistic regression models were studied to determine MDR's risk factors. Results: Of 107 gram-negative bacteria, 41 (38.3%) accounted for Enterobacter, 30 (28%) for Klebsiella pneumonia, and 22 (20.6%) for Escherichia coli. Additionally, 61 (56.5%) were MDR microorganisms. Among the susceptibility tests performed for selected isolates, 41 (77.4%) had resistance to Piperacillin, 57 (75%) showed resistance to amoxiclav, and 16 (72.7%) had cefoxitin resistance. In addition, carbapenemase resistance was found in 24 (43.6%) and meropenem resistance in 13 (36.1%). Colistin, aztreonam, and tigecycline resistances were the least frequent. The following dependent risk factors increased the multidrug resistance risk in gram-negative infections; late-onset sepsis 3.547 fold (p=0.005), use of mechanical ventilation 3.143 fold (p=0.007), blood culture positivity 3.587-fold (p=0.013), bronchopulmonary dysplasia 6.702 fold, (p= 0.015) and total parenteral nutrition 5.591 fold (p=0.001), lower gestational age 1.122 (1/0.891) fold (p=0.026), and birth weight 1.001 (1/0.999) fold, (p=0.013). Similarly, anti-biotherapy duration was significantly higher in the MDR group than in the non-MDR group. Conclusions: The reported risk factors for MDR in gram-negative neonatal infections are all dependent risk factors. Hence clinicians must be alert to all potential risk factors.
新生儿重症监护室耐多药革兰氏阴性菌发生率和危险因素:单中心十年经验
背景:新生儿革兰阴性感染的多药耐药性(MDR)难以控制,不同研究的危险因素不同。我们的目的是调查革兰氏阴性分离株的人口统计学、死亡率、耐多药状态以及耐多药革兰氏阴性感染的危险因素。材料方法:我们在土耳其Duzce大学医院对2012年1月至2022年1月期间新生儿耐多药革兰氏阴性感染进行了一项回顾性单中心研究。本研究评估新生儿耐多药革兰氏阴性感染的危险因素和临床特征。所有分析均使用IBM SPSS V23进行。研究了单变量分析和多变量逻辑回归模型来确定MDR的危险因素。结果:107株革兰氏阴性菌中,肠杆菌41株(38.3%),肺炎克雷伯菌30株(28%),大肠杆菌22株(20.6%)。此外,61种(56.5%)为耐多药微生物。在对所选分离株进行的药敏试验中,41株(77.4%)对哌拉西林耐药,57株(75%)对阿莫西林耐药,16株(72.7%)对头孢西丁耐药。此外,碳青霉烯酶耐药性24例(43.6%),美罗培南耐药性13例(36.1%)。粘菌素、氨曲南和替加环素耐药性最不常见。以下依赖性危险因素增加了革兰氏阴性感染的多药耐药性风险;晚发性败血症3.547倍(p=0.005),使用机械通气3.143倍(p=0.007),血液培养阳性3.587倍(p=0.013),支气管肺发育不良6.702倍(p=0.015)和全胃肠外营养5.591倍(p=0.001),低胎龄1.122倍(1/0.891)倍(p=0.026),出生体重1.001倍(1/0.999)倍(p=0.013)。类似地,MDR组的抗生物治疗持续时间显著高于非MDR组。结论:报道的新生儿革兰阴性感染MDR的危险因素均为依赖性危险因素。因此临床医生必须警惕所有潜在的风险因素。
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Konuralp Tip Dergisi
Konuralp Tip Dergisi MEDICINE, GENERAL & INTERNAL-
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