重症监护病房中抗微生物药物的使用和耐抗生素细菌和真菌感染的其他危险因素

A. Cheng, Jesse Chou, Robert G Sawyer
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摘要

耐药感染在重症监护病房(ICU)尤其成问题,但危险因素尚不清楚。我们假设耐药革兰氏阴性杆状体(rGNR)、耐药革兰氏阳性球菌(rGPC)和继发性真菌感染的危险因素不同。材料与方法:对1997 - 2017年icu获得性感染患者进行单中心队列研究。纳入条件是rGNR、rGPC或真菌的存在。研究的危险因素包括人口统计学、医学合并症、急性生理和慢性健康评估(APACHE) II评分和既往抗微生物药物暴露。结果:共发现重症监护病房获得性感染43,199例。其中有一千九百九十八种被认为具有抗药性,2321种被认为没有抗药性。任何耐药菌的鉴定与女性、非创伤性诊断、APACHE II评分、肝脏疾病、慢性类固醇使用、任何既往感染史和耐药感染史显著相关,但与既往抗菌药物使用天数无关。rGNR感染与既往感染给予治疗性抗菌药物的天数有关,但与住院期间既往抗菌药物的总天数无关。rGPC感染与先前使用抗菌素治疗的感染和住院期间使用抗菌素的总天数有关。真菌感染与任何先前的抗微生物药物暴露都没有关联。控制疾病的严重程度和人口统计,与非耐药感染相比,耐药感染与死亡率无关。结论:rGNR感染的可能性与最近的抗菌药物暴露密切相关,而rGPC感染似乎与先前的抗菌药物暴露有关。真菌感染可能与先前的抗微生物接触无关。这些发现表明不同种类的耐药病原体的不同的生态失调机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobial use and other risk factors for infections with antimicrobial-resistant bacteria and fungi bacteria and fungi in an intensive care unit
Introduction: Resistant infections are especially problematic in the intensive care unit (ICU), but risk factors remain unclear. We hypothesized that the risk factors for resistant Gram-negative rods (rGNR), resistant Gram-positive cocci (rGPC), and secondary fungal infections differed. Materials and Methods: A single-center cohort study of patients with ICU-acquired infections from 1997 to 2017 was performed. Inclusion was conditioned on the presence of rGNR, rGPC, or fungi. Risk factors studied included demographics, medical comorbidities, Acute Physiology and Chronic Health Evaluation (APACHE) II score, and previous antimicrobial exposure. Results: Four thousand three hundred and nineteen ICU-acquired infections were identified. One thousand nine hundred and ninety-eight were considered resistant and 2321 were considered nonresistant. Identification of any resistant organism was significantly associated with female sex, nontrauma diagnosis, APACHE II score, liver disease, chronic steroid use, history of any prior infection, and history of a resistant infection, but not days of prior antimicrobial use. Infections with rGNR were associated with days of therapeutic antimicrobials given for a previous infection, but not total prior antimicrobial days during hospitalization. rGPC infections were associated with both previous infections treated with antimicrobials and total prior antimicrobial days during hospitalization. Fungal infections were not associated with any measure of prior antimicrobial exposure. Controlling for the severity of illness and demographics, resistant infections were not associated with mortality compared to nonresistant infections. Conclusions: The likelihood of rGNR infection is closely linked to recent antimicrobial exposure, while rGPC infection appears to be associated with prior antimicrobial exposure. Fungal infections may not be associated with prior antimicrobial exposure. These findings suggest disparate mechanisms of dysbiosis for different classes of resistant pathogens.
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