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摘要:
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| 目的: 探讨碳青霉烯耐药肠杆菌科细菌(CRE)中blaNDM和blaOXA基因型分布特征,评估基因型检测在区域传播监控中的临床价值,为临床精准治疗和感染控制提供科学依据。方法: 采用回顾性队列研究方法,纳入2024年1月至2025年3月期间本院365例CRE感染住院患者。采用MALDI-TOF MS进行细菌鉴定,VITEK 2系统检测药敏,多重PCR技术检测blaNDM、blaOXA、blaKPC、blaVIM、blaIMP等碳青霉烯酶基因,阳性产物测序分析基因亚型。收集患者临床资料,分析不同基因型CRE的临床特征、抗菌药物敏感性、传播特征及患者预后。采用多因素Logistic回归分析影响患者30 d死亡的独立危险因素。结果: 365株CRE中肺炎克雷伯菌278株(76.2%),其次为大肠埃希菌49株(13.4%)。blaNDM基因阳性324株(88.8%),主要为blaNDM-1亚型286株(88.3%);blaOXA基因阳性267株(73.2%),主要为blaOXA-48亚型176株(65.9%);双基因阳性248株(67.9%)。双基因阳性组患者恶性肿瘤比例(46.8% vs 32.6%,P=0.021)、ICU住院比例(73.8% vs 52.6%,P<0.001)及机械通气使用率(48.4% vs 29.5%,P=0.003)均显著高于单基因组。与blaNDM单基因阳性组比,双基因阳性菌株对替加环素(58.9% vs 77.6%,P=0.003)和多黏菌素B(54.8% vs 71.1%,P=0.013)的敏感率显著降低。研究期间识别出6起聚集性传播事件,涉及83例患者(22.7%),重症医学科、血液科为高风险科室。双基因阳性组30 d病死率(24.2% vs 13.7%,P=0.029)和住院天数[(31.4±19.8)d vs(22.1±15.3)d,P<0.001]均显著高于单基因组。多因素分析显示,双基因阳性(OR=2.34,95%CI:1.21~4.52,P=0.012)是患者30 d死亡的独立危险因素。结论: blaNDM/blaOXA基因型检测在CRE区域传播监控中具有重要临床价值。双基因阳性CRE感染患者表现出更广泛的耐药性、更高的病死率和更差的临床预后,提示需要更加积极的治疗策略和严格的感染控制措施。基因型检测不仅能够指导精准治疗,还是院内感染控制和流行病学监测的重要工具。 |
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