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新生儿肠道CRKP定植和继发感染的影响因素

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目的 分析新生儿耐碳青霉烯类肺炎克雷伯菌(CRKP)肠道定植与定植后继发感染的影响因素,为制定CRKP感染的防控策略提供依据。方法 选取2021年1月-2022年10月入住某院新生儿病房的新生儿为研究对象,入院后48 h内进行CRKP首次筛查,此外在住院期间每周进行一次耐碳青霉烯类肠杆菌(CRE)肛拭子主动筛查,并监测CRKP菌株感染情况。分析定植组、非定植组和感染组新生儿临床数据。对肠道定植菌及定植后继发感染新生儿临床标本中分离的非重复CRKP菌株进行碳青霉烯酶基因检测与多位点序列分型(MLST)和脉冲场凝胶电泳(PFGE)分析。结果 共有1 438例新生儿进行了 CRE主动筛查,174例新生儿CRKP阳性,CRKP定植率为12。1%。174例定植新生儿中有35例继发感染,发病率为20。1%。新生儿CRKP肠道定植的独立危险因素为剖宫产(OR=2。050,95%CI:1。200~3。504,P=0。009)、使用头孢菌素类抗生素(OR=1。889,95%CI:1。086~3。288,P=0。024)、鼻胃管喂养(OR=2。317,95%CI:1。155~4。647,P=0。018);保护因素为母乳喂养(OR=0。506,95%CI:0。284~0。901,P=0。021)、口服益生菌(OR=0。307,95%CI:0。147~0。643,P=0。002)、灌肠(OR=0。334,95%CI:0。171~0。656,P=0。001)。新生儿CRKP肠道定植继发感染的独立危险因素为使用碳青霉烯类抗生素(OR=19。869,95%CI:1。778~222。029,P=0。015)和住院时间延长(OR=1。118,95%CI:1。082~1。157,P<0。001)。耐药基因结果显示CRKP菌株产碳青霉烯酶基因均为blaKPC-2,且同属于ST11型。同源性关系结果分析显示肠道CRKP定植与定植后继发感染菌株高度同源。结论 新生儿住院期间CRKP肠道定植可能会增加CRKP感染的风险。因此,可通过重点关注新生儿肠道定植及定植后继发感染的危险与保护因素,并采取相应的预防控制措施,减少CRKP医院感染的发生和传播。
Influencing factors for intestinal colonization and secondary infection of CRKP in neonates
Objective To analyze the influencing factors for intestinal colonization and secondary infection of car-bapenem-resistant Klebsiella pneumoniae(CRKP)in neonates,and provide a basis for formulating prevention and control strategies for CRKP infection.Methods Neonates who were admitted to the neonatal ward of a hospital from January 2021 to October 2022 were selected as the study subjects,and the first screening of CRKP was con-ducted within 48 hours after admission.In addition,active anal swab screening for carbapenem-resistant Ente-robacterales(CRE)was performed weekly during hospitalization,and the infection status of CRKP strains was mo-nitored.Clinical data of neonates in the colonization group,non-colonization group,and infection group were ana-lyzed.Intestinal colonized strains and the non-repetitive CRKP strains isolated from clinical specimens of neonates with secondary infection after colonization were performed carbapenemase gene detection,multilocus sequence ty-ping(MLST)and pulsed-field gel electrophoresis(PFGE)analysis.Results A total of 1 438 neonates were active-ly screened for CRE,174 were CRKP positive,CRKP colonization rate was 12.1%.Among 174 neonates,35 were with secondary infection,with the incidence of 20.1%.The independent risk factors for neonatal CRKP intestinal colonization were cesarean section(OR=2.050,95%CI:1.200-3.504,P=0.009),use of cephalosporins(OR=1.889,95%CI:1.086-3.288,P=0.024),nasogastric tube feeding(OR=2.317,95%CI:1.155-4.647,P=0.018).Protective factors were breast-feeding(OR=0.506,95%CI:0.284-0.901,P=0.021),oral probiotics(OR=0.307,95%CI:0.147-0.643,P=0.002),and enema(OR=0.334,95%CI:0.171-0.656,P=0.001).Independent risk factors for secondary infection after intestinal colonization of neonatal CRKP were carbapenem anti-biotic use(OR=19.869,95%CI:1.778-222.029,P=0.015)and prolonged hospital stay(OR=1.118,95%CI:1.082-1.157,P<0.001).The detection results of drug resistance genes showed that carbapenemase-producing genes of CRKP strains were all blaKPC-2,all belonged to type ST11.Homologous analysis showed that intestinal CRKP colonization was highly homologous with the secondary infection strains after colonization.Conclusion CRKP intestinal colonization during neonatal hospitalization may increase the risk of CRKP infection.Risk and pro-tective factors of neonatal intestinal colonization and secondary infections after colonization should be paid attention,and corresponding preventive and control measures should be taken,so as to reduce the occurrence and transmission CRKP healthcare-associated infection.

carbapenem-resistant Klebsiella pneumoniaecolonizationinfectionneonateprotective factorrisk factorhomology

翟誉、李庆蓉、李江、何薇、和平安、吕梅、杨旭

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昆明医科大学第二附属医院检验科,云南昆明 650032

耐碳青霉烯类肺炎克雷伯菌 定植 感染 新生儿 保护因素 危险因素 同源性

国家自然科学基金项目云南省科技厅基础研究专项面上项目云南省教育厅科学研究基金项目昆明医科大学第二附属医院院内科技计划项目昆明医科大学2023年硕士研究生创新基金立项项目

82060669202101AT0702562023Y06412021yk0022023S315

2024

中国感染控制杂志
中南大学

中国感染控制杂志

CSTPCD北大核心
影响因子:2.112
ISSN:1671-9638
年,卷(期):2024.23(2)
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