Intestinal Carriage of Carbapenemase-Producing Enterobacteriaceae Members in Immunocompromised Children During COVID-19 Pandemic

IF 0.5 Q4 PEDIATRICS Archives of Pediatric Infectious Diseases Pub Date : 2023-01-02 DOI:10.5812/pedinfect-127183
Nasim Almasian Tehrani, M. Alebouyeh, S. Armin, N. Soleimani, A. Karimi, B. Shamsian, S. Nazari, L. Azimi
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Abstract

Background: Hospital-acquired infection with carbapenem-resistant Enterobacteriaceae (CRE) is a global concern. The administration of antibiotics among the infected and non-infected immunocompromised children with SARS-CoV-2 is associated with an increased risk of intestinal CRE colonization and bacteremia during hospitalization. Objectives: The present study aimed to detect the correlation between the intestinal colonization of carbapenemase encoding Enterobacteriaceae with SARS-CoV-2 infection and antibiotic prescription among immunocompromised children admitted to the oncology and Bone Marrow Transplantation (BMT) wards. Methods: Stool samples were collected from the immunocompromised children, and the members of Enterobacteriaceae were isolated using standard microbiological laboratory methods. Carbapenem resistance isolates were initially characterized by the disc diffusion method according to CLSI 2021 and further confirmed by the PCR assay. SARS-CoV-2 infection was also recorded according to documented real-time PCR results. Results: In this study, 102 Enterobacteriaceae isolates were collected from the stool samples. The isolates were from Escherichia spp. (59/102, 57.8%), Klebsiella spp. (34/102, 33.3%), Enterobacter spp. (5/102, 4.9%), Citrobacter spp. (2/102, 1.9%), and Serratia spp. (2/102, 1.9%). The carbapenem resistance phenotype was detected among 42.37%, 73.52%, 40%, 50%, and 100% of Escherichia spp., Klebsiella spp., Enterobacter spp., Citrobacter spp., and Serratia spp., respectively. Moreover, blaOXA-48 (49.1%) and blaNDM-1 (29.4%), as well as blaVIM (19.6%) and blaKPC (17.6%) were common in the CRE isolates. SARS-CoV-2 infection was detected in 50% of the participants; however, it was confirmed in 65.45% (36/55) of the intestinal CRE carriers. The administration of antibiotics, mainly broad-spectrum antibiotics, had a significant correlation with the CRE colonization in both the infected and non-infected children with SARS-CoV-2 infection. Conclusions: Regardless of the COVID-19 status, prolonged hospitalization and antibiotic prescription are major risk factors associated with the CRE intestinal colonization in immunocompromised children.
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在COVID-19大流行期间免疫功能低下儿童中产碳青霉烯酶肠杆菌科成员的肠道运输
背景:医院获得性感染碳青霉烯耐药肠杆菌科(CRE)是一个全球关注的问题。感染和未感染的免疫功能低下的SARS-CoV-2患儿在住院期间使用抗生素与肠道CRE定植和菌血症的风险增加有关。目的:本研究旨在检测肿瘤和骨髓移植(BMT)病房免疫功能低下儿童肠道碳青霉烯酶编码肠杆菌科与SARS-CoV-2感染的定殖与抗生素处方的相关性。方法:收集免疫功能低下儿童的粪便样本,采用标准微生物实验室方法分离肠杆菌科成员。对碳青霉烯类耐药菌株采用圆盘扩散法进行初步鉴定,并采用PCR法进行进一步鉴定。根据记录的实时PCR结果也记录了SARS-CoV-2感染。结果:本研究共检出102株肠杆菌科分离株。分离株分别为埃希氏菌(59/ 102,57.8%)、克雷伯氏菌(34/ 102,33.3%)、肠杆菌(5/ 102,4.9%)、柠檬酸杆菌(2/ 102,1.9%)和沙雷氏菌(2/ 102,1.9%)。埃希氏菌、克雷伯氏菌、肠杆菌、柠檬酸杆菌和沙雷氏菌的耐药表型分别为42.37%、73.52%、40%、50%和100%。此外,blaOXA-48(49.1%)和blaNDM-1(29.4%)以及blaVIM(19.6%)和blaKPC(17.6%)在CRE分离株中普遍存在。50%的参与者检测到SARS-CoV-2感染;65.45%(36/55)肠道CRE携带者确诊。抗生素(主要是广谱抗生素)的使用与感染和未感染的SARS-CoV-2感染儿童的CRE定植均有显著相关。结论:无论是否感染COVID-19,长期住院和抗生素处方是免疫功能低下儿童CRE肠道定植的主要危险因素。
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来源期刊
CiteScore
1.80
自引率
14.30%
发文量
22
期刊介绍: Archives Of Pediatric Infectious Disease is a clinical journal which is informative to all practitioners like pediatric infectious disease specialists and internists. This authoritative clinical journal was founded by Professor Abdollah Karimi in 2012. The Journal context is devoted to the particular compilation of the latest worldwide and interdisciplinary approach and findings including original manuscripts, meta-analyses and reviews, health economic papers, debates and consensus statements of clinical relevance to pediatric disease field, especially infectious diseases. In addition, consensus evidential reports not only highlight the new observations, original research and results accompanied by innovative treatments and all the other relevant topics but also include highlighting disease mechanisms or important clinical observations and letters on articles published in the journal.
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