中国西部地区儿童支原体社区获得性肺炎合并病毒和细菌感染的临床影响

Zhuoxin Liang, Wenqiang Zhang, Yongjiang Jiang, Ping Wu, Sen Zhang, Shaolin Xu, Jinjian Fu, E. McGrath
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摘要

社区获得性肺炎(CAP)是指在医院外感染,导致肺实质炎症。CAP患者肺炎支原体(肺炎支原体)感染的临床特征很少报道。本研究的目的是描述中国柳州住院CAP儿童肺炎支原体与病毒和细菌病原体共同感染的临床特征和影响。本研究回顾了在三级妇幼保健医院因肺炎支原体感染而被诊断为CAP的儿童。从该医院的电子医疗系统中收集与共感染病原体、人口统计、临床特征和住院费用相关的数据。2017年,共有983名儿童被诊断为支原体CAP。其中细菌性M型占18.2%。肺炎合并感染11.3%为病毒性M型。肺炎合并感染。肺炎支原体感染率最高的是2月和3月的19.1%,而细菌-M感染率最高。肺炎和病毒-M。肺炎合并感染在12月和1月分别为3.6%和2.3%。咳嗽和喘息的患病率在细菌或病毒-M之间存在显著差异。肺炎合并感染组和单感染组。此外,呼吸道病毒和细菌-M的胸部X光检查进展、胸腔积液、呼吸衰竭和通气率较高。肺炎合并感染组比单纯感染组多。与肺炎支原体单感染的儿童相比,细菌或呼吸道病毒共同感染的儿童住院时间更长,治疗费用也更多(P值<0.001),将有严重的疾病进展,应该进行专门的治疗和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Impact of Combined Viral and Bacterial Infection in Pediatric Mycoplasmal Community-Acquired Pneumonia in Western China
Community-acquired pneumonia (CAP) refers to an infection contracted outside the hospital that leads to lung parenchyma inflammation. The clinical characteristics of Mycoplasma pneumoniae (M. pneumoniae) infection in CAP patients were rarely reported. The aim of this study was to describe the clinical characteristic and the impact of co-infections of M. pneumoniae with viral and bacterial pathogens in hospitalized children with CAP in Liuzhou, China. This study retrospects children diagnosed with CAP due to M. pneumoniae infection at a tertiary maternal and child health care hospital. Data related to co-infection pathogens, demographics, clinical characteristics, and hospitalization cost were collected from the electronic medical system in this hospital. A total of 983 children were diagnosed with mycoplasmal CAP in 2017. Among them, 18.2% had a bacterial-M. pneumoniae co-infection and 11.3% had a viral-M. pneumoniae co-infection. The highest infection rate of M. pneumoniae was 19.1% in February and March, while the highest rates of bacterial-M. pneumoniae and viral-M. pneumoniae co-infections were 3.6% in December and 2.3% in January, respectively. The prevalence of coughing and wheezing had significant differences between the bacterial- or viral-M. pneumoniae co-infections and the mono-infection groups. Furthermore, the chest X-ray progression, pleural effusions, respiratory failure, and ventilation rates were higher in the respiratory viral- and bacterial-M. pneumoniae co-infection groups than in the mono-infection group. Children with a bacterial or respiratory viral co-infection had a longer hospitalization and spent more on treatment fees than those with a M. pneumoniae mono-infection (P value <0.001). We conclude that children with mycoplasmal CAP, either with a bacterial or viral co-infection, who show signs of coughing and wheezing and have a radiographic progression, will have a severe disease progression and should be specifically treated and managed.
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Nanoscience and Nanotechnology Letters
Nanoscience and Nanotechnology Letters Physical, Chemical & Earth Sciences-MATERIALS SCIENCE, MULTIDISCIPLINARY
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