Ma Yun-Ju, Wang Shih-Min, Cho Yu-Hao, Shen Ching-Fen, Liu Ching-Chuan, Chi Hsin, Huang Yi-Chuan, Huang Li-Min, Huang Yhu-Chering, Lin Hsiao-Chuan, Ho Yu-Huai, Mu Jung-Jung
Department of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan City, Taiwan.
Department of Emergency Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan City, Taiwan; Center of Infectious Disease and Signaling Research, National Cheng Kung University, Tainan City, Taiwan; Taiwan Pediatric Infectious Disease Alliance, Taiwan.
J Microbiol Immunol Infect. 2015 Dec;48(6):632-8. doi: 10.1016/j.jmii.2014.08.003. Epub 2014 Oct 11.
Community-acquired pneumonia (CAP) is the leading cause of hospitalization of children. Mycoplasma pneumoniae is one of the most common pathogens. The disease severity is diverse, and the diagnosis remains a challenge to clinical pediatricians. The aims of this study are to provide a nationwide surveillance of the epidemiology and clinical manifestations of community-acquired mycoplasma pneumonia (CAMP) in children in Taiwan.
The medical records of children enrolled by the Taiwan Pediatric Infectious Disease Alliance (TPIDA) project during 2010-2011 were reviewed. Hospitalized children with segmental or lobar pneumonia were included. The demographic, clinical, laboratory and radiographic data were analyzed. Nasopharyngeal swabs, pleural effusion, and serum were collected for multiplex viral and bacterial polymerase chain reaction (PCR), mycoplasma immunoglobulin M (IgM), or paired immunoglobulin G (IgG) titer.
There were overall 127 children with CAMP. Among them, 16 (12.6%) children had PCR and IgM positivity, 74 (58.3%) children had a positive serologic study, 34 (27.8%) children had positive PCR detection, and three (2.4%) children had paired IgG above a four-fold increase. Enrolled patients were divided into two groups before and after the age of 5 years. Children younger than 5 years or younger had a significantly longer hospitalization, higher intensive care unit (ICU) admission rates, and more complications. They were more frequent to receive oxygen supplementation and even surgical intervention. The white blood cell counts and C-reactive protein levels were higher in children 5 years old or younger.
Mycoplasma pneumoniae is an important etiology of CAP in children 5 years or younger. They had a longer length of hospitalization, higher inflammatory responses, and more complications, compared to children older than 5 years.
社区获得性肺炎(CAP)是儿童住院的主要原因。肺炎支原体是最常见的病原体之一。该病严重程度各异,诊断对临床儿科医生而言仍是一项挑战。本研究旨在对台湾地区儿童社区获得性支原体肺炎(CAMP)的流行病学和临床表现进行全国性监测。
回顾了台湾儿科传染病联盟(TPIDA)项目在2010 - 2011年期间登记的儿童病历。纳入患有节段性或大叶性肺炎的住院儿童。对人口统计学、临床、实验室和影像学数据进行分析。采集鼻咽拭子、胸腔积液和血清进行多重病毒和细菌聚合酶链反应(PCR)、支原体免疫球蛋白M(IgM)或配对免疫球蛋白G(IgG)滴度检测。
共有127例CAMP患儿。其中,16例(12.6%)患儿PCR和IgM呈阳性,74例(58.3%)患儿血清学检查呈阳性,34例(27.8%)患儿PCR检测呈阳性,3例(2.4%)患儿配对IgG升高四倍以上。纳入的患者按5岁前后分为两组。5岁及以下的儿童住院时间明显更长,重症监护病房(ICU)入住率更高,并发症更多。他们更频繁地接受吸氧甚至手术干预。5岁及以下儿童的白细胞计数和C反应蛋白水平更高。
肺炎支原体是5岁及以下儿童CAP的重要病因。与5岁以上儿童相比,他们住院时间更长,炎症反应更强烈,并发症更多。