张夏,孙静,古绍敏.小儿MPP合并EB病毒感染的临床表现及危险因素Logistic回归分析.[J].中南医学科学杂志.,2022,(3):435-437.
小儿MPP合并EB病毒感染的临床表现及危险因素Logistic回归分析
Clinical manifestations of children with MPP and EB virus infection and Logistic regression analysis of risk factors
投稿时间:2021-09-10  修订日期:2021-11-08
DOI:10.15972/j.cnki.43-1509/r.2022.03.032
中文关键词:  肺炎支原体肺炎  EB病毒  危险因素
英文关键词:mycoplasma pneumoniae pneumonia  EB virus  risk factor
基金项目:重庆市永川区科技局自然科技基金(YCstc,2020n60234) 作者简介:张夏,硕士,副主任检验师,研究方向为临床检验医学、临床生化及分子生物学,E-mail为3587737176@qq.com。通信作者古绍敏,主任医师,研究方向为儿科的临床诊断和冶疗,E-mail为gushaomin123@163.com。
作者单位E-mail
张夏 重庆市永川区妇幼保健院,重庆市 402160 e-mail为3587737176@qq.com,e-mail为gushaomin123@163.com 
孙静 四川大学华西第二医院麻醉科,四川省成都市 610041  
古绍敏 重庆医药高等专科学校附属第一医院,重庆市 402160 e-mail为3587737176@qq.com,e-mail为gushaomin123@163.com 
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中文摘要:
      目的探讨小儿肺炎支原体肺炎(MPP)合并EB病毒感染的临床表现并分析其危险因素。方法选取164例MPP合并EB病毒感染的患儿作为研究组,95例单纯EB病毒感染的上呼吸道感染患儿作为对照组,收集所有患儿的一般资料、临床特征,进行Logistic回归分析危险因素。结果两组患儿在年龄、发病季节、出生低体质量、流行接触史、免疫力低下、高热、呼吸困难、发热时间≥10天、肺部阴影≥2/3肺叶、胸腔积液、血沉≥50 mm/h、C反应蛋白≥8 mg/L上的差异有统计学意义(P<0.05);余指标差异无显著性。Logistic回归分析显示流行接触史(OR=2.438)、免疫力低下(OR=3.808)、发热时间≥10天(OR=2.000)、肺部阴影≥2/3肺叶(OR=1.772)、血沉≥50 mm/h(OR=3.062)、C反应蛋白≥8 mg/L(OR=2.192)是MPP合并EB病毒感染的危险因素。结论小儿MPP合并EB病毒感染有明显的临床表现及流行病学特征,降低高危因素有助于MPP合并EB病毒感染的防治。
英文摘要:
      To explore the clinical manifestations of children with Mycoplasma pneumoniae pneumonia (MPP) and EB virus infection and analyze the risk factors. MethodsA total of 164 children with MPP and EB virus infection (study group) and 95 children with upper respiratory tract infection infected with simple EB virus were used as the control group. The general data and clinical characteristics of all children were collected. Logistic regression analysis was conducted to analyze the risk factors. ResultsThere were significant differences in age, onset season, low birth weight, epidemic exposure history, low immunity, hyperpyrexia, dyspnea, fever time not shorter than 10d, lung shadow not smaller than 2/3 lung lobe, pleural effusion, erythrocyte sedimentation rate not lower than 50 mm/h and C-reactive protein not lower than 8 mg/L between the two groups (P<0.05), while there were no significant difference in gender, cesarean section, vomiting, lymphadenopathy and rash. Logistic regression analysis showed that epidemic exposure history (OR=2.438), low immunity (OR=3.808), fever time not shorter than 10 day (OR=2.000), lung shadow not smaller than 2/3 lung lobe (OR=1.772), erythrocyte sedimentation rate not lower than 50 mm/h (OR=3.062) and C-reactive protein not lower than 8 mg/L (OR=2.192) were the risk factors of MPP combined with EB virus infection. ConclusionsThere are significant clinical manifestations and epidemiological characteristics in children with MPP and EB virus infection. Reducing high-risk factors is conductive to the prevention of MPP combined with EB virus infection.
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