石伟先, 董梅, 龚成, 李茂中, 张铁钢, 李爱华, 罗明, 刘医萌, 赵佳琛, 黄芳. 2015-2016年北京市急性呼吸道感染病例肺炎支原体流行特征分析[J]. 疾病监测, 2018, 33(4): 306-311. DOI: 10.3784/j.issn.1003-9961.2018.04.011
引用本文: 石伟先, 董梅, 龚成, 李茂中, 张铁钢, 李爱华, 罗明, 刘医萌, 赵佳琛, 黄芳. 2015-2016年北京市急性呼吸道感染病例肺炎支原体流行特征分析[J]. 疾病监测, 2018, 33(4): 306-311. DOI: 10.3784/j.issn.1003-9961.2018.04.011
Shi Weixian, Dong Mei, Gong Cheng, Li Maozhong, Zhang Tiegang, Li Aihua, Luo Ming, Liu Yimeng, Zhao Jiachen, Huang Fang. Analysis of Mycoplasma pneumoniae infection in acute respiratory infection cases in Beijing,2015-2016[J]. Disease Surveillance, 2018, 33(4): 306-311. DOI: 10.3784/j.issn.1003-9961.2018.04.011
Citation: Shi Weixian, Dong Mei, Gong Cheng, Li Maozhong, Zhang Tiegang, Li Aihua, Luo Ming, Liu Yimeng, Zhao Jiachen, Huang Fang. Analysis of Mycoplasma pneumoniae infection in acute respiratory infection cases in Beijing,2015-2016[J]. Disease Surveillance, 2018, 33(4): 306-311. DOI: 10.3784/j.issn.1003-9961.2018.04.011

2015-2016年北京市急性呼吸道感染病例肺炎支原体流行特征分析

Analysis of Mycoplasma pneumoniae infection in acute respiratory infection cases in Beijing,2015-2016

  • 摘要: 目的 分析北京市2015-2016年急性呼吸道感染病例中肺炎支原体的流行特征,为其防控提供科学依据。方法 以2015年1月至2016年12月就诊于北京市各区哨点医院的急性呼吸道感染病例为研究对象,收集其咽拭子、痰、鼻咽抽吸物等呼吸道样本。采用实时荧光PCR法检测样本中肺炎支原体及其基因型别,病例性别、年龄、发病时间、临床表现的不同基因型肺炎支原体阳性率的比较采用χ2检验。结果 所有样本中的肺炎支原体阳性率为4.69%(652/13 904),其中P1-Ⅰ、P1-Ⅱ和未分型阳性样本分别为238、230和184份;经χ2检验,P1-Ⅰ型与P1-Ⅱ型阳性率差异无统计学意义(χ2=0.139,P=0.709)。男、女性病例阳性率分别为4.35%(342/7 866)和5.13%(310/6 038),差异有统计学意义(χ2=4.726,P=0.030)。6~岁年龄组阳性率最高,60~岁最低,各年龄组阳性率差异有统计学意义(χ2=347.600,P=0.001)。2016年肺炎支原体阳性率(5.18%)高于2015年(4.11%)(χ2=8.889,P=0.003),10- 12月阳性率高于其他月份(χ2=225.000,P=0.001)。肺炎病例中肺炎支原体阳性率(6.45%)高于急性上呼吸道感染病例(1.65%)(χ2=166.800,P=0.001)。结论 2015-2016年北京市急性呼吸道感染病例中,P1-Ⅰ型与P1-Ⅱ型肺炎支原体同时流行,女性患者、6~岁儿童与青少年为肺炎支原体感染的高发人群,不同年龄组病例易感基因型不同,2016年较2015年高发,各季节均有散发病例,10-12月为流行高峰,肺炎支原体的感染更易导致肺炎。

     

    Abstract: Objective By monitoring the infection status of Mycoplasma pneumoniae in patients with acute respiratory tract infection during 2015-2016 in Beijing,the epidemiological characteristics for M. pneumoniae infection were analyzed. Methods A total of 13 904 respiratory samples,including throat swabs,sputum and nasopharyngeal aspiration,were collected from the acute respiratory infections cases in sentinel hospitals in all districts in Beijing from January 2015 to December 2016. Real-time fluorescence PCR was used to detect M. pneumoniae and its genotypes in samples,and χ2 test was used to compare the positive detection rate of M. pneumoniae among different genotypes according to sex,age,onset time and clinical manifestations. Results A total 652 M. pneumoniae positive samples were detected in 13 904 samples,the positive detection rate was 4.69%,of which 238 (36.50%)were positive for genotype P1-Ⅰ,230 (35.28%)for genotype P1-Ⅱ,but 184 (28.22%)samples were failed in genotyping. There was no significant difference in positive detection rates between P1-Ⅰ and P1-Ⅱ(χ2=0.139,P=0.709). The positive rates of male and female patients were 4.35%(342/7 866)and 5.13%(310/6 038), respectively,with significant difference(χ2=4.726,P=0.030). The positive rate was highest in age group 6-years(10.23%, 150/1 466)and lowest in age group 60-years(1.43%,62/4 346),and the differences in positive detection rate among all age groups were significant (χ2=347.600,P=0.001). The positive rate of M. pneumoniae was 5.18% in 2016,which was significantly higher than 4.11% in 2015 (χ2=8.889,P=0.003). The positive detection rate in October-December was significantly higher than that in other months(χ2=225.000,P=0.001). The positive rate in pneumonia cases was 6.45%, significantly higher than 1.65% in cases of acute upper respiratory tract infection(χ2=166.800,P=0.001). Conclusion From 2015 to 2016,both P1-Ⅰ and P1-Ⅱ M. pneumoniae were prevalent in the acute respiratory infection cases in Beijing. Females,people aged 6-15 years were at high risk. The susceptible genotypes were different in patients in different age groups. The positive detection rate of M. pneumoniae was higher in 2016 than in 2015. M. pneumoniae infection occurred in all seasons,but peaked from October to December. M. pneumoniae infection is prone to cause pneumonia.

     

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