文章摘要
儿童肺泡灌洗液RT-PCR检测对支原体感染的辅助诊断价值探讨
Analysis of bronchoalveolar lavage fluid MP-DNA detection by RT-PCR for aided diagnosis in children with mycoplasma infection
投稿时间:2017-10-09  
DOI:10.3969/j.issn.1000-0399.2018.03.012
中文关键词: 肺炎支原体  肺泡灌洗液  DNA  IgM抗体  儿童
英文关键词: Mycoplasma pneumoniae  Bronchoalveolar lavage fluid  DNA  IgM antibody  Children
基金项目:
作者单位E-mail
张晨宇 230051 合肥 安徽省儿童医院医学检验中心  
刘海鹏 230051 合肥 安徽省儿童医院医学检验中心 itishaipeng@yeah.net 
朱丽娟 230051 合肥 安徽省儿童医院医学检验中心  
刘红娟 230051 合肥 安徽省儿童医院医学检验中心  
裘肃霆 230051 合肥 安徽省儿童医院医学检验中心  
苏晓霁 230051 合肥 安徽省儿童医院医学检验中心  
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中文摘要:
      目的 探讨支原体感染儿童肺泡灌洗液RT-PCR检测的早期诊断和病情评估。方法 选取2016年1月至12月安徽省儿童医院收治的235例感染肺炎支原体(MP)的患儿,检测重症肺炎和轻症肺炎肺泡灌洗液MP-DNA和血清MP-IgM,根据2项指标的差异和MP-DNA拷贝量的高低,分析MP-DNA与病情的关系。结果 男患儿MP-IgM阳性率低于女患儿,>3~14岁患儿MP-DNA阳性率高于1~3岁患儿,入院前病程≤ 7 d患儿MP-IgM阳性率低于入院前病程>7 d患儿,差异有统计学意义(P<0.05)。重症肺炎患儿中,MP-DNA高拷贝量占85.71%,高于轻症肺炎患儿,差异有统计学意义(P<0.05);重症肺炎的MP-DNA拷贝量高于轻症肺炎患儿,差异有统计学意义(P<0.05)。结论 RT-PCR法检测支原体肺炎患儿肺泡灌洗液MP-DNA拷贝量可为快速确诊和判断患儿病情提供参考。
英文摘要:
      Objective To evaluate the diagnostic value of real time fluorescence quantitative PCR (RT-PCR) applied in bronchoalveolar lavage fluid MP-DNA detection in children with mycoplasma infection at the early stage. Methods The bronchoalveolar lavage fluid MP-DNA and serum MP-IgM from 235children with mycoplasma pneumoniae were deeply measured,and these indexes were further used to evaluate the relationship with the state of an illness. Results The positive rates of MP-IgM in male were lower than those in female, the positive rates of MP-DNA in >3~14 years old were higher than those in 1~3 years old, the positive rates of MP-IgM in children with a course of diseaseless than and equal to 7 days from onset to hospital admission were significantly lower than those in a course of disease more than 7 days, and the difference was statistically significant (P<0.05). The high-copy MP-DNA accounted for 85.71% in children with severe pneumonia, and the proportions of the high-copy MP-DNA in children with severe pneumonia were higher than those in children with mild pneumonia, and there was a significant statistical difference(P<0.05); the copy numbers of MP-DNA in children with severe pneumonia were higher than those in children with mild pneumonia, and there was a significant statisticaldifference(P<0.05) Conclusion The RT-PCR method to check the copies of bronchoalveolar lavage fluid MP-DNA provides a reference for fast and accurate diagnosis of the severity of children disease.
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