期刊文献+

GeneXpert法检测痰液在肺结核诊断中的价值

The value of sputum detection by GeneXpert method in the diagnosis of pulmonary tuberculosis
下载PDF
导出
摘要 目的:探讨Gene Xper t法检测痰液在肺结核诊断中的临床价值。方法:选取2020年12月—2021年3月在滨州市结核病防治院确诊的住院肺结核患者123例,123例患者各留取晨痰3~5 m L于无菌痰盒中,分别采用GeneXpert法、痰TB-DNA定性法、痰培养法、痰抗酸染色涂片法进行检测,对比不同组别中的诊断结果。结果:123例肺结核患者GeneXpert法阳性89例(72.36%),痰TB-DNA定性法阳性76例(61.79%),痰培养法阳性56例(45.53%),痰抗酸染色涂片法阳性49例(39.84%)。GeneXpert法和痰培养法结果比较,差异有统计学意义(χ^(2)=18.293,P<0.001);痰TB-DNA定性法和痰培养法结果比较,差异有统计学意义(χ^(2)=6.539,P=0.011);痰抗酸染色涂片法和痰培养法结果比较,差异无统计学意义(χ^(2)=0.814,P=0.367);GeneXpert法和痰TB-DNA定性法结果比较,差异无统计学意义(χ^(2)=3.11,P=0.078)。123例患者经痰液检测,菌阳组阳性检出率显著高于菌阴组,菌阳和菌阴组GeneXpert法检测结果比较,差异有统计学意义(χ^(2)=18.229,P<0.001)。结论:GeneXpert法检测患者痰液在肺结核诊断中有较高应用价值,且快速、简便,值得临床应用。 Objective To explore the clinical application value of sputum detection by GeneXpert in the diagnosis of pulmonary tuberculosis.Methods From December 2020 to March 2021,a total of 123 inpatients with confirmed tuberculosis in Binzhou Tuberculosis Hospital were enrolled,morning sputum 3 to 5 mL samples were collected from each patient and detected Mycobacterium tuberculosis by GeneXpert method,Sputum TB-DNA qualitative method,sputum culture and acid-fast staining smear,respectively,the diagnostic efficacy of different groups was compared.Results Among the samples from 123 patients,89(72.36%)were positive by GeneXpert method,76(61.79%)were positive by Sputum TB-DNA qualitative method,56(45.53%)were positive by sputum culture,and 49(39.84%)were positive by sputum acid-fast staining smear.There was significant difference between GeneXpert method and sputum culture results(χ^(2)=18.293,P<0.001);The results of Sputum TB-DNA qualitative method and sputum culture method were significantly different(χ^(2)=6.539,P=0.011);The results of acid-fast staining smear and sputum culture method were significantly no different(χ^(2)=0.814 P=0.367);There was no significant difference between the results of GeneXpert method and sputum TB-DNA qualitative method(χ^(2)=3.11,P=0.078).The 123 sputum samples were then divided into two groups,bacteria positive group and bacteria negative group.The positive rate of the bacteria positive group was significantly higher than bacteria negative group.The results of GeneXpert method were statistically significant(χ^(2)=18.229,P<0.001)between bacteria positive group and bacteria negative group.Conclusion GeneXpert method has great application value in the diagnosis of pulmonary tuberculosis,and it is rapid,simple and worthy of popularization and application.
作者 郭新军 杜小倩 GUO Xinjun;DU Xiaoqian(Department of Laboratory,Binzhou Central Hospital<Binzhou Tuberculosis Prevention and Control Hospital>,Binzhou,Shandong 251700,China)
出处 《医药前沿》 2022年第34期12-14,共3页 Journal of Frontiers of Medicine
关键词 GeneXpert法 肺结核 诊断 GeneXpert method Tuberculosis(TB) Diagnosis
  • 相关文献

参考文献7

二级参考文献56

  • 1闵春燕,时翠林,叶志坚,陈兴年,吴妹英.气管镜多指标联合检测对菌阴支气管结核患者的诊断价值[J].结核病与肺部健康杂志,2013,2(2). 被引量:5
  • 2潘毓萱,赵雁林.菌阴肺结核的细菌学含义[J].中华结核和呼吸杂志,2005,28(10):671-674. 被引量:29
  • 3中国疾病预防控制中心.痰涂片镜检实验室质量保证手册.北京:中国协和医科大学出版社,2004:5-18.
  • 4赵雁林,尚美.我国当前结核病实验室诊断的现状[J].结核病与胸部肿瘤,2007(4):310-314. 被引量:5
  • 5赵雁林,王黎霞,成诗明,等.结核分枝杆菌药物敏感性试验标准化操作程序及质量保证手册.北京:人民卫生出版社,2012.
  • 6赵雁林,王黎霞,成诗明,等.分枝杆菌分离培养标准化操作程序及质量保证手册.北京:人民卫生出版社,2012:26-30.
  • 7Lawn SD, Nicol MP. Xpert MTB/RIF assay: development, evaluation and implementation of a new rapid molecular diag- nostic for tuberculosis and rifampicin resistance. Future Microbiol, 2011, 6(9):1067-1082.
  • 8Blakemore R, Story E, Helb D, et al. Evaluation of the ana- lytical performance of the Xpert MTB/RIF assay. J Clin Microbiol, 2010, 48(7):2495-2501.
  • 9Moure R, Munoz L, Tortes M, et al. Rapid detection of My- cobacterium tuberculosis complex and rifampin resistance in smear-negatlve clinical samples by use of an integrated real- time PCR method. J Clin Microbiol, 2011,49(3):1137-1139.
  • 10Armand S, Vanhuls P, Delcroix G, et al. Comparison of the Xpert MTB/RIF test with an IS6110 TaqMan real-time PCR assay for direct detection of Mycobacterium tuberculosis in re- spiratory and nonrespiratory specimens. J Clin Microbiol, 2011, 49(5):1772-1776.

共引文献697

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部