首页> 外文OA文献 >PCR-Single-Strand Conformational Polymorphism Method for Rapid Detection of Rifampin-Resistant Mycobacterium tuberculosis: Systematic Review and Meta-Analysis▿ †
【2h】

PCR-Single-Strand Conformational Polymorphism Method for Rapid Detection of Rifampin-Resistant Mycobacterium tuberculosis: Systematic Review and Meta-Analysis▿ †

机译:PCR-单链构象多态性法快速检测耐利福平的结核分枝杆菌:系统评价和荟萃分析▿†

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The reference standard methods for drug susceptibility testing of Mycobacterium tuberculosis, such as culture on Lowenstein-Jensen or Middlebrook 7H10/11 medium, are very slow to give results; and due to the emergence of multidrug-resistant M. tuberculosis and extensively drug-resistant M. tuberculosis, there is an urgent demand for new, rapid, and accurate drug susceptibility testing methods. PCR-single-strand conformational polymorphism (PCR-SSCP) analysis has been proposed as a rapid method for the detection of resistance to rifampin, but its accuracy has not been systematically evaluated. We performed a systematic review and meta-analysis to evaluate the accuracy of PCR-SSCP analysis for the detection of rifampin-resistant tuberculosis. We searched the Medline, Embase, Web of Science, BIOSIS, and LILACS databases and contacted authors if additional information was required. Ten studies met our inclusion criteria for rifampin resistance detection. We applied the summary receiver operating characteristic (SROC) curve to perform the meta-analysis and to summarize diagnostic accuracy. The sensitivity of PCR-SSCP analysis for the rapid detection of rifampin-resistant tuberculosis was 0.79 (95% confidence interval [CI], 0.75 to 0.82), the specificity was 0.96 (95% CI, 0.94 to 0.98), the positive likelihood ratio was 16.10 (95% CI, 5.87 to 44.13), the negative likelihood ratio was 0.20 (95% CI, 0.10 to 0.40), and the diagnostic odds ratio was 100.93 (95% CI, 31.95 to 318.83). PCR-SSCP analysis is a sensitive and specific test for the rapid detection of rifampin-resistant M. tuberculosis. Additional studies in countries with a high prevalence of multidrug-resistant M. tuberculosis and also cost-effectiveness analysis are required in order to obtain a complete picture on the utility of this method for rapid drug resistance detection in M. tuberculosis.
机译:结核分枝杆菌药敏试验的参考标准方法,例如在Lowenstein-Jensen或Middlebrook 7H10 / 11培养基上的培养,效果很慢。由于出现了多药耐药性结核分枝杆菌和广泛耐药的结核分枝杆菌,迫切需要新的,快速而准确的药敏试验方法。已经提出PCR-单链构象多态性(PCR-SSCP)分析作为检测对利福平的抗性的快速方法,但是其准确性尚未得到系统的评价。我们进行了系统的综述和荟萃分析,以评估PCR-SSCP分析检测耐利福平的结核病的准确性。我们搜索了Medline,Embase,Web of Science,BIOSIS和LILACS数据库,并在需要其他信息时与作者联系。十项研究符合我们对利福平耐药性检测的纳入标准。我们应用摘要接收器操作特性(SROC)曲线进行荟萃分析并总结诊断准确性。 PCR-SSCP分析对快速检测耐利福平结核病的敏感性为0.79(95%置信区间[CI],0.75至0.82),特异性为0.96(95%CI,0.94至0.98),阳性似然比为16.10(95%CI,5.87至44.13),负似然比为0.20(95%CI,0.10至0.40),诊断比值比为100.93(95%CI,31.95至318.83)。 PCR-SSCP分析是快速检测耐利福平的结核分枝杆菌的灵敏且特异的测试。为了对这种方法在结核分枝杆菌中快速耐药性检测的实用性有一个完整的了解,需要在具有高耐药性结核分枝杆菌的国家中进行进一步的研究,并进行成本效益分析。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号