摘要
目的评估多色巢式荧光定量PCR(Xpert MTB/RIF)的半定量水平与MGIT 960液体培养的报阳率、报阳时间和利福平的耐药情况之间的关系。方法回顾性收集同时行痰液Xpert MTB/RIF及MGIT 960液体培养检测的患者共376例,根据Xpert MTB/RIF检测阈值将其分为4组进行比较。结果高含量组(98.1%)和中含量组(95.3%)的MGIT 960报阳率均较极低含量组(39.2%)和低含量组(66.1%)显著增高(P <0.01)。同时中等含量组(16.0 d)和高含量组(13.0 d)的报阳时间均较极低含量组(23.0 d)和低含量组(20.0 d)显著更短(P <0.01)。此外,以MGIT 960药敏试验结果为金标准,高含量组(96.2%)和中含量组(92.1%)耐药基因检测的准确度均较极低含量组(35.4%)和低含量组(63.6%)显著增高(P <0.01)。结论 Xpert MTB/RIF试验半定量结果为中等含量及以上时,液体培养的报阳率更高、报阳时间也更短,并且利福平的耐药基因检测的准确度也更高。
Objective To evaluate the relationship between semi-quantitative Xpert MTB/RIF level and the positive rate,reporting time and rifampicin resistance in MGIT 960 liquid culture. Methods The retrospective study enrolled 376 patients,the specimens of who were detected by Xpert MTB/RIF and MGIT 960 rapid liquid culture at the same time. The patients were separated in four groups for comparison according to semi-quantitative Xpert MTB/RIF level. Results The positive rate in MGIT 960 liquid culture of the very medium( 95. 3%) and high content group( 98. 1%) were both significantly higher than that in the very low( 66. 1%) and low content group( 39. 2%)( P < 0. 01). Meanwhile,the reporting time in MGIT 960 liquid culture of the medium( 16. 0 d) and high content group( 13. 0 d) were significantly shorter than that in the very low( 23. 0 d) and low content group( 20. 0 d)( P < 0. 01). With the drug sensitivity test of MGIT 960 liquid culture as the gold standard,the accuracy in the very low,low,medium and high content group were respectively 35. 4%( 28/79),63. 6%( 75/118),92. 1%( 117/127),96. 2%( 50/52). The accuracy of rifampicin detection in the medium( 92. 1%) and high content group( 96. 2%) were significantly higher than that in the very low( 35. 4%) and low content group( 63. 6%)( P <0. 01). Conclusion When the semi-quantitative results of Xpert MTB/RIF are at medium level and above,the positive rate of liquid culture is higher,the time of reporting positive is shorter,and the accuracy of rifampicin resistance gene detection is also higher.
作者
陈菊萍
范超明
CHEN Ju-ping;FAN Chao-ming(Clinical Laboratory,the Affiliated Hospital of Hangzhou Normal University,Hangzhou,Zhejiang 310011,China)
出处
《中国卫生检验杂志》
CAS
2020年第22期2714-2716,2719,共4页
Chinese Journal of Health Laboratory Technology
基金
杭州市科技发展计划项目(20191203B102)
浙江省医药卫生科技项目(2019KY500)。