检验医学
檢驗醫學
검험의학
LABORATORY MEDICINE
2014年
6期
590-592
,共3页
陈旭%董丹凤%韩立中%倪语星
陳旭%董丹鳳%韓立中%倪語星
진욱%동단봉%한립중%예어성
艰难梭菌%快速检测%实时荧光定量聚合酶链反应
艱難梭菌%快速檢測%實時熒光定量聚閤酶鏈反應
간난사균%쾌속검측%실시형광정량취합매련반응
Clostridium difficile%Rapid detection%Real-time fluorescence quantitation polymerase chain reaction
目的:对GeneXpert实时荧光定量聚合酶链反应(PCR)在快速检测临床粪便标本中艰难梭菌的应用进行评估。方法采用双拭子蘸取临床未成形粪便标本,一支拭子用于GeneXpert实时荧光定量PCR检测艰难梭菌毒素基因tcdB,另一支用于常规厌氧菌培养检测;对GeneXpert实时荧光定量PCR检测结果与常规厌氧菌培养结果的一致性进行统计学分析,并计算GeneXpert实时荧光定量PCR的敏感性、特异性、阳性预测值和阴性预测值等参数。结果临床收集到141例未成形粪便标本,GeneXpert实时荧光定量PCR检出艰难梭菌毒素基因tcdB阳性42例,其中常规厌氧菌培养阳性34例,两者一致性较好(Kappa=0.7750,P<0.01),GeneXpert实时荧光定量PCR的敏感性、特异性、阳性预测值和阴性预测值分别为87.2%、92.2%、81.0%和94.9%。结论GeneXpert实时荧光定量PCR直接检测粪便标本中的艰难梭菌具有检测快速、操作简便等优点,有重要的临床应用价值。
目的:對GeneXpert實時熒光定量聚閤酶鏈反應(PCR)在快速檢測臨床糞便標本中艱難梭菌的應用進行評估。方法採用雙拭子蘸取臨床未成形糞便標本,一支拭子用于GeneXpert實時熒光定量PCR檢測艱難梭菌毒素基因tcdB,另一支用于常規厭氧菌培養檢測;對GeneXpert實時熒光定量PCR檢測結果與常規厭氧菌培養結果的一緻性進行統計學分析,併計算GeneXpert實時熒光定量PCR的敏感性、特異性、暘性預測值和陰性預測值等參數。結果臨床收集到141例未成形糞便標本,GeneXpert實時熒光定量PCR檢齣艱難梭菌毒素基因tcdB暘性42例,其中常規厭氧菌培養暘性34例,兩者一緻性較好(Kappa=0.7750,P<0.01),GeneXpert實時熒光定量PCR的敏感性、特異性、暘性預測值和陰性預測值分彆為87.2%、92.2%、81.0%和94.9%。結論GeneXpert實時熒光定量PCR直接檢測糞便標本中的艱難梭菌具有檢測快速、操作簡便等優點,有重要的臨床應用價值。
목적:대GeneXpert실시형광정량취합매련반응(PCR)재쾌속검측림상분편표본중간난사균적응용진행평고。방법채용쌍식자잠취림상미성형분편표본,일지식자용우GeneXpert실시형광정량PCR검측간난사균독소기인tcdB,령일지용우상규염양균배양검측;대GeneXpert실시형광정량PCR검측결과여상규염양균배양결과적일치성진행통계학분석,병계산GeneXpert실시형광정량PCR적민감성、특이성、양성예측치화음성예측치등삼수。결과림상수집도141례미성형분편표본,GeneXpert실시형광정량PCR검출간난사균독소기인tcdB양성42례,기중상규염양균배양양성34례,량자일치성교호(Kappa=0.7750,P<0.01),GeneXpert실시형광정량PCR적민감성、특이성、양성예측치화음성예측치분별위87.2%、92.2%、81.0%화94.9%。결론GeneXpert실시형광정량PCR직접검측분편표본중적간난사균구유검측쾌속、조작간편등우점,유중요적림상응용개치。
Objective To evaluate the clinical application of GeneXpert real-time fluorescence quantitation polymerase chain reaction (PCR)in rapid detection of Clostridium difficile from stool.Methods Two-head swab was dipped in clinical stool specimens,one-head swab was used for GeneXpert real-time fluorescence quantitation PCR in detecting toxity gene tcdB ,and the other was used for anaerobic culture.The results of these 2 methods were compared and analyzed statistically,and the sensitivity,specificity,positive predictive value and negative predictive value of GeneXpert real-time fluorescence quantitation PCR were calculated.Results Totally 1 41 clinical stool specimens were collected,and GeneXpert real-time fluorescence quantitation PCR revealed that Clostridium difficile was positive in 42 cases,among which Clostridium difficile was cultured in 34 cases.GeneXpert real-time fluorescence quantitation PCR was well consistent with the culture method (Kappa=0.775 0,P<0.01 ),and the sensitivity,specificity,positive predictive value and negative predictive value of GeneXpert real-time fluorescence quantitation PCR were 87.2%, 92.2%,81 .0% and 94.9%,respectively.Conclusions GeneXpert real-time fluorescence quantitation PCR could detect Clostridium difficile from stool specimens directly and accurately,and it has a prospective potential for clinical application.