湖南师范大学学报(医学版)
湖南師範大學學報(醫學版)
호남사범대학학보(의학판)
JOURNAL OF HUNAN NORMAL UNIVERSITY(MEDICAL SCIENCE)
2013年
4期
33-35
,共3页
徐明忠%晏群%邹明祥%李虹玲
徐明忠%晏群%鄒明祥%李虹玲
서명충%안군%추명상%리홍령
肺炎支原体%MP快速培养法%酶联免疫吸附实验
肺炎支原體%MP快速培養法%酶聯免疫吸附實驗
폐염지원체%MP쾌속배양법%매련면역흡부실험
Mycoplasma pneumoniae%MP rapid culture method%enzyme-linked immunosorbent assay
目的:评价肺炎支原体快速培养法在小儿肺炎支原体(MP)肺炎诊断中的应用价值。方法:采用咽拭子MP快速培养法和ELISA半定量检测血清MP-IgM抗体同时检测248例呼吸道感染小儿患者,对检查结果进行统计学分析。结果:248例患儿中,快速培养法检出21例阳性,阳性率22.98%;ELISA法检出MP-IgM阳性25例,阳性率27.42%,两种方法检测阳性检出数差异有统计学意义(P=0.000);两种方法一致性较好(kappa=0.819>0.75, T=12.982,P=0.000);以临床诊断结果评价两种实验室检测方法绘制ROC曲线,AUC快速培养=0.880,AUC血清MP-IgM=0.820。结论:MP快速培养快速简便,较血清MP-IgM检测更适用于早期和免疫系统尚未发育完善及免疫缺陷患者的诊断,与血清MP-IgM检测联合应用可提高MP的诊断效率。
目的:評價肺炎支原體快速培養法在小兒肺炎支原體(MP)肺炎診斷中的應用價值。方法:採用嚥拭子MP快速培養法和ELISA半定量檢測血清MP-IgM抗體同時檢測248例呼吸道感染小兒患者,對檢查結果進行統計學分析。結果:248例患兒中,快速培養法檢齣21例暘性,暘性率22.98%;ELISA法檢齣MP-IgM暘性25例,暘性率27.42%,兩種方法檢測暘性檢齣數差異有統計學意義(P=0.000);兩種方法一緻性較好(kappa=0.819>0.75, T=12.982,P=0.000);以臨床診斷結果評價兩種實驗室檢測方法繪製ROC麯線,AUC快速培養=0.880,AUC血清MP-IgM=0.820。結論:MP快速培養快速簡便,較血清MP-IgM檢測更適用于早期和免疫繫統尚未髮育完善及免疫缺陷患者的診斷,與血清MP-IgM檢測聯閤應用可提高MP的診斷效率。
목적:평개폐염지원체쾌속배양법재소인폐염지원체(MP)폐염진단중적응용개치。방법:채용인식자MP쾌속배양법화ELISA반정량검측혈청MP-IgM항체동시검측248례호흡도감염소인환자,대검사결과진행통계학분석。결과:248례환인중,쾌속배양법검출21례양성,양성솔22.98%;ELISA법검출MP-IgM양성25례,양성솔27.42%,량충방법검측양성검출수차이유통계학의의(P=0.000);량충방법일치성교호(kappa=0.819>0.75, T=12.982,P=0.000);이림상진단결과평개량충실험실검측방법회제ROC곡선,AUC쾌속배양=0.880,AUC혈청MP-IgM=0.820。결론:MP쾌속배양쾌속간편,교혈청MP-IgM검측경괄용우조기화면역계통상미발육완선급면역결함환자적진단,여혈청MP-IgM검측연합응용가제고MP적진단효솔。
Objective To evaluation the Mycoplasma pneumoniae rapid culture method in detection of my-coplasma pneumonia (MP) application value. Methods Using the throat swab MP rapid culture assay for simulta-neous detection and ELISA method for quantitative of serum MP-IgM antibodies detection of 248 cases of respi-ratory tract infections in pediatric patients , the test was used for statistical analysis. Results In all the 248 cases, rapid culture assay for detection of 21 positive cases, the positive rate of 22.98%;ELISA method for detection of MP-IgM was positive in 25 cases, the positive rate was 27.42%, two kinds of methods for detection of the positive number of MP had significant difference (P=0.000). two kinds of methodshad better consistency (kappa=0.819>0.75,T=12.982,P=0.000);Using the results of clinical diagnosis to evaluatetwo kinds of laboratory testing methods and draw the ROC curve, AUCrapid culture=0.880,AUCserum MP-IgM=0.820. Conclusion MP rapid culture is a quick and convenientmethod, especially in the early, immune system not yet mature and immunodeficiencypa-tients is better thanserum MP-IgM,can improve the diagnosis efficiency by combined with serum MP-IgM.