中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2001年
3期
181-183
,共3页
王宝玺%倪安平%郑和义%朱学骏%秦俭%叶顺章%王千秋%乐嘉豫%汤全贵%刘全中
王寶璽%倪安平%鄭和義%硃學駿%秦儉%葉順章%王韆鞦%樂嘉豫%湯全貴%劉全中
왕보새%예안평%정화의%주학준%진검%협순장%왕천추%악가예%탕전귀%류전중
沙眼衣原体%聚合酶链反应%连接酶链反应%培养
沙眼衣原體%聚閤酶鏈反應%連接酶鏈反應%培養
사안의원체%취합매련반응%련접매련반응%배양
目的与细胞培养和连接酶链反应 (LCR)比较考察 6种国产聚合酶链反应 (PCR)试剂盒在检测性传播疾病门诊患者标本沙眼衣原体的诊断价值。方法在北京、上海、南京、天津 5家临床医院性病门诊收集到 673份尿道 /宫颈拭子标本,分别进行沙眼衣原体培养和 PCR检测,对结果不相符合的标本采用 LCR复检,将各种 PCR检测结果分别与培养、 LCR以及综合结果进行比较分析。结果合格病例 616例,培养法检测阳性率 6.3%, PCR检测阳性率分别为 23.5%~ 28.7%。与培养结果比较,各种 PCR检测的敏感性均在 90%以上,其中 PCR1、 PCR2和 PCR5均达到 100%。 LCR复核标本 200份,与之相比, PCR检测的敏感性为 83.9%~ 98.6%,特异性 66.7%~ 94.7%, YI指数 0.523~ 0.881。其中 PCR2结果符合性最好,其它依次为 PCR4、 PCR1、 PCR5、 PCR3及 PCR6。综合分析证明国产 PCR检测沙眼衣原体的敏感性均在 85%以上,特异性均在 95%以上。 YI指数由高到低分别为 PCR2、 PCR1、 PCR3、 PCR5、 PCR4、 PCR6。结论国产 PCR检测尿道 /宫颈拭子沙眼衣原体具有较高的敏感性与特异性,可以用于临床检验,实验室质控与监督是本方法得以正确应用的关键。
目的與細胞培養和連接酶鏈反應 (LCR)比較攷察 6種國產聚閤酶鏈反應 (PCR)試劑盒在檢測性傳播疾病門診患者標本沙眼衣原體的診斷價值。方法在北京、上海、南京、天津 5傢臨床醫院性病門診收集到 673份尿道 /宮頸拭子標本,分彆進行沙眼衣原體培養和 PCR檢測,對結果不相符閤的標本採用 LCR複檢,將各種 PCR檢測結果分彆與培養、 LCR以及綜閤結果進行比較分析。結果閤格病例 616例,培養法檢測暘性率 6.3%, PCR檢測暘性率分彆為 23.5%~ 28.7%。與培養結果比較,各種 PCR檢測的敏感性均在 90%以上,其中 PCR1、 PCR2和 PCR5均達到 100%。 LCR複覈標本 200份,與之相比, PCR檢測的敏感性為 83.9%~ 98.6%,特異性 66.7%~ 94.7%, YI指數 0.523~ 0.881。其中 PCR2結果符閤性最好,其它依次為 PCR4、 PCR1、 PCR5、 PCR3及 PCR6。綜閤分析證明國產 PCR檢測沙眼衣原體的敏感性均在 85%以上,特異性均在 95%以上。 YI指數由高到低分彆為 PCR2、 PCR1、 PCR3、 PCR5、 PCR4、 PCR6。結論國產 PCR檢測尿道 /宮頸拭子沙眼衣原體具有較高的敏感性與特異性,可以用于臨床檢驗,實驗室質控與鑑督是本方法得以正確應用的關鍵。
목적여세포배양화련접매련반응 (LCR)비교고찰 6충국산취합매련반응 (PCR)시제합재검측성전파질병문진환자표본사안의원체적진단개치。방법재북경、상해、남경、천진 5가림상의원성병문진수집도 673빈뇨도 /궁경식자표본,분별진행사안의원체배양화 PCR검측,대결과불상부합적표본채용 LCR복검,장각충 PCR검측결과분별여배양、 LCR이급종합결과진행비교분석。결과합격병례 616례,배양법검측양성솔 6.3%, PCR검측양성솔분별위 23.5%~ 28.7%。여배양결과비교,각충 PCR검측적민감성균재 90%이상,기중 PCR1、 PCR2화 PCR5균체도 100%。 LCR복핵표본 200빈,여지상비, PCR검측적민감성위 83.9%~ 98.6%,특이성 66.7%~ 94.7%, YI지수 0.523~ 0.881。기중 PCR2결과부합성최호,기타의차위 PCR4、 PCR1、 PCR5、 PCR3급 PCR6。종합분석증명국산 PCR검측사안의원체적민감성균재 85%이상,특이성균재 95%이상。 YI지수유고도저분별위 PCR2、 PCR1、 PCR3、 PCR5、 PCR4、 PCR6。결론국산 PCR검측뇨도 /궁경식자사안의원체구유교고적민감성여특이성,가이용우림상검험,실험실질공여감독시본방법득이정학응용적관건。
Objective To evaluate the diagnostic value of six home made PCR kits for the detection of Chlamydia trachomatis in patients with sexually transmitted diseases, cell culture and LCR were used as references. Methods Endocervical or urethral swab specimens were collected from 673 patients attending STD clinics in Beijing, Shanghai, Nanjing and Tianjin. C. trachomatis culture and PCR were performed with specimens from all patients while LCR was performed only with specimens which the culture and PCR gave discrepant results. Results Among 616 eligible patients thirty- nine (6.3% ) cases were culture positive, and PCRs revealed positive rates from 23.5% to 28.7% . In comparison with cell culture, the sensitivity of PCRs were 90% or higher. In 200 cases which the culture and PCR gave discrepant results, LCR and PCR showed excellent consistency (YI index: 0.523~ 0.881 ), the sensitivity and specificity of PCRs ranged from 83.9% ~ 98.6% and 66.7% ~ 94.7% respectively, while PCR2 showed the highest YI index (0.881). With an expanded gold standard for discrepant results, we found that the specificity and sensitivity of PCRs were higher than 95% and 85% , respectively. Conclusions Domestic produced PCR kits for Chlamydia trachomatis detection are highly sensitive and specific, however, the quality control of laboratory still remains important in the clinical application.