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首页> 外文期刊>Journal of cataract and refractive surgery >Laboratory diagnosis of endophthalmitis: comparison of microbiology and molecular methods in the European Society of Cataract & Refractive Surgeons multicenter study and susceptibility testing.
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Laboratory diagnosis of endophthalmitis: comparison of microbiology and molecular methods in the European Society of Cataract & Refractive Surgeons multicenter study and susceptibility testing.

机译:眼内炎的实验室诊断:欧洲白内障和屈光外科医师协会多中心研究和药敏试验中微生物学和分子方法的比较。

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PURPOSE: To investigate and compare the use of molecular biology with the use of traditional Gram stain and organism culture for the laboratory diagnosis of postoperative endophthalmitis. SETTING: Twenty-four ophthalmology units together with 9 microbiology laboratories and 2 European reference molecular biology laboratories. METHODS: A prospective randomized partially masked multicenter cataract surgery study recruited 16 603 patients. This resulted in 29 cases of presumed postoperative endophthalmitis. Gram stain and culture were performed in the local laboratory according to agreed protocols. Samples of aqueous and/or vitreous were transported to the first referenced molecular biology laboratory (Regensburg, Germany) for polymerase chain reaction (PCR) testing, and an extracted aliquot of DNA was then referred to the second laboratory (Alicante, Spain) for PCR. RESULTS: Of the 29 who presented with presumed postoperative endophthalmitis, 20 were classified as proven infective endophthalmitis with positive Gram stain, culture, or PCR. Fourteen patients were culture-positive; all but 1 of these was also positive by PCR. Six patients were positive by PCR but negative by Gram stain or culture. Nine patients were negative by both microbiology and PCR testing. CONCLUSIONS: Use of molecular biology technique increased the laboratory rate of identifying the pathogen by 20%, confirming the technique is very useful for the endophthalmitis specimen. Samples of both aqueous and vitreous should be collected and stored at -20 degrees C for PCR at the time of the diagnostic taps.
机译:目的:调查和比较分子生物学与传统革兰氏染色法和生物培养法在术后眼内炎实验室诊断中的应用。地点:二十四个眼科单位以及9个微生物实验室和2个欧洲参考分子生物学实验室。方法:一项前瞻性随机部分掩盖的多中心白内障手术研究招募了16603名患者。这导致了29例术后眼内炎的推测。革兰氏染色和培养是根据当地规定的协议在当地实验室进行的。将水性和/或玻璃态样品送至第一个参考的分子生物学实验室(德国雷根斯堡)进行聚合酶链反应(PCR)测试,然后将提取的DNA等分试样转交给第二个实验室(西班牙阿利坎特)进行PCR 。结果:在29名假定的术后眼内炎患者中,有20人被归类为经证实的感染性眼内炎,革兰氏染色,培养或PCR阳性。 14例患者培养阳性。除1个以外,所有这些均通过PCR呈阳性。 PCR阳性6例,革兰氏染色或培养阴性。通过微生物学和PCR测试,九名患者均为阴性。结论:分子生物学技术的使用使鉴定病原体的实验室速度提高了20%,证明该技术对眼内炎标本非常有用。诊断水龙头时,应收集水样和玻璃样的样品,并保存在-20摄氏度下进行PCR。

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