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多中心临床评估 illumigene 组 A 链球菌 DNA 扩增检测试剂盒用于咽拭子中检测组 A 链球菌。

Multicenter clinical evaluation of the illumigene group A Streptococcus DNA amplification assay for detection of group A Streptococcus from pharyngeal swabs.

机构信息

Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

出版信息

J Clin Microbiol. 2013 May;51(5):1474-7. doi: 10.1128/JCM.00176-13. Epub 2013 Feb 27.

Abstract

Acute pharyngitis is a nonspecific symptom that can result from a number of viral or bacterial infections. For most etiologies, symptoms are self-limited and resolve without lasting effects; however, pharyngitis resulting from infection with Streptococcus pyogenes (a group A Streptococcus [GAS]) can be associated with serious sequelae, including acute rheumatic fever and acute glomerulonephritis. Rapid accurate detection of GAS in pharyngeal specimens from individuals suffering from pharyngitis aids in the management and selection of antibiotic therapy for these patients. A total of 796 pharyngeal swabs were collected at three separate clinical centers. Each specimen was analyzed using the illumigene group A strep DNA amplification assay (Meridian Bioscience Inc., Cincinnati, OH). To confirm GAS identification, the results were compared to those from direct and extracted culture methods using Gram staining and a GAS-specific latex agglutination test. Discrepant results were resolved using an alternative nucleic acid amplification test. The prevalence of culture-detected GAS in this study was 12.8% (102/796 specimens). The illumigene assay detected GAS in 74/74 direct culture-positive specimens (100% sensitivity) and 100/102 extracted culture-positive specimens (98.0% sensitivity). GAS was detected by the illumigene assay in an additional 42 specimens that were direct culture negative (94.2% specificity) and 16 specimens that were extracted culture negative (97.7% specificity). Discrepant analysis using an alternative molecular assay detected GAS nucleic acid in 13/16 (81.3%) false-positive specimens and 1/2 false-negative specimens, resulting in a final sensitivity of 99.0% and a specificity of 99.6% for the detection of GAS in pharyngeal swabs using the illumigene assay.

摘要

急性咽炎是一种非特异性症状,可由多种病毒或细菌感染引起。对于大多数病因,症状是自限性的,没有持久的影响就会自行消退;然而,由 A 组链球菌(酿脓链球菌)感染引起的咽炎可导致严重的后遗症,包括风湿热和急性肾小球肾炎。快速准确地检测咽炎患者咽拭子中的酿脓链球菌有助于管理和选择这些患者的抗生素治疗。在三个不同的临床中心共采集了 796 份咽拭子。每份标本均采用 illumigene 组 A 链球菌 DNA 扩增检测法(美国俄亥俄州辛辛那提市美迪亚诊断公司)进行分析。为了确认 GAS 的鉴定结果,将结果与直接和提取培养方法的结果进行比较,使用革兰氏染色和 GAS 特异性乳胶凝集试验。通过替代核酸扩增试验解决不一致的结果。在这项研究中,培养检测到的 GAS 患病率为 12.8%(796 份标本中的 102 份)。illumigene 检测法在 74/74 份直接培养阳性标本中检测到 GAS(100%敏感性)和 100/102 份提取培养阳性标本(98.0%敏感性)。illumigene 检测法还在 42 份直接培养阴性标本(94.2%特异性)和 16 份提取培养阴性标本(97.7%特异性)中检测到 GAS。使用替代分子检测法进行不一致分析,在 16 份(81.3%)假阳性标本和 1 份(81.3%)假阴性标本中检测到 GAS 核酸,最终使用 illumigene 检测法检测咽拭子中 GAS 的灵敏度为 99.0%,特异性为 99.6%。

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