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在一般医疗实践中,通过用添加杆菌肽纸片的链球菌培养基培养咽拭子对β溶血性链球菌进行初步分组时缺乏可靠性。

Lack of reliability of primary grouping of beta-hemolytic streptococci by culture of throat swabs with streptocult supplemented with bacitracin disks in general practice.

作者信息

Hoffmann S

出版信息

J Clin Microbiol. 1985 Oct;22(4):497-500. doi: 10.1128/jcm.22.4.497-500.1985.

Abstract

Fifty-eight general practitioners took throat swabs from 434 patients with sore throats. Office cultures were performed on Streptocult supplemented with bacitracin disks in an attempt to carry out primary grouping of beta-hemolytic streptococci (BHS). In 424 cases the findings were compared with those obtained in a microbiological laboratory. Streptocult showed a sensitivity of 75% and a specificity of 84% in the detection of BHS. The office-performed grouping procedure of the correctly detected BHS, however, only had a sensitivity of 65% and a specificity of 87%. Overall, as many as 45% of the patients with BHS group A were misdiagnosed. The unsatisfactory results obtained with primary grouping of BHS may be due partly to incorrect determinations of the diameter of the inhibition zone around the bacitracin disks and partly to an inappropriate choice of breakpoint. It is concluded that cultures of throat swabs on Streptocult in general practice should not be accompanied by attempts to carry out primary grouping with bacitracin disks. A laboratory investigation showed that incubation at room temperature for 48 h and at 35 degrees C for 24 h gave identical BHS positivity rates.

摘要

58名全科医生从434名咽痛患者处采集了咽拭子。在补充了杆菌肽纸片的链球菌培养基(Streptocult)上进行门诊培养,试图对β溶血性链球菌(BHS)进行初步分组。在424例病例中,将结果与微生物实验室的结果进行了比较。链球菌培养基在检测BHS时的敏感性为75%,特异性为84%。然而,门诊对正确检测出的BHS进行的分组程序,敏感性仅为65%,特异性为87%。总体而言,多达45%的A组BHS患者被误诊。BHS初步分组结果不理想,部分原因可能是杆菌肽纸片周围抑菌圈直径测定错误,部分原因可能是断点选择不当。得出的结论是,在全科医疗中,用链球菌培养基对咽拭子进行培养时,不应尝试使用杆菌肽纸片进行初步分组。一项实验室研究表明,在室温下孵育48小时和在35摄氏度下孵育24小时,BHS阳性率相同。

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