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在全科医疗中使用五种诊断试剂盒从咽喉拭子中检测A组链球菌抗原

Detection of group A streptococcal antigen from throat swabs with five diagnostic kits in general practice.

作者信息

Hoffmann S

机构信息

Streptococcus Department, Statens Seruminstitut, Copenhagen, Denmark.

出版信息

Diagn Microbiol Infect Dis. 1990 May-Jun;13(3):209-15. doi: 10.1016/0732-8893(90)90061-y.

Abstract

During a 5-month period, 248 general practitioners from 164 general practice offices obtained duplicate throat swabs from 2469 patients with acute pharyngotonsillitis. At the general practice office, one of the swabs was assayed for the presence of group A streptococcal antigen, using one of five commercially available diagnostic kits. (The participants did not receive instruction in the use of the kits). The other swab was cultured in our laboratory for the presence of group A streptococci. The diagnostic parameters for the five kits were as follows: Abbott TestPack Strep A--sensitivity, 79% (110/139) and specificity, 98% (490/501); Direct Strep A EIA (Roche)--sensitivity, 79% (104/132) and specificity, 63% (178/281); Respirastick--sensitivity, 55% (46/84) and specificity, 96% (298/309); Reveal Colour Strep A--sensitivity, 82% (114/139) and specificity, 83% (223/268); Tandem ICON Strep A--sensitivity, 78% (111/143) and specificity, 98% (362/368). The antigen detection test results were heavily influenced by the clinical prediction of a streptococcal or viral etiology. It is concluded that in the absence of a standard throat culture, the Abbott TestPack Strep A kit and the Tandem ICON Strep A kit both offer a more safe diagnostic alternative than clinical assessment. Depending on the current prevalence of group A streptococci, the additional use of a throat swab culture should be considered in case of negative antigen detection test results.

摘要

在5个月的时间里,来自164个全科诊所的248名全科医生从2469例急性咽扁桃体炎患者身上采集了重复的咽拭子。在全科诊所,使用五种市售诊断试剂盒中的一种对其中一份拭子检测A组链球菌抗原的存在情况。(参与者未接受试剂盒使用方面的指导)。另一份拭子在我们实验室培养以检测A组链球菌的存在情况。五种试剂盒的诊断参数如下:雅培TestPack A群链球菌检测试剂盒——灵敏度79%(110/139),特异性98%(490/501);直接A群链球菌酶免疫分析试剂盒(罗氏公司)——灵敏度79%(104/132),特异性63%(178/281);呼吸棒——灵敏度55%(46/84),特异性96%(298/309);显色A群链球菌检测试剂盒——灵敏度82%(114/139),特异性83%(223/268);串联式ICON A群链球菌检测试剂盒——灵敏度78%(111/143),特异性98%(362/368)。抗原检测试验结果受链球菌或病毒病因临床预测的严重影响。得出的结论是,在没有标准咽拭子培养的情况下,雅培TestPack A群链球菌检测试剂盒和串联式ICON A群链球菌检测试剂盒都比临床评估提供了更安全的诊断选择。根据当前A组链球菌的流行情况,在抗原检测试验结果为阴性时应考虑额外进行咽拭子培养。

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