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[用于肺炎支原体感染血清学诊断的微粒凝集Serodia-Myco II试验的商业实用性评估]

[Evaluation of commercial usefulness for microparticle agglutination Serodia-Myco II test for serodiagnosis of Mycoplasma pneumonia infections].

作者信息

Rastawicki Waldemar, Kałuzewski Stanisław, Jagielski Marek, Gierczyński Rafał

机构信息

Zakład Bakteriologii PZH w Warszawie.

出版信息

Med Dosw Mikrobiol. 2002;54(1):67-73.

Abstract

The usefulness of Serodia-Myco II agglutination test (Fujirebio, Japan) for diagnosis of the M. pneumoniae infections was evaluated. A total of 66 serum samples obtained from patients with respiratory tract infections were tested by Serodia-Myco II test, complement fixation (CF) test, ELISA-IgG/-IgM, and by latex agglutination (LA) test prepared in our laboratory. Using CF test and ELISA as the reference tests, Serodia-Myco II test gave too many false positive results. This test in relation to CF test, ELISA-IgM, ELISA-IgG, and LA test showed a very high sensitivity, virtually 100%, with a low specificity, below 50%. It seems that oversensitivity of the Serodia-Myco II test is caused by too low cut off (40) value recommended by the manufacturer. The Serodia-Myco II test may be used in routine serodiagnosis of mycoplasmosis under condition that cut off value will be raised to 160 and the positive results of this test will be confirmed by the CF test or ELISA.

摘要

评估了Serodia-Myco II凝集试验(富士瑞必欧株式会社,日本)对肺炎支原体感染的诊断价值。对66份来自呼吸道感染患者的血清样本进行了Serodia-Myco II试验、补体结合(CF)试验、ELISA-IgG/IgM以及本实验室制备的乳胶凝集(LA)试验。以CF试验和ELISA作为参考试验,Serodia-Myco II试验出现了太多假阳性结果。该试验与CF试验、ELISA-IgM、ELISA-IgG和LA试验相比,显示出非常高的敏感性,几乎为100%,但特异性较低,低于50%。似乎Serodia-Myco II试验的过度敏感性是由制造商推荐的截断值(40)过低所致。在将截断值提高到160且该试验的阳性结果通过CF试验或ELISA确认的条件下,Serodia-Myco II试验可用于支原体病的常规血清学诊断。

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