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沙眼的实验室诊断:一项合作研究。

Laboratory diagnosis of trachoma: a collaborative study.

作者信息

Schachter J, Mordhorst C H, Moore B W, Tarizzo M L

出版信息

Bull World Health Organ. 1973 May;48(5):509-15.

Abstract

A collaborative study on the laboratory diagnosis of trachoma was carried out in three laboratories. A standardized complement fixation (CF) test with chlamydial (bedsonial) group antigen was found to be highly reproducible. The results obtained by different laboratories using the method and reagents suggested by the WHO International Reference Centre for Trachoma and other Chlamydial Infections agreed in more than 95% of the tests. Similar agreement was observed between the results obtained with these reagents and those routinely used in one of these laboratories. In confirmation of previous studies, the CF test was found to give positive results in only a limited proportion of trachoma cases. However, in an area where the disease is hyperendemic the rates showed good correlation with the intensity of clinical signs. A comparison was also made between Giemsa staining and a fluorescent antibody (FA) technique for the cytological examination of conjunctival scrapings. The results obtained with the former method correlated well with clinical activity but the positivity rate was lower than that obtained by the FA technique. The FA results, however, were not an accurate indicator of clinical intensity. These results suggest that the Giemsa method may detect only the most heavily infected individuals.

摘要

在三个实验室开展了一项关于沙眼实验室诊断的合作研究。发现采用衣原体(贝氏属)群抗原进行标准化补体结合(CF)试验具有高度可重复性。不同实验室使用世界卫生组织沙眼和其他衣原体感染国际参考中心推荐的方法和试剂所获得的结果,在超过95%的检测中是一致的。在这些试剂所获结果与这些实验室之一常规使用的试剂所获结果之间也观察到了类似的一致性。正如之前研究证实的那样,CF试验仅在有限比例的沙眼病例中呈阳性结果。然而,在疾病高度流行的地区,阳性率与临床体征的严重程度显示出良好的相关性。还对吉姆萨染色法和荧光抗体(FA)技术用于结膜刮片细胞学检查进行了比较。前一种方法所获结果与临床活动情况相关性良好,但阳性率低于FA技术所获结果。然而,FA结果并非临床严重程度的准确指标。这些结果表明,吉姆萨方法可能只能检测出感染最严重的个体。

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Diagnosis and assessment of trachoma.沙眼的诊断与评估
Clin Microbiol Rev. 2004 Oct;17(4):982-1011, table of contents. doi: 10.1128/CMR.17.4.982-1011.2004.

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