...
首页> 外文期刊>Journal of Clinical Microbiology >Lack of utility of a Limulus amoebocyte lysate assay in the diagnosis of urethral discharges in men.
【24h】

Lack of utility of a Limulus amoebocyte lysate assay in the diagnosis of urethral discharges in men.

机译:Li变形细胞裂解物测定法在诊断男性尿道排出物中缺乏实用性。

获取原文
           

摘要

We evaluated a Limulus amoebocyte lysate assay (LALA) test kit for the diagnosis of gonorrhea in 883 unselected men with urethral discharge. Results were compared with those of Gram-stained smears and Martin-Lewis cultures. Of 331 men with gonococcal urethritis and 552 men with nongonoccal urethritis, 125 (37.8%) and 503 (91.1%), respectively, could not be evaluated by LALA owing either to insufficient discharge specimen to perform the test (569 or 64.4%) or to other exclusion criteria (59 or 6.7%). Of 255 LALA-evaluable discharges, LALA correctly diagnosed 252 (98.8%), compared with 244 (95.7%) for the Gram-stained smear. However, the Gram-stained smear also correctly diagnosed 96.5% of 456 men with insufficient discharge for LALA testing. The clinical utility of the LALA test kit is severely limited by performance criteria that exclude the majority of unselected men with urethritis. In addition, it is more technically cumbersome, time consuming, and costly than Gram-stained smears. Further test modifications are unlikely to overcome these inherent disadvantages of LALA.
机译:我们评估了Li气变形细胞溶解物测定法(LALA)测试试剂盒,以诊断883名未经选择的尿道分泌物男子的淋病。将结果与革兰氏染色涂片和马丁-刘易斯文化的结果进行比较。在331例淋球菌性尿道炎男性和552例非淋球菌性尿道炎男性中,分别由于出院样本不足以进行测试而无法对LALA进行评估(分别为125(37.8%)和503(91.1%))(569或64.4%)或其他排除标准(59或6.7%)。在255次LALA可评估的分泌物中,LALA正确诊断出252次(98.8%),而革兰氏染色涂片诊断为244次(95.7%)。但是,革兰氏染色涂片还可以正确诊断出456名男性中的96.5%,出院不足以进行LALA测试。 LALA检测试剂盒的临床实用性受到性能标准的严重限制,该性能标准排除了大多数未选择的患有尿道炎的男性。另外,与革兰氏染色涂片相比,它在技术上更加繁琐,耗时且昂贵。进一步的测试修改不可能克服LALA的这些固有缺点。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号