首页> 外文OA文献 >Limulus amoebocyte lysate assay in the diagnosis of peritonitis in patients receiving continuous ambulatory peritoneal dialysis.
【2h】

Limulus amoebocyte lysate assay in the diagnosis of peritonitis in patients receiving continuous ambulatory peritoneal dialysis.

机译:continuous变形细胞溶胞产物测定法在连续性非卧床腹膜透析患者的腹​​膜炎诊断中。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

AIMS: To evaluate the Limulus amoebocyte lysate (LAL) assay for differentiating Gram positive from Gram negative peritonitis in patients receiving continuous ambulatory peritoneal dialysis (CAPD). METHODS: One hundred and six patients with suspected peritonitis were studied. LAL assay was performed by adding 0.1 ml of CAPD fluid to 0.1 ml of LAL reagent and incubating in a heating block for 60 minutes at 37 degrees C. The sensitivity of the reaction was determined by: (i) diluting endotoxin in distilled water and used (filter sterilised) peritoneal dialysis fluid; and (ii) diluting a broth culture of E coli used in peritoneal dialysis fluid. A positive LAL assay was defined as the constant stability of the clot through an inversion of 180 degrees. RESULTS: Compared with bacterial culture, the LAL assay had a sensitivity of 65% and a specificity of 98%. The sensitivity of microscopy compared with culture of Gram negative organisms was 76%; overall sensitivity of microscopy in comparison was 80%. CONCLUSIONS: The Gram stain was more sensitive than has previously been reported; the LAL assay was specific but insensitive for the diagnosis of CAPD peritonitis. There was a correlation between reduced leucocyte count and culture; this was reduced in cases from which Gram negative organisms had been isolated. It is recommended that laboratories evaluate their Gram stain procedure to improve its sensitivity because the LAL assay is not a satisfactory substitute.
机译:目的:评估Li连续性腹膜透析(CAPD)患者中革兰氏阳性和阴性革兰性腹膜炎的溶血性变形细胞溶解(LAL)测定。方法:对106例疑似腹膜炎患者进行了研究。通过将0.1 ml的CAPD液添加到0.1 ml的LAL试剂中,并在加热块中于37摄氏度温育60分钟,进行LAL测定。反应的敏感性通过以下方法确定:(i)将内毒素稀释在蒸馏水中并使用(过滤器灭菌)腹膜透析液; (ii)稀释用于腹膜透析液的大肠杆菌的肉汤培养物。阳性LAL测定定义为凝块通过反转180度的恒定稳定性。结果:与细菌培养相比,LAL测定的敏感性为65%,特异性为98%。与革兰氏阴性菌培养相比,显微镜的敏感性为76%;相比之下,显微镜的总灵敏度为80%。结论:革兰氏染色比以前报道的更敏感。 LAL检测对CAPD腹膜炎的诊断具有特异性,但不敏感。白细胞数量减少与培养之间存在相关性;如果从中分离出革兰氏阴性菌,则减少了这种情况。建议实验室评估革兰氏染色程序以提高其灵敏度,因为LAL分析不是令人满意的替代方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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