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五种粪便浓缩系统的寄生虫检测效率

Parasite detection efficiencies of five stool concentration systems.

作者信息

Perry J L, Matthews J S, Miller G R

机构信息

Department of Veterans Affairs Medical Center, Wichita, Kansas.

出版信息

J Clin Microbiol. 1990 Jun;28(6):1094-7. doi: 10.1128/jcm.28.6.1094-1097.1990.

Abstract

Fresh fecal material that was free of ova and parasites was pooled with 10% Formalin in a 1:4 ratio to prepare a standard specimen. Portions of 100 ml of this specimen were individually seeded with Cryptosporidium oocysts, Entamoeba coli, Entamoeba histolytica, and Giardia lamblia cysts; ova of Necator americanus; and Strongyloides larvae. Appropriate volumes of each parasite suspension were used to evaluate the Fecal Concentrator Kit (Remel, Lenexa, Kans.), Fecal Parasite Concentrator (Evergreen Scientific, Los Angeles, Calif.), Para-Pak Macro-Con (Meridian Diagnostics, Inc., Cincinnati, Ohio), and Trend FeKal CON-Trate (Trend Scientific, Inc., St. Paul, Minn.). A standardized gauze filtration method was used as the reference procedure. Tests were performed in triplicate with each individual parasite-concentrator combination, with three slides examined from each sediment. All of the systems effectively concentrated parasites compared with direct examination of unconcentrated fecal material. The Fecal Concentrator Kit provided the best overall performance. Clarity of sediment, lack of debris, and uniformity of background material were found to be important considerations for microscopic detection of parasites in concentrated specimens.

摘要

将不含虫卵和寄生虫的新鲜粪便样本与10%福尔马林按1:4的比例混合,以制备标准样本。将100毫升该样本分别接种隐孢子虫卵囊、结肠内阿米巴、溶组织内阿米巴和蓝氏贾第鞭毛虫包囊;美洲板口线虫卵;以及类圆线虫幼虫。使用每种寄生虫悬液的适当体积来评估粪便浓缩试剂盒(Remel公司,堪萨斯州莱尼克斯)、粪便寄生虫浓缩器(长青科学公司,加利福尼亚州洛杉矶)、Para-Pak Macro-Con(子午线诊断公司,俄亥俄州辛辛那提)和Trend FeKal CON-Trate(Trend科学公司,明尼苏达州圣保罗)。采用标准化纱布过滤方法作为参考程序。对每种寄生虫浓缩器组合进行三次重复测试,从每份沉淀物中检查三张载玻片。与直接检查未浓缩的粪便样本相比,所有系统都能有效浓缩寄生虫。粪便浓缩试剂盒的总体性能最佳。发现沉淀物的清晰度、无碎片以及背景材料的均匀性是在浓缩样本中显微镜检测寄生虫的重要考虑因素。

相似文献

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Parasite detection efficiencies of five stool concentration systems.五种粪便浓缩系统的寄生虫检测效率
J Clin Microbiol. 1990 Jun;28(6):1094-7. doi: 10.1128/jcm.28.6.1094-1097.1990.

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