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Luminex xTAG-GPP(胃肠道病原体检测试剂盒)在急性腹泻疾病诊断中的评估

Evaluation of the Luminex xTAG-GPP (Gastrointestinal Pathogen Panel) in the diagnosis of diseases with acute diarrhoea.

作者信息

Casañ Cristina, Ocete María Dolores, Medina Rafael, Gimeno Concepción

机构信息

Área Clínica de Microbiología, Enfermedades Infecciosas y Medicina Preventiva, Servicio de Microbiología, Consorcio Hospital General Universitario de Valencia, Valencia, España.

Área Clínica de Microbiología, Enfermedades Infecciosas y Medicina Preventiva, Servicio de Microbiología, Consorcio Hospital General Universitario de Valencia, Valencia, España.

出版信息

Enferm Infecc Microbiol Clin. 2017 Nov;35(9):574-577. doi: 10.1016/j.eimc.2016.02.022. Epub 2016 Apr 6.

Abstract

INTRODUCTION

Most Microbiology laboratories use different techniques for the diagnosis of gastrointestinal infections. Some of which require at least 72 hours to obtain final results.

MATERIAL AND METHODS

The gastrointestinal panel Luminex (xTAG-GPP, Luminex Molecular Diagnostics, Toronto, Canada) is a qualitative multiplex fast and sensitive assay able to detect and to identify the 15 most common pathogens causing gastrointestinal infection simultaneously. We evaluated this multiplex panel comparing it with conventional methods used in our laboratory.

RESULTS

We analyzed 225 samples of feces. Through the conventional methods were positive 74 samples (32.9%). Through the Luminex method were positive 137 samples (60.9%).

CONCLUSIONS

The use of the xTAG GPP system in Clinical Microbiology can improve the diagnosis of gastrointestinal infectious because it provides results in less than 8 hours. Some pathogens should be applied with caution and should be interpreted based on the patient́s clinical data.

摘要

引言

大多数微生物实验室使用不同技术诊断胃肠道感染。其中一些技术至少需要72小时才能获得最终结果。

材料与方法

胃肠道检测Luminex(xTAG-GPP,Luminex分子诊断公司,加拿大多伦多)是一种定性多重快速且灵敏的检测方法,能够同时检测和鉴定导致胃肠道感染的15种最常见病原体。我们将这种多重检测方法与我们实验室使用的传统方法进行了比较评估。

结果

我们分析了225份粪便样本。通过传统方法有74份样本呈阳性(32.9%)。通过Luminex方法有137份样本呈阳性(60.9%)。

结论

在临床微生物学中使用xTAG GPP系统可改善胃肠道感染的诊断,因为它能在不到8小时内得出结果。对于某些病原体应谨慎应用,并应根据患者的临床数据进行解读。

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