Binnicker Matthew J
J Clin Microbiol. 2015 Dec;53(12):3723-8. doi: 10.1128/JCM.02103-15.
Gastrointestinal disease is a major cause of morbidity and mortality worldwide, especially among young children and immunocompromised patients. Diarrhea may result from infection with a variety of microbial pathogens, including bacteria, viruses, or parasites. Historically, the diagnosis of infectious diarrhea has been made using microscopy, antigen tests, culture, and real-time PCR. A combination of these traditional tests is often required due to the inability to distinguish between infectious etiologies based on the clinical presentation alone. Recently, several multiplex molecular assays have been developed for the detection of gastrointestinal pathogens directly from clinical stool samples. These panels allow for the detection and identification of up to 20 pathogens in as little as 1 h. This review will focus on the multiplex molecular panels that have received clearance from the FDA for the diagnosis of diarrheal disease and will highlight issues related to test performance, result interpretation, and cost-effectiveness of these new molecular diagnostic tools.
胃肠道疾病是全球发病和死亡的主要原因,在幼儿和免疫功能低下患者中尤为如此。腹泻可能由多种微生物病原体感染引起,包括细菌、病毒或寄生虫。从历史上看,感染性腹泻的诊断一直通过显微镜检查、抗原检测、培养和实时聚合酶链反应(PCR)进行。由于仅根据临床表现无法区分感染病因,通常需要结合这些传统检测方法。最近,已经开发了几种多重分子检测方法,用于直接从临床粪便样本中检测胃肠道病原体。这些检测板能够在短短1小时内检测和鉴定多达20种病原体。本综述将重点关注已获得美国食品药品监督管理局(FDA)批准用于诊断腹泻病的多重分子检测板,并将突出与这些新分子诊断工具的检测性能、结果解读和成本效益相关的问题。