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非O157产志贺毒素大肠杆菌日益凸显的临床重要性。

The emerging clinical importance of non-O157 Shiga toxin-producing Escherichia coli.

作者信息

Johnson Kristine E, Thorpe Cheleste M, Sears Cynthia L

机构信息

Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

出版信息

Clin Infect Dis. 2006 Dec 15;43(12):1587-95. doi: 10.1086/509573. Epub 2006 Nov 9.

Abstract

In 1982, hemorrhagic colitis and hemolytic-uremic syndrome were linked to infection with Escherichia coli O157:H7, a serotype now classified as Shiga toxin-producing E. coli (STEC). Thereafter, hemorrhagic colitis and hemolytic-uremic syndrome associated with non-O157 STEC serogroups were reported, with the frequency of non-O157 STEC illness rivaling that of O157:H7 in certain geographic regions. In the United States, non-O157 E. coli may account for up to 20%-50% of all STEC infections. A high index of suspicion, paired with options to test for non-O157 STEC infection, are necessary for early recognition and appropriate treatment of these infections. Supportive care without the use of antibiotics is currently considered to be optimal treatment for all STEC infections. This commentary provides a perspective on the non-O157 STEC as human pathogens, how and when the clinician should approach the diagnosis of these organisms, and the challenges ahead.

摘要

1982年,出血性结肠炎和溶血尿毒综合征与感染大肠杆菌O157:H7有关,该血清型现归类为产志贺毒素大肠杆菌(STEC)。此后,有报道称非O157 STEC血清群也会引发出血性结肠炎和溶血尿毒综合征,在某些地理区域,非O157 STEC疾病的发生率与O157:H7相当。在美国,非O157大肠杆菌感染可能占所有STEC感染的20% - 50%。高度的怀疑指数以及检测非O157 STEC感染的方法,对于这些感染的早期识别和恰当治疗至关重要。目前认为,不使用抗生素的支持性治疗是所有STEC感染的最佳治疗方法。本评论阐述了非O157 STEC作为人类病原体的情况、临床医生应如何以及何时对这些病原体进行诊断,以及未来面临的挑战。

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