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克雅氏病:了解克雅氏病

CJD: Understanding Creutzfeldt-Jakob disease.

作者信息

Vacca Vincent M

机构信息

Vincent M. Vacca, Jr., is Clinical Nurse Educator, Neuroscience Intensive Care Unit, at Brigham & Women's Hospital in Boston, Mass.

出版信息

Nursing. 2016 Mar;46(3):36-42; quiz 42-3. doi: 10.1097/01.NURSE.0000480598.84274.0f.

Abstract

Rare, transmissible, and rapidly progressive, Creutzfeldt-Jakob disease (CJD) is an ultimately fatal central nervous system infection caused by accumulation of abnormally shaped prion proteins in neurons (see Understanding prion proteins). Although categorized as an infection, CJD doesn't lead to the immune system or inflammatory response typical of most infectious diseases. This article discusses the pathophysiology and diagnosis of this terminal illness and nursing care for patients with suspected or confirmed CJD.

摘要

克雅氏病(CJD)罕见、具有传染性且病情进展迅速,是一种最终致命的中枢神经系统感染,由神经元中异常形状的朊病毒蛋白积累引起(见了解朊病毒蛋白)。尽管被归类为感染性疾病,但克雅氏病不会引发大多数传染病典型的免疫系统或炎症反应。本文讨论了这种绝症的病理生理学、诊断方法以及对疑似或确诊克雅氏病患者的护理。

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