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史蒂文斯-约翰逊综合征:发病机制、诊断与管理

Stevens-Johnson syndrome: pathogenesis, diagnosis, and management.

作者信息

Hazin Ribhi, Ibrahimi Omar A, Hazin Moustafa I, Kimyai-Asadi Arash

机构信息

Harvard University, Faculty of Arts and Sciences, Cambridge, MA, USA.

出版信息

Ann Med. 2008;40(2):129-38. doi: 10.1080/07853890701753664.

Abstract

Cutaneous drug reactions are the most common type of adverse drug reaction. These reactions, ranging from simple pruritic eruptions to potentially life-threatening events, are a significant cause of iatrogenic morbidity and mortality. Stevens-Johnson syndrome (SJS) is a serious and potentially life-threatening cutaneous drug reaction. Although progress has been made in the management of SJS through early detection, prompt hospitalization, and immediate cessation of offending agents, the prevalence of permanent disabilities associated with SJS remains unchanged. Nevertheless, despite being a problem that is global in scope, government and health care agencies worldwide have yet to find a consensus on either diagnostic criteria or therapy for this disorder. Here, we provide the internist and emergency room physician with a brief review the SJS literature and summarize the latest recommended interventions with the hope of improving early recognition of this disease and prevention of permanent sequelae and mortality that frequently complicate SJS.

摘要

皮肤药物反应是最常见的药物不良反应类型。这些反应范围从简单的瘙痒性皮疹到潜在的危及生命的事件,是医源性发病和死亡的重要原因。史蒂文斯 - 约翰逊综合征(SJS)是一种严重且潜在危及生命的皮肤药物反应。尽管通过早期检测、及时住院和立即停用致病药物,在SJS的管理方面已取得进展,但与SJS相关的永久性残疾患病率仍未改变。然而,尽管这是一个全球性问题,但全球范围内的政府和医疗保健机构尚未就该疾病的诊断标准或治疗达成共识。在此,我们为内科医生和急诊室医生简要回顾SJS的文献,并总结最新推荐的干预措施,希望能提高对该疾病的早期识别,并预防经常使SJS复杂化的永久性后遗症和死亡率。

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