灾难性抗磷脂综合征
医学
抗磷脂综合征
重症监护医学
协商一致会议
多器官衰竭
系统性红斑狼疮
外科
血栓形成
内科学
疾病
作者
Ronald A. Asherson,Ricard Cervera,P G de Groot,Doruk Erkan,MC Boffa,J.C. Piette,Munther A. Khamashta,Yehuda Shoenfeld
出处
期刊:Lupus
[SAGE]
日期:2003-07-01
卷期号:12 (7): 530-534
被引量:799
标识
DOI:10.1191/0961203303lu394oa
摘要
The term ‘catastrophic’ antiphospholipid syndrome (APS) is used to define an accelerated form of APS resulting in multiorgan failure. Although catastrophicAPS patients represent less than 1% of all patients with APS, they are usually in a life-threatening medical situation that requires high clinical awareness. The careful and open discussion of several proposals by all participants in the pre-symposium workshop on APS consensus, held in Taormina on occasion of the 10th International Congress on aPL and chaired by Munther A Khamashta and Yehuda Shoenfeld (29 September 2002), has allowed the acceptation of a preliminary set of classification criteria. On the other hand, the optimal management of catastrophicAPS must have three clear aims: to treat any precipitating factors (prompt use of antibioticsif infection is suspected, amputation for any necrotic organ, high awareness in patients with APS who undergo an operation or an invasive procedure), to prevent and to treat the ongoing thrombotic events and to suppress the excessive cytokine ‘storm’. Anticoagulation (usually intravenous heparin followed by oral anticoagulants), corticosteroids, plasma exchange, intravenous gammaglobulins and, if associated with lupus flare, cyclophosphamide, are the most commonly used treatments for catastrophic APS patients.
科研通智能强力驱动
Strongly Powered by AbleSci AI