Suppr超能文献

灾难性抗磷脂综合征幸存者的长期预后。

Long term outcome of catastrophic antiphospholipid syndrome survivors.

作者信息

Erkan D, Asherson R A, Espinosa G, Cervera R, Font J, Piette J-C, Lockshin M D

机构信息

Hospital for Special Surgery, Weill Medical College of Cornell University, New York, NY, USA.

出版信息

Ann Rheum Dis. 2003 Jun;62(6):530-3. doi: 10.1136/ard.62.6.530.

Abstract

BACKGROUND

Catastrophic antiphospholipid syndrome (APS) is defined as life threatening multiple organ thromboses developing simultaneously or over a short period. The survival rate of catastrophic APS is about 50%, but the long term outcome of patients who survive is unknown.

OBJECTIVE

To determine the long term outcome of patients with catastrophic APS and provide further information on patients who survived.

PATIENTS AND METHODS

The clinical characteristics and outcomes of 130 patients with catastrophic APS have been reported previously. Six new cases were recently added to this series. Based on these publications, the authors who reported patients who had survived were contacted. Each author was asked (a) what treatment they gave their patients after the catastrophic APS; (b) if their patients had any further thrombosis.

RESULTS

63/136 (46%) patients died at the initial event. Of the remaining 73 patients, information was available for 58 (79%). Thirty eight (66%) patients did not develop further APS related events during an average follow up of 67.2 months. Eleven (19%) patients developed further APS related events but were still alive. No patients developed further catastrophic APS. Nine (16%) patients died: due to multiple organ failure (three patients); myelofibrosis (one); pneumonia (one); and APS related events (four).

CONCLUSION

Sixty six per cent of patients who survive an initial catastrophic APS event remained symptom free with anticoagulation during an average follow up of 67.2 months. Twenty six per cent of the survivors developed further APS related events and the mortality rate of these patients was about 25%.

摘要

背景

灾难性抗磷脂综合征(APS)定义为在短时间内同时发生或出现危及生命的多器官血栓形成。灾难性APS的生存率约为50%,但存活患者的长期预后尚不清楚。

目的

确定灾难性APS患者的长期预后,并提供关于存活患者的更多信息。

患者与方法

先前已报道130例灾难性APS患者的临床特征和预后。本系列最近新增6例。基于这些报道,与报道存活患者的作者取得联系。每位作者被问及:(a)在灾难性APS发生后他们给予患者何种治疗;(b)他们的患者是否有进一步的血栓形成。

结果

63/136(46%)例患者在初次发病时死亡。其余73例患者中,58例(79%)有可用信息。在平均67.2个月的随访期间,38例(66%)患者未发生进一步的APS相关事件。11例(19%)患者发生了进一步的APS相关事件,但仍存活。无患者发生进一步的灾难性APS。9例(16%)患者死亡,原因分别为多器官功能衰竭(3例)、骨髓纤维化(1例)、肺炎(1例)和APS相关事件(4例)。

结论

在初次灾难性APS事件中存活的患者,66%在平均67.2个月的抗凝随访期间无症状。26%的幸存者发生了进一步的APS相关事件,这些患者的死亡率约为25%。

相似文献

5
Cessation of oral anticoagulants in antiphospholipid syndrome.抗磷脂综合征中口服抗凝剂的停用
Lupus. 2017 Oct;26(12):1291-1296. doi: 10.1177/0961203317699285. Epub 2017 Mar 29.
8
Antiphospholipid syndrome - an update.抗磷脂综合征——最新进展
Vasa. 2018 Oct;47(6):451-464. doi: 10.1024/0301-1526/a000723. Epub 2018 Sep 12.
9
Management of refractory cases of catastrophic antiphospholipid syndrome.灾难性抗磷脂综合征难治病例的处理。
Autoimmun Rev. 2011 Sep;10(11):664-8. doi: 10.1016/j.autrev.2011.04.031. Epub 2011 May 1.
10
Clinical course of high-risk patients diagnosed with antiphospholipid syndrome.诊断为抗磷脂综合征的高危患者的临床病程。
J Thromb Haemost. 2010 Feb;8(2):237-42. doi: 10.1111/j.1538-7836.2009.03674.x. Epub 2009 Oct 30.

引用本文的文献

6
Systemic sclerosis. Part II: perioperative considerations.系统性硬化症。第二部分:围手术期注意事项。
BJA Educ. 2023 Mar;23(3):101-109. doi: 10.1016/j.bjae.2022.10.003. Epub 2023 Jan 4.
8
Catastrophic Antiphospholipid Syndrome after Orthotopic Liver Transplant.原位肝移植术后灾难性抗磷脂综合征
Case Rep Transplant. 2022 May 5;2022:6209300. doi: 10.1155/2022/6209300. eCollection 2022.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验