The challenge of bleeding in antiphospholipid antibody-positive patients.

IF 3.9 2区 医学 Q1 RHEUMATOLOGY Current Rheumatology Reports Pub Date : 2015-02-01 DOI:10.1007/s11926-014-0481-0
Giulia Pazzola, Stéphane Zuily, Doruk Erkan
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引用次数: 38

Abstract

Antiphospholipid antibody-positive patients can develop bleeding due to capillaritis, microthrombosis, antiprothrombin antibodies, thrombocytopenia, and/or excessive antithrombotic therapy. Clinical characteristics of patients, e.g., renal impairment, elderly, or concomitant medications, are closely related to the risk of bleeding. The management of bleeding in antiphospholipid antibody (aPL)-positive patients is challenging due to the baseline increased risk of thrombosis. If anticoagulation is stopped, it should be restarted as soon as possible once the acute bleeding is controlled; the continuation of anticoagulation despite active bleeding may be required in selected cases. High-dose corticosteroid is the mainstay treatment for diffuse alveolar hemorrhage, lupus anticoagulant-hypoprothrombinemia syndrome, and severe thrombocytopenia; immunosuppressive drugs are also required to improve the long-term outcomes. Hydrocortisone is critical in adrenal hemorrhage patients due to concomitant adrenal insufficiency; despite bleeding, anticoagulation should be maintained as much as possible. Plasma exchange should be considered in catastrophic antiphospholipid syndrome patients with concurrent bleeding. This article will review the causes of bleeding in aPL-positive patients as well as the management strategies.

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抗磷脂抗体阳性患者出血的挑战。
抗磷脂抗体阳性的患者可因毛细血管炎、微血栓形成、抗凝血酶原抗体、血小板减少症和/或过度抗血栓治疗而出血。患者的临床特征,如肾功能不全、老年或合并用药,与出血风险密切相关。由于血栓形成的基线风险增加,抗磷脂抗体(aPL)阳性患者的出血管理具有挑战性。如果停用抗凝,一旦急性出血得到控制,应尽快重新开始;在某些情况下,尽管活动性出血仍需要继续抗凝治疗。大剂量皮质类固醇是弥漫性肺泡出血、狼疮抗凝-低凝血原血症综合征和严重血小板减少症的主要治疗方法;免疫抑制药物也需要改善长期预后。氢化可的松是关键的肾上腺出血患者由于合并肾上腺功能不全;尽管有出血,仍应尽可能保持抗凝。并发出血的灾难性抗磷脂综合征患者应考虑血浆置换。本文将回顾apl阳性患者出血的原因及处理策略。
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来源期刊
CiteScore
11.20
自引率
0.00%
发文量
41
期刊介绍: This journal aims to review the most important, recently published research in the field of rheumatology. By providing clear, insightful, balanced contributions by international experts, the journal intends to serve all those involved in the care and prevention of rheumatologic conditions. We accomplish this aim by appointing international authorities to serve as Section Editors in key subject areas such as the many forms of arthritis, osteoporosis and metabolic bone disease, and systemic lupus erythematosus. Section Editors, in turn, select topics for which leading experts contribute comprehensive review articles that emphasize new developments and recently published papers of major importance, highlighted by annotated reference lists. An international Editorial Board reviews the annual table of contents, suggests articles of special interest to their country/region, and ensures that topics are current and include emerging research. Commentaries from well-known figures in the field are also occasionally provided.
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