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抗磷脂综合征中直接口服抗凝剂:一个真实病例系列

Direct oral anticoagulants in antiphospholipid syndrome: a real life case series.

作者信息

Betancur J F, Bonilla-Abadía F, Hormaza A A, Jaramillo F J, Cañas C A, Tobón G J

机构信息

Department of Internal Medicine, Fundación Valle del Lili, Cali, Colombia. CES University School of Medicine, Medellín, Colombia

Department of Internal Medicine, Division of Rheumatology, Fundación Valle del Lili Cali, Colombia. ICESI University, School of Medicine, Cali, Colombia.

出版信息

Lupus. 2016 May;25(6):658-62. doi: 10.1177/0961203315624555. Epub 2016 Jan 6.

Abstract

AIM

The aim of this study was to describe a case series of patients with primary or secondary antiphospholipid syndrome (APS) treated with direct oral anticoagulants (DOACs).

PATIENTS AND METHODS

Clinical charts of eight patients with thrombotic primary or secondary APS treated with direct oral anticoagulants (DOACs) between January 2012 and May 2015 were reviewed.

RESULTS

The mean age was 45 ± 14.36 (range 27-69 years). Four patients had secondary APS (50%). All patients were initially treated with warfarin by a mean time of 70.87 ± 57.32 months (range 17-153 months). Changes in anticoagulation were defined by recurring thrombosis in five patients (62.5%) and life-threatening bleeding in the other three cases. Seven patients (87.5%) received rivaroxaban treatment and one patient (12.5%) apixaban. The mean follow-up period with DOACs was 19 ± 10.06 months (range 2-36 months). There was no recurrence of thrombosis by the time of data collection.

CONCLUSIONS

Despite not being the standard treatment in APS, we propose DOACs as a rational alternative for the management of patients with this diagnosis. Further interventional clinical studies are necessary for possible standardization of this therapy in APS patients.

摘要

目的

本研究旨在描述一系列接受直接口服抗凝剂(DOACs)治疗的原发性或继发性抗磷脂综合征(APS)患者。

患者与方法

回顾了2012年1月至2015年5月期间8例接受直接口服抗凝剂(DOACs)治疗的血栓形成性原发性或继发性APS患者的临床病历。

结果

平均年龄为45±14.36岁(范围27 - 69岁)。4例患者患有继发性APS(50%)。所有患者最初均接受华法林治疗,平均治疗时间为70.87±57.32个月(范围17 - 153个月)。抗凝治疗的改变是由5例患者(62.5%)复发性血栓形成和其他3例患者危及生命的出血所决定的。7例患者(87.5%)接受利伐沙班治疗,1例患者(12.5%)接受阿哌沙班治疗。接受DOACs治疗的平均随访期为19±10.06个月(范围2 - 36个月)。在收集数据时无血栓形成复发。

结论

尽管DOACs并非APS的标准治疗方法,但我们建议将其作为该诊断患者管理的合理替代方案。对于APS患者这种治疗方法的可能标准化,还需要进一步的介入性临床研究。

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