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Chest:肥厚型心肌病合并房颤患者服用非维生素K拮抗剂的疗效和安全性

2018-11-23 xing.T MedSci原创

由此可见,与华法林相比,采用NOAC治疗的HCM合并AF患者具有相似的卒中和大出血风险,但全因死亡率和复合致命性心血管事件均较低。该研究的数据表明HCM合并AF患者可以安全有效地服用NOAC治疗。

对于肥厚型心肌病(HCM)合并房颤(AF)患者建议进行慢性抗凝治疗。非维生素K拮抗剂口服抗凝剂(NOACs)是华法林的替代品,但支持其用于HCM合并AF患者的数据有限。近日,呼吸领域权威杂志chest上发表了一篇研究文章,研究人员旨在比较HCM合并AF患者服用NOAC和华法林之间的血栓栓塞事件、出血和死亡率。

研究人员从2011年1月1日至2016年12月31日期间的韩国国民健康保险服务(NHIS)数据库中确定了华法林治疗组的HCM合并AF患者(n=955),并以1:2的比例倾向匹配了NOAC治疗组(n=1504)。

中位随访15个月后,服用NOAC和华法林治疗的HCM合并AF患者缺血性卒中和大出血的发生率相似。NOAC治疗的患者全因死亡率(NOAC组和华法林组每100人每年发生5.11和10.13次事件)和致命血管事件的综合发生率(每100人每年发生0.77和1.80次事件)较低。与华法林相比,服用NOACs可显著降低全因死亡(风险比[HR]:0.43,95%置信区间[CI]:0.32-0.57)和复合致命性血管事件(HR:0.39,95%CI:0.18-0.82)风险。

由此可见,与华法林相比,采用NOAC治疗的HCM合并AF患者具有相似的卒中和大出血风险,但全因死亡率和复合致命性心血管事件均较低。该研究的数据表明HCM合并AF患者可以安全有效地服用NOAC治疗。

原始出处:

Hyunjean Jung,et al.Effectiveness and Safety of Non-Vitamin K Antagonist Oral Anticoagulants in Atrial Fibrillation Patients with Hypertrophic Cardiomyopathy: A Nationwide Cohort Study.chest.2018.https://doi.org/10.1016/j.chest.2018.11.009

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    2019-01-15 Smile2680
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attachment=null, authenticateStatus=null, createdAvatar=, createdBy=395f25, createdName=爆笑小医, createdTime=Sun Nov 25 11:27:00 CST 2018, time=2018-11-25, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1031983, encodeId=edba103198316, content=谢谢梅斯提供这么好的信息,学到很多, beContent=null, objectType=article, channel=null, level=null, likeNumber=90, replyNumber=0, topicName=null, topicId=null, topicList=[], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=f0620, createdName=内科新手, createdTime=Fri Nov 23 23:27:00 CST 2018, time=2018-11-23, status=1, ipAttribution=)]
    2018-11-23 内科新手

    谢谢梅斯提供这么好的信息,学到很多

    0

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肥厚型心肌病患儿的晚期存活和症状状态尚无明确研究。现有研究人员对儿童肥厚型心肌病的长期预后进行研究。澳大利亚国家儿童心肌病研究是一项纵向的基于人群的队列研究,研究人群为1987年-1996年间确诊的心肌病患儿(0-10岁)。主要结点是确诊到死亡或心脏移植的时间。共有80位肥厚型心肌病患者,确诊时的中位年龄为0.48岁(四分位间距 0.1、2.5)。确诊后1年、10年和20年时未死亡/移植的患者分别

JACC:保留收缩功能的肥厚型心肌病患者的晚期钆增强

在保留收缩功能的低/中危成年HCM患者中(阻塞性、肌切除和非阻塞性亚组),%LGE与更高的复合终点发生率显著相关。

Circulation:心脏磁共振晚期钆增强在肥厚型心肌病儿童和青少年患者中的发生率和发展

目前认为心脏磁共振(CMR)晚期钆增强(LGE)代表致密心肌纤维化。可在约60%的肥厚型心肌病(HCM)成年患者中见到。但是,LGE在HCM的儿童和青少年患者中的发生率尚未明确。此外,目前还缺乏关于LGE在儿科HCM中的发展和演变的纵向研究。现Anna Axelsson Raja等人对LGE在有无患HCM的遗传倾向的儿童和青少年中的患病率、进展和临床相关性进行评估。研究人员开展一观察性的回顾性研究

JACC:FHOD3是肥厚型心肌病的新致病基因

肥厚型心肌病的遗传学机制尚不清楚,甲酸同系物2结构域3(FHOD3)在心肌肥厚的发生中可能起到重要作用,但其对肥厚型心肌病发生的影响尚不清楚。本研究的目的旨在探索FHOD3基因突变与肥厚型心肌病发生的关系。本研究对3189名不相关的肥厚型心肌病先证者和2777名无心肌病患者(病例对照)的FHOD3基因进行大规模平行测序。最终,在132名先证者中筛出94个候选突变,这些突变在肥厚型心肌病患者的频率要

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