• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

V1至V3导联出现右束支传导阻滞及ST段抬高:无明显结构性心脏病患者猝死的一个标志物。

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease.

作者信息

Brugada J, Brugada R, Brugada P

机构信息

Arrhythmia Unit, Cardiovascular Institute, Hospital Clínic, University of Barcelona, Spain.

出版信息

Circulation. 1998 Feb 10;97(5):457-60. doi: 10.1161/01.cir.97.5.457.

DOI:10.1161/01.cir.97.5.457
PMID:9490240
Abstract

BACKGROUND

Five years ago, we described a specific ECG pattern of right bundle-branch block and ST-segment elevation in leads V1 through V3 associated with sudden death in patients without demonstrable structural heart disease. Information on long-term outcome has become available due to pooled data on a large cohort of patients with this syndrome who are followed at 33 centers worldwide.

METHODS AND RESULTS

Data on 63 patients (57 men; mean age, 38+/-17 years) with the described ECG pattern were analyzed in terms of arrhythmic events and sudden death. Events were analyzed for patients with at least one episode of aborted sudden death or syncope of unknown origin before recognition of the syndrome (symptomatic patients, n=41) and for patients in whom the ECG pattern was recognized by chance or because of screening related to sudden death of a relative (asymptomatic patients, n=22). During a mean follow-up of 34+/-32 months, an arrhythmic event occurred in 14 symptomatic patients (34%) and 6 asymptomatic patients (27%). An automatic defibrillator was implanted in 35 patients, 15 received pharmacological therapy with beta-blockers and/or amiodarone, and 13 did not receive treatment The incidence of arrhythmic events was similar in all therapy groups (log-rank 0.86); however, total mortality was 0% in the implantable defibrillator group, 26% in the pharmacological group, and 31% in the no therapy group (log-rank 0.0005). All mortality was due to sudden death.

CONCLUSIONS

Patients without demonstrable structural heart disease and an ECG pattern of right bundle-branch block and ST-segment elevation in leads V1 through V3 are at risk for sudden death. Amiodarone and/or beta-blockers do not protect them against sudden death, and an implantable defibrillator seems to be the present treatment of choice.

摘要

背景

五年前,我们描述了一种特殊的心电图模式,即右束支传导阻滞以及V1至V3导联ST段抬高,这与无明显结构性心脏病患者的猝死相关。由于对一大群患有该综合征的患者进行汇总数据,这些患者在全球33个中心接受随访,因此现在有了关于长期预后的信息。

方法与结果

对63例(57例男性;平均年龄38±17岁)具有上述心电图模式的患者的数据进行心律失常事件和猝死方面的分析。对在该综合征被识别之前至少有一次不明原因的猝死未遂或晕厥发作的患者(有症状患者,n = 41)以及因亲属猝死筛查偶然发现或因筛查而识别出该心电图模式的患者(无症状患者,n = 22)的事件进行分析。在平均34±32个月的随访期间,14例有症状患者(34%)和6例无症状患者(27%)发生了心律失常事件。35例患者植入了自动除颤器,15例接受了β受体阻滞剂和/或胺碘酮的药物治疗,13例未接受治疗。所有治疗组的心律失常事件发生率相似(对数秩检验P = 0.86);然而,植入式除颤器组的总死亡率为0%,药物治疗组为26%,未治疗组为31%(对数秩检验P = 0.0005)。所有死亡均为猝死。

结论

无明显结构性心脏病且具有V1至V3导联右束支传导阻滞和ST段抬高心电图模式的患者有猝死风险。胺碘酮和/或β受体阻滞剂不能保护他们免于猝死,植入式除颤器似乎是目前的首选治疗方法。

相似文献

1
Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease.V1至V3导联出现右束支传导阻滞及ST段抬高:无明显结构性心脏病患者猝死的一个标志物。
Circulation. 1998 Feb 10;97(5):457-60. doi: 10.1161/01.cir.97.5.457.
2
Further characterization of the syndrome of right bundle branch block, ST segment elevation, and sudden cardiac death.右束支传导阻滞、ST段抬高与心源性猝死综合征的进一步特征分析
J Cardiovasc Electrophysiol. 1997 Mar;8(3):325-31. doi: 10.1111/j.1540-8167.1997.tb00796.x.
3
Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report.右束支传导阻滞、持续性ST段抬高与心源性猝死:一种独特的临床和心电图综合征。一项多中心报告。
J Am Coll Cardiol. 1992 Nov 15;20(6):1391-6. doi: 10.1016/0735-1097(92)90253-j.
4
[Right bundle branch block, ST segment elevation and sudden cardiac death. A clinical and electrocardiographic syndrome--Brugada syndrome].[右束支传导阻滞、ST段抬高与心源性猝死。一种临床及心电图综合征——Brugada综合征]
Ugeskr Laeger. 1999 Feb 22;161(8):1120-2.
5
Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men.泰国男性不明原因猝死综合征的致心律失常标志物。
Circulation. 1997 Oct 21;96(8):2595-600. doi: 10.1161/01.cir.96.8.2595.
6
[Right bundle branch block and ST-segment elevation in right precordial leads: a marker for sudden cardiac death].[右束支传导阻滞及右胸导联ST段抬高:心脏性猝死的一个标志物]
Orv Hetil. 2000 Mar 19;141(12):615-7.
7
Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts.钠通道阻滞剂可识别ST段抬高及右束支传导阻滞但心脏结构正常的患者发生猝死的风险。
Circulation. 2000 Feb 8;101(5):510-5. doi: 10.1161/01.cir.101.5.510.
8
The syndrome of right bundle branch block ST segment elevation in V1 to V3 and sudden death--the Brugada syndrome.V1至V3导联右束支传导阻滞伴ST段抬高及猝死综合征——布加综合征
Europace. 1999 Jul;1(3):156-66. doi: 10.1053/eupc.1999.0033.
9
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families.右束支传导阻滞与ST段抬高综合征的临床及遗传异质性:对52个家庭的前瞻性评估
Circulation. 2000 Nov 14;102(20):2509-15. doi: 10.1161/01.cir.102.20.2509.
10
What to do in patients with no structural heart disease and sudden arrhythmic death?无结构性心脏病且发生心律失常性猝死的患者该如何处理?
Am J Cardiol. 1996 Sep 12;78(5A):69-75. doi: 10.1016/s0002-9149(96)00505-x.

引用本文的文献

1
Genetic insights into cardiac conduction disorders from genome-wide association studies.全基因组关联研究对心脏传导障碍的遗传学见解。
Hum Genomics. 2025 Feb 28;19(1):20. doi: 10.1186/s40246-025-00732-x.
2
Zebrafish as a Model System for Brugada Syndrome.斑马鱼作为布加综合征的模型系统
Rev Cardiovasc Med. 2024 Sep 5;25(9):313. doi: 10.31083/j.rcm2509313. eCollection 2024 Sep.
3
Unconventional diagnosis of bradyarrhythmic syncope in Brugada syndrome: a case report.Brugada综合征中缓慢性心律失常性晕厥的非常规诊断:一例报告
Eur Heart J Case Rep. 2024 Apr 22;8(5):ytae201. doi: 10.1093/ehjcr/ytae201. eCollection 2024 May.
4
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.转录失调是单基因心律失常综合征和心脏复极常见调节剂的共同基础。
Circulation. 2023 Mar 7;147(10):824-840. doi: 10.1161/CIRCULATIONAHA.122.062193. Epub 2022 Dec 16.
5
Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome.俄罗斯布加综合征患者中编码Nav1.5通道基因的诊断率及变异重新评估
Front Pharmacol. 2022 Aug 24;13:984299. doi: 10.3389/fphar.2022.984299. eCollection 2022.
6
Risk stratification of sudden cardiac death in Brugada syndrome: an updated review of literature.Brugada综合征心脏性猝死的危险分层:文献综述更新
Egypt Heart J. 2022 Apr 11;74(1):25. doi: 10.1186/s43044-022-00267-9.
7
Brugada syndrome: should we be screening patients before prescribing psychotropic medication?Brugada综合征:在开具精神药物之前我们应该对患者进行筛查吗?
Ther Adv Psychopharmacol. 2022 Jan 28;12:20451253211067017. doi: 10.1177/20451253211067017. eCollection 2022.
8
Why Is Only Type 1 Electrocardiogram Diagnostic of Brugada Syndrome? Mechanistic Insights From Computer Modeling.为何只有 1 型心电图可诊断 Brugada 综合征?计算机建模的机制见解。
Circ Arrhythm Electrophysiol. 2022 Jan;15(1):e010365. doi: 10.1161/CIRCEP.121.010365. Epub 2021 Dec 29.
9
2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.2020年亚太心律学会/美国心律学会关于不明原因猝死死者及心脏骤停患者及其家属调查的专家共识声明
J Arrhythm. 2021 Apr 8;37(3):481-534. doi: 10.1002/joa3.12449. eCollection 2021 Jun.
10
Long-term follow-up in patients with Brugada Syndrome in South China.华南地区 Brugada 综合征患者的长期随访。
Ann Noninvasive Electrocardiol. 2021 May;26(3):e12823. doi: 10.1111/anec.12823. Epub 2021 Jan 8.