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本文引用的文献

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Natural history of Brugada syndrome: insights for risk stratification and management.Brugada综合征的自然病史:对风险分层和管理的见解
Circulation. 2002 Mar 19;105(11):1342-7. doi: 10.1161/hc1102.105288.
2
Na(+) channel mutation that causes both Brugada and long-QT syndrome phenotypes: a simulation study of mechanism.导致Brugada综合征和长QT综合征表型的钠离子通道突变:机制的模拟研究
Circulation. 2002 Mar 12;105(10):1208-13. doi: 10.1161/hc1002.105183.
3
Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.不明原因夜间猝死综合征(SUNDS)的遗传和生物物理基础,SUNDS是一种与Brugada综合征等位基因相关的疾病。
Hum Mol Genet. 2002 Feb 1;11(3):337-45. doi: 10.1093/hmg/11.3.337.
4
Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome.与布加迪综合征相关的SCN5A双突变体R1232W/T1620M的表达及细胞内定位
Circ Res. 2002 Jan 11;90(1):E11-6.
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Long-term follow-up of individuals with the electrocardiographic pattern of right bundle-branch block and ST-segment elevation in precordial leads V1 to V3.对心电图表现为右束支传导阻滞及胸前导联V1至V3 ST段抬高的个体进行长期随访。
Circulation. 2002 Jan 1;105(1):73-8. doi: 10.1161/hc0102.101354.
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Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.在一个法国家族中发现的新型SCN5A突变,该突变可导致孤立性心脏传导缺陷或Brugada综合征。
Circulation. 2001 Dec 18;104(25):3081-6. doi: 10.1161/hc5001.100834.
7
Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).Brugada综合征的新机制:SCN5A突变体(R1432G)的表面定位缺陷
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Three-year follow-up of patients with right bundle branch block and ST segment elevation in the right precordial leads: Japanese Registry of Brugada Syndrome. Idiopathic Ventricular Fibrillation Investigators.右束支传导阻滞合并右胸前导联ST段抬高患者的三年随访:日本Brugada综合征注册研究。特发性室颤研究人员。
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9
Assessment of noninvasive markers in identifying patients at risk in the Brugada syndrome: insight into risk stratification.
J Am Coll Cardiol. 2001 May;37(6):1628-34. doi: 10.1016/s0735-1097(01)01197-4.
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Brugada综合征中ST段形态与信号平均心电图检测到的传导障碍之间的关系。

Relationship between ST-segment morphology and conduction disturbances detected by signal-averaged electrocardiography in Brugada syndrome.

作者信息

Takami Mitsuaki, Ikeda Takanori, Enjoji Yoshihisa, Sugi Kaoru

机构信息

Third Department of Internal Medicine, Ohashi Hospital, Toho University School of Medicine, Tokyo, Japan.

出版信息

Ann Noninvasive Electrocardiol. 2003 Jan;8(1):30-6. doi: 10.1046/j.1542-474x.2003.08106.x.

DOI:10.1046/j.1542-474x.2003.08106.x
PMID:12848811
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6932588/
Abstract

BACKGROUND

Although arrhythmogenesis of Brugada syndrome is still unknown, it has been reported to be associated with conduction disturbances. Two ST-segment morphologies (coved and saddle-back patterns) have been described in this syndrome. No study has sought to determine which morphology has stronger conduction disturbances, thereby associating with life-threatening events.

METHODS

Forty-six patients who presented the Brugada-type ECG with either of a characteristic coved (n = 25) or saddle-back (n = 21) pattern of ST-segment morphology underwent signal-averaged ECG (SAECG). SAECG parameters, and the history of life-threatening events defined as syncope or aborted sudden death, were compared between groups.

RESULTS

Although filtered QRS duration did not differ between groups, the incidence of late potentials in the coved group was higher than in the saddle-back group (22 patients (88%) versus 4 patients (19%); P < 0.01), showing lower RMS40 and longer LAS40. Life-threatening events occurred in 17 patients (68%) in the coved group and 7 patients (33%) in the saddle-back group (P = 0.02).

CONCLUSION

The coved pattern of ST segment was more closely related to conduction disturbances than the saddle-back pattern in patients with Brugada-type ECG. Life-threatening events were more common in patients with the coved ST-segment elevation. Conduction disturbances in the coved pattern of ST segment may reflect a substrate of arrhythmogenesis in Brugada syndrome.

摘要

背景

尽管布加综合征的心律失常机制尚不清楚,但据报道其与传导障碍有关。该综合征已描述了两种ST段形态(穹窿型和马鞍型)。尚无研究试图确定哪种形态的传导障碍更强,进而与危及生命的事件相关联。

方法

46例呈现布加综合征特征性心电图的患者,其中25例为穹窿型ST段形态,21例为马鞍型ST段形态,均接受了信号平均心电图(SAECG)检查。比较两组的SAECG参数以及定义为晕厥或心脏骤停的危及生命事件的病史。

结果

尽管两组间滤波后的QRS波时限无差异,但穹窿型组的晚电位发生率高于马鞍型组(22例(88%)对4例(19%);P<0.01),表现为较低的RMS40和较长的LAS40。穹窿型组17例(68%)发生危及生命事件,马鞍型组7例(33%)发生危及生命事件(P=0.02)。

结论

在布加综合征心电图患者中,ST段穹窿型比马鞍型与传导障碍的关系更密切。ST段穹窿型抬高的患者发生危及生命事件更为常见。ST段穹窿型的传导障碍可能反映了布加综合征心律失常的基质。