Progressive outcomes of bundle branch reentrant ventricular tachycardia in patients without structural heart disease

被引:3
作者
Li, Zhaomin [1 ]
Peng, Xiafeng [1 ]
Cui, Chang [1 ]
Zhang, Yike [1 ]
Ju, Weizhu [1 ]
Zhang, Fengxiang [1 ]
Yang, Gang [1 ]
Gu, Kai [1 ]
Liu, Hailei [1 ]
Wang, Zidun [1 ]
Jiang, Xiaohong [1 ]
Li, Mingfang [1 ]
Chen, Hongwu [1 ]
Chen, Minglong [1 ]
机构
[1] Nanjing Med Univ, Dept Cardiol, Affiliated Hosp 1, Guangzhou Rd, Nanjing 210029, Jiangsu, Peoples R China
关键词
Bundle branch reentrant ventricular tachycardia; Follow-up; Genetic testing; Left bundle branch; Right bundle branch; RADIOFREQUENCY CATHETER ABLATION; HIS-PURKINJE SYSTEM; MECHANISM; GUIDELINES; DYSTROPHY;
D O I
10.1016/j.hrthm.2023.02.027
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Ablation strategies to treat bundle branch reen-trant ventricular tachycardia (BBRT) are well described. However, reports of long-term follow-up outcomes in BBRT patients without structural heart disease (SHD) are limited.OBJECTIVE The purpose of this study was to investigate the long-term follow-up prognosis of BBRT patients without SHD.METHODS Changes in electrocardiographic and echocardiographic parameters were used to evaluate progression during follow-up. Po-tential pathogenic candidate variants were screened using a specific gene panel.RESULTS Eleven consecutive BBRT patients without obvious SHD based on echocardiographic and cardiovascular magnetic resonance imaging results were enrolled. Median age was 20 (11-48) years, and median follow-up time was 72 months. During follow-up, PR in-terval [206 (158-360) ms vs 188 (158-300) ms; P = .018] and QRS duration [187 (155-240) ms vs 164 (130-178) ms; P = .008] each increased significantly compared with postablation. Right-and left-sided chamber dilation and reduced left ventricular ejection fraction (LVEF) also were observed. Clinical deterioration or events occurred in 8 patients: 1 sudden death; 3 both complete heart block and reduced LVEF; 2 significantly reduced LVEF; and 2 prolonged PR in-terval. Genetic testing results showed that 6 of 10 patients (excluding the patient with sudden death) had >1 potential path-ogenic candidate variants.CONCLUSION Further deterioration of His-Purkinje system con-duction was observed in young BBRT patients without SHD after ablation. The His-Purkinje system may be the first target of genetic predisposition.
引用
收藏
页码:815 / 821
页数:7
相关论文
共 27 条
[21]   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology [J].
Richards, Sue ;
Aziz, Nazneen ;
Bale, Sherri ;
Bick, David ;
Das, Soma ;
Gastier-Foster, Julie ;
Grody, Wayne W. ;
Hegde, Madhuri ;
Lyon, Elaine ;
Spector, Elaine ;
Voelkerding, Karl ;
Rehm, Heidi L. .
GENETICS IN MEDICINE, 2015, 17 (05) :405-424
[22]  
Roberts Jason D, 2017, JACC Clin Electrophysiol, V3, P276, DOI [10.1016/j.jacep.2016.09.019, 10.1016/j.jacep.2016.09.019]
[23]   An unusual form of bundle branch reentrant tachycardia [J].
Sarkozy, Andrea ;
Boussy, Tim ;
Chierchia, Gian-Battista ;
Geelen, Peter ;
Brugada, Pedro .
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2006, 17 (08) :902-906
[24]   Left bundle branch-Purkinje system in patients with bundle branch reentrant tachycardia: Lessons from catheter ablation and electroanatomic mapping [J].
Schmidt, Boris ;
Tang, Min ;
Chun, Julian ;
Antz, Matthias ;
Tilz, Roland R. ;
Metzner, Andreas ;
Koektuerk, Bulent ;
Xie, Ping ;
Kuck, Karl-Heinz ;
Ouyang, Feifan .
HEART RHYTHM, 2009, 6 (01) :51-58
[25]   Bundle branch re-entry ventricular tachycardia in a patient with myotonic dystrophy [J].
Takeda, Kotaro ;
Takemoto, Masao ;
Mukai, Yasushi ;
Seto, Taku ;
Ohwaki, Kazuo ;
Kaji, Yoshikazu ;
Chishaki, Akiko ;
Sunagawa, Kenji .
JOURNAL OF CARDIOLOGY, 2009, 53 (03) :463-466
[26]   TRANSCATHETER ELECTRICAL ABLATION OF RIGHT BUNDLE-BRANCH - A METHOD OF TREATING MACROREENTRANT VENTRICULAR-TACHYCARDIA ATTRIBUTED TO BUNDLE-BRANCH REENTRY [J].
TCHOU, P ;
JAZAYERI, M ;
DENKER, S ;
DONGAS, J ;
CACERES, J ;
AKHTAR, M .
CIRCULATION, 1988, 78 (02) :246-257
[27]   Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification [J].
Yao, Xiang-Ping ;
Cheng, Xuewen ;
Wang, Chong ;
Zhao, Miao ;
Guo, Xin-Xin ;
Su, Hui-Zhen ;
Lai, Lu-Lu ;
Zou, Xiao-Huan ;
Chen, Xue-Jiao ;
Zhao, Yuying ;
Dong, En-Lin ;
Lu, Ying-Qian ;
Wu, Shuang ;
Li, Xiaojuan ;
Fan, Gaofeng ;
Yu, Hongjie ;
Xu, Jianfeng ;
Wang, Ning ;
Xiong, Zhi-Qi ;
Chen, Wan-Jin .
NEURON, 2018, 98 (06) :1116-+