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The appearance of new accessory pathway after the Cone procedure.
Nguyen, Dinh Son Ngoc; Chang, Shih-Lin; Weng, Chi-Jen; Wu, Fei-Yi; Chen, Shih-Ann.
Afiliação
  • Nguyen DSN; Division of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Chang SL; Cardiovascular Research Center, National Yang-Ming Chiao Tung University, Taipei, Taiwan.
  • Weng CJ; Division of Cardiology, Department of Medicine, Heart Rhythm Center, Taipei Veterans General Hospital, Taipei, Taiwan.
  • Wu FY; Cardiovascular Research Center, National Yang-Ming Chiao Tung University, Taipei, Taiwan.
  • Chen SA; School of Medicine, College of Medicine, National Yang-Ming Chiao Tung University, Taipei, Taiwan.
J Cardiovasc Electrophysiol ; 34(12): 2617-2620, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37964504
ABSTRACT

INTRODUCTION:

Acquired Wolff-Parkinson-White (WPW) syndrome can occur after congenital heart disease (CHD) surgery. METHODS AND

RESULTS:

A 27-year-old male with Ebstein's anomaly and manifest WPW syndrome received catheter ablation twice. The first electrophysiology study (EPS) induced orthodromic atrioventricular reentrant tachycardia and successfully eliminated the posteroseptal accessory pathway (AP). Six months after the Cone procedure, the patient suffered from palpitation. The second EPS was performed and abolished the right lateral AP.

CONCLUSION:

The appearance of a new AP after the reconstruction of CHD is a rare finding and should raise suspicion of an acquired AP connection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Wolff-Parkinson-White / Taquicardia Supraventricular / Ablação por Cateter / Anomalia de Ebstein / Feixe Acessório Atrioventricular / Cardiopatias Congênitas Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Wolff-Parkinson-White / Taquicardia Supraventricular / Ablação por Cateter / Anomalia de Ebstein / Feixe Acessório Atrioventricular / Cardiopatias Congênitas Idioma: En Ano de publicação: 2023 Tipo de documento: Article