Chakrabarti Apurba, Giudicessi John R, Ezzeddine Fatima M, Delling Francesca N, Dixit Shalini, Lee Yoo Jin, Muser Daniele, Magnani Silvia, Van Wijngaarden Aniek, Ajmone Marsan Nina, Miller Marc A, Gandhi Jonathan, Trivieri Maria G, Font Jonaz, Martins Raphael, McCaffrey James A, Santangeli Pasquale, Marchlinski Francis E, Chapagain Himal, Mathew Don, Kancharla Krishna, Syed Faisal F, Abid Ahad, Cerbin Lukasz, Tzou Wendy S, Garg Lohit, Della Rocca Domenico G, Natale Andrea, Mohanty Sanghamitra, Sheldon Seth H, Kuo Ling, Haugaa Kristina H, Aabel Eivind W, Enriquez Andres, Maeda Shingo, Deshmukh Amrish, Ghannam Michael, Bogun Frank, Ackerman Michael J, Liang Jackson J
Division of Cardiovascular Medicine, University of Michigan, Ann Arbor (A.C., A.D., M.G., F.B., J.J.L.).
Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN (J.R.G., F.M.E., M.J.A.).
Circ Arrhythm Electrophysiol. 2025 Mar;18(3):e013099. doi: 10.1161/CIRCEP.124.013099. Epub 2025 Feb 20.
Patients with arrhythmogenic mitral valve prolapse syndrome are at increased risk for life-threatening ventricular arrhythmias, but studies have been limited by small sample sizes. We sought to assemble an international arrhythmogenic mitral valve prolapse syndrome registry to delineate the clinical, imaging, and treatment characteristics of patients with arrhythmogenic mitral valve prolapse syndrome who survived sudden cardiac arrest (SCA) or had sustained ventricular tachycardia (VT) or ventricular fibrillation.
In this descriptive registry, we characterized patients with arrhythmogenic mitral valve prolapse syndrome who survived SCA, sustained VT, or ventricular fibrillation. Deidentified data were abstracted locally and combined centrally.
We included 148 patients who had SCA or VT/ventricular fibrillation. Patients had a mean age of 43.7±15.4 years; 68% were women, 73% had bileaflet prolapse, 65% had mitral annular disjunction, 67% had nonsustained VT, and 59% had inferolateral T-wave inversions. Syncope (n=54, 48%) and anterolateral T-wave inversion (n=26, 22%) were relatively common. Catheter ablation was performed in 50 (35%) patients for premature ventricular complexes and in 18 (17.7%) patients for VT. Sites of origin for arrhythmias were commonly in the papillary muscles, fascicles, mitral annulus, and inferior/inferolateral left ventricle.
In this international descriptive registry of patients with arrhythmogenic mitral valve prolapse syndrome and SCA, patients were young, women, and had bileaflet mitral valve prolapse, mitral annular disjunction, inferolateral T-wave inversions, and nonsustained VT. A history of syncope and anterolateral T-wave inversions was relatively common in patients who survived SCA or sustained VT/ventricular fibrillation.
致心律失常性二尖瓣脱垂综合征患者发生危及生命的室性心律失常的风险增加,但此前的研究因样本量小而受到限制。我们试图建立一个国际致心律失常性二尖瓣脱垂综合征注册库,以描述那些经历过心脏骤停(SCA)存活、或有持续性室性心动过速(VT)或心室颤动的致心律失常性二尖瓣脱垂综合征患者的临床、影像学和治疗特征。
在这个描述性注册研究中,我们对经历过SCA、持续性VT或心室颤动的致心律失常性二尖瓣脱垂综合征患者进行了特征描述。去识别化的数据在当地提取并集中汇总。
我们纳入了148例发生过SCA或VT/心室颤动的患者。患者的平均年龄为43.7±15.4岁;68%为女性,73%有双叶脱垂,65%有二尖瓣环分离,67%有非持续性VT,59%有下外侧T波倒置。晕厥(n = 54,48%)和前外侧T波倒置(n = 26,22%)相对常见。50例(35%)患者因室性早搏接受了导管消融,18例(17.7%)患者因VT接受了导管消融。心律失常的起源部位通常在乳头肌、束支、二尖瓣环和左心室下壁/下外侧壁。
在这个关于致心律失常性二尖瓣脱垂综合征和SCA患者的国际描述性注册研究中,患者多为年轻女性,有双叶二尖瓣脱垂、二尖瓣环分离、下外侧T波倒置和非持续性VT。晕厥病史和前外侧T波倒置在经历过SCA存活或持续性VT/心室颤动的患者中相对常见。