Lopez Jose, Duarte Gustavo J, Colombo Rosario A, Folds Andrea, Losiniecki Fergie J, Chait Robert
Department of Internal Medicine, HCA Florida Aventura Hospital, Aventura, FL, United States.
Department of Medicine, Jacobi Medical Center/Albert Einstein College of Medicine, New York, NY, United States.
Int J Cardiol Heart Vasc. 2022 Sep 22;43:101123. doi: 10.1016/j.ijcha.2022.101123. eCollection 2022 Dec.
Left bundle branch block (LBBB) causes left ventricular dyssynchrony, and its presence with concomitant left ventricular dysfunction has been proven to play a synergistic role, worsening ventricular function. Our study seeks to further explore the association between LBBB and various in-hospital outcomes in patients with takotsubo syndrome (TTS).
The national inpatient sample was queried from 2016 to 2019 to identify all admissions with a primary diagnosis of TTS. International classification of diseases, tenth revision codes were used to divide patients based on the presence or absence of LBBB. Multivariate regression analysis was performed to assess the effect of LBBB among all the pre-specified outcomes.
A total of 26,615 admissions were included in the analysis. Admissions with LBBB were more likely to be older (72.2 vs. 66.2 years) and have a higher burden of comorbidities. The presence of a LBBB was associated with ventricular arrhythmias (OR = 1.97, 95% CI 1.08-3.61, p = 0.028) but not with sudden cardiac arrest (SCA), acute heart failure, cardiogenic shock, and all-cause intra-hospital mortality.
Intraventricular dyssynchrony appears to play a significant role in ventricular arrhythmogenesis and SCA, as several trials have demonstrated that cardiac resynchronization therapy alone without defibrillator function reduces the rate of ventricular arrhythmias and SCA in patients with heart failure with systolic dysfunction and a widened QRS complex. The most likely mechanism of arrhythmia development in TTS is related to the elevated plasma levels of catecholamines and their proarrhythmic effects in the ventricular myocardium.
左束支传导阻滞(LBBB)可导致左心室不同步,且已证实其与左心室功能障碍并存时会起协同作用,使心室功能恶化。我们的研究旨在进一步探讨LBBB与应激性心肌病(TTS)患者各种院内结局之间的关联。
查询2016年至2019年的全国住院患者样本,以确定所有以TTS为主要诊断的入院病例。使用国际疾病分类第十版编码,根据是否存在LBBB对患者进行分组。进行多变量回归分析,以评估LBBB在所有预先设定结局中的作用。
分析共纳入26615例入院病例。合并LBBB的入院患者年龄更大(72.2岁对66.2岁),合并症负担更高。LBBB的存在与室性心律失常相关(OR = 1.97,95% CI 1.08 - 3.61,p = 0.028),但与心搏骤停(SCA)、急性心力衰竭、心源性休克和全因院内死亡率无关。
心室内不同步似乎在室性心律失常的发生和SCA中起重要作用,因为多项试验表明,单独的心脏再同步治疗(无除颤器功能)可降低收缩功能障碍且QRS波增宽的心力衰竭患者的室性心律失常和SCA发生率。TTS中心律失常发生的最可能机制与血浆儿茶酚胺水平升高及其在心室心肌中的促心律失常作用有关。