MacLachlan H, Antonakaki A, Bhatia R, Fyazz S, Chatrath N, Androulakis E, Marawaha S, Basu J, Miles C, Dhutia H, Zaidi A, Chandra N, Sheikh N, Gati S, Malhotra A, Finocchiaro G, Sharma S, Papadakis M
Cardiovascular Clinical Academic Group, St George's, University of London, London, UK.
Department of Cardiology, Glenfield Hospital, Leicester, UK.
Eur J Prev Cardiol. 2024 Feb 27. doi: 10.1093/eurjpc/zwae082.
There is limited information on the clinical significance of complete right bundle branch block (CRBBB) in young individuals. The aim of this study was to determine the prevalence and significance of CRBBB in a large cohort of young individuals aged 14-35 years old.
From 2008 to 2018, 104,369 consecutive individuals underwent a cardiovascular assessment with a health questionnaire, electrocardiogram, clinical consultation, and selective echocardiography. Follow-up was obtained via direct telephone consultations. Mean follow-up was 7.3 ± 2.7 years.
CRBBB was identified in 154 (0.1%) individuals and was more prevalent in males compared with females (0.20% vs. 0.06%; p<0.05) and in athletes compared with non-athletes (0.25% vs. 0.14%; p<0.05). CRBBB-related cardiac conditions were identified in 7 (5%) individuals (4 with atrial septal defect, 1 with Brugada syndrome, 1 with progressive cardiac conduction disease and 1 with atrial fibrillation). Pathology was more frequently identified in individuals with non-isolated CRBBB compared with individuals with isolated CRBBB (14% vs 1%; p < 0.05) and in individuals with a QRS duration of ≥130 milliseconds (ms) compared with individuals with a QRS of <130ms (10% vs 1%; p<0.05).
The prevalence of CRBBB in young individuals was 0.1% and was more prevalent in males and athletes. CRBBB-related conditions were identified in 5% of individuals and were more common in individuals with non-isolated CRBBB and more pronounced intraventricular conduction delay (QRS duration of ≥130ms). Secondary evaluation should be considered for young individuals with CRBBB with symptoms, concerning family history, additional electrocardiographic anomalies or significant QRS prolongation (≥130ms).
关于年轻人完全性右束支传导阻滞(CRBBB)的临床意义,相关信息有限。本研究的目的是确定在一大群14至35岁的年轻人中CRBBB的患病率及其意义。
从2008年到2018年,104369名连续的个体接受了心血管评估,包括健康问卷、心电图、临床会诊和选择性超声心动图检查。通过直接电话会诊进行随访。平均随访时间为7.3±2.7年。
在154名(0.1%)个体中发现了CRBBB,男性比女性更常见(0.20%对0.06%;p<0.05),运动员比非运动员更常见(0.25%对0.14%;p<0.05)。在7名(5%)个体中发现了与CRBBB相关的心脏疾病(4例房间隔缺损、1例Brugada综合征、1例进行性心脏传导疾病和1例心房颤动)。与孤立性CRBBB个体相比,非孤立性CRBBB个体更常发现病变(14%对1%;p<0.05),QRS时限≥130毫秒(ms)的个体比QRS<130ms的个体更常发现病变(10%对1%;p<0.05)。
年轻人中CRBBB的患病率为0.1%,在男性和运动员中更常见。5%的个体发现了与CRBBB相关的疾病,在非孤立性CRBBB个体和更明显的室内传导延迟(QRS时限≥130ms)个体中更常见。对于有症状、有家族病史、有其他心电图异常或QRS明显延长(≥130ms)的CRBBB年轻个体,应考虑进行进一步评估