University Hospitals Leuven, Belgium.
Int J Cardiol. 2013 Apr 15;164(3):318-22. doi: 10.1016/j.ijcard.2011.07.010. Epub 2011 Jul 29.
To develop a quantitative event-free prediction model of late atrial arrhythmia after atrial septal defect (ASD) repair.
The clinical management of ASD is driven by risk factors that determine the occurrence of late atrial arrhythmia.
Data from ASD type secundum patients, included in the Belgian Congenital Heart Disease Registry, were analyzed. Based on review of the literature, age at repair, gender, pulmonary hypertension, atrial arrhythmia before and within one month after repair were included in the model. Using Cox-regression analysis, a weighted risk score was derived, which was validated using the Brier score.
A total of 155 patients (117 women; median age at follow-up 53.9 years, range 18.0-78.8) having 349 follow-up years was included. Thirty-nine patients (25.2%) presented with late atrial arrhythmia. Multivariate analysis showed that a mPAP ≥ 25 mmHg (HR 4.39; 95%CI 2.17-9.09; P<0.0001), the presence of atrial arrhythmia before (HR 3.52; 95%CI 1.75-7.14; P=0.002) and ≤ 1month after repair (HR 6.62; 95%CI 2.38-20.00; P<0.0001) and gender (HR 2.18 95%CI 1.11-4.35) were associated with late atrial arrhythmia. A risk score (0 to 28 points) to predict atrial arrhythmia free survival was derived for follow-up times ranging from one to 5 years. Mean Brier score for the model was 0.10.
We formulated a well validated risk model to predict arrhythmia-free survival in ASD patients undergoing ASD repair. Further research is needed whether this model can be used for individual clinical risk stratification and whether the model can be adapted for application in other congenital heart defects.
开发一种用于预测房间隔缺损(ASD)修补术后晚期房性心律失常的定量无事件预测模型。
ASD 的临床管理取决于决定晚期房性心律失常发生的风险因素。
分析了包含在比利时先天性心脏病注册中心的 ASD 型 II 孔患者的数据。基于文献回顾,纳入了修复时的年龄、性别、肺动脉高压、修复前和修复后一个月内的房性心律失常等因素。采用 Cox 回归分析得出加权风险评分,并使用 Brier 评分进行验证。
共纳入 155 例患者(117 例女性;中位随访时间为 53.9 岁,范围为 18.0-78.8),随访时间共 349 年。39 例(25.2%)患者出现晚期房性心律失常。多变量分析显示,mPAP≥25mmHg(HR 4.39;95%CI 2.17-9.09;P<0.0001)、修复前(HR 3.52;95%CI 1.75-7.14;P=0.002)和≤1 个月后存在房性心律失常(HR 6.62;95%CI 2.38-20.00;P<0.0001)以及性别(HR 2.18 95%CI 1.11-4.35)与晚期房性心律失常相关。为随访时间 1 至 5 年,建立了一个预测房性心律失常无事件生存的风险评分(0 至 28 分)。模型的平均 Brier 评分是 0.10。
我们制定了一个经过良好验证的风险模型,用于预测 ASD 患者接受 ASD 修补术后无心律失常生存。需要进一步研究该模型是否可用于个体临床风险分层,以及该模型是否可适用于其他先天性心脏病。