修复后法洛四联症心源性猝死的危险分层

Jayant Kakarla MBBS, Nathan C. Denham BM, PhD, Ayako Ishikita MD, PhD, Erwin Oechslin MD, Rafael Alonso-Gonzalez MD, Krishnakumar Nair MD
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引用次数: 1

摘要

法洛四联症修复后心脏性猝死的预防已取得重大进展。当代队列报告更高的生存率归因于改进的手术技术,心力衰竭管理,以及包括除颤器植入和消融技术在内的前瞻性风险分层和室性心律失常管理策略。在过去的25年里,我们对预测风险因素的理解也从侵入性和更有限的措施提高到基于广泛的人口统计、成像、电生理和功能数据的个性化风险预测评分。尽管这些现代评分系统都能改善预测,但研究队列之间存在重要差异,包括危险因素和成像方式,这些差异会显著影响个体患者的解释和实施。此外,疾病复杂性的准确表型和解剖修复实质上调节了这种风险和猝死的机制。在修复的法洛四联症治疗中,常规实施风险分层是重要的,它直接影响了一级预防除颤器植入,以及考虑主动侵入策略,包括室性心动过速消融和肺动脉瓣置换术。由多学科专家团队对成人先天性心脏病进行评估和风险分层是至关重要的。尽管我们对这些复杂因素的了解有所增加,但对个体患者的协调仍然具有挑战性,通常需要与多学科团队、患者及其家属仔细考虑和讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk Stratification for Sudden Cardiac Death in Repaired Tetralogy of Fallot

There has been significant progress in the prevention of sudden cardiac death in repaired tetralogy of Fallot. Contemporary cohorts report greater survival attributable to improved surgical techniques, heart failure management, and proactive strategies for risk stratification and management of ventricular arrhythmias including defibrillator implantation and ablation technology. Over the last 25 years, our understanding of predictive risk factors has also improved from invasive and more limited measures to individualized risk prediction scores based on extensive demographic, imaging, electrophysiological, and functional data. Although each of these contemporary scoring systems improves prediction, there are important differences between the study cohorts, included risk factors, and imaging modalities that can significantly affect interpretation and implementation for the individual patient. In addition, accurate phenotyping of disease complexity and anatomic repair substantially modulates this risk and the mechanism of sudden death. Routine implementation of risk stratification within repaired tetralogy of Fallot management is important and directly informs primary prevention defibrillator implantation as well as consideration for proactive invasive strategies including ventricular tachycardia ablation and pulmonary valve replacement. Assessment and risk stratification by a multidisciplinary team of experts in adult congenital heart disease are crucial and critical. Although we have increased understanding, reconciliation of these complex factors for the individual patient remains challenging and often requires careful consideration and discussion with multidisciplinary teams, patients, and their families.

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