Dan Gheorghe-Andrei
Carol Davila University of Medicine and Pharmacy Bucharest, Romania.
Colentina University Hospital Bucharest, Romania.
Eur Cardiol. 2019 Jul 11;14(2):77-81. doi: 10.15420/ecr.2019.8.1. eCollection 2019 Jul.
AF is a worldwide epidemic, affecting approximately 33 million people, and its rising prevalence is expected to account for increasing clinical and public health costs. AF is associated with an increased risk of MI, heart failure, stroke, dementia, chronic kidney disease and mortality. Preserving sinus rhythm is essential for a better outcome. However, because of the inherent limits of both pharmacological and interventional methods, rhythm strategy management is reserved for symptom and quality-of-life improvement. While 'classical' antiarrhythmic drug therapy remains the first-line therapy for rhythm control, its efficacy and safety are limited by empirical use, proarrhythmic risk and organ toxicity. Ablative techniques have had an impressive development, but AF ablation still failed to demonstrate a significant impact on hard endpoints. Understanding of the complex mechanisms of AF will help to develop new vulnerable targets to therapy. Promising molecules are under development, intended to fill the gap between the current pharmacological treatment aimed at maintaining sinus rhythm and the expectations from rhythm strategy.
房颤是一种全球性的流行病,影响着约3300万人,其患病率不断上升,预计将导致临床和公共卫生成本增加。房颤与心肌梗死、心力衰竭、中风、痴呆、慢性肾病及死亡率风险增加相关。维持窦性心律对于取得更好的治疗效果至关重要。然而,由于药物和介入方法的固有局限性,节律策略管理仅用于改善症状和生活质量。虽然“经典”抗心律失常药物治疗仍是节律控制的一线治疗方法,但其疗效和安全性受到经验性使用、促心律失常风险和器官毒性的限制。消融技术有了令人瞩目的发展,但房颤消融仍未能对硬性终点产生显著影响。了解房颤的复杂机制将有助于开发新的治疗脆弱靶点。有前景的分子正在研发中,旨在填补目前旨在维持窦性心律的药物治疗与节律策略期望之间的差距。