Ng Fu Siong, Handa Balvinder S, Li Xinyang, Peters Nicholas S
National Heart & Lung Institute, Imperial College London, London, United Kingdom.
Front Physiol. 2020 Aug 28;11:987. doi: 10.3389/fphys.2020.00987. eCollection 2020.
Current treatment approaches for persistent atrial fibrillation (AF) have a ceiling of success of around 50%. This is despite 15 years of developing adjunctive ablation strategies in addition to pulmonary vein isolation to target the underlying arrhythmogenic substrate in AF. A major shortcoming of our current approach to AF treatment is its predominantly empirical nature. This has in part been due to a lack of consensus on the mechanisms that sustain human AF. In this article, we review evidence suggesting that the previous debates on AF being an organized arrhythmia with a focal driver a disorganized rhythm sustained by multiple wavelets, may prove to be a false dichotomy. Instead, a range of fibrillation electrophenotypes exists along a continuous spectrum, and the predominant mechanism in an individual case is determined by the nature and extent of remodeling of the underlying substrate. We propose moving beyond the current empirical approach to AF treatment, highlight the need to prescribe AF treatments based on the underlying AF electrophenotype, and review several possible novel mapping algorithms that may be useful in discerning the AF electrophenotype to guide tailored treatments, including Granger Causality mapping.
目前针对持续性心房颤动(AF)的治疗方法成功率上限约为50%。尽管在肺静脉隔离之外,为了针对房颤潜在的致心律失常基质,已经开展了15年的辅助消融策略研究,但情况依然如此。我们目前治疗房颤的方法的一个主要缺点是其主要基于经验。部分原因是对于维持人类房颤的机制缺乏共识。在本文中,我们回顾了相关证据,表明之前关于房颤是由局灶驱动因素引起的有组织的心律失常还是由多个小波维持的无序节律的争论,可能是一个错误的二分法。相反,沿着连续谱存在一系列颤动电生理表型,个体病例中的主要机制由潜在基质重塑的性质和程度决定。我们建议超越目前针对房颤治疗的经验方法,强调根据潜在的房颤电生理表型来制定房颤治疗方案的必要性,并回顾几种可能有助于识别房颤电生理表型以指导个性化治疗的新型标测算法,包括格兰杰因果关系标测。