Schwartz Peter J, Dagradi Federica, Giovenzana Fulvio L F, Cerea Paolo
Center for Cardiac Arrhythmias of Genetic Origin, Istituto Auxologico Italiano IRCCS, Via Pier Lombardo 22, 20135 Milan, Italy.
Eur Heart J Suppl. 2025 Feb 19;27(Suppl 1):i47-i50. doi: 10.1093/eurheartjsupp/suae085. eCollection 2025 Feb.
This essay stems from a controversial recommendation present in the 2022 European Guidelines which indicated the appropriateness of considering an implantable cardioverter defibrillator (ICD) implant even for still asymptomatic long QT syndrome (LQTS) patients deemed to be at high risk by the 1-2-3 LQTS score based on QTc and genotype calculated prior to the institution of therapy. As 15 years ago, we also had proposed, but never used, a risk score called M-FACT to identify patients at high risk of an appropriate ICD shock, we felt the responsibility of assessing what would have happened to our patients if we had rigorously used that score. We performed a study recently published in the which brought to general attention two concepts important for clinical management. One is that all LQTS patients should be seen at least once a year for a reassessment of arrhythmic risk based on standard electrocardiogram, 12-lead 24 h Holter recording and an exercise stress test. The other is that, based on these yearly visits, we perform 'therapy optimization' by adding to the standard β-blocker therapy either left cardiac sympathetic denervation or mexiletine or an ICD implant. On almost 1000 LQTS patients, all genotyped, this dynamic approach was accompanied by not a single death, few events, and out of 142 patients who should have received an ICD based on the score, only 22 did and only 3 had an ICD shock. These data and concepts call for a reconsideration of the recommendation made by the guidelines.
本文源于2022年欧洲指南中一项有争议的建议,该建议指出,对于仍无症状的长QT综合征(LQTS)患者,即使根据治疗前计算的QTc和基因型得出的1-2-3 LQTS评分被认为处于高风险,考虑植入植入式心脏复律除颤器(ICD)也是合适的。15年前,我们也曾提出但从未使用过一种名为M-FACT的风险评分来识别有适当ICD电击高风险的患者,我们觉得有责任评估如果我们严格使用该评分,我们的患者会发生什么情况。我们最近进行了一项研究并发表在[期刊名称未给出]上,该研究引起了临床管理中两个重要概念的广泛关注。一个是所有LQTS患者每年至少应就诊一次,以便根据标准心电图、12导联24小时动态心电图记录和运动应激试验重新评估心律失常风险。另一个是,基于这些年度就诊,我们通过在标准β受体阻滞剂治疗基础上增加左心交感神经去神经术、美西律或ICD植入来进行“治疗优化”。在近1000名所有已进行基因分型的LQTS患者中,这种动态方法没有导致一例死亡,很少发生事件,在根据评分应该接受ICD治疗的142名患者中,只有22名接受了ICD治疗,只有3名发生了ICD电击。这些数据和概念促使人们重新考虑指南提出的建议。