儿科心脏植入式电子装置新指南:临床实践有何变化?

M. Silvetti, D. Colonna, Fulvio Gabbarini, Giulio Porcedda, Alessandro Rimini, A. D'Onofrio, L. Leoni
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摘要

指南是指导病人诊断和治疗的重要工具,可改善医疗专业人员的决策过程。指南根据新证据定期更新。2021 年、2022 年和 2023 年的四份新指南涉及儿科起搏和除颤。在永久起搏方面有一些相关变化。对于房室传导阻滞患者,降低了建议植入起搏器的心率限制,以减少过早植入起搏器的情况。但需要强调的是,心率标准并不是绝对的,因为血流动力学不能耐受的心动过缓迹象或症状甚至可能出现在更高的心率下。在窦房结功能障碍中,有症状的心动过缓是起搏的最相关建议。当推测心室起搏量较大时,越来越多地使用和推荐使用生理起搏。新的建议表明,循环记录器可指导遗传性心律失常综合征的治疗,并可用于严重但不频繁的心悸。关于除颤器植入,主要变化在于一级预防建议。对于肥厚型心肌病,《指南》中加入了儿科风险计算器。在扩张型心肌病方面,由于儿科心源性猝死的罕见性,低射血分数标准被降为二级。在长 QT 综合征方面,新的标准包括 QTc 严重延长,根据基因型和一些特定的突变而有不同的限制。在心律失常性心肌病中,血流动力学可耐受的室性心动过速和心律失常性晕厥被降为 II 级推荐标准。总之,这些新指南旨在评估心脏植入式电子设备的各个方面,并改进治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Guidelines of Pediatric Cardiac Implantable Electronic Devices: What Is Changing in Clinical Practice?
Guidelines are important tools to guide the diagnosis and treatment of patients to improve the decision-making process of health professionals. They are periodically updated according to new evidence. Four new Guidelines in 2021, 2022 and 2023 referred to pediatric pacing and defibrillation. There are some relevant changes in permanent pacing. In patients with atrioventricular block, the heart rate limit in which pacemaker implantation is recommended was decreased to reduce too-early device implantation. However, it was underlined that the heart rate criterion is not absolute, as signs or symptoms of hemodynamically not tolerated bradycardia may even occur at higher rates. In sinus node dysfunction, symptomatic bradycardia is the most relevant recommendation for pacing. Physiological pacing is increasingly used and recommended when the amount of ventricular pacing is presumed to be high. New recommendations suggest that loop recorders may guide the management of inherited arrhythmia syndromes and may be useful for severe but not frequent palpitations. Regarding defibrillator implantation, the main changes are in primary prevention recommendations. In hypertrophic cardiomyopathy, pediatric risk calculators have been included in the Guidelines. In dilated cardiomyopathy, due to the rarity of sudden cardiac death in pediatric age, low ejection fraction criteria were demoted to class II. In long QT syndrome, new criteria included severely prolonged QTc with different limits according to genotype, and some specific mutations. In arrhythmogenic cardiomyopathy, hemodynamically tolerated ventricular tachycardia and arrhythmic syncope were downgraded to class II recommendation. In conclusion, these new Guidelines aim to assess all aspects of cardiac implantable electronic devices and improve treatment strategies.
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