El Assaad Iqbal, Heilbronner Alison K, Zahka Kenneth, Hammond Benjamin, Patel Akash, Aziz Peter F
Children's Institute Department of Heart, Vascular & Thoracic, Division of Cardiology & Cardiovascular Medicine, Cleveland Clinic Children's, Cleveland, Ohio, USA.
Cleveland Clinic Lerner College of Medicine, Cleveland, Ohio, USA.
J Cardiovasc Electrophysiol. 2025 Sep;36(9):2287-2295. doi: 10.1111/jce.70001. Epub 2025 Jul 14.
Currently, there is no specific standard to assess beta blocker efficacy in long QT syndrome (LQTS).
To describe our institutional experience with utilizing cardiopulmonary exercise testing (CPET) to assess for chronotropic suppression and to compare frequency of life-threatening events (LTEs) on intentional "submaximal" treatment to those on maximal treatment.
We queried our Inherited Arrhythmia Registry and identified patients with LQTS who were on "submaximal" beta blocker doses (nadolol < 0.75-mg/kg/day & propranolol < 2 mg/kg/day) with at least 6 months follow up. Adequate beta blockade effect was defined as at least 15% decrease from maximal HR.
The study included 127 LQTS patients: 47% on maximal therapy, 43% on submaximal therapy, and 10% not receiving treatment. Thirty three percent of patients were on submaximal therapy due to side effects, none in patients less than 10 years of age. Baseline characteristics were similar between the groups. There was no significant difference in LTEs between maximal and submaximal therapy (8% vs. 5.4%, p = 0.72). During CPET, patients on maximal therapy were more likely to exhibit adequate chronotropic suppression (60% vs. 40%, p = 0.01). None of the patients on submaximal therapy with adequate chronotropic effect experienced LTEs during follow-up.
Adequate chronotropic suppression was achieved with "submaximal" beta blocker dose in 40%. Despite similar baseline risk profiles, LTEs were not significantly different in patients with submaximal versus maximal therapy. CPET may be a useful modality to devise an individualized treatment plan, especially in those who cannot tolerate the recommended guideline directed dose.
目前,尚无评估β受体阻滞剂对长QT综合征(LQTS)疗效的具体标准。
描述我们利用心肺运动试验(CPET)评估变时性抑制的机构经验,并比较“次最大剂量”治疗与最大剂量治疗时危及生命事件(LTE)的发生频率。
我们查询了遗传性心律失常登记处,确定了接受“次最大剂量”β受体阻滞剂治疗(纳多洛尔<0.75mg/kg/天和普萘洛尔<2mg/kg/天)且随访至少6个月的LQTS患者。充分的β受体阻滞剂阻滞效应定义为心率较最大值降低至少15%。
该研究纳入了127例LQTS患者:47%接受最大剂量治疗,43%接受次最大剂量治疗,10%未接受治疗。33%的患者因副作用接受次最大剂量治疗,10岁以下患者中无人出现这种情况。各组间基线特征相似。最大剂量治疗与次最大剂量治疗的LTE发生率无显著差异(8%对5.4%,p=0.72)。在CPET期间,接受最大剂量治疗的患者更有可能表现出充分的变时性抑制(60%对40%,p=0.01)。在随访期间,变时性效应充分的次最大剂量治疗患者均未发生LTE。
40%的患者使用“次最大剂量”β受体阻滞剂可实现充分的变时性抑制。尽管基线风险特征相似,但次最大剂量治疗与最大剂量治疗患者的LTE发生率无显著差异。CPET可能是制定个体化治疗方案的有用方法,尤其是对于那些无法耐受推荐的指南指导剂量的患者。