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伊伐布雷定单药治疗局灶性房性心动过速的儿科患者:一项单中心研究。

Ivabradine monotherapy in pediatric patients with focal atrial tachycardia: a single-center study.

机构信息

Department of Cardiology, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, 1678 Dong Fang Road, Shanghai, 200127, China.

出版信息

Eur J Pediatr. 2023 May;182(5):2265-2271. doi: 10.1007/s00431-023-04891-8. Epub 2023 Mar 4.

Abstract

UNLABELLED

This study investigated the efficacy of ivabradine monotherapy in pediatric patients with focal atrial tachycardia (FAT). We prospectively enrolled 12 pediatric patients (7.5 ± 4.5 years; six girls) with FAT who were resistant to conventional antiarrhythmics and received ivabradine as monotherapy. Patients were classified as having tachycardia-induced cardiomyopathy (TIC) if they had a left ventricular ejection fraction (LVEF) of < 50% and a left ventricular end-diastolic dimension (LVDD) z-score of > 2 due to tachycardia. Oral ivabradine was initiated at 0.1 mg/kg every 12 h, increased to 0.2 mg/kg every 12 h if no restoration of stable sinus rhythm was observed after two doses, and discontinued after 48 h if neither rhythm nor heart rate control was observed. Of these patients, six (50%) had incessant atrial tachycardia, and 6 had frequent short episodes of FAT. Six patients were diagnosed with TIC, and their mean LVEF and mean LVDD z-score were 36.2 ± 8.7% (range, 27-48%) and 4.2 ± 1.7 (range, 2.2-7.3), respectively. Finally, six patients achieved either rhythm (n = 3) or heart rate control (n = 3) within 48 h of ivabradine monotherapy. One patient achieved rhythm/heart rate control with ivabradine at a dose of 0.1 mg/kg every 12 h, while the others achieved rhythm/heart rate control at a dose of 0.2 mg/kg every 12 h. Five patients received ivabradine monotherapy for chronic therapy, one (20%) of whom had FAT breakthrough 1 month after discharge, and metoprolol was added. Neither FAT recurrence nor adverse effect (with or without beta-blocker) was observed during a median follow-up of 5 months.

CONCLUSION

Ivabradine is well-tolerated and may provide early heart rate control in pediatric FAT and can be considered early, especially in the presence of left ventricular dysfunction. Further investigations are deserved to confirm the optimal dose and long-term efficacy in this population.

WHAT IS KNOWN

• Focal atrial tachycardia (FAT) is the most common arrhythmia associated with tachycardia-induced cardiomyopathy (TIC) in children, and the efficacy of conventional antiarrhythmic medications in the treatment of FAT is poor. • Ivabradine is currently the only selective hyperpolarization-activated cyclic nucleotide-gated (HCN) inhibitor, which can effectively low HR without negative effect on blood pressure or inotropy.

WHAT IS NEW

• Ivabradine (0.1-0.2 mg/kg every 12 h) can effectively suppress focal atrial tachycardia in 50% of pediatric patients. • Ivabradine provides early control of heart rate and hemodynamic stabilization in children with severe left ventricular dysfunction due to atrial tachycardia within 48 h.

摘要

目的

研究伊伐布雷定单药治疗局灶性房性心动过速(FAT)的疗效。

方法

前瞻性纳入 12 例对常规抗心律失常药物耐药且接受伊伐布雷定单药治疗的 FAT 患儿(7.5±4.5 岁;6 名女性)。如果患儿因心动过速而出现左心室射血分数(LVEF)<50%和左心室舒张末期内径(LVDD)z 评分>2,则被归类为心动过速性心肌病(TIC)。如果在两剂后未恢复稳定窦性心律,则起始口服伊伐布雷定 0.1mg/kg,每 12 小时 1 次;如果未观察到节律或心率控制,则停止使用伊伐布雷定。

结果

其中 6 例(50%)患儿存在无休止性房性心动过速,6 例患儿存在频繁的 FAT 短阵发作。6 例患儿诊断为 TIC,其平均 LVEF 和平均 LVDD z 评分分别为 36.2±8.7%(范围 27-48%)和 4.2±1.7(范围 2.2-7.3)。

最终,6 例患儿在伊伐布雷定单药治疗 48 小时内均实现了节律或心率控制。1 例患儿以 0.1mg/kg,每 12 小时 1 次的剂量实现了节律/心率控制,而其他患儿以 0.2mg/kg,每 12 小时 1 次的剂量实现了节律/心率控制。

5 例患儿接受伊伐布雷定单药进行慢性治疗,其中 1 例(20%)患儿在出院后 1 个月 FAT 复发,加用美托洛尔。在平均 5 个月的随访期间,均未观察到 FAT 复发或不良事件(有无β受体阻滞剂)。

结论

伊伐布雷定耐受性良好,可早期控制儿科 FAT 的心率,可考虑早期使用,特别是在存在左心室功能障碍时。进一步的研究值得开展,以证实该药在该人群中的最佳剂量和长期疗效。

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