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J Clin Med Res. 2023 Jun;15(6):336-339. doi: 10.14740/jocmr4940. Epub 2023 Jun 29.
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本文引用的文献

1
The Clinical Use of Ivabradine.依伐布雷定的临床应用。
J Am Coll Cardiol. 2017 Oct 3;70(14):1777-1784. doi: 10.1016/j.jacc.2017.08.038.
2
Inappropriate sinus tachycardia: focus on ivabradine.不适当窦性心动过速:关注伊伐布雷定。
Intern Med J. 2016 Aug;46(8):875-83. doi: 10.1111/imj.13093.
3
Hyperthyroidism and cardiovascular complications: a narrative review on the basis of pathophysiology.甲状腺功能亢进症与心血管并发症:基于病理生理学的叙述性综述。
Arch Med Sci. 2013 Oct 31;9(5):944-52. doi: 10.5114/aoms.2013.38685. Epub 2013 Nov 5.
4
Ivabradine in combination with metoprolol succinate in the treatment of inappropriate sinus tachycardia.伊伐布雷定联合琥珀酸美托洛尔治疗不适当窦性心动过速。
J Cardiovasc Pharmacol Ther. 2013 Jul;18(4):338-44. doi: 10.1177/1074248413478172. Epub 2013 Feb 19.
5
Heart rate reduction with ivabradine prevents thyroid hormone-induced cardiac remodeling in rat.伊伐布雷定降低心率可预防甲状腺激素诱导的大鼠心脏重塑。
Heart Vessels. 2013 Jul;28(4):524-35. doi: 10.1007/s00380-012-0304-z. Epub 2012 Nov 11.
6
Heart rate as a risk factor in chronic heart failure (SHIFT): the association between heart rate and outcomes in a randomised placebo-controlled trial.心率作为慢性心力衰竭的危险因素(SHIFT):一项随机安慰剂对照试验中心率与结局的关系。
Lancet. 2010 Sep 11;376(9744):886-94. doi: 10.1016/S0140-6736(10)61259-7.
7
Distinct regulation of cardiac I(f) current via thyroid receptors alpha1 and beta1.通过甲状腺受体α1和β1对心脏If电流进行不同调节。
Pflugers Arch. 2009 Oct;458(6):1061-8. doi: 10.1007/s00424-009-0691-x. Epub 2009 Jul 22.
8
The funny current: cellular basis for the control of heart rate.滑稽电流:心率控制的细胞基础。
Drugs. 2007;67 Suppl 2:15-24. doi: 10.2165/00003495-200767002-00003.
9
Ivabradine -- the first selective sinus node I(f) channel inhibitor in the treatment of stable angina.伊伐布雷定——首个用于治疗稳定型心绞痛的选择性窦房结I(f)通道抑制剂。
Int J Clin Pract. 2006 Feb;60(2):222-8. doi: 10.1111/j.1742-1241.2006.00817.x.
10
Endogenous subclinical hyperthyroidism affects quality of life and cardiac morphology and function in young and middle-aged patients.内源性亚临床甲状腺功能亢进影响中青年患者的生活质量以及心脏形态和功能。
J Clin Endocrinol Metab. 2000 Dec;85(12):4701-5. doi: 10.1210/jcem.85.12.7085.

伊伐布雷定治疗继发于甲状腺功能亢进的窦性心动过速的疗效

Resolution of Sinus Tachycardia Secondary to Hyperthyroidism With Ivabradine.

作者信息

Medina Yelizaveta, Khan Asif, Spagnola Jonathon, Lafferty James

机构信息

Department of Medicine, Staten Island University Hospital, Staten Island, NY 10305, USA.

Department of Cardiology, Staten Island University Hospital, Staten Island, NY 10305, USA.

出版信息

J Clin Med Res. 2023 Jun;15(6):336-339. doi: 10.14740/jocmr4940. Epub 2023 Jun 29.

DOI:10.14740/jocmr4940
PMID:37434775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10332879/
Abstract

Currently, ivabradine is not approved for the treatment of sinus tachycardia secondary to hyperthyroidism. We aimed to increase the recognition of ivabradine as an effective alternative to, or combination with, beta-blockers in controlling sinus tachycardia secondary to hyperthyroidism. Elevated thyroid hormone levels enhance cardiac performance through a positive chronotropic effect, resulting in an increased heart rate (HR), an effect brought on by increasing the funny current at sinoatrial node (SAN). Ivabradine is a novel, dose-dependent selective inhibitor of channels. By decreasing SAN pacemaker activity, ivabradine allows for selective reduction of HR with a resultant increase in ventricular filling time. This mechanism sets ivabradine apart from the typical rate-reducing medications, namely beta-blockers and calcium channel blockers, which simultaneously decrease HR and myocardial contractility. We describe a case of hyperthyroidism-induced sinus tachycardia, resistant to maximal doses of beta-blocker, which was successfully managed by ivabradine. After excluding other causes of tachycardia, such as anemia, hypovolemic states, structural heart disease, drug abuse, and infection, ivabradine was given off-label for symptomatic relief of hyperthyroidism-induced sinus tachycardia. Within 24 h, HR steadily decreased to the low 80s. Our patient had a unique presentation in which he presented with hyperthyroidism-induced sinus tachycardia with no relief after administration of maximal dose of beta-blocker. Ivabradine was then given, with resolution of sinus tachycardia within 24 h.

摘要

目前,伊伐布雷定未被批准用于治疗继发于甲状腺功能亢进的窦性心动过速。我们旨在提高对伊伐布雷定的认识,它可作为β受体阻滞剂的有效替代药物或与之联合使用,用于控制继发于甲状腺功能亢进的窦性心动过速。甲状腺激素水平升高通过正性变时作用增强心脏功能,导致心率(HR)增加,这种作用是通过增加窦房结(SAN)的If电流实现的。伊伐布雷定是一种新型的、剂量依赖性的I f通道选择性抑制剂。通过降低窦房结起搏细胞的活性,伊伐布雷定可选择性降低心率,从而增加心室充盈时间。这一机制使伊伐布雷定有别于典型的降低心率药物,即β受体阻滞剂和钙通道阻滞剂,后两者会同时降低心率和心肌收缩力。我们描述了一例继发于甲状腺功能亢进的窦性心动过速病例,该病例对最大剂量的β受体阻滞剂耐药,但使用伊伐布雷定成功得到了控制。在排除心动过速的其他原因,如贫血、低血容量状态、结构性心脏病、药物滥用和感染后,伊伐布雷定被用于对症缓解继发于甲状腺功能亢进的窦性心动过速,但属于超适应症用药。在24小时内,心率稳步降至80次/分低位。我们的患者有独特的临床表现,即表现为继发于甲状腺功能亢进的窦性心动过速,在给予最大剂量的β受体阻滞剂后无缓解。随后给予伊伐布雷定,窦性心动过速在24小时内得到缓解。