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静脉注射索他洛尔在儿科和先天性心脏病患者中的应用:一项多中心注册研究。

IV Sotalol Use in Pediatric and Congenital Heart Patients: A Multicenter Registry Study.

机构信息

Children`s Mercy Hospital Kansas City MO.

University of Wisconsin Madison WI.

出版信息

J Am Heart Assoc. 2022 May 3;11(9):e024375. doi: 10.1161/JAHA.121.024375. Epub 2022 May 2.

DOI:10.1161/JAHA.121.024375
PMID:35491986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9238590/
Abstract

Background There is limited information regarding the clinical use and effectiveness of IV sotalol in pediatric patients and patients with congenital heart disease, including those with severe myocardial dysfunction. A multicenter registry study was designed to evaluate the safety, efficacy, and dosing of IV sotalol. Methods and Results A total of 85 patients (age 1 day-36 years) received IV sotalol, of whom 45 (53%) had additional congenital cardiac diagnoses and 4 (5%) were greater than 18 years of age. In 79 patients (93%), IV sotalol was used to treat supraventricular tachycardia and 4 (5%) received it to treat ventricular arrhythmias. Severely decreased cardiac function by echocardiography was seen before IV sotalol in 7 (9%). The average dose was 1 mg/kg (range 0.5-1.8 mg/kg/dose) over a median of 60 minutes (range 30-300 minutes). Successful arrhythmia termination occurred in 31 patients (49%, 95% CI [37%-62%]) with improvement in rhythm control defined as rate reduction permitting overdrive pacing in an additional 18 patients (30%, 95% CI [19%-41%]). Eleven patients (16%) had significant QTc prolongation to >465 milliseconds after the infusion, with 3 (4%) to >500 milliseconds. There were 2 patients (2%) for whom the infusion was terminated early. Conclusions IV sotalol was safe and effective for termination or improvement of tachyarrhythmias in 79% of pediatric patients and patients with congenital heart disease, including those with severely depressed cardiac function. The most common dose, for both acute and maintenance dosing, was 1 mg/kg over ~60 minutes with rare serious complications.

摘要

背景 关于静脉注射索他洛尔在儿科患者和先天性心脏病患者中的临床应用和疗效,包括那些心肌功能严重受损的患者,相关信息有限。一项多中心注册研究旨在评估静脉注射索他洛尔的安全性、疗效和剂量。

方法和结果 共有 85 名患者(年龄 1 天至 36 岁)接受了静脉注射索他洛尔治疗,其中 45 名(53%)患者还存在其他先天性心脏疾病诊断,4 名(5%)患者年龄大于 18 岁。在 79 名(93%)患者中,静脉注射索他洛尔用于治疗室上性心动过速,4 名(5%)患者用于治疗室性心律失常。在开始静脉注射索他洛尔之前,7 名(9%)患者的超声心动图显示心脏功能严重下降。平均剂量为 1mg/kg(剂量范围 0.5-1.8mg/kg/dose),中位输注时间为 60 分钟(输注时间范围 30-300 分钟)。31 名患者(49%,95%CI [37%-62%])心律失常终止成功,18 名患者(30%,95%CI [19%-41%])的节律控制得到改善,定义为降低心率,允许超速起搏。11 名患者(16%)在输注后 QTc 延长>465 毫秒,其中 3 名(4%)患者>500 毫秒。有 2 名患者(2%)提前终止了输液。

结论 静脉注射索他洛尔在 79%的儿科患者和先天性心脏病患者中安全且有效,可终止或改善心动过速,包括那些心肌功能严重受损的患者。急性和维持剂量最常见的剂量为 1mg/kg,约 60 分钟,很少出现严重并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/7f04f7c11d97/JAH3-11-e024375-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/6bbc5a6e0c66/JAH3-11-e024375-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/fa6c3a8a0cd5/JAH3-11-e024375-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/b0c375a6f53e/JAH3-11-e024375-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/7f04f7c11d97/JAH3-11-e024375-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/6bbc5a6e0c66/JAH3-11-e024375-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/fa6c3a8a0cd5/JAH3-11-e024375-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/b0c375a6f53e/JAH3-11-e024375-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53ae/9238590/7f04f7c11d97/JAH3-11-e024375-g004.jpg

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本文引用的文献

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2
Intravenous Sotalol for the Treatment of Ventricular Dysrhythmias in an Infant on Extracorporeal Membrane Oxygenation.静脉注射索他洛尔治疗接受体外膜肺氧合的婴儿室性心律失常
Pediatr Cardiol. 2020 Feb;41(2):418-422. doi: 10.1007/s00246-019-02225-w. Epub 2019 Oct 29.
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Outpatient intravenous sotalol load to replace 3-day admission oral sotalol load.
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HeartRhythm Case Rep. 2019 Apr 24;5(7):382-383. doi: 10.1016/j.hrcr.2019.04.005. eCollection 2019 Jul.
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Moving beyond P values: data analysis with estimation graphics.超越P值:使用估计图进行数据分析。
Nat Methods. 2019 Jul;16(7):565-566. doi: 10.1038/s41592-019-0470-3.
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