Digoxin Loading Doses and Serum Digoxin Concentrations for Rate Control of Atrial Arrhythmias in Critically Ill Patients.

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Tania Ahuja, Raghad Saadi, John Papadopoulos, Samuel Bernard, Raymond Pashun, James Horowitz, Eugene Yuriditsky, Cristian Merchan
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引用次数: 0

Abstract

Intravenous (IV) digoxin loading dose recommendations for rate control of atrial arrhythmias in critically ill patients are not well studied. When using digoxin in the setting of atrial fibrillation/atrial flutter (AF/AFL), a loading dose (LD) in either a fixed-dose regimen, weight-based dose, or pharmacokinetic-based calculation to target a serum digoxin concentration (SDC) of 0.8-1.5 ng/mL is recommended. The objective of this study was to assess the safety and effectiveness of digoxin LD used in critically ill patients for rate control of AF/AFL and to assess the SDC achieved. This single center retrospective cohort study included patients who received IV digoxin and had a SDC drawn. The primary endpoint was the median SDC achieved after a digoxin LD. Secondary outcomes included the frequency of SDCs ≥1.5 ng/mL and heart rate (HR) control. A total of 92 patients were included. The median total LD of digoxin for the entire cohort was 11mcg/kg (750 mcg). For 61% of the cohort, the LD was distributed over six-hour intervals. The median SDC after completion of the IV digoxin LD was 1.3 ng/mL (0.9, 1.7). The incidence of supratherapeutic SDC was 36% for the total cohort. A target HR < 110 beats per minute within 24 hours from digoxin LD was achieved in 60% of the cohort. In conclusion, a median total digoxin LD of 750 mcg in critically ill patients with AF/AFL, targeting a SDC < 1.5ng/mL may be considered for acute rate control, taking into account drug-drug interactions in the cardiac intensive care unit. Future studies are necessary to confirm our findings.

用于控制重症患者房性心律失常的地高辛负荷剂量和血清地高辛浓度。
目前尚未对用于控制重症患者房性心律失常的静脉注射(IV)地高辛负荷剂量建议进行充分研究。在心房颤动/心房扑动(AF/AFL)情况下使用地高辛时,建议采用固定剂量方案、基于体重的剂量或基于药代动力学的计算方法来计算负荷剂量(LD),目标血清地高辛浓度(SDC)为 0.8-1.5 纳克/毫升。本研究旨在评估重症患者使用地高辛 LD 控制房颤/心律失常的安全性和有效性,并评估所达到的 SDC。这项单中心回顾性队列研究纳入了接受静脉注射地高辛并提取了 SDC 的患者。主要终点是地高辛 LD 后达到的 SDC 中位数。次要结果包括SDC≥1.5纳克/毫升的频率和心率(HR)控制。共纳入 92 名患者。整个组群的地高辛总LD中位数为11mcg/kg(750微克)。其中 61% 的患者的 LD 分布在 6 小时内。完成静脉注射地高辛 LD 后的 SDC 中位数为 1.3 纳克/毫升(0.9, 1.7)。在所有组群中,超治疗量 SDC 的发生率为 36%。有 60% 的患者在地高辛 LD 24 小时内达到目标心率 < 110 次/分。总之,考虑到心脏重症监护病房中药物间的相互作用,房颤/房颤重症患者的地高辛总LD中位数为750微克,目标SDC<1.5ng/mL,可以考虑用于急性心率控制。未来的研究有必要证实我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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