Trials on Timing of Cardiovascular Medication Administration

Manan Pareek MD, MSc, PhD , Niklas Dyrby Johansen MD, PhD , Sine Højlund Christensen MSc , Anna Meta Dyrvig Kristensen MD , Majid Afzal MD , Johanna Maria Christina Frary MD , Muthiah Vaduganathan MD, MPH , Michael Hecht Olsen MD, PhD, DMSc , Pradeesh Sivapalan MD, PhD , Jens Ulrik Stæhr Jensen MD, PhD , Deepak L. Bhatt MD, MPH, MBA , Tor Biering-Sørensen MD, MSc, MPH, PhD
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引用次数: 0

Abstract

The incidence of certain disease events such as myocardial infarction, stroke, aortic rupture, and sudden cardiac death is affected by the time of day. It is thus theorized that synchronization of medication timing with circadian rhythmicity (or at the minimum, clock time) may improve treatment efficacy and/or reduce the risk of serious adverse events. We launched the C3 (Cardiovascular Circadian Chronotherapy) trial concept to efficiently conduct randomized, controlled, clinical outcome trials of the timing of medication administration. This concept takes advantage of the Danish nationwide administrative health registries for participant identification and collection of baseline and follow-up data as well as the mandatory governmental electronic letter system. Although many of these interventions may only provide small effect sizes, any positive effects from simple changes in the timing of drug administration could potentially lead to large, worldwide prognostic improvements.
心血管药物给药时间的试验:心血管昼夜节律时间疗法试验概念。
某些疾病事件的发生率,如心肌梗死、中风、主动脉破裂和心源性猝死,受一天中的时间的影响。因此,从理论上讲,与昼夜节律性(或至少是时钟时间)同步的用药时间可以提高治疗效果和/或降低严重不良事件的风险。我们推出了C3(心血管昼夜节律治疗)试验概念,以有效地进行随机、对照、临床结果的给药时间试验。这一概念利用了丹麦全国卫生行政登记处的参与者身份识别和基线和后续数据的收集,以及强制性的政府电子信件系统。虽然这些干预措施中的许多可能只提供小的效果,但药物给药时间的简单改变所产生的任何积极影响都可能导致全球范围内的巨大预后改善。
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来源期刊
JACC advances
JACC advances Cardiology and Cardiovascular Medicine
CiteScore
1.90
自引率
0.00%
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