Habel Nicole, Infeld Margaret, Bernknopf Jacob, Meyer Markus, Lustgarten Daniel
Department of Medicine, Larner College of Medicine, University of Vermont, Burlington, Vermont.
Cardiovascular Center, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts.
Heart Rhythm O2. 2023 Dec 8;5(1):41-49. doi: 10.1016/j.hroo.2023.12.001. eCollection 2024 Jan.
In heart failure with preserved ejection fraction (HFpEF), it has been assumed that pharmacologic heart rate suppression should provide clinical benefits through an increase in diastolic filling time. Contrary to this assumption, heart rate lowering in patients with preserved left ventricular ejection fraction and hypertension or coronary artery disease results in adverse outcomes and suggests that the opposite may be beneficial. Namely, shortening the diastolic filling time with a higher heart rate might normalize the elevated filling pressures that are the of HFpEF. Initial clinical studies that assessed the effects of accelerated heart rates in pacemaker patients with preclinical and overt HFpEF provide support for this latter hypothesis, having shown improvements in quality of life, natriuretic peptide and activity levels, and atrial fibrillation burden.
The study sought to determine the effects of continued resting heart rate elevation with and without superimposed nocturnal pacing in HFpEF patients without standard pacing indication.
The physiologic accelerated pacing as treatment for heart failure with preserved ejection fraction (PACE HFpEF) trial is an investigator-initiated, prospective, patient-blinded multiple crossover pilot study that assesses the impact of accelerated pacing on quality of life, physical activity, N-terminal pro-B-type natriuretic peptide, and echocardiographic measures of cardiac structure and function.
Twenty patients were enrolled and underwent dual-chamber pacemaker implantation under U.S. Food and Drug Administration investigational device exemption with both atrial and ventricular physiologic lead placement targeting the Bachmann bundle and the His bundle.
This manuscript describes the rationale and design of the PACE HFpEF trial, which tests the safety and feasibility of continuous accelerated physiological pacing as a treatment strategy in HFpEF.
在射血分数保留的心力衰竭(HFpEF)中,一直认为药物性心率抑制应通过增加舒张期充盈时间来提供临床益处。与这一假设相反,左心室射血分数保留且患有高血压或冠状动脉疾病的患者心率降低会导致不良后果,这表明相反的情况可能有益。也就是说,较高心率缩短舒张期充盈时间可能会使HFpEF中升高的充盈压恢复正常。最初评估心率加快对临床前期和显性HFpEF起搏器患者影响的临床研究为后一种假设提供了支持,这些研究显示生活质量、利钠肽和活动水平以及房颤负担均有改善。
本研究旨在确定在无标准起搏指征的HFpEF患者中,持续静息心率升高以及叠加夜间起搏的影响。
生理性加速起搏治疗射血分数保留的心力衰竭(PACE HFpEF)试验是一项由研究者发起的前瞻性、患者盲法的多次交叉试点研究,评估加速起搏对生活质量、身体活动、N末端B型利钠肽原以及心脏结构和功能的超声心动图指标的影响。
20名患者入组,并在美国食品药品监督管理局的研究器械豁免下接受了双腔起搏器植入,心房和心室生理性电极均放置在针对巴赫曼束和希氏束的位置。
本手稿描述了PACE HFpEF试验的原理和设计,该试验测试了持续加速生理性起搏作为HFpEF治疗策略的安全性和可行性。