Department of Pharmacy, West Virginia University Hospitals, Morgantown, WV, USA.
West Virginia Clinical and Translational Science Institute, Morgantown, WV, USA.
J Pharm Pract. 2024 Dec;37(6):1245-1251. doi: 10.1177/08971900241247932. Epub 2024 Apr 21.
Limited data exists to evaluate the optimal management of outpatient beta blocker therapy when patients with heart failure with reduced ejection fraction (HFrEF) are admitted for acute decompensated heart failure (ADHF). This study aimed to compare the effects of holding or decreasing the dose of outpatient beta blocker therapy vs continuation of therapy on rates of tachyarrhythmias during admission for ADHF. This single-center, retrospective cohort study divided patients with HFrEF (left ventricular ejection fraction less than or equal to 40%) admitted for ADHF into two cohorts: one that had their outpatient beta blocker continued at the same dose upon admission and one that had it held or dose decreased. The primary outcome was a composite of non-sustained or sustained ventricular tachycardia, ventricular fibrillation, or atrial fibrillation or flutter with rapid ventricular response during the hospitalization. Secondary outcomes included the individual tachyarrhythmias in the primary outcome, in-hospital mortality, and 90-day re-admission for heart failure. Of the 137 patients included, 82 were in the continuation cohort and 55 in the discontinuation/reduction cohort. The median length of stay was 5.3 days (interquartile range, 3.8-7.6). No significant difference in the primary composite outcome was found between the discontinuation/reduction and continuation cohorts (29.1% vs 22.0%; relative risk [95% confidence interval], 1.33 [.74-2.37]; P = .420). No significant differences were seen between the two cohorts for any of the secondary outcomes. Beta blocker therapy adjustment on admission for ADHF may not affect the occurrence of tachyarrhythmias in patients with HFrEF.
当射血分数降低的心力衰竭 (HFrEF) 患者因急性失代偿性心力衰竭 (ADHF) 入院时,评估门诊β受体阻滞剂治疗的最佳管理方法的数据有限。本研究旨在比较在 ADHF 入院时停用或减少门诊β受体阻滞剂剂量与继续治疗对心律失常发生率的影响。这项单中心回顾性队列研究将因 ADHF 入院的 HFrEF 患者(左心室射血分数小于或等于 40%)分为两组:一组在入院时继续使用相同剂量的门诊β受体阻滞剂,另一组则停药或减少剂量。主要结局是住院期间发生非持续或持续性室性心动过速、心室颤动或心房颤动或快速心室反应的房扑的复合结果。次要结局包括主要结局中的个体性心律失常、院内死亡率和 90 天心力衰竭再入院。在纳入的 137 例患者中,82 例在继续组,55 例在停药/减量组。中位住院时间为 5.3 天(四分位间距,3.8-7.6)。停药/减量组与继续组在主要复合结局方面无显著差异(29.1% vs 22.0%;相对风险[95%置信区间],1.33[0.74-2.37];P=0.420)。两组在任何次要结局方面均无显著差异。ADHF 入院时调整β受体阻滞剂治疗可能不会影响 HFrEF 患者心律失常的发生。