Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada; Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada.
J Card Fail. 2022 Aug;28(8):1298-1308. doi: 10.1016/j.cardfail.2022.04.015. Epub 2022 May 16.
Patients with heart failure (HF) and a reduced ejection fraction (HFrEF) who experience worsening HF (WHF) events are at increased risk of adverse outcomes and experience significant morbidity and mortality. We herein describe the epidemiology of these patients and identify those potentially eligible for vericiguat therapy in this population-based study.
This retrospective cohort study included hospitalized or emergency department patients with a primary diagnosis of HF and a left ventricular ejection fraction (LVEF) of less than 45% diagnosed between April 1, 2009, and March 31, 2019 in Alberta, Canada, with follow-up to March 31, 2020. Inclusion criteria from the VerICiguaT Global Study in Subjects with Heart Failure with Reduced Ejection (VICTORIA) trial were applied to explore eligibility for vericiguat. Among 25,629 patients with HF and LVEF data, 9948 (38.8%) had HFrEF, of which 5259 (52.8%) experienced WHF at some point during a median 5.8 years of follow-up, and 38.3% of those met the vericiguat trial eligibility criteria. Compared with patients with HFrEF without WHF, those with WHF were older, with more comorbidities, worse renal function, and similar LVEF status, but greater use of HF medications at baseline. At the time of WHF, 27% of those with HFrEF and WHF were on triple therapy, 50.6% were on dual therapy, and 15.4% were on monotherapy. All-cause mortality and the composite outcome of all-cause mortality or cardiovascular hospitalization at 1-year of follow-up were higher in the HFrEF with WHF cohort compared with HFrEF without WHF (adjusted hazard ratios of 1.92 and 1.51, respectively, both P < .0001).
Approximately one-half of patients with HFrEF experienced WHF over the long-term follow-up. Most were not on triple therapy, highlighting the underuse of the existing standard-of-care treatments and opportunities for application of newer therapies; more than one-third of patients with HFrEF may be eligible for vericiguat.
Among patients with heart failure (HF), those who experience worsening HF (WHF) are at increased risk of adverse outcomes. A few new therapies, including vericiguat, have emerged recently for patients with HF and reduced ejection fraction. However, the epidemiology, treatment patterns, and outcomes of patients with WHF in large representative populations is unclear. In the current study, approximately one-half of the patients with HF and reduced ejection fraction experienced WHF and 38.3% were potentially eligible for vericiguat therapy. The guideline-recommended therapies were under-utilized among patients with WHF, which highlights the need for initiatives to address this care gap.
射血分数降低的心力衰竭(HFrEF)患者如果出现心力衰竭恶化(WHF)事件,其发生不良结局的风险会增加,并经历显著的发病率和死亡率。本研究旨在描述这些患者的流行病学情况,并确定在这一基于人群的研究中可能适合接受维立西呱治疗的人群。
这是一项回顾性队列研究,纳入了 2009 年 4 月 1 日至 2019 年 3 月 31 日期间在加拿大阿尔伯塔省因主要诊断为心力衰竭且左心室射血分数(LVEF)<45%而住院或在急诊就诊的患者,并在 2020 年 3 月 31 日之前进行随访。应用来自 VerICiguaT 全球研究(VICTORIA)的维立西呱在射血分数降低的心力衰竭患者中的应用试验的纳入标准,来探索维立西呱的使用资格。在 25629 例有心力衰竭和 LVEF 数据的患者中,有 9948 例(38.8%)为 HFrEF,其中 5259 例(52.8%)在中位 5.8 年的随访期间发生了 WHF,其中 38.3%的患者符合维立西呱试验的纳入标准。与无 WHF 的 HFrEF 患者相比,WHF 患者年龄更大,合并症更多,肾功能更差,LVEF 状态相似,但基线时心力衰竭药物的使用更多。在发生 WHF 时,有 27%的 HFrEF 合并 WHF 患者接受三联治疗,50.6%接受双联治疗,15.4%接受单药治疗。与无 WHF 的 HFrEF 患者相比,WHF 合并 HFrEF 患者在 1 年随访时全因死亡率和全因死亡率或心血管住院的复合结局更高(校正后的危险比分别为 1.92 和 1.51,均 P<0.0001)。
在长期随访中,约有一半的 HFrEF 患者出现 WHF。大多数患者未接受三联治疗,这突出了现有标准治疗方法的使用不足以及应用新疗法的机会;超过三分之一的 HFrEF 患者可能适合接受维立西呱治疗。
在心力衰竭(HF)患者中,那些出现 HF 恶化(WHF)的患者发生不良结局的风险会增加。最近出现了一些新的治疗方法,包括维立西呱,用于治疗射血分数降低的心力衰竭患者。然而,在大型代表性人群中,WHF 患者的流行病学、治疗模式和结局尚不清楚。在当前的研究中,约有一半的 HF 合并射血分数降低的患者出现 WHF,其中 38.3%可能适合接受维立西呱治疗。WHF 患者的指南推荐疗法使用不足,这突显了需要采取措施来解决这一治疗空白。