Department of Pharmacy Practice, School of Pharmacy-Boston, Massachusetts College of Pharmacy and Health Sciences, Boston, MA, USA.
Department of Pharmacy, Brigham and Women's Hospital, Boston, MA, USA.
Ann Pharmacother. 2023 Nov;57(11):1291-1301. doi: 10.1177/10600280231154021. Epub 2023 Feb 17.
Results from large placebo-controlled randomized trials in patients with heart failure with mid-range ejection fraction (HFmrEF) and HF with preserved EF (HFpEF) have become available recently. This article discusses results of these clinical trials.
Peer-reviewed articles were identified from MEDLINE (1966 to December 31, 2022) using search terms dapagliflozin, empagliflozin, SGLT-2Is, HFmrEF, and HFpEF.
Eight completed, pertinent clinical trials were included.
EMPEROR-Preserved, and DELIVER demonstrated that empagliflozin and dapagliflozin reduce CV death and heart failure hospitalization (HHF) in patients with HFmrEF and HFpEF, with/without diabetes when added to a standard heart failure (HF) regimen. The benefit is primarily due to reduction in HHF. Additional data from post hoc analyses of trials of dapagliflozin, ertugliflozin, and sotagliflozin suggest that these benefits may be a class effect. Benefits appear greatest in patients with left ventricular ejection fraction 41% up to about 65%.
While many pharmacologic treatments have been proven to reduce mortality and improve cardiovascular (CV) outcomes in people with HFmrEF and HF with reduced EF (HFrEF), there are few therapy which improve CV outcome in people with HFpEF. SGLT-2I become one of the first class of pharmacologic agent that can be used to reduce HHF and CV mortality.
Studies showed that empagliflozin and dapagliflozin reduce the combined risk of CV death or HHF in patients with HFmrEF and HFpEF when added to a standard HF regimen. Given that benefit has now been demonstrated across the spectrum of HF, SGLT-2Is should be considered one of the standard HF pharmacotherapy.
最近,有大量心力衰竭伴中间射血分数(HFmrEF)和射血分数保留的心力衰竭(HFpEF)的安慰剂对照随机临床试验结果问世。本文讨论了这些临床试验的结果。
通过 MEDLINE(1966 年至 2022 年 12 月 31 日)使用达格列净、恩格列净、SGLT-2Is、HFmrEF 和 HFpEF 等检索词,确定了同行评议文章。
纳入了 8 项已完成的相关临床试验。
EMPEROR-Preserved 和 DELIVER 研究表明,当加用标准心力衰竭(HF)治疗方案时,恩格列净和达格列净可降低 HFmrEF 和 HFpEF 患者(伴或不伴糖尿病)的心血管死亡和心力衰竭住院(HHF)风险。获益主要归因于 HHF 的减少。来自达格列净、埃曲格列净和索格列净试验事后分析的额外数据表明,这些获益可能是一类药物的作用。获益在左心室射血分数为 41%至约 65%的患者中最大。
虽然许多药物治疗已被证明可降低 HFmrEF 和射血分数降低的心力衰竭(HFrEF)患者的死亡率并改善心血管(CV)结局,但很少有治疗方法可改善 HFpEF 患者的 CV 结局。SGLT-2I 成为可用于减少 HHF 和 CV 死亡率的首批药物之一。
研究表明,当加用标准 HF 治疗方案时,恩格列净和达格列净可降低 HFmrEF 和 HFpEF 患者的 CV 死亡或 HHF 复合风险。鉴于获益已在整个 HF 范围内得到证实,SGLT-2I 应被视为 HF 标准药物治疗之一。