Division of Cardiology, Department of Internal Medicine, Texas Tech University Health Sciences Center, El Paso, Texas, United States.
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Texas Tech University Health Sciences Center, El Paso, Texas, United States.
Cardiovasc Hematol Disord Drug Targets. 2022;22(2):87-95. doi: 10.2174/1871529X22666220630164630.
Heart failure is the leading cause of morbidity and mortality worldwide. With improved longevity, the incidence and prevalence of heart failure continue to rise with an estimated prevalence of around 26 million worldwide. Heart failure with preserved ejection fraction (HFpEF) constitutes around 50% of the total heart failure cases and is the most common cause of heart failure in the elderly population. The cost of heart failure care continues to rise with care for heart failure hospitalization taking the major bulk. The cost was around 30 billion in the US in 2012 and is projected to reach 70 billion by 2030.
This study aims to provide updated pharmacotherapy of heart failure with a preserved ejection fraction (HFpEF).
We performed a comprehensive literature review to examine the available pharmacotherapeutics in the management of heart failure with a preserved ejection fraction using online databases (PubMed and Embase).
We reviewed multiple studies examining pharmacotherapeutics in the management of HFpEF and reducing heart failure hospitalizations in this cohort. Until recently, our management mainly focused on aggressively managing diabetes, hypertension, atrial fibrillation, and coronary artery disease anticipating improving the outcome. Beta-blockers, Angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, sildenafil, digoxin, vericiguat, praliciguat, and Ivabradine did not improve heart failure hospitalization in this cohort.
EMPEROR-PRESERVED (Empagliflozin) and PRESERVED-HF (Dapagliflozin) results in the management of HFpEF look promising irrespective of diabetes status. Sacubitrilvalsartan and Empagliflozon are the only medications approved for its management as per the PARAGON-HF and EMPEROR-PRESERVED studies, respectively.
心力衰竭是全球发病率和死亡率的主要原因。随着寿命的延长,心力衰竭的发病率和患病率继续上升,估计全球约有 2600 万人患病。射血分数保留的心力衰竭(HFpEF)约占心力衰竭总病例的 50%,是老年人群中最常见的心力衰竭原因。心力衰竭治疗的费用持续上升,心力衰竭住院治疗占大部分。2012 年美国的心力衰竭治疗费用约为 300 亿美元,预计到 2030 年将达到 700 亿美元。
本研究旨在提供射血分数保留的心力衰竭(HFpEF)的最新药物治疗方法。
我们使用在线数据库(PubMed 和 Embase)全面审查了有关管理射血分数保留的心力衰竭的现有药物治疗方法的文献。
我们审查了多项研究,研究了管理 HFpEF 和减少该队列中心力衰竭住院的药物治疗方法。直到最近,我们的管理主要集中在积极管理糖尿病、高血压、心房颤动和冠状动脉疾病,期望改善结果。在该队列中,β受体阻滞剂、血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂、西地那非、地高辛、维立西呱、普拉西胍和伊伐布雷定并未改善心力衰竭住院率。
EMPEROR-PRESERVED(恩格列净)和 PRESERVED-HF(达格列净)在 HFpEF 管理中的结果看起来很有希望,无论糖尿病状况如何。依普利酮和恩格列净是根据 PARAGON-HF 和 EMPEROR-PRESERVED 研究分别批准用于其管理的唯一药物。