急性和慢性射血分数保留型心力衰竭合并高血压的药物治疗:最新研究综述

IF 2.8 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Hiroaki Hiraiwa, Takahiro Okumura, Toyoaki Murohara
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引用次数: 0

摘要

在这篇全面的最新综述中,我们对目前针对射血分数保留型心力衰竭(HFpEF)急性期和慢性期并发高血压患者的药物疗法进行了循证分析。此外,我们还探讨了治疗高血压合并射血分数保留型心力衰竭(HFpEF)的常用药物和新型药物在疗效、安全性和临床结果方面的最新进展和证据。在 HFpEF 的急性期,静脉注射利尿剂、矿物质皮质激素受体拮抗剂 (MRA) 和血管扩张剂至关重要,而在慢性期,血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂已被证明能有效提高临床疗效。然而,由于钙通道阻滞剂具有潜在的负性肌力作用,因此在合并高血压的高频血友病患者中使用时应谨慎。我们还探讨了治疗 HFpEF 的新兴药物疗法,如钠糖共转运体 2(SGLT2)抑制剂、血管紧张素受体-去甲肾素抑制剂(ARNI)、可溶性鸟苷酸环化酶(sGC)刺激剂、新型 MRA 和伊伐布雷定。值得注意的是,SGLT2 抑制剂在减少高频心衰患者的心衰住院率和心血管死亡率方面已显示出希望,无论其是否患有糖尿病。此外,ARNI 和 sGC 刺激剂在改善症状、功能能力和生活质量方面也显示出潜力。尽管如此,仍有必要开展更多研究,以确定针对并发高血压的高频心衰的最佳治疗策略。此外,长期研究对于评估新兴药物疗法的持久性和持续疗效也至关重要。确定 HFpEF 病理生理学的新靶点和机制将为治疗并发高血压的 HFpEF 的创新药物开发方法铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Drug Therapy for Acute and Chronic Heart Failure with Preserved Ejection Fraction with Hypertension: A State-of-the-Art Review

Drug Therapy for Acute and Chronic Heart Failure with Preserved Ejection Fraction with Hypertension: A State-of-the-Art Review

In this comprehensive state-of-the-art review, we provide an evidence-based analysis of current drug therapies for patients with heart failure with preserved ejection fraction (HFpEF) in the acute and chronic phases with concurrent hypertension. Additionally, we explore the latest developments and emerging evidence on the efficacy, safety, and clinical outcomes of common and novel drug treatments in the management of HFpEF with concurrent hypertension. During the acute phase of HFpEF, intravenous diuretics, mineralocorticoid receptor antagonists (MRAs), and vasodilators are pivotal, while in the chronic phase, angiotensin-converting enzyme inhibitors and angiotensin receptor blockers have proven effective in enhancing clinical outcomes. However, the use of calcium channel blockers in HFpEF with hypertension should be approached with caution, owing to their potential negative inotropic effects. We also explored emerging drug therapies for HFpEF, such as sodium–glucose co-transporter 2 (SGLT2) inhibitors, angiotensin receptor–neprilysin inhibitor (ARNI), soluble guanylate cyclase (sGC) stimulators, novel MRAs, and ivabradine. Notably, SGLT2 inhibitors have shown promise in reducing heart failure hospitalizations and cardiovascular mortality in patients with HFpEF, regardless of their diabetic status. Additionally, ARNI and sGC stimulators have demonstrated potential in improving symptoms, functional capacity, and quality of life. Nonetheless, additional research is necessary to pinpoint optimal treatment strategies for HFpEF with concurrent hypertension. Furthermore, long-term studies are essential to assess the durability and sustained benefits of emerging drug therapies. Identification of novel targets and mechanisms underlying HFpEF pathophysiology will pave the way for innovative drug development approaches in the management of HFpEF with concurrent hypertension.

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来源期刊
CiteScore
6.70
自引率
3.30%
发文量
38
审稿时长
>12 weeks
期刊介绍: Promoting rational therapy within the discipline of cardiology, the American Journal of Cardiovascular Drugs covers all aspects of the treatment of cardiovascular disorders, particularly the place in therapy of newer and established agents. Via a program of reviews and original clinical research articles, the journal addresses major issues relating to treatment of these disorders, including the pharmacology, efficacy and adverse effects of the major classes of drugs; information on newly developed drugs and drug classes; the therapeutic implications of latest research into the aetiology of cardiovascular disorders; and the practical management of specific clinical situations. The American Journal of Cardiovascular Drugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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