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The Epidemic of Heart Failure: A Lucid Approach to Stemming the Rising Tide

机译:心力衰竭的流行:一种遏制潮流上升的清晰方法

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At least 1 in 5 Canadians will experience heart failure (HF) during their lifetimes, with an average 1-year mortality rate of 23.4%. Hospitalizations for HF are projected to increase 3-fold from 1996 to 2050. HF can be associated with either reduced ejection fraction (HFrEF) or preserved ejection fraction (HFpEF), with the latter becoming increasingly common. The prognosis of both groups is equally concerning, but clinical trials testing pharmacologic therapies for HFpEF have been disappointing. We briefly discuss established therapies for HF and then focus on emerging therapies, challenges, and opportunities. Areas covered include practical pathophysiology; health care organization; monitoring and new technologies; pharmacogenomics, biomarkers, and personalized therapy; novel pharmacologic approaches; special considerations in acutely decompensated HF; revascularization; managing valve dysfunction; refining cardiac resynchronization therapy and device therapies; and cell therapy for cardiac repair. Among the novel pharmacologic directions we address are approaches to reducing oxidative stress, improving myocardial metabolism, new mineralocorticoid receptor antagonists, restoring vasoconstrictor-vasodilator balance, increasing cyclic guanosine monophosphate levels, and positive inotropic agents. Modifications in the organization of health care are particularly important, with an emerging hub-and-spokes model involving engaged patients cared for by primary care teams, with ready access to specialized HF clinics. Biomarkers have contributed to better understanding of the pathophysiology of HFrEF as well as HFpEF and will eventually allow much more effective and personalized management. Considering the vast array of areas in development, we can look forward to continuing improvements in the care and outcomes of patients with HF in the future.
机译:至少五分之一的加拿大人一生中都会经历心力衰竭(HF),平均1年死亡率为23.4%。预计从1996年到2050年,HF的住院治疗将增加3倍。HF可能与射血分数降低(HFrEF)或射血分数保留(HFpEF)相关,后者越来越普遍。两组的预后都同样令人担忧,但是测试HFpEF药物治疗的临床试验令人失望。我们简要讨论了HF的既定疗法,然后重点介绍了新兴疗法,挑战和机遇。涵盖的领域包括实用的病理生理学;卫生保健组织;监测和新技术;药物基因组学,生物标志物和个性化治疗;新的药理学方法;严重代偿性HF的特殊考虑;血运重建处理瓣膜功能障碍;完善心脏再同步疗法和器械疗法;和用于心脏修复的细胞疗法。在我们解决的新药理方向中,包括减少氧化应激,改善心肌代谢,新盐皮质激素受体拮抗剂,恢复血管收缩剂-血管扩张剂平衡,增加环鸟苷单磷酸水平和正性肌力药物的方法。卫生保健组织的修改尤为重要,因为出现了一种新兴的“轮辐式”模式,其中涉及由初级保健团队照顾的敬业患者,并且可以随时进入专业的HF诊所。生物标志物有助于更好地了解HFrEF以及HFpEF的病理生理,最终将允许更有效和个性化的管理。考虑到发展中的广泛领域,我们可以期待将来在HF患者的护理和转归方面继续得到改善。

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