Vericiguat—Filling the Gaps in Heart Failure Management

B. Rao
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Abstract

Corresponding author: B Hygriv Rao, KIMS Hospitals, Hyderabad, Telangana 500003, India. E-mail: hygriv@hotmail.com Left ventricular dysfunction is an established marker in heart failure (HF) patients predicting poor clinical outcomes, sudden death, and overall mortality.1 Over the last few decades, various pharmacological agents as guideline directed medical treatment (GDMT) have been introduced serially in the management of HF resulting in incremental benefit in HF hospitalizations, quality of life, symptom alleviation, and mortality. Large data has established the use of beta blockers, angiotensin converting enzyme inhibitors, angiotensin receptor blockers, angiotensin receptor– neprilysin inhibitors, and mineralocorticoid receptor antagonists, in these patients. The ongoing battle against HF was consolidated by amalgamation of sacubitril–valsartan and SGLT-2 inhibitors in the GDMT by data from large trials—PARDIGM HF, DAPA HF, EMPEROR Reduced. 2,3,4 Despite the scintillating advances in pharmacotherapy in this area, the twin clinical problems of worsening HF and renal failure continue to cause abundant frustration in patient management. Patients with a recent HF hospitalization or worsening HF constitute a particularly vulnerable cohort as they are associated with high subsequent event rates and mortality. Moreover HF is frequently associated with impaired renal function and/or high serum potassium concentrations. Kidney is truly the Achilles heel in the management of HF as almost all the routine medications used in these patients require monitoring of renal function and electrolytes.5 Impaired estimated glomerular filtration rate (eGFR), with HF, presents a serious therapeutic challenge as it precludes prescription of all components of GDMT, makes it difficult to up-titrate them to optimal doses, and frequently results in their discontinuation. The most difficult cohort of patients to initiate and maintain GDMT are patients with a lower eGFR, higher N-terminal probrain natriuretic peptide (NTproBNP), and elevated serum potassium concentrations. These are the patients who have a higher risk of cardiovascular death and hospitalizations for HF and in a greater need for these treatments. Accordingly, an unmet need exists for effective therapies in patients with severe heart failure with reduced ejection fraction (HFrEF) and advanced chronic
vericiguat -填补心力衰竭管理的空白
通讯作者:B Hygriv Rao, kim医院,海德拉巴,泰伦加纳500003,印度。E-mail: hygriv@hotmail.com左心室功能障碍是心衰(HF)患者临床预后不良、猝死和总死亡率的一个既定指标在过去的几十年里,各种药理学药物作为指导药物治疗(GDMT)被陆续引入心衰治疗,导致心衰住院、生活质量、症状缓解和死亡率的增加。大量数据已经证实在这些患者中使用-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、血管紧张素受体- neprilysin抑制剂和矿皮质激素受体拮抗剂。pardigm HF、DAPA HF、EMPEROR Reduced等大型临床试验的数据表明,沙比替-缬沙坦和SGLT-2抑制剂在GDMT中的合并治疗巩固了对HF的持续斗争。2,3,4尽管该领域的药物治疗取得了突破性进展,但HF恶化和肾衰竭的双重临床问题继续给患者管理带来巨大挫折。最近住院的HF患者或恶化的HF患者是一个特别脆弱的群体,因为他们与高的后续事件发生率和死亡率相关。此外,心衰常与肾功能受损和/或血清钾浓度高有关。肾脏确实是心衰治疗的致命弱点,因为几乎所有用于心衰患者的常规药物都需要监测肾功能和电解质心衰患者估计肾小球滤过率(eGFR)受损,这是一个严重的治疗挑战,因为它排除了GDMT所有成分的处方,使其难以提高剂量至最佳剂量,并经常导致停药。启动和维持GDMT最困难的患者队列是eGFR较低、n端脑钠肽前体(NTproBNP)较高和血清钾浓度升高的患者。这些患者因心衰有较高的心血管死亡和住院风险,更需要这些治疗。因此,对严重心力衰竭伴射血分数降低(HFrEF)和晚期慢性心力衰竭患者的有效治疗存在未满足的需求
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