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Effects of Sacubitril/Valsartan Across the Spectrum of Renal Impairment in Patients With Heart Failure

医学 沙库比林 肾脏疾病 肾功能 缬沙坦 内科学 依那普利 肌酐 蛋白尿 心力衰竭 沙库比林、缬沙坦 心脏病学 重症监护医学 血管紧张素转换酶 血压
作者
Safia Chatur,Brendon L. Neuen,Brian Claggett,Iris E. Beldhuis,Finnian R. Mc Causland,Akshay S. Desai,Jean L. Rouleau,Michael R. Zile,Martin Lefkowitz,Milton Packer,John J.V. McMurray,Scott D. Solomon,Muthiah Vaduganathan
出处
期刊:Journal of the American College of Cardiology [Elsevier BV]
卷期号:83 (22): 2148-2159 被引量:18
标识
DOI:10.1016/j.jacc.2024.03.392
摘要

The Kidney Disease Improving Global Outcomes (KDIGO) classification integrates both estimated glomerular filtration rate(eGFR) and urine-albumin-creatinine-ratio to stratify risk more comprehensively in patients with chronic kidney disease. There are limited data assessing whether this classification system is associated with prognosis and treatment response in heart failure populations. PARADIGM-HF was a global RCT evaluating sacubitril/valsartan vs. enalapril in patients with HFrEF. Patients were classified according to low, moderate, and high/very high KDIGO risk. Treatment responses were assessed according to baseline KDIGO risk. The primary outcome was a composite of CV death or HF hospitalization. A renal composite outcome was defined as sustained decline in eGFR by ≥40% or end stage kidney disease. Among 1,910 (23% of total) participants with available data, 42%, 32%, and 26% were classified as low, moderate, and high/very high KDIGO risk, respectively. Patients in the highest KDIGO risk categories experienced the highest rates of the primary composite outcome (7.6[6.5-9.0], 9.4[7.9-11.2], 14.9[12.7-17.6] per 100py; P<0.001). Sacubitril/valsartan had a similar safety profile and similarly reduced the risk of both the primary outcome (PInteraction=0.31) and the renal composite outcome (PInteraction=0.50) across the spectrum of KDIGO risk. One in 4 patients with HFrEF were classified as at least high KDIGO kidney risk; these individuals faced concordantly the highest risks of CV events. Sacubitril/valsartan exhibited consistent CV and kidney protective benefits as well as safety across the spectrum of baseline kidney risk. These data further support initiation of sacubitril/valsartan in HFrEF across a broad range of kidney risk.
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