Division of Nephrology, Department of Medicine Taipei Veterans General Hospital Taipei Taiwan.
School of Medicine National Yang-Ming Chiao-Tung University Taipei Taiwan.
J Am Heart Assoc. 2022 Sep 20;11(18):e026407. doi: 10.1161/JAHA.122.026407. Epub 2022 Sep 5.
Background Heart failure with reduced ejection fraction (HFrEF) is a chronic disease with substantial mortality. Management of HFrEF has seen significant breakthrough after the launch of neprilysin inhibitor. The PARADIGM-HF (Prospective Comparison of ARNI with ACEI to Determine Impacton Global Mortality and Morbidity in Heart Failure) trial showed that sacubitril/valsartan significantly reduces HFrEF mortality and the heart failure hospitalization rate. However, in patients with advanced kidney disease, who have the highest prevalence of heart failure, the efficacy and safety of sacubitril/valsartan remains uncertain. We aim to study the efficiency of sacubitril/valsartan in patients with end-stage kidney disease. Methods and Results Heart function was screened by echocardiogram among all patients with end-stage kidney disease in 2 hospitals. Patients with HFrEF received either sacubitril/valsartan or conventional treatment. Fifteen echocardiographic parameters were compared before and after treatment. After 1-year sacubitril/valsartan treatment, parameters of systolic (left ventricular ejection fraction 31.3% to 45.1%, <0.0001; left ventricular end-systolic volume 95.7 to 70.1 mL, =0.006; left ventricular internal diameter at end-systole phase 47.2 to 40.1 mm, =0.005), and diastolic (E/A ratio 1.3 to 0.8, =0.009; E/Med e' ratio 25.3 to 18.8, =0.010) function improved in patients with HFrEF and end-stage kidney disease. These parameters were unchanged in the conventional treatment group. Serum potassium did not increase in the sacubitril/valsartan group. Conclusions Sacubitril/valsartan improves left ventricular systolic and diastolic function in patients with HFrEF and end-stage kidney disease.
射血分数降低的心力衰竭(HFrEF)是一种死亡率较高的慢性疾病。在肾素-血管紧张素-醛固酮系统抑制剂上市后,HFrEF 的治疗取得了显著进展。PARADIGM-HF(血管紧张素受体脑啡肽酶抑制剂与血管紧张素转换酶抑制剂治疗心力衰竭的前瞻性比较)试验表明,沙库巴曲缬沙坦可显著降低 HFrEF 患者的死亡率和心力衰竭住院率。然而,在患有晚期肾病(心力衰竭患病率最高的疾病)的患者中,沙库巴曲缬沙坦的疗效和安全性尚不确定。我们旨在研究沙库巴曲缬沙坦在终末期肾病患者中的疗效。
在 2 家医院的所有终末期肾病患者中进行了超声心动图筛查心功能。HFrEF 患者接受沙库巴曲缬沙坦或常规治疗。比较治疗前后 15 项超声心动图参数。沙库巴曲缬沙坦治疗 1 年后,患者的收缩功能参数(左心室射血分数从 31.3%升至 45.1%,<0.0001;左心室收缩末期容积从 95.7 降至 70.1ml,=0.006;左心室收缩末期内径从 47.2 降至 40.1mm,=0.005)和舒张功能参数(E/A 比值从 1.3 降至 0.8,=0.009;E/Med e' 比值从 25.3 降至 18.8,=0.010)均得到改善。常规治疗组患者的这些参数则无变化。沙库巴曲缬沙坦组患者的血清钾未升高。
沙库巴曲缬沙坦可改善 HFrEF 合并终末期肾病患者的左心室收缩和舒张功能。