Carvedilol Combined With Ivabradine Improves Left Ventricular Diastolic Dysfunction, Clinical Progression, and Survival in Cirrhosis

被引:27
|
作者
Premkumar, Madhumita [1 ]
Rangegowda, Devaraja [1 ]
Vyas, Tanmay [1 ]
Khumuckham, Jelen S. [2 ]
Shasthry, Saggere M. [1 ]
Thomas, Sherin S. [3 ]
Goyal, Ritu [3 ]
Kumar, Guresh [4 ]
Sarin, Shiv K. [1 ]
机构
[1] Inst Liver & Biliary Sci, Dept Hepatol, D1 Vasant Kunj, New Delhi 110070, India
[2] Inst Liver & Biliary Sci, Dept Cardiol, New Delhi, India
[3] Inst Liver & Biliary Sci, Dept Biochem, New Delhi, India
[4] Inst Liver & Biliary Sci, Dept Epidemiol, New Delhi, India
关键词
left ventricular diastolic dysfunction; cirrhotic cardiomyopathy; nonselective; beta-blocker; cirrhosis; carvedilol; ivabradine; CHRONIC HEART-FAILURE; NONSELECTIVE BETA-BLOCKERS; CORONARY-ARTERY-DISEASE; EUROPEAN-SOCIETY; RATE REDUCTION; POOR SURVIVAL; DOUBLE-BLIND; PROPRANOLOL; DIAGNOSIS; ECHOCARDIOGRAPHY;
D O I
10.1097/MCG.0000000000001219
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Left ventricular diastolic dysfunction (LVDD) refers to impaired cardiac diastolic relaxation and may be improved by targeted heart rate reduction (THR). The authors evaluated whether a combination of carvedilol and ivabradine, an I(f)channel blocker that reduces heart rate without affecting blood pressure, could improve LVDD and outcomes in cirrhosis. Patients and Methods: THR was defined as heart rate reduction to 55 to 65 beats per minute. Of 260 patients with cirrhosis, 189 (72%) with LVDD were randomized to THR [group (Gr.)A; n=94; carvedilol +/- ivabradine)] or standard care (Gr.B; n=95; no beta-blockers) and followed for 12 months. Results: In Gr.A, THR was achieved at 4 weeks in 88 (93%) patients (responders, R): 48 (61.5%) with carvedilol alone and 40 (86.9%) of 46 patients with additional ivabradine. In Gr.A, LVDD reversed in 16 (20.5%) and improved from grade 2 to 1 in 34 (35.4%)], whereas in Gr.B, it progressed from grade 1 to 2 in 10 (10.5%) patients. At 12 months, 21 (11.1%) patients died, 6 (14%) in Gr.A and 15 (18%) in Gr.B (P=0.240), but no mortality was seen in those who had persistent THR at 1 year (n=78;P=0.000). In multivariate analysis, model for end-stage liver disease [hazard ratio (HR), 1.52; 95% confidence interval (CI), 1.22-2.75;P=0.034] and E-wave transmitral/early diastolic mitral annular velocity (HR, 1.28; 95% CI, 1.23-2.42;P=0.048) predicted 1-year mortality. Nonresponders had an increased mortality risk (HR, 1.3; 95% CI, 1.2-1.8;P=0.046) independent of age, gender, and baseline model for end-stage liver disease. Levels of norepinephrine, N terminal brain natriuretic peptide, plasma renin activity, and aldosterone were reduced (P<0.01) in responders. More patients in Gr.B developed acute kidney injury (odds ratio, 4.2; 95% CI, 2.8-10.5;P=0.027) and encephalopathy (odds ratio, 6.6; 95% CI, 1.9-9.7;P=0.040). Conclusions: Ivabradine combined with carvedilol improves LVDD, achieves THR more often and reduces risk of encephalopathy, acute kidney injury with improved survival in patients with cirrhosis.
引用
收藏
页码:561 / 568
页数:8
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