Recovery of left ventricular dysfunction after sacubitril/valsartan: predictors and management

被引:27
作者
Chang, Hung-Yu [1 ,2 ]
Chen, Kuan-Chun [1 ,3 ,4 ]
Fong, Man-Cai [1 ,3 ]
Feng, An-Ning [1 ,2 ]
Fu, Hao-Neng [1 ]
Huang, Kuan-Chih [1 ]
Chong, Eric [5 ]
Yin, Wei-Hsian [1 ,2 ]
机构
[1] Cheng Hsin Gen Hosp, Heart Ctr, 45 Cheng Hsin St, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Fac Med, Sch Med, Taipei, Taiwan
[3] Natl Def Med Ctr, Taipei, Taiwan
[4] Natl Yang Ming Univ, Inst Emergency & Crit Care Med, Taipei, Taiwan
[5] Farrer Pk Hosp, Div Cardiol, Singapore, Singapore
关键词
Heart failure; Left ventricular ejection fraction; Sacubitril/valsartan; CONGESTIVE-HEART-FAILURE; CARDIAC RESYNCHRONIZATION THERAPY; REDUCED EJECTION FRACTION; LONG-TERM; MORTALITY; ENALAPRIL; SURVIVAL; TRIAL; SPIRONOLACTONE; IMPROVEMENT;
D O I
10.1016/j.jjcc.2019.08.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Literature describing recovery of left ventricular (LV) function post sacubitril/valsartan treatment and the optimal management of heart failure (HF) patients receiving sacubitril/valsartan remain sparse. Methods: We recruited 437 consecutive chronic HF patients with baseline left ventricular ejection fraction (LVEF) less than 40%, who were treated with sacubitril/valsartan. All patients underwent routine echocardiographic measurement. Results: During treatment period, recovery of LVEF to 50% or greater was observed in 77 (17.6%) patients. After multivariate analysis, recovery of LV dysfunctionwas associated with non-ischemic etiology of HF, smaller baseline LV end-diastolic diameter (LVEDD), and higher initial dosage of sacubitril/valsartan. Compared to those without recovery of LV dysfunction, death from cardiovascular causes or first unplanned hospitalization for HF (CVD/HFH) were significantly lower in patients with LVEF recovery [11.7% vs. 24.4%, hazard ratio (HR) 0.42, p = 0.014]. Among patients with recovery of LVEF, 51 patients continued to receive the same dosage of sacubitril/valsartan had higher LVEF and were less likely to have deterioration of LVEF than the other 26 patients who received either tapering dose of sacubitril/valsartan or switching from sacubitril/valsartan to renin-angiotensin-system blockers (LVEF 56.4 +/- 5.3% vs. 45.0 +/- 12.8%, p< 0.001; Delta LVEF 1.2 +/- 5.1% vs. 9.3 +/- 12.0%, p < 0.001). CVD/HFH occurred more frequently in the taper group than the maintenance group (23.1% vs. 5.9%, HR 0.22, p = 0.035). Conclusions: Non-ischemic etiology of HF, smaller baseline LVEDD, and higher initial dosage of sacubitril/ valsartan could predict better recovery of LV function. Among patients with functional recovery, tapering sacubitril/valsartan dose was associated with deterioration of recovered heart function and had less favorable prognosis during follow-up. (C) 2019 Published by Elsevier Ltd on behalf of Japanese College of Cardiology.
引用
收藏
页码:233 / 241
页数:9
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