Your browser doesn't support javascript.
loading
Long-Term Outcomes of Sacubitril/Valsartan in Heart Failure with Reduced Ejection Fraction and Coexisting End-Stage Renal Disease.
Lin, Wan-Ying; Shao, Yu-Hsuan Joni; Chiang, Andy F; Huang, Chih-Chieh; Chiang, Kim F; Chan, Chao-Shun; Huang, Chun-Yao; Hsiao, Bu-Yuan.
Affiliation
  • Lin WY; Department of Family Medicine, Taipei Medical University Hospital, Taipei, Taiwan.
  • Shao YJ; Graduate Institute of Biomedical Informatics, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan.
  • Chiang AF; Office of Data Science, Health Data Analytics and Statistics Center, Taipei Medical University, Taipei, Taiwan.
  • Huang CC; Clinical Big Data Research Center, Taipei Medical University Hospital, Taipei, Taiwan.
  • Chiang KF; Department of Family Medicine, Taipei Medical University Hospital, Taipei, Taiwan.
  • Chan CS; Office of Data Science, Taipei Medical University, Taipei, Taiwan.
  • Huang CY; Department of Medicine, Stanford University School of Medicine, Stanford, California, USA.
  • Hsiao BY; Division of Cardiology and Cardiovascular Research Center, Department of Internal Medicine, Taipei Medical University Hospital, Taipei, Taiwan.
Clin Pharmacol Ther ; 116(2): 471-477, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38880970
ABSTRACT
Sacubitril/valsartan (Entresto) has proven therapeutic effects in heart failure (HF) patients, but its impact on those with advanced chronic kidney disease (CKD) remains unclear, particularly in HF patients with coexisting end-stage renal disease (ESRD). This study aims to assess the long-term survival of patients with heart failure with reduced ejection fraction (HFrEF) and coexisting ESRD treated with sacubitril/valsartan. A retrospective cohort study included 2,860 HFrEF and ESRD patients between January 2008 and December 2020. After propensity score matching, data from a sacubitril/valsartan group (n = 61) and a candesartan or valsartan group (n = 117) were analyzed. Patients on sacubitril/valsartan for at least 9 months had significantly lower 5-year all-cause mortality (39.3%) compared with the non-sacubitril/valsartan group (54.7%) (HR 0.46; 95% CI, 0.25-0.82; P = 0.0094). Left ventricular ejection fraction (LVEF) improvement after 3 years in the sacubitril/valsartan group (14.51 ±18.98) was significantly greater than the non-sacubitril/valsartan group (6.91 ±18.44) (P = 0.0408). Average hospitalizations in sacubitril/valsartan and non-sacubitril/valsartan groups were 1.39 and 0.97, respectively (incidence rate ratio, 1.59; 95% CI, 0.90-2.82; P = 0.1106). Sacubitril/valsartan treatment demonstrated significantly lower 5-year mortality rates and greater LVEF improvement in HFrEF patients with coexisting ESRD compared with candesartan or valsartan. These findings suggest that sacubitril/valsartan is a beneficial treatment option for this patient population.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stroke Volume / Biphenyl Compounds / Drug Combinations / Angiotensin Receptor Antagonists / Valsartan / Aminobutyrates / Heart Failure / Kidney Failure, Chronic Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Clin Pharmacol Ther Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stroke Volume / Biphenyl Compounds / Drug Combinations / Angiotensin Receptor Antagonists / Valsartan / Aminobutyrates / Heart Failure / Kidney Failure, Chronic Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Clin Pharmacol Ther Year: 2024 Document type: Article Affiliation country: Country of publication: