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Clinical evidence of initiating a very low dose of sacubitril/valsartan: a prospective observational analysis

Authors
 Hyoeun Kim  ;  Jaewon Oh  ;  Sanghyup Lee  ;  Jaehyung Ha  ;  Minjae Yoon  ;  Kyeong-Hyeon Chun  ;  Chan Joo Lee  ;  Sungha Park  ;  Sang-Hak Lee  ;  Seok-Min Kang 
Citation
 SCIENTIFIC REPORTS, Vol.11(1) : 16335, 2021-08 
Journal Title
SCIENTIFIC REPORTS
Issue Date
2021-08
MeSH
Aminobutyrates / administration & dosage* ; Angiotensin Receptor Antagonists / administration & dosage* ; Biphenyl Compounds / administration & dosage* ; Drug Combinations ; Enalapril / therapeutic use ; Female ; Heart Failure / drug therapy* ; Heart Failure / metabolism ; Hospitalization ; Humans ; Male ; Middle Aged ; Natriuretic Peptide, Brain / metabolism ; Prospective Studies ; Stroke Volume / drug effects ; Valsartan / administration & dosage* ; Valsartan / therapeutic use ; Ventricular Function, Left / drug effects
Abstract
Sacubitril/valsartan is superior to enalapril in reducing the risks of cardiovascular death and preventing hospitalization in patients with heart failure and reduced ejection fraction (HFrEF). However, patients often do not receive sacubitril/valsartan because of concerns about hypotension. We examined the feasibility of initiating sacubitril/valsartan at a very low dose (VLD) in potentially intolerant patients with HFrEF and subsequent dose up-titration, treatment persistence and outcomes. We analyzed 206 patients with HFrEF grouped according to starting sacubitril/valsartan dose. The VLD group (n = 106) commenced 25 mg twice daily, and the standard-dose (SD) group (n = 100) started on ≥ 50 mg twice daily. Baseline systolic blood pressure was 103 ± 12 mmHg vs. 119 ± 14 mmHg in the SD group (P < 0.001). The maximal target dose achievement rate was higher in the SD group (27.0% vs 9.4%, p = 0.001) and the VLD group experienced more dose up-titrations and fewer down-titrations than the SD group. The VLD group had a decrease in N-terminal prohormone of brain natriuretic peptide (NT-proBNP) similar to the SD group and a similar increase in left ventricular ejection fraction. There were no significant differences in symptomatic hypotension, worsening renal function, hyperkalemia, cardiovascular mortality, and rehospitalization due to HF between the two groups during follow-up period. In patients considered by the treating physician likely to be intolerant of sacubitril/valsartan, initiation with 25 mg twice daily was generally possible and patients remained in therapy, with similar decreases in NT-proBNP and increases in left ventricular ejection fraction to those observed in patients receiving SD sacubitril/valsartan.
Files in This Item:
T202104775.pdf Download
DOI
10.1038/s41598-021-95787-w
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kang, Seok Min(강석민) ORCID logo https://orcid.org/0000-0001-9856-9227
Kim, Hyoeun(김효은) ORCID logo https://orcid.org/0000-0002-7334-9700
Park, Sung Ha(박성하) ORCID logo https://orcid.org/0000-0001-5362-478X
Oh, Jae Won(오재원) ORCID logo https://orcid.org/0000-0002-4585-1488
Yoon, Minjae(윤민재)
Lee, Sang Hak(이상학) ORCID logo https://orcid.org/0000-0002-4535-3745
Lee, Sanghyup(이상협)
Lee, Chan Joo(이찬주) ORCID logo https://orcid.org/0000-0002-8756-409X
Chun, Kyeong Hyeon(전경현) ORCID logo https://orcid.org/0000-0002-7798-658X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/186876
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