2021
DOI: 10.4236/crcm.2021.107025
|View full text |Cite
|
Sign up to set email alerts
|

The Effect of Sacubitril/Valsartan in a Dialysis Patient with Severe Heart Failure

Abstract: Heart failure (HF) is a major comorbidity in patients with end-stage renal disease (ESRD). The pathogenesis of HF in patients on renal replacement therapy represents the confluence of several traditional and nontraditional vascular risk factors, unique to the milieu of chronic kidney disease and the dialysis modality [1]. The purpose of this report is to describe the efficacy and safety of sacubitril/valsartan for an ESRD patient on hemodialysis therapy conmbined with heart failure with reduced ejection fracti… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

1
0
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 9 publications
(9 reference statements)
1
0
0
Order By: Relevance
“…There was no difference in chronic renal events (OR 0.92 (0.8-1.05)) or hyperkalemia (OR 1.02 (0.84-1.23)), suggesting that neutral endopeptidase inhibitors (NEPi)+ ACEi/ARBs have a safe record at the renal level. In line with our findings, Kong et al [ 14 ] demonstrated that administration of Sac/Val (50 mg twice a day) for one year improved the symptoms of HF and reduced NT-proBNP levels, accompanied by a decrease in blood pressure in a single HD patient with HFrEF. Although the authors attributed these cardiac beneficial effects to Sac/Val, it should be emphasized that the drug was given along with spironolactone at a dose of 20 mg three times a day and metoprolol at a dose of 23.75 mg once daily.…”
Section: Discussionsupporting
confidence: 92%
“…There was no difference in chronic renal events (OR 0.92 (0.8-1.05)) or hyperkalemia (OR 1.02 (0.84-1.23)), suggesting that neutral endopeptidase inhibitors (NEPi)+ ACEi/ARBs have a safe record at the renal level. In line with our findings, Kong et al [ 14 ] demonstrated that administration of Sac/Val (50 mg twice a day) for one year improved the symptoms of HF and reduced NT-proBNP levels, accompanied by a decrease in blood pressure in a single HD patient with HFrEF. Although the authors attributed these cardiac beneficial effects to Sac/Val, it should be emphasized that the drug was given along with spironolactone at a dose of 20 mg three times a day and metoprolol at a dose of 23.75 mg once daily.…”
Section: Discussionsupporting
confidence: 92%