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Evaluating Sacubitril/Valsartan Dose Dependence on Clinical Outcomes in Patients With Heart Failure With Reduced
Kazuhiko Kido1, Christopher Bianco2, Marco Caccamo2
1West Virginia University School of Pharmacy, Morgantown, WV, USA.
Insights
Higher doses of sacubitril/valsartan (97/103 mg or 49/51 mg) significantly reduced heart failure (HF) hospitalization and all-cause mortality compared to the lowest dose (24/26 mg) in patients with HF with reduced ejection fraction (HFrEF).
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Limited evidence exists for low (24/26 mg) and moderate (49/51 mg) doses of sacubitril/valsartan.
- Understanding dose-response relationships is crucial for optimizing heart failure treatment.
Purpose of the Study:
- To evaluate the impact of different sacubitril/valsartan dosages on heart failure (HF) hospitalization and mortality.
- To compare the efficacy of 24/26 mg, 49/51 mg, and 97/103 mg doses in patients with HF with reduced ejection fraction (HFrEF).
Main Methods:
- Retrospective multicenter cohort study involving patients with HFrEF.
- Compared three doses of sacubitril/valsartan: 24/26 mg, 49/51 mg, and 97/103 mg.
- Utilized propensity matching analysis to control for confounding factors; coprimary outcomes were all-cause mortality and HF rehospitalization.
Main Results:
- Higher doses of sacubitril/valsartan were associated with reduced HF hospitalization rates.
- The 97/103-mg group showed the lowest hospitalization rate (16.10%), followed by the 49/51-mg group (19.51%), compared to the 24/26-mg group (29.14%).
- All-cause mortality was significantly lower in the 49/51-mg (17.58%) and 97/103-mg (9.27%) groups compared to the 24/26-mg group (29.63%).
Conclusions:
- Sacubitril/valsartan at 97/103 mg or 49/51 mg is associated with significantly lower rates of HF hospitalization and all-cause mortality.
- The findings support the use of higher doses of sacubitril/valsartan for improved outcomes in HFrEF patients.
- Optimizing sacubitril/valsartan dosage is essential for managing heart failure effectively.
Background:
Limited evidence is available regarding low (24/26 mg) and middle (49/51 mg) doses of sacubitril/valsartan.
Objectives:
The purpose of this study was to investigate the effect of sacubitril/valsartan dose on heart failure (HF) hospitalization and mortality in patients with HF with reduced ejection fraction (HFrEF).
Methods:
A retrospective multicenter cohort study compared 3 doses of sacubitril/valsartan in patients with HFrEF. The coprimary outcomes were all-cause mortality and rehospitalization for HF. Propensity matching analysis was performed.
Results:
Of 721 eligible patients, propensity matching created a cohort with an effective sample size of 652 (24/26-mg group [n = 326], 49/51-mg group [n = 147], 97/103-mg group [n = 179]). The HF hospitalization rates were 29.14% in the 24/26-mg group, 19.51% in the 49/51-mg group, and 16.10% in the 97/103-mg group (24/26 vs 49/51 mg: HR = 1.56, 95% CI = 1.04-2.34; 24/26 vs 97/103 mg: HR = 1.79, 95% CI = 1.18-2.73; 49/51 vs 97/103 mg: HR = 1.15, 95% CI = 0.70-1.89). All-cause mortality rates were 29.63% in the 24/26-mg group, 17.58% in the 49/51-mg group, and 9.27% in the 97/103-mg group (24/26 vs 49/51 mg: HR = 1.67, 95% CI = 1.07-2.59; 24/26 vs 97/103 mg: HR = 2.56, 95% CI = 1.54-4.24; 49/51 vs 97/103 mg: HR = 1.54, 95% CI = 0.84-2.82).
Conclusion And Relevance:
Sacubitril/valsartan 97/103- or 49/51-mg dose is associated with a lower mortality or hospitalization rate for HF in patients receiving sacubitril/valsartan compared with the 24/26-mg dose group.
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