Sacubitril/Valsartan is useful and safe in elderly people with heart failure and reduced ejection fraction. Data from a real-word cohort
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Updated: Dec 31, 2025

Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
Alberto Esteban-Fernández1, Pablo Díez-Villanueva2, Lourdes Vicent3
1Servicio de Cardiología, Hospital Universitario de Móstoles, Madrid, Spain; Universidad Rey Juan Carlos, Madrid, Spain.
Insights
Sacubitril/Valsartan is safe and effective in elderly heart failure patients in real-world practice. Treatment withdrawal in elderly individuals is linked to a poorer prognosis, highlighting the importance of continued therapy.
Area of Science:
- Cardiology
- Pharmacology
- Geriatrics
Background:
- Elderly patients with heart failure (HF) are underrepresented in Sacubitril/Valsartan trials.
- The real-world effectiveness and safety of Sacubitril/Valsartan in advanced age are not well-established.
Purpose of the Study:
- To evaluate the use and safety of Sacubitril/Valsartan in a real-world cohort of elderly patients.
- To compare adverse events and reasons for withdrawal based on age groups.
Main Methods:
- Prospective registry of patients initiating Sacubitril/Valsartan in clinical practice.
- Comparison of baseline characteristics, adverse events, and withdrawal causes across different age groups.
Main Results:
- Sacubitril/Valsartan was well-tolerated across all age groups, with no significant age-related differences in adverse events.
- Symptomatic hypotension showed a trend towards higher frequency in older patients.
- Treatment withdrawal was less frequent in older patients and associated with a poorer prognosis.
Conclusions:
- Sacubitril/Valsartan is a safe and useful treatment for elderly patients with heart failure with reduced ejection fraction (HF-rEF) in real-world settings.
- Treatment withdrawal in elderly patients is linked to a poor prognosis.
- Lower doses of Sacubitril/Valsartan were achieved in elderly individuals.
Background:
HF elderly patients are underrepresented in Sacubitril/Valsartan HF trials, and the effect of S/V in real-life patients with advanced age is unknown. The aim of this study was to evaluate the use and safety of S/V in a real-word cohort of elderly patients.
Methods:
We performed a prospective registry of patients who started S/V in clinical practice. We compared baseline characteristics, adverse events during follow-up and causes of S/V withdrawal according to age.
Results:
A total of 427 patients started treatment with S/V: 222 (52.0%)<70 years old, 140 (32.8%) between 70 and 79 and 65 (15.2%)≥80. During a mean follow-up of 7.0±0.1months S/V was well tolerated, with no age-related differences in adverse events (26.8%, 25.9%, 23.1% respectively; p=0.83). Symptomatic hypotension tended to be more frequent in the elderly (19.8%, 25.6%, 33.3% respectively; p=0.17). The withdrawal of S/V was more frequent in younger patients (14.4%, 10.0%, 4.6% respectively; p=0.05) and related to poor prognosis (HR 13.51, 95% CI 3.22-56.13, p<0.001).
Conclusions:
Sacubitril/Valsartan is useful and safe in elderly people with HF-rEF in real-life clinical practice, and withdrawal is associated to poor prognosis. The doses achieved are lower in elderly people.
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