Abstract
Background
Frailty is associated with worse clinical outcomes in heart failure (HF) patients [1]. The benefits of sacubitril/valsartan in frail HF patients are unclear [2]. This study explored whether use of sacubitril/valsartan leads to improved clinical outcomes in frail hospitalised HF patients.
Methods
This cross-sectional multicentre study included all HF admissions over a period of 7 years at two tertiary hospitals in Australia. Frailty status was determined by use of the Hospital Frailty Risk Score (HFRS) [3] and patients with a score of ≥5 were classified as frail. The primary outcome for this study was the days-alive-and-out-of-hospital at 90 days of hospital discharge (DAOH90). Multilevel multivariable Poisson regression model determined whether frail patients who were on sacubitril/valsartan had increased DAOH90 after adjustment for age, sex, Charlson index (CCI), creatinine, brain natriuretic peptide (BNP), haemoglobin, albumin, C-reactive protein (CRP), and use of other heart failure-specific medications.
Results
There were 5,734 HF admissions during the study period and 1,406 (24.5%) were classified as frail, of whom 22 (1.6%) patients were on sacubitril/valsartan. Frail patients who were on sacubitril/valsartan were significantly younger, with a higher CCI and lower creatinine levels than those who were not on this treatment (p<0.05). The mean (SD) DAOH90 was significantly increased in frail patients who were on sacubitril/valsartan than those who were not on this treatment (84.6 (16.5) vs 61.7 (36.6) days, respectively). After adjusted analysis frail patients on sacubitril/valsartan were 22% more likely to have an increased DAOH90 than those without this treatment (IRR 1.22, 95% CI 1.16–1.29, p<0.001).
Conclusion
Use of sacubitril/valsartan is associated with improved clinical outcomes in frail HF patients.
Frailty is associated with worse clinical outcomes in heart failure (HF) patients [1]. The benefits of sacubitril/valsartan in frail HF patients are unclear [2]. This study explored whether use of sacubitril/valsartan leads to improved clinical outcomes in frail hospitalised HF patients.
Methods
This cross-sectional multicentre study included all HF admissions over a period of 7 years at two tertiary hospitals in Australia. Frailty status was determined by use of the Hospital Frailty Risk Score (HFRS) [3] and patients with a score of ≥5 were classified as frail. The primary outcome for this study was the days-alive-and-out-of-hospital at 90 days of hospital discharge (DAOH90). Multilevel multivariable Poisson regression model determined whether frail patients who were on sacubitril/valsartan had increased DAOH90 after adjustment for age, sex, Charlson index (CCI), creatinine, brain natriuretic peptide (BNP), haemoglobin, albumin, C-reactive protein (CRP), and use of other heart failure-specific medications.
Results
There were 5,734 HF admissions during the study period and 1,406 (24.5%) were classified as frail, of whom 22 (1.6%) patients were on sacubitril/valsartan. Frail patients who were on sacubitril/valsartan were significantly younger, with a higher CCI and lower creatinine levels than those who were not on this treatment (p<0.05). The mean (SD) DAOH90 was significantly increased in frail patients who were on sacubitril/valsartan than those who were not on this treatment (84.6 (16.5) vs 61.7 (36.6) days, respectively). After adjusted analysis frail patients on sacubitril/valsartan were 22% more likely to have an increased DAOH90 than those without this treatment (IRR 1.22, 95% CI 1.16–1.29, p<0.001).
Conclusion
Use of sacubitril/valsartan is associated with improved clinical outcomes in frail HF patients.
Original language | English |
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Pages (from-to) | S72 |
Number of pages | 1 |
Journal | Heart, Lung and Circulation |
Volume | 31 |
Issue number | Suppl. 3 |
DOIs | |
Publication status | Published - 2 Aug 2022 |
Keywords
- Heart failure
- Frailty
- sacubitril/valsartan
- clinical outcomes