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Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial

AIMS: Dapagliflozin reduced the combined risk of worsening heart failure or cardiovascular death among patients with heart failure with mildly reduced or preserved ejection fraction. In this study, the safety and efficacy of dapagliflozin according to background diuretic therapy and the influence of...

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Autores principales: Chatur, Safia, Vaduganathan, Muthiah, Claggett, Brian, Vardeny, Orly, Desai, Akshay S, Jhund, Pardeep S, de Boer, Rudolf A, Lam, Carolyn S P, Kosiborod, Mikhail N, Shah, Sanjiv J, Martinez, Felipe, Inzucchi, Silvio E, Hernandez, Adrian F, Haddad, Tariq, Mitter, Sumeet S, Miao, Zi Michael, Petersson, Magnus, Maria Langkilde, Anna, McMurray, John J V, Solomon, Scott D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484057/
https://www.ncbi.nlm.nih.gov/pubmed/37220093
http://dx.doi.org/10.1093/eurheartj/ehad283
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author Chatur, Safia
Vaduganathan, Muthiah
Claggett, Brian
Vardeny, Orly
Desai, Akshay S
Jhund, Pardeep S
de Boer, Rudolf A
Lam, Carolyn S P
Kosiborod, Mikhail N
Shah, Sanjiv J
Martinez, Felipe
Inzucchi, Silvio E
Hernandez, Adrian F
Haddad, Tariq
Mitter, Sumeet S
Miao, Zi Michael
Petersson, Magnus
Maria Langkilde, Anna
McMurray, John J V
Solomon, Scott D
author_facet Chatur, Safia
Vaduganathan, Muthiah
Claggett, Brian
Vardeny, Orly
Desai, Akshay S
Jhund, Pardeep S
de Boer, Rudolf A
Lam, Carolyn S P
Kosiborod, Mikhail N
Shah, Sanjiv J
Martinez, Felipe
Inzucchi, Silvio E
Hernandez, Adrian F
Haddad, Tariq
Mitter, Sumeet S
Miao, Zi Michael
Petersson, Magnus
Maria Langkilde, Anna
McMurray, John J V
Solomon, Scott D
author_sort Chatur, Safia
collection PubMed
description AIMS: Dapagliflozin reduced the combined risk of worsening heart failure or cardiovascular death among patients with heart failure with mildly reduced or preserved ejection fraction. In this study, the safety and efficacy of dapagliflozin according to background diuretic therapy and the influence of dapagliflozin on longitudinal diuretic use were evaluated. METHODS AND RESULTS: In this pre-specified analysis of the Dapagliflozin Evaluation to Improve the LIVEs of Patients With Preserved Ejection Fraction Heart Failure (DELIVER) trial, the effects of dapagliflozin vs. placebo were assessed in the following subgroups: no diuretic, non-loop diuretic, and loop diuretic furosemide equivalent doses of <40, 40, and >40 mg, respectively. Of the 6263 randomized patients, 683 (10.9%) were on no diuretic, 769 (12.3%) were on a non-loop diuretic, and 4811 (76.8%) were on a loop diuretic at baseline. Treatment benefits of dapagliflozin on the primary composite outcome were consistent by diuretic use categories (P  (interaction) = 0.64) or loop diuretic dose (P  (interaction) = 0.57). Serious adverse events were similar between dapagliflozin and placebo arms, irrespective of diuretic use or dosing. Dapagliflozin reduced new initiation of loop diuretics by 32% [hazard ratio (HR) 0.68; 95% confidence interval (CI): 0.55–0.84, P < 0.001] but did not influence discontinuations/disruptions (HR 0.98; 95% CI: 0.86–1.13, P = 0.83) in follow-up. First sustained loop diuretic dose increases were less frequent, and sustained dose decreases were more frequent in patients treated with dapagliflozin: net difference of −6.5% (95% CI: −9.4 to −3.6; P < 0.001). The mean dose of loop diuretic increased over time in the placebo arm, a longitudinal increase that was significantly attenuated with treatment with dapagliflozin (placebo-corrected treatment effect of −2.5 mg/year; 95% CI: −1.5, −3.7, P < 0.001). CONCLUSION: In patients with heart failure with mildly reduced or preserved ejection fraction, the clinical benefits of dapagliflozin relative to placebo were consistent across a wide range of diuretic categories and doses with a similar safety profile. Treatment with dapagliflozin significantly reduced new loop diuretic requirement over time.
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spelling pubmed-104840572023-09-08 Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial Chatur, Safia Vaduganathan, Muthiah Claggett, Brian Vardeny, Orly Desai, Akshay S Jhund, Pardeep S de Boer, Rudolf A Lam, Carolyn S P Kosiborod, Mikhail N Shah, Sanjiv J Martinez, Felipe Inzucchi, Silvio E Hernandez, Adrian F Haddad, Tariq Mitter, Sumeet S Miao, Zi Michael Petersson, Magnus Maria Langkilde, Anna McMurray, John J V Solomon, Scott D Eur Heart J Fast Track Clinical Research AIMS: Dapagliflozin reduced the combined risk of worsening heart failure or cardiovascular death among patients with heart failure with mildly reduced or preserved ejection fraction. In this study, the safety and efficacy of dapagliflozin according to background diuretic therapy and the influence of dapagliflozin on longitudinal diuretic use were evaluated. METHODS AND RESULTS: In this pre-specified analysis of the Dapagliflozin Evaluation to Improve the LIVEs of Patients With Preserved Ejection Fraction Heart Failure (DELIVER) trial, the effects of dapagliflozin vs. placebo were assessed in the following subgroups: no diuretic, non-loop diuretic, and loop diuretic furosemide equivalent doses of <40, 40, and >40 mg, respectively. Of the 6263 randomized patients, 683 (10.9%) were on no diuretic, 769 (12.3%) were on a non-loop diuretic, and 4811 (76.8%) were on a loop diuretic at baseline. Treatment benefits of dapagliflozin on the primary composite outcome were consistent by diuretic use categories (P  (interaction) = 0.64) or loop diuretic dose (P  (interaction) = 0.57). Serious adverse events were similar between dapagliflozin and placebo arms, irrespective of diuretic use or dosing. Dapagliflozin reduced new initiation of loop diuretics by 32% [hazard ratio (HR) 0.68; 95% confidence interval (CI): 0.55–0.84, P < 0.001] but did not influence discontinuations/disruptions (HR 0.98; 95% CI: 0.86–1.13, P = 0.83) in follow-up. First sustained loop diuretic dose increases were less frequent, and sustained dose decreases were more frequent in patients treated with dapagliflozin: net difference of −6.5% (95% CI: −9.4 to −3.6; P < 0.001). The mean dose of loop diuretic increased over time in the placebo arm, a longitudinal increase that was significantly attenuated with treatment with dapagliflozin (placebo-corrected treatment effect of −2.5 mg/year; 95% CI: −1.5, −3.7, P < 0.001). CONCLUSION: In patients with heart failure with mildly reduced or preserved ejection fraction, the clinical benefits of dapagliflozin relative to placebo were consistent across a wide range of diuretic categories and doses with a similar safety profile. Treatment with dapagliflozin significantly reduced new loop diuretic requirement over time. Oxford University Press 2023-05-23 /pmc/articles/PMC10484057/ /pubmed/37220093 http://dx.doi.org/10.1093/eurheartj/ehad283 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Fast Track Clinical Research
Chatur, Safia
Vaduganathan, Muthiah
Claggett, Brian
Vardeny, Orly
Desai, Akshay S
Jhund, Pardeep S
de Boer, Rudolf A
Lam, Carolyn S P
Kosiborod, Mikhail N
Shah, Sanjiv J
Martinez, Felipe
Inzucchi, Silvio E
Hernandez, Adrian F
Haddad, Tariq
Mitter, Sumeet S
Miao, Zi Michael
Petersson, Magnus
Maria Langkilde, Anna
McMurray, John J V
Solomon, Scott D
Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial
title Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial
title_full Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial
title_fullStr Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial
title_full_unstemmed Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial
title_short Dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the DELIVER trial
title_sort dapagliflozin and diuretic utilization in heart failure with mildly reduced or preserved ejection fraction: the deliver trial
topic Fast Track Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484057/
https://www.ncbi.nlm.nih.gov/pubmed/37220093
http://dx.doi.org/10.1093/eurheartj/ehad283
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