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Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis

BACKGROUND: Heart failure (HF) is a major cause of recurrent hospitalization and death worldwide. Sodium-glucose cotransporter-2 inhibitors including dapagliflozin are anti-diabetic drugs with promising cardiovascular (CV) effects. We performed systematic review and meta-analysis of randomized contr...

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Autores principales: Ali, Ahmed E., Mazroua, Muhammad Sabry, ElSaban, Mariam, Najam, Nadia, Kothari, Aditi S., Mansoor, Taha, Amal, Tanya, Lee, Joanna, Kashyap, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ubiquity Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453961/
https://www.ncbi.nlm.nih.gov/pubmed/37636033
http://dx.doi.org/10.5334/gh.1258
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author Ali, Ahmed E.
Mazroua, Muhammad Sabry
ElSaban, Mariam
Najam, Nadia
Kothari, Aditi S.
Mansoor, Taha
Amal, Tanya
Lee, Joanna
Kashyap, Rahul
author_facet Ali, Ahmed E.
Mazroua, Muhammad Sabry
ElSaban, Mariam
Najam, Nadia
Kothari, Aditi S.
Mansoor, Taha
Amal, Tanya
Lee, Joanna
Kashyap, Rahul
author_sort Ali, Ahmed E.
collection PubMed
description BACKGROUND: Heart failure (HF) is a major cause of recurrent hospitalization and death worldwide. Sodium-glucose cotransporter-2 inhibitors including dapagliflozin are anti-diabetic drugs with promising cardiovascular (CV) effects. We performed systematic review and meta-analysis of randomized controlled trials investigating the effects of dapagliflozin in heart failure patients. METHODS: We searched PubMed, Scopus and ScienceDirect databases. A total of 1,567 studies from January 2017 to September 10, 2022, were screened. After applying exclusion criteria, 22 studies were retrieved for full-text screening, and nine of them were eligible for this meta-analysis. Effect estimates for dichotomous variables were expressed as risk ratio (RR) and 95% CI. The primary outcomes were the incidence of all-cause mortality, hospitalization due to HF, and CV death. This review was registered on PROSPERO with ID CRD42022347793. RESULTS: A total of 14,032 patients were included. The overall risk ratio of all-cause mortality favored the dapagliflozin group over the placebo/standard therapy group (RR = 0.89, 95% CI: 0.82–0.97, P = 0.006) and the pooled studies were not heterogenous (I(2) = 0%). Additionally, dapagliflozin significantly reduced the hospitalization due to heart failure (RR = 0.76, 95% CI: 0.70–0.84, P > 0.00001, I(2) = 0%), cardiovascular death (RR = 0.87, 95% CI: 0.78–0.97, P = 0.01, I(2) = 0%) and their composite outcomes. CONCLUSION: Dapagliflozin reduces the risk of all-cause mortality, heart failure hospitalizations and cardiovascular death in a wide range of heart failure patients.
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spelling pubmed-104539612023-08-26 Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis Ali, Ahmed E. Mazroua, Muhammad Sabry ElSaban, Mariam Najam, Nadia Kothari, Aditi S. Mansoor, Taha Amal, Tanya Lee, Joanna Kashyap, Rahul Glob Heart Review BACKGROUND: Heart failure (HF) is a major cause of recurrent hospitalization and death worldwide. Sodium-glucose cotransporter-2 inhibitors including dapagliflozin are anti-diabetic drugs with promising cardiovascular (CV) effects. We performed systematic review and meta-analysis of randomized controlled trials investigating the effects of dapagliflozin in heart failure patients. METHODS: We searched PubMed, Scopus and ScienceDirect databases. A total of 1,567 studies from January 2017 to September 10, 2022, were screened. After applying exclusion criteria, 22 studies were retrieved for full-text screening, and nine of them were eligible for this meta-analysis. Effect estimates for dichotomous variables were expressed as risk ratio (RR) and 95% CI. The primary outcomes were the incidence of all-cause mortality, hospitalization due to HF, and CV death. This review was registered on PROSPERO with ID CRD42022347793. RESULTS: A total of 14,032 patients were included. The overall risk ratio of all-cause mortality favored the dapagliflozin group over the placebo/standard therapy group (RR = 0.89, 95% CI: 0.82–0.97, P = 0.006) and the pooled studies were not heterogenous (I(2) = 0%). Additionally, dapagliflozin significantly reduced the hospitalization due to heart failure (RR = 0.76, 95% CI: 0.70–0.84, P > 0.00001, I(2) = 0%), cardiovascular death (RR = 0.87, 95% CI: 0.78–0.97, P = 0.01, I(2) = 0%) and their composite outcomes. CONCLUSION: Dapagliflozin reduces the risk of all-cause mortality, heart failure hospitalizations and cardiovascular death in a wide range of heart failure patients. Ubiquity Press 2023-08-22 /pmc/articles/PMC10453961/ /pubmed/37636033 http://dx.doi.org/10.5334/gh.1258 Text en Copyright: © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Ali, Ahmed E.
Mazroua, Muhammad Sabry
ElSaban, Mariam
Najam, Nadia
Kothari, Aditi S.
Mansoor, Taha
Amal, Tanya
Lee, Joanna
Kashyap, Rahul
Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis
title Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis
title_full Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis
title_fullStr Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis
title_full_unstemmed Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis
title_short Effect of Dapagliflozin in Patients with Heart Failure: A Systematic Review and Meta-Analysis
title_sort effect of dapagliflozin in patients with heart failure: a systematic review and meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453961/
https://www.ncbi.nlm.nih.gov/pubmed/37636033
http://dx.doi.org/10.5334/gh.1258
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