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Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study
AIMS: To evaluate effectiveness and healthcare resource utilization (HCRU) of empagliflozin versus dipeptidyl peptidase‐4 inhibitors (DPP‐4i) in Swedish clinical practice, as part of the EMPRISE EU study (EUPAS27606, NCT03817463). MATERIALS AND METHODS: A non‐interventional, cohort study using retro...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092061/ https://www.ncbi.nlm.nih.gov/pubmed/36097728 http://dx.doi.org/10.1111/dom.14870 |
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author | Nyström, Thomas Toresson Grip, Emilie Gunnarsson, Joel Casajust, Paula Karlsdotter, Kristina Skogsberg, Josefin Ustyugova, Anastasia |
author_facet | Nyström, Thomas Toresson Grip, Emilie Gunnarsson, Joel Casajust, Paula Karlsdotter, Kristina Skogsberg, Josefin Ustyugova, Anastasia |
author_sort | Nyström, Thomas |
collection | PubMed |
description | AIMS: To evaluate effectiveness and healthcare resource utilization (HCRU) of empagliflozin versus dipeptidyl peptidase‐4 inhibitors (DPP‐4i) in Swedish clinical practice, as part of the EMPRISE EU study (EUPAS27606, NCT03817463). MATERIALS AND METHODS: A non‐interventional, cohort study using retrospectively collected data from Swedish national registries. Adults with type 2 diabetes newly initiated on empagliflozin or DPP‐4i from May 2014 to December 2018 were matched 1:1 using propensity scores based on >180 covariates. Cardiovascular outcomes included hospitalization for heart failure (HHF), all‐cause mortality (ACM), myocardial infarction (MI), stroke and cardiovascular mortality (CVM), as well as their composite outcomes. Renal outcomes included end‐stage renal disease (ESRD), estimated glomerular filtration rate (eGFR) decline to <60 ml/min/1.73 m(2) and progression to micro/macroalbuminuria. HCRU outcomes were also assessed. Comparisons were done using Cox proportional hazards and Poisson regression models. RESULTS: Overall, 15,785 matched‐pairs were identified, with a mean follow‐up of 6.4 and 9.7 months for patients initiating empagliflozin versus DPP‐4i, respectively. Empagliflozin was associated with significant reduction in rates of HHF (hazard ratio [HR] = 0.67; 95% confidence interval: 0.49‐0.91), ACM (HR = 0.53; 0.41‐0.68), HHF + ACM (HR = 0.59; 0.48‐0.73), MI + stroke + ACM (HR = 0.68; 0.57‐0.81), CVM (HR = 0.46; 0.29‐0.73), HHF + CVM (HR = 0.61; 0.47‐0.79) and MI + stroke + CVM (HR = 0.79; 0.63‐0.98) versus DPP‐4i. Empagliflozin also reduced the rates of ESRD (HR = 0.13; 0.03‐0.57) and eGFR decline (HR = 0.83; 0.70‐0.99). Regarding HCRU, empagliflozin was associated with lower risk of first inpatient stay (HR = 0.87; 0.81‐0.93), and lower rate of inpatient and outpatient visits (rate ratio [RR] = 0.85; 0.80‐0.89 and RR = 0.96; 0.94‐0.98) than DPP‐4i. CONCLUSIONS: Empagliflozin treatment compared to DPP‐4i reduced cardiorenal events and overall mortality, which may explain lower HCRU among empagliflozin users in Sweden. |
format | Online Article Text |
id | pubmed-10092061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-100920612023-04-13 Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study Nyström, Thomas Toresson Grip, Emilie Gunnarsson, Joel Casajust, Paula Karlsdotter, Kristina Skogsberg, Josefin Ustyugova, Anastasia Diabetes Obes Metab Original Articles AIMS: To evaluate effectiveness and healthcare resource utilization (HCRU) of empagliflozin versus dipeptidyl peptidase‐4 inhibitors (DPP‐4i) in Swedish clinical practice, as part of the EMPRISE EU study (EUPAS27606, NCT03817463). MATERIALS AND METHODS: A non‐interventional, cohort study using retrospectively collected data from Swedish national registries. Adults with type 2 diabetes newly initiated on empagliflozin or DPP‐4i from May 2014 to December 2018 were matched 1:1 using propensity scores based on >180 covariates. Cardiovascular outcomes included hospitalization for heart failure (HHF), all‐cause mortality (ACM), myocardial infarction (MI), stroke and cardiovascular mortality (CVM), as well as their composite outcomes. Renal outcomes included end‐stage renal disease (ESRD), estimated glomerular filtration rate (eGFR) decline to <60 ml/min/1.73 m(2) and progression to micro/macroalbuminuria. HCRU outcomes were also assessed. Comparisons were done using Cox proportional hazards and Poisson regression models. RESULTS: Overall, 15,785 matched‐pairs were identified, with a mean follow‐up of 6.4 and 9.7 months for patients initiating empagliflozin versus DPP‐4i, respectively. Empagliflozin was associated with significant reduction in rates of HHF (hazard ratio [HR] = 0.67; 95% confidence interval: 0.49‐0.91), ACM (HR = 0.53; 0.41‐0.68), HHF + ACM (HR = 0.59; 0.48‐0.73), MI + stroke + ACM (HR = 0.68; 0.57‐0.81), CVM (HR = 0.46; 0.29‐0.73), HHF + CVM (HR = 0.61; 0.47‐0.79) and MI + stroke + CVM (HR = 0.79; 0.63‐0.98) versus DPP‐4i. Empagliflozin also reduced the rates of ESRD (HR = 0.13; 0.03‐0.57) and eGFR decline (HR = 0.83; 0.70‐0.99). Regarding HCRU, empagliflozin was associated with lower risk of first inpatient stay (HR = 0.87; 0.81‐0.93), and lower rate of inpatient and outpatient visits (rate ratio [RR] = 0.85; 0.80‐0.89 and RR = 0.96; 0.94‐0.98) than DPP‐4i. CONCLUSIONS: Empagliflozin treatment compared to DPP‐4i reduced cardiorenal events and overall mortality, which may explain lower HCRU among empagliflozin users in Sweden. Blackwell Publishing Ltd 2022-10-10 2023-01 /pmc/articles/PMC10092061/ /pubmed/36097728 http://dx.doi.org/10.1111/dom.14870 Text en © 2022 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Nyström, Thomas Toresson Grip, Emilie Gunnarsson, Joel Casajust, Paula Karlsdotter, Kristina Skogsberg, Josefin Ustyugova, Anastasia Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study |
title | Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study |
title_full | Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study |
title_fullStr | Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study |
title_full_unstemmed | Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study |
title_short | Empagliflozin reduces cardiorenal events, healthcare resource use and mortality in Sweden compared to dipeptidyl peptidase‐4 inhibitors: Real world evidence from the Nordic EMPRISE study |
title_sort | empagliflozin reduces cardiorenal events, healthcare resource use and mortality in sweden compared to dipeptidyl peptidase‐4 inhibitors: real world evidence from the nordic emprise study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092061/ https://www.ncbi.nlm.nih.gov/pubmed/36097728 http://dx.doi.org/10.1111/dom.14870 |
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