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Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin

Background Previously, dapagliflozin was limited to patients with an estimated glomerular filtration rate (eGFR) ≥ 60 mL/min/1.73 m(2), while empagliflozin can be used for those with an eGFR ≥ 45 mL/min/1.73 m(2). Therefore dapagliflozin was switched to empagliflozin in many patients when eGFR decre...

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Autores principales: Yang, Ai-Yu, Chen, Hung-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352843/
https://www.ncbi.nlm.nih.gov/pubmed/33258006
http://dx.doi.org/10.1007/s11096-020-01210-1
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author Yang, Ai-Yu
Chen, Hung-Chun
author_facet Yang, Ai-Yu
Chen, Hung-Chun
author_sort Yang, Ai-Yu
collection PubMed
description Background Previously, dapagliflozin was limited to patients with an estimated glomerular filtration rate (eGFR) ≥ 60 mL/min/1.73 m(2), while empagliflozin can be used for those with an eGFR ≥ 45 mL/min/1.73 m(2). Therefore dapagliflozin was switched to empagliflozin in many patients when eGFR decreased. However, the clinical efficacy and safety of these switcfhes are not clear. Objective In this study, we compared the efficacy and renal safety between patients switching from dapagliflozin to empagliflozin in patients. Setting This is a retrospective study of adult patients (aged ≥ 20 years) who had attended the Kaohsiung Medical University Hospital. Method This retrospective observational study included patients who were switched from dapagliflozin to empagliflozin. To assess the effect of other hypoglycemic drugs on efficacy, the types and dose alterations of other hypoglycemic drugs were classified on the defined daily dose (DDD). Main outcome measure The primary outcome measure was the change in hemoglobin A1c (HbA1c) level after 6 months. Patients with HbA1c levels at or lower than the baseline value after 6 months were defined as effective and patients with levels higher than the baseline were defined as invalid. Safety was evaluated by comparing the difference of eGFR between the baseline value and 6 months after treatment. Results Overall, 111 patients were enrolled in the study. Six months after switching from dapagliflozin to empagliflozin, HbA1c significantly reduced, with no statistically significant difference observed in eGFR. In our study, 78 patients were assigned to the effective group (70.3%) and 33 patients were invalid (29.7%). When the other hypoglycemic drugs were grouped by total dosage, fasting plasma glucose and HbA1c only decreased significantly in the "DDD decrease" and "DDD increase" groups. Conclusion Our study showed that switching from dapagliflozin to empagliflozin in patients with type 2 diabetes was effective for blood glucose maintenance and caused no significant changes in renal function. In addition, compared to similar sodium-glucose co-transporter-2 inhibitors, other hypoglycemic drugs may be factors that influence the efficacy of sugar-lowering treatments.
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spelling pubmed-83528432021-08-24 Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin Yang, Ai-Yu Chen, Hung-Chun Int J Clin Pharm Research Article Background Previously, dapagliflozin was limited to patients with an estimated glomerular filtration rate (eGFR) ≥ 60 mL/min/1.73 m(2), while empagliflozin can be used for those with an eGFR ≥ 45 mL/min/1.73 m(2). Therefore dapagliflozin was switched to empagliflozin in many patients when eGFR decreased. However, the clinical efficacy and safety of these switcfhes are not clear. Objective In this study, we compared the efficacy and renal safety between patients switching from dapagliflozin to empagliflozin in patients. Setting This is a retrospective study of adult patients (aged ≥ 20 years) who had attended the Kaohsiung Medical University Hospital. Method This retrospective observational study included patients who were switched from dapagliflozin to empagliflozin. To assess the effect of other hypoglycemic drugs on efficacy, the types and dose alterations of other hypoglycemic drugs were classified on the defined daily dose (DDD). Main outcome measure The primary outcome measure was the change in hemoglobin A1c (HbA1c) level after 6 months. Patients with HbA1c levels at or lower than the baseline value after 6 months were defined as effective and patients with levels higher than the baseline were defined as invalid. Safety was evaluated by comparing the difference of eGFR between the baseline value and 6 months after treatment. Results Overall, 111 patients were enrolled in the study. Six months after switching from dapagliflozin to empagliflozin, HbA1c significantly reduced, with no statistically significant difference observed in eGFR. In our study, 78 patients were assigned to the effective group (70.3%) and 33 patients were invalid (29.7%). When the other hypoglycemic drugs were grouped by total dosage, fasting plasma glucose and HbA1c only decreased significantly in the "DDD decrease" and "DDD increase" groups. Conclusion Our study showed that switching from dapagliflozin to empagliflozin in patients with type 2 diabetes was effective for blood glucose maintenance and caused no significant changes in renal function. In addition, compared to similar sodium-glucose co-transporter-2 inhibitors, other hypoglycemic drugs may be factors that influence the efficacy of sugar-lowering treatments. Springer International Publishing 2020-11-30 2021 /pmc/articles/PMC8352843/ /pubmed/33258006 http://dx.doi.org/10.1007/s11096-020-01210-1 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Yang, Ai-Yu
Chen, Hung-Chun
Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin
title Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin
title_full Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin
title_fullStr Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin
title_full_unstemmed Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin
title_short Study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin
title_sort study comparing the efficacy and renal safety for patients with diabetes switching from dapagliflozin to empagliflozin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8352843/
https://www.ncbi.nlm.nih.gov/pubmed/33258006
http://dx.doi.org/10.1007/s11096-020-01210-1
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