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Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study

BACKGROUND: Sodium-glucose cotransporter 2 inhibitor (SGLT2i) should be considered for patients with type 2 diabetes (T2D) and chronic kidney disease (CKD) having estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m(2) and urine albumin-to-creatinine ratio (UACR) > 30 mg/g. However, SGL...

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Autores principales: Jeong, Su Jin, Lee, Seung Eun, Shin, Dong Hyun, Park, Ie Byung, Lee, Hui Seung, Kim, Kyoung-Ah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122538/
https://www.ncbi.nlm.nih.gov/pubmed/33990175
http://dx.doi.org/10.1186/s12882-021-02381-3
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author Jeong, Su Jin
Lee, Seung Eun
Shin, Dong Hyun
Park, Ie Byung
Lee, Hui Seung
Kim, Kyoung-Ah
author_facet Jeong, Su Jin
Lee, Seung Eun
Shin, Dong Hyun
Park, Ie Byung
Lee, Hui Seung
Kim, Kyoung-Ah
author_sort Jeong, Su Jin
collection PubMed
description BACKGROUND: Sodium-glucose cotransporter 2 inhibitor (SGLT2i) should be considered for patients with type 2 diabetes (T2D) and chronic kidney disease (CKD) having estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m(2) and urine albumin-to-creatinine ratio (UACR) > 30 mg/g. However, SGLT2i is currently underprescribed among eligible, at-risk patients for CKD progression. We analyzed prescription patterns and barriers to initiating SGLT2i in patients with T2D and CKD in real practice. METHODS: A total of 3,703 consecutive outpatients with T2D from four teaching hospitals during six months (2019 ~ 2020) were reviewed. Five eGFR categories (G1, ≥ 90; G2, 60–89; G3ab, 30–59; G4-5, < 30 mL/min/1.73 m(2)) and three UACR categories (A1, < 30; A2, 30–300; A3, > 300 mg/g) were used to define CKD status. RESULTS: Overall, 25.8 % patients received SGLT2i in the following eGFR and albuminuria categories: G1 (A1, 31 %; A2, 48 %; A3, 45 %); G2 (A1, 18 %; A2, 24 %; A3, 30%); and G3 (A1, 9 %; A2, 7 %; A3, 13 %). Total prevalence estimate of CKD was 33.8 % (n = 1,253), of whom 25.6 % patients received SGLT2i. We defined eGFR ≥ 45 mL/min/1.73 m(2) and UACR ≥ 30 mg/g as high-risk CKD group eligible for SGLT2i (n = 905), of whom 32.9 % patients were treated with an SGLT2i. In this high-risk group, SGLT2i initiation showed negative correlations with age ≥ 65 years and recent hospitalization. Conversely, HbA1c level, body mass index (BMI), presence of diabetic retinopathy, and previous heart failure events were positively correlated with SGLT2i initiation. CONCLUSIONS: Only 32.9 % of T2D with CKD eligible for SGLT2i is currently treated with SGLT2i in real-world clinical practice. The older patient group and clinical inertia are the main barriers to initiate SGLT2i for eligible patients. Clinicians should change the glucocentric approach and focus on reducing renal events in T2D. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-021-02381-3.
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spelling pubmed-81225382021-05-17 Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study Jeong, Su Jin Lee, Seung Eun Shin, Dong Hyun Park, Ie Byung Lee, Hui Seung Kim, Kyoung-Ah BMC Nephrol Research BACKGROUND: Sodium-glucose cotransporter 2 inhibitor (SGLT2i) should be considered for patients with type 2 diabetes (T2D) and chronic kidney disease (CKD) having estimated glomerular filtration rate (eGFR) ≥ 30 mL/min/1.73 m(2) and urine albumin-to-creatinine ratio (UACR) > 30 mg/g. However, SGLT2i is currently underprescribed among eligible, at-risk patients for CKD progression. We analyzed prescription patterns and barriers to initiating SGLT2i in patients with T2D and CKD in real practice. METHODS: A total of 3,703 consecutive outpatients with T2D from four teaching hospitals during six months (2019 ~ 2020) were reviewed. Five eGFR categories (G1, ≥ 90; G2, 60–89; G3ab, 30–59; G4-5, < 30 mL/min/1.73 m(2)) and three UACR categories (A1, < 30; A2, 30–300; A3, > 300 mg/g) were used to define CKD status. RESULTS: Overall, 25.8 % patients received SGLT2i in the following eGFR and albuminuria categories: G1 (A1, 31 %; A2, 48 %; A3, 45 %); G2 (A1, 18 %; A2, 24 %; A3, 30%); and G3 (A1, 9 %; A2, 7 %; A3, 13 %). Total prevalence estimate of CKD was 33.8 % (n = 1,253), of whom 25.6 % patients received SGLT2i. We defined eGFR ≥ 45 mL/min/1.73 m(2) and UACR ≥ 30 mg/g as high-risk CKD group eligible for SGLT2i (n = 905), of whom 32.9 % patients were treated with an SGLT2i. In this high-risk group, SGLT2i initiation showed negative correlations with age ≥ 65 years and recent hospitalization. Conversely, HbA1c level, body mass index (BMI), presence of diabetic retinopathy, and previous heart failure events were positively correlated with SGLT2i initiation. CONCLUSIONS: Only 32.9 % of T2D with CKD eligible for SGLT2i is currently treated with SGLT2i in real-world clinical practice. The older patient group and clinical inertia are the main barriers to initiate SGLT2i for eligible patients. Clinicians should change the glucocentric approach and focus on reducing renal events in T2D. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12882-021-02381-3. BioMed Central 2021-05-14 /pmc/articles/PMC8122538/ /pubmed/33990175 http://dx.doi.org/10.1186/s12882-021-02381-3 Text en © The Author(s) 2021 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jeong, Su Jin
Lee, Seung Eun
Shin, Dong Hyun
Park, Ie Byung
Lee, Hui Seung
Kim, Kyoung-Ah
Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study
title Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study
title_full Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study
title_fullStr Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study
title_full_unstemmed Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study
title_short Barriers to initiating SGLT2 inhibitors in diabetic kidney disease: a real-world study
title_sort barriers to initiating sglt2 inhibitors in diabetic kidney disease: a real-world study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122538/
https://www.ncbi.nlm.nih.gov/pubmed/33990175
http://dx.doi.org/10.1186/s12882-021-02381-3
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