2019 update to: Management of hyperglycaemia in type 2 diabetes, 2018. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)

被引:0
作者
John B. Buse
Deborah J. Wexler
Apostolos Tsapas
Peter Rossing
Geltrude Mingrone
Chantal Mathieu
David A. D’Alessio
Melanie J. Davies
机构
[1] University of North Carolina School of Medicine,Department of Medicine
[2] Massachusetts General Hospital,Department of Medicine and Diabetes Unit
[3] Harvard Medical School,Second Medical Department
[4] Aristotle University Thessaloniki,Diabetes and Nutritional Sciences
[5] Steno Diabetes Center Copenhagen,Clinical and Experimental Endocrinology, UZ Gasthuisberg
[6] University of Copenhagen,Department of Medicine
[7] Fondazione Policlinico Universitario A. Gerelli IRCCS,undefined
[8] Università Cattolica del Sacro Cuore,undefined
[9] King’s College London,undefined
[10] KU Leuven,undefined
[11] Duke University School of Medicine,undefined
[12] Diabetes Research Centre,undefined
[13] University of Leicester,undefined
[14] Leicester General Hospital,undefined
来源
Diabetologia | 2020年 / 63卷
关键词
Cardiovascular disease; Chronic kidney disease; Glucose-lowering therapy; Guidelines; Heart failure; Hypoglycaemia; Patient-centred care; Type 2 diabetes mellitus;
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摘要
The American Diabetes Association and the European Association for the Study of Diabetes have briefly updated their 2018 recommendations on management of hyperglycaemia, based on important research findings from large cardiovascular outcomes trials published in 2019. Important changes include: (1) the decision to treat high-risk individuals with a glucagon-like-peptide 1 (GLP-1) receptor agonist or sodium–glucose cotransporter 2 (SGLT2) inhibitor to reduce major adverse cardiovascular events (MACE), hospitalisation for heart failure (hHF), cardiovascular death or chronic kidney disease (CKD) progression should be considered independently of baseline HbA1c or individualised HbA1c target; (2) GLP-1 receptor agonists can also be considered in patients with type 2 diabetes without established cardiovascular disease (CVD) but with the presence of specific indicators of high risk; and (3) SGLT2 inhibitors are recommended in patients with type 2 diabetes and heart failure, particularly those with heart failure with reduced ejection fraction, to reduce hHF, MACE and CVD death, as well as in patients with type 2 diabetes with CKD (eGFR 30 to ≤60 ml min−1 [1.73 m]−2 or urinary albumin-to-creatinine ratio >30 mg/g, particularly >300 mg/g) to prevent the progression of CKD, hHF, MACE and cardiovascular death.
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页码:221 / 228
页数:7
相关论文
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