Worldwide inertia to the use of cardiorenal protective glucose-lowering drugs (SGLT2i and GLP-1 RA) in high-risk patients with type 2 diabetes
Language English Country England, Great Britain Media electronic
Document type Journal Article
PubMed
33097060
PubMed Central
PMC7585305
DOI
10.1186/s12933-020-01154-w
PII: 10.1186/s12933-020-01154-w
Knihovny.cz E-resources
- Keywords
- Cardiorenal protection, Clinical inertia, Glucose lowering drugs, Type 2 diabetes,
- MeSH
- Glucagon-Like Peptide-1 Receptor Agonists MeSH
- Biomarkers blood MeSH
- Global Health MeSH
- Diabetes Mellitus, Type 2 * blood diagnosis drug therapy epidemiology MeSH
- Sodium-Glucose Transporter 2 Inhibitors * adverse effects therapeutic use MeSH
- Risk Assessment MeSH
- Incretins * adverse effects therapeutic use MeSH
- Cardiovascular Diseases * diagnosis epidemiology prevention & control MeSH
- Clinical Decision-Making MeSH
- Blood Glucose * drug effects metabolism MeSH
- Practice Patterns, Physicians' MeSH
- Humans MeSH
- Evidence-Based Medicine MeSH
- Kidney Diseases * diagnosis epidemiology prevention & control MeSH
- Protective Factors MeSH
- Glycemic Control * adverse effects MeSH
- Risk Factors MeSH
- Practice Guidelines as Topic MeSH
- Treatment Outcome MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Glucagon-Like Peptide-1 Receptor Agonists MeSH
- Biomarkers MeSH
- Sodium-Glucose Transporter 2 Inhibitors * MeSH
- GLP1R protein, human MeSH Browser
- Incretins * MeSH
- Blood Glucose * MeSH
The disclosure of proven cardiorenal benefits with certain antidiabetic agents was supposed to herald a new era in the management of type 2 diabetes (T2D), especially for the many patients with T2D who are at high risk for cardiovascular and renal events. However, as the evidence in favour of various sodium-glucose transporter-2 inhibitor (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP-1 RA) accumulates, prescriptions of these agents continue to stagnate, even among eligible, at-risk patients. By contrast, dipeptidyl peptidase-4 inhibitors (DPP-4i) DPP-4i remain more widely used than SGLT2i and GLP-1 RA in these patients, despite a similar cost to SGLT2i and a large body of evidence showing no clear benefit on cardiorenal outcomes. We are a group of diabetologists united by a shared concern that clinical inertia is preventing these patients from receiving life-saving treatments, as well as placing them at greater risk of hospitalisation for heart failure and progression of renal disease. We propose a manifesto for change, in order to increase uptake of SGLT2i and GLP-1 RA in appropriate patients as a matter of urgency, especially those who could be readily switched from an agent without proven cardiorenal benefit. Central to our manifesto is a shift from linear treatment algorithms based on HbA1c target setting to parallel, independent considerations of atherosclerotic cardiovascular disease, heart failure and renal risks, in accordance with newly updated guidelines. Finally, we call upon all colleagues to play their part in implementing our manifesto at a local level, ensuring that patients do not pay a heavy price for continued clinical inertia in T2D.
Department of Diabetes Carol Davila University of Medicine and Pharmacy Bucharest Romania
Department of Diabetology National Medical Academy for Postgraduate Education Kiev Ukraine
Department of Endocrinology Medical University Sofia 2 Zdrave Street Sofia Bulgaria
Division of Endocrinology Diabetes and Metabolism University Hospital Basel Basel Switzerland
Faculty of Medicine Josip Juraj Strossmayer University of Osijek Osijek Croatia
Medical University of Vienna Vienna Austria
National Institute of Endocrinology and Diabetology Lubochna Slovak Republic
Riga East Clinical Hospital Riga Latvia
Riga Stradins University Riga Latvia
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The management of type 2 diabetes before, during and after Covid-19 infection: what is the evidence?