HbA1c and beyond
Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt
The Kidney Disease: Improving Global Outcomes (KDIGO) Clinical Practice Guideline on Diabetes Management in Chronic Kidney Disease from 2020 comes at an opportune time when progress in diabetes technology and therapeutics offers new options to manage the large population of patients with diabetes and chronic kidney disease (CKD) at high risk of poor health outcomes. Management of haemoglobin A1c is important in diabetes, but an enlarging base of evidence from large clinical trials has demonstrated important new treatments offering organ protection and not just glucose management, such as sodium-glucose cotransporter 2 inhibitors and glucagon-like peptide-1 receptor agonists. It is the ambition that the guideline can help to optimize the clinical care of people with diabetes and CKD by integrating new options with existing management strategies based on high-quality evidence. Here, the focus has been on comprehensive care of patients with diabetes and CKD, glycaemic monitoring and targets, antihyperglycaemic therapies in patients with diabetes and CKD, and new developments since the guideline was published offering new opportunities and a wider target population for the new interventions.
Originalsprog | Engelsk |
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Tidsskrift | Nephrology Dialysis Transplantation |
Vol/bind | 38 |
Udgave nummer | 1 |
Sider (fra-til) | 34-40 |
Antal sider | 7 |
ISSN | 0931-0509 |
DOI | |
Status | Udgivet - 2023 |
Bibliografisk note
Funding Information:
ACKNOWLEDGEMENTS This review was written on the occasion of a presentation at ERA-EDTA 2021. I am indebted to the hard work of the KDIGO staff, evidence review team and the Work Group for diabetes and CKD guideline that were involved in developing the KDIGO guideline for management of diabetes in CKD [2]. FUNDING P.R. has been funded by the Novo Nordisk Foundation grant PROTON on Personalised Treatment of Diabetic Nephropathy NNF14OC0013659 and PRIMETIME NNF19OC0058900.
Publisher Copyright:
© 2021 The Author(s). Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved.
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