2022 Canadian Cardiovascular Society Guideline for Use of GLP-1 Receptor Agonists and SGLT2 Inhibitors for Cardiorenal Risk Reduction in Adults.

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Clinical Guidelines
Authored By
"Mancini, G B John , O'Meara, Eileen , Zieroth, Shelley , Bernier, Mathieu , Cheng, Alice Y Y , Cherney, David Z I , Connelly, Kim A , Ezekowitz, Justin , Goldenberg, Ronald M , Leiter, Lawrence A , Nesrallah, Gihad , Paty, Breay W , Piché, Marie-Eve , Senior, Peter , Sharma, Abhinav , Verma, Subodh , Woo, Vincent , Darras, Pol , Grégoire, Jean , Lonn, Eva , Stone, James A , Yale, Jean-François , Yeung, Colin , Zimmerman, Deborah"
Interests
Endocrinology
Cardiology
Speciality
Cardiology
Endocrinology
Book Detail
Publisher
Elsevier
volume
38
ISSN
1916-7075 ; Electronic
No. of pages
15
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Event Data
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ISSN
1916-7075 ; Electronic
IS_Ebsco
true
Description

This guideline synthesizes clinical trial data supporting the role of glucagon-like peptide-1 receptor agonists and sodium-glucose co-transporter 2 inhibitors (SGLT2i) for treatment of heart failure (HF), chronic kidney disease, and for optimizing prevention of cardiorenal morbidity and mortality in patients with type 2 diabetes. It is on the basis of a companion systematic review and meta-analysis guided by a focused set of population, intervention, control, and outcomes (PICO) questions that address priority cardiorenal end points. The Grading of Recommendations, Assessment, Development, and Evaluation (GRADE) system and a modified Delphi process were used. We encourage comprehensive assessment of cardiovascular (CV) patients with routine measurement of estimated glomerular filtration rate, urinary albumin-creatinine ratio, glycosylated hemoglobin (A1c), and documentation of left ventricular ejection fraction (LVEF) when evaluating symptoms of HF. For patients with HF, we recommend integration of SGLT2i with other guideline-directed pharmacotherapy for the reduction of hospitalization for HF when LVEF is > 40% and for the reduction of all-cause and CV mortality, hospitalization for HF, and renal protection when LVEF is ≤ 40%. In patients with albuminuric chronic kidney disease, we recommend integration of SGLT2i with other guideline-directed pharmacotherapy to reduce all-cause and CV mortality, nonfatal myocardial infarction, and hospitalization for HF. We provide recommendations and algorithms for the selection of glucagon-like peptide-1 receptor agonists and SGLT2i for patients with type 2 diabetes and either established atherosclerotic CV disease or risk factors for atherosclerotic CV disease to reduce all-cause and CV mortality, nonfatal stroke, and for the prevention of hospitalization for HF and decline in renal function. We offer practical advice for safe use of these diabetes-associated agents with profound cardiorenal benefits.

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