View the presentations in this CME activity and complete the evaluation. Your certificate will be mailed to you upon satisfactory completion of these documents.
Introduction & Pre-CME Questions
Matthew R. Weir, MD
Diabetes, Kidney and Heart Disease- Overview
Matthew R. Weir, MD
Pathogenesis of CKD in Diabetes
Susanne B. Nicholas, MD
Management Diabetic Kidney Disease- Circa 2022
Peter Rossing, MD, DMSc
Panel Discussion and Q&A - Closing the Loop- the Management of CKD in DM
Panel:
Peter Rossing, MD • DMSc • Matthew R. Weir, MD • Yehuda Handelsman, MD
Moderator: Mikhail Kosiborod, MD
Professor and Chief
Division of Nephrology
Department of Medicine
University of Maryland School of Medicine
Baltimore, Maryland
Research leader, professor
Complications Research
Copenhagen, Denmark
Diabetic kidney disease (DKD), type 2 diabetes (T2D) cardiovascular disease (CVD), and heart failure (HF) share a common etiology involving hyperglycemia, hypertension, inflammation, fibrosis, oxidative stress, and increased renin-angiotensinaldosterone system (RAAS) activity. Both CKD and T2D are common, affecting 14% and 11% of the US population, respectively. 36% of patients with diabetes also have DKD, which is the leading cause of end-stage renal disease (ESRD) and more than doubles their risk of cardiovascular events and triples the risk of heart failure (HF). Traditional approach to management of CKD has been based on blocking RAAS with ACE and ARB inhibitors. Yet, achieving optimal outcomes from treating DKD and T2D remains a challenge. Identifying patients with eGFR and spot urinary albumin-creatinine ratio is valuable and would support early intervention. Recently sodium glucose cotransporter 2 (SGLT2) inhibitors were added to the management of these patients. Diabetes kidney disease progression is also driven by inflammation and fibrosis underscoring the need for newer medications. A new class the nonsteroidal MRAs specifically finerenone has shown significant clinical benefits with reduced side effect profile as seen by the recent CVOTs FIDELIO and FIGARO. In these studies, finerenone improved CKD and heart disease in patients with DKD. In this CME symposium we will explore these issues addressing the pathophysiology of DKD and the contemporary role of its management with focus on the role of the new class of non-steroidal MRA CKD, CVD and HF outcome.
Upon completion of this CME symposium, participants should be able to:
This educational initiative is designed for cardiologists, nephrologists, endocrinologists, primary care physicians, internists, and other healthcare professionals interested in the Epidemiology, pathophysiology, prevention, and treatment of diabetes with CKD and prevention of related morbidity and mortality.
This activity has been planned and implemented in accordance with the Essential Areas and Policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of PESI Inc., and Metabolic Endocrine Education Foundation (MEEF). PESI Inc., is accredited by the ACCME to provide continuing medical education for physicians.
PESI, Inc, designated this live educational activity for a maximum of 1.75 AMA PRA Category 1 Credit(s).
For information please contact: [email protected] or 818 342 1889
This is a CME Program Supported by an Educational Grant from Bayer