CME

CME


Latest Episodes

A Clinical Guide to the Role of Iron in HF Pathophysiology
August 30, 2021

Host: Robert J. Mentz, MD, FHFSA, FACC, FAHA Guest: Peter van der Meer, MD, PhD Iron deficiency is an extremely common comorbidity for 50% to 70% of our patients with heart failure in both the acute and chronic settings. It’s associated with poor e

RCC Treatment Strategies in a Poor-Risk Patient
August 27, 2021

Host: Jay Raman, MD, FACS Guest: Oguz Akin, MD Guest: Robert J. Motzer, MD Guest: Elizabeth Plimack, MD, MS Did you know that the current 5-year survival rate for patients diagnosed with metastatic RCC is only 12% despite advances in molecular

Counseling Your Patients At Risk of HDFN
August 27, 2021

Host: Lee P. Shulman, MD, FACMG, FACOG Guest: Michelle Y. Owens, MD OB-GYN clinicians can improve how they communicate with their patients about hemolytic disease of the fetus and newborn or HDFN. Strategies include encouraging patients to talk abo

Elevated Creatinine and AKI Are NOT Synonymous: Optimal RAASi Therapy Is Always the Goal
August 26, 2021

Host: George L. Bakris, MD Guest: Biykem Bozkurt, MD, PhD, FHFSA, FACC, FAHA, FACP Guest: Robert Toto, MD When treating patients with heart failure and chronic kidney disease, RAASi therapy should be continued if at all possible. One thing to kee

Optimizing RAASi Therapy in Patients with Hyperkalemia: The Role of Potassium Binders
August 25, 2021

Host: Javed Butler, MD, MBA, MPH Guest: Giuseppe M.C. Rosano, MD, PhD, FESC, FHFA It is well understood that RAASi therapy is critical in the management of patients with heart failure. However, hyperkalemia is common in these patients, and its pres

Practicing Precision in ALK and ROS1 Rearrangement Positive NSCLC: Testing, Targets, and Treatments
August 25, 2021

Guest: Maria E. Arcila, MD Guest: Alexander Drilon, MD Capitalizing on the advances in identification of oncogenic driver mutations, genetic testing, and therapeutic approaches that target actionable mutations, targeted therapy is the current stand

Optimizing the Care and Quality of Life for Patients with ADPKD – Part 3: Management
August 16, 2021

Guest: Michel Chonchol, MD Guest: Frederic Rahbari-Oskoui, MD, MS This Expert Exchange webcast aims to improve clinicians’ ability to manage patients diagnosed with ADPKD.

Recognizing & Treating Alpha-1 Antitrypsin Deficiency (AATD)
August 12, 2021

Guest: Cheryl Pirozzi, MD, MS Guest: Charlie Strange, MD Alpha-1 antitrypsin deficiency (AATD) is a common yet underdiagnosed genetic disorder. Led by 2 AATD experts, this activity will address the most current information on the screening, diagnos

Optimizing the Care and Quality of Life for Patients with ADPKD – Part 2: Progression and Prognostication
August 05, 2021

Guest: Matthew B. Lanktree, MD, PhD Guest: Neera Dahl, MD, PhD This Expert Exchange webcast aims to improve clinicians’ ability to properly monitor disease progression and make treatment decisions based on prognostic indicators.

Optimizing the Care and Quality of Life for Patients with ADPKD – Part 1: Detection and Diagnosis
August 04, 2021

Guest: Arlene B. Chapman, MD Guest: Matthew B. Lanktree, MD, PhD This Expert Exchange webcast aims to improve clinicians’ ability to detect and diagnose ADPKD in at-risk patients.