Listen to this expert discussion on identifying and managing PAH, including earlier and accurate diagnosis, treatment approaches, and the impact of disease progression.

Acid sphingomyelinase deficiency (ASMD), also known as Niemann-Pick disease, is a rare autosomal recessive lysosomal storage disorder (LSD) which can be challenging to diagnose and manage. This activity will offer access to the latest information and best practices to facilitate the early recognition of signs and symptoms and accurate diagnosis of ASMD.

This activity has been designed to address the educational needs of cardiologists, interventional cardiologists, primary care providers, allied healthcare professionals (ie, nurse practitioners, PAs, and pharmacists), and other clinicians involved in the care of patients with cardiovascular disease.

Recognize the varied phenotypic presentation and underlying genotypes of hATTR amyloidosis

Demonstrate appropriate, guideline-based decision-making related to the selection, initiation, and duration of pharmacotherapy for patients with VTE

With the expanding use of SGLT2 inhibitors beyond glucose control, this AI-driven activity will inform clinicians about the available evidence assessing their efficacy and safety in CKD, renoprotective benefits in patients with CKD with and without T2DM, evolving practice standards, and their relevance to patient care.

This case-based enduring simulcast will cover the treatment and management of patients with type 2 diabetes mellitus.