Significant disparities in the healthcare system limit access to specialized care, advanced diagnostics, and novel treatments for hypertrophic cardiomyopathy (HCM), particularly affecting patients in rural, underserved, and minority communities. Barriers such as inadequate referral pathways, insurance coverage issues, and socioeconomic factors delay diagnosis and hinder access to advanced and disease-modifying therapies. Additionally, the underrepresentation of minority populations in HCM clinical trials compromises the applicability of research findings to diverse patient groups, further exacerbating inequities in care.
Join our esteemed panel of experts to learn about HCM in underserved and minority populations focusing on key diagnostic challenges, access to medical therapy and emerging treatments, and how to address systemic inequities through shared decision making to improve outcomes and quality of life for all patients with HCM.
CHAIRPERSON
Carolyn Y. Ho, MD
Professor of Medicine, Harvard Medical School
Medical Director, Cardiovascular Genetics Center
Brigham and Women’s Hospital
Boston, Massachusetts
PANELIST
Sharon Cresci, MD
Professor of Medicine and Genetics
Associate director, WUMS/BJH Hypertrophic Cardiomyopathy Center
Director, IMPACT (Initiative for Mentoring, Promoting Networking and Advocacy for Cardiology Trainees)
Washington University
Cardiovascular Division
St Louis, Missouri
PANELIST
Nosheen Reza, MD, MS, FACC, FHFSA
Assistant Professor of Medicine
Penn Center for Inherited Cardiovascular Disease
Section of Advanced Heart Failure, Transplantation, and Mechanical Support
University of Pennsylvania
Philadelphia, Pennsylvania
2121 S Prairie Ave, Chicago, Illinois, 60616
Room: Grand Horizon BC