Bradley B. Keller, MD
- Medical Director, Greater Louisville and Western KY Practice, Heart Institute
- Professor, UC Department of Pediatrics
- brad.keller@cchmc.org
- 502-584-3200
- 502-584-3333
- Board Certified
About
Biography
I am a clinician-investigator providing care to children and adults with congenital heart disease throughout Kentucky. I specialize in understanding the causes of congenital heart disease and developing and testing novel technologies for heart disease patients. On March 1, 2020, I joined the Cincinnati Children's Heart Institute and Dr. Juan Villafañe as co-director of Cincinnati Children’s Heart Institute – Greater Louisville and Western Kentucky practices. I work at our offices throughout the region.
With over 30 years of clinical and administrative congenital heart care experience, I have previously served as division chief of Pediatric Cardiology at the University of Kentucky and at the Children’s Hospital of Pittsburgh.
Pediatric Cardiology Fellowship: University of Rochester Medical Center, Rochester, NY, 1988-1991.
Pediatric Residency: Johns Hopkins Hospital, Baltimore, MD, 1985-1988.
MD: Pennsylvania State University School of Medicine, Hershey, PA, 1981-1985.
BS: University of Pennsylvania, Philadelphia, PA, 1977-1981.
Interests
Pediatric and adult congenital heart disease
Interests
Clinical translation of outpatient telemedicine
Research Areas
Insurance Information
Cincinnati Children's strives to accept a wide variety of health plans. Please contact your health insurance carrier to verify coverage for your specific benefit plan.
Publications
Treprostinil Effectiveness in Higher-Risk Pediatric Patients With Idiopathic and Heritable Pulmonary Arterial Hypertension. Canadian Journal of Cardiology. 2024; 40:613-621.
Percutaneous coronary intervention combined with treat-repair-treat strategy in a patient with pulmonary arterial hypertension associated with atrial septal defect and left main coronary compression syndrome. International Journal of Cardiology Congenital Heart Disease. 2023; 13:100458.
Right Heart Catheterization in Pediatric Pulmonary Arterial Hypertension: Insights and Outcome from a Large Tertiary Center. Journal of Clinical Medicine. 2022; 11:5374.
Sulforaphane Does Not Protect Right Ventricular Systolic and Diastolic Functions in Nrf2 Knockout Pulmonary Artery Hypertension Mice. Cardiovascular Drugs and Therapy. 2022; 36:425-436.
Isolated Coarctation of the Aorta: Current Concepts and Perspectives. Frontiers in Cardiovascular Medicine. 2022; 9:817866.
Pulmonary hypertensive crisis in children with pulmonary arterial hypertension undergoing cardiac catheterization. Pulmonary Circulation. 2022; 12:e12067.
Ferroptosis is essential for diabetic cardiomyopathy and is prevented by sulforaphane via AMPK/NRF2 pathways. Acta Pharmaceutica Sinica B. 2022; 12:708-722.
Better Outcomes in Pulmonary Arterial Hypertension After Repair of Congenital Heart Disease, Compared With Idiopathic Pulmonary Arterial Hypertension. CJC Open. 2021; 3:872-879.
Emerging roles of microRNA-208a in cardiology and reverse cardio-oncology. Medicinal Research Reviews. 2021; 41:2172-2194.
Engineered cardiac tissues: a novel in vitro model to investigate the pathophysiology of mouse diabetic cardiomyopathy. Acta Pharmacologica Sinica. 2021; 42:932-941.
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