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
Services and Specialties
Adolescent and Adult Congenital Heart Disease, Heart Institute, Cardiology Clinic
Interests
Clinical translation of outpatient telemedicine
Research Areas
Heart
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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