As a practicing pediatric hematologist for 30 years, I provide care for children with a wide variety of hematological disorders. My primary focus is the evaluation and management of care for children with sickle cell anemia and other hemolytic anemias. I also treat children who present with other forms of anemia, as well as neutropenia or thrombocytopenia.
When I began my career, there were almost no treatments available for sickle cell anemia. We now have many new diagnostic tools and novel approaches to help improve our young patients' lives. I have always enjoyed providing direct clinical care as well as performing laboratory investigations that lead to more effective care and improved outcomes for our children.
My research goals are to determine the best ways to use hydroxyurea for children with sickle cell anemia and to understand why some children respond better than others. I’m investigating the genetic basis for treatment outcomes and hope to optimize hydroxyurea treatment for each patient. Transforming the clinical care of children with sickle cell anemia across the world, through the widespread use of hydroxyurea, is my long-term research goal.
Our studies include both translational and clinical research. I have led several National Institutes of Health (NIH)-funded trials of hydroxyurea to prevent stroke in children with sickle cell anemia, demonstrating the efficacy of this simple daily oral medication. I’m also investigating the use of hydroxyurea in low-resource settings, focusing on sub-Saharan Africa and the Caribbean. Our exciting results have shown the feasibility, safety and benefits of hydroxyurea in these settings, which could potentially transform the treatment landscape for sickle cell anemia worldwide. Some of my research trials also include point-of-care diagnostics and optimizing hydroxyurea treatment through individualized dosing.
Improving the care and health of children with sickle cell anemia has been a rewarding career goal. However, taking what we have learned in the United States and bringing this knowledge to low-resource countries has been even more gratifying. With support from the Cincinnati Children's Research Foundation, we have established productive global partnerships with local partners in six sub-Saharan countries and two Caribbean islands. These collaborations are changing the approach to diagnosing and treating sickle cell anemia worldwide.
MD: Duke University School of Medicine, Durham, NC, 1979-83
Residency: Baylor College of Medicine, Houston, TX, 1983-86
Fellowship: Duke Medical Center, Durham, NC, 1986-89
PhD: Duke University School of Medicine, Durham, NC, 1987-1991
Certifications: Pediatric Hematology/Oncology
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High early mortality among Ugandan children with sickle cell anemia and congenital HIV identified by newborn screening. Blood Glob Hematol. 2026; 2(2):100093.
The role of outer setting health system factors in the use of hydroxyurea for Ugandan children with sickle cell anemia. Blood Glob Hematol. 2026; 2(2):100091.
Ten Years of Hydroxyurea for Ugandan Children with Sickle Cell Anemia. New England Journal of Medicine. 2026; 394(20):2059-2061.
Newborn screening results for sickle cell disease from the ASH Consortium on Newborn Screening in Africa (CONSA). Blood advances. 2026; 10(9):3200-3206.
Artificial Intelligence-Based Analysis of Central Nervous System Vasculopathy in Pediatric Sickle Cell Anemia. American Journal of Hematology. 2026; 101(5):998-1004.
Persistent Splenomegaly is associated with Morbidity in Tanzanian Children with Sickle Cell Anemia: Secondary Analysis of the SPHERE Trial. Acta Haematologica. 2026; 1-18.
Growth and puberty in African children with sickle cell anemia treated with hydroxyurea. Blood advances. 2026.
Sickle Cell Disease in Sub-Saharan Africa: Progress and Potential. American Journal of Hematology. 2026; 101 Suppl 1:3-4.
Prolonged, Unintentional Overdose of Hydroxyurea in a Child With Sickle Cell Anemia. Pediatric Blood and Cancer. 2026; 73(2):e70076.
Hydroxyurea pharmacokinetics in children with sickle cell anemia across different global populations. Blood advances. 2026; 10(2):418-427.
Russell E. Ware, MD, PhD6/3/2026
Russell E. Ware, MD, PhD12/9/2024
Russell E. Ware, MD, PhD, Adam Lane, PhD3/22/2021
Russell E. Ware, MD, PhD, Luke R. Smart, MD12/10/2020
Russell E. Ware, MD, PhD6/25/2020
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