Overview
Dr. Tanabe is the Laurel B. Chadwick Distinguished Professor in the Schools of Nursing and Medicine at Duke at the Duke University School of Nursing. Dr. Tanabe is a clinical and health services researcher. Her program of research focuses on improving systems of healthcare and patient outcomes for persons with sickle cell disease, a primarily minority and under-served population. Dr. Tanabe has received funding from the Agency for Health Care Research and Quality, the National Institute of Heart, Lung, and Blood, National Institute of Minority Health and Health Disparities and the National Institute of Nursing Research. Her work is advancing the care of individuals with sickle cell disease with a strong focus on improving pain management in the emergency department during a vaso-occlusive crisis. Her methodological expertise includes conducting multi-site clinical RCT’s, survey methods, qualitative research, quality improvement and implementation science. Dr. Tanabe has a strong passion for her work, individuals with sickle cell disease, and for mentoring students and faculty to conduct important, meaningful work to improve the health and well being of individuals and families.
Current Appointments & Affiliations
Laurel Chadwick Distinguished Professor of Nursing
·
2019 - Present
School of Nursing
Professor in the School of Nursing
·
2017 - Present
School of Nursing
Vice Dean, Research and Regulatory Affairs
·
2020 - Present
School of Nursing
Professor of Medicine
·
2017 - Present
Medicine, Hematology,
Medicine
Assistant Professor in Surgery
·
2017 - Present
Emergency Medicine,
Clinical Science Departments
Affiliate Faculty Member, Duke-Margolis Institute for Health Policy
·
2024 - Present
Duke-Margolis Institute for Health Policy,
University Institutes and Centers
Recent Publications
Improving the Quality of Whole-Person Healthcare Delivery: Critical Components of a Sickle Cell Disease Nurse Navigator Role.
Journal Article Prof Case Manag · November 2025 PURPOSE/OBJECTIVES: Sickle cell disease (SCD) is a complex genetic hemoglobinopathy which is associated with a severely shortened lifespan; the median age of death remains in the low 50's. Individuals living with SCD have complex medical, psychological, an ... Full text Link to item CiteProvider Implicit Racial Bias in Pediatric Sickle Cell Disease.
Journal Article Journal of racial and ethnic health disparities · August 2025 Background/objectivesThis study is to (1) assess implicit racial bias among pediatric providers and (2) use virtual patient (VP) vignettes to determine the impact of implicit racial bias on clinical decision-making in pediatric sickle cell disease ... Full text CiteOpioid-related Transitions for Chronic Pain Management: A Concept Analysis.
Journal Article Pain management nursing : official journal of the American Society of Pain Management Nurses · August 2025 BackgroundPeople who are prescribed opioids for pain management may undergo transitions of care. However, little is known about transitions of care that involve a prescribed opioid, which may have significant consequences for people with chronic p ... Full text CiteRecent Grants
Nurse LEADS: Training in Nurse-LEd models of care ADdressing the Social Determinants of Health
Inst. Training Prgm or CMEMentor · Awarded by National Institute of Nursing Research · 2024 - 2029Predictors of Pain Severity and Pain-Related Outcomes in Individuals with Sickle Cell Disease
ResearchAdvisor · Awarded by National Heart, Lung, and Blood Institute · 2023 - 2025North Carolina Sickle Cell Data Collection
Public ServiceCo Investigator · Awarded by NC Department of Health and Human Services · 2024 - 2024View All Grants
Education, Training & Certifications
University of Illinois ·
1996
Ph.D.
Loyola University, Chicago ·
1990
M.S.N.
Rush University ·
1987
B.S.