Overview
Dr. Kayle’s program of research aims to improve health outcomes among people with childhood-onset complex chronic conditions, with a focus on sickle cell disease (SCD). In partnership with the North Carolina Department of Health and Human Services, Division of Public Health, she co-leads the North Carolina Sickle Cell Data Collection Program (NC SCDC), a state-level surveillance program funded by the Centers for Disease Control and Prevention. NC SCDC curates and analyzes multi-source, population-level datasets to describe the epidemiology, health outcomes, and social determinants of health influencing SCD. Dr. Kayle collaborates with national and state partners to disseminate surveillance findings informing practice, research, and policy for SCD.
Dr. Kayle teaches Nursing Care of Infants, Children, and Adolescents in the Accelerated Bachelor of Nursing program. Her service contributions include several state-level committees on SCD.
Dr. Kayle completed her Bachelor of Science in Nursing at the American University of Beirut, her Master's in Pediatric Acute and Critical Care and her Doctor of Philosophy in Nursing at Duke University School of Nursing, and her Postdoctoral Fellowship in Health Services and Outcomes Research at Northwestern University, Feinberg School of Medicine. She has over twelve years of pediatric acute and critical care clinical experience.
Current Appointments & Affiliations
Recent Publications
Gaps during pediatric to adult care transfer escalate acute resource utilization in sickle cell disease.
Journal Article Blood Adv · July 23, 2024 Guidelines recommend transfer to adult health care within 6 months of completing pediatric care; however, this has not been studied in sickle cell disease (SCD). We hypothesized that longer transfer gaps are associated with increased resource utilization. ... Full text Link to item CiteBurden of Aging: Health Outcomes Among Adolescents and Young Adults With Sickle Cell Disease
Journal Article HemaSphere · August 13, 2023 Full text CiteCommon data model for sickle cell disease surveillance: considerations and implications.
Journal Article JAMIA Open · July 2023 OBJECTIVE: Population-level data on sickle cell disease (SCD) are sparse in the United States. The Centers for Disease Control and Prevention (CDC) is addressing the need for SCD surveillance through state-level Sickle Cell Data Collection Programs (SCDC). ... Full text Open Access Link to item CiteRecent Grants
North Carolina Sickle Cell Data Collection
Public ServicePrincipal Investigator · Awarded by NC Department of Health and Human Services · 2024 - 2024NCDHHS Sickle Cell Data Collection Program in North Carolina Year 3
Public ServicePrincipal Investigator · Awarded by NC Department of Health and Human Services · 2022 - 2023Improving SCD Care using Web-based Guidelines, Nurse Care Managers and Peer Mentors in Parimary Care Emergency Departments in Central North Carolina
ResearchCo Investigator · Awarded by National Institutes of Health · 2016 - 2023View All Grants