Date of Award

2024

Document Type

Dissertation

Degree Name

Doctor of Philosophy (PhD)

Program

Health Outcomes and Policy Research

Track

Health Services Research

Research Advisor

James Bailey, MD

Committee

Jane Hankins, MD; Justin Gatwood, PhD; Kenneth Ataga, MD; Min Zhang, PhD

Keywords

Longitudinal study, Real-world evidence, Risk factors, Survival analysis

Abstract

Sickle cell disease (SCD) is an inherited disease characterized by sickle-shaped red blood cells that can slow or block blood flow. It affects about 100,000 people in the United States, and occurs more commonly in people of African descent. SCD is considered as a hypercoagulable state and venous thromboembolism (VTE) is a serious disease-specific complication. However, there have been limited real-world studies on VTE in SCD patients. This work aims to provide a comprehensive assessment of the risk factors and treatment of VTE in adults with SCD by using longitudinal real-world data. First, a retrospective cohort study on 30-day readmission was conducted to give a general understanding of the treatment of SCD. It was found that SCD patients were at high risk of readmission, and younger adults had higher risk than older adults. The risk factors vary significantly by age. These findings suggest that multifaceted, age-specific interventions are needed to improve the clinical outcomes of SCD patients. Second, the treatment patterns of pharmacological anticoagulation in adults with SCD was studied by using a retrospective, repeated cross-sectional design. The results may contribute to the optimal selection of regimens or dosing and informed decision making on anticoagulant utilization in routine care. Third, the incidence of VTE and its associated risk factors and clinical outcomes were examined. Several SCD-related complications and treatments were found to be significantly associated with VTE. Landmark survival analysis demonstrated that early management of VTE may improve the overall survival of SCD patients.

Declaration of Authorship

Declaration of Authorship is included in the supplemental files.

ORCID

0000-0003-3215-8657

DOI

10.21007/etd.cghs.2024.0669

2024-016-Chen-DOA.pdf (189 kB)
Declaration of Authorship

Available for download on Sunday, August 09, 2026

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