Identification of Risk Factors For an Unsuccessful Transition From Pediatric to Adult Sickle cell Disease Care.
Publication/Presentation Date
12-18-2013
Abstract
Background
A successful transition from pediatric to adult sickle cell disease (SCD) care is paramount to continued improvements in survival. In order to enhance transition success, our pediatric SCD transition process was modified to include combined adult and pediatric provider clinics that incorporated participation by our local SCD community‐based organization. All children ages 16 and over participated in this newly‐formed transition program.
Procedure
After 5 years of implementation of the modified SCD transition program, we retrospectively studied clinical and non‐clinical risk factors for an unsuccessful transition. Risk factor categories studied included patient demographics, transition clinic attendance, and disease severity.
Results
Thirty‐two percent of patients did not transition successfully. Demographic factors such as gender, race, and type of insurance did not influence transition outcome, although travel distance to the adult SCD center was an identifiable risk factor for an unsuccessful transition. While transition clinic attendance rate did not affect transition outcomes, older age at first modified combined transition clinic visit was a significant risk factor for lack of transition. Patients with clinical markers of milder disease severity (SC and Sβ+ genotypes and no chronic transfusion therapy) were at higher risk for an unsuccessful transition than patients with severe disease.
Conclusions
We have identified several risk factors for lack of transition success which will allow us to modify our transition efforts going forward to capture this highest risk subset. Pediatr Blood Cancer 2014;61:697–701. © 2013 Wiley Periodicals, Inc.
Volume
61
Issue
4
First Page
697
Last Page
701
Published In/Presented At
Andemariam, B., Owarish-Gross, J., Grady, J., Boruchov, D., Thrall, R., & Hagstrom, J. (2014). Identification of risk factors for an unsuccessful transition from pediatric to adult sickle cell disease care. Pediatric Blood & Cancer, 61(4), 697-701. doi:10.1002/pbc.24870
Disciplines
Medicine and Health Sciences | Pediatrics
PubMedID
24347402
LVHN link
http://search.ebscohost.com/login.aspx?direct=true&db=mnh&AN=24347402&site=ehost-live&scope=site
Department(s)
Department of Pediatrics Faculty, Department of Pediatrics Residents
Document Type
Article