Document Type
Journal Article
Publication Date
7-1-2016
Journal
American Journal of Preventive Medicine
Volume
51
Issue
1S1
Inclusive Pages
S17-S23
DOI
10.1016/j.amepre.2016.02.004
Abstract
Introduction
Transitions between inpatient and outpatient care and pediatric to adult care are associated with increased mortality for sickle cell disease (SCD) patients. As accurate and timely sharing of health information is essential during transitions, a health information technology (HIT)-enabled tool holds promise to improve care transitions.
Methods
From 2012 through 2014, the team conducted and analyzed data from an environmental scan, key informant interviews, and focus groups to inform the development of an HIT-enabled tool for SCD patients’ use during care transitions. The scan included searches of peer-reviewed and gray literature to understand SCD patient needs, transition concerns, and best practices in mobile health applications, and searches of websites and online stores to identify existing transition tools and their features. Eleven focus groups consisted of four groups of SCD patients of varying ages (≥9 years); three groups of parents/caregivers of SCD patients; three groups of providers; and one with IT developers.
Results
In focus groups, patients and caregivers reported that the transition from home to the emergency department (ED) was the most challenging; the ED was also where transitions from pediatric to adult care usually occurred. Patients felt they were not taken seriously by unfamiliar ED providers, and their inability to convey their diagnosis, pain regimen, and detailed medical history while in significant pain hindered care.
Conclusions
The environmental scan did not reveal an existing suitable transition tool, but patients, parents, providers, and IT experts saw the potential and appeal of creating a tool to meet ED health information needs to improve care transitions.
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 4.0 License.
APA Citation
Frost, J., Cherry, R., Oyeku, S., Faro, E., Crosby, L., Britto, M., Tuchman, L. K., Horn, I. B., Homer, C., & Jain, A. (2016). Improving Sickle Cell Transitions of Care Through Health Information Technology.. American Journal of Preventive Medicine, 51 (1S1). http://dx.doi.org/10.1016/j.amepre.2016.02.004
Peer Reviewed
1
Open Access
1
Comments
Reproduced with permission of Elsevier. American Journal of Preventive Medicine.