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University of Pennsylvania

SOCIAL DISPARITIES IN HEALTHCARE UTILIZATION FOR CHILDREN AND ADOLESCENTS WITH MIGRAINE DISEASE

Abstract

dc:description.abstract

Headache disorders are very common among youth but remain underdiagnosed and undertreated especially in emergency department (ED) where providers must worry about serious causes of headache. This disproportionately affects patients from marginalized communities who tend to visit the ED for chronic conditions. While prior research found disparities in migraine treatment, we suspect that these disparities might also involve migraine diagnosis. If so, the biases one aims to explore may also lead to selection bias for studies that identify patients by diagnosis. Migraine care also faces obstacles unique to headache especially relating to patient-provider communication. In this thesis, we looked at nationwide trends in racial/ethnic disparities in headache management in pediatric EDs. As we found migraine was underdiagnosed for children from marginalized groups, we developed several language-learning models to identify migraine independent of diagnostic coding. We explored which patient traits were associated with the thoroughness of clinical documentation. Amongst patients with model-identified migraine, we explored socioeconomic trends in migraine care during and after the ED visit. Continuing on to outpatient care, we explored the feasibility of adopting a text message-based headache diary. Using diary-collected data, we determined the level of agreement between participants’ self-reported migraine attacks and attacks determined by diagnostic criteria. In the nationwide study, Non-Hispanic Black (NHB) children diagnosed with headache in the ED received fewer migraine-specific diagnoses and lower rates of testing, neuroimaging, and intravenous medications. At our institution, we found that boys and younger patients tended to have less thorough clinical notes. However, notes were sufficient to train several models to identify migraine. For children with model-identified migraine, we again found that NHB children received less intensive care and fewer migraine diagnoses even after accounting for potential confounders. For the text message-based diary, participants displayed high completion rates; however, participants tended to underestimate which headaches were actually migraine attacks. Overall, these findings suggest that there are significant barriers to migraine care that are felt disproportionately by children from marginalized communities.

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Kellier, Danielle, Joy
Advisors dc:contributor.advisor
  • Farrar, John, T
  • Szperka, Christina, L

Subjects

dc:subject × 2

Rights

Language dc:language.iso
en

Identifiers

dc:identifier.*
Repository record dc:identifier.uri
https://repository.upenn.edu/handle/20.500.14332/62745
OAI identifier oai:identifier
oai:repository.upenn.edu:20.500.14332/62745

Chain of custody

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Harvested from
University of Pennsylvania
Base URL
repository.upenn.edu/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Kellier, Danielle, Joy. SOCIAL DISPARITIES IN HEALTHCARE UTILIZATION FOR CHILDREN AND ADOLESCENTS WITH MIGRAINE DISEASE. 2026. https://repository.upenn.edu/handle/20.500.14332/62745