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University of Texas Health Science Center at Houston

Evaluating Insurance Approval Rates of Exome Sequencing and Its Effect On Minority Patients' Access to Genetic Care

Abstract

dc:description.abstract

<p>Exome sequencing (ES) is often a standard step in the genetic testing process for patients with rare or complex disease. Despite clinical implementation of ES, insurance companies (payers) continue to deny this test. We investigated if the payer barrier is influenced by payer type, and if other demographic or clinical information correlated to ES approval and obtainment. To do this, a retrospective chart and clinical database review was completed on patients seen at a tertiary care center and community-based clinic. Patient demographics, clinical indications, and testing recommendations and outcomes were used to assess ES approval and obtainment. We found that patients with a public payer were 91% less likely to have ES approved, and 76% less likely to obtain ES compared to patients with a private payer. In our cohort, all minority patients were more likely to have a public payer compared to white patients. A consistent approach to ES recommendation was observed regardless of patient demographic or clinical information. In conclusion, having a public payer significantly impacts a patient’s ability to obtain ES and access the downstream benefits of testing. Additionally, the public payer barrier disproportionately effects minority patients as they are more likely to hold public payer options. Collectively, this information can support the development of payer policies and initiatives that promote equitable care of patients with rare diseases.</p>

Degree

thesis:*
Name thesis:degree_name
Masters of Science (MS)
Level thesis:degree_level
Thesis (MS)
Year dc:date.available
2021

Author and committee

dc:creator, dc:contributor.*
Authors dc:creator
  • Frane, Katlyn
  • <p>https://orcid.org/0000-0001-5441-3677</p>
Contributors dc:contributor
  • Chelsea Wagner, M.S., CGC
  • Paul Hillman, M.D., Ph.D
  • Leslie Dunnington, M.S., CGC

Subjects

dc:subject × 10

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:digitalcommons.library.tmc.edu:utgsbs_dissertations-2135

Chain of custody

source
Harvested from
University of Texas Health Science Center at Houston
Base URL
digitalcommons.library.tmc.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Frane, Katlyn; <p>https://orcid.org/0000-0001-5441-3677</p>. Evaluating Insurance Approval Rates of Exome Sequencing and Its Effect On Minority Patients' Access to Genetic Care. Thesis (MS) thesis, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/1079