Access to clinical genetic services: An evaluation of patient referral characteristics and identifying barriers in Michigan.

Autor: Lemke LN; Department of Public Health, Grand Valley State University, Grand Rapids, Michigan, USA.; Division of Quality and Infection Prevention, Northern Arizona Healthcare, Flagstaff, Arizona, USA., Bupp CP; Division of Medical Genetics and Genomics, Corewell Health Helen DeVos Children's Hospital (Previously Known as Spectrum Health Helen DeVos Children's Hospital), Grand Rapids, Michigan, USA., Niemchick KL; Department of Public Health, Grand Valley State University, Grand Rapids, Michigan, USA.
Jazyk: angličtina
Zdroj: Journal of genetic counseling [J Genet Couns] 2024 Jul 10. Date of Electronic Publication: 2024 Jul 10.
DOI: 10.1002/jgc4.1947
Abstrakt: The utilization of genetics in medical care has enhanced the utility of precision medicine and hence increased the need for clinical genetic services. These services have reduced the costs and expanded the availability of genetic testing, but their use is limited in certain populations. This study explores the access to clinical genetic services for Michigan patients referred to a genetics clinic on the western side of the state. Factors included the travel distance (miles), wait time for appointment (days from the referral date to the date of first appointment), population demographics, and cultural characteristics. A retrospective record review of all aged patients (n = 568) referred to a genetics clinic in 2018 demonstrated that all patients were insured (100%), of which majority were white-non-Hispanic (90.7%), more than half were < 10 years of age at referral (53.3%), and most of them kept their first appointment (93.5%). Our analysis showed that the wait time was associated with referral non-compliance, p < 0.01. Adjusting for all variables, for each additional day in wait time, patients had 1% increased risk of not seeking clinical genetic services (OR = 1.01, 90% CI [1.01, 1.02]). Policies to encourage genetic service utilization and improve equitable access to precision health are needed. An opportunity exists for strategies that broaden and add diverse populations to those receiving genetic services.
(© 2024 National Society of Genetic Counselors.)
Databáze: MEDLINE
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