Date of Award

8-2026

Document Type

Independent Study

Degree Name

Masters of Science in Medical Laboratory Science (MS)

Department

Medical Laboratory Science

First Advisor

Heather Langerud

Second Advisor

Samantha Peterson

Abstract

Hepatitis C virus (HCV) remains a major public health concern, particularly among marginalized and high-risk populations who experience barriers to timely diagnosis, treatment initiation, and linkage to care. Traditional laboratory-based HCV testing often requires multistep workflows and follow-up visits, contributing to delayed confirmation of active infection and loss to care. This literature review examines how point-of-care HCV ribonucleic acid (RNA) testing affects time to diagnosis, treatment initiation, and linkage to care compared with standard laboratory-based testing. Evidence from systematic reviews, community-based trials, correctional settings, supervised consumption sites, diagnostic performance studies, and cost-effectiveness analyses indicates that point-of-care RNA testing shortens turnaround times, supports same-day or rapid treatment initiation, and improves engagement across the HCV care cascade. However, implementation challenges remain, including cost, regulatory considerations, workforce training, assay sensitivity limitations, and the need to address social determinants of health that affect treatment completion. Overall, point-of-care HCV RNA testing is a promising strategy for reducing diagnostic delays and improving access to care, especially when integrated into comprehensive, low-barrier models designed for underserved populations.

Creative Commons License

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

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