Author:
Klaman Stacey L.,Godino Job G.,Northrup Adam,Lewis Sydney V.,Tam Aaron,Carrillo Carolina,Lewis Robert,Matthews Eva,Mendez Blanca,Reyes Letty,Rojas Sarah,Ramers Christian
Abstract
Abstract
Background
As many as 2.4 million Americans are affected by chronic Hepatitis C Virus (HCV) in the United States.In 2018, the estimated number of adults with a history of HCV infection in San Diego County was 55,354 (95% CI: 25,411–93,329). This corresponded to a seroprevalence of 2.1% (95% CI: 2.1–3.4%). One-third of infections were among PWID. Published research has demonstrated that direct-acting antivirals (DAAs) have high efficacy and can now be used by primary care providers to treat HCV. In addition, limited evidence exists to support the effectiveness of simplified algorithms in clinical trial and real-world settings. Even with expanded access to HCV treatment in primary care settings, there are still groups, especially people who inject drugs (PWID) and people experiencing homelessness, who experience treatment disparities due to access and treatment barriers. The current study extends the simplified algorithm with a streetside ‘one-stop-shop’ approach with integrated care (including the offer of buprenorphine prescriptions and abscess care) using a mobile clinic situated adjacent to a syringe service program serving many homeless populations. Rates of HCV treatment initiation and retention will be compared between patients offered HCV care in a mobile clinic adjacent to a syringe services program (SSP) and homeless encampment versus those who are linked to a community clinic’s current practice of usual care, which includes comprehensive patient navigation.
Methods
A quasi-experimental, prospective, interventional, comparative effectiveness trial with allocation of approximately 200 patients who inject drugs and have chronic HCV to the "simplified care" pathway (intervention group) or the "usual care" pathway (control group). Block randomization will be performed with a 1:1 randomization.
Discussion
Previous research has demonstrated acceptable outcomes for patients treated using simplified algorithms for DAAs and point-of-care testing in mobile medical clinics; however, there are opportunities to explore how these new, innovative systems of care impact treatment initiation rates or other HCV care cascade outcomes among PWID.
Trial registration
We have registered our study with ClinicalTrials.gov, a resource of the United States National Library of Medicine. This database contains research studies from United States and other countries around the world. Our study has not been previously published. The ClinicalTrials.gov registration identifier is NCT04741750.
Publisher
Springer Science and Business Media LLC
Reference26 articles.
1. Hofmesiter MG, Rosenthal EM, Barker LK, Rosenberg ES, Barranco MA, Hall EW, Edlin BR, Mermin J, Ward JW, Ryerson AB. Estimating prevalence of hepatitis C virus infection in the United States, 2013–2016. Hepatology. 2019;69(3):1020–31.
2. Cunningham EB, Wheeler A, Hajarizadeh B, French CE, Roche R, Marshall AD. Interventions to enhance testing, linkage to care, and treatment initiation for hepatitis C virus infection: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2022;7(5):426–45. https://doi.org/10.1016/S2468-1253(21)00471-4.
3. Trickey A, Fajardo E, Alemu D, Artenie AA, Easterbrook P. Impact of hepatitis C virus point-of-care RNA viral load testing compared with laboratory-based testing on uptake of RNA testing and treatment, and turnaround times: a systematic review and meta-analysis. Lancet Gastroenterol Hepatol. 2023;8(3):253–70. https://doi.org/10.1016/S2468-1253(22)00346-6.
4. Surveillance for Viral Hepatitis – United States, 2017. Centers for Disease Control and Prevention. https://www.cdc.gov/hepatitis/statistics/2017surveillance/index.htm. Accessed 26 Sept 2019.
5. New Hepatitis C Cases Rise for Seventh Year in a row. September 10, 2019 Press Release. AIDS Institute. http://www.theaidsinstitute.org/sites/default/files/attachments/CDC%20hepatitis%20data%20press%20release.pdf. Accessed 26 Sept 2019.