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. 2023 Apr 10;13(4):e068604.
doi: 10.1136/bmjopen-2022-068604.

Mixed-methods evaluation of point-of-care hepatitis C virus RNA testing in a Scottish prison

Affiliations

Mixed-methods evaluation of point-of-care hepatitis C virus RNA testing in a Scottish prison

Christopher J Byrne et al. BMJ Open. .

Abstract

Objectives: Hepatitis C virus (HCV) poses a global public health threat. Prisons are a focus of prevention efforts due to high infection burdens. Expedition of treatment for incarcerated people is critical, as many are short-term sentenced. We evaluated point-of-care (PoC) HCV RNA testing in a maximum-security Scottish prison and assessed its impact on transition to treatment. We also evaluated costs and determinants of implementation.

Design: Mixed-methods evaluation of a single-centre care pathway pilot using National Health Service (NHS) data from 2018 to 2021. Descriptive statistics and survival analysis were undertaken. Cost analysis was assessed from a provider perspective. Healthcare staff participated in semistructured interviews and thematic analysis with a deductive approach was undertaken to identify implementation determinants.

Setting: A large maximum-security Scottish prison health centre administered by the NHS.

Participants: 296 incarcerated NHS patients (all men) and six NHS staff members (two men and four women).

Interventions: HCV testing using the Cepheid GeneXpert platform with Xpert HCV VL Fingerstick assay.

Outcome measures: The main outcome was survival (in days) from HCV test to treatment initiation. Secondary outcomes were cost-per-cure obtained and implementation determinants.

Results: During the pilot, 167 Xpert tests were administered, with an 84% completion rate, and treatment transition was superior for those who received it (p=0.014). Where PoC tests were administered, shorter survival to treatment was observed (19 vs 33 days: adjusted HR (aHR) 1.91 (1.03-3.55), p=0.040; 19 vs 50 days; aHR 3.76 (1.67-8.46), p=0.001). PoC was costlier than conventional testing. In qualitative analysis, most facilitators were observed among characteristics of individual domain while most barriers were noted in the inner setting.

Conclusions: Integrating PoC HCV RNA diagnosis into nurse-led HCV care in a maximum-security prison health centre shortens survival to HCV treatment. However, there are cost implications to this approach and multiple determinants that impact on implementation should be addressed.

Keywords: Hepatology; INFECTIOUS DISEASES; Organisation of health services; PUBLIC HEALTH; Public health; QUALITATIVE RESEARCH.

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Conflict of interest statement

Competing interests: CJB, AM and SKI have no disclosures. JFD reports grants and personal fees from AbbVie; grants and personal fees from Gilead; and grants and personal fees from MSD, outside the submitted work.

Figures

Figure 1
Figure 1
Summary of observation dates and study activities. Conventional testing was by whole blood sent to a laboratory for analysis and dried blood spot methods.
Figure 2
Figure 2
Target cohort profile with related clinical outcomes and censoring. *Cases received treatment but excluded from cost and time-to-treatment analyses, as their testing data were unavailable or unverifiable. All censored in survival analysis at relevant decease, liberation, transfer or follow-up censor dates. Group 1 are those tested conventionally from 2018 to 19 (reference period); group 2 are those conventionally tested during the pilot phase (2019–21); group 3 are those tested with the GeneXpert during the pilot phase (2019–21). LTFU, lost to follow-up; PoC, point of care; RNA, ribonucleic acid; RNA+, RNA positive (actively infected); SVR, sustained virologic response.

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References

    1. Gallacher J, McPherson S. Progress towards micro-elimination of hepatitis C in the custodial setting. J Viral Hepat 2021;28:300–1. 10.1111/jvh.13428 - DOI - PubMed
    1. Degenhardt L, Peacock A, Colledge S, et al. . Global prevalence of injecting drug use and sociodemographic characteristics and prevalence of HIV, HBV, and HCV in people who inject drugs: a multistage systematic review. Lancet Glob Health 2017;5:e1192–207. 10.1016/S2214-109X(17)30375-3 - DOI - PMC - PubMed
    1. Kronfli N, Linthwaite B, Kouyoumdjian F, et al. . Interventions to increase testing, linkage to care and treatment of hepatitis C virus (HCV) infection among people in prisons: a systematic review. Int J Drug Policy 2018;57:95–103. 10.1016/j.drugpo.2018.04.003 - DOI - PubMed
    1. Altice FL, Azbel L, Stone J, et al. . The perfect storm: incarceration and the high-risk environment perpetuating transmission of HIV, hepatitis C virus, and tuberculosis in Eastern Europe and central Asia. Lancet 2016;388:1228–48. 10.1016/S0140-6736(16)30856-X - DOI - PMC - PubMed
    1. Taylor A, Munro A, Allen E, et al. . Low incidence of hepatitis C virus among prisoners in Scotland. Addiction 2013;108:1296–304. 10.1111/add.12107 - DOI - PubMed

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