Single-visit hepatitis C point-of-care testing, linkage to nursing care, and peer-supported treatment among people with recent injecting drug use at a peer-led needle and syringe program: The TEMPO Pilot Study.
Grebely, J
Gilliver, R
McNaughton, T
Conway, A
Cunningham, E
Henderson, C
Hadlow, B
Molloy, K
Doab, A
Tillakeratne, S
Pepolim, L
Harrod, ME
Dore, GJ
Read, P
- Publisher:
- Elsevier
- Publication Type:
- Journal Article
- Citation:
- Int J Drug Policy, 2023, 114, pp. 103982
- Issue Date:
- 2023-04
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Grebely, J | |
dc.contributor.author | Gilliver, R | |
dc.contributor.author | McNaughton, T | |
dc.contributor.author | Conway, A | |
dc.contributor.author | Cunningham, E | |
dc.contributor.author | Henderson, C | |
dc.contributor.author | Hadlow, B | |
dc.contributor.author | Molloy, K | |
dc.contributor.author |
Doab, A https://orcid.org/0000-0002-8204-2217 |
|
dc.contributor.author | Tillakeratne, S | |
dc.contributor.author | Pepolim, L | |
dc.contributor.author | Harrod, ME | |
dc.contributor.author | Dore, GJ | |
dc.contributor.author | Read, P | |
dc.date.accessioned | 2024-01-15T06:27:46Z | |
dc.date.available | 2023-02-16 | |
dc.date.available | 2024-01-15T06:27:46Z | |
dc.date.issued | 2023-04 | |
dc.identifier.citation | Int J Drug Policy, 2023, 114, pp. 103982 | |
dc.identifier.issn | 0955-3959 | |
dc.identifier.issn | 1873-4758 | |
dc.identifier.uri | http://hdl.handle.net/10453/174498 | |
dc.description.abstract | BACKGROUND: Point-of-care hepatitis C virus (HCV) RNA testing can facilitate single-visit diagnosis and treatment. This study evaluated a single-visit test and treat intervention integrating point-of-care HCV RNA testing, linkage to nursing care, and peer-supported engagement/delivery of treatment among people with recent injecting drug use at a peer-led needle and syringe program (NSP). METHODS: TEMPO Pilot is an interventional cohort study of people with recent injecting drug use (previous month) recruited between September 2019-February 2021 from one peer-led NSP in Sydney, Australia. Participants received point-of-care HCV RNA testing (Xpert HCV Viral Load Fingerstick), linkage to nursing care, and peer-supported engagement/delivery of treatment. The primary endpoint was the proportion initiating HCV therapy. RESULTS: Among 101 people with recent injecting drug use (median age 43; 31% female), 27% (n = 27) were HCV RNA detectable. Treatment uptake was 74% (20 of 27; sofosbuvir/velpatasvir, n = 8; glecaprevir/pibrentasvir, n = 12). Among people initiating treatment (n = 20), 45% (n = 9) initiated treatment at the same visit, 50% (n = 10) in the next 1-2 days, and 5% on day 7 (n = 1). Two participants initiated treatment outside the study (overall treatment uptake 81%). Reasons for not initiating treatment included loss to follow-up (n = 2), no reimbursement (n = 1), not suitable for treatment (mental health) (n = 1), and inability to perform liver disease assessment (n = 1). In the full analysis set, 60% (12 of 20) completed treatment and 40% (8 of 20) had a sustained virological response (SVR). In the evaluable population (excluding people without an SVR test), SVR was 89% (8 of 9). CONCLUSION: Point-of-care HCV RNA testing, linkage to nursing, and peer-supported engagement/delivery led to high HCV treatment uptake (majority single-visit) among people with recent injecting drug use attending a peer-led NSP. The lower proportion of people with SVR highlights the need for further interventions to support treatment completion. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Elsevier | |
dc.relation.ispartof | Int J Drug Policy | |
dc.relation.isbasedon | 10.1016/j.drugpo.2023.103982 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 11 Medical and Health Sciences, 16 Studies in Human Society, 17 Psychology and Cognitive Sciences | |
dc.subject.classification | Substance Abuse | |
dc.subject.classification | 4206 Public health | |
dc.subject.classification | 4407 Policy and administration | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Female | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Male | |
dc.subject.mesh | Antiviral Agents | |
dc.subject.mesh | Hepacivirus | |
dc.subject.mesh | Pilot Projects | |
dc.subject.mesh | Cohort Studies | |
dc.subject.mesh | Hepatitis C, Chronic | |
dc.subject.mesh | Syringes | |
dc.subject.mesh | Substance Abuse, Intravenous | |
dc.subject.mesh | Hepatitis C | |
dc.subject.mesh | Substance-Related Disorders | |
dc.subject.mesh | RNA | |
dc.subject.mesh | Point-of-Care Testing | |
dc.subject.mesh | Nursing Care | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Hepacivirus | |
dc.subject.mesh | Hepatitis C | |
dc.subject.mesh | Hepatitis C, Chronic | |
dc.subject.mesh | Substance-Related Disorders | |
dc.subject.mesh | Substance Abuse, Intravenous | |
dc.subject.mesh | RNA | |
dc.subject.mesh | Antiviral Agents | |
dc.subject.mesh | Nursing Care | |
dc.subject.mesh | Cohort Studies | |
dc.subject.mesh | Pilot Projects | |
dc.subject.mesh | Syringes | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Female | |
dc.subject.mesh | Male | |
dc.subject.mesh | Point-of-Care Testing | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Female | |
dc.subject.mesh | Adult | |
dc.subject.mesh | Male | |
dc.subject.mesh | Antiviral Agents | |
dc.subject.mesh | Hepacivirus | |
dc.subject.mesh | Pilot Projects | |
dc.subject.mesh | Cohort Studies | |
dc.subject.mesh | Hepatitis C, Chronic | |
dc.subject.mesh | Syringes | |
dc.subject.mesh | Substance Abuse, Intravenous | |
dc.subject.mesh | Hepatitis C | |
dc.subject.mesh | Substance-Related Disorders | |
dc.subject.mesh | RNA | |
dc.subject.mesh | Point-of-Care Testing | |
dc.subject.mesh | Nursing Care | |
dc.title | Single-visit hepatitis C point-of-care testing, linkage to nursing care, and peer-supported treatment among people with recent injecting drug use at a peer-led needle and syringe program: The TEMPO Pilot Study. | |
dc.type | Journal Article | |
utslib.citation.volume | 114 | |
utslib.location.activity | Netherlands | |
utslib.for | 11 Medical and Health Sciences | |
utslib.for | 16 Studies in Human Society | |
utslib.for | 17 Psychology and Cognitive Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Health | |
pubs.organisational-group | /University of Technology Sydney/Strength - CHSP - Health Services and Practice | |
utslib.copyright.status | open_access | * |
dc.date.updated | 2024-01-15T06:27:44Z | |
pubs.publication-status | Published | |
pubs.volume | 114 |
Abstract:
BACKGROUND: Point-of-care hepatitis C virus (HCV) RNA testing can facilitate single-visit diagnosis and treatment. This study evaluated a single-visit test and treat intervention integrating point-of-care HCV RNA testing, linkage to nursing care, and peer-supported engagement/delivery of treatment among people with recent injecting drug use at a peer-led needle and syringe program (NSP). METHODS: TEMPO Pilot is an interventional cohort study of people with recent injecting drug use (previous month) recruited between September 2019-February 2021 from one peer-led NSP in Sydney, Australia. Participants received point-of-care HCV RNA testing (Xpert HCV Viral Load Fingerstick), linkage to nursing care, and peer-supported engagement/delivery of treatment. The primary endpoint was the proportion initiating HCV therapy. RESULTS: Among 101 people with recent injecting drug use (median age 43; 31% female), 27% (n = 27) were HCV RNA detectable. Treatment uptake was 74% (20 of 27; sofosbuvir/velpatasvir, n = 8; glecaprevir/pibrentasvir, n = 12). Among people initiating treatment (n = 20), 45% (n = 9) initiated treatment at the same visit, 50% (n = 10) in the next 1-2 days, and 5% on day 7 (n = 1). Two participants initiated treatment outside the study (overall treatment uptake 81%). Reasons for not initiating treatment included loss to follow-up (n = 2), no reimbursement (n = 1), not suitable for treatment (mental health) (n = 1), and inability to perform liver disease assessment (n = 1). In the full analysis set, 60% (12 of 20) completed treatment and 40% (8 of 20) had a sustained virological response (SVR). In the evaluable population (excluding people without an SVR test), SVR was 89% (8 of 9). CONCLUSION: Point-of-care HCV RNA testing, linkage to nursing, and peer-supported engagement/delivery led to high HCV treatment uptake (majority single-visit) among people with recent injecting drug use attending a peer-led NSP. The lower proportion of people with SVR highlights the need for further interventions to support treatment completion.
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