TY - JOUR
T1 - The impact of point-of-care hepatitis C testing in needle and syringe exchange programs on linkage to care and treatment uptake among people who inject drugs
T2 - An Australian pilot study
AU - Howell, Jessica
AU - Traeger, Michael W.
AU - Williams, Bridget
AU - Layton, Chloe
AU - Doyle, Joseph S.
AU - Latham, Ned
AU - Draper, Bridget
AU - Bramwell, Frances
AU - Membrey, Dean
AU - McPherson, Maggie
AU - Roney, Janine
AU - Stoové, Mark
AU - Thompson, Alexander J.
AU - Hellard, Margaret E.
AU - Pedrana, Alisa
N1 - Funding Information:
We would like to gratefully acknowledge the support and time of all the participants of the Rapid EC study and involved healthworkers. The Rapid EC study was funded by Gastroenterology Society of Australia, Gilead Sciences (Gilead Australia Fellowship JH), St Vincent’s Foundation and the Shepherd Foundation. JH is supported by a Gilead Sciences Australia fellowship, University of Melbourne Faculty Trust fellowship and NHMRC Program grant.
Funding Information:
The Burnet receives funding support from Gilead Sciences, Abbvie, GSK and Merck for investigator‐initiated research. MH, JD, AT and MS receive funding support from Gilead Sciences, Abbvie and GSK for investigator‐initiated research. JH received funding from Gilead Sciences via the Australia Gilead Research Fellowship (2017) and honoraria from Gilead Sciences and Eisai. AP receives funding support from Gilead Sciences and MSD for investigator‐initiated research. JD’s institution has received honoraria from Merck, Gilead and BMS. Cepheid provided loan of three GeneXpert machines and 300 cartridges for the study.
Publisher Copyright:
© 2022 John Wiley & Sons Ltd.
PY - 2022/5
Y1 - 2022/5
N2 - Point-of-care (POC) diagnostics overcome barriers to conventional hepatitis C (HCV) testing in people who inject drugs. This study assessed impact on hepatitis C treatment uptake of POC HCV testing in needle and syringe exchange programs (NSPs). Rapid EC was a single-arm interventional pilot study of HCV POC testing conducted in three inner-city community clinics with NSPs. Twelve months after the POC testing, a retrospective medical record and Pharmaceutical Benefits Scheme audit was performed to determine the number of HCV RNA-positive participants who were prescribed HCV treatment. 70 HCV RNA-positive Rapid EC study participants were included. 44 (63%) were prescribed DAAs; 26 (59%) completed treatment and 15 (34%) had SVR testing, all of whom were cured. Age ≥ 40 years (aOR 3.45, 95% CI 1.10–11.05, p =.03) and secondary school education (aOR 5.8, 95% CI 1.54–21.80, p =.009) had higher likelihood of being prescribed DAAs, whereas homelessness was inversely associated with prescription of DAAs (aOR 0.30, 95% CI 0.09–1.04, p =.057). Median time to receive a DAA script from date of diagnosis was seven days (IQR 0 to 14 days), and time to filling the DAA prescription was 2 days (IQR 0–12 days). In conclusion, provision of POC testing through NSPs was effective for linking new clients to HCV treatment and reduced the time to treatment. Further studies are needed to define the most cost-effective use of POC testing in models of care for people who inject drugs to increase HCV treatment uptake.
AB - Point-of-care (POC) diagnostics overcome barriers to conventional hepatitis C (HCV) testing in people who inject drugs. This study assessed impact on hepatitis C treatment uptake of POC HCV testing in needle and syringe exchange programs (NSPs). Rapid EC was a single-arm interventional pilot study of HCV POC testing conducted in three inner-city community clinics with NSPs. Twelve months after the POC testing, a retrospective medical record and Pharmaceutical Benefits Scheme audit was performed to determine the number of HCV RNA-positive participants who were prescribed HCV treatment. 70 HCV RNA-positive Rapid EC study participants were included. 44 (63%) were prescribed DAAs; 26 (59%) completed treatment and 15 (34%) had SVR testing, all of whom were cured. Age ≥ 40 years (aOR 3.45, 95% CI 1.10–11.05, p =.03) and secondary school education (aOR 5.8, 95% CI 1.54–21.80, p =.009) had higher likelihood of being prescribed DAAs, whereas homelessness was inversely associated with prescription of DAAs (aOR 0.30, 95% CI 0.09–1.04, p =.057). Median time to receive a DAA script from date of diagnosis was seven days (IQR 0 to 14 days), and time to filling the DAA prescription was 2 days (IQR 0–12 days). In conclusion, provision of POC testing through NSPs was effective for linking new clients to HCV treatment and reduced the time to treatment. Further studies are needed to define the most cost-effective use of POC testing in models of care for people who inject drugs to increase HCV treatment uptake.
KW - community-based testing
KW - diagnostics
KW - models of care
KW - viral hepatitis
UR - http://www.scopus.com/inward/record.url?scp=85126749666&partnerID=8YFLogxK
U2 - 10.1111/jvh.13664
DO - 10.1111/jvh.13664
M3 - Article
C2 - 35274403
AN - SCOPUS:85126749666
SN - 1352-0504
VL - 29
SP - 375
EP - 384
JO - Journal of Viral Hepatitis
JF - Journal of Viral Hepatitis
IS - 5
ER -