The population level care cascade for hepatitis C in British Columbia, Canada as of 2018: Impact of direct acting antivirals.


Journal

Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857

Informations de publication

Date de publication:
12 2019
Historique:
received: 11 03 2019
revised: 14 08 2019
accepted: 19 08 2019
pubmed: 25 8 2019
medline: 6 10 2020
entrez: 25 8 2019
Statut: ppublish

Résumé

Population-level monitoring of hepatitis C virus (HCV) infected people across cascades of care identifies gaps in access and engagement in care and treatment. We characterized the population-level care cascade for HCV in British Columbia (BC), Canada before and after introduction of Direct Acting Antiviral (DAA) treatment. BC Hepatitis Testers Cohort (BC-HTC) includes 1.7 million individuals tested for HCV, HIV, reported cases of hepatitis B, and active tuberculosis in BC from 1990 to 2018 linked to medical visits, hospitalizations, cancers, prescription drugs and mortality data. We defined six HCV care cascade stages: (a) antibody diagnosed; (b) RNA tested; (c) RNA positive; (d) genotyped; (e) initiated treatment; and (f) achieved sustained virologic response (SVR). We estimated 61 127 people were HCV antibody positive in BC in 2018 (undiagnosed: 7686, 13%; diagnosed: 53 441, 87%). Of those diagnosed, 83% (44 507) had HCV RNA testing, and of those RNA positive, 90% (28 716) were genotyped. Of those genotyped, 61% (17 441) received therapy, with 90% (15 672) reaching SVR. Individuals from older birth cohorts had lower progression to HCV RNA testing. While people who currently inject drugs had the highest proportional progression to RNA testing, this group had the lowest proportional treatment uptake. Although gaps in HCV RNA and genotype testing after antibody diagnosis exist, the largest gap in the care cascade is treatment initiation, despite introduction of DAA treatment and removal of treatment eligibility restrictions. Further interventions are required to ensure testing and treatment is equitably accessible in BC.

Sections du résumé

BACKGROUND
Population-level monitoring of hepatitis C virus (HCV) infected people across cascades of care identifies gaps in access and engagement in care and treatment. We characterized the population-level care cascade for HCV in British Columbia (BC), Canada before and after introduction of Direct Acting Antiviral (DAA) treatment.
METHODS
BC Hepatitis Testers Cohort (BC-HTC) includes 1.7 million individuals tested for HCV, HIV, reported cases of hepatitis B, and active tuberculosis in BC from 1990 to 2018 linked to medical visits, hospitalizations, cancers, prescription drugs and mortality data. We defined six HCV care cascade stages: (a) antibody diagnosed; (b) RNA tested; (c) RNA positive; (d) genotyped; (e) initiated treatment; and (f) achieved sustained virologic response (SVR).
RESULTS
We estimated 61 127 people were HCV antibody positive in BC in 2018 (undiagnosed: 7686, 13%; diagnosed: 53 441, 87%). Of those diagnosed, 83% (44 507) had HCV RNA testing, and of those RNA positive, 90% (28 716) were genotyped. Of those genotyped, 61% (17 441) received therapy, with 90% (15 672) reaching SVR. Individuals from older birth cohorts had lower progression to HCV RNA testing. While people who currently inject drugs had the highest proportional progression to RNA testing, this group had the lowest proportional treatment uptake.
CONCLUSIONS
Although gaps in HCV RNA and genotype testing after antibody diagnosis exist, the largest gap in the care cascade is treatment initiation, despite introduction of DAA treatment and removal of treatment eligibility restrictions. Further interventions are required to ensure testing and treatment is equitably accessible in BC.

Identifiants

pubmed: 31444846
doi: 10.1111/liv.14227
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2261-2272

Subventions

Organisme : CIHR
ID : PHE-141773
Pays : Canada
Organisme : CIHR
ID : NHC - 142832
Pays : Canada
Organisme : CIHR
ID : PJT-156066
Pays : Canada

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

Sofia R Bartlett (SR)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.
Kirby Institute, University of New South Wales Australia, Sydney, NSW, Australia.

Amanda Yu (A)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.

Nuria Chapinal (N)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.

Carmine Rossi (C)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.

Zahid Butt (Z)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.

Stanley Wong (S)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.

Maryam Darvishian (M)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.

Mark Gilbert (M)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.

Jason Wong (J)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.

Mawuena Binka (M)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.

Maria Alvarez (M)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.

Mark Tyndall (M)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.

Mel Krajden (M)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC, Canada.

Naveed Z Janjua (NZ)

British Columbia Centre for Disease Control (BCCDC), Vancouver, BC, Canada.
School of Population and Public Health, University of British Columbia, Vancouver, BC, Canada.

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