A systematic review and meta-analysis of community and primary-care-based hepatitis C testing and treatment services that employ direct acting antiviral drug treatments.


Journal

BMC health services research
ISSN: 1472-6963
Titre abrégé: BMC Health Serv Res
Pays: England
ID NLM: 101088677

Informations de publication

Date de publication:
28 Oct 2019
Historique:
received: 20 12 2018
accepted: 14 10 2019
entrez: 30 10 2019
pubmed: 30 10 2019
medline: 23 1 2020
Statut: epublish

Résumé

Direct Acting Antiviral (DAAs) drugs have a much lower burden of treatment and monitoring requirements than regimens containing interferon and ribavirin, and a much higher efficacy in treating hepatitis C (HCV). These characteristics mean that initiating treatment and obtaining a virological cure (Sustained Viral response, SVR) on completion of treatment, in non-specialist environments should be feasible. We investigated the English-language literature evaluating community and primary care-based pathways using DAAs to treat HCV infection. Databases (Cinahl; Embase; Medline; PsycINFO; PubMed) were searched for studies of treatment with DAAs in non-specialist settings to achieve SVR. Relevant studies were identified including those containing a comparison between a community and specialist services where available. A narrative synthesis and linked meta-analysis were performed on suitable studies with a strength of evidence assessment (GRADE). Seventeen studies fulfilled the inclusion criteria: five from Australia; two from Canada; two from UK and eight from USA. Seven studies demonstrated use of DAAs in primary care environments; four studies evaluated integrated systems linking specialists with primary care providers; three studies evaluated services in locations providing care to people who inject drugs; two studies evaluated delivery in pharmacies; and one evaluated delivery through telemedicine. Sixteen studies recorded treatment uptake. Patient numbers varied from around 60 participants with pathway studies to several thousand in two large database studies. Most studies recruited less than 500 patients. Five studies reported reduced SVR rates from an intention-to-treat analysis perspective because of loss to follow-up before the final confirmatory SVR test. GRADE assessments were made for uptake of HCV treatment (medium); completion of HCV treatment (low) and achievement of SVR at 12 weeks (medium). Services sited in community settings are feasible and can deliver increased uptake of treatment. Such clinics are able to demonstrate similar SVR rates to published studies and real-world clinics in secondary care. Stronger study designs are needed to confirm the precision of effect size seen in current studies. Prospero: CRD42017069873.

Sections du résumé

BACKGROUND BACKGROUND
Direct Acting Antiviral (DAAs) drugs have a much lower burden of treatment and monitoring requirements than regimens containing interferon and ribavirin, and a much higher efficacy in treating hepatitis C (HCV). These characteristics mean that initiating treatment and obtaining a virological cure (Sustained Viral response, SVR) on completion of treatment, in non-specialist environments should be feasible. We investigated the English-language literature evaluating community and primary care-based pathways using DAAs to treat HCV infection.
METHODS METHODS
Databases (Cinahl; Embase; Medline; PsycINFO; PubMed) were searched for studies of treatment with DAAs in non-specialist settings to achieve SVR. Relevant studies were identified including those containing a comparison between a community and specialist services where available. A narrative synthesis and linked meta-analysis were performed on suitable studies with a strength of evidence assessment (GRADE).
RESULTS RESULTS
Seventeen studies fulfilled the inclusion criteria: five from Australia; two from Canada; two from UK and eight from USA. Seven studies demonstrated use of DAAs in primary care environments; four studies evaluated integrated systems linking specialists with primary care providers; three studies evaluated services in locations providing care to people who inject drugs; two studies evaluated delivery in pharmacies; and one evaluated delivery through telemedicine. Sixteen studies recorded treatment uptake. Patient numbers varied from around 60 participants with pathway studies to several thousand in two large database studies. Most studies recruited less than 500 patients. Five studies reported reduced SVR rates from an intention-to-treat analysis perspective because of loss to follow-up before the final confirmatory SVR test. GRADE assessments were made for uptake of HCV treatment (medium); completion of HCV treatment (low) and achievement of SVR at 12 weeks (medium).
CONCLUSION CONCLUSIONS
Services sited in community settings are feasible and can deliver increased uptake of treatment. Such clinics are able to demonstrate similar SVR rates to published studies and real-world clinics in secondary care. Stronger study designs are needed to confirm the precision of effect size seen in current studies. Prospero: CRD42017069873.

Identifiants

pubmed: 31660966
doi: 10.1186/s12913-019-4635-7
pii: 10.1186/s12913-019-4635-7
pmc: PMC6819346
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

765

Références

Eur J Epidemiol. 2015 Feb;30(2):115-29
pubmed: 25385677
Lancet Gastroenterol Hepatol. 2017 Nov;2(11):832-836
pubmed: 28802815
BMJ. 2009 Jul 21;339:b2700
pubmed: 19622552
Lancet Gastroenterol Hepatol. 2017 Mar;2(3):161-176
pubmed: 28404132
Ann Intern Med. 2017 May 2;166(9):637-648
pubmed: 28319996
BMJ Innov. 2017 Jul;3(3):144-151
pubmed: 29445515
J Int AIDS Soc. 2017 Jul 28;20(1):22146
pubmed: 28782335
BMJ Open. 2018 Dec 14;8(12):e021443
pubmed: 30552244
Clin Infect Dis. 2019 Jun 22;:null
pubmed: 31233117
PLoS One. 2015 Mar 11;10(3):e0116963
pubmed: 25760440
Int J Drug Policy. 2017 Sep;47:26-33
pubmed: 28888558
J Viral Hepat. 2018 Sep;25(9):1089-1098
pubmed: 29660212
Int J Drug Policy. 2017 Sep;47:34-46
pubmed: 28797498
Int J Drug Policy. 2017 Sep;47:196-201
pubmed: 28811158
Ann Intern Med. 2017 Sep 5;167(5):311-318
pubmed: 28785771
Hepatology. 2013 Nov;58(5):1598-609
pubmed: 23553643
J Clin Epidemiol. 2015 Nov;68(11):1312-24
pubmed: 25721570
Can Commun Dis Rep. 2018 Jul 05;44(7-8):166-172
pubmed: 31011297
J Viral Hepat. 2018 May;25(5):482-490
pubmed: 29239130
J Virus Erad. 2018 Apr 1;4(2):118-122
pubmed: 29682305
Int J Drug Policy. 2014 Mar;25(2):204-11
pubmed: 24332457
Harm Reduct J. 2013 May 07;10:7
pubmed: 23651646
BMC Infect Dis. 2016 May 16;16:202
pubmed: 27184661
Ann Hepatol. 2017 Aug 8;16(5):749-758
pubmed: 28809740
Expert Rev Gastroenterol Hepatol. 2018 Mar;12(3):303-314
pubmed: 29300496
J Subst Abuse Treat. 2017 Apr;75:49-53
pubmed: 28237054
Can J Gastroenterol Hepatol. 2017;2017:3268650
pubmed: 28529936
Int J Drug Policy. 2017 Sep;47:126-136
pubmed: 28647161
Ann Hepatol. 2017 Oct 16;16(6):874-880
pubmed: 29055923
Int J Drug Policy. 2017 Sep;47:209-215
pubmed: 28587943
Am J Med. 2017 Apr;130(4):432-438.e3
pubmed: 27998682
Int J Drug Policy. 2017 Sep;47:216-220
pubmed: 28666635

Auteurs

Andrew Radley (A)

NHS Tayside, Directorate of Public Health, Kings Cross Hospital, Clepington Road, Dundee, DD3 8EA, UK. aradley@dundee.ac.uk.
University of Dundee, Division of Cardiovascular Medicines and Diabetes Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK. aradley@dundee.ac.uk.

Emma Robinson (E)

University of Dundee, Division of Cardiovascular Medicines and Diabetes Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.

Esther J Aspinall (EJ)

School of Health and Life Sciences, Glasgow Caledonian University Glasgow and Health Protection Scotland, NHS National Services, Scotland, UK.

Kathryn Angus (K)

Institute for Social Marketing, Faculty of Health Sciences and Sport University of Stirling, Stirling, FK9 4LA, UK.

Lex Tan (L)

University of Dundee, Division of Cardiovascular Medicines and Diabetes Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.

John F Dillon (JF)

University of Dundee, Division of Cardiovascular Medicines and Diabetes Ninewells Hospital and Medical School, Dundee, DD1 9SY, UK.

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Classifications MeSH