Toward microelimination of hepatitis C and HIV coinfection in NHS Tayside, Scotland: Real-world outcomes.
HIV
Injecting
PWID
Scotland; direct Acting Antivirals
coinfection
drug users
elimination
hepatitis C
microelimination
people Who Inject Drugs
Journal
Health science reports
ISSN: 2398-8835
Titre abrégé: Health Sci Rep
Pays: United States
ID NLM: 101728855
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
received:
24
04
2020
revised:
30
07
2020
accepted:
18
08
2020
entrez:
9
10
2020
pubmed:
10
10
2020
medline:
10
10
2020
Statut:
epublish
Résumé
NHS Tayside is a health board in Scotland which serves around 400 000 residents. Approximately, 2761 are estimated to be persons who inject drugs (PWID), and therefore at risk of infections such as hepatitis C (HCV) and HIV. There are few studies exploring mechanisms and success of eliminating HCV in HIV co-infected PWID using real-world data. This study aims to empirically assess HCV treatment outcomes in people living with HIV (PLHIV) to evaluate progress toward microelimination of HCV in the HIV-positive population in Tayside. HCV testing and treatment details for PLHIV stored on clinical databases dating from 2001 were extracted and anonymized. HCV treatment uptake among co-infected patients eligible for HCV treatment was calculated. Reinfection incidence was calculated in person years. Confidence intervals were calculated assuming Poisson distribution. Caldicott Guardian approval was obtained to access patient data (ref: IGTCAL 5677). Ninety-six percent of PLHIV were tested for HCV across nine services and aware of their HCV status. From 2001 to 2019, 58 PLHIV were HCV co-infected. Four left the area and five died prior to HCV treatment. Forty-nine were eligible for HCV treatment. Thirty were treated with PEGylated interferon (Peg-IFN); 18 with direct acting antivirals (DAA). One is yet to be treated. Twelve treated with Peg-IFN did not achieve sustained viral response (SVR12); 10 were retreated, two died prior to re-treatment. Injecting drug use was the mode of HCV transmission for 39 of 49 patients. Proportion who achieved SVR12 is 75%; 92% if treated with DAAs. Annual proportions of PLHIV treated for HCV increased from 3.57% in the Peg-IFN era to 66.67% in the DAA era. Reinfection incidence is 0.2 per 100 person years (CI -0.3 to 0.7). NHS Tayside has made progress toward microelimination of HCV among PLHIV. The most common mode of HCV transmission in PLHIV in NHS Tayside is injecting drug use. DAAs increased the proportion of co-infected PLHIV treated for HCV and produced superior SVR12 results compared to Peg-IFN.
Sections du résumé
BACKGROUND AND AIMS
OBJECTIVE
NHS Tayside is a health board in Scotland which serves around 400 000 residents. Approximately, 2761 are estimated to be persons who inject drugs (PWID), and therefore at risk of infections such as hepatitis C (HCV) and HIV. There are few studies exploring mechanisms and success of eliminating HCV in HIV co-infected PWID using real-world data. This study aims to empirically assess HCV treatment outcomes in people living with HIV (PLHIV) to evaluate progress toward microelimination of HCV in the HIV-positive population in Tayside.
METHODS
METHODS
HCV testing and treatment details for PLHIV stored on clinical databases dating from 2001 were extracted and anonymized. HCV treatment uptake among co-infected patients eligible for HCV treatment was calculated. Reinfection incidence was calculated in person years. Confidence intervals were calculated assuming Poisson distribution. Caldicott Guardian approval was obtained to access patient data (ref: IGTCAL 5677).
RESULTS
RESULTS
Ninety-six percent of PLHIV were tested for HCV across nine services and aware of their HCV status. From 2001 to 2019, 58 PLHIV were HCV co-infected. Four left the area and five died prior to HCV treatment. Forty-nine were eligible for HCV treatment. Thirty were treated with PEGylated interferon (Peg-IFN); 18 with direct acting antivirals (DAA). One is yet to be treated. Twelve treated with Peg-IFN did not achieve sustained viral response (SVR12); 10 were retreated, two died prior to re-treatment. Injecting drug use was the mode of HCV transmission for 39 of 49 patients. Proportion who achieved SVR12 is 75%; 92% if treated with DAAs. Annual proportions of PLHIV treated for HCV increased from 3.57% in the Peg-IFN era to 66.67% in the DAA era. Reinfection incidence is 0.2 per 100 person years (CI -0.3 to 0.7).
CONCLUSIONS
CONCLUSIONS
NHS Tayside has made progress toward microelimination of HCV among PLHIV. The most common mode of HCV transmission in PLHIV in NHS Tayside is injecting drug use. DAAs increased the proportion of co-infected PLHIV treated for HCV and produced superior SVR12 results compared to Peg-IFN.
Identifiants
pubmed: 33033752
doi: 10.1002/hsr2.191
pii: HSR2191
pmc: PMC7534516
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e191Informations de copyright
© 2020 The Authors. Health Science Reports published by Wiley Periodicals LLC.
Déclaration de conflit d'intérêts
John F. Dillon has received personal honoraria for lectures and institutional research grants from MSD, AbbVie, Gilead, Roche, and Janssen. All authors declare no conflict of interest.
Références
Hepat Mon. 2015 Jul 22;15(7):e27740
pubmed: 26300929
Lancet Gastroenterol Hepatol. 2017 Mar;2(3):161-176
pubmed: 28404132
J Acquir Immune Defic Syndr. 2015 Apr 1;68(4):456-62
pubmed: 25559606
Lancet Gastroenterol Hepatol. 2018 Aug;3(8):559-565
pubmed: 29859740
Int J Drug Policy. 2018 Dec;62:74-77
pubmed: 30368101
J Assoc Nurses AIDS Care. 2016 Sep-Oct;27(5):574-84
pubmed: 27080926
Open Forum Infect Dis. 2018 May 23;5(6):ofy120
pubmed: 29992173
AIDS. 2007 Oct 18;21(16):2209-16
pubmed: 18090048
Pharmacol Ther. 2018 Mar;183:118-126
pubmed: 29024739
Semin Liver Dis. 2018 Aug;38(3):181-192
pubmed: 29986353
Lancet HIV. 2018 Nov;5(11):e605
pubmed: 30507440
Infect Dis Clin North Am. 2018 Jun;32(2):371-393
pubmed: 29778261
Lancet Infect Dis. 2016 Jul;16(7):797-808
pubmed: 26922272
AIDS. 2013 Oct 23;27(16):2551-7
pubmed: 23736152
PLoS One. 2018 Jul 25;13(7):e0198520
pubmed: 30044779
Open Forum Infect Dis. 2019 Aug 14;:
pubmed: 31412130
J Int AIDS Soc. 2018 Apr;21 Suppl 2:e25062
pubmed: 29633560
Frontline Gastroenterol. 2013 Oct;4(4):255-262
pubmed: 28839735
Clin Infect Dis. 2009 Nov 15;49(10):1605-15
pubmed: 19842982
J Hepatol. 2016 May;64(5):1020-1026
pubmed: 26780289
Clin Infect Dis. 2020 Sep 12;71(6):1502-1510
pubmed: 31585005