Hepatitis C care cascade among patients with and without tuberculosis: Nationwide observational cohort study in the country of Georgia, 2015-2020.
Journal
PLoS medicine
ISSN: 1549-1676
Titre abrégé: PLoS Med
Pays: United States
ID NLM: 101231360
Informations de publication
Date de publication:
05 2023
05 2023
Historique:
received:
03
10
2022
accepted:
13
04
2023
revised:
18
05
2023
medline:
22
5
2023
pubmed:
4
5
2023
entrez:
4
5
2023
Statut:
epublish
Résumé
The Eastern European country of Georgia initiated a nationwide hepatitis C virus (HCV) elimination program in 2015 to address a high burden of infection. Screening for HCV infection through antibody testing was integrated into multiple existing programs, including the National Tuberculosis Program (NTP). We sought to compare the hepatitis C care cascade among patients with and without tuberculosis (TB) diagnosis in Georgia between 2015 and 2019 and to identify factors associated with loss to follow-up (LTFU) in hepatitis C care among patients with TB. Using national ID numbers, we merged databases of the HCV elimination program, NTP, and national death registry from January 1, 2015 to September 30, 2020. The study population included 11,985 adults (aged ≥18 years) diagnosed with active TB from January 1, 2015 through December 31, 2019, and 1,849,820 adults tested for HCV antibodies between January 1, 2015 and September 30, 2020, who were not diagnosed with TB during that time. We estimated the proportion of patients with and without TB who were LTFU at each step of the HCV care cascade and explored temporal changes. Among 11,985 patients with active TB, 9,065 (76%) patients without prior hepatitis C treatment were tested for HCV antibodies, of which 1,665 (18%) had a positive result; LTFU from hepatitis C care was common, with 316 of 1,557 (20%) patients with a positive antibody test not undergoing viremia testing and 443 of 1,025 (43%) patients with viremia not starting treatment for hepatitis C. Overall, among persons with confirmed viremic HCV infection, due to LTFU at various stages of the care cascade only 28% of patients with TB had a documented cure from HCV infection, compared to 55% among patients without TB. LTFU after positive antibody testing substantially decreased in the last 3 years, from 32% among patients diagnosed with TB in 2017 to 12% among those diagnosed in 2019. After a positive HCV antibody test, patients without TB had viremia testing sooner than patients with TB (hazards ratio [HR] = 1.46, 95% confidence intervals [CI] [1.39, 1.54], p < 0.001). After a positive viremia test, patients without TB started hepatitis C treatment sooner than patients with TB (HR = 2.05, 95% CI [1.87, 2.25], p < 0.001). In the risk factor analysis adjusted for age, sex, and case definition (new versus previously treated), multidrug-resistant (MDR) TB was associated with an increased risk of LTFU after a positive HCV antibody test (adjusted risk ratio [aRR] = 1.41, 95% CI [1.12, 1.76], p = 0.003). The main limitation of this study was that due to the reliance on existing electronic databases, we were unable to account for the impact of all confounding factors in some of the analyses. LTFU from hepatitis C care after a positive antibody or viremia test was high and more common among patients with TB than in those without TB. Better integration of TB and hepatitis C care systems can potentially reduce LTFU and improve patient outcomes both in Georgia and other countries that are initiating or scaling up their nationwide hepatitis C control efforts and striving to provide personalized TB treatment.
Sections du résumé
BACKGROUND
The Eastern European country of Georgia initiated a nationwide hepatitis C virus (HCV) elimination program in 2015 to address a high burden of infection. Screening for HCV infection through antibody testing was integrated into multiple existing programs, including the National Tuberculosis Program (NTP). We sought to compare the hepatitis C care cascade among patients with and without tuberculosis (TB) diagnosis in Georgia between 2015 and 2019 and to identify factors associated with loss to follow-up (LTFU) in hepatitis C care among patients with TB.
METHODS AND FINDINGS
Using national ID numbers, we merged databases of the HCV elimination program, NTP, and national death registry from January 1, 2015 to September 30, 2020. The study population included 11,985 adults (aged ≥18 years) diagnosed with active TB from January 1, 2015 through December 31, 2019, and 1,849,820 adults tested for HCV antibodies between January 1, 2015 and September 30, 2020, who were not diagnosed with TB during that time. We estimated the proportion of patients with and without TB who were LTFU at each step of the HCV care cascade and explored temporal changes. Among 11,985 patients with active TB, 9,065 (76%) patients without prior hepatitis C treatment were tested for HCV antibodies, of which 1,665 (18%) had a positive result; LTFU from hepatitis C care was common, with 316 of 1,557 (20%) patients with a positive antibody test not undergoing viremia testing and 443 of 1,025 (43%) patients with viremia not starting treatment for hepatitis C. Overall, among persons with confirmed viremic HCV infection, due to LTFU at various stages of the care cascade only 28% of patients with TB had a documented cure from HCV infection, compared to 55% among patients without TB. LTFU after positive antibody testing substantially decreased in the last 3 years, from 32% among patients diagnosed with TB in 2017 to 12% among those diagnosed in 2019. After a positive HCV antibody test, patients without TB had viremia testing sooner than patients with TB (hazards ratio [HR] = 1.46, 95% confidence intervals [CI] [1.39, 1.54], p < 0.001). After a positive viremia test, patients without TB started hepatitis C treatment sooner than patients with TB (HR = 2.05, 95% CI [1.87, 2.25], p < 0.001). In the risk factor analysis adjusted for age, sex, and case definition (new versus previously treated), multidrug-resistant (MDR) TB was associated with an increased risk of LTFU after a positive HCV antibody test (adjusted risk ratio [aRR] = 1.41, 95% CI [1.12, 1.76], p = 0.003). The main limitation of this study was that due to the reliance on existing electronic databases, we were unable to account for the impact of all confounding factors in some of the analyses.
CONCLUSIONS
LTFU from hepatitis C care after a positive antibody or viremia test was high and more common among patients with TB than in those without TB. Better integration of TB and hepatitis C care systems can potentially reduce LTFU and improve patient outcomes both in Georgia and other countries that are initiating or scaling up their nationwide hepatitis C control efforts and striving to provide personalized TB treatment.
Identifiants
pubmed: 37141386
doi: 10.1371/journal.pmed.1004121
pii: PMEDICINE-D-22-03278
pmc: PMC10194957
doi:
Substances chimiques
Hepatitis C Antibodies
0
Types de publication
Observational Study
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1004121Subventions
Organisme : FIC NIH HHS
ID : D43 TW007124
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI111211
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI168386
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI050409
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI114444
Pays : United States
Informations de copyright
Copyright: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
Références
PLoS One. 2019 Apr 29;14(4):e0216123
pubmed: 31034530
Subst Abuse Treat Prev Policy. 2022 Mar 28;17(1):23
pubmed: 35346265
Am J Epidemiol. 2010 Mar 1;171(5):624-32
pubmed: 20106935
MMWR Morb Mortal Wkly Rep. 2017 Jul 28;66(29):773-776
pubmed: 28749925
Nat Med. 2020 Feb;26(2):157-160
pubmed: 32047317
BMC Infect Dis. 2016 Nov 25;16(1):712
pubmed: 27887646
J Clin Oncol. 2008 Aug 20;26(24):4027-34
pubmed: 18711194
World J Hepatol. 2015 Jun 8;7(10):1377-89
pubmed: 26052383
Lancet Infect Dis. 2012 Nov;12(11):859-70
pubmed: 22914343
Lancet Infect Dis. 2020 Feb;20(2):e47-e53
pubmed: 31740252
J Viral Hepat. 2021 Oct;28(10):1340-1354
pubmed: 34310812
Liver Int. 2022 Apr;42(4):775-786
pubmed: 35129278
Lancet HIV. 2019 Mar;6(3):e201-e204
pubmed: 30846058
Int J Tuberc Lung Dis. 2006 Apr;10(4):396-401
pubmed: 16602403
Hepatology. 2004 Apr;39(4):1147-71
pubmed: 15057920
MMWR Morb Mortal Wkly Rep. 2015 Jul 24;64(28):753-7
pubmed: 26203628
Clin Infect Dis. 2020 Aug 22;71(5):1263-1268
pubmed: 31563938
BMC Public Health. 2019 May 10;19(Suppl 3):480
pubmed: 32326913
Epidemiology. 1999 Jan;10(1):37-48
pubmed: 9888278
J Virus Erad. 2019 Jan 1;5(1):60-66
pubmed: 30800429
Lancet Respir Med. 2020 Apr;8(4):383-394
pubmed: 32192585
J Hepatol. 2019 Oct;71(4):645-647
pubmed: 31356831
Antimicrob Agents Chemother. 2019 Oct 7;:
pubmed: 31591118
Hepatology. 2018 Sep;68(3):827-838
pubmed: 29377196
MMWR Morb Mortal Wkly Rep. 2019 Jul 26;68(29):637-641
pubmed: 31344021
PLoS One. 2013 Dec 19;8(12):e83892
pubmed: 24367617
Curr Opin HIV AIDS. 2019 Jan;14(1):66-70
pubmed: 30489347
BMC Infect Dis. 2017 Nov 1;17(Suppl 1):699
pubmed: 29143676
J Hepatol. 2020 Apr;72(4):680-687
pubmed: 31811882
J Chin Med Assoc. 2018 Feb;81(2):111-118
pubmed: 29198550
Prev Med. 2020 Sep;138:106153
pubmed: 32473265
J Hepatol. 2014 Nov;61(1 Suppl):S58-68
pubmed: 25443346
Hepatol Med Policy. 2017 Jun 13;2:9
pubmed: 30288322
BMC Public Health. 2019 May 10;19(Suppl 3):466
pubmed: 32326938
Open Forum Infect Dis. 2021 Jan 04;8(2):ofaa653
pubmed: 33634203
Clin Liver Dis. 1997 Nov;1(3):543-57, vi
pubmed: 15560057
Int J Tuberc Lung Dis. 2016 Apr;20(4):430-4
pubmed: 26970149
Pharmacol Ther. 2018 Mar;183:118-126
pubmed: 29024739
J Viral Hepat. 2020 Dec;27(12):1270-1283
pubmed: 32964615
Clin Infect Dis. 2015 Jun 15;60(12):1829-36
pubmed: 25761867
Int J Tuberc Lung Dis. 2014 Dec;18(12):1479-84
pubmed: 25517815
Curr Hepatol Rep. 2018 Dec;17(4):377-384
pubmed: 30923667
Transfusion. 2020 Jun;60(6):1243-1252
pubmed: 32542715
BMJ Open. 2020 Feb 2;10(1):e032027
pubmed: 32014870
Semin Liver Dis. 2018 Aug;38(3):181-192
pubmed: 29986353
Clin Infect Dis. 2019 Nov 27;69(12):2218-2227
pubmed: 31352481
Lancet. 2016 Sep 17;388(10050):1228-48
pubmed: 27427455
Int J Drug Policy. 2020 Oct;84:102893
pubmed: 32739613
J Infect. 2022 Jun;84(6):834-872
pubmed: 35271917
Clin Gastroenterol Hepatol. 2023 Apr;21(4):988-994.e2
pubmed: 35577048