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Trends in cause-specific mortality in HIV-hepatitis C coinfection following hepatitis C treatment scale-up.

Authors :
Kronfli N
Bhatnagar SR
Hull MW
Moodie EEM
Cox J
Walmsley S
Gill J
Cooper C
Martel-Laferrière V
Pick N
Klein MB
Source :
AIDS (London, England) [AIDS] 2019 May 01; Vol. 33 (6), pp. 1013-1022.
Publication Year :
2019

Abstract

Objective: Hepatitis C virus (HCV) treatment may reduce liver-related mortality but with competing risks, other causes of mortality may undermine benefits. We examined changes in cause-specific mortality among HIV-HCV coinfected patients before and after scale-up of HCV treatment.<br />Design: Prospective multicentre HIV-HCV cohort study in Canada.<br />Methods: Cause-specific deaths, classified using a modified 'Coding of Cause of Death in HIV' protocol, were determined for two time periods, 2003-2012 and 2013-2017, stratified by age (20-49; 50-80 years). Comparison of trends between periods was performed using Poisson regression. To account for competing risks, multinomial regression was used to estimate the cause-specific hazard ratios of time and age on cause of death, from which end-stage liver disease (ESLD)-specific 5-year cumulative incidence functions were estimated.<br />Results: Overall, 1634 participants contributed 8248 person-years of follow-up; 273 (17%) died. Drug overdose was the most common cause of death overall, followed by ESLD and smoking-related deaths. In 2013-2017, ESLD was surpassed by drug overdose and smoking-related deaths among those aged 20-49 and 50-80, respectively. After accounting for competing risks, comparing 2003-2012 to 2013-2017, ESLD deaths declined (adjusted hazards ratio: 0.18, 95% confidence interval 0.05-0.62). However, both early and late period cumulative incidence functions demonstrated increased risk of death from ESLD for patients with poor HIV control and advanced fibrosis.<br />Conclusion: The gains made in overall mortality with HCV therapy may be thwarted if modifiable harms are not addressed. Although ESLD-related deaths have decreased over time, treatment should be further expanded, prioritizing those with advanced fibrosis.

Details

Language :
English
ISSN :
1473-5571
Volume :
33
Issue :
6
Database :
MEDLINE
Journal :
AIDS (London, England)
Publication Type :
Academic Journal
Accession number :
30946155
Full Text :
https://doi.org/10.1097/QAD.0000000000002156