» Articles » PMID: 37532284

Mortality Rates Among Patients Successfully Treated for Hepatitis C in the Era of Interferon-free Antivirals: Population Based Cohort Study

Abstract

Objectives: To quantify mortality rates for patients successfully treated for hepatitis C in the era of interferon-free, direct acting antivirals and compare these rates with those of the general population.

Design: Population based cohort study.

Setting: British Columbia, Scotland, and England (England cohort consists of patients with cirrhosis only).

Participants: 21 790 people who were successfully treated for hepatitis C in the era of interferon-free antivirals (2014-19). Participants were divided into three liver disease severity groups: people without cirrhosis (pre-cirrhosis), those with compensated cirrhosis, and those with end stage liver disease. Follow-up started 12 weeks after antiviral treatment completion and ended on date of death or 31 December 2019.

Main Outcome Measures: Crude and age-sex standardised mortality rates, and standardised mortality ratio comparing the number of deaths with that of the general population, adjusting for age, sex, and year. Poisson regression was used to identify factors associated with all cause mortality rates.

Results: 1572 (7%) participants died during follow-up. The leading causes of death were drug related mortality (n=383, 24%), liver failure (n=286, 18%), and liver cancer (n=250, 16%). Crude all cause mortality rates (deaths per 1000 person years) were 31.4 (95% confidence interval 29.3 to 33.7), 22.7 (20.7 to 25.0), and 39.6 (35.4 to 44.3) for cohorts from British Columbia, Scotland, and England, respectively. All cause mortality was considerably higher than the rate for the general population across all disease severity groups and settings; for example, all cause mortality was three times higher among people without cirrhosis in British Columbia (standardised mortality ratio 2.96, 95% confidence interval 2.71 to 3.23; P<0.001) and more than 10 times higher for patients with end stage liver disease in British Columbia (13.61, 11.94 to 15.49; P<0.001). In regression analyses, older age, recent substance misuse, alcohol misuse, and comorbidities were associated with higher mortality rates.

Conclusion: Mortality rates among people successfully treated for hepatitis C in the era of interferon-free, direct acting antivirals are high compared with the general population. Drug and liver related causes of death were the main drivers of excess mortality. These findings highlight the need for continued support and follow-up after successful treatment for hepatitis C to maximise the impact of direct acting antivirals.

Citing Articles

Long-term Effect of the HCV Elimination With Direct-acting Antivirals on the Progression of Gastroesophageal Varices.

Yuri Y, Nishimura T, Ikeda N, Takashima T, Aizawa N, Kimura T In Vivo. 2024; 38(6):2968-2972.

PMID: 39477391 PMC: 11535916. DOI: 10.21873/invivo.13779.


Review of the Effects of Antiviral Therapy on Hepatitis B/C-Related Mortality and the Regression of Fibrosis.

Sinclair 3rd S, Shearen S, Ghobrial Y, Trad G, Abdul Basit S, Shih D Viruses. 2024; 16(10).

PMID: 39459866 PMC: 11512229. DOI: 10.3390/v16101531.


Hazardous Alcohol Use and Its Effect on Direct-Acting Antiviral Therapy Initiation among People with Active Injection Drug Use and Current Hepatitis C Infection.

Karimi-Sari H, Lucas G, Zook K, Weir B, Landry M, Sherman S Viruses. 2024; 16(9).

PMID: 39339891 PMC: 11437464. DOI: 10.3390/v16091416.


Trends in viral hepatitis liver-related morbidity and mortality in New South Wales, Australia.

Tillakeratne S, Pearson S, Alavi M, Hajarizadeh B, Martinello M, Law M Lancet Reg Health West Pac. 2024; 51:101185.

PMID: 39282135 PMC: 11402402. DOI: 10.1016/j.lanwpc.2024.101185.


Results from a retrospective case finding and re-engagement exercise for people previously diagnosed with hepatitis C virus to increase uptake of directly acting antiviral treatment.

Etoori D, Simmons R, Desai M, Foster G, Stuart A, Sabin C BMC Public Health. 2024; 24(1):2427.

PMID: 39243047 PMC: 11378625. DOI: 10.1186/s12889-024-19919-3.


References
1.
Fried M . Side effects of therapy of hepatitis C and their management. Hepatology. 2002; 36(5 Suppl 1):S237-44. DOI: 10.1053/jhep.2002.36810. View

2.
McDonald S, Hutchinson S, Innes H, Allen S, Bramley P, Bhattacharyya D . Attendance at specialist hepatitis clinics and initiation of antiviral treatment among persons chronically infected with hepatitis C: examining the early impact of Scotland's Hepatitis C Action Plan. J Viral Hepat. 2014; 21(5):366-76. DOI: 10.1111/jvh.12153. View

3.
Thomson B, Kwong G, Ratib S, Sweeting M, Ryder S, De Angelis D . Response rates to combination therapy for chronic HCV infection in a clinical setting and derivation of probability tables for individual patient management. J Viral Hepat. 2007; 15(4):271-8. DOI: 10.1111/j.1365-2893.2007.00941.x. View

4.
Goh E, Morgan M . Review article: pharmacotherapy for alcohol dependence - the why, the what and the wherefore. Aliment Pharmacol Ther. 2017; 45(7):865-882. DOI: 10.1111/apt.13965. View

5.
Omland L, Osler M, Jepsen P, Krarup H, Weis N, Christensen P . Socioeconomic status in HCV infected patients - risk and prognosis. Clin Epidemiol. 2013; 5:163-72. PMC: 3678712. DOI: 10.2147/CLEP.S43926. View