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Challenges in hepatitis C elimination despite highly effective antiviral agents in patients with and without intravenous drug use

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Summary

Aim

To assess the adherence to treatment, sustained virologic response (SVR) rate, and reinfection rate in hepatitis C patients with and without intravenous drug use.

Methods

This retrospective study included hepatitis C patients, evaluated and treated in our hepatology outpatient clinic between January 2014 and October 2019.

The following information was extracted from the patient’s file: the presence of positive viral load for hepatitis C virus (HCV), active and recent (in the last 6 months) use of i.v. drugs, HCV genotype, treatment regimen, SVR, HCV reinfection rate, coinfection with human immunodeficiency virus (HIV) and ongoing opioid substitution therapy (OST).

Results

We included 431 hepatitis C patients, 234 people who inject drugs (PWID) and 197 non-PWID. Most patients were treated with direct-acting antivirals (DAA) only.

The rate of documented SVR by treated patients was significantly higher in the non-PWID cohort (91.5% vs. 61.5%, p < 0.0001), while noncompliance (did not show up to start treatment) rate or refusal of treatment was significantly higher in the PWID cohort (19.4% vs. 8.9%, p = 0.004).

In the PWID cohort, younger age and recent (in the last 6 months) or ongoing i.v. drug use was associated with noncompliance: 31.1 ± 8.4 years vs. 35.8 ± 10.6 years (p = 0.02) and 33.3% vs. 12.8% (p = 0.0008), respectively.

Ongoing OST was associated with better compliance: 61.1% vs. 46.1% (p = 0.04).

Conclusion

To achieve elimination of hepatitis C better treatment strategies are needed, especially in PWIDs.

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Abbreviations

DAA:

Direct-acting antivirals

EOT:

End of treatment

HCV:

Hepatitis C virus

HIV:

Human immunodeficiency virus

Non-PWID:

People who do not inject drugs

OST:

Opioid substitution therapy

PegIFN:

Pegylated interferon

PWID:

People who inject drugs

SVR:

Sustained virologic response

WHO:

World Health Organization

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Correspondence to Markus Peck-Radosavljevic.

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Conflict of interest

M. Peck-Radosavljevic declares consultation and speaker fees from AbbVie, Gilead, MSD. S. Bota: declares speaker fees from AbbVie. F. Hucke, C. Urak, K. Flatscher and M. Razpotnik declare that they have no competing interests.

Ethical standards

This study was approved by the ethics committee of our institution (approval number A38/18), and the study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki as reflected in a priori approval by the institution’s human research committee.

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Bota, S., Razpotnik, M., Hucke, F. et al. Challenges in hepatitis C elimination despite highly effective antiviral agents in patients with and without intravenous drug use. Wien Klin Wochenschr 133, 641–646 (2021). https://doi.org/10.1007/s00508-021-01868-1

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