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Clinical Experience of Patients With Hepatitis C Treated With Direct-Acting Antivirals After Heart Transplantation

Authors :
Chia-Ying Liu
Wei-Ling Yang
Hou-Sheng Yang
Jeng Wei
Chung-Yi Chang
You-Min Lu
Sheng-Ming Ling
Source :
Transplantation Proceedings. 53:665-672
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Background Hepatitis C increases the mortality and morbidity of patients after heart transplant. Direct-acting antivirals (DAAs) are the primary drugs for hepatitis C treatment. However, such drugs are expensive and frequently unaffordable for patients. In DAA treatment, the assessment of drug interaction is crucial. Methods We investigated a retrospective case series study from January 2017 to December 2019. Sustained virologic response 12 (SVR12) was used to assess the effectiveness of DAA treatment. Data on patients’ demographic information, timing of hepatitis C virus (HCV) infection (before or after heart transplant), HCV genotypes and viral loads, DAAs used (branded drugs or generic drugs), and drug interaction assessments were collected. Results Fifteen heart transplant patients received hepatitis C treatments during the study period, 11 of whom were infected because their donors had hepatitis C. After DAA treatment, HCV was undetectable in all patients, and 93.3% of them achieved SVR12. Nine patients used the generic sofosbuvir/velpatasvir, and 88.9% of them achieved SVR12. A total of 256 drugs were used with DAAs; 51 records of drug interactions were noted, 3 of which were contraindications, and the remaining records were potential interactions. Patients who used sofosbuvir or elbasvir/grazoprevir experienced fewer drug interactions. Conclusions DAA treatment is effective for hepatitis C treatment in patients after heart transplant. Patients who cannot afford branded drugs because of their prices can use generic drugs as an alternative. Drug interactions must be surveyed during DAA treatment.

Details

ISSN :
00411345
Volume :
53
Database :
OpenAIRE
Journal :
Transplantation Proceedings
Accession number :
edsair.doi.dedup.....9fe3b49175661b5e2a1195dd6e900b55