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Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison

BACKGROUND: Prisoners are at risk of hepatitis C virus (HCV) infection, especially among the people who inject drugs (PWID). We implemented an outreach strategy in combination with universal mass screening and immediate onsite treatment with a simplified pan-genotypic direct-acting antivirals (DAA)...

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Autores principales: Chen, Chun-Ting, Lu, Ming-Ying, Hsieh, Meng-Hsuan, Tsai, Pei-Chien, Hsieh, Tsai-Yuan, Yeh, Ming-Lun, Huang, Ching-I, Tsai, Yi-Shan, Ko, Yu-Min, Lin, Ching-Chih, Chen, Kuan-Yu, Wei, Yu-Ju, Hsu, Po-Yao, Hsu, Cheng-Ting, Jang, Tyng-Yuan, Liu, Ta-Wei, Liang, Po-Cheng, Hsieh, Ming-Yen, Lin, Zu-Yau, Huang, Chung-Feng, Huang, Jee-Fu, Dai, Chia-Yen, Chuang, Wan-Long, Shih, Yu-Lueng, Yu, Ming-Lung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776526/
https://www.ncbi.nlm.nih.gov/pubmed/35110949
http://dx.doi.org/10.3748/wjg.v28.i2.263
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author Chen, Chun-Ting
Lu, Ming-Ying
Hsieh, Meng-Hsuan
Tsai, Pei-Chien
Hsieh, Tsai-Yuan
Yeh, Ming-Lun
Huang, Ching-I
Tsai, Yi-Shan
Ko, Yu-Min
Lin, Ching-Chih
Chen, Kuan-Yu
Wei, Yu-Ju
Hsu, Po-Yao
Hsu, Cheng-Ting
Jang, Tyng-Yuan
Liu, Ta-Wei
Liang, Po-Cheng
Hsieh, Ming-Yen
Lin, Zu-Yau
Huang, Chung-Feng
Huang, Jee-Fu
Dai, Chia-Yen
Chuang, Wan-Long
Shih, Yu-Lueng
Yu, Ming-Lung
author_facet Chen, Chun-Ting
Lu, Ming-Ying
Hsieh, Meng-Hsuan
Tsai, Pei-Chien
Hsieh, Tsai-Yuan
Yeh, Ming-Lun
Huang, Ching-I
Tsai, Yi-Shan
Ko, Yu-Min
Lin, Ching-Chih
Chen, Kuan-Yu
Wei, Yu-Ju
Hsu, Po-Yao
Hsu, Cheng-Ting
Jang, Tyng-Yuan
Liu, Ta-Wei
Liang, Po-Cheng
Hsieh, Ming-Yen
Lin, Zu-Yau
Huang, Chung-Feng
Huang, Jee-Fu
Dai, Chia-Yen
Chuang, Wan-Long
Shih, Yu-Lueng
Yu, Ming-Lung
author_sort Chen, Chun-Ting
collection PubMed
description BACKGROUND: Prisoners are at risk of hepatitis C virus (HCV) infection, especially among the people who inject drugs (PWID). We implemented an outreach strategy in combination with universal mass screening and immediate onsite treatment with a simplified pan-genotypic direct-acting antivirals (DAA) regimen, 12 wk of sofosbuvir/velpatasvir, in a PWID-dominant prison in Taiwan. AIM: To implement an outreach strategy in combination with universal mass screening and immediate onsite treatment with a simplified pan-genotypic DAA regimen in a PWID-dominant prison in Taiwan. METHODS: HCV-viremic patients were recruited for onsite treatment program for HCV micro-elimination with a pangenotypic DAA regimen, 12 wk of sofosbuvir/ velpatasvir, from two cohorts in Penghu Prison, either identified by mass screen or in outpatient clinics, in September 2019. Another group of HCV-viremic patients identified sporadically in outpatient clinics before mass screening were enrolled as a control group. The primary endpoint was sustained virological response (SVR12, defined as undetectable HCV ribonucleic acid (RNA) 12 wk after end-of-treatment). RESULTS: A total of 212 HCV-viremic subjects were recruited for HCV micro-elimination campaign; 91 patients treated with sofosbuvir/Ledipasvir or glecaprevir/ pibrentasvir before mass screening were enrolled as a control. The HCV micro-elimination group had significantly lower proportion of diabetes, hypertension, hyperlipidemia, advanced fibrosis and chronic kidney diseases, but higher levels of HCV RNA. The SVR12 rate was comparable between the HCV micro-elimination and control groups, 95.8% (203/212) vs 94.5% (86/91), respectively, in intent-to-treat analysis, and 100% (203/203) vs 98.9% (86/87), respectively, in per-protocol analysis. There was no virological failure, treatment discontinuation, and serious adverse event among sofosbuvir/velpatasvir-treated patients in the HCV micro-elimination group. CONCLUSION: Outreach mass screening followed by immediate onsite treatment with a simplified pangenotypic DAA regimen, sofosbuvir/velpatasvir, provides successful strategies toward HCV micro-elimination among prisoners.
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spelling pubmed-87765262022-02-01 Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison Chen, Chun-Ting Lu, Ming-Ying Hsieh, Meng-Hsuan Tsai, Pei-Chien Hsieh, Tsai-Yuan Yeh, Ming-Lun Huang, Ching-I Tsai, Yi-Shan Ko, Yu-Min Lin, Ching-Chih Chen, Kuan-Yu Wei, Yu-Ju Hsu, Po-Yao Hsu, Cheng-Ting Jang, Tyng-Yuan Liu, Ta-Wei Liang, Po-Cheng Hsieh, Ming-Yen Lin, Zu-Yau Huang, Chung-Feng Huang, Jee-Fu Dai, Chia-Yen Chuang, Wan-Long Shih, Yu-Lueng Yu, Ming-Lung World J Gastroenterol Prospective Study BACKGROUND: Prisoners are at risk of hepatitis C virus (HCV) infection, especially among the people who inject drugs (PWID). We implemented an outreach strategy in combination with universal mass screening and immediate onsite treatment with a simplified pan-genotypic direct-acting antivirals (DAA) regimen, 12 wk of sofosbuvir/velpatasvir, in a PWID-dominant prison in Taiwan. AIM: To implement an outreach strategy in combination with universal mass screening and immediate onsite treatment with a simplified pan-genotypic DAA regimen in a PWID-dominant prison in Taiwan. METHODS: HCV-viremic patients were recruited for onsite treatment program for HCV micro-elimination with a pangenotypic DAA regimen, 12 wk of sofosbuvir/ velpatasvir, from two cohorts in Penghu Prison, either identified by mass screen or in outpatient clinics, in September 2019. Another group of HCV-viremic patients identified sporadically in outpatient clinics before mass screening were enrolled as a control group. The primary endpoint was sustained virological response (SVR12, defined as undetectable HCV ribonucleic acid (RNA) 12 wk after end-of-treatment). RESULTS: A total of 212 HCV-viremic subjects were recruited for HCV micro-elimination campaign; 91 patients treated with sofosbuvir/Ledipasvir or glecaprevir/ pibrentasvir before mass screening were enrolled as a control. The HCV micro-elimination group had significantly lower proportion of diabetes, hypertension, hyperlipidemia, advanced fibrosis and chronic kidney diseases, but higher levels of HCV RNA. The SVR12 rate was comparable between the HCV micro-elimination and control groups, 95.8% (203/212) vs 94.5% (86/91), respectively, in intent-to-treat analysis, and 100% (203/203) vs 98.9% (86/87), respectively, in per-protocol analysis. There was no virological failure, treatment discontinuation, and serious adverse event among sofosbuvir/velpatasvir-treated patients in the HCV micro-elimination group. CONCLUSION: Outreach mass screening followed by immediate onsite treatment with a simplified pangenotypic DAA regimen, sofosbuvir/velpatasvir, provides successful strategies toward HCV micro-elimination among prisoners. Baishideng Publishing Group Inc 2022-01-14 2022-01-14 /pmc/articles/PMC8776526/ /pubmed/35110949 http://dx.doi.org/10.3748/wjg.v28.i2.263 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Prospective Study
Chen, Chun-Ting
Lu, Ming-Ying
Hsieh, Meng-Hsuan
Tsai, Pei-Chien
Hsieh, Tsai-Yuan
Yeh, Ming-Lun
Huang, Ching-I
Tsai, Yi-Shan
Ko, Yu-Min
Lin, Ching-Chih
Chen, Kuan-Yu
Wei, Yu-Ju
Hsu, Po-Yao
Hsu, Cheng-Ting
Jang, Tyng-Yuan
Liu, Ta-Wei
Liang, Po-Cheng
Hsieh, Ming-Yen
Lin, Zu-Yau
Huang, Chung-Feng
Huang, Jee-Fu
Dai, Chia-Yen
Chuang, Wan-Long
Shih, Yu-Lueng
Yu, Ming-Lung
Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison
title Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison
title_full Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison
title_fullStr Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison
title_full_unstemmed Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison
title_short Outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis C virus micro-elimination in a prison
title_sort outreach onsite treatment with a simplified pangenotypic direct-acting anti-viral regimen for hepatitis c virus micro-elimination in a prison
topic Prospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8776526/
https://www.ncbi.nlm.nih.gov/pubmed/35110949
http://dx.doi.org/10.3748/wjg.v28.i2.263
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