Loading…
Real-world direct-acting antiviral treatment in kidney transplant and hemodialysis patients: the EpiTer-2 multicenter observational study
Patients who undergo hemodialysis (HD) or kidney transplantation (KTx) previously had limited possibilities for treatment of hepatitis C virus (HCV) infection. Direct-acting antivirals (DAA) give these patients a chance of virus eradication and safe transplantation. The aim of this study was to eval...
Saved in:
Published in: | Annals of gastroenterology 2021, Vol.34 (3), p.438-446 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c390t-9b71052ba2bf75f166050e95ada51837a23123510ba666a48ae6465cece9dadf3 |
---|---|
cites | |
container_end_page | 446 |
container_issue | 3 |
container_start_page | 438 |
container_title | Annals of gastroenterology |
container_volume | 34 |
creator | Tronina, Olga Durlik, Magdalena Orłowska, Iwona Lorenc, Beata Łapiński, Tadeusz W Garlicki, Aleksander Dybowska, Dorota Zarębska-Michaluk, Dorota Tudrujek-Zdunek, Magdalena Citko, Jolanta Janczewska, Ewa Kaczmarczyk, Marcin Jaroszewicz, Jerzy Krygier, Rafał Klapaczyński, Jakub Dobracka, Beata Białkowska-Warzecha, Jolanta Piekarska, Anna Simon, Krzysztof Halota, Waldemar Pawłowska, Małgorzata Tomasiewicz, Krzysztof Flisiak, Robert |
description | Patients who undergo hemodialysis (HD) or kidney transplantation (KTx) previously had limited possibilities for treatment of hepatitis C virus (HCV) infection. Direct-acting antivirals (DAA) give these patients a chance of virus eradication and safe transplantation. The aim of this study was to evaluate the effectiveness and safety of DAA in KTx and HD patients in real-world settings.
Sustained virologic response (SVR) and treatment safety were analyzed in KTx and HD patients from the EpiTer-2 database, which included HCV-infected subjects treated with DAA between 2015 and 2019. Additionally, for KTx patients, changes in creatinine concentration, estimated glomerular filtration rate (eGFR), proteinuria within a year after treatment, and changes in the need for calcineurin inhibitors were assessed.
Among 10,152 patients from the EpiTer-2 database 148 were selected, 85 after KTx and 63 undergoing HD. The most common genotype, 1b HCV, was found in 73% and 86% of patients, respectively. Cirrhosis was noted in 10% and 19%, respectively. The most common DAA regimen after KTx was sofosbuvir/ledipasvir (54%), whereas in HD patients it was ombitasvir/paritaprevir/ritonavir +/- dasabuvir (56%). All patients with available follow-up results achieved SVR. No deaths, kidney loss or acute rejection episodes were noted. The most common adverse effects in both groups were anemia and weakness. One year after treatment, creatinine concentration, eGFR and proteinuria remained stable in the majority of patients.
DAA treatment of HCV infection demonstrated high effectiveness and safety in hemodialyzed patients and patients who had undergone KTx in this real-world study. |
doi_str_mv | 10.20524/aog.2021.0595 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8079881</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2522392363</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-9b71052ba2bf75f166050e95ada51837a23123510ba666a48ae6465cece9dadf3</originalsourceid><addsrcrecordid>eNpVkctu1DAUhi0EoqWwZYm8ZJPBl9iJWSChqlykSkhVu7ZO4pMZQxIH25lqHoG3xkNL1a78y-c715-Qt5xtBFOi_gBhW5TgG6aMekZOeWNE1dRaPi-as7bohp-QVyn9ZEzppq5fkhMpTd2yhp-SP1cIY3Ub4uio8xH7XEGf_bylMGe_9xFGmiNCnnDO1M_0l3czHsofzGkZC1RAR3c4BedhPCSf6ALZFzp9pHmH9GLx1xgrQad1zL4vAYw0dAnjvnBhLg1SXt3hNXkxwJjwzf17Rm6-XFyff6suf3z9fv75suqlYbkyXcPL4h2IbmjUwLVmiqFR4EDxVjYgJBdScdaB1hrqFlDXWvXYo3HgBnlGPt3VXdZuQnccqCxpl-gniAcbwNunkdnv7DbsbTmYaVteCry_LxDD7xVTtpNPPY7lGBjWZIUSQhohtSzo5g7tY0gp4vDQhjP7zz9b_LNH_-zRv5Lw7vFwD_h_w-RfFJybOg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2522392363</pqid></control><display><type>article</type><title>Real-world direct-acting antiviral treatment in kidney transplant and hemodialysis patients: the EpiTer-2 multicenter observational study</title><source>NCBI_PubMed Central(免费)</source><creator>Tronina, Olga ; Durlik, Magdalena ; Orłowska, Iwona ; Lorenc, Beata ; Łapiński, Tadeusz W ; Garlicki, Aleksander ; Dybowska, Dorota ; Zarębska-Michaluk, Dorota ; Tudrujek-Zdunek, Magdalena ; Citko, Jolanta ; Janczewska, Ewa ; Kaczmarczyk, Marcin ; Jaroszewicz, Jerzy ; Krygier, Rafał ; Klapaczyński, Jakub ; Dobracka, Beata ; Białkowska-Warzecha, Jolanta ; Piekarska, Anna ; Simon, Krzysztof ; Halota, Waldemar ; Pawłowska, Małgorzata ; Tomasiewicz, Krzysztof ; Flisiak, Robert</creator><creatorcontrib>Tronina, Olga ; Durlik, Magdalena ; Orłowska, Iwona ; Lorenc, Beata ; Łapiński, Tadeusz W ; Garlicki, Aleksander ; Dybowska, Dorota ; Zarębska-Michaluk, Dorota ; Tudrujek-Zdunek, Magdalena ; Citko, Jolanta ; Janczewska, Ewa ; Kaczmarczyk, Marcin ; Jaroszewicz, Jerzy ; Krygier, Rafał ; Klapaczyński, Jakub ; Dobracka, Beata ; Białkowska-Warzecha, Jolanta ; Piekarska, Anna ; Simon, Krzysztof ; Halota, Waldemar ; Pawłowska, Małgorzata ; Tomasiewicz, Krzysztof ; Flisiak, Robert</creatorcontrib><description>Patients who undergo hemodialysis (HD) or kidney transplantation (KTx) previously had limited possibilities for treatment of hepatitis C virus (HCV) infection. Direct-acting antivirals (DAA) give these patients a chance of virus eradication and safe transplantation. The aim of this study was to evaluate the effectiveness and safety of DAA in KTx and HD patients in real-world settings.
Sustained virologic response (SVR) and treatment safety were analyzed in KTx and HD patients from the EpiTer-2 database, which included HCV-infected subjects treated with DAA between 2015 and 2019. Additionally, for KTx patients, changes in creatinine concentration, estimated glomerular filtration rate (eGFR), proteinuria within a year after treatment, and changes in the need for calcineurin inhibitors were assessed.
Among 10,152 patients from the EpiTer-2 database 148 were selected, 85 after KTx and 63 undergoing HD. The most common genotype, 1b HCV, was found in 73% and 86% of patients, respectively. Cirrhosis was noted in 10% and 19%, respectively. The most common DAA regimen after KTx was sofosbuvir/ledipasvir (54%), whereas in HD patients it was ombitasvir/paritaprevir/ritonavir +/- dasabuvir (56%). All patients with available follow-up results achieved SVR. No deaths, kidney loss or acute rejection episodes were noted. The most common adverse effects in both groups were anemia and weakness. One year after treatment, creatinine concentration, eGFR and proteinuria remained stable in the majority of patients.
DAA treatment of HCV infection demonstrated high effectiveness and safety in hemodialyzed patients and patients who had undergone KTx in this real-world study.</description><identifier>ISSN: 1108-7471</identifier><identifier>ISSN: 1792-7463</identifier><identifier>EISSN: 1792-7463</identifier><identifier>DOI: 10.20524/aog.2021.0595</identifier><identifier>PMID: 33948071</identifier><language>eng</language><publisher>Greece: Hellenic Society of Gastroenterology</publisher><subject>Original</subject><ispartof>Annals of gastroenterology, 2021, Vol.34 (3), p.438-446</ispartof><rights>Copyright: © 2021 Hellenic Society of Gastroenterology.</rights><rights>Copyright: © 2021 Hellenic Society of Gastroenterology 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-9b71052ba2bf75f166050e95ada51837a23123510ba666a48ae6465cece9dadf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079881/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079881/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,4010,27904,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33948071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tronina, Olga</creatorcontrib><creatorcontrib>Durlik, Magdalena</creatorcontrib><creatorcontrib>Orłowska, Iwona</creatorcontrib><creatorcontrib>Lorenc, Beata</creatorcontrib><creatorcontrib>Łapiński, Tadeusz W</creatorcontrib><creatorcontrib>Garlicki, Aleksander</creatorcontrib><creatorcontrib>Dybowska, Dorota</creatorcontrib><creatorcontrib>Zarębska-Michaluk, Dorota</creatorcontrib><creatorcontrib>Tudrujek-Zdunek, Magdalena</creatorcontrib><creatorcontrib>Citko, Jolanta</creatorcontrib><creatorcontrib>Janczewska, Ewa</creatorcontrib><creatorcontrib>Kaczmarczyk, Marcin</creatorcontrib><creatorcontrib>Jaroszewicz, Jerzy</creatorcontrib><creatorcontrib>Krygier, Rafał</creatorcontrib><creatorcontrib>Klapaczyński, Jakub</creatorcontrib><creatorcontrib>Dobracka, Beata</creatorcontrib><creatorcontrib>Białkowska-Warzecha, Jolanta</creatorcontrib><creatorcontrib>Piekarska, Anna</creatorcontrib><creatorcontrib>Simon, Krzysztof</creatorcontrib><creatorcontrib>Halota, Waldemar</creatorcontrib><creatorcontrib>Pawłowska, Małgorzata</creatorcontrib><creatorcontrib>Tomasiewicz, Krzysztof</creatorcontrib><creatorcontrib>Flisiak, Robert</creatorcontrib><title>Real-world direct-acting antiviral treatment in kidney transplant and hemodialysis patients: the EpiTer-2 multicenter observational study</title><title>Annals of gastroenterology</title><addtitle>Ann Gastroenterol</addtitle><description>Patients who undergo hemodialysis (HD) or kidney transplantation (KTx) previously had limited possibilities for treatment of hepatitis C virus (HCV) infection. Direct-acting antivirals (DAA) give these patients a chance of virus eradication and safe transplantation. The aim of this study was to evaluate the effectiveness and safety of DAA in KTx and HD patients in real-world settings.
Sustained virologic response (SVR) and treatment safety were analyzed in KTx and HD patients from the EpiTer-2 database, which included HCV-infected subjects treated with DAA between 2015 and 2019. Additionally, for KTx patients, changes in creatinine concentration, estimated glomerular filtration rate (eGFR), proteinuria within a year after treatment, and changes in the need for calcineurin inhibitors were assessed.
Among 10,152 patients from the EpiTer-2 database 148 were selected, 85 after KTx and 63 undergoing HD. The most common genotype, 1b HCV, was found in 73% and 86% of patients, respectively. Cirrhosis was noted in 10% and 19%, respectively. The most common DAA regimen after KTx was sofosbuvir/ledipasvir (54%), whereas in HD patients it was ombitasvir/paritaprevir/ritonavir +/- dasabuvir (56%). All patients with available follow-up results achieved SVR. No deaths, kidney loss or acute rejection episodes were noted. The most common adverse effects in both groups were anemia and weakness. One year after treatment, creatinine concentration, eGFR and proteinuria remained stable in the majority of patients.
DAA treatment of HCV infection demonstrated high effectiveness and safety in hemodialyzed patients and patients who had undergone KTx in this real-world study.</description><subject>Original</subject><issn>1108-7471</issn><issn>1792-7463</issn><issn>1792-7463</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVkctu1DAUhi0EoqWwZYm8ZJPBl9iJWSChqlykSkhVu7ZO4pMZQxIH25lqHoG3xkNL1a78y-c715-Qt5xtBFOi_gBhW5TgG6aMekZOeWNE1dRaPi-as7bohp-QVyn9ZEzppq5fkhMpTd2yhp-SP1cIY3Ub4uio8xH7XEGf_bylMGe_9xFGmiNCnnDO1M_0l3czHsofzGkZC1RAR3c4BedhPCSf6ALZFzp9pHmH9GLx1xgrQad1zL4vAYw0dAnjvnBhLg1SXt3hNXkxwJjwzf17Rm6-XFyff6suf3z9fv75suqlYbkyXcPL4h2IbmjUwLVmiqFR4EDxVjYgJBdScdaB1hrqFlDXWvXYo3HgBnlGPt3VXdZuQnccqCxpl-gniAcbwNunkdnv7DbsbTmYaVteCry_LxDD7xVTtpNPPY7lGBjWZIUSQhohtSzo5g7tY0gp4vDQhjP7zz9b_LNH_-zRv5Lw7vFwD_h_w-RfFJybOg</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Tronina, Olga</creator><creator>Durlik, Magdalena</creator><creator>Orłowska, Iwona</creator><creator>Lorenc, Beata</creator><creator>Łapiński, Tadeusz W</creator><creator>Garlicki, Aleksander</creator><creator>Dybowska, Dorota</creator><creator>Zarębska-Michaluk, Dorota</creator><creator>Tudrujek-Zdunek, Magdalena</creator><creator>Citko, Jolanta</creator><creator>Janczewska, Ewa</creator><creator>Kaczmarczyk, Marcin</creator><creator>Jaroszewicz, Jerzy</creator><creator>Krygier, Rafał</creator><creator>Klapaczyński, Jakub</creator><creator>Dobracka, Beata</creator><creator>Białkowska-Warzecha, Jolanta</creator><creator>Piekarska, Anna</creator><creator>Simon, Krzysztof</creator><creator>Halota, Waldemar</creator><creator>Pawłowska, Małgorzata</creator><creator>Tomasiewicz, Krzysztof</creator><creator>Flisiak, Robert</creator><general>Hellenic Society of Gastroenterology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2021</creationdate><title>Real-world direct-acting antiviral treatment in kidney transplant and hemodialysis patients: the EpiTer-2 multicenter observational study</title><author>Tronina, Olga ; Durlik, Magdalena ; Orłowska, Iwona ; Lorenc, Beata ; Łapiński, Tadeusz W ; Garlicki, Aleksander ; Dybowska, Dorota ; Zarębska-Michaluk, Dorota ; Tudrujek-Zdunek, Magdalena ; Citko, Jolanta ; Janczewska, Ewa ; Kaczmarczyk, Marcin ; Jaroszewicz, Jerzy ; Krygier, Rafał ; Klapaczyński, Jakub ; Dobracka, Beata ; Białkowska-Warzecha, Jolanta ; Piekarska, Anna ; Simon, Krzysztof ; Halota, Waldemar ; Pawłowska, Małgorzata ; Tomasiewicz, Krzysztof ; Flisiak, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-9b71052ba2bf75f166050e95ada51837a23123510ba666a48ae6465cece9dadf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tronina, Olga</creatorcontrib><creatorcontrib>Durlik, Magdalena</creatorcontrib><creatorcontrib>Orłowska, Iwona</creatorcontrib><creatorcontrib>Lorenc, Beata</creatorcontrib><creatorcontrib>Łapiński, Tadeusz W</creatorcontrib><creatorcontrib>Garlicki, Aleksander</creatorcontrib><creatorcontrib>Dybowska, Dorota</creatorcontrib><creatorcontrib>Zarębska-Michaluk, Dorota</creatorcontrib><creatorcontrib>Tudrujek-Zdunek, Magdalena</creatorcontrib><creatorcontrib>Citko, Jolanta</creatorcontrib><creatorcontrib>Janczewska, Ewa</creatorcontrib><creatorcontrib>Kaczmarczyk, Marcin</creatorcontrib><creatorcontrib>Jaroszewicz, Jerzy</creatorcontrib><creatorcontrib>Krygier, Rafał</creatorcontrib><creatorcontrib>Klapaczyński, Jakub</creatorcontrib><creatorcontrib>Dobracka, Beata</creatorcontrib><creatorcontrib>Białkowska-Warzecha, Jolanta</creatorcontrib><creatorcontrib>Piekarska, Anna</creatorcontrib><creatorcontrib>Simon, Krzysztof</creatorcontrib><creatorcontrib>Halota, Waldemar</creatorcontrib><creatorcontrib>Pawłowska, Małgorzata</creatorcontrib><creatorcontrib>Tomasiewicz, Krzysztof</creatorcontrib><creatorcontrib>Flisiak, Robert</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tronina, Olga</au><au>Durlik, Magdalena</au><au>Orłowska, Iwona</au><au>Lorenc, Beata</au><au>Łapiński, Tadeusz W</au><au>Garlicki, Aleksander</au><au>Dybowska, Dorota</au><au>Zarębska-Michaluk, Dorota</au><au>Tudrujek-Zdunek, Magdalena</au><au>Citko, Jolanta</au><au>Janczewska, Ewa</au><au>Kaczmarczyk, Marcin</au><au>Jaroszewicz, Jerzy</au><au>Krygier, Rafał</au><au>Klapaczyński, Jakub</au><au>Dobracka, Beata</au><au>Białkowska-Warzecha, Jolanta</au><au>Piekarska, Anna</au><au>Simon, Krzysztof</au><au>Halota, Waldemar</au><au>Pawłowska, Małgorzata</au><au>Tomasiewicz, Krzysztof</au><au>Flisiak, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Real-world direct-acting antiviral treatment in kidney transplant and hemodialysis patients: the EpiTer-2 multicenter observational study</atitle><jtitle>Annals of gastroenterology</jtitle><addtitle>Ann Gastroenterol</addtitle><date>2021</date><risdate>2021</risdate><volume>34</volume><issue>3</issue><spage>438</spage><epage>446</epage><pages>438-446</pages><issn>1108-7471</issn><issn>1792-7463</issn><eissn>1792-7463</eissn><abstract>Patients who undergo hemodialysis (HD) or kidney transplantation (KTx) previously had limited possibilities for treatment of hepatitis C virus (HCV) infection. Direct-acting antivirals (DAA) give these patients a chance of virus eradication and safe transplantation. The aim of this study was to evaluate the effectiveness and safety of DAA in KTx and HD patients in real-world settings.
Sustained virologic response (SVR) and treatment safety were analyzed in KTx and HD patients from the EpiTer-2 database, which included HCV-infected subjects treated with DAA between 2015 and 2019. Additionally, for KTx patients, changes in creatinine concentration, estimated glomerular filtration rate (eGFR), proteinuria within a year after treatment, and changes in the need for calcineurin inhibitors were assessed.
Among 10,152 patients from the EpiTer-2 database 148 were selected, 85 after KTx and 63 undergoing HD. The most common genotype, 1b HCV, was found in 73% and 86% of patients, respectively. Cirrhosis was noted in 10% and 19%, respectively. The most common DAA regimen after KTx was sofosbuvir/ledipasvir (54%), whereas in HD patients it was ombitasvir/paritaprevir/ritonavir +/- dasabuvir (56%). All patients with available follow-up results achieved SVR. No deaths, kidney loss or acute rejection episodes were noted. The most common adverse effects in both groups were anemia and weakness. One year after treatment, creatinine concentration, eGFR and proteinuria remained stable in the majority of patients.
DAA treatment of HCV infection demonstrated high effectiveness and safety in hemodialyzed patients and patients who had undergone KTx in this real-world study.</abstract><cop>Greece</cop><pub>Hellenic Society of Gastroenterology</pub><pmid>33948071</pmid><doi>10.20524/aog.2021.0595</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1108-7471 |
ispartof | Annals of gastroenterology, 2021, Vol.34 (3), p.438-446 |
issn | 1108-7471 1792-7463 1792-7463 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8079881 |
source | NCBI_PubMed Central(免费) |
subjects | Original |
title | Real-world direct-acting antiviral treatment in kidney transplant and hemodialysis patients: the EpiTer-2 multicenter observational study |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T07%3A34%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Real-world%20direct-acting%20antiviral%20treatment%20in%20kidney%20transplant%20and%20hemodialysis%20patients:%20the%20EpiTer-2%20multicenter%20observational%20study&rft.jtitle=Annals%20of%20gastroenterology&rft.au=Tronina,%20Olga&rft.date=2021&rft.volume=34&rft.issue=3&rft.spage=438&rft.epage=446&rft.pages=438-446&rft.issn=1108-7471&rft.eissn=1792-7463&rft_id=info:doi/10.20524/aog.2021.0595&rft_dat=%3Cproquest_pubme%3E2522392363%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c390t-9b71052ba2bf75f166050e95ada51837a23123510ba666a48ae6465cece9dadf3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2522392363&rft_id=info:pmid/33948071&rfr_iscdi=true |