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    <responseDate>2026-10-15T17:14:46Z</responseDate>
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                <identifier>oai:data.mendeley.com/n3w628yk3t.1</identifier>
                <datestamp>2023-05-03T11:40:11Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Czarnecka, Paulina</dc:creator>
    <dc:title>Evaluation of long-term outcomes of direct acting antiviral agents in chronic kidney disease subjects: a single center cohort study.</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Abstract: Background: Chronic kidney disease (CKD) population, including kidney transplant recipients (KTRs) and subjects on renal replacement therapy, is particularly vulnerable to unfa-vorable outcomes of chronic hepatitis C (CHC). Currently, there are oral direct- acting antiviral agents (DAAs) available to eradicate the virus with favorable short-terms outcomes, however long-term effects are lacking. The aim of the study was to assess long-term efficacy and safety of DAA therapy in CKD population. Methods: An observational, cohort single-center study was performed. Fifty-nine CHC subjects with CKD, treated with DAAs between 2016 and 2018 were enrolled to the study. Safety and efficacy profiles were assessed, including sustained virologic response (SVR), occult hepatitis C infection (OCI) incidence and liver fibrosis. Results: SVR was achieved in 96 % of cases (n=57). OCI was diagnosed only in one subject following SVR. Signifi-cant Liver stiffness regression has been observed 4 years following SVR compered to baseline values (Mdn = 6.1 kPa, IQR = 3.75 kPa; 4.9 kPa,IQR = 2.9 kPa), p &lt;0.001. Most common adverse events were anemia, weakness and urinary tract infection. Conclusion: DAAs provide a safe and effective cure for CHC in both CKD patients and KTRs with favorable safety profile in the long-term follow-up.</dc:description>
    <dc:subject>Fibrosis</dc:subject>
    <dc:subject>Hepatitis C</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/n3w628yk3t.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/n3w628yk3t.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
    <dc:rights>http://creativecommons.org/licenses/by/4.0</dc:rights>
    <dc:relation>https://data.mendeley.com/datasets/n3w628yk3t</dc:relation>
    <dc:date>2023-05-03T11:40:11Z</dc:date>
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