Clinical Results of Tenofovir Disoproxil Fumarate in a Hemodialysis Patient with Chronic Hepatitis B
A male hepatitis B virus (HBV) carrier in his 40s under hemodialysis treatment exhibited chronic hepatitis (alanine aminotransferase: 41 IU/L, HBV-DNA: >9.1 log copies/mL). Following discontinuation of the initial treatment with pegylated interferon-α-2a at 24 weeks due to adverse effects, the ad...
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description | A male hepatitis B virus (HBV) carrier in his 40s under hemodialysis treatment exhibited chronic hepatitis (alanine aminotransferase: 41 IU/L, HBV-DNA: >9.1 log copies/mL). Following discontinuation of the initial treatment with pegylated interferon-α-2a at 24 weeks due to adverse effects, the administration of tenofovirdisoproxil fumarate (TDF) (300 mg/week) led to a rapid improvement in hepatitis markers: HBV DNA became undetectable at month 34, and seroconversion of hepatitis B envelope antigen was confirmed at 45 months. No side effects were recorded during TDF treatment. TDF is a newly approved nucleoside analogue that may cause severe side effects via proximal tubular injury in patients with renal dysfunction. However, few reports have described its use in hemodialysis patients, whose anuric state may render them less susceptible to side effects including kidney injury. Hepatitis improved remarkably without any adverse drug reactions in the present case. TDF may therefore be considered for chronic hepatitis B patients receiving hemodialysis. |
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Following discontinuation of the initial treatment with pegylated interferon-α-2a at 24 weeks due to adverse effects, the administration of tenofovirdisoproxil fumarate (TDF) (300 mg/week) led to a rapid improvement in hepatitis markers: HBV DNA became undetectable at month 34, and seroconversion of hepatitis B envelope antigen was confirmed at 45 months. No side effects were recorded during TDF treatment. TDF is a newly approved nucleoside analogue that may cause severe side effects via proximal tubular injury in patients with renal dysfunction. However, few reports have described its use in hemodialysis patients, whose anuric state may render them less susceptible to side effects including kidney injury. Hepatitis improved remarkably without any adverse drug reactions in the present case. TDF may therefore be considered for chronic hepatitis B patients receiving hemodialysis.</description><identifier>ISSN: 2296-9705</identifier><identifier>EISSN: 2296-9705</identifier><identifier>DOI: 10.1159/000508806</identifier><identifier>PMID: 33251250</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Antigens ; Antiretroviral drugs ; Care and treatment ; Case Report ; Case reports ; Case studies ; chronic hepatitis b ; Chronic kidney failure ; Drug resistance ; Drug therapy ; end-stage renal disease ; Hemodialysis ; Hemodialysis patients ; Hepatitis ; Hepatitis B ; Infections ; Kidney diseases ; Liver cancer ; Mortality ; nucleoside analogue ; Patient outcomes ; Patients ; Serology ; Tenofovir ; tenofovirdisoproxil fumarate</subject><ispartof>Case Reports in Nephrology and Dialysis, 2020-09, Vol.10 (3), p.130-138</ispartof><rights>2020 The Author(s). Published by S. Karger AG, Basel</rights><rights>COPYRIGHT 2020 S. 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Karger AG, Basel 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c489t-7a9370bb4559a093636cc57fefbda2f3fb740a520140c76ea6615122ee1b7b1e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670323/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670323/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2096,27612,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Aomura, Daiki</creatorcontrib><creatorcontrib>Tachibana, Naoki</creatorcontrib><creatorcontrib>Komatsu, Michiharu</creatorcontrib><creatorcontrib>Kobayashi, Masakazu</creatorcontrib><title>Clinical Results of Tenofovir Disoproxil Fumarate in a Hemodialysis Patient with Chronic Hepatitis B</title><title>Case Reports in Nephrology and Dialysis</title><addtitle>Case Rep Nephrol Dial</addtitle><description>A male hepatitis B virus (HBV) carrier in his 40s under hemodialysis treatment exhibited chronic hepatitis (alanine aminotransferase: 41 IU/L, HBV-DNA: >9.1 log copies/mL). Following discontinuation of the initial treatment with pegylated interferon-α-2a at 24 weeks due to adverse effects, the administration of tenofovirdisoproxil fumarate (TDF) (300 mg/week) led to a rapid improvement in hepatitis markers: HBV DNA became undetectable at month 34, and seroconversion of hepatitis B envelope antigen was confirmed at 45 months. No side effects were recorded during TDF treatment. TDF is a newly approved nucleoside analogue that may cause severe side effects via proximal tubular injury in patients with renal dysfunction. However, few reports have described its use in hemodialysis patients, whose anuric state may render them less susceptible to side effects including kidney injury. Hepatitis improved remarkably without any adverse drug reactions in the present case. TDF may therefore be considered for chronic hepatitis B patients receiving hemodialysis.</description><subject>Antigens</subject><subject>Antiretroviral drugs</subject><subject>Care and treatment</subject><subject>Case Report</subject><subject>Case reports</subject><subject>Case studies</subject><subject>chronic hepatitis b</subject><subject>Chronic kidney failure</subject><subject>Drug resistance</subject><subject>Drug therapy</subject><subject>end-stage renal disease</subject><subject>Hemodialysis</subject><subject>Hemodialysis patients</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>Infections</subject><subject>Kidney diseases</subject><subject>Liver cancer</subject><subject>Mortality</subject><subject>nucleoside analogue</subject><subject>Patient outcomes</subject><subject>Patients</subject><subject>Serology</subject><subject>Tenofovir</subject><subject>tenofovirdisoproxil fumarate</subject><issn>2296-9705</issn><issn>2296-9705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>M--</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><sourceid>DOA</sourceid><recordid>eNptks9rFDEUxwdRbKk9ePcQ6MnD1pdkkmwuQp3aH1BUpJ5Dfu5mnZ2MyWy1_71ppywWJIeE9z758L7wmuYthlOMmfwAAAyWS-AvmkNCJF9IAezlP--D5riUTcVwyyhn8Lo5oJQwTBgcNq7r4xCt7tF3X3b9VFAK6NYPKaS7mNF5LGnM6U_s0cVuq7OePIoD0ujKb5OLur8vsaBveop-mNDvOK1Rt86pGisx1vJU25_eNK-C7os_frqPmh8Xn2-7q8XN18vr7uxmYdulnBZCSyrAmJYxqUFSTrm1TAQfjNMk0GBEC5qRGgSs4F5zjmsM4j02wmBPj5rr2euS3qgxxzrxvUo6qsdCyiul8xRt7xUXQJbUBGnBtcxxSQyz3EiBW0NacNX1cXaNO7P1ztZ8WffPpM87Q1yrVbpToqopoVVw8iTI6dfOl0lt0i4PNb8iTAAQEJhV6nSmVrpOFYeQqszW4_w22jT4EGv9jLdVyzh-0L6fP9icSsk-7EfCoB4WQu0XorLvZvanziuf9-S-ffLfdvflfCbU6AL9C1zRupw</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Aomura, Daiki</creator><creator>Tachibana, Naoki</creator><creator>Komatsu, Michiharu</creator><creator>Kobayashi, Masakazu</creator><general>S. 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Following discontinuation of the initial treatment with pegylated interferon-α-2a at 24 weeks due to adverse effects, the administration of tenofovirdisoproxil fumarate (TDF) (300 mg/week) led to a rapid improvement in hepatitis markers: HBV DNA became undetectable at month 34, and seroconversion of hepatitis B envelope antigen was confirmed at 45 months. No side effects were recorded during TDF treatment. TDF is a newly approved nucleoside analogue that may cause severe side effects via proximal tubular injury in patients with renal dysfunction. However, few reports have described its use in hemodialysis patients, whose anuric state may render them less susceptible to side effects including kidney injury. Hepatitis improved remarkably without any adverse drug reactions in the present case. TDF may therefore be considered for chronic hepatitis B patients receiving hemodialysis.</abstract><cop>Basel, Switzerland</cop><pub>S. 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subjects | Antigens Antiretroviral drugs Care and treatment Case Report Case reports Case studies chronic hepatitis b Chronic kidney failure Drug resistance Drug therapy end-stage renal disease Hemodialysis Hemodialysis patients Hepatitis Hepatitis B Infections Kidney diseases Liver cancer Mortality nucleoside analogue Patient outcomes Patients Serology Tenofovir tenofovirdisoproxil fumarate |
title | Clinical Results of Tenofovir Disoproxil Fumarate in a Hemodialysis Patient with Chronic Hepatitis B |
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