PS-077 Long term hepatotoxicity outcome of endothelin receptor antagonists as treatment in pulmonary arterial hypertension

BackgroundBosentan and ambrisentan, endothelin receptor antagonists, are used as treatment for pulmonary arterial hypertension (PAH), alone or in combination. It is known that elevations in liver aminotransferases (AST/ALT) associated with bosentan and ambrisetan are dose dependent, and hence aminot...

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Veröffentlicht in:European journal of hospital pharmacy. Science and practice 2017-03, Vol.24 (Suppl 1), p.A261-A261
Hauptverfasser: Gómez, G Calzado, Nicolás, F Gutiérrez, Eguilior, N Yurrebaso, Casariego, GJ Nazco, Romero, MM Viña, Gil, S García, Rodríguez, J Ramos, de la Fuente, GA González
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container_end_page A261
container_issue Suppl 1
container_start_page A261
container_title European journal of hospital pharmacy. Science and practice
container_volume 24
creator Gómez, G Calzado
Nicolás, F Gutiérrez
Eguilior, N Yurrebaso
Casariego, GJ Nazco
Romero, MM Viña
Gil, S García
Rodríguez, J Ramos
de la Fuente, GA González
description BackgroundBosentan and ambrisentan, endothelin receptor antagonists, are used as treatment for pulmonary arterial hypertension (PAH), alone or in combination. It is known that elevations in liver aminotransferases (AST/ALT) associated with bosentan and ambrisetan are dose dependent, and hence aminotransferases levels must be monitored.PurposeTo analyse hepatotoxicity in patients diagnosed with PAH treated with bosentan or ambrisentan.Material and methodsA retrospective observational study was conducted from 2010 to 2016. We included all patients receiving treatment with bosentan or ambrisentan for at least 2 months. We registered AST and ALT levels prior to initiation of treatment, at 2 and 8 weeks after initiation and then monthly. Based on the summary of product characteristics, we considered aminotransferases levels 3 times the upper limit of normal (ULN) as hepatotoxicity. Information was obtained from electronic medical records (SAP). ResultsWe enrolled 39 patients (37 women, 2 men) with a mean age of 57 years (20–85) at the start of treatment with bosentan. The mean period of treatment until the end of the study was 57.2 months (2–146). During the study period, we registered 3×ULN in 18% of patients; 57% required a reduced dose, 14% stop treatment and the rest did not required modification of treatment. 6 patients (5 women, 1 man), with a mean age of 51 years (45–77) (at the start of treatment) were treated with ambrisentan. At the end of period of study, mean time of treatment was 18.5 months. We registered 3×ULN in 33% of patients; in any case, medical prescription changed treatment.ConclusionThe hepatotoxicity results registered in our study were very similar to outcomes from clinical trials. The pharmacist must check the correct dose, based on AST/ALT level. Also, side effect are dose dependent and mainly asymptomatic, but nevertheless some cases of liver cirrhosis and liver failure have been reported.No conflict of interest
doi_str_mv 10.1136/ejhpharm-2017-000640.583
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It is known that elevations in liver aminotransferases (AST/ALT) associated with bosentan and ambrisetan are dose dependent, and hence aminotransferases levels must be monitored.PurposeTo analyse hepatotoxicity in patients diagnosed with PAH treated with bosentan or ambrisentan.Material and methodsA retrospective observational study was conducted from 2010 to 2016. We included all patients receiving treatment with bosentan or ambrisentan for at least 2 months. We registered AST and ALT levels prior to initiation of treatment, at 2 and 8 weeks after initiation and then monthly. Based on the summary of product characteristics, we considered aminotransferases levels 3 times the upper limit of normal (ULN) as hepatotoxicity. Information was obtained from electronic medical records (SAP). ResultsWe enrolled 39 patients (37 women, 2 men) with a mean age of 57 years (20–85) at the start of treatment with bosentan. The mean period of treatment until the end of the study was 57.2 months (2–146). During the study period, we registered 3×ULN in 18% of patients; 57% required a reduced dose, 14% stop treatment and the rest did not required modification of treatment. 6 patients (5 women, 1 man), with a mean age of 51 years (45–77) (at the start of treatment) were treated with ambrisentan. At the end of period of study, mean time of treatment was 18.5 months. We registered 3×ULN in 33% of patients; in any case, medical prescription changed treatment.ConclusionThe hepatotoxicity results registered in our study were very similar to outcomes from clinical trials. The pharmacist must check the correct dose, based on AST/ALT level. Also, side effect are dose dependent and mainly asymptomatic, but nevertheless some cases of liver cirrhosis and liver failure have been reported.No conflict of interest</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2017-000640.583</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Liver cirrhosis ; Pulmonary hypertension</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2017-03, Vol.24 (Suppl 1), p.A261-A261</ispartof><rights>2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2017 (c) 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2017 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Gómez, G Calzado</creatorcontrib><creatorcontrib>Nicolás, F Gutiérrez</creatorcontrib><creatorcontrib>Eguilior, N Yurrebaso</creatorcontrib><creatorcontrib>Casariego, GJ Nazco</creatorcontrib><creatorcontrib>Romero, MM Viña</creatorcontrib><creatorcontrib>Gil, S García</creatorcontrib><creatorcontrib>Rodríguez, J Ramos</creatorcontrib><creatorcontrib>de la Fuente, GA González</creatorcontrib><title>PS-077 Long term hepatotoxicity outcome of endothelin receptor antagonists as treatment in pulmonary arterial hypertension</title><title>European journal of hospital pharmacy. Science and practice</title><description>BackgroundBosentan and ambrisentan, endothelin receptor antagonists, are used as treatment for pulmonary arterial hypertension (PAH), alone or in combination. It is known that elevations in liver aminotransferases (AST/ALT) associated with bosentan and ambrisetan are dose dependent, and hence aminotransferases levels must be monitored.PurposeTo analyse hepatotoxicity in patients diagnosed with PAH treated with bosentan or ambrisentan.Material and methodsA retrospective observational study was conducted from 2010 to 2016. We included all patients receiving treatment with bosentan or ambrisentan for at least 2 months. We registered AST and ALT levels prior to initiation of treatment, at 2 and 8 weeks after initiation and then monthly. Based on the summary of product characteristics, we considered aminotransferases levels 3 times the upper limit of normal (ULN) as hepatotoxicity. Information was obtained from electronic medical records (SAP). ResultsWe enrolled 39 patients (37 women, 2 men) with a mean age of 57 years (20–85) at the start of treatment with bosentan. The mean period of treatment until the end of the study was 57.2 months (2–146). During the study period, we registered 3×ULN in 18% of patients; 57% required a reduced dose, 14% stop treatment and the rest did not required modification of treatment. 6 patients (5 women, 1 man), with a mean age of 51 years (45–77) (at the start of treatment) were treated with ambrisentan. At the end of period of study, mean time of treatment was 18.5 months. We registered 3×ULN in 33% of patients; in any case, medical prescription changed treatment.ConclusionThe hepatotoxicity results registered in our study were very similar to outcomes from clinical trials. The pharmacist must check the correct dose, based on AST/ALT level. Also, side effect are dose dependent and mainly asymptomatic, but nevertheless some cases of liver cirrhosis and liver failure have been reported.No conflict of interest</description><subject>Liver cirrhosis</subject><subject>Pulmonary hypertension</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kctKxDAYhYMoOIy-Q8B1x9yTLmXwBgMK6jqkaWaaoU1qmoIDLtz4oj6JHUZduvrP4vD9HD4AIEYLjKm4dNumb0zqCoKwLBBCgqEFV_QIzAhisihLwY7_Mhen4HwYfIU4papktJyB98enAkn59fG5imEDs0sdbFxvcszxzVufdzCO2cbOwbiGLtQxN671ASZnXZ9jgiZks4nBD3mAZoA5OZM7FzKcSv3YdjGYtIMmTWhvWtjsejflMPgYzsDJ2rSDO_-5c_Byc_28vCtWD7f3y6tVUeFpUmGtEVQxwq2oKywUVoSQCnPErKtKJGhdUokUqljJaltKIQxTSNE1U85iTOgcXBy4fYqvoxuy3sYxhemlJpwTKTgW4r8WVpJSSvbQOaCHVtVtdZ98N63TGOm9D_3rQ-996IMPPfmg33-hgb8</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Gómez, G Calzado</creator><creator>Nicolás, F Gutiérrez</creator><creator>Eguilior, N Yurrebaso</creator><creator>Casariego, GJ Nazco</creator><creator>Romero, MM Viña</creator><creator>Gil, S García</creator><creator>Rodríguez, J Ramos</creator><creator>de la Fuente, GA González</creator><general>BMJ Publishing Group LTD</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201703</creationdate><title>PS-077 Long term hepatotoxicity outcome of endothelin receptor antagonists as treatment in pulmonary arterial hypertension</title><author>Gómez, G Calzado ; Nicolás, F Gutiérrez ; Eguilior, N Yurrebaso ; Casariego, GJ Nazco ; Romero, MM Viña ; Gil, S García ; Rodríguez, J Ramos ; de la Fuente, GA González</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1006-cca638425c6db16818222b1504ceb9063d937080b494dc9766a48083f48ec1123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Liver cirrhosis</topic><topic>Pulmonary hypertension</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gómez, G Calzado</creatorcontrib><creatorcontrib>Nicolás, F Gutiérrez</creatorcontrib><creatorcontrib>Eguilior, N Yurrebaso</creatorcontrib><creatorcontrib>Casariego, GJ Nazco</creatorcontrib><creatorcontrib>Romero, MM Viña</creatorcontrib><creatorcontrib>Gil, S García</creatorcontrib><creatorcontrib>Rodríguez, J Ramos</creatorcontrib><creatorcontrib>de la Fuente, GA González</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>European journal of hospital pharmacy. Science and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gómez, G Calzado</au><au>Nicolás, F Gutiérrez</au><au>Eguilior, N Yurrebaso</au><au>Casariego, GJ Nazco</au><au>Romero, MM Viña</au><au>Gil, S García</au><au>Rodríguez, J Ramos</au><au>de la Fuente, GA González</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PS-077 Long term hepatotoxicity outcome of endothelin receptor antagonists as treatment in pulmonary arterial hypertension</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2017-03</date><risdate>2017</risdate><volume>24</volume><issue>Suppl 1</issue><spage>A261</spage><epage>A261</epage><pages>A261-A261</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>BackgroundBosentan and ambrisentan, endothelin receptor antagonists, are used as treatment for pulmonary arterial hypertension (PAH), alone or in combination. It is known that elevations in liver aminotransferases (AST/ALT) associated with bosentan and ambrisetan are dose dependent, and hence aminotransferases levels must be monitored.PurposeTo analyse hepatotoxicity in patients diagnosed with PAH treated with bosentan or ambrisentan.Material and methodsA retrospective observational study was conducted from 2010 to 2016. We included all patients receiving treatment with bosentan or ambrisentan for at least 2 months. We registered AST and ALT levels prior to initiation of treatment, at 2 and 8 weeks after initiation and then monthly. Based on the summary of product characteristics, we considered aminotransferases levels 3 times the upper limit of normal (ULN) as hepatotoxicity. Information was obtained from electronic medical records (SAP). ResultsWe enrolled 39 patients (37 women, 2 men) with a mean age of 57 years (20–85) at the start of treatment with bosentan. The mean period of treatment until the end of the study was 57.2 months (2–146). During the study period, we registered 3×ULN in 18% of patients; 57% required a reduced dose, 14% stop treatment and the rest did not required modification of treatment. 6 patients (5 women, 1 man), with a mean age of 51 years (45–77) (at the start of treatment) were treated with ambrisentan. At the end of period of study, mean time of treatment was 18.5 months. We registered 3×ULN in 33% of patients; in any case, medical prescription changed treatment.ConclusionThe hepatotoxicity results registered in our study were very similar to outcomes from clinical trials. The pharmacist must check the correct dose, based on AST/ALT level. Also, side effect are dose dependent and mainly asymptomatic, but nevertheless some cases of liver cirrhosis and liver failure have been reported.No conflict of interest</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/ejhpharm-2017-000640.583</doi></addata></record>
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subjects Liver cirrhosis
Pulmonary hypertension
title PS-077 Long term hepatotoxicity outcome of endothelin receptor antagonists as treatment in pulmonary arterial hypertension
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