4CPS-051 Pharmacokinetics alterations in two critically ill patients on extracorporeal membrane oxygenation receiving isavuconazol
Background and importanceExtracorporeal membrane oxygenation (ECMO) can modify drug pharmacokinetics and pharmacodynamics. We report two cases of critically ill patients on ECMO receiving isavuconazol.Aim and objectivesPrimary aim: to assess the correlation between the dose of isavuconazol administe...
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description | Background and importanceExtracorporeal membrane oxygenation (ECMO) can modify drug pharmacokinetics and pharmacodynamics. We report two cases of critically ill patients on ECMO receiving isavuconazol.Aim and objectivesPrimary aim: to assess the correlation between the dose of isavuconazol administered and its plasma drug concentrations (IsaPlasmConc). Secondary aim: to analyse differences in IsaPlasm at different points in the ECMO circuit to study drug sequestration.Material and methodsProspective study in critically ill patients treated with intravenous isavuconazol and receiving ECMO in the intensive care unit (ICU) from August to October 2021. Isavuconazol area under the curve (AUCisa) was calculated using the trapezoidal method. Blood samples were drawn from an arterial catheter and from ECMO circuit pre- and post-oxygenator at 0 (predose) and 1 hour (end of infusion), and from an arterial catheter at 2, 4, 6 and 12 hours after isavuconazol infusion.A therapeutic goal of IsaPlasmConc 2.5–10 µg/mL was established. The analytical method used was high-pressure liquid chromatography. Differences greater than 10% on ECMO sites were considered as possible drug sequestration.ResultsBoth patients received a loading dose of isavuconazole 200 mg/8 hours over 48 hours. No relevant drug interactions were identified.Patient 1: male, 61 years, 65 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/24 hours intravenously (IV). On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenator) were: C0h: 1.39, 1.36 and 1.34, respectively; C1h: 2.83, 2.64 and 3.02; C2h: 2.28; C4h: 1.6; C6h: 1.61; C12h: 1.06 µg/mL. AUCisa was 36.8 µg/hour/mL. It was considered infra-therapeutic, so the isavuconazol dosage was increased to 200 mg/12 hours. On day 10, IsaPlasmConc were: C0h: 2.16, 2.17 and 2.09; C1h: 3.17, 2.99 and 2.96; C2h: 3.10; C4h: 2.67; C6h: 2.41; C12h: 2.24. AUCisa was 144.3µg/hour/mL. The patient achieved negative cultures and clinical improvement.Patient 2: male, 65 years, 84 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/12 hours IV. On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenatore) were: C0h: 2.00, 1.95 and 1.86, respectively, C1h: 3.01, 3.34 and 3.21; C2h: 3.00; C4h: 2.44; C6h: 2.34; C12h: 3.09. AUCisa was 125.2 µg/hour/mL. The patient died due to external causes.Conclusion and relevanceIn our patients there was not a significant sequestration of isavuconazole in the ECMO circuit. However, patients required hi |
doi_str_mv | 10.1136/ejhpharm-2022-eahp.94 |
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fullrecord | <record><control><sourceid>proquest_bmj_j</sourceid><recordid>TN_cdi_proquest_journals_2672362196</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2672362196</sourcerecordid><originalsourceid>FETCH-LOGICAL-b1174-17f4b49e2ef873441e03d4d5e54f76d616f4cfb8d96eb5c950086cb40a018d2c3</originalsourceid><addsrcrecordid>eNpFkMtKw0AUhoMoWGofQRhwnTq3TDJLKd6gYEFdh5nJSTs1nYmTtLauXOiL-iQm1svqHPi_8x_4ouiU4DEhTJzDclEvVFjFFFMag1rUY8kPogHFPI2lFPzwb0_EcTRqGqtxwlgmOZOD6J1PZvcxTsjn28es71HGP1kHrTUNUlULQbXWuwZZh9oXj0ywXaSqaodsVaG6S8G1DfIOwbYN3XWofQBVoRWsdFAOkN_u5uC-a1AAA3Zj3RzZRm3Wxjv16quT6KhUVQOjnzmMHq8uHyY38fTu-nZyMY01ISmPSVpyzSVQKLOUcU4As4IXCSS8TEUhiCi5KXVWSAE6MTLBOBNGc6wwyQpq2DA62_fWwT-voWnzpV8H173MqUgpE5RI0VFkT-nV8h8gOO9957--89533vvOO5NfFOp7Fg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2672362196</pqid></control><display><type>article</type><title>4CPS-051 Pharmacokinetics alterations in two critically ill patients on extracorporeal membrane oxygenation receiving isavuconazol</title><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Doménech, L ; Garcia-Garcia, S ; Miarons, M ; Gomez-Domingo, MR ; Riera, J ; Bonilla, C ; Gallart, E ; Mateos, C ; Gorgas Torner, MQ</creator><creatorcontrib>Doménech, L ; Garcia-Garcia, S ; Miarons, M ; Gomez-Domingo, MR ; Riera, J ; Bonilla, C ; Gallart, E ; Mateos, C ; Gorgas Torner, MQ</creatorcontrib><description>Background and importanceExtracorporeal membrane oxygenation (ECMO) can modify drug pharmacokinetics and pharmacodynamics. We report two cases of critically ill patients on ECMO receiving isavuconazol.Aim and objectivesPrimary aim: to assess the correlation between the dose of isavuconazol administered and its plasma drug concentrations (IsaPlasmConc). Secondary aim: to analyse differences in IsaPlasm at different points in the ECMO circuit to study drug sequestration.Material and methodsProspective study in critically ill patients treated with intravenous isavuconazol and receiving ECMO in the intensive care unit (ICU) from August to October 2021. Isavuconazol area under the curve (AUCisa) was calculated using the trapezoidal method. Blood samples were drawn from an arterial catheter and from ECMO circuit pre- and post-oxygenator at 0 (predose) and 1 hour (end of infusion), and from an arterial catheter at 2, 4, 6 and 12 hours after isavuconazol infusion.A therapeutic goal of IsaPlasmConc 2.5–10 µg/mL was established. The analytical method used was high-pressure liquid chromatography. Differences greater than 10% on ECMO sites were considered as possible drug sequestration.ResultsBoth patients received a loading dose of isavuconazole 200 mg/8 hours over 48 hours. No relevant drug interactions were identified.Patient 1: male, 61 years, 65 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/24 hours intravenously (IV). On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenator) were: C0h: 1.39, 1.36 and 1.34, respectively; C1h: 2.83, 2.64 and 3.02; C2h: 2.28; C4h: 1.6; C6h: 1.61; C12h: 1.06 µg/mL. AUCisa was 36.8 µg/hour/mL. It was considered infra-therapeutic, so the isavuconazol dosage was increased to 200 mg/12 hours. On day 10, IsaPlasmConc were: C0h: 2.16, 2.17 and 2.09; C1h: 3.17, 2.99 and 2.96; C2h: 3.10; C4h: 2.67; C6h: 2.41; C12h: 2.24. AUCisa was 144.3µg/hour/mL. The patient achieved negative cultures and clinical improvement.Patient 2: male, 65 years, 84 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/12 hours IV. On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenatore) were: C0h: 2.00, 1.95 and 1.86, respectively, C1h: 3.01, 3.34 and 3.21; C2h: 3.00; C4h: 2.44; C6h: 2.34; C12h: 3.09. AUCisa was 125.2 µg/hour/mL. The patient died due to external causes.Conclusion and relevanceIn our patients there was not a significant sequestration of isavuconazole in the ECMO circuit. However, patients required higher isavuconazole doses to achieve IsaPlasmConc therapeutic goals. Therapeutic drug monitoring during ECMO is appropriate to assure therapeutic efficacy and security.References and/or acknowledgementsConflict of interestNo conflict of interest</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2022-eahp.94</identifier><language>eng</language><publisher>London: British Medical Journal Publishing Group</publisher><subject>Aspergillosis ; Catheters ; Conflicts of interest ; Drug dosages ; Extracorporeal membrane oxygenation ; Patients ; Pharmacokinetics ; Section 4: Clinical pharmacy services ; Surgical apparatus & instruments</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2022-03, Vol.29 (Suppl 1), p.A44-A45</ispartof><rights>European Association of Hospital Pharmacists 2022. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2022 European Association of Hospital Pharmacists 2022. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><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>Doménech, L</creatorcontrib><creatorcontrib>Garcia-Garcia, S</creatorcontrib><creatorcontrib>Miarons, M</creatorcontrib><creatorcontrib>Gomez-Domingo, MR</creatorcontrib><creatorcontrib>Riera, J</creatorcontrib><creatorcontrib>Bonilla, C</creatorcontrib><creatorcontrib>Gallart, E</creatorcontrib><creatorcontrib>Mateos, C</creatorcontrib><creatorcontrib>Gorgas Torner, MQ</creatorcontrib><title>4CPS-051 Pharmacokinetics alterations in two critically ill patients on extracorporeal membrane oxygenation receiving isavuconazol</title><title>European journal of hospital pharmacy. Science and practice</title><addtitle>Eur J Hosp Pharm</addtitle><description>Background and importanceExtracorporeal membrane oxygenation (ECMO) can modify drug pharmacokinetics and pharmacodynamics. We report two cases of critically ill patients on ECMO receiving isavuconazol.Aim and objectivesPrimary aim: to assess the correlation between the dose of isavuconazol administered and its plasma drug concentrations (IsaPlasmConc). Secondary aim: to analyse differences in IsaPlasm at different points in the ECMO circuit to study drug sequestration.Material and methodsProspective study in critically ill patients treated with intravenous isavuconazol and receiving ECMO in the intensive care unit (ICU) from August to October 2021. Isavuconazol area under the curve (AUCisa) was calculated using the trapezoidal method. Blood samples were drawn from an arterial catheter and from ECMO circuit pre- and post-oxygenator at 0 (predose) and 1 hour (end of infusion), and from an arterial catheter at 2, 4, 6 and 12 hours after isavuconazol infusion.A therapeutic goal of IsaPlasmConc 2.5–10 µg/mL was established. The analytical method used was high-pressure liquid chromatography. Differences greater than 10% on ECMO sites were considered as possible drug sequestration.ResultsBoth patients received a loading dose of isavuconazole 200 mg/8 hours over 48 hours. No relevant drug interactions were identified.Patient 1: male, 61 years, 65 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/24 hours intravenously (IV). On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenator) were: C0h: 1.39, 1.36 and 1.34, respectively; C1h: 2.83, 2.64 and 3.02; C2h: 2.28; C4h: 1.6; C6h: 1.61; C12h: 1.06 µg/mL. AUCisa was 36.8 µg/hour/mL. It was considered infra-therapeutic, so the isavuconazol dosage was increased to 200 mg/12 hours. On day 10, IsaPlasmConc were: C0h: 2.16, 2.17 and 2.09; C1h: 3.17, 2.99 and 2.96; C2h: 3.10; C4h: 2.67; C6h: 2.41; C12h: 2.24. AUCisa was 144.3µg/hour/mL. The patient achieved negative cultures and clinical improvement.Patient 2: male, 65 years, 84 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/12 hours IV. On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenatore) were: C0h: 2.00, 1.95 and 1.86, respectively, C1h: 3.01, 3.34 and 3.21; C2h: 3.00; C4h: 2.44; C6h: 2.34; C12h: 3.09. AUCisa was 125.2 µg/hour/mL. The patient died due to external causes.Conclusion and relevanceIn our patients there was not a significant sequestration of isavuconazole in the ECMO circuit. However, patients required higher isavuconazole doses to achieve IsaPlasmConc therapeutic goals. Therapeutic drug monitoring during ECMO is appropriate to assure therapeutic efficacy and security.References and/or acknowledgementsConflict of interestNo conflict of interest</description><subject>Aspergillosis</subject><subject>Catheters</subject><subject>Conflicts of interest</subject><subject>Drug dosages</subject><subject>Extracorporeal membrane oxygenation</subject><subject>Patients</subject><subject>Pharmacokinetics</subject><subject>Section 4: Clinical pharmacy services</subject><subject>Surgical apparatus & instruments</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpFkMtKw0AUhoMoWGofQRhwnTq3TDJLKd6gYEFdh5nJSTs1nYmTtLauXOiL-iQm1svqHPi_8x_4ouiU4DEhTJzDclEvVFjFFFMag1rUY8kPogHFPI2lFPzwb0_EcTRqGqtxwlgmOZOD6J1PZvcxTsjn28es71HGP1kHrTUNUlULQbXWuwZZh9oXj0ywXaSqaodsVaG6S8G1DfIOwbYN3XWofQBVoRWsdFAOkN_u5uC-a1AAA3Zj3RzZRm3Wxjv16quT6KhUVQOjnzmMHq8uHyY38fTu-nZyMY01ISmPSVpyzSVQKLOUcU4As4IXCSS8TEUhiCi5KXVWSAE6MTLBOBNGc6wwyQpq2DA62_fWwT-voWnzpV8H173MqUgpE5RI0VFkT-nV8h8gOO9957--89533vvOO5NfFOp7Fg</recordid><startdate>20220323</startdate><enddate>20220323</enddate><creator>Doménech, L</creator><creator>Garcia-Garcia, S</creator><creator>Miarons, M</creator><creator>Gomez-Domingo, MR</creator><creator>Riera, J</creator><creator>Bonilla, C</creator><creator>Gallart, E</creator><creator>Mateos, C</creator><creator>Gorgas Torner, MQ</creator><general>British Medical Journal Publishing Group</general><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>20220323</creationdate><title>4CPS-051 Pharmacokinetics alterations in two critically ill patients on extracorporeal membrane oxygenation receiving isavuconazol</title><author>Doménech, L ; Garcia-Garcia, S ; Miarons, M ; Gomez-Domingo, MR ; Riera, J ; Bonilla, C ; Gallart, E ; Mateos, C ; Gorgas Torner, MQ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1174-17f4b49e2ef873441e03d4d5e54f76d616f4cfb8d96eb5c950086cb40a018d2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Aspergillosis</topic><topic>Catheters</topic><topic>Conflicts of interest</topic><topic>Drug dosages</topic><topic>Extracorporeal membrane oxygenation</topic><topic>Patients</topic><topic>Pharmacokinetics</topic><topic>Section 4: Clinical pharmacy services</topic><topic>Surgical apparatus & instruments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Doménech, L</creatorcontrib><creatorcontrib>Garcia-Garcia, S</creatorcontrib><creatorcontrib>Miarons, M</creatorcontrib><creatorcontrib>Gomez-Domingo, MR</creatorcontrib><creatorcontrib>Riera, J</creatorcontrib><creatorcontrib>Bonilla, C</creatorcontrib><creatorcontrib>Gallart, E</creatorcontrib><creatorcontrib>Mateos, C</creatorcontrib><creatorcontrib>Gorgas Torner, MQ</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health & 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 & 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>Doménech, L</au><au>Garcia-Garcia, S</au><au>Miarons, M</au><au>Gomez-Domingo, MR</au><au>Riera, J</au><au>Bonilla, C</au><au>Gallart, E</au><au>Mateos, C</au><au>Gorgas Torner, MQ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>4CPS-051 Pharmacokinetics alterations in two critically ill patients on extracorporeal membrane oxygenation receiving isavuconazol</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><stitle>Eur J Hosp Pharm</stitle><date>2022-03-23</date><risdate>2022</risdate><volume>29</volume><issue>Suppl 1</issue><spage>A44</spage><epage>A45</epage><pages>A44-A45</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>Background and importanceExtracorporeal membrane oxygenation (ECMO) can modify drug pharmacokinetics and pharmacodynamics. We report two cases of critically ill patients on ECMO receiving isavuconazol.Aim and objectivesPrimary aim: to assess the correlation between the dose of isavuconazol administered and its plasma drug concentrations (IsaPlasmConc). Secondary aim: to analyse differences in IsaPlasm at different points in the ECMO circuit to study drug sequestration.Material and methodsProspective study in critically ill patients treated with intravenous isavuconazol and receiving ECMO in the intensive care unit (ICU) from August to October 2021. Isavuconazol area under the curve (AUCisa) was calculated using the trapezoidal method. Blood samples were drawn from an arterial catheter and from ECMO circuit pre- and post-oxygenator at 0 (predose) and 1 hour (end of infusion), and from an arterial catheter at 2, 4, 6 and 12 hours after isavuconazol infusion.A therapeutic goal of IsaPlasmConc 2.5–10 µg/mL was established. The analytical method used was high-pressure liquid chromatography. Differences greater than 10% on ECMO sites were considered as possible drug sequestration.ResultsBoth patients received a loading dose of isavuconazole 200 mg/8 hours over 48 hours. No relevant drug interactions were identified.Patient 1: male, 61 years, 65 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/24 hours intravenously (IV). On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenator) were: C0h: 1.39, 1.36 and 1.34, respectively; C1h: 2.83, 2.64 and 3.02; C2h: 2.28; C4h: 1.6; C6h: 1.61; C12h: 1.06 µg/mL. AUCisa was 36.8 µg/hour/mL. It was considered infra-therapeutic, so the isavuconazol dosage was increased to 200 mg/12 hours. On day 10, IsaPlasmConc were: C0h: 2.16, 2.17 and 2.09; C1h: 3.17, 2.99 and 2.96; C2h: 3.10; C4h: 2.67; C6h: 2.41; C12h: 2.24. AUCisa was 144.3µg/hour/mL. The patient achieved negative cultures and clinical improvement.Patient 2: male, 65 years, 84 kg. Pulmonary aspergillosis treated with isavuconazole 200 mg/12 hours IV. On day 4, IsaPlasmConc (arterial, pre-oxygenator and post-oxygenatore) were: C0h: 2.00, 1.95 and 1.86, respectively, C1h: 3.01, 3.34 and 3.21; C2h: 3.00; C4h: 2.44; C6h: 2.34; C12h: 3.09. AUCisa was 125.2 µg/hour/mL. The patient died due to external causes.Conclusion and relevanceIn our patients there was not a significant sequestration of isavuconazole in the ECMO circuit. However, patients required higher isavuconazole doses to achieve IsaPlasmConc therapeutic goals. Therapeutic drug monitoring during ECMO is appropriate to assure therapeutic efficacy and security.References and/or acknowledgementsConflict of interestNo conflict of interest</abstract><cop>London</cop><pub>British Medical Journal Publishing Group</pub><doi>10.1136/ejhpharm-2022-eahp.94</doi><oa>free_for_read</oa></addata></record> |
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subjects | Aspergillosis Catheters Conflicts of interest Drug dosages Extracorporeal membrane oxygenation Patients Pharmacokinetics Section 4: Clinical pharmacy services Surgical apparatus & instruments |
title | 4CPS-051 Pharmacokinetics alterations in two critically ill patients on extracorporeal membrane oxygenation receiving isavuconazol |
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