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Evaluation of an ex-vivo neonatal extracorporeal membrane oxygenation circuit on antiepileptic drug sequestration
Antiepileptic dosing information used to manage neonatal patients receiving extracorporeal membrane oxygenation (ECMO) is limited. The objective of this study is to quantify the extent of sequestration of various antiepileptic drugs using an ex-vivo neonatal ECMO circuit. Two neonatal closed-loop EC...
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Published in: | Perfusion 2022-11, Vol.37 (8), p.812-818 |
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creator | Kalaria, Shamir N Kishk, Omayma A Gopalakrishnan, Mathangi Bagdure, Dayanand N |
description | Antiepileptic dosing information used to manage neonatal patients receiving extracorporeal membrane oxygenation (ECMO) is limited. The objective of this study is to quantify the extent of sequestration of various antiepileptic drugs using an ex-vivo neonatal ECMO circuit. Two neonatal closed-loop ECMO circuits were prepared using a Rotaflow centrifugal pump, custom polyvinylchloride tubing and a Quadrox-i Neonatal membrane oxygenator. After 5 minutes of circuit priming and stabilization with normal saline/albumin or expired human whole blood, single boluses of levetiracetam (200 mg), lacosamide (20 mg), and phenytoin (200 mg) were injected into the circuit. To account for spontaneous drug degradation, two polyvinylchloride beakers were filled with normal saline/albumin or expired human whole blood and equivalent antiepileptic drug doses were prepared. Simultaneous pharmacokinetic samples were collected from the control solution and the pre-centrifugal pump, pre-oxygenator, and post-oxygenator sampling ports from each circuit. Similar drug recovery profiles were observed among the three sampling sites investigated. Percent drug sequestration after a 24-hour circuit flow period was relatively similar between the two different circuits and ranged between 5.5%–13.2% for levetiracetam, 18.4%–22.3% for lacosamide, and 24.5%–30.2% for phenytoin. A comparison at 12 and 24 hours demonstrated similar percent drug sequestration across all three drugs in each circuit. Percent drug sequestrations for levetiracetam and lacosamide were less than 20% and for phenytoin were as high as 30% based on the sampling following single bolus dose administration into a neonatal ECMO circuit. Careful consideration of patient clinical status should be taken in consideration when optimizing antiepileptic therapy in neonates receiving ECMO. |
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The objective of this study is to quantify the extent of sequestration of various antiepileptic drugs using an ex-vivo neonatal ECMO circuit. Two neonatal closed-loop ECMO circuits were prepared using a Rotaflow centrifugal pump, custom polyvinylchloride tubing and a Quadrox-i Neonatal membrane oxygenator. After 5 minutes of circuit priming and stabilization with normal saline/albumin or expired human whole blood, single boluses of levetiracetam (200 mg), lacosamide (20 mg), and phenytoin (200 mg) were injected into the circuit. To account for spontaneous drug degradation, two polyvinylchloride beakers were filled with normal saline/albumin or expired human whole blood and equivalent antiepileptic drug doses were prepared. Simultaneous pharmacokinetic samples were collected from the control solution and the pre-centrifugal pump, pre-oxygenator, and post-oxygenator sampling ports from each circuit. Similar drug recovery profiles were observed among the three sampling sites investigated. Percent drug sequestration after a 24-hour circuit flow period was relatively similar between the two different circuits and ranged between 5.5%–13.2% for levetiracetam, 18.4%–22.3% for lacosamide, and 24.5%–30.2% for phenytoin. A comparison at 12 and 24 hours demonstrated similar percent drug sequestration across all three drugs in each circuit. Percent drug sequestrations for levetiracetam and lacosamide were less than 20% and for phenytoin were as high as 30% based on the sampling following single bolus dose administration into a neonatal ECMO circuit. 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The objective of this study is to quantify the extent of sequestration of various antiepileptic drugs using an ex-vivo neonatal ECMO circuit. Two neonatal closed-loop ECMO circuits were prepared using a Rotaflow centrifugal pump, custom polyvinylchloride tubing and a Quadrox-i Neonatal membrane oxygenator. After 5 minutes of circuit priming and stabilization with normal saline/albumin or expired human whole blood, single boluses of levetiracetam (200 mg), lacosamide (20 mg), and phenytoin (200 mg) were injected into the circuit. To account for spontaneous drug degradation, two polyvinylchloride beakers were filled with normal saline/albumin or expired human whole blood and equivalent antiepileptic drug doses were prepared. Simultaneous pharmacokinetic samples were collected from the control solution and the pre-centrifugal pump, pre-oxygenator, and post-oxygenator sampling ports from each circuit. Similar drug recovery profiles were observed among the three sampling sites investigated. Percent drug sequestration after a 24-hour circuit flow period was relatively similar between the two different circuits and ranged between 5.5%–13.2% for levetiracetam, 18.4%–22.3% for lacosamide, and 24.5%–30.2% for phenytoin. A comparison at 12 and 24 hours demonstrated similar percent drug sequestration across all three drugs in each circuit. Percent drug sequestrations for levetiracetam and lacosamide were less than 20% and for phenytoin were as high as 30% based on the sampling following single bolus dose administration into a neonatal ECMO circuit. Careful consideration of patient clinical status should be taken in consideration when optimizing antiepileptic therapy in neonates receiving ECMO.</description><subject>Albumin</subject><subject>Albumins</subject><subject>Antiepileptic agents</subject><subject>Blood</subject><subject>Centrifugal pumps</subject><subject>Circuits</subject><subject>Dosage</subject><subject>Drugs</subject><subject>Etiracetam</subject><subject>Extracorporeal membrane oxygenation</subject><subject>Information management</subject><subject>Membranes</subject><subject>Neonates</subject><subject>Newborn babies</subject><subject>Oxygenation</subject><subject>Patients</subject><subject>Pharmacokinetics</subject><subject>Phenytoin</subject><subject>Polyvinyl chloride</subject><subject>Priming</subject><subject>Sampling</subject><subject>Surgical apparatus & instruments</subject><issn>0267-6591</issn><issn>1477-111X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kM1OwzAQhC0EoqXwAFyQJc4pXjuJkyOq-JMqcQGJW-Q4TuUqtVM7qdq3xyEFDojT2rvfztiD0DWQOQDnd4SmPE1yoACEZpCxEzSFmPMIAD5O0XSYRwMwQRferwkhcRyzczRhMeQ0z2CKtg870fSi09ZgW2NhsNpHO72z2ChrRCea0OickNa11qlw3ahN6YRR2O4PK2XGVamd7HWHw1GYTqtWN6rttMSV61fYq22vfFAZ2Et0VovGq6tjnaH3x4e3xXO0fH16WdwvIxle1kUVY1QoSEMBmSakLqUKX8wTAlyIUpYgmazTNKtpBWWZQEXDgORJmgkgPGYzdDvqts5-2Rdr2zsTLAvKaR4nOWEDBSMlnfXeqbpond4IdyiAFEPIxZ-Qw87NUbkvN6r62fhONQDzEfBipX5t_1f8BCvAhkg</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>Kalaria, Shamir N</creator><creator>Kishk, Omayma A</creator><creator>Gopalakrishnan, Mathangi</creator><creator>Bagdure, Dayanand N</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>NAPCQ</scope><orcidid>https://orcid.org/0000-0001-7980-4236</orcidid></search><sort><creationdate>20221101</creationdate><title>Evaluation of an ex-vivo neonatal extracorporeal membrane oxygenation circuit on antiepileptic drug sequestration</title><author>Kalaria, Shamir N ; Kishk, Omayma A ; Gopalakrishnan, Mathangi ; Bagdure, Dayanand N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c298t-d332ae163321c650fbce81895017aabcb1c3cf668f2d1bb51d217a09568a10743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Albumin</topic><topic>Albumins</topic><topic>Antiepileptic agents</topic><topic>Blood</topic><topic>Centrifugal pumps</topic><topic>Circuits</topic><topic>Dosage</topic><topic>Drugs</topic><topic>Etiracetam</topic><topic>Extracorporeal membrane oxygenation</topic><topic>Information management</topic><topic>Membranes</topic><topic>Neonates</topic><topic>Newborn babies</topic><topic>Oxygenation</topic><topic>Patients</topic><topic>Pharmacokinetics</topic><topic>Phenytoin</topic><topic>Polyvinyl chloride</topic><topic>Priming</topic><topic>Sampling</topic><topic>Surgical apparatus & instruments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kalaria, Shamir N</creatorcontrib><creatorcontrib>Kishk, Omayma A</creatorcontrib><creatorcontrib>Gopalakrishnan, Mathangi</creatorcontrib><creatorcontrib>Bagdure, Dayanand N</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Perfusion</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kalaria, Shamir N</au><au>Kishk, Omayma A</au><au>Gopalakrishnan, Mathangi</au><au>Bagdure, Dayanand N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of an ex-vivo neonatal extracorporeal membrane oxygenation circuit on antiepileptic drug sequestration</atitle><jtitle>Perfusion</jtitle><addtitle>Perfusion</addtitle><date>2022-11-01</date><risdate>2022</risdate><volume>37</volume><issue>8</issue><spage>812</spage><epage>818</epage><pages>812-818</pages><issn>0267-6591</issn><eissn>1477-111X</eissn><abstract>Antiepileptic dosing information used to manage neonatal patients receiving extracorporeal membrane oxygenation (ECMO) is limited. The objective of this study is to quantify the extent of sequestration of various antiepileptic drugs using an ex-vivo neonatal ECMO circuit. Two neonatal closed-loop ECMO circuits were prepared using a Rotaflow centrifugal pump, custom polyvinylchloride tubing and a Quadrox-i Neonatal membrane oxygenator. After 5 minutes of circuit priming and stabilization with normal saline/albumin or expired human whole blood, single boluses of levetiracetam (200 mg), lacosamide (20 mg), and phenytoin (200 mg) were injected into the circuit. To account for spontaneous drug degradation, two polyvinylchloride beakers were filled with normal saline/albumin or expired human whole blood and equivalent antiepileptic drug doses were prepared. Simultaneous pharmacokinetic samples were collected from the control solution and the pre-centrifugal pump, pre-oxygenator, and post-oxygenator sampling ports from each circuit. Similar drug recovery profiles were observed among the three sampling sites investigated. Percent drug sequestration after a 24-hour circuit flow period was relatively similar between the two different circuits and ranged between 5.5%–13.2% for levetiracetam, 18.4%–22.3% for lacosamide, and 24.5%–30.2% for phenytoin. A comparison at 12 and 24 hours demonstrated similar percent drug sequestration across all three drugs in each circuit. Percent drug sequestrations for levetiracetam and lacosamide were less than 20% and for phenytoin were as high as 30% based on the sampling following single bolus dose administration into a neonatal ECMO circuit. Careful consideration of patient clinical status should be taken in consideration when optimizing antiepileptic therapy in neonates receiving ECMO.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>34192981</pmid><doi>10.1177/02676591211028183</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7980-4236</orcidid></addata></record> |
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subjects | Albumin Albumins Antiepileptic agents Blood Centrifugal pumps Circuits Dosage Drugs Etiracetam Extracorporeal membrane oxygenation Information management Membranes Neonates Newborn babies Oxygenation Patients Pharmacokinetics Phenytoin Polyvinyl chloride Priming Sampling Surgical apparatus & instruments |
title | Evaluation of an ex-vivo neonatal extracorporeal membrane oxygenation circuit on antiepileptic drug sequestration |
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