The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy

Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of thi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Brain & development (Tokyo. 1979) 2016-09, Vol.38 (8), p.723-730
Hauptverfasser: Takeuchi, Tomoya, Natsume, Jun, Kidokoro, Hiroyuki, Ishihara, Naoko, Yamamoto, Hiroyuki, Azuma, Yoshiteru, Ito, Yuji, Kurahashi, Naoko, Tsuji, Takeshi, Suzuki, Motomasa, Itomi, Kazuya, Yamada, Keitaro, Kurahashi, Hirokazu, Abe, Shinpei, Okumura, Akihisa, Maruyama, Koichi, Negoro, Tamiko, Watanabe, Kazuyoshi, Kojima, Seiji
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 730
container_issue 8
container_start_page 723
container_title Brain & development (Tokyo. 1979)
container_volume 38
creator Takeuchi, Tomoya
Natsume, Jun
Kidokoro, Hiroyuki
Ishihara, Naoko
Yamamoto, Hiroyuki
Azuma, Yoshiteru
Ito, Yuji
Kurahashi, Naoko
Tsuji, Takeshi
Suzuki, Motomasa
Itomi, Kazuya
Yamada, Keitaro
Kurahashi, Hirokazu
Abe, Shinpei
Okumura, Akihisa
Maruyama, Koichi
Negoro, Tamiko
Watanabe, Kazuyoshi
Kojima, Seiji
description Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range.
doi_str_mv 10.1016/j.braindev.2016.03.004
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1808386575</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0387760416300213</els_id><sourcerecordid>1808386575</sourcerecordid><originalsourceid>FETCH-LOGICAL-c531t-31240f631b34c4368750e13327235eaa3a2bc8f04f777c5575e22db1fd1fc6d93</originalsourceid><addsrcrecordid>eNqFkUFv1DAQhS1ERbeFv1D5yCXpjJ3E4YJAVWlBlThQDpwsxxmzXrJ2sLNF--_r1bYcuHAazei9Gft7jF0g1AjYXW7qIRkfRnqoRelrkDVA84KtsFeiUijxJVuB7FWlOmhO2VnOGwBAgfCKnQoFUmKLK_bjfk2cnCO7ZB4dt7Ha0uitWXwMZRL4ZLZxSf6nD8TtRCaZYIn7wL-Y2QTKZbr205go8D9-WXOa_URz3r9mJ85Mmd481XP2_dP1_dVtdff15vPVx7vKthKXSqJowHUSB9nYRna9aoFQSqGEbMkYacRgeweNU0rZtlUtCTEO6EZ0thvfyXP29rh3TvH3jvKitz5bmqbyuLjLGnvoZd8VY5F2R6lNMedETs_Jb03aawR9wKo3-hmrPmDVIHXBWowXTzd2Q8Hz1_bMsQg-HAVUfvrgKelsPRVQo08FrR6j__-N9_-ssJMPJYnpF-0pb-IuhcJRo85Cg_52CPeQLXYSQBRijwtwoNI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1808386575</pqid></control><display><type>article</type><title>The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Takeuchi, Tomoya ; Natsume, Jun ; Kidokoro, Hiroyuki ; Ishihara, Naoko ; Yamamoto, Hiroyuki ; Azuma, Yoshiteru ; Ito, Yuji ; Kurahashi, Naoko ; Tsuji, Takeshi ; Suzuki, Motomasa ; Itomi, Kazuya ; Yamada, Keitaro ; Kurahashi, Hirokazu ; Abe, Shinpei ; Okumura, Akihisa ; Maruyama, Koichi ; Negoro, Tamiko ; Watanabe, Kazuyoshi ; Kojima, Seiji</creator><creatorcontrib>Takeuchi, Tomoya ; Natsume, Jun ; Kidokoro, Hiroyuki ; Ishihara, Naoko ; Yamamoto, Hiroyuki ; Azuma, Yoshiteru ; Ito, Yuji ; Kurahashi, Naoko ; Tsuji, Takeshi ; Suzuki, Motomasa ; Itomi, Kazuya ; Yamada, Keitaro ; Kurahashi, Hirokazu ; Abe, Shinpei ; Okumura, Akihisa ; Maruyama, Koichi ; Negoro, Tamiko ; Watanabe, Kazuyoshi ; Kojima, Seiji</creatorcontrib><description>Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range.</description><identifier>ISSN: 0387-7604</identifier><identifier>EISSN: 1872-7131</identifier><identifier>DOI: 10.1016/j.braindev.2016.03.004</identifier><identifier>PMID: 27033151</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject><![CDATA[Adolescent ; Anticonvulsants - administration & dosage ; Anticonvulsants - pharmacokinetics ; Benzodiazepines - administration & dosage ; Carbamazepine - administration & dosage ; Child ; Child, Preschool ; Clonazepam - administration & dosage ; Co-medication ; Drug concentration ; Drug interaction ; Drug Interactions ; Drug Therapy, Combination ; Epilepsy ; Epilepsy - blood ; Epilepsy - drug therapy ; Female ; Humans ; Infant ; Infant, Newborn ; Isoxazoles - administration & dosage ; Japan ; Lamotrigine ; Male ; Neurology ; Phenobarbital - administration & dosage ; Phenytoin - administration & dosage ; Piracetam - administration & dosage ; Piracetam - analogs & derivatives ; Triazines - administration & dosage ; Triazines - pharmacokinetics ; Valproic Acid - administration & dosage ; Young Adult]]></subject><ispartof>Brain &amp; development (Tokyo. 1979), 2016-09, Vol.38 (8), p.723-730</ispartof><rights>The Japanese Society of Child Neurology</rights><rights>2016 The Japanese Society of Child Neurology</rights><rights>Copyright © 2016 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-31240f631b34c4368750e13327235eaa3a2bc8f04f777c5575e22db1fd1fc6d93</citedby><cites>FETCH-LOGICAL-c531t-31240f631b34c4368750e13327235eaa3a2bc8f04f777c5575e22db1fd1fc6d93</cites><orcidid>0000-0002-6006-5258</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.braindev.2016.03.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27033151$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeuchi, Tomoya</creatorcontrib><creatorcontrib>Natsume, Jun</creatorcontrib><creatorcontrib>Kidokoro, Hiroyuki</creatorcontrib><creatorcontrib>Ishihara, Naoko</creatorcontrib><creatorcontrib>Yamamoto, Hiroyuki</creatorcontrib><creatorcontrib>Azuma, Yoshiteru</creatorcontrib><creatorcontrib>Ito, Yuji</creatorcontrib><creatorcontrib>Kurahashi, Naoko</creatorcontrib><creatorcontrib>Tsuji, Takeshi</creatorcontrib><creatorcontrib>Suzuki, Motomasa</creatorcontrib><creatorcontrib>Itomi, Kazuya</creatorcontrib><creatorcontrib>Yamada, Keitaro</creatorcontrib><creatorcontrib>Kurahashi, Hirokazu</creatorcontrib><creatorcontrib>Abe, Shinpei</creatorcontrib><creatorcontrib>Okumura, Akihisa</creatorcontrib><creatorcontrib>Maruyama, Koichi</creatorcontrib><creatorcontrib>Negoro, Tamiko</creatorcontrib><creatorcontrib>Watanabe, Kazuyoshi</creatorcontrib><creatorcontrib>Kojima, Seiji</creatorcontrib><title>The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy</title><title>Brain &amp; development (Tokyo. 1979)</title><addtitle>Brain Dev</addtitle><description>Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range.</description><subject>Adolescent</subject><subject>Anticonvulsants - administration &amp; dosage</subject><subject>Anticonvulsants - pharmacokinetics</subject><subject>Benzodiazepines - administration &amp; dosage</subject><subject>Carbamazepine - administration &amp; dosage</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Clonazepam - administration &amp; dosage</subject><subject>Co-medication</subject><subject>Drug concentration</subject><subject>Drug interaction</subject><subject>Drug Interactions</subject><subject>Drug Therapy, Combination</subject><subject>Epilepsy</subject><subject>Epilepsy - blood</subject><subject>Epilepsy - drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Isoxazoles - administration &amp; dosage</subject><subject>Japan</subject><subject>Lamotrigine</subject><subject>Male</subject><subject>Neurology</subject><subject>Phenobarbital - administration &amp; dosage</subject><subject>Phenytoin - administration &amp; dosage</subject><subject>Piracetam - administration &amp; dosage</subject><subject>Piracetam - analogs &amp; derivatives</subject><subject>Triazines - administration &amp; dosage</subject><subject>Triazines - pharmacokinetics</subject><subject>Valproic Acid - administration &amp; dosage</subject><subject>Young Adult</subject><issn>0387-7604</issn><issn>1872-7131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFv1DAQhS1ERbeFv1D5yCXpjJ3E4YJAVWlBlThQDpwsxxmzXrJ2sLNF--_r1bYcuHAazei9Gft7jF0g1AjYXW7qIRkfRnqoRelrkDVA84KtsFeiUijxJVuB7FWlOmhO2VnOGwBAgfCKnQoFUmKLK_bjfk2cnCO7ZB4dt7Ha0uitWXwMZRL4ZLZxSf6nD8TtRCaZYIn7wL-Y2QTKZbr205go8D9-WXOa_URz3r9mJ85Mmd481XP2_dP1_dVtdff15vPVx7vKthKXSqJowHUSB9nYRna9aoFQSqGEbMkYacRgeweNU0rZtlUtCTEO6EZ0thvfyXP29rh3TvH3jvKitz5bmqbyuLjLGnvoZd8VY5F2R6lNMedETs_Jb03aawR9wKo3-hmrPmDVIHXBWowXTzd2Q8Hz1_bMsQg-HAVUfvrgKelsPRVQo08FrR6j__-N9_-ssJMPJYnpF-0pb-IuhcJRo85Cg_52CPeQLXYSQBRijwtwoNI</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Takeuchi, Tomoya</creator><creator>Natsume, Jun</creator><creator>Kidokoro, Hiroyuki</creator><creator>Ishihara, Naoko</creator><creator>Yamamoto, Hiroyuki</creator><creator>Azuma, Yoshiteru</creator><creator>Ito, Yuji</creator><creator>Kurahashi, Naoko</creator><creator>Tsuji, Takeshi</creator><creator>Suzuki, Motomasa</creator><creator>Itomi, Kazuya</creator><creator>Yamada, Keitaro</creator><creator>Kurahashi, Hirokazu</creator><creator>Abe, Shinpei</creator><creator>Okumura, Akihisa</creator><creator>Maruyama, Koichi</creator><creator>Negoro, Tamiko</creator><creator>Watanabe, Kazuyoshi</creator><creator>Kojima, Seiji</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6006-5258</orcidid></search><sort><creationdate>20160901</creationdate><title>The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy</title><author>Takeuchi, Tomoya ; Natsume, Jun ; Kidokoro, Hiroyuki ; Ishihara, Naoko ; Yamamoto, Hiroyuki ; Azuma, Yoshiteru ; Ito, Yuji ; Kurahashi, Naoko ; Tsuji, Takeshi ; Suzuki, Motomasa ; Itomi, Kazuya ; Yamada, Keitaro ; Kurahashi, Hirokazu ; Abe, Shinpei ; Okumura, Akihisa ; Maruyama, Koichi ; Negoro, Tamiko ; Watanabe, Kazuyoshi ; Kojima, Seiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-31240f631b34c4368750e13327235eaa3a2bc8f04f777c5575e22db1fd1fc6d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Anticonvulsants - administration &amp; dosage</topic><topic>Anticonvulsants - pharmacokinetics</topic><topic>Benzodiazepines - administration &amp; dosage</topic><topic>Carbamazepine - administration &amp; dosage</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Clonazepam - administration &amp; dosage</topic><topic>Co-medication</topic><topic>Drug concentration</topic><topic>Drug interaction</topic><topic>Drug Interactions</topic><topic>Drug Therapy, Combination</topic><topic>Epilepsy</topic><topic>Epilepsy - blood</topic><topic>Epilepsy - drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Isoxazoles - administration &amp; dosage</topic><topic>Japan</topic><topic>Lamotrigine</topic><topic>Male</topic><topic>Neurology</topic><topic>Phenobarbital - administration &amp; dosage</topic><topic>Phenytoin - administration &amp; dosage</topic><topic>Piracetam - administration &amp; dosage</topic><topic>Piracetam - analogs &amp; derivatives</topic><topic>Triazines - administration &amp; dosage</topic><topic>Triazines - pharmacokinetics</topic><topic>Valproic Acid - administration &amp; dosage</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takeuchi, Tomoya</creatorcontrib><creatorcontrib>Natsume, Jun</creatorcontrib><creatorcontrib>Kidokoro, Hiroyuki</creatorcontrib><creatorcontrib>Ishihara, Naoko</creatorcontrib><creatorcontrib>Yamamoto, Hiroyuki</creatorcontrib><creatorcontrib>Azuma, Yoshiteru</creatorcontrib><creatorcontrib>Ito, Yuji</creatorcontrib><creatorcontrib>Kurahashi, Naoko</creatorcontrib><creatorcontrib>Tsuji, Takeshi</creatorcontrib><creatorcontrib>Suzuki, Motomasa</creatorcontrib><creatorcontrib>Itomi, Kazuya</creatorcontrib><creatorcontrib>Yamada, Keitaro</creatorcontrib><creatorcontrib>Kurahashi, Hirokazu</creatorcontrib><creatorcontrib>Abe, Shinpei</creatorcontrib><creatorcontrib>Okumura, Akihisa</creatorcontrib><creatorcontrib>Maruyama, Koichi</creatorcontrib><creatorcontrib>Negoro, Tamiko</creatorcontrib><creatorcontrib>Watanabe, Kazuyoshi</creatorcontrib><creatorcontrib>Kojima, Seiji</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Brain &amp; development (Tokyo. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takeuchi, Tomoya</au><au>Natsume, Jun</au><au>Kidokoro, Hiroyuki</au><au>Ishihara, Naoko</au><au>Yamamoto, Hiroyuki</au><au>Azuma, Yoshiteru</au><au>Ito, Yuji</au><au>Kurahashi, Naoko</au><au>Tsuji, Takeshi</au><au>Suzuki, Motomasa</au><au>Itomi, Kazuya</au><au>Yamada, Keitaro</au><au>Kurahashi, Hirokazu</au><au>Abe, Shinpei</au><au>Okumura, Akihisa</au><au>Maruyama, Koichi</au><au>Negoro, Tamiko</au><au>Watanabe, Kazuyoshi</au><au>Kojima, Seiji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy</atitle><jtitle>Brain &amp; development (Tokyo. 1979)</jtitle><addtitle>Brain Dev</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>38</volume><issue>8</issue><spage>723</spage><epage>730</epage><pages>723-730</pages><issn>0387-7604</issn><eissn>1872-7131</eissn><abstract>Abstract Purpose Although it has been reported that some antiepileptic drugs have inducing or inhibiting effects on lamotrigine (LTG) clearance, whether they have the same effects in Asian epilepsy patients as in those in other countries has not been clarified, especially in children. The aim of this study was to determine the effects of co-medications on LTG clearance in Japanese children with epilepsy. Methods A total of 342 routine serum concentration measurements of LTG in 102 Japanese epilepsy patients under 20 years of age were reviewed. The dose-corrected concentration (DCC) of LTG was calculated as [concentration]/[dose/(body weight)], and the DCC of LTG was compared by co-medication. The difference in the DCC of LTG was compared between patients with and without valproic acid (VPA) and between those with and without drugs inducing glucuronic acid conjugation (phenytoin (PHT), carbamazepine (CBZ), and phenobarbital (PB)). Results The DCC of LTG was significantly higher in patients on VPA and significantly lower in patients on drugs inducing glucuronic acid conjugation than in patients on LTG monotherapy. The DCC of LTG was significantly higher in patients on CBZ than in patients on PHT or PB. There was no correlation between the DCC of LTG and the concentration of VPA or metabolic inducers within the therapeutic range. Other antiepileptic drugs including clobazam, clonazepam, zonisamide, and levetiracetam had little effect on LTG concentration. Conclusion LTG concentration changes dramatically with concomitant antiepileptic drugs in Japanese children, as previously reported from other countries, and special attention is required. Although the dose of LTG should be adjusted when starting or discontinuing VPA or metabolic inducers, no adjustment is needed when changing the dose of VPA or metabolic inducers in the therapeutic range.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27033151</pmid><doi>10.1016/j.braindev.2016.03.004</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6006-5258</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0387-7604
ispartof Brain & development (Tokyo. 1979), 2016-09, Vol.38 (8), p.723-730
issn 0387-7604
1872-7131
language eng
recordid cdi_proquest_miscellaneous_1808386575
source MEDLINE; Elsevier ScienceDirect Journals Complete
subjects Adolescent
Anticonvulsants - administration & dosage
Anticonvulsants - pharmacokinetics
Benzodiazepines - administration & dosage
Carbamazepine - administration & dosage
Child
Child, Preschool
Clonazepam - administration & dosage
Co-medication
Drug concentration
Drug interaction
Drug Interactions
Drug Therapy, Combination
Epilepsy
Epilepsy - blood
Epilepsy - drug therapy
Female
Humans
Infant
Infant, Newborn
Isoxazoles - administration & dosage
Japan
Lamotrigine
Male
Neurology
Phenobarbital - administration & dosage
Phenytoin - administration & dosage
Piracetam - administration & dosage
Piracetam - analogs & derivatives
Triazines - administration & dosage
Triazines - pharmacokinetics
Valproic Acid - administration & dosage
Young Adult
title The effects of co-medications on lamotrigine clearance in Japanese children with epilepsy
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T23%3A01%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20effects%20of%20co-medications%20on%20lamotrigine%20clearance%20in%20Japanese%20children%20with%20epilepsy&rft.jtitle=Brain%20&%20development%20(Tokyo.%201979)&rft.au=Takeuchi,%20Tomoya&rft.date=2016-09-01&rft.volume=38&rft.issue=8&rft.spage=723&rft.epage=730&rft.pages=723-730&rft.issn=0387-7604&rft.eissn=1872-7131&rft_id=info:doi/10.1016/j.braindev.2016.03.004&rft_dat=%3Cproquest_cross%3E1808386575%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1808386575&rft_id=info:pmid/27033151&rft_els_id=1_s2_0_S0387760416300213&rfr_iscdi=true