<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Xia Y</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Valproic acid (VPA) is a widely used antiseizure medication and its dosing needs to be tailored individually through therapeutic drug monitoring (TDM) to avoid or prevent toxicity. Currently, immune-enzymatic assays such as Enzyme Multiplied Immunoassay Technique (EMIT), and Liquid Chromatography (LC)-based techniques, particularly coupled to Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS), resulting a potential lack of concordance between laboratories. &lt;b>Methods:&lt;/b> In this study, plasma VPA concentrations were determined for 711 pediatric patients with epilepsy by a routine EMIT assay and by a validated in-house LC-ESI-MS/MS method on the same group of samples, aimed to address the aforementioned concern. Consistency between two assays was evaluated u</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>750744</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8650496</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Switching Between LC-ESI-MS/MS and EMIT Methods for Routine TDM of Valproic Acid in Pediatric Patients With Epilepsy: What Clinicians and Researchers Need to Know.</pubmed_title><pmcid>PMC8650496</pmcid><pubmed_authors>Xia Y</pubmed_authors><pubmed_authors>Shen MY</pubmed_authors><pubmed_authors>Long JY</pubmed_authors><pubmed_authors>Guo HL</pubmed_authors><pubmed_authors>Chen F</pubmed_authors><pubmed_authors>Qiu JC</pubmed_authors><pubmed_authors>Dong N</pubmed_authors><pubmed_authors>Lu XP</pubmed_authors><pubmed_authors>Hu YH</pubmed_authors><pubmed_authors>Ding XS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Switching Between LC-ESI-MS/MS and EMIT Methods for Routine TDM of Valproic Acid in Pediatric Patients With Epilepsy: What Clinicians and Researchers Need to Know.</name><description>&lt;b>Background:&lt;/b> Valproic acid (VPA) is a widely used antiseizure medication and its dosing needs to be tailored individually through therapeutic drug monitoring (TDM) to avoid or prevent toxicity. Currently, immune-enzymatic assays such as Enzyme Multiplied Immunoassay Technique (EMIT), and Liquid Chromatography (LC)-based techniques, particularly coupled to Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS), resulting a potential lack of concordance between laboratories. &lt;b>Methods:&lt;/b> In this study, plasma VPA concentrations were determined for 711 pediatric patients with epilepsy by a routine EMIT assay and by a validated in-house LC-ESI-MS/MS method on the same group of samples, aimed to address the aforementioned concern. Consistency between two assays was evaluated u</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-08T05:02:06.703Z</modification><creation>2025-06-01T02:42:58.64Z</creation></dates><accession>S-EPMC8650496</accession><cross_references><pubmed>34887756</pubmed><doi>10.3389/fphar.2021.750744</doi></cross_references></HashMap>