{"title":"系统性方法在癫痫长期药物治疗中的应用:丙戊酸一例报告","authors":"Captain Manvikram Singh Gill","doi":"10.5530/amdhs.2020.2.7","DOIUrl":null,"url":null,"abstract":"This is a case of breakthrough seizure and use of valproic acid (VPA) in management. Objective is to discuss the systematic approach in pharmacological treatment of epilepsy. Day one, patient was initiated with intravenous infusion of phenytoin 800mg, tablet phenytoin 300mg OD and tablet VPA 400mg TDS. Tablet VPA doses were withheld at Day 2 after Therapeutic Drug Monitoring (TDM) toxic levels. Patient was discharged with tablet VPA 400mg BD and tablet levetiracetam 500mg BD. In the beginning of therapy, a single pharmacotherapeutic agent is introduced cautiously to reduce any unwanted incidences of idiosyncratic and dose related toxicity. The pharmaco therapeutic agent dose must then be increased gradually to a maximum tolerated drug-dose therapeutic response. If this agent is not tolerated, it can be substituted with another agent for efficacious mono therapy. If seizures prevail, despite adequate trials of two appropriate agents, then poly therapy should be initiated. Patients need to be informed about the objectives of therapy and","PeriodicalId":237766,"journal":{"name":"Advances in Medical, Dental and Health Sciences","volume":"32 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Systematic Approach in Long Term Pharmacological Treatment of Epilepsy: A Case Report on the Use of Valproic Acid\",\"authors\":\"Captain Manvikram Singh Gill\",\"doi\":\"10.5530/amdhs.2020.2.7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This is a case of breakthrough seizure and use of valproic acid (VPA) in management. Objective is to discuss the systematic approach in pharmacological treatment of epilepsy. Day one, patient was initiated with intravenous infusion of phenytoin 800mg, tablet phenytoin 300mg OD and tablet VPA 400mg TDS. Tablet VPA doses were withheld at Day 2 after Therapeutic Drug Monitoring (TDM) toxic levels. Patient was discharged with tablet VPA 400mg BD and tablet levetiracetam 500mg BD. In the beginning of therapy, a single pharmacotherapeutic agent is introduced cautiously to reduce any unwanted incidences of idiosyncratic and dose related toxicity. The pharmaco therapeutic agent dose must then be increased gradually to a maximum tolerated drug-dose therapeutic response. If this agent is not tolerated, it can be substituted with another agent for efficacious mono therapy. If seizures prevail, despite adequate trials of two appropriate agents, then poly therapy should be initiated. Patients need to be informed about the objectives of therapy and\",\"PeriodicalId\":237766,\"journal\":{\"name\":\"Advances in Medical, Dental and Health Sciences\",\"volume\":\"32 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-07-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advances in Medical, Dental and Health Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5530/amdhs.2020.2.7\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Medical, Dental and Health Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5530/amdhs.2020.2.7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Systematic Approach in Long Term Pharmacological Treatment of Epilepsy: A Case Report on the Use of Valproic Acid
This is a case of breakthrough seizure and use of valproic acid (VPA) in management. Objective is to discuss the systematic approach in pharmacological treatment of epilepsy. Day one, patient was initiated with intravenous infusion of phenytoin 800mg, tablet phenytoin 300mg OD and tablet VPA 400mg TDS. Tablet VPA doses were withheld at Day 2 after Therapeutic Drug Monitoring (TDM) toxic levels. Patient was discharged with tablet VPA 400mg BD and tablet levetiracetam 500mg BD. In the beginning of therapy, a single pharmacotherapeutic agent is introduced cautiously to reduce any unwanted incidences of idiosyncratic and dose related toxicity. The pharmaco therapeutic agent dose must then be increased gradually to a maximum tolerated drug-dose therapeutic response. If this agent is not tolerated, it can be substituted with another agent for efficacious mono therapy. If seizures prevail, despite adequate trials of two appropriate agents, then poly therapy should be initiated. Patients need to be informed about the objectives of therapy and