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新一代抗癫痫药物对成人全面强直阵挛发作单药治疗保留率的比较 被引量:7

The Retention Rate of New Antiepileptic Drugs in Treating Adults with Generalized Tonic-clonic Seizure
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摘要 目的比较5种新一代抗癫痫药物对成人全面强直阵挛发作单药治疗的保留率。方法选择2010年7月-2011年6月354例确诊为癫痫全面强直阵挛发作患者,分别采用拉莫三嗪、左乙拉西坦、奥卡西平、托吡酯、加巴喷丁5种药物进行单药治疗,对其5种药物的6、12个月保留率进行比较。结果 5种药物的6、12个月保留率分别为:拉莫三嗪90.8%、79.8%,左乙拉西坦88.0%、66.7%,奥卡西平82.1%、58.2%,托吡酯81.2%、58.0%,加巴喷丁26.5%、20.6%。6个月保留率加巴喷丁与其他4种药物比较差异有统计学意义(P<0.001),其他药物之间差异无统计学意义。12个月保留率拉莫三嗪与其他4种药物比较差异有统计学意义(P<0.005),其他药物之间差异无统计学意义。结论拉莫三嗪对成人全面强直阵挛发作单药治疗12个月保留率最高。通过对5种新一代抗癫痫药物12个月保留率比较研究,可以对临床单药治疗癫痫药物选择提供一定参考。 Objective To compare the retention rate of five new antiepileptic drugs (AEDs) in treating adults with generalized tonic-clonic seizure. Methods A total of 354 patients diagnosed with generalized tonic-clonic seizure were treated with five AEDs separately, including lamotrigine (LTG), levetiracetam (LEV), oxcabazepine (OXC), topiramate (TPM), and gabapentin (GAB). The 6- and 12-month retention rates of these five drug treatments were compared. Results The 6- and 12-month retention rates were respectively LTG (90.8%, 79.8%), LEV (88.0%, 66.7%), OXC (82.1%, 58.2%), TPM (81.2%, 58.0%) and GAB (26.5%, 20.6%). For 6-month retention rate, the lowest was GAB, which was significantly different from others (P 〈 0.001); no difference was found among the other AEDs. For 12-month retention rate, the highest was LTG, which was significantly different from others (P 〈 0.005); no difference was found among the other AEDs. Conclusions LTG has the highest one-year retention rate in treating adults with generalized tonic-clonic seizure. The comparison of retention rates among the new AEDs can provide useful insight for the choice of antiepileptic drugs for adults with generalized tonic-clonic seizure.
出处 《华西医学》 CAS 2012年第6期855-858,共4页 West China Medical Journal
关键词 抗癫痫药物 单药治疗 保留率 Antiepileptic drugs Monotherapy Retention rate
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  • 1陈永久.难治性癫痫的治疗[J].中国基层医药,1996,4(4):63-63. 被引量:1
  • 2蒋万书,陈石金,李明伟,谢廷风,代素芳,吕孟达.选择性杏仁海马切除治疗颞叶癫痫[J].中国神经精神疾病杂志,1989,15(6):330-332. 被引量:7
  • 3徐姜定.难治性癫痫治疗进展[J].浙江临床医学,2006,8(10):1009-1010. 被引量:13
  • 4[1]Taylor CT. Energing perspectives or the mechanism of action of gabapentin. Neurology 1994,44(Sup5):10
  • 5[2]Harden CL. New anticpileptic drugs Neurology 1994,44:787
  • 6May TW, KornMerker E, Rambeck B. Clinical pharmacokinetics of Oxcarbazepine. Clin Pharmacokinet, 2003, 42 (12) : 1023-1042.
  • 7Flesch G. Overview of the clinical pharmacokinetics of Oxcarbazepine. Clin Drug Invest, 2004, 24(4) : 185-203.
  • 8Freidel M, Krause E, Kuhn K, et al. Oxcarbazepine in the treatment of epilepsy. Fort Schr Neurol Psychiatr, 2007, 75 (2) : 100-106.
  • 9Chung S, Wang N, Hank N. Comparative retention rates and long-term tolerability of new antiepileptic drugs. Seizure, 2007, 16: 296-304.
  • 10Kutluay E, Mccague KD, Souza J, et al. Safety and tolerability of oxcarbazepine in elderly patients with epilepsy. Epilepsy Behav, 2003, 4(2) : 175-180.

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同被引文献58

  • 1刘姜冰,石静萍,赵薛旭.托吡酯神经保护作用的研究进展[J].临床神经病学杂志,2005,18(4):317-318. 被引量:13
  • 2岳英,徐一峰,孙鹏.舍曲林的临床应用[J].上海精神医学,2007,19(2):122-124. 被引量:20
  • 3梁颖华,王冬梅,杨得坡,郭镇明,李文敏.贯叶金丝桃素及其衍生物的合成与神经药理学研究进展[J].中草药,2007,38(5):789-791. 被引量:35
  • 4中国医药工业信息中心.中国新药研发监测数据库[EB/OL].http://cpm.pharmadl.com.
  • 5Kerchner GA, Boxer AL. Bapineuzumab [J]. Expert Opin Biol Ther, 2010, 10(7) : 1121-1130.
  • 6Lobello K, Ryan JM, Liu E, et al. Targeting beta amyloid: a clinical review of immunotherapeutic approaches in Alzheimer's Disease[J]. Int J Alzheimers Dis, 2012, http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3265072/ ?tool=pmcentrez.
  • 7Alzheimer's Association. 2009 Alzheimer's Disease Facts and Figures [EB/OL]. (2012-08-10) [2012-08-14] .http://www.alz. org/national/documents/report alzfactsfigures2009 .pdf.
  • 8中华医学会编著.临床诊疗指南-癫痫间病分册[M].北京:人民卫生出版社,2002: 45-47.
  • 9Evans BK, KustraRP, Hammer AE, et al. Assessment of tolerability inelderly patients: changing toLamotrigine therapy [J]. Am J Ger-iatrPharmacother, 2007,5(1): 112-119.
  • 10Sun W, Wang Y,Wang W, et al. Attention changes in epilepsypa-tients following 3-month topiramate or valproate treatment re-vealed by event-related potential [J]. Int J Psychophysiol, 2008, 68(3):235-241.

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