期刊文献+

新诊断癫痫患者的规范化药物治疗 被引量:49

Standardized medication strategy for new diagnosed epilepsy
原文传递
导出
摘要 目的评估新诊断癫痫患者的规范化药物治疗方法、疗效和安全性。方法对278例新诊断癫痫患者制订规范化药物治疗方法,在治疗24个月后评价疗效、保留率和安全性。结果278例新诊断患者中235例采用单药治疗,43例采用联合治疗。单药治疗以卡马西平和丙戊酸钠为主。24个月时总无发作率76.3%(212/278),有效率22.7%(63/278)。单药治疗保留率卡马西平为69.8%,丙戊酸钠为76.2%,奥卡西平为68.0%,托吡酯为69.6%,拉莫三嗪为83.3%,左乙拉西坦为85.7%,苯妥英钠为100%。结论患者经规范治疗后均得到满意的控制,表明规范治疗方法具有较好的临床实用价值,值得进一步推广。 Objective To formulate and detect the efficacy and safety of standardized medication strategy of epilepsy. Methods The normalized medication strategy was worked out in 278 new diagnosed patients, whose effect, retention rate and safety were evaluated after 24 months of treatment. Results Of all the 278 patients, 235 patients were taken mono-therapy while other 43 patients used therapeutic alliance. Most patients took CBZ or VPA as mono-therapy drugs. At the time after 24 months, almost 76. 3% (212/278) patients got seizure free, and the effectiveness was 22. 7% (63/278). The retention rate of those mono-therapy drugs were investigated respectively. CBZ presented 69. 8% , VPA presented 76. 2% , OXC was 68.0%, TPM was 69. 6%, LTG was 83.3%, LEV presented 85.7%, and 100% for PHT. Conclusions All epileptic patients were well-controlled after taking standardized medication. The standardized medication strategy of epilepsy possesses valuable importance in clinical practice, which deserves further popularization.
出处 《中华神经科杂志》 CAS CSCD 北大核心 2011年第1期6-9,共4页 Chinese Journal of Neurology
基金 基金项目:上海市卫生局重点学科建设项目
关键词 癫痫 药物疗法 临床方案 Epilepsy Drug therapy Clinical protocols
  • 相关文献

参考文献19

  • 1Proposal for revised clinical and electroencephalographic classification of epileptic seizures. From the Commission on Classification and Terminology of the International League Against Epilepsy. Epilepsia, 1981, 22 : 489-501.
  • 2Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy. Epilepsia, 1989, 30: 389- 399.
  • 3National Institute for Clinical Excellence. The epilepsies: the diagnosis and management of the epilepsies in aduhs and children in primary and secondary care [ R/OL ]. London: National Institute for Clinical Excellence, 2004. [ 2010-09-01 ]. http :// www. nice. org. uk/CG020aduhsquickrefguide.
  • 4French JA, Kanner AM, Bautista J, et al. Efficacy and tolerability of the new antiepileptic drugs I : treatment of new onset epilepsy: report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neum|ogy and the American Epilepsy Society. Neurology, 2004, 62: 1252-1260.
  • 5Marson AG, Williamson PR, Clough H, et al. Carbamazepine versus valproate monotherapy for epilepsy: a meta-analysis. Epilepsia, 2002, 43: 505-513.
  • 6Tudur Smith C, Marson AG, Williamson PR. Phenytoin versus valproate monotherapy for partial onset seizures and generalized onset tonic-clonic seizures. Cochrane Database Syst Rev, 2001, (4) : CD001769.
  • 7Posner EB, Mohamed K, Marson AG. Ethosuximide, sodium valproate or lamotrigine for absence seizures in children and adolescents. Cochrane Database Syst Rev, 2005, ( 4 ) : CD003032.
  • 8] Nicolson A, Appleton RE, Chadwick DW, et al. The relationship between treatment with valproate, lamotrigine, and topiramate and the prognosis of the idiopathic generalised epilepsies. J Neurol Neurosurg Psychiatry, 2004, 75: 75-79.
  • 9Kwan P, Brodie MJ. Epilepsy after the first drug fails : substitution or add-on? Seizure, 2000, 9: 464-468.
  • 10Morrow J, Russell A, Guthrie E, et al. Malformation risks of antiepileptic drugs in pregnancy: a prospective study from the UK Epilepsy and Pregnancy Register. J Neurol Neurosurg Psychiatry, 2006, 77 : 193-198.

二级参考文献13

  • 1Abou-Khalil B, Hemdal P, Privitera MD. An open-label study of levetiracetam at individualized doses between 1000 and 3000 mg·day^-1 in adult patients with refractory epilepsy. Seizure,2003, 12: 141-149.
  • 2Beran RG, Berkovic SF, Black AB, et al. Efficacy and safety of levetiracetam 1000-3000 mg/day in patients with refractory partialonset seizures: a muhicenter, open-label single-arm study.Epilepsy Res, 2005, 63: 1-9.
  • 3Patsalos PN. Pharmacokinetic profile of levetiracetam: toward ideal characteristics. Pharmacol Ther, 2000, 85: 77-85.
  • 4Klitgaard H. Levetiracetam: the preclinical profile of a new class of antiepileptic drugs? Epilepsia, 2001, 42 Suppl 4: 13-18.
  • 5Rigo JM, Nguyen L, Belachew S, et al. Levetiracetam: novel modulation of ionotropic inhibitory receptors. Epilepsia, 2000, 41Suppl 7 :S35.
  • 6Zona C, Niespodziany I, Marchetti C, et al. Levetiracetam does not modulate neuronal voltage-gated Na^+ and T-type Ca^2+ currents. Seizure, 2001, 10: 279-286.
  • 7Noyer M, Gillard M, Matagne A, et al. The novel antiepileptic drug levetiracetam (ucb 1.059 ) appears to act via a specific binding site in CNS membranes. Eur J Pharmacol, 1995, 286:137-146.
  • 8Niespodziany I, Kltigaard H, Margineanu DG. Levetiracetam:modulation of high voltage-activated Ca^2+ current in CA1 pyramidal neurons of rat hippocampal slices. Epilepsia, 2000, 41 Suppl 7 : 37.
  • 9Madeja M, Margineanu DG, Gorji A, et al. Reduction of voltage-operated potassium currents by levetiracetam: a novel antiepileptic mechanism of act on? Neuropharmacology, 2003, 45 : 661-667.
  • 10Shorvon SD, Lowenthal A, Janz D, et al. Multicenter double-blind randomized, placebo-controlled trial of levetiracetam as addon therapy in patients with refractory partial seizures. European Levetiracetam Study Group. Epilepsia, 2000, 41 : 1179-1186.

共引文献43

同被引文献465

引证文献49

二级引证文献396

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部