期刊文献+

基于冶疗药物监测的拉莫三嗪个体化用药分析 被引量:5

Individualized medication analysis of lamotrigine based on therapeutic drug monitoring
下载PDF
导出
摘要 目的:探讨拉莫三嗪(LTG)血药浓度与剂量对其疗效的影响,为临床个体化用药提供参考。方法:收集服用LTG的癫痫患者资料,共计67例,分析LTG血药浓度、给药剂量、疗效及不良反应的相关性,对血药浓度和剂量进行回归分析,并对血药浓度、日剂量和疗效进行对比。结果:4例患者发生过敏而停药,56例患者血药浓度处于治疗窗内(3~15μg·mL^(-1)),7例患者血药浓度低于治疗窗,两者给药剂量差异无统计学意义;给药剂量与血药浓度在一定范围内呈正相关。治疗窗组的总有效率为91.07%,显著高于低治疗窗组的57.14%;控制组和显效组的血药浓度显著高于有效组和无效组,有效组的给药剂量显著低于显效组(P <0.05)。3例低治疗窗患者和5例治疗窗内患者联用丙戊酸钠进行治疗。结论:TDM对LTG的治疗有重要指导意义,LTG用药存在个体差异,临床应基于TDM进行LTG个体化用药,以提高疗效,降低不良反应的发生。 Objective: To investigate the influence of the plasma concentration and dose of lamotrigine (LTG) on its efficacy, and provide reference for rational drug use. Methods: Data of 67 epileptic patients taking LTG were collected and the correlation of plasma concentration, clinical effect and adverse reactions were analyzed by regression analysis. Results: Four patients developed allergies resulted in LTG withdrawl. 56 patients had the blood concentrations in the treatment window (3 – 15 μg·mL^-1) except 7 patients. There was no significant difference in dose between the two groups. The plasma concentration of LTG was positively correlated with the dose of LTG. The total effective rate was 91.07% in the treatment window group, which was significantly higher than that of the low treatment window group (57.14%). The blood concentration of LTG in the control and the excellence group was significantly higher than that in the effective and the ineffective group. The dose of the effective group was significantly lower than that of the excellence group (P < 0.05). 3 patients in the low treatment window group and 5 patients in the treatment window group were treated together with sodium valproate. Conclusion: TDM had great significance in the treatment of LTG. There were individual differences in the use of LTG. Individualized use of LTG based on TDM could improve the efficacy and avoid the occurrence of adverse drug reactions.
作者 周甜甜 王夏红 张慧芝 张颖 王录 ZHOU Tian-tian;WANG Xia-hong;ZHANG Hui-zhi;ZHANG Ying;WANG Lu(Department of Pharmacy, Zhengzhou Second Hospital, Zhengzhou 450000, China;Department of Neurology, Zhengzhou Second Hospital, Zhengzhou 450000, China)
出处 《中国药物应用与监测》 CAS 2019年第2期75-77,92,共4页 Chinese Journal of Drug Application and Monitoring
基金 河南省医学科技攻关计划项目(2018020740)
关键词 治疗药物监测 拉莫三嗪 疗效 药品不良反应 Therapeutic drug monitoring Lamotrigine Curative effect Adverse drug reaction
  • 相关文献

参考文献8

二级参考文献73

  • 1袁洪波,朱毅,陈力.拉莫三嗪片不良反应回顾性分析[J].现代预防医学,2012,39(22):6088-6090. 被引量:10
  • 2葛茂振.癫痫的分类与治疗[J].黑龙江医药,1991,0(5):8-9. 被引量:1
  • 3陈子怡,周列民,周珏倩,李伟峰,程芙蓉,潘军利.抗癫痫药物所致重型药疹及危险因素分析[J].医学信息(西安上半月),2006,19(11):1989-1990. 被引量:15
  • 4易娟,周宏灏.UGT1A基因的遗传多态性对底物代谢的影响[J].生理科学进展,2007,38(3):235-238. 被引量:2
  • 5Maekenziea P1,Bock K'W,Burchell B,et al. Ncmendamre update for the mammalian UDP glycosyhransferase(UGT) gene supeffamily[ J ]. Phanm- eogenet Genomics, 2005,15(10) : 677.
  • 6Miyagi SJ , Collier AC. Pediatric devdopment d glucuronidation: the ontogeny cf hepatic UGT1A4[J]. Drug Metab Dispos ,2007,35(9): 1587.
  • 7Sun DX,Chen C., Ddlingelr RW,et al. Characterimtion of tanofen and 4-hydrm7 tamoxlfen glucuronidaticn by human UGT1M variants[J]. Breast Cancer Pes, 2006,8(4):P,50.
  • 8Ehmer U, Vogel A,Sehutte JK,et al. Variation of hepatic glucuronida-tion: novel functional polymoisms of the UDP-glucuronosyltranserase UGT1A4[J]. Hepatology ,2004,39(4):970.
  • 9Moil A,Mamo Y,lwai M,et al. UDP-glucuronosyltranerase 1A4 poly- morphisms in a Jatmnese population and kinetics of clozapine[ J]. Drug Metab Dispcs ,2005,33(5) :672.
  • 10M&tard V, Girard H, Harvey M, et al. Analysis d inherited genetic variations at the UGTI locus in the French-Camadian polmlion[J]. Hum Mutat,2009,30(4) :677.

共引文献178

同被引文献45

引证文献5

二级引证文献13

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