期刊文献+

美多芭联合恩他卡朋对中晚期帕金森患者的临床疗效研究 被引量:10

Clinical Curative Effect of Madopar Combining Entacapone in Patients with Middle-late Parkinson's Patients
下载PDF
导出
摘要 目的:对美多芭联合恩他卡朋治疗中晚期帕金森患者的临床疗效进行观察和总结。方法:65例临床确诊为原发性帕金森病的患者,随机分为美多芭组32例,单独给予美多芭治疗,联合组33例,在美多芭组用药的基础上联用恩他卡朋治疗。两组患者均治疗12周。对比治疗前后外周血中LD的血药浓度、UPDRS评分及血浆SOD、MDA、GSH、GSH-PX水平。结果:对比美多芭组,联合组治疗后能提高LD的血药浓度,降低UPDRS评分,抗氧化能力有所改善,差异有统计学意义(P<0.05);美多芭组治疗后血药浓度较治疗前有所下降,但差异无统计学意义。结论:联合用药能提高中晚期PD患者外周血中的LD血药浓度,改善症状,提高机体抗氧化水平。 Objective: To observe and summarize the clinical curative effect of madopar combining en-tacapone in middle-late Parkinson's disease ( PD) patients. Methods: Sixty-five cases of clinically diagnosed idiopathic Parkinson's disease were randomly divided, 32 subjects were treated with madopar (madopar group) and 33 subjects were treated with madopar combining entacapone (combination group). The two groups of patients were treated for 12 weeks. Before and after treatment, levodopa ( LD) concentration in peripheral blood, UPDRS scores and levels of SOD, MDA, GSH and GSH-PX in peripheral blood were recorded and compared. Results: Compared with the madopar group, the combination group showed higher blood LD concentrations and antioxidant capacity, lower UPDRS scores, the differences were statistically significant ( P〈0.05). Conclusion: Madopar combining entacapone can improve clinical symptoms and raise blood LD concentrations and antioxidant levels in middle-late Parkinson's patients.
出处 《药学与临床研究》 2017年第2期121-123,共3页 Pharmaceutical and Clinical Research
基金 南京药学会-常州四药医院药学科研基金(2014YX003)
关键词 帕金森病 美多芭 恩他卡朋 血药浓度 Parkinson's Disease Madopar Entacapone Blood concentration
  • 相关文献

参考文献3

二级参考文献45

  • 1Nutt JG.On-off phenomenon:relation to levodopa pharmacokinetics and pharmacodynamics[J].Ann Neurol,1987,22:535-540.
  • 2Tolokan A,Klebovich I,Balogh-Nemes K,et al.Automated determination of levodopa and carbidopa in plasma by high-performance liquid chromatography-electrochemical detection using an on-line flow injection analysis sample pretreatment unit[J].J Chromatogr B Biomed Sci Appl,1997,698(1-2):201-207.
  • 3Schimiet RF,Thew G.Human physiology,springer-verlay,Berlin Heiderg[Z].New York,1983,681.Albert J S. Physiopathology of the cardiovascular system.Little Brown and company Boston/Toronto.
  • 4Yeh KC,August TF,et al.Pharmacokinetics and bioavailability of Sinemet CR:A summary of human studies[J].Neurology 39(Suppl 2),1989,11:25-37.
  • 5Zhang ZX, Roman GC, Hong Z, et al. Parkinson's disease in China: prevalence in Beijing, Xi'an, and Shanghai[J]. Lancet,2005,365: 595-597
  • 6Verhagen Metman L. Recognition and treatment of response fluctuations in Parkinson's disease[J]. Amino Acids, 2002, 23(1-3) : 141-145
  • 7KerAnen T, Gordin A, Karlsson M, et al. Inhibition of soluble catechol-O-methyltransferase and single-dose pharmacokinetics after oral and intravenous administration of entacapone[J]. Eur J Clin Pharmacol, 1994, 46:151-157
  • 8Ruottinen HM, Rinne UK. A double-blind pharmacokinetic and clinical dose-response study of entacapone as an adjuvant to levodopa therapy in advanced Parkinson' s disease[J]. Clin Neuropharmacol, 1996, 19:283-296
  • 9Muller T, Erdmann C, Muhlack S, et al. Inhibition of catechol-O- methyltransferase contributes to more stable levodopa plasma levels [J]. Mov Disord, 2006, 21:332-336
  • 10Heikkinen H, Varhe A, Laine T, et al. Entacapone improves the availability of L-dopa in plasma by decreasing its peripheral metabolism independent of L-dopa/carbidopa dose[J]. Br J Clin Pharmacol, 2002, 54:363-371

共引文献24

同被引文献91

引证文献10

二级引证文献44

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