• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

溴隐亭在晚期帕金森病长期管理中的应用

Bromocriptine in the long-term management of advanced Parkinson's disease.

作者信息

Grimes J D, Hassan M N

出版信息

Can J Neurol Sci. 1983 May;10(2):86-90. doi: 10.1017/s0317167100044693.

DOI:10.1017/s0317167100044693
PMID:6861013
Abstract

Thirty-seven patients with advanced Parkinson's disease who initially tolerated, and responded to bromocriptine therapy were followed for 12 to 50 (mean 28) months. Using a method of gradual increase of bromocriptine, with concomitant levodopa reduction, the peak effect of the drug was apparent by three months, at which time the mean daily dose of bromocriptine was 23.9 mg and Sinemet (levodopa + carbidopa) had been reduced by 34 percent. Eight patients had sustained improvement without further drug changes for an average of 29 (range 14-50) months. After periods of improvement varying between 3 and 30 months, 29 patients had a fall-off from peak effect. Peak effect was regained in 21 of these 29 patients for an average of 16 additional months by initially increasing bromocriptine or Sinemet, or by eventually increasing both drugs. The main adverse effect was a confusional state which necessitated late withdrawal of bromocriptine in four patients. The best results were in younger patients with end-of-dose deterioration and levodopa induced dyskinesias. With cautious introduction, and intermittent dosage adjustment, bromocriptine can be of long-term benefit to patients with advance Parkinson's disease. The majority of patients have a gradual late fall-off in effect which can frequently be reversed with dosage adjustment.

摘要

37例晚期帕金森病患者最初耐受溴隐亭治疗且有反应,随访12至50(平均28)个月。采用逐渐增加溴隐亭剂量并同时减少左旋多巴用量的方法,3个月时药物达到最大效应,此时溴隐亭平均日剂量为23.9mg,息宁(左旋多巴+卡比多巴)已减少34%。8例患者持续改善,未再调整药物,平均持续29(14至50)个月。在3至30个月不等的改善期后,29例患者从最大效应下降。这29例患者中有21例通过最初增加溴隐亭或息宁,或最终同时增加两种药物,平均又恢复最大效应16个月。主要不良反应是意识模糊状态,4例患者因此不得不停用溴隐亭。效果最佳的是有剂末恶化和左旋多巴诱发异动症的年轻患者。谨慎用药并间断调整剂量,溴隐亭对晚期帕金森病患者可产生长期益处。大多数患者效应会逐渐后期下降,常可通过调整剂量逆转。

相似文献

1
Bromocriptine in the long-term management of advanced Parkinson's disease.溴隐亭在晚期帕金森病长期管理中的应用
Can J Neurol Sci. 1983 May;10(2):86-90. doi: 10.1017/s0317167100044693.
2
Method of addition of bromocriptine to the drug regime of patients with advanced Parkinson's disease.在晚期帕金森病患者的药物治疗方案中添加溴隐亭的方法。
Can J Neurol Sci. 1981 Feb;8(1):31-4. doi: 10.1017/s0317167100042803.
3
Bromocriptine in the management of end of dose deterioration in Parkinson's disease.溴隐亭在帕金森病剂末恶化管理中的应用
Can J Neurol Sci. 1984 Nov;11(4):452-6. doi: 10.1017/s0317167100045996.
4
Long-term treatment with high-dosage bromocriptine in advanced Parkinson's disease.高剂量溴隐亭对晚期帕金森病的长期治疗
Adv Neurol. 1987;45:539-42.
5
Bromocriptine: problems with low-dose de novo therapy in Parkinson's disease.溴隐亭:帕金森病低剂量起始治疗的问题
Clin Neuropharmacol. 1985;8(1):73-7.
6
Long-term efficacy of bromocriptine in Parkinson disease.溴隐亭治疗帕金森病的长期疗效
Neurology. 1980 May;30(5):518-23. doi: 10.1212/wnl.30.5.518.
7
A comparison of bromocriptine (Parlodel) and levodopa-carbidopa (Sinemet) for treatment of "de novo" Parkinson's disease patients.溴隐亭(帕罗西汀)与左旋多巴-卡比多巴(息宁)治疗“初发”帕金森病患者的比较。
Can J Neurol Sci. 1987 Nov;14(4):576-80.
8
Adjuvant treatment of Parkinson's disease with dopamine agonists: open trial with bromocriptine and CU 32-085.多巴胺激动剂辅助治疗帕金森病:溴隐亭和CU 32 - 085的开放试验
J Neurol. 1982;227(2):75-88. doi: 10.1007/BF00313773.
9
Low-dosage treatment in de novo patients with Parkinson's disease: a prospective study.帕金森病初发患者的低剂量治疗:一项前瞻性研究。
Adv Neurol. 1987;45:529-34.
10
Treatment of parkinson's disease with bromocriptine.用溴隐亭治疗帕金森病。
N Engl J Med. 1976 Dec 16;295(25):1400-4. doi: 10.1056/NEJM197612162952504.

引用本文的文献

1
Description of the time course of the prolactin suppressant effect of the dopamine agonist CQP201-403 by an integrated pharmacokinetic-pharmacodynamic model.通过整合药代动力学-药效学模型描述多巴胺激动剂CQP201-403催乳素抑制作用的时间过程。
Br J Clin Pharmacol. 1986 Jul;22(1):1-13. doi: 10.1111/j.1365-2125.1986.tb02872.x.
2
Bromocriptine induced pleuropulmonary fibrosis.溴隐亭诱发胸膜肺纤维化。
Thorax. 1986 Apr;41(4):328-30. doi: 10.1136/thx.41.4.328.