Suppr超能文献

[重症肌无力患者血清吡啶斯的明水平:方法及临床意义]

[Serum levels of pyridostigmine in myasthenia gravis: methods and clinical significance].

作者信息

Schumm F, Gaertner H J, Wiatr G, Dichgans J

出版信息

Fortschr Neurol Psychiatr. 1985 Jun;53(6):201-11. doi: 10.1055/s-2007-1001967.

Abstract

Correlation studies on patients with myasthenia gravis are reported in which clinical assessment of fatigue and neurophysiological findings are compared to blood levels of pyridostigmine. Measurements using a high-pressure liquid chromatography method (HPLC), give reproducible results. The levels of pyridostigmine in the serum or plasma of healthy controls and of patients show no essential differences. Components of coffee, tea, chocolate and cigarettes can markedly disturb the chromatography by adding additional peaks, so that interpretation becomes difficult or impossible. Blood levels can be measured approximately one hour after oral intake of 60 mg pyridostigmine. Concentrations rise for two to four hours and then decline exponentially. The half-life of pyridostigmine was between 156 and 210 minutes. Despite identical oral dosages, the concentration differed intraindividually and interindividually among patients. While the blood level does not reach its maximum value for 1-1 1/2 to 3 hours, the maximum clinical and neurophysiological effect of pyridostigmine appears 30-60 minutes after ingestion. Variable distribution of cholinesterase inhibitors over the different compartments (blood, synaptic region) is assumed to cause this temporal lag. If the total amount of pyridostigmine is divided into 4-5 doses, the concentration profiles over the course of a day are relatively stable. There is no significant correlation between the variations in blood level throughout one day, and changes in myasthenic symptomatology. Effects of pyridostigmine can be measured at levels as low as 5 ng/ml; at levels above 40 ng/ml further improvement can be detected only rarely. Blood levels were lower if corticosteroids were administered simultaneously; azathioprine had no influence on blood levels. Blood levels assays allow better differentiation of cholinergic and myasthenic crises and the identification of disturbed absorption and interactions with other medications.

摘要

报告了对重症肌无力患者的相关性研究,其中将疲劳的临床评估和神经生理学检查结果与血液中吡啶斯的明水平进行了比较。使用高压液相色谱法(HPLC)进行测量可得到可重复的结果。健康对照者和患者血清或血浆中吡啶斯的明水平无本质差异。咖啡、茶、巧克力和香烟的成分会通过增加额外的峰而显著干扰色谱分析,从而使解释变得困难或无法进行。口服60毫克吡啶斯的明后约一小时可测量血液水平。浓度在两到四个小时内上升,然后呈指数下降。吡啶斯的明的半衰期在156至210分钟之间。尽管口服剂量相同,但患者体内的浓度在个体内和个体间存在差异。虽然血液水平在1至1.5到3小时内未达到最大值,但吡啶斯的明的最大临床和神经生理学效应在摄入后30至60分钟出现。胆碱酯酶抑制剂在不同隔室(血液、突触区域)中的可变分布被认为是造成这种时间延迟的原因。如果将吡啶斯的明的总量分为4至5剂,则一天中的浓度曲线相对稳定。一天中血液水平的变化与肌无力症状的变化之间没有显著相关性。吡啶斯的明的作用在低至5纳克/毫升的水平即可测量;在高于40纳克/毫升的水平,仅很少能检测到进一步改善。如果同时给予皮质类固醇,血液水平会降低;硫唑嘌呤对血液水平没有影响。血液水平检测有助于更好地区分胆碱能危象和肌无力危象,并识别吸收障碍以及与其他药物的相互作用。

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