{"title":"[直立功能障碍的治疗方面]。","authors":"H Rieckert","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>In two open intraindividual controlled clinical trials efficacy of placebo, Dihydergot and etilefrine as well as a combination of Dihydergot and etilefrine on the parameters \"venous capacity\", \"circulatory response to orthostatic stress\" and \"blood pressure\" was compared under acute and chronic therapy. Under acute conditions (15 healthy individuals; medication: placebo 0.25 Dihydergot i.v., 15 mg etilefrine p.o., 0.25 mg Dihydergot plus 15 mg etilefrine p.o.) superiority of the combination could be demonstrated concerning tonisation of the capacitance vessels and improvement of circulatory regulation during orthostasis, as indicated by less pronounced increase in heart rate. In a further study, in which 14 healthy individuals with relatively low blood pressure (RR syst./RR diast. 114/78 mm Hg) received each for one week 20 mg etilefrine, 2 mg Dihydergot or the combination (Dihydergot plus), blood pressure increased significantly (p less than or equal to 0.05) under the combination. The effect was due to the etilefrine component of the combination as could be inferred from the assessment of efficacy.</p>","PeriodicalId":79233,"journal":{"name":"Medizinische Klinik (Praxis-Ausg.)","volume":"77 5","pages":"48-52"},"PeriodicalIF":0.0000,"publicationDate":"1982-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Therapeutic aspects of orthostatic dysfunction].\",\"authors\":\"H Rieckert\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In two open intraindividual controlled clinical trials efficacy of placebo, Dihydergot and etilefrine as well as a combination of Dihydergot and etilefrine on the parameters \\\"venous capacity\\\", \\\"circulatory response to orthostatic stress\\\" and \\\"blood pressure\\\" was compared under acute and chronic therapy. Under acute conditions (15 healthy individuals; medication: placebo 0.25 Dihydergot i.v., 15 mg etilefrine p.o., 0.25 mg Dihydergot plus 15 mg etilefrine p.o.) superiority of the combination could be demonstrated concerning tonisation of the capacitance vessels and improvement of circulatory regulation during orthostasis, as indicated by less pronounced increase in heart rate. In a further study, in which 14 healthy individuals with relatively low blood pressure (RR syst./RR diast. 114/78 mm Hg) received each for one week 20 mg etilefrine, 2 mg Dihydergot or the combination (Dihydergot plus), blood pressure increased significantly (p less than or equal to 0.05) under the combination. The effect was due to the etilefrine component of the combination as could be inferred from the assessment of efficacy.</p>\",\"PeriodicalId\":79233,\"journal\":{\"name\":\"Medizinische Klinik (Praxis-Ausg.)\",\"volume\":\"77 5\",\"pages\":\"48-52\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1982-02-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medizinische Klinik (Praxis-Ausg.)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medizinische Klinik (Praxis-Ausg.)","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
在两项开放的个体内对照临床试验中,比较了安慰剂、双氢化氢和依替弗林以及双氢化氢和依替弗林在急慢性治疗下对“静脉容量”、“体位应激循环反应”和“血压”等参数的疗效。在急性情况下(15名健康个体;药物:安慰剂0.25双氢化氢滴注,15毫克替替林p.o., 0.25毫克双氢化氢加15毫克替替林p.o.),这种组合的优势可以证明在直立时对容性血管的张力和循环调节的改善,如心率不太明显的增加所示。在一项进一步的研究中,14名血压相对较低(RR系统)的健康个体。/ RR diast。(114/78 mm Hg)各组分别给予乙曲林20 mg、双氢化氢2 mg或联合用药(双氢化氢加)1周后,血压显著升高(p <或等于0.05)。从疗效评估中可以推断,这种效果是由于联合用药中的etilefrine成分。
In two open intraindividual controlled clinical trials efficacy of placebo, Dihydergot and etilefrine as well as a combination of Dihydergot and etilefrine on the parameters "venous capacity", "circulatory response to orthostatic stress" and "blood pressure" was compared under acute and chronic therapy. Under acute conditions (15 healthy individuals; medication: placebo 0.25 Dihydergot i.v., 15 mg etilefrine p.o., 0.25 mg Dihydergot plus 15 mg etilefrine p.o.) superiority of the combination could be demonstrated concerning tonisation of the capacitance vessels and improvement of circulatory regulation during orthostasis, as indicated by less pronounced increase in heart rate. In a further study, in which 14 healthy individuals with relatively low blood pressure (RR syst./RR diast. 114/78 mm Hg) received each for one week 20 mg etilefrine, 2 mg Dihydergot or the combination (Dihydergot plus), blood pressure increased significantly (p less than or equal to 0.05) under the combination. The effect was due to the etilefrine component of the combination as could be inferred from the assessment of efficacy.