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[前列腺素E1动脉内灌注治疗间歇性跛行患者]

[Intra-arterial infusion treatment with prostaglandin E1 in patients with intermittent claudication].

作者信息

Rudofsky G

机构信息

Innere Medizin, Bundeswehrkrankenhaus Ulm, Bundesrepublik Deutschland.

出版信息

Wien Klin Wochenschr. 1988 Jul 15;100(14):484-8.

PMID:3062906
Abstract

In a double-blind, placebo-controlled study 50 patients with peripheral arterial occlusive disease stage IIb were given daily or intra-arterial infusion of either 1 ampoule of Prostavasin (20 micrograms PGE 1) or 1 ampoule of placebo (646.7 micrograms alpha-cyclodextrin), each dissolved in 50 ml saline, over 60-120 min. Weekends excepted, the therapy was continued for three weeks. Under PGE 1 therapy the maximum ergometric walking distance increased by 146% (mean: from 109 m to 268 m), as opposed to 40% in the placebo group (mean: from 101.5 m to 142 m). Furthermore, significant improvements were seen with regard to painfree walking capacity (PGE 1: + 170%; placebo: + 49%). Free maximum and pain-free walking distances were increased as well (PGE 1: + 131% and 48%; placebo: + 26% and 27%). Haemorrheological parameters, e.g. plasma and whole blood viscosity, haematocrit and erythrocyte aggregation decreased (p less than 0.01) after PGE 1, whereas a significant increase (p less than 0.01) in acral digital temperature, blood flow and ultrasonic Doppler values was seen. No side-effects were observed.

摘要

在一项双盲、安慰剂对照研究中,50例IIb期外周动脉闭塞性疾病患者接受每日或动脉内输注1安瓿前列腺素(20微克前列腺素E1)或1安瓿安慰剂(646.7微克α-环糊精),每种药物均溶于50毫升生理盐水中,输注时间为60 - 120分钟。除周末外,治疗持续三周。在前列腺素E1治疗下,最大运动耐力步行距离增加了146%(平均:从109米增至268米),而安慰剂组为40%(平均:从101.5米增至142米)。此外,无痛步行能力也有显著改善(前列腺素E1组:+170%;安慰剂组:+49%)。自由最大步行距离和无痛步行距离也有所增加(前列腺素E1组:+131%和48%;安慰剂组:+26%和27%)。前列腺素E1治疗后血液流变学参数,如血浆和全血粘度、血细胞比容和红细胞聚集性降低(p<0.01),而指端温度、血流和超声多普勒值则显著升高(p<0.01)。未观察到副作用。

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