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[多利普强效片——6个月给药期的用药经验]

[Duolip Forte--experience during a 6-month period of administration].

作者信息

Toschnerová H, Ceska R, Sobra J, Traurig J

机构信息

II. interní klinika 1. LF UK, Praha.

出版信息

Cas Lek Cesk. 1993 May 18;132(10):308-10.

PMID:8513467
Abstract

Duolip forte (ethophylline clofibrate, tablets à 500 mg) produced by Merckle Austria was administered to 20 patients with different types of hyperlipoproteinaemia for a 6-month period in amounts of 500 mg/day. Before onset of treatment and during treatment the patients adhered to a defined hypolipidaemic diet. The total cholesterol level during administration increased from 7.71 +/- 1.71 mmol/l to 8.23 +/- 1.34 mmol/l (p = 0.05). The LDL cholesterol level rose from 4.93 +/- 1.70 mmol/l to 5.53 +/- 1.34 mmol/l (n.s.). Apolipoprotein B declined from 1.99 +/- 0.39 g/l to 1.80 +/- 0.30 g/l (n.s.). HDL cholesterol rose from 1.09 +/- 0.32 mmol/l to 1.53 +/- 0.56 mmol/l (p = 0.01). The triglyceride level declined from 5.71 +/- 5.60 mmol/1 to 3.72 +/- 4.32 mmol/1 (n.s.). The lipid metabolism parameters were evaluated already after three months of Duolip treatment but the values did not differ significantly from values assessed after 6 months of administration; therefore only the final values are given. In the course of six months of Duolip administration the body weight of the patients did not change and no serious side-effects were observed which would call for discontinuation of treatment. Duolip forte is evaluated as a safe, but as compared with other available drugs of the clofibrate series, less effective hypolipidaemic agent.

摘要

奥地利默克公司生产的多利平酯(益多酯,500毫克片剂),以每日500毫克的剂量给予20名不同类型高脂蛋白血症患者,为期6个月。在治疗开始前及治疗期间,患者遵循特定的降血脂饮食。给药期间,总胆固醇水平从7.71±1.71毫摩尔/升升至8.23±1.34毫摩尔/升(p = 0.05)。低密度脂蛋白胆固醇水平从4.93±1.70毫摩尔/升升至5.53±1.34毫摩尔/升(无统计学意义)。载脂蛋白B从1.99±0.39克/升降至1.80±0.30克/升(无统计学意义)。高密度脂蛋白胆固醇从1.09±0.32毫摩尔/升升至1.53±0.56毫摩尔/升(p = 0.01)。甘油三酯水平从5.71±5.60毫摩尔/升降至3.72±4.32毫摩尔/升(无统计学意义)。在多利平治疗三个月后就对脂质代谢参数进行了评估,但这些值与给药6个月后评估的值没有显著差异;因此只给出了最终值。在多利平给药的六个月期间,患者体重没有变化,也未观察到需要停药的严重副作用。多利平酯被评估为一种安全的降血脂药物,但与氯贝丁酯系列的其他现有药物相比,效果较差。

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