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盐酸匹卡司特长期用于常年性支气管哮喘患者的可接受性、安全性及有效性。

Acceptability, safety and efficacy of picumast dihydrochloride on long-term use in patients with perennial bronchial asthma.

作者信息

Boerner D, Metz K, Eberhardt R

机构信息

Department of Product Development, Boehringer Mannheim GmbH, Fed Rep. of Germany.

出版信息

Arzneimittelforschung. 1989 Oct;39(10A):1372-4.

PMID:2576367
Abstract

104 adult patients with predominantly extrinsic perennial asthma who were maintained on bronchodilator or glucocorticoid therapy, were entered into a one-year open study designed to evaluate the efficacy, safety and acceptability of picumast dihydrochloride (3,4-dimethyl-7-[4-(4-chlorobenzyl)piperazine-1-yl]propoxycoumarin dihydrochloride) (2 mg twice daily). 74 patients completed the 12-month treatment period and a further 18 (total 92) were followed up for at least 2 months. Adverse drug reactions were reported in 14 patients and 5 of them were withdrawn from the trial for only non serious reactions. 12 patients were excluded from the analysis of efficacy because they dropped out early and no sufficient data were available for a judgement. Although this was an open study, analysis of diary card measurements and clinical assessments indicate that picumast dihydrochloride could represent a new and effective prophylactic therapy in the long-term management of bronchial asthma. Picumast dihydrochloride improved forced expiratory volume in 1 s (FEV1), peak flow and subjective asthmatic symptoms in 51%, 64% and 70% of the patients, respectively. 92% of those who participated in this study were willing to take the study drug again.

摘要

104例主要患有外源性常年性哮喘且维持使用支气管扩张剂或糖皮质激素治疗的成年患者,进入了一项为期一年的开放性研究,该研究旨在评估盐酸匹卡司特(3,4 - 二甲基 - 7 - [4 - (4 - 氯苄基)哌嗪 - 1 - 基]丙氧基香豆素二盐酸盐)(每日两次,每次2毫克)的疗效、安全性和可接受性。74例患者完成了12个月的治疗期,另有18例(共92例)至少随访了2个月。14例患者报告了药物不良反应,其中5例因仅出现非严重反应而退出试验。12例患者因提前退出且没有足够数据进行判断而被排除在疗效分析之外。尽管这是一项开放性研究,但对日记卡测量值和临床评估的分析表明,盐酸匹卡司特在支气管哮喘的长期管理中可能代表一种新的有效预防性治疗方法。盐酸匹卡司特分别使51%、64%和70%的患者一秒用力呼气量(FEV1)、峰值流速和主观哮喘症状得到改善。参与本研究的患者中有92%愿意再次服用研究药物。

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