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吸入用糠酸莫米松:用于成人和青少年持续性哮喘的应用综述

Inhaled mometasone furoate: a review of its use in adults and adolescents with persistent asthma.

作者信息

Sharpe M, Jarvis B

机构信息

Adis International Limited, Mairangi Bay, Auckland, New Zealand.

出版信息

Drugs. 2001;61(9):1325-50. doi: 10.2165/00003495-200161090-00011.

Abstract

UNLABELLED

Mometasone furoate is a corticosteroid with relatively high in vitro potency. Recent randomised, double-blind, multicentre trials have assessed the efficacy of mometasone furoate delivered by dry powder inhaler over 12 weeks in adults and adolescents with mild to severe persistent asthma. Mometasone furoate 200 microg twice daily or 400 microg once daily in the morning or 200 microg once daily in the evening improved lung function, asthma symptom scores and use of rescue medication to a significantly greater extent than placebo in patients who had previously received only short-acting inhaled beta2-adrenoceptor agonists alone as treatment in 3 trials (n = 195 to 306). In studies in 227 to 733 patients with mild to moderate asthma who were receiving ongoing treatment with inhaled corticosteroids prior to enrolment, mometasone furoate 100 to 400 microg twice daily was consistently better at improving the above indicators of asthma than placebo. Mometasone furoate 100 to 200 microg twice daily was as effective as beclomethasone dipropionate 200 microg twice daily or budesonide 400 microg twice daily and mometasone furoate 200 microg twice daily was as effective as fluticasone propionate 250 microg twice daily. Mometasone furoate 400 or 800 microg twice daily was also consistently more effective than placebo in reducing oral corticosteroid dosages and improving lung function and asthma symptoms in 132 patients with oral corticosteroid-dependent asthma. Once daily administration of mometasone furoate 400 microg appears to be as effective at improving indicators of asthma as twice daily administration of 200 microg. Patients receiving mometasone furoate < or =800 microg/day and recipients of placebo experienced a similar overall incidence of adverse events considered to be related to treatment. The most common of these events were oral candidiasis, headache, pharyngitis and dysphonia. Mometasone furoate 100 to 400 microg twice daily, beclomethasone dipropionate 200 microg twice daily, budesonide 400 microg twice daily or fluticasone propionate 250 microg twice daily were similarly tolerated.

CONCLUSION

Inhaled mometasone furoate is well tolerated, with minimal systemic activity and is equally effective when administered as a divided dose or as a single daily dose. Use of the drug can result in a decrease in requirements for oral corticosteroids in patients with oral corticosteroid-dependent asthma and is as effective as other inhaled corticosteroids currently used in the treatment of mild to moderate persistent asthma. Thus mometasone furoate is suitable for the control of mild to severe persistent asthma in adults or adolescents.

摘要

未标注

糠酸莫米松是一种体外效力相对较高的皮质类固醇。最近的随机、双盲、多中心试验评估了干粉吸入器递送的糠酸莫米松在12周内对轻至重度持续性哮喘成人和青少年的疗效。在3项试验(n = 195至306)中,对于之前仅接受短效吸入β2肾上腺素能激动剂作为治疗的患者,每天两次200微克或每天一次400微克早晨给药或每天一次200微克晚上给药的糠酸莫米松在改善肺功能、哮喘症状评分和急救药物使用方面比安慰剂有显著更大程度的改善。在对227至733名轻度至中度哮喘患者进行的研究中,这些患者在入组前正在接受吸入性皮质类固醇的持续治疗,每天两次100至400微克的糠酸莫米松在改善上述哮喘指标方面始终比安慰剂更好。每天两次100至200微克的糠酸莫米松与每天两次200微克的二丙酸倍氯米松或每天两次400微克的布地奈德效果相同,每天两次200微克的糠酸莫米松与每天两次250微克的丙酸氟替卡松效果相同。在132名依赖口服皮质类固醇的哮喘患者中,每天两次400微克或800微克的糠酸莫米松在减少口服皮质类固醇剂量、改善肺功能和哮喘症状方面也始终比安慰剂更有效。每天一次400微克的糠酸莫米松给药在改善哮喘指标方面似乎与每天两次200微克给药效果相同。接受每天≤800微克糠酸莫米松的患者和接受安慰剂的患者经历的被认为与治疗相关的不良事件总体发生率相似。这些事件中最常见的是口腔念珠菌病、头痛、咽炎和发音困难。每天两次100至400微克的糠酸莫米松、每天两次200微克的二丙酸倍氯米松、每天两次400微克的布地奈德或每天两次250微克的丙酸氟替卡松耐受性相似。

结论

吸入性糠酸莫米松耐受性良好,全身活性最小,分剂量给药或每日单次给药效果相同。使用该药物可使依赖口服皮质类固醇的哮喘患者对口服皮质类固醇的需求减少,并且与目前用于治疗轻至中度持续性哮喘的其他吸入性皮质类固醇效果相同。因此,糠酸莫米松适用于控制成人或青少年的轻至重度持续性哮喘。

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