首页> 外文期刊>Respiration: International Review of Thoracic Diseases >A new beclomethasone dipropionate multidose powder inhaler in the treatment of bronchial asthma.
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A new beclomethasone dipropionate multidose powder inhaler in the treatment of bronchial asthma.

机译:一种新的倍氯米松双丙酸酯多剂量粉末吸入器,用于治疗支气管哮喘。

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摘要

The clinical efficacy, tolerability and acceptability of a new multidose powder inhaler (MDPI) containing beclomethasone dipropionate (BDP) were compared with those of a BDP aerosol administered with a large volume spacer (MDI-spacer) among adult asthmatics currently receiving from 500 to 1,000 microgram/day of an inhaled corticosteroid. During the study, the dosage of BDP from both devices was 400 microgram twice daily. Ninety-one patients were randomized to the MDPI group and 42 to the MDI-spacer group. The trial was performed as an open, randomized, parallel group multicenter study. The duration of the treatment period was 12 weeks, and the study was preceded by a 2-week run-in period. During the run-in period, the mean morning peak expiratory flow (PEF) was 487 and 466 1/min in the MDPI and MDI-spacer groups, respectively. After the 12-week treatment, the morning PEF was 491 1/min in the MDPI group and 463 1/min in the MDI-spacer group. The evening values were 500 and 479 1/min during the run-in period and 496 and 476 1/min after the 12-week treatment, respectively. Asthma symptom scores and the use of rescue medication were low in both groups, indicating good efficacy of the preparations tested. The median dose of histamine required to decrease forced expiratory volume in 1 s by 15% increased during the study from 800 to 1,098 microgram in the MDPI group and from 795 to 960 microgram in the MDI-spacer group. The most frequent adverse events in both groups were hoarseness and sore throat. There were no statistically significant differences between the treatment groups in serum cortisol values or in the number of patients with thrush. Seventy-two percent of the patients regarded the MDPI easier to use while 95% considered it more portable. Over 80% of the patients felt that the MDPI was also easier to clean and as easy or easier to learn to use than the MDI-spacer. To conclude, the novel powder inhaler is well tolerated and at least equally effective as the conventional MDI-spacer combination in the treatment of asthma with BDP. However, in everyday use, patients clearly favored the powder inhaler.
机译:在目前接受500至1,000例成年哮喘的成年哮喘患者中,比较了一种含有倍氯米松二丙酸酯(BDP)的新型多剂量粉末吸入器(MDPI)的临床疗效,耐受性和可接受性,并与采用大剂量间隔物(MDI-spacer)的BDP气雾剂进行了比较。微克/天吸入皮质类固醇。在研究期间,两种设备的BDP剂量均为每天两次400微克。将91例患者随机分为MDPI组和42例MDI垫片组。该试验以开放,随机,平行组多中心研究的形式进行。治疗期为12周,在研究之前进行了2周的磨合期。在磨合期间,MDPI和MDI垫片组的平均早晨峰值呼气流量(PEF)分别为487和466 1 / min。经过12周的治疗后,MDPI组的早晨PEF为491 1 / min,MDI垫片组的早晨PEF为463 1 / min。在磨合期间,夜间值分别为500和479 1 / min,在12周治疗后,分别为496和476 1 / min。两组的哮喘症状评分和急救药物使用率均较低,表明所测制剂的疗效良好。在研究中,组胺的中位数剂量在1 s内降低15%所需的呼气量,在MDPI组中从800微克增加到1,098微克,在MDI垫片组中从795微克增加到960微克。两组中最常见的不良事件是声音嘶哑和喉咙痛。在治疗组之间,血清皮质醇值或鹅口疮患者的数量均无统计学差异。 72%的患者认为MDPI更易于使用,而95%的患者认为MDPI更易携带。超过80%的患者认为MDPI较MDI垫片更易于清洁,易于使用。综上所述,新型粉末吸入器在BDP哮喘治疗中具有良好的耐受性,并且至少与常规MDI-间隔剂组合等效。但是,在日常使用中,患者显然偏爱粉末吸入器。

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