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奈多罗米钠及奈多罗米钠/沙丁胺醇组合的依从性。依从性工作组。

Compliance with nedocromil sodium and a nedocromil sodium/salbutamol combination. Compliance Working Group.

作者信息

Braunstein G L, Trinquet G, Harper A E

机构信息

Laboratoires Fisons S.A., Tour PFA, Paris la Défense, France.

出版信息

Eur Respir J. 1996 May;9(5):893-8. doi: 10.1183/09031936.96.09050893.

Abstract

Nonadherence to prescribed preventive medication is common in asthma. We wanted to assess whether the combination of a beta 2-bronchodilator with an anti-inflammatory treatment in the same metered-dose inhaler (MDI) with a regular dosing schedule might improve compliance. A double-blind study was used to compare use (two actuations four times daily for 12 weeks) of 2 mg nedocromil sodium (n = 101) with a combination of 2 mg nedocromil sodium and 100 micrograms salbutamol (n = 100) in mild-to-moderate asthma patients (mean age 42 +/- 14 yrs; 98 males and 103 females). Compliance was measured using the electronic Nebulizer Chronolog (NC) device, change in MDI canister weight, patient questionnaire and physician assessment. The mean +/- SD number of actuations per day for nedocromil sodium and the combination during the primary period of assessment (Weeks 11-12) was 4.2 +/- 2.6 and 4.6 +/- 2.5 (NC), 5.3 +/- 2.1 and 5.3 +/- 2.0 (canister weight), and 7.5 +/- 1.3 and 7.4 +/- 1.3 (questionnaire), respectively. Physician assessment rated compliance as "good" to "excellent". The first and final days of the period were not used in the NC analysis to exclude part-days of treatment and drug-dumping (repeated actuations without inhalation), and may account for the difference between NC and canister weight results. The mean number of two-actuation doses per day determined from the NC was 2.1 +/- 1.3 for nedocromil sodium and 2.4 +/- 2.1 for the combination. Thirty five percent (nedocromil sodium) and 34% (combination) of the patients were compliant (6-10 actuations per day for > or = 60% of the days). We conclude that compliance is poor in asthma, electronic recording revealed the dumping phenomenon and, in this study, the combination of an inhaled beta 2-bronchodilator with a preventive treatment did not improve compliance over a three month period in patients with mild-to-moderate asthma.

摘要

在哮喘患者中,不遵医嘱使用预防性药物的情况很常见。我们想评估在同一定量吸入器(MDI)中,将β2-支气管扩张剂与抗炎治疗药物按常规给药方案联合使用是否能提高依从性。采用双盲研究比较了2毫克奈多罗米钠(n = 101)与2毫克奈多罗米钠和100微克沙丁胺醇联合用药(n = 100)在轻至中度哮喘患者(平均年龄42±14岁;男性98例,女性103例)中的使用情况(每天4次,每次按压2下,持续12周)。使用电子雾化器计时仪(NC)、MDI药罐重量变化、患者问卷和医生评估来衡量依从性。在评估的主要阶段(第11 - 12周),奈多罗米钠组和联合用药组每天平均±标准差的按压次数分别为:通过NC测量为4.2±2.6和4.6±2.5,通过药罐重量测量为5.3±2.1和5.3±2.0,通过问卷测量为7.5±1.3和7.4±1.3。医生评估将依从性评为“良好”至“优秀”。NC分析未使用该阶段的第一天和最后一天的数据,以排除部分天数的治疗和药物倾倒情况(重复按压但未吸入),这可能是NC与药罐重量结果存在差异的原因。根据NC测定,奈多罗米钠组每天两次按压剂量的平均数为2.1±1.3,联合用药组为2.4±2.1。35%(奈多罗米钠组)和34%(联合用药组)的患者依从性良好(≥60%的天数每天按压6 - 10次)。我们得出结论,哮喘患者的依从性较差,电子记录显示存在药物倾倒现象,并且在本研究中,对于轻至中度哮喘患者,吸入性β2-支气管扩张剂与预防性治疗联合使用在三个月内并未提高依从性。

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