Chung K F, Naya I
National Heart and Lung Institute, Imperial College School of Medicine & Royal Brompton & Harefield Hospital, London, UK.
Respir Med. 2000 Sep;94(9):852-8. doi: 10.1053/rmed.2000.0813.
Compliance with prescribed asthma medication is commonly estimated from tablet counts for oral medications and canister weights for inhaled medications. Recently, electronic medication monitoring devices, developed to evaluate numerical compliance as well as drug use patterns, were used to assess compliance with inhaled steroids and beta2-agonists. This was the first study to electronically assess compliance with an oral asthma medication. Fifty-seven asthmatic patients, stable on inhaled beta2-agonists only with a mean FEV1 of 77% predicted (+/- 13%, SD) began 12 weeks of treatment with zafirlukast 20 mg twice daily. The monitoring device, an electronic TrackCap, recorded the date and time on each occasion that patients removed and replaced their medication bottle caps. Patients were told that compliance would be assessed as part of the study, but patients were not told about the specifics of the TrackCap. Compliance was defined: 1. as the number of TrackCap events per number of prescribed tablets; and 2. as the difference between number of tablets dispensed and number returned per number prescribed. Adherence was defined as the number of days with two TrackCap events at least 8 h apart per the total number of days' dosing. Forty-seven patients completed the study with a median compliance of 89% (mean. 80%) and a median adherence of 71% (mean, 64%) as measured by TrackCap events. Compliance as estimated from return-tablet count was slightly higher (median, 92%). High rates of compliance were maintained throughout the trial. These results show that compliance with and adherence to a treatment of an oral, twice-daily, maintenance asthma medication, such as zafirlukast, is high.
通常根据口服药物的药片计数和吸入药物的药罐重量来估算哮喘患者对规定药物的依从性。最近,为评估数值依从性以及药物使用模式而开发的电子药物监测设备被用于评估吸入性类固醇和β2激动剂的依从性。这是第一项以电子方式评估口服哮喘药物依从性的研究。57名仅使用吸入性β2激动剂病情稳定的哮喘患者,其平均第一秒用力呼气容积(FEV1)为预测值的77%(±13%,标准差),开始接受为期12周的扎鲁司特治疗,每日两次,每次20毫克。监测设备为电子追踪帽,记录患者每次取下和更换药瓶盖的日期和时间。患者被告知依从性将作为研究的一部分进行评估,但未被告知追踪帽的具体情况。依从性定义为:1. 追踪帽事件数与规定药片数之比;2. 配药片数与按规定应归还片数之差与规定片数之比。坚持性定义为两次追踪帽事件间隔至少8小时的天数与总给药天数之比。47名患者完成了研究,通过追踪帽事件测量,依从性中位数为89%(平均值80%),坚持性中位数为71%(平均值64%)。根据归还药片计数估算的依从性略高(中位数92%)。在整个试验过程中依从率都很高。这些结果表明,对于口服、每日两次的维持性哮喘药物如扎鲁司特的治疗,其依从性和坚持性都很高。