Centre of Academic Primary Care, University of Aberdeen, Foresterhill Health Centre, Aberdeen, UK.
BMC Pulm Med. 2010 Jan 5;10:1. doi: 10.1186/1471-2466-10-1.
Poor adherence with prescribed asthma medication is a major barrier to positive treatment outcomes. This study was designed to determine the effect of a once-daily administration of mometasone furoate administered via a dry powder inhaler (MF-DPI) on treatment adherence compared with a twice-daily administration.
This was a 12-week open-label study designed to mimic an actual clinical setting in patients >or=12 years old with mild-to-moderate persistent asthma. Patients were randomized to receive MF-DPI 400 microg once-daily in the evening or MF-DPI 200 microg twice-daily. Adherence was assessed primarily using the number of actual administered doses reported from the device counter divided by the number of scheduled doses. Self-reports were also used to determine adherence. Health-related quality of life, healthcare resource utilization, and days missed from work or school were also reported.
1233 patients were randomized. The mean adherence rates, as measured by the automatic dose counter, were significantly better (P < 0.001) with MF-DPI 400 microg once-daily in the evening (93.3%) than with MF-DPI 200 microg twice-daily (89.5%). Mean adherence rates based on self-reports were also significantly better (P < 0.001) with MF-DPI 400 microg QD PM (97.2%) than with MF-DPI 200 microg twice-daily (95.3%). Adherence rates were lower in adolescents (12-17 years old). Health-related quality of life improved by 20% in patients using MF-DPI once-daily in the evening and by 14% in patients using MF-DPI twice-daily. Very few (<8%) patients missed work/school.
Mean adherence rates were greater with a once-daily dosing regimen of MF-DPI than with a twice-daily dosing regimen.This trial was completed prior to the ISMJE requirements for trial registration.
未遵医嘱使用规定剂量的哮喘药物是积极治疗结果的主要障碍。本研究旨在确定每日一次使用糠酸莫米松干粉吸入剂(MF-DPI)与每日两次相比对治疗依从性的影响。
这是一项为期 12 周的开放性标签研究,旨在模仿 12 岁以上轻至中度持续性哮喘患者的实际临床环境。患者被随机分为每日一次接受 MF-DPI 400μg (晚上)或 MF-DPI 200μg 每日两次。依从性主要通过设备计数器报告的实际给药次数除以计划剂量次数来评估。也使用自我报告来确定依从性。还报告了健康相关生活质量、医疗资源利用和旷工/缺课天数。
1233 名患者被随机分组。使用自动剂量计数器测量的平均依从率,每日一次接受 MF-DPI 400μg (晚上)显著更好(P < 0.001)(93.3%),而每日两次接受 MF-DPI 200μg (89.5%)。基于自我报告的平均依从率也显著更好(P < 0.001),每日一次接受 MF-DPI 400μg (晚上)(97.2%)显著优于每日两次接受 MF-DPI 200μg (95.3%)。青少年(12-17 岁)的依从率较低。使用 MF-DPI 每日一次的患者健康相关生活质量提高了 20%,而使用 MF-DPI 每日两次的患者提高了 14%。很少有(<8%)患者旷工/缺课。
与每日两次给药方案相比,MF-DPI 每日一次给药方案的平均依从率更高。本试验是在 ISMJE 对试验注册的要求之前完成的。