Friedman Howard S, Navaratnam Prakash, McLaughlin John
Analytic Solutions, LLC, New York, NY 10012, USA.
J Asthma. 2010 Nov;47(9):994-1000. doi: 10.1080/02770903.2010.513076.
Because adherence to asthma controller medication among adolescents and young adults is poor but critical for asthma control, strategies are needed to improve adherence. One strategy is to reduce the number of daily doses necessary to maintain adequate control. Mometasone furoate delivered through a dry powder inhaler (MF-DPI) is an inhaled corticosteroid (ICS) approved for once-daily dosing in most patients. Fluticasone propionate (FP) is an ICS approved for twice-daily dosing. A retrospective claims analysis was performed to assess treatment adherence and markers of asthma control in adolescent and young adult patients with mild asthma who began treatment with MF-DPI or FP.
Data from approximately 37 million patients in an administrative insurance claims database in the United States were analyzed. Patients, 12-25 years, with mild asthma and previous asthma medication use were assigned an index date based on their first prescription fill of MF-DPI or FP between 1 January 2005 and 10 October 2008. Demographics, prescription claims, and health care utilization data were captured in the 365-day period before (preindex) and after (postindex) the index date. Patients from each cohort were propensity score-matched 1:1 based on preindex data. Adherence was measured by prescription fills and percentage of days covered (PDC); asthma control was measured by exacerbations and short-acting β₂-agonist (SABA) canister claims. Bivariate and multivariate generalized linear model (GLM) analyses were conducted to determine differences in outcomes between the cohorts.
After matching, 692 patients per group (average age - 16 years) were analyzed. Adherence in the postindex period was significantly higher in the MF-DPI cohort compared with the FP cohort as measured by PDC (23.5% vs. 14.5%; p< .0001) and prescription fills (2.70 vs. 1.91; p< .0001). The mean number of postindex SABA canister claims was significantly lower in the MF-DPI cohort compared with the FP cohort (1.04 vs. 1.40; p< .0001). There was no significant difference in the mean number of postindex exacerbations between the cohorts.
Adolescent/young adult patients with mild asthma who received MF-DPI had better postindex adherence and fewer SABA canister claims than patients receiving FP.
由于青少年和年轻成年人对哮喘控制药物的依从性较差,但这对哮喘控制至关重要,因此需要采取策略来提高依从性。一种策略是减少维持充分控制所需的每日剂量数。通过干粉吸入器递送的糠酸莫米松(MF-DPI)是一种吸入性糖皮质激素(ICS),大多数患者批准每日给药一次。丙酸氟替卡松(FP)是一种批准每日给药两次的ICS。进行了一项回顾性索赔分析,以评估开始使用MF-DPI或FP治疗的轻度哮喘青少年和年轻成年患者的治疗依从性和哮喘控制指标。
分析了美国一个行政保险索赔数据库中约3700万患者的数据。年龄在12-25岁、患有轻度哮喘且之前使用过哮喘药物的患者,根据其在2005年1月1日至2008年10月10日期间首次开具MF-DPI或FP处方的时间确定索引日期。在索引日期之前(索引前)和之后(索引后)的365天内收集人口统计学、处方索赔和医疗保健利用数据。根据索引前数据,对每个队列的患者进行1:1倾向得分匹配。通过处方配药和覆盖天数百分比(PDC)来衡量依从性;通过加重发作次数和短效β₂激动剂(SABA)吸入器索赔来衡量哮喘控制情况。进行双变量和多变量广义线性模型(GLM)分析以确定队列之间结果的差异。
匹配后,每组分析692名患者(平均年龄16岁)。通过PDC(23.5%对14.5%;p<0.0001)和处方配药(2.70对1.91;p<0.0001)衡量,MF-DPI队列在索引后时期的依从性显著高于FP队列。与FP队列相比,MF-DPI队列索引后SABA吸入器索赔的平均数显著更低(1.04对1.40;p<0.0001)。队列之间索引后加重发作的平均数没有显著差异。
与接受FP的患者相比,接受MF-DPI的轻度哮喘青少年/年轻成年患者在索引后具有更好的依从性且SABA吸入器索赔更少。