Department of Medicine, Mayo Clinic, Phoenix, AZ.
Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, MN; Department of Health Sciences Research, Division of Health Care Policy and Research, Mayo Clinic, Rochester, MN.
Chest. 2021 Mar;159(3):924-932. doi: 10.1016/j.chest.2020.10.050. Epub 2020 Oct 24.
Little is known about adherence to asthma biologics.
Is adherence to inhaled corticosteroid (ICS) associated with subsequent asthma biologic adherence?
We analyzed individuals with asthma who started asthma biologics in the OptumLab Data Warehouse and used that data until October 2019. We calculated proportion days covered (PDC) for ICS ± long-acting β-agonists in the 6 months before and after asthma biologics were started and asthma biologic PDC for the first 6 months of use. We performed a multivariable analysis to identify factors associated with asthma biologic PDC ≥0.75, ICS PDC ≥0.75 during the 6-month period after asthma biologic were started, and achievement of a ≥50% reduction in asthma exacerbations during the first 6 months of asthma biologic use.
We identified 5,319 people who started asthma biologics. The mean PDC for asthma biologics was 0.76 (95% CI, 0.75-0.77) in the first 6 months after starting, higher than the mean PDCs for ICS in the 6 months before (0.44 [95% CI, 0.43-0.45]) and after (0.40 [95% CI, 0.39-0.40]) starting the asthma biologic. PDC ≥0.75 for ICS 6 months before index biologic use is associated with PDC for asthma biologics ≥0.75 (OR, 1.25; 95% CI, 1.10-1.43) and for ICS during the first 6 months of biologic use (OR, 9.93; 95% CI, 8.55-11.53). Neither ICS PDC ≥0.75 (OR, 0.92; 95% CI, 0.74-1.14) nor asthma biologic PDC ≥0.75 (OR, 1.15; 95% CI, 0.97-1.36) is associated with a statistically significant reduction in asthma exacerbations during the first 6 months of asthma biologic use among people with any exacerbation in the 6 months before first use.
Adherence to asthma biologic is higher than to ICS and is associated with different factors.
关于哮喘生物制剂的依从性知之甚少。
吸入皮质类固醇(ICS)的依从性是否与随后的哮喘生物制剂依从性相关?
我们分析了在 OptumLab 数据仓库中开始使用哮喘生物制剂的哮喘患者,并在 2019 年 10 月之前使用该数据。我们计算了在开始使用哮喘生物制剂前 6 个月内 ICS±长效β激动剂的比例天数覆盖(PDC)和使用哮喘生物制剂的前 6 个月内哮喘生物制剂的 PDC。我们进行了多变量分析,以确定与哮喘生物制剂 PDC≥0.75、开始使用哮喘生物制剂后 6 个月内 ICS PDC≥0.75 以及在使用哮喘生物制剂的前 6 个月内哮喘加重减少≥50%相关的因素。
我们确定了 5319 名开始使用哮喘生物制剂的患者。开始使用后第 1 至 6 个月,哮喘生物制剂的平均 PDC 为 0.76(95%CI,0.75-0.77),高于开始使用前 6 个月 ICS 的平均 PDC(0.44 [95%CI,0.43-0.45])和开始使用后(0.40 [95%CI,0.39-0.40])。开始索引生物制剂前 6 个月 ICS PDC≥0.75 与哮喘生物制剂 PDC≥0.75(OR,1.25;95%CI,1.10-1.43)和生物制剂使用的前 6 个月期间的 ICS PDC 相关(OR,9.93;95%CI,8.55-11.53)。ICS PDC≥0.75(OR,0.92;95%CI,0.74-1.14)和哮喘生物制剂 PDC≥0.75(OR,1.15;95%CI,0.97-1.36)均与开始使用哮喘生物制剂前 6 个月内哮喘加重减少无统计学意义相关在首次使用前 6 个月内有任何加重的人群中。
对哮喘生物制剂的依从性高于对 ICS 的依从性,且与不同因素相关。