Department of Pharmacy Systems Outcomes and Policy, School of Pharmacy, University of Illinois Chicago, 833 S Wood St, Chicago, IL 60612. Email:
Am J Manag Care. 2024 Aug 1;30(8):e226-e232. doi: 10.37765/ajmc.2024.89591.
Adherence to medications is important for the management of chronic diseases. Although the proportion of days covered (PDC) is a common metric for measuring adherence, it may be insufficient to distinguish relevant differences in medication-taking behavior. Group-based trajectory models (GBTMs) have been used to better represent adherence over time. This study aims to examine adherence patterns 1 year after initiation among users of sodium-glucose cotransporter 2 (SGLT2) inhibitors using GBTMs and evaluate the ability of baseline characteristics to predict adherence trajectory.
SGLT2 inhibitor new-user cohort study from 2014 to 2018.
We calculated 12-month PDC and categorized patients with PDC of 80% or greater as adherent. We performed multivariable logistic regression on adherence status controlling for baseline covariates. GBTMs were fit to identify adherence patterns 12 months following SGLT2 inhibitor initiation. Five multinomial logistic regression models including different subsets of predictors were used to predict adherence trajectory group assignment.
In a cohort of 228,363 SGLT2 inhibitor users, the mean PDC was 57%, with 36% of the cohort being adherent. Overall, women and patients with anxiety or depression were less likely to be adherent. Six patterns of SGLT2 inhibitor adherence were identified with GBTMs: 1 fill (PDC = 0.08), early discontinuation (PDC = 0.22), consistently low adherence (PDC = 0.35), moderate adherence (PDC = 0.48), high adherence (PDC = 0.79), and near-perfect adherence (PDC = 0.95). All prediction models showed poor predictive accuracy (0.35).
We found wide variation in adherence patterns among SGLT2 inhibitor users in a national cohort. Predictors from a health care claims database were unable to accurately predict adherence trajectory.
药物依从性对于慢性病的管理非常重要。尽管比例天数覆盖(PDC)是衡量依从性的常用指标,但它可能不足以区分药物使用行为的相关差异。基于群组的轨迹模型(GBTM)已被用于更好地表示随时间的依从性。本研究旨在使用 GBTM 检查 SGLT2 抑制剂使用者在起始治疗后 1 年的依从模式,并评估基线特征预测依从轨迹的能力。
2014 年至 2018 年 SGLT2 抑制剂新使用者队列研究。
我们计算了 12 个月的 PDC,并将 PDC 达到 80%或更高的患者归类为依从者。我们通过多变量逻辑回归控制基线协变量来对依从状态进行分析。使用 GBTM 来确定 SGLT2 抑制剂起始后 12 个月的依从模式。使用 5 个包含不同预测变量子集的多项逻辑回归模型来预测依从轨迹组分配。
在 228363 例 SGLT2 抑制剂使用者的队列中,平均 PDC 为 57%,其中 36%的患者依从性较好。总体而言,女性和患有焦虑或抑郁的患者不太可能依从。通过 GBTM 确定了 SGLT2 抑制剂依从的 6 种模式:1 次填充(PDC=0.08)、早期停药(PDC=0.22)、持续低依从(PDC=0.35)、中度依从(PDC=0.48)、高依从(PDC=0.79)和近乎完美依从(PDC=0.95)。所有预测模型的预测准确性都较差(0.35)。
我们在一个全国性队列中发现 SGLT2 抑制剂使用者的依从模式存在广泛差异。来自医疗保健索赔数据库的预测因子无法准确预测依从轨迹。