a Formerly Global Health Economics and Outcomes Research Analytics , AbbVie, Inc. , North Chicago , IL , USA.
b Division of Endocrinology, Diabetes & Metabolism , The Ohio State University Wexner Medical Center , Columbus , OH , USA.
Curr Med Res Opin. 2018 Sep;34(9):1673-1678. doi: 10.1080/03007995.2018.1486293. Epub 2018 Jun 25.
The objective of this analysis was to compare adherence at 6 months and 12 months across levothyroxine formulations for patients with hypothyroidism.
This retrospective analysis utilized insurance claims data from a commercially insured population from January 1, 2000 through March 31, 2016. Patients were included if they were diagnosed with hypothyroidism and initiated treatment with generic levothyroxine, Levoxyl, Synthroid, Unithroid, or Tirosint. Patients were excluded if they were younger than age 18, were diagnosed with thyroid cancer, received a prescription for liothyronine, or did not have continuous insurance coverage over the study period. Adherence, defined by the proportion of days covered (PDC) ≥ 80%, was examined using multivariable analyses for both 6 and 12 months post-initiation on therapy Results: The study identified 580,331 patients who fit the study criteria. At 6 months, 40.3% of patients were found to be non-adherent, while 51.9% were non-adherent at 12 months. Synthroid was associated with significantly higher adherence compared to all other levothyroxine formulations at both 6 and 12 months. Compared to generic levothyroxine, the likelihood of being adherent at 12 months was highest for Synthroid (OR = 1.44; 95% CI = 1.43-1.46), followed by Levoxyl (OR = 1.20 95% CI = 1.17-1.23). Tirosint and Unithroid were associated with significantly lower adherence at 12 months compared to generic levothyroxine (OR = 0.65; 95% CI = 0.57-0.75 and OR = 0.79; 95% CI = 0.71-0.89, respectively).
This large, retrospective real-world study demonstrated that adherence to levothyroxine remains a concern among patients with hypothyroidism, and that differences in adherence may exist across levothyroxine formulations.
本分析旨在比较甲状腺功能减退症患者使用左甲状腺素的不同制剂在 6 个月和 12 个月时的依从性。
本回顾性分析利用了 2000 年 1 月 1 日至 2016 年 3 月 31 日商业保险人群的保险索赔数据。如果患者被诊断患有甲状腺功能减退症且开始接受左甲状腺素通用制剂、Levoxyl、Synthroid、Unithroid 或 Tirosint 治疗,则将其纳入研究。如果患者年龄小于 18 岁、被诊断为甲状腺癌、接受左三碘甲状腺氨酸处方或在研究期间没有连续的保险覆盖,则将其排除在外。使用多变量分析检查治疗开始后 6 个月和 12 个月时的依从性,定义为比例天数覆盖(PDC)≥80%。
研究确定了 580331 名符合研究标准的患者。在 6 个月时,发现 40.3%的患者不符合依从性标准,而在 12 个月时,51.9%的患者不符合依从性标准。与所有其他左甲状腺素制剂相比,Synthroid 在 6 个月和 12 个月时均与更高的依从性相关。与通用左甲状腺素相比,Synthroid 在 12 个月时的依从性最高(OR=1.44;95%CI=1.43-1.46),其次是 Levoxyl(OR=1.20;95%CI=1.17-1.23)。与通用左甲状腺素相比,Tirosint 和 Unithroid 在 12 个月时的依从性显著较低(OR=0.65;95%CI=0.57-0.75 和 OR=0.79;95%CI=0.71-0.89)。
这项大型回顾性真实世界研究表明,甲状腺功能减退症患者的左甲状腺素依从性仍然是一个问题,并且不同左甲状腺素制剂之间可能存在依从性差异。