Colantonio Lisandro D, Kent Shia T, Huang Lei, Chen Ligong, Monda Keri L, Serban Maria-Corina, Manthripragada Angelika, Kilgore Meredith L, Rosenson Robert S, Muntner Paul
Department of Epidemiology, University of Alabama at Birmingham, 1700 University Boulevard, LHL 450, Birmingham, AL, 35294, USA.
Center for Observational Research, Amgen, Inc, Thousand Oaks, CA, USA.
Cardiovasc Drugs Ther. 2016 Oct;30(5):525-533. doi: 10.1007/s10557-016-6680-3.
To compare characteristics of patients with possible statin intolerance identified using different claims-based algorithms versus patients with high adherence to statins.
We analyzed 134,863 Medicare beneficiaries initiating statins between 2007 and 2011. Statin intolerance and discontinuation, and high adherence to statins, defined by proportion of days covered ≥80 %, were assessed during the 365 days following statin initiation. Definition 1 of statin intolerance included statin down-titration or discontinuation with ezetimibe initiation, having a claim for a rhabdomyolysis or antihyperlipidemic event followed by statin down-titration or discontinuation, or switching between ≥3 types of statins. Definition 2 included beneficiaries who met Definition 1 and those who down-titrated statin intensity. We also analyzed beneficiaries who met Definition 2 of statin intolerance or discontinued statins.
The prevalence of statin intolerance was 1.0 % (n = 1320) and 5.2 % (n = 6985) using Definitions 1 and 2, respectively. Overall, 45,266 (33.6 %) beneficiaries had statin intolerance by Definition 2 or discontinued statins and 55,990 (41.5 %) beneficiaries had high adherence to statins. Compared with beneficiaries with high adherence to statins, those with statin intolerance and who had statin intolerance or discontinued statins were more likely to be female versus male, and black, Hispanic or Asian versus white. The multivariable adjusted odds ratio for statin intolerance by Definitions 1 and 2 comparing patients initiating high versus low/moderate intensity statins were 2.82 (95%CI: 2.42-3.29), and 8.58 (8.07-9.12), respectively, and for statin intolerance or statin discontinuation was 2.35 (2.25-2.45).
Definitions of statin intolerance presented herein can be applied to analyses using administrative claims data.
比较使用不同基于索赔算法识别出的可能存在他汀类药物不耐受的患者与他汀类药物高依从性患者的特征。
我们分析了2007年至2011年间开始使用他汀类药物的134,863名医疗保险受益人。在开始使用他汀类药物后的365天内,评估他汀类药物不耐受和停药情况,以及他汀类药物高依从性(定义为覆盖天数比例≥80%)。他汀类药物不耐受的定义1包括他汀类药物减量或停药并开始使用依折麦布、有横纹肌溶解或抗高脂血症事件的索赔记录随后他汀类药物减量或停药,或在≥3种他汀类药物之间切换。定义2包括符合定义1的受益人以及他汀类药物强度减量的受益人。我们还分析了符合他汀类药物不耐受定义2或停用他汀类药物的受益人。
使用定义1和定义2时,他汀类药物不耐受的患病率分别为1.0%(n = 1320)和5.2%(n = 6985)。总体而言,45,266名(33.6%)受益人根据定义2存在他汀类药物不耐受或停用他汀类药物,55,990名(41.5%)受益人对他汀类药物有高依从性。与他汀类药物高依从性的受益人相比,他汀类药物不耐受以及存在他汀类药物不耐受或停用他汀类药物的受益人更有可能是女性而非男性,是黑人、西班牙裔或亚裔而非白人。比较开始使用高强度与低/中等强度他汀类药物的患者,定义1和定义2下他汀类药物不耐受的多变量调整优势比分别为2.82(95%CI:2.42 - 3.29)和8.58(8.07 - 9.12),他汀类药物不耐受或他汀类药物停药的多变量调整优势比为2.35(2.25 - 2.45)。
本文提出的他汀类药物不耐受定义可应用于使用行政索赔数据的分析。