Center for Pharmacoeconomic Studies, College of Pharmacy, The University of Texas, Austin, TX 78712, USA.
Clin Ther. 2012 Apr;34(4):944-956.e4. doi: 10.1016/j.clinthera.2012.02.021. Epub 2012 Mar 22.
Some previously published research on treatment utilization patterns in patients with attention deficit/hyperactivity disorder (ADHD) has been focused on data from commercial health plans, whereas research in the Medicaid population is lacking. Thus, little is known about these utilization patterns in Medicaid populations, which typically have demographic and clinical characteristics that differ from those of employer-based groups.
The objectives of the present retrospective data analysis were to evaluate the associations of medication groups (categorized by stimulant type [methylphenidate or amphetamine] and duration of action [short-acting (SA) or long-acting (LA)]) with measures of stimulant utilization patterns (adherence, persistence, and switching) in children, adolescents, and adults with ADHD enrolled in the fee-for-service delivery model within the Texas Medicaid Program.
Texas Medicaid fee-for-service claims data were analyzed retrospectively. Data from enrollees with ADHD (6-63 years) were included if patients were newly initiated on medication from January 2006 to September 2007, had ≥1 medical claim with a code for ADHD, and had continuous Medicaid eligibility 6 months before and after treatment initiation. Adherence, persistence, and switching were compared by initial stimulant medication group (SA methylphenidate [SA-M], LA-M, SA amphetamine [SA-A], and LA-A). Rates were compared overall and by age group (children, adolescents, and adults). Multivariate models were used to control for demographic, clinical, and utilization covariates.
Of 15,055 eligible patients, mostly children, 71% were initiated on methylphenidate; 90% received LA formulations (LA-M, 65%; LA-A, 25%). Most children (66%) and adolescents (65%) were initiated on LA-M, followed by LA-A (23% and 29%, respectively). Among adults, 38% each were initiated on LA-M and LA-A. Overall adherence (measured using the days in possession ratio [DPR]) and persistence were significantly greater with the LA versus the SA formulations (mean DPR, 0.497-0.504 vs 0.407-0.418, respectively; mean persistence, 81 vs 66-67 days; both, P < 0.001), and the rates of switching were lower with the LA versus the SA formulations (12.3%-14% vs 27%-28%; P < 0.001). On multivariate analyses, the likelihoods of adherence and persistence were significantly greater with the LA formulations, and the likelihood of being switched was significantly greater with the SA formulations (P < 0.001). These analyses also showed that medication utilization was significantly related to demographic and clinical characteristics.
Based on the findings from this retrospective analysis, ADHD treatment utilization patterns varied by formulation in this Texas Medicaid population. Persistence at 180 days was poor regardless of the stimulant used. Consideration of stimulant formulations and demographic characteristics in patients in whom long-term ADHD management is being initiated may assist in optimum utilization, perhaps leading to better symptom control and more efficient resource utilization.
一些之前发表的关于注意力缺陷/多动障碍(ADHD)患者治疗利用模式的研究主要集中在商业健康计划的数据上,而关于医疗补助计划(Medicaid)人群的研究则有所欠缺。因此,对于 Medicaid 人群的这些利用模式知之甚少,后者通常具有与雇主群体不同的人口统计学和临床特征。
本回顾性数据分析的目的是评估药物类别(按兴奋剂类型[哌醋甲酯或安非他命]和作用持续时间[短效(SA)或长效(LA)]分类)与 ADHD 儿童、青少年和成年人在德克萨斯州医疗补助计划下接受服务付费模式治疗时的兴奋剂利用模式(依从性、持久性和转换)之间的相关性。
对德克萨斯州医疗补助计划的服务付费数据进行回顾性分析。如果患者在 2006 年 1 月至 2007 年 9 月期间新开始服用药物,有≥1 次与 ADHD 相关的医疗索赔,并且在治疗开始前和开始后 6 个月内连续获得医疗补助资格,则纳入 ADHD 患者(6-63 岁)的数据。通过初始兴奋剂药物类别(SA 哌醋甲酯[SA-M]、LA-M、SA 安非他命[SA-A]和 LA-A)比较依从性、持久性和转换。总体上和按年龄组(儿童、青少年和成年人)进行比较。使用多变量模型控制人口统计学、临床和利用方面的协变量。
在 15055 名符合条件的患者中,大多数为儿童,71%的患者开始服用哌醋甲酯;90%的患者使用 LA 制剂(LA-M,65%;LA-A,25%)。大多数儿童(66%)和青少年(65%)开始服用 LA-M,其次是 LA-A(分别为 23%和 29%)。在成年人中,LA-M 和 LA-A 的起始率各为 38%。总体而言,与 SA 制剂相比,LA 制剂的依从性(通过占有日比值[DPR]衡量)和持久性显著更高(平均 DPR,0.497-0.504 对 0.407-0.418,分别;平均持久性,81 天对 66-67 天;均 P < 0.001),且 LA 制剂的转换率更低(12.3%-14%对 27%-28%;均 P < 0.001)。在多变量分析中,与 LA 制剂相比,依从性和持久性的可能性显著更高,而与 SA 制剂相比,转换的可能性显著更高(P < 0.001)。这些分析还表明,药物利用与人口统计学和临床特征显著相关。
根据本回顾性分析的结果,在德克萨斯州 Medicaid 人群中,ADHD 治疗利用模式因制剂而异。无论使用何种兴奋剂,180 天的持久性都很差。在开始长期 ADHD 管理时,考虑兴奋剂制剂和人口统计学特征,可能有助于最佳利用,从而可能更好地控制症状和更有效地利用资源。