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考察德克萨斯州医疗补助计划人群中儿童和青少年注意缺陷多动障碍治疗模式的异质性:模型分析治疗反应欠佳。

Examining the heterogeneity of treatment patterns in attention deficit hyperactivity disorder among children and adolescents in the Texas Medicaid population: modeling suboptimal treatment response.

机构信息

a Global Outcomes Research and Epidemiology , Shire, Lexington , MA , USA.

b Health Outcomes Division , The University of Texas at Austin, College of Pharmacy , Austin , TX , USA.

出版信息

J Med Econ. 2019 Aug;22(8):788-797. doi: 10.1080/13696998.2019.1606814. Epub 2019 May 8.

Abstract

To examine suboptimal responses (SR) in attention deficit hyperactivity disorder (ADHD) among pediatric patients in the Texas Medicaid program receiving osmotic-release oral system methylphenidate (OROS-MPH) or lisdexamfetamine (LDX) and apply an SR prediction model to identify patients most likely to experience an SR to either OROS-MPH or LDX therapies. A retrospective cohort study was conducted using Texas Medicaid claims data of ADHD children and adolescents (6-17 years of age) initiating OROS-MPH or LDX. Primary SR endpoints were drug discontinuation, switching, and augmentation 12-months post-ADHD drug initiation. Logistic regression models were developed to predict SR to OROS-MPH and LDX in 1:1 matched groups of children and adolescent cohorts. A total of 3,633 children and 1,611 adolescents were matched for each cohort. SR was observed among more children (76.4% vs 72.3%;  < 0.001) and adolescents (82.7% vs 78.2%;  = 0.002) initiating OROS-MPH compared to LDX. Patient sub-groups with the highest predicted risk of OROS-MPH SR experienced significantly lower observed SR rates ( < 0.05) when initiating LDX (children: 80.6% for OROS-MPH vs 75.8% for LDX; OR = 0.75, 95% CI = 0.60-0.94; adolescents: 87.2% for OROS-MPH vs 80.6% for LDX; OR = 0.61, 95% CI = 0.41-0.89). For patients with highest predicted SR rates to LDX, observed SR rates were not significantly different between patients initiating LDX or OROS-MPH. This study demonstrated how a personalized medicine approach using administrative claims data can be used to identify sub-groups of child and adolescent ADHD patients with different risks for suboptimal response with OROS-MPH or LDX in a Medicaid population.

摘要

为了研究在德克萨斯州医疗补助计划中接受渗透压控释口服系统哌甲酯(OROS-MPH)或 lisdexamfetamine(LDX)的儿科患者中注意力缺陷多动障碍(ADHD)的亚最佳反应(SR),并应用 SR 预测模型来识别最有可能对 OROS-MPH 或 LDX 治疗产生 SR 的患者。使用德克萨斯州医疗补助计划中 ADHD 儿童和青少年(6-17 岁)开始接受 OROS-MPH 或 LDX 的索赔数据,进行了一项回顾性队列研究。主要的 SR 终点是药物停药、换药和 12 个月后 ADHD 药物开始时的药物增强。建立了逻辑回归模型,以预测 1:1 匹配的儿童和青少年队列中 OROS-MPH 和 LDX 的 SR。每个队列匹配了 3633 名儿童和 1611 名青少年。与接受 LDX 的儿童(76.4%对 72.3%;  < 0.001)和青少年(82.7%对 78.2%;  = 0.002)相比,接受 OROS-MPH 的儿童和青少年中观察到的 SR 发生率更高。预测 OROS-MPH SR 风险最高的患者亚组在开始接受 LDX 时,观察到的 SR 率明显较低( < 0.05)(儿童:OROS-MPH 为 80.6%,LDX 为 75.8%;OR=0.75,95%CI=0.60-0.94;青少年:OROS-MPH 为 87.2%,LDX 为 80.6%;OR=0.61,95%CI=0.41-0.89)。对于预测 LDX 发生 SR 率最高的患者,开始接受 LDX 或 OROS-MPH 的患者之间的观察到的 SR 率没有显著差异。这项研究表明,如何使用基于行政索赔数据的个性化医疗方法,在 Medicaid 人群中识别接受 OROS-MPH 或 LDX 治疗的儿童和青少年 ADHD 患者亚组,这些患者对 OROS-MPH 或 LDX 的亚最佳反应风险不同。

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