Imagawa Hideyuki, Nagar Saurabh P, Montgomery William, Nakamura Tomomi, Sato Masayo, Davis Keith L
Medical Development Unit Japan, Eli Lilly Japan K.K., Kobe, Japan.
RTI Health Solutions, Research Triangle Park, NC, USA.
Neuropsychiatr Dis Treat. 2018 Feb 22;14:611-621. doi: 10.2147/NDT.S150261. eCollection 2018.
To describe the characteristics and medication treatment patterns of adult patients with attention-deficit/hyperactivity disorder (ADHD) prescribed atomoxetine in Japan.
A retrospective analysis of insurance claims data was conducted using the Japan Medical Data Center database. Adults (≥18 years) with ADHD who had ≥1 atomoxetine claim from January 1, 2013 to December 31, 2014, and ≥180 to ≤900 days of follow-up were included. First atomoxetine claim defined the index date. Patient characteristics included age, gender, and comorbid conditions. Treatment patterns assessed included rates of atomoxetine discontinuation, switching, persistence, adherence (assessed via the medication possession ratio), and use of concomitant medications.
A total of 457 adults met all the inclusion criteria. Mean (SD) age was 32.7 (10.4) years, and 61.0% of patients were male. Nearly 72.0% of the patients had at least one comorbid mental health condition in the baseline period; depression (43.8%) and insomnia (40.7%) were the most common mental health comorbidities. Most common physical comorbidities were chronic obstructive pulmonary disease (14.4%) and diabetes (12.9%). Non-ADHD-specific psychotropics were prescribed to 59.7% of patients during the baseline period and to 65.9% during the follow-up period; 6.6% were prescribed non-ADHD-specific psychotropics concomitantly with atomoxetine. Overall, 40.0% of adults discontinued atomoxetine during the entire follow-up period and 65.9% were persistent with atomoxetine therapy at 3 months post-index date. Mean (SD) atomoxetine medication possession ratio was 0.57 (0.25), and 25.4% switched to an alternative ADHD therapy; methylphenidate (22.4%) and non-ADHD-specific psychotropics (77.6%) were the most common medication alternatives. Nearly 8% augmented atomoxetine with methylphenidates, non-stimulants, or non-ADHD-specific psychotropics.
In this observational study, a majority of adults with ADHD treated with atomoxetine were still persistent with therapy at 3 months post-index date, with one quarter switching to alternative ADHD therapy. High proportions of mental health comorbidities, along with high use of non-ADHD-specific psychotropic medications in both the baseline and follow-up periods, were observed among patients with ADHD prescribed atomoxetine.
描述在日本接受托莫西汀治疗的成人注意力缺陷多动障碍(ADHD)患者的特征及药物治疗模式。
使用日本医疗数据中心数据库对保险理赔数据进行回顾性分析。纳入2013年1月1日至2014年12月31日期间有≥1次托莫西汀理赔记录且随访时间≥180天至≤900天的成年(≥18岁)ADHD患者。首次托莫西汀理赔日期定义为索引日期。患者特征包括年龄、性别和共病情况。评估的治疗模式包括托莫西汀停药率、换药率、持续用药率、依从性(通过药物持有率评估)以及合并用药情况。
共有457名成年人符合所有纳入标准。平均(标准差)年龄为32.7(10.4)岁,61.0%的患者为男性。近72.0%的患者在基线期至少有一种合并的心理健康状况;抑郁症(43.8%)和失眠(40.7%)是最常见的心理健康合并症。最常见的躯体合并症是慢性阻塞性肺疾病(14.4%)和糖尿病(12.9%)。在基线期,59.7%的患者使用了非ADHD特异性精神药物,随访期为65.9%;6.6%的患者在使用托莫西汀的同时还使用了非ADHD特异性精神药物。总体而言,在整个随访期内,40.0%的成年人停用了托莫西汀,在索引日期后3个月,65.9%的患者持续接受托莫西汀治疗。托莫西汀的平均(标准差)药物持有率为0.57(0.25),25.4%的患者换用了另一种ADHD治疗药物;哌甲酯(22.4%)和非ADHD特异性精神药物(77.6%)是最常见的替代药物。近8%的患者使用哌甲酯、非兴奋剂或非ADHD特异性精神药物与托莫西汀联合用药。
在这项观察性研究中,大多数接受托莫西汀治疗的成年ADHD患者在索引日期后3个月仍持续接受治疗,四分之一的患者换用了其他ADHD治疗药物。在接受托莫西汀治疗的ADHD患者中,观察到心理健康合并症的比例较高,且在基线期和随访期使用非ADHD特异性精神药物的比例也较高。