Van Brunt David L, Johnston Joseph A, Ye Wenyu, Pohl Gerhardt M, Sun Pei J, Sterling Kimberly L, Davis Martha E
Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, USA.
Pharmacotherapy. 2005 Nov;25(11):1541-9. doi: 10.1592/phco.2005.25.11.1541.
To investigate predictors of beginning treatment with atomoxetine, a new attention-deficit-hyperactivity disorder (ADHD) drug, shortly after it was introduced into the marketplace compared with well-established stimulants for children in a managed care setting.
Retrospective cohort analysis.
Managed care claims database.
A total of 45,144 patients aged 18 years or younger who filled a prescription for an ADHD-specific drug.
For each patient, the most recent start of therapy between April 1 and December 31, 2003, was categorized by drug: atomoxetine; any stimulant; or short-, intermediate-, or long-acting stimulant. The categories were based on the first use of the drug without use of a drug in that same category in the previous 3 months. Logistic regression analysis of past-year administrative claims was applied to determine predictors of the start of specific pharmacotherapy. Patients with a claim of ADHD with hyperactivity were 1.50 times more likely to begin therapy with atomoxetine than with any stimulant (95% confidence interval [CI] 1.42-1.58). Patients with a history of tics (odds ratio [OR] 3.11, 95% CI 2.54-3.82), anxiety (OR 1.35, 95% CI 1.24-1.48), pervasive developmental disorders (OR 2.00, 95% CI 1.69-2.37), or frequent use of behavioral care services (OR 1.34, 95% CI 1.21-1.48) were predisposed to starting treatment with atomoxetine relative to any stimulant, but patients with obesity were not (OR 0.68, 95% CI 0.53-0.87). A short-acting stimulant was specifically preferred for patients with narcolepsy or hypersomnolence (OR 0.33, 95% CI 0.20-0.56). Alcohol dependence, but not drug dependence or drug abuse, was predictive of the selection of atomoxetine over a short-acting stimulant (OR 2.98, 95% CI 1.25-7.09).
Atomoxetine therapy was systematically preferred for patients with psychiatric comorbidities, contraindications to stimulants, or relatively heavy use of behavioral health care.
调查在管理式医疗环境中,与已广泛使用的儿童兴奋剂相比,新型注意力缺陷多动障碍(ADHD)药物托莫西汀在进入市场后不久即开始使用的预测因素。
回顾性队列分析。
管理式医疗理赔数据库。
共有45144名18岁及以下开具ADHD特异性药物处方的患者。
对于每位患者,将2003年4月1日至12月31日期间最近一次开始治疗的药物分类为:托莫西汀;任何一种兴奋剂;或短效、中效或长效兴奋剂。分类依据是在前3个月内首次使用该药物且未使用过同一类别的其他药物。应用对过去一年行政理赔数据的逻辑回归分析来确定特定药物治疗开始的预测因素。有ADHD伴多动症状理赔记录的患者开始使用托莫西汀治疗的可能性是使用任何一种兴奋剂的1.50倍(95%置信区间[CI]1.42 - 1.58)。有抽动症病史(优势比[OR]3.11,95%CI 2.54 - 3.82)、焦虑症(OR 1.35,95%CI 1.24 - 1.48)、广泛性发育障碍(OR 2.00,95%CI 1.69 - 2.37)或频繁使用行为护理服务(OR 1.34,95%CI 1.21 - 1.48)的患者相对于任何一种兴奋剂更倾向于开始使用托莫西汀治疗,但肥胖患者并非如此(OR 0.68,95%CI 0.53 - 0.87)。对于发作性睡病或嗜睡症患者,特别倾向于选择短效兴奋剂(OR 0.33,95%CI 0.20 - 0.56)。酒精依赖而非药物依赖或药物滥用可预测选择托莫西汀而非短效兴奋剂(OR 2.98,95%CI 1.25 - 7.09)。
对于有精神疾病共病、兴奋剂禁忌证或行为健康护理使用相对较多的患者,系统性地更倾向于使用托莫西汀治疗。