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Medications for attention-deficit/hyperactivity disorder in individuals with or without coexisting autism spectrum disorder: analysis of data from the Swedish prescribed drug register

机译:有或没有共存自闭症谱系障碍的个人注意力/多动障碍的药物:瑞典规定药物登记册的数据分析

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Clinical studies found that medication for attention-deficit/hyperactivity disorder (ADHD) is effective in coexisting autism spectrum disorder (ASD), but current research is based on small clinical studies mainly performed on children or adolescents. We here use register data to examine if individuals with ADHD and coexisting ASD present differences in the prescribing patterns of ADHD medication when compared to individuals with pure ADHD. Data with information on filled prescriptions and diagnoses was retrieved from the Swedish Prescribed Drug Register and the National Patient Register. We identified 34,374 individuals with pure ADHD and 5012 individuals with ADHD and coexisting ASD, aged between 3 and 80?years. The first treatment episode with ADHD medications (≥ 2 filled prescriptions within 90?days) and daily doses of methylphenidate during a 3-year period was measured. Odds ratios (ORs) were calculated for the likelihood of being prescribed ADHD medication in individuals with and without ASD and Wilcoxon rank-sum test was used to compare group differences in dose per day. Individuals with ADHD and coexisting ASD were less likely to start continuous treatment with ADHD medication (ADHD 80.5%; ADHD with ASD 76.2%; OR, 0.80; 95% confidence interval, 0.75-0.86), were less likely to be prescribed methylphenidate, and were more commonly prescribed second line treatments such as dexamphetamine, amphetamine, or modafinil. No group difference was observed for atomoxetine. In adults with ADHD and coexisting ASD, methylphenidate was prescribed in lower daily doses over three?years as compared to individuals with pure ADHD. The findings indicate that there are differences in the medical treatment of individuals with or without ASD. If these differences are due to different medication responses in ASD or due to other factors such as clinicians’ perceptions of medication effects in patients with ASD, needs to be further studied.
机译:临床研究发现,注意力缺陷/多动障碍(ADHD)的药物在共存自闭症谱系(ASD)中是有效的,但目前的研究基于主要对儿童或青少年进行的小临床研究。我们在这里使用寄存器数据来检查具有ADHD和共存ASD的个体是否与具有纯ADHD的个体相比的ADHD药物的处方模式的差异。从瑞典规定的药物寄存器和国家患者登记册中检索有关填充处方和诊断信息的数据。我们确定了34,374名以纯粹的ADHD和5012名拥有ADHD和共存ASD的个人,年龄在3到80岁之间进行了3至80人。测定了第一次处理ADHD药物(≥2次填充的处方)和每日剂量的甲基酚依赖于3年期间的治疗。计算赔率比(或)用于在具有并且没有ASD中的个体中规定的ADHD药物的可能性,并且使用WILCOXON RANK-SUM试验来比较每天剂量的群体差异。具有ADHD和共存ASD的个体不太可能与ADHD药物进行连续治疗(ADHD 80.5%; ADHD,ASD 76.2%;或,0.80; 95%置信区间,0.75-0.86)不太可能被规定甲基透明剂,更常见的第二线治疗如德克胺,安非他明,或Modafinil。未经氧杂志观察到群体差异。在具有ADHD和ASD的成年人中,与纯ADHD的个体相比,在3年内,甲基酚在较低的每日剂量中规定。调查结果表明,有或没有ASD的个体的医学治疗存在差异。如果这些差异是由于ASD中的不同药物反应或由于临床医生的其他因素,例如临床医生对ASD患者的药物作用的看法,需要进一步研究。

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