Tool for Converting ADHD Rating Scales Scores Based on Individual Participant Data from 53 Randomized Controlled Trials of ADHD Medications.

IF 1.8 4区 医学 Q2 PEDIATRICS
Christos Christogiannis, Miguel Garcia-Argibay, Anneka Tomlinson, Sulagna Roy, Luis C Farhat, Guilherme Fusetto Veronesi, Valeria Parlatini, Alessio Bellato, Corentin J Gosling, Dimitris Mavridis, Orestis Efthimiou, Edoardo G Ostinelli, Andrea Cipriani, Samuele Cortese
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引用次数: 0

Abstract

Introduction: A variety of rating scales are currently being used to assess symptom severity and quantify symptoms change in attention-deficit/hyperactivity disorder (ADHD) research and clinical practice. This poses difficulties in interpreting scores from different scales in clinical practice and synthesizing data from studies using different scales. We aimed to develop algorithms for converting scores across the ADHD scales most often used in randomized controlled trials (RCTs) of ADHD medications in children/adolescents and adults, and to develop an online tool for implementing the algorithms.

Methods: We analyzed individual participant data from RCTs of ADHD medications (32 RCTs in children/adolescents, 21 in adults), with data on at least two scales per participant at the same timepoint. We applied a series of competing models, that is, univariable and multivariable regression, random forests, and an equipercentile linkage approach, to link pairs of scales. To assess the error of the linking procedure and identify the optimal model, we calculated the median absolute error and R2 of all approaches by comparing the values predicted from the models to the observed ones. We subsequently developed a tool to implement the best algorithms.

Results: We linked six commonly used ADHD scales, such as the ADHD Rating Scale (ADHD-RS-IV; investigator-rated) and the Conners' Parent Rating Scale (CPRS-R:S). Spline models most frequently yielded the lowest prediction error, outperforming alternative conversion algorithms for absolute scores in 6 out of 12 univariable models and 8 out of 12 multivariable models. The tool for scores conversion is available at ADHD_Scale_Conversion_Tool.

Conclusions: Our linkage algorithms enable the comparison and harmonization of findings across studies using different ADHD rating scales. Translating scores across scales improves the interpretability of research findings, facilitates future evidence synthesis across studies, and may support clinical practice. Our online tool supports the practical uptake of our results.

基于53个ADHD药物随机对照试验的个体参与者数据转换ADHD评定量表得分的工具。
在注意力缺陷/多动障碍(ADHD)的研究和临床实践中,各种评定量表目前被用于评估症状严重程度和量化症状变化。这在解释临床实践中不同量表的得分和综合使用不同量表的研究数据时造成了困难。我们的目标是开发一种算法,用于转换儿童/青少年和成人ADHD药物随机对照试验(rct)中最常用的ADHD量表得分,并开发一种在线工具来实现该算法。方法:我们分析了来自ADHD药物随机对照试验的个体参与者数据(32项儿童/青少年随机对照试验,21项成人随机对照试验),每个参与者在同一时间点至少有两个量表的数据。我们应用了一系列相互竞争的模型,即单变量和多变量回归、随机森林和等百分位链接方法,来连接对尺度。为了评估连接过程的误差并确定最优模型,我们通过将模型预测值与观测值进行比较,计算了所有方法的中位数绝对误差和R2。我们随后开发了一个工具来实现最好的算法。结果:我们将ADHD评定量表(ADHD- rs - iv;调查者评定)和Conners父母评定量表(CPRS-R:S)等六种常用的ADHD量表进行了关联。样条模型通常产生最低的预测误差,在12个单变量模型中的6个和12个多变量模型中的8个中,其绝对分数优于替代转换算法。分数转换工具可在adhd_scale_converversion_tool中获得。结论:我们的关联算法能够比较和协调使用不同ADHD评定量表的研究结果。跨量表翻译分数提高了研究结果的可解释性,促进了未来跨研究的证据合成,并可能支持临床实践。我们的在线工具支持我们的结果的实际吸收。
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来源期刊
CiteScore
3.60
自引率
5.30%
发文量
61
审稿时长
>12 weeks
期刊介绍: Journal of Child and Adolescent Psychopharmacology (JCAP) is the premier peer-reviewed journal covering the clinical aspects of treating this patient population with psychotropic medications including side effects and interactions, standard doses, and research on new and existing medications. The Journal includes information on related areas of medical sciences such as advances in developmental pharmacokinetics, developmental neuroscience, metabolism, nutrition, molecular genetics, and more. Journal of Child and Adolescent Psychopharmacology coverage includes: New drugs and treatment strategies including the use of psycho-stimulants, selective serotonin reuptake inhibitors, mood stabilizers, and atypical antipsychotics New developments in the diagnosis and treatment of ADHD, anxiety disorders, schizophrenia, autism spectrum disorders, bipolar disorder, eating disorders, along with other disorders Reports of common and rare Treatment Emergent Adverse Events (TEAEs) including: hyperprolactinemia, galactorrhea, weight gain/loss, metabolic syndrome, dyslipidemia, switching phenomena, sudden death, and the potential increase of suicide. Outcomes research.
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