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在临床样本中对脑电图(EEG)和评定量表在识别注意力缺陷多动障碍(ADHD)方面进行盲法多中心验证。

Blinded, multi-center validation of EEG and rating scales in identifying ADHD within a clinical sample.

作者信息

Snyder Steven M, Quintana Humberto, Sexson Sandra B, Knott Peter, Haque A F M, Reynolds Donald A

机构信息

Department of Psychology, University of North Texas Health Science Center at Fort Worth, Fort Worth, TX 76107, USA.

出版信息

Psychiatry Res. 2008 Jun 30;159(3):346-58. doi: 10.1016/j.psychres.2007.05.006. Epub 2008 Apr 18.

Abstract

Previous validation studies of attention deficit/hyperactivity disorder (ADHD) assessment by rating scales or EEG have provided Class-IV evidence per standards of the American Academy of Neurology. To investigate clinical applications, we collected Class-I evidence, namely from a blinded, prospective, multi-center study of a representative clinical sample categorized with a clinical standard. Participating males (101) and females (58) aged 6 to 18 had presented to one of four psychiatric and pediatric clinics because of the suspected presence of attention and behavior problems. DSM-IV diagnosis was performed by clinicians assisted with a semi-structured clinical interview. EEG (theta/beta ratio) and ratings scales (Conners Rating Scales-Revised and ADHD Rating Scales-IV) were collected separately in a blinded protocol. ADHD prevalence in the clinical sample was 61%, whereas the remainder had other childhood/adolescent disorders or no diagnosis. Comorbidities were observed in 66% of ADHD patients and included mood, anxiety, disruptive, and learning disorders at rates similar to previous findings. EEG identified ADHD with 87% sensitivity and 94% specificity. Rating scales provided sensitivity of 38-79% and specificity of 13-61%. While parent or teacher identification of ADHD by rating scales was reduced in accuracy when applied to a diverse clinical sample, theta/beta ratio changes remained consistent with the clinician's ADHD diagnosis. Because theta/beta ratio changes do not identify comorbidities or alternative diagnoses, the results do not support the use of EEG as a stand-alone diagnostic and should be limited to the interpretation that EEG may complement a clinical evaluation for ADHD.

摘要

先前通过评定量表或脑电图对注意力缺陷多动障碍(ADHD)进行评估的验证研究,按照美国神经病学学会的标准提供了IV级证据。为了研究临床应用,我们收集了I级证据,即来自一项针对具有代表性临床样本的盲法、前瞻性、多中心研究,该样本按照临床标准进行分类。参与研究的6至18岁男性(101名)和女性(58名)因疑似存在注意力和行为问题,前往四家精神科和儿科诊所之一就诊。DSM-IV诊断由临床医生在半结构化临床访谈的协助下进行。脑电图(θ/β比值)和评定量表(康纳斯修订评定量表和ADHD评定量表-IV)按照盲法方案分别收集。临床样本中ADHD的患病率为61%,其余患者患有其他儿童期/青少年期疾病或未确诊。66%的ADHD患者存在共病,包括情绪、焦虑、破坏性行为和学习障碍,其发生率与先前研究结果相似。脑电图诊断ADHD的敏感性为87%,特异性为94%。评定量表的敏感性为38%-79%,特异性为13%-61%。当应用于多样化的临床样本时,通过评定量表由家长或教师识别ADHD的准确性会降低,而θ/β比值的变化与临床医生对ADHD的诊断仍保持一致。由于θ/β比值的变化无法识别共病或其他诊断,因此这些结果不支持将脑电图作为独立诊断方法,其应用应限于脑电图可辅助ADHD临床评估的解释。

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