The World Health Organization adult ADHD self-report scale (ASRS): a short screening scale for use in the general population
1968/10/31 by RONALD C. KESSLER, Ronald C. Kessler, Lenard A. Adler +21 · 3,439 citations
Energy · Medicine · Neuroscience · Psychology · #Attention Deficit Hyperactivity Disorder #Clinical psychology #Coal and Coke Industries Research #Cohen's kappa #Comorbidity #Concordance #Functional Brain Connectivity Studies #Internal medicine #Kappa #Logistic regression #Medicine #Neural and Behavioral Psychology Studies #Population #Psychiatry #Psychology #Rating scale #Statistics
paper · doi:10.1017/s0033291704002892
published in Psychological Medicine 35(2), 245-256 (Cambridge University Press)
openalex publication_date 2005/01/21 · openalex created_date 2016/06/24 · openalex updated_date 2026/08/05
Abstract
BACKGROUND: A self-report screening scale of adult attention-deficit/hyperactivity disorder (ADHD), the World Health Organization (WHO) Adult ADHD Self-Report Scale (ASRS) was developed in conjunction with revision of the WHO Composite International Diagnostic Interview (CIDI). The current report presents data on concordance of the ASRS and of a short-form ASRS screener with blind clinical diagnoses in a community sample. METHOD: The ASRS includes 18 questions about frequency of recent DSM-IV Criterion A symptoms of adult ADHD. The ASRS screener consists of six out of these 18 questions that were selected based on stepwise logistic regression to optimize concordance with the clinical classification. ASRS responses were compared to blind clinical ratings of DSM-IV adult ADHD in a sample of 154 respondents who previously participated in the US National Comorbidity Survey Replication (NCS-R), oversampling those who reported childhood ADHD and adult persistence. RESULTS: Each ASRS symptom measure was significantly related to the comparable clinical symptom rating, but varied substantially in concordance (Cohen's kappa in the range 0.16-0.81). Optimal scoring to predict clinical syndrome classifications was to sum unweighted dichotomous responses across all 18 ASRS questions. However, because of the wide variation in symptom-level concordance, the unweighted six-question ASRS screener outperformed the unweighted 18-question ASRS in sensitivity (68.7% v. 56.3%), specificity (99.5% v. 98.3%), total classification accuracy (97.9% v. 96.2%), and kappa (0.76 v. 0.58). CONCLUSIONS: Clinical calibration in larger samples might show that a weighted version of the 18-question ASRS outperforms the six-question ASRS screener. Until that time, however, the unweighted screener should be preferred to the full ASRS, both in community surveys and in clinical outreach and case-finding initiatives.
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