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The current study aimed to assess this association between <jats:styled-content style=\"fixed-case\">ADHD<\/jats:styled-content> symptoms and drug\u2010specific <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content> complexity and chronicity.<\/jats:p><\/jats:sec><jats:sec><jats:title>Design and Methods<\/jats:title><jats:p>A cross\u2010sectional survey was administered to a convenience sample of 489 adults receiving <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content> treatment at 16 <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>ustralian drug and alcohol treatment centres between <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>eptember 2010 and <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>ugust 2011. Participants were screened for adult <jats:styled-content style=\"fixed-case\">ADHD<\/jats:styled-content> symptoms using the <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>dult <jats:styled-content style=\"fixed-case\">ADHD S<\/jats:styled-content>elf\u2010<jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>eport <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>cale. Associations between <jats:styled-content style=\"fixed-case\">ADHD<\/jats:styled-content> screening status and drug\u2010specific <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content> complexity and chronicity were assessed using multivariate logistic and modified <jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>oisson regression analysis, controlling for a range of potential confounders.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Overall, 215 (44%) patients screened positive for concurrent adult <jats:styled-content style=\"fixed-case\">ADHD<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content>. After <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>imes' correction, a significant positive association was observed between <jats:styled-content style=\"fixed-case\">ADHD<\/jats:styled-content> screening status and <jats:italic>current<\/jats:italic> amphetamine <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content> (odds ratio (<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>)\u2009=\u20091.85; 95% confidence interval (<jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>): 1.19\u20132.36). Patients who screened positive for <jats:styled-content style=\"fixed-case\">ADHD<\/jats:styled-content> were significantly more likely to report <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content>\u2005<jats:italic>history<\/jats:italic> for heavy alcohol use (<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\u2009=\u20092.05; 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>: 1.21\u20133.45) and amphetamine (<jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\u2009=\u20091.96; 95% <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>: 1.26\u20133.06) as well as significantly increased risk of moderate (3\u20134 years) duration for benzodiazepine and amphetamine <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content>s and long (\u22655 years) duration for alcohol, opiates other than heroin or methadone, and amphetamine <jats:styled-content style=\"fixed-case\">SUDs<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Discussion and Conclusions<\/jats:title><jats:p>The findings provide evidence that there is increased drug dependence complexity and chronicity in treatment\u2010seeking <jats:styled-content style=\"fixed-case\">SUD<\/jats:styled-content> patients who screen positively for <jats:styled-content style=\"fixed-case\">ADHD<\/jats:styled-content>, specifically for amphetamine, alcohol, opiates other than heroin or methadone, and benzodiazepines. <jats:italic>[Young JT, Carruthers S, Kaye S, Allsop S, Gilsenan J, Degenhardt L, van de Glind G, van den Brink W, Preen D. 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