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EDITORIALS |
MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, London
Glyncynffig Hostel, Bridgend
MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, London, UK
Correspondence: Philip Asherson, MRC Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Denmark Hill, London SE5 8AF, UK. Email: p.Asherson{at}iop.kcl.ac.uk
Declaration of interest The authors research is funded by the UKMedical Research Council, the Wellcome Trust and the US National Institute of Mental Health. P.A. received unrestricted research funds from Janssen-Cilag and has spoken at meetings sponsored by Janssen-Cilag and Eli Lilly.
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ABSTRACT |
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INTRODUCTION |
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A good deal of the justification for this therapeutic activity is the demonstration that ADHD is a predictor of adult mental health problems. Furthermore, effective treatment with stimulant medication increases the immediate value of the clinical diagnosis (Taylor et al, 2004). General adult psychiatry, however, has not yet followed suit in identifying and treating substantial numbers of affected people. Yet it is likely that an increasing load in adult psychiatry will develop. Young people are entering adult life while still receiving medication for ADHD, and adult psychiatrists are needed to take over psychiatric treatment when symptoms persist. An increasing number of adults are recognising themselves or being recognised by family members, general practitioners, probation officers, drug and alcohol specialists, psychologists and others as being disabled by ADHD and requiring assistance. In addition there is a pool of adult psychiatric patients in whom the diagnosis of ADHD has gone unrecognised and for whom treatments put in place for alternative diagnoses, such as anxiety, depression, cyclothymia and personality disorder, are ineffective.
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VALIDITY OF THE ADULT DIAGNOSIS |
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Furthermore, it is well established that ADHD symptoms in adults show the same responsiveness to stimulant and non-stimulant medications as that seen in children (Faraone et al, 2004; Simpson & Plosker, 2004). For these reasons UK and European experts in a recent review of available data on the efficacy of extended-release preparations in the treatment of ADHD include recommendations for their use in adults (Banaschewski et al, 2006).
A key question is the number of children with ADHD who continue to show ADHD in adult life. Studies that followed children identified with ADHD, as well as controls, into adulthood have been included in a meta-analysis of 32 publications (Faraone et al, 2006). When the ADHD samples included only those who met full diagnostic criteria for ADHD the rate of persistence was approximately 15% at age 25 years. However, the rate was far higher approximately 65% when individuals fulfilling the DSMIV definition of ADHD in partial remission were included, referring to the persistence of some symptoms associated with significant clinical impairments.
Our own data support this conclusion. In an epidemiological survey of school-children from the London district of Newham, E.T. and colleagues measured ADHD behaviours at ages 7 and 17 years. Levels of inattentive and restless activity had indeed diminished. However, 17-year-olds previously characterised as hyperactive showed a level of hyperactivity similar to that seen in the control group of normal 7-year-olds. Although this meant that most no longer met full diagnostic criteria, the relative distance between them and controls was unchanged. Importantly, the degree to which hyperactive behaviour was above the age norm was strongly related to poor social adjustment in terms of lack of friends, occupation and constructive activity. Deficits associated with high levels of psychiatric morbidity were also seen when the same people were followed up at age 26 years (further information available on request) and these are all the more significant because of increasing demands in adult life for self-organisation and the ability to plan ahead.
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DIAGNOSIS IN ADULTS |
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Although most people experience such symptoms at times, individuals with ADHD experience these to a severe degree most of the time. As in other common adult psychiatric disorders, such as anxiety and depression, ADHD symptoms are continuously distributed throughout the population (Asherson, 2004). Clinical thresholds are therefore determined on the basis of usual clinical practice, which recognises disorder when the symptoms are sufficiently frequent or severe to cause personal distress, distress to others, interference with psychosocial function or health complications.
In making the correct diagnosis there are potential traps for the inexperienced ADHD diagnostician. First, ADHD symptoms may be not be evident in the clinic or other highly structured environments. The reason is that ADHD symptoms may respond to (decrease in) situations that are highly novel or salient to the individual, such as an important psychiatric evaluation. It is therefore important to base mental state descriptions on a typical week and a variety of normal situations. Second, ADHD symptoms start early in life, by definition before the age of 7 years, and are persistent and non-episodic. They are therefore more trait-like than symptom-like, since there is no clear change from a premorbid state, and can therefore be mistaken for character traits that may be deemed resistant to psychopharmacological intervention. Third, mood instability is extremely common in adult ADHD and can lead to diagnoses of minor affective disorders or personality disorder. Clinical experience suggests that mood instability in the context of ADHD frequently responds to stimulants in the same timescale as core symptoms of the disorder.
Many adults with ADHD have other problems: antisocial personality, alcohol misuse, substance dependence, dysthymia, cyclothymia, anxiety disorders and general and specific learning difficulties. Early-onset and persistent antisocial behaviour is a particularly common association that sometimes leads to persistent impulsive antisocial behaviour in adult life. Longitudinal studies show that ADHD comes first and may then lead to development of antisocial behaviour, a trajectory thought to be mediated by prominent shared environmental influences.
Bipolar affective disorder includes some symptoms that are very similar to those of ADHD. Both are characterised by overactivity, distractibility, inattentiveness and mood changes. The definitions were not framed with the purpose of distinguishing between these two disorders; however, the distinction is usually not difficult. The mood state of ADHD is irritable and volatile, rather than containing elements of euphoria and grandiosity. The course of adult ADHD is one of a persisting trait, very different from the episodes of mania and/or depression characteristic of bipolar disorder. Follow-up studies of typical ADHD cases have not observed the development of classic adult bipolar disorder (Type 1). Recent changes have taken place in the concept of juvenile mania. It has been argued that mania of very early onset is characterised by a mood of irritability rather than euphoria, and by chronicity rather than fluctuation. If this change of definition is accepted, then the distinction from ADHD becomes difficult indeed. In people with a pattern of ADHD symptoms, emotional instability and irritability in childhood, the mood symptoms tend to persist in the same form rather than becoming more like classic bipolar disorder.
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CLINICAL IMPLICATIONS |
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REFERENCES |
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Asherson, P. (2005) Clinical assessment and treatment of attention deficit hyperactivity disorder in adults. Expert Review of Neurotherapeutics, 5, 525 539.
Banaschewski, T., Coghill, D., Santosh, P., et al (2006) Long-acting medications for the hyperkinetic disorders: a systematic review and European treatment guideline. European Child and Adolescent Psychiatry, in press.
Faraone, S. V., Biederman, J., Spencer, T., et al (2000) Attention-deficit/hyperactivity disorder in adults: an overview. Biological Psychiatry, 48, 9 20.[CrossRef][Medline]
Faraone, S. V., Spencer, T., Aleardi, M., et al (2004) Meta-analysis of the efficacy of methylphenidate for treating adult attention-deficit/hyperactivity disorder. Journal of Clinical Psychopharmacology, 24, 24 29.[CrossRef][Medline]
Faraone, S. V., Biederman, J. & Mick, E. (2006) The age-dependent decline of attention deficit hyperactivity disorder: a meta-analysis of follow-up studies. Psychological Medicine, 36, 159 165.[CrossRef][Medline]
Simpson, D. & Plosker, G. L. (2004) Atomoxetine: a review of its use in adults with attention deficit hyperactivity disorder. Drugs, 64, 205 222.[CrossRef][Medline]
Taylor, E., Dopfner, M., Sergeant, J., et al (2004) European clinical guidelines for hyperkinetic disorder first upgrade. European Child and Adolescent Psychiatry, 13 (suppl. 1), i7i30.
Weiss, M. & Murray, C. (2003) Assessment
and management of attention-deficit hyperactivity disorder in adults.
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Weiss, M., Murray, C. & Weiss, G. (2002) Adults with attention-deficit/hyperactivity disorder: current concepts. Journal of Psychiatric Practice, 8, 99 111.[CrossRef][Medline]
Wender, P. H. (1998) Attention-deficit hyperactivity disorder in adults. Psychiatric Clinics of North America, 21, 761 774.[CrossRef][Medline]
Received for publication May 15, 2006. Accepted for publication August 18, 2006.
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