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Updated European Consensus Statement on diagnosis and treatment of adult ADHD

Published online by Cambridge University Press:  16 November 2018

J.J.S. Kooij
Affiliation:
aPsyQ Psycho-Medical Programs, Expertise Center Adult ADHD, Carel Reinierszkade 197, 2593 HRThe Hague, The Netherlands bAmsterdam UMC, LocationVUMc, Dept. of Psychiatry, Amsterdam, the Netherlands
D. Bijlenga
Affiliation:
aPsyQ Psycho-Medical Programs, Expertise Center Adult ADHD, Carel Reinierszkade 197, 2593 HRThe Hague, The Netherlands
L. Salerno
Affiliation:
INS, Institute of Neuroscience, Florence, Italy
R. Jaeschke
Affiliation:
Jagiellonian University Medical College, Section of Affective Disorders, Department of Psychiatry, Krakow, Poland
I. Bitter
Affiliation:
JSemmelweis University, Department of Psychiatry, Budapest, Hungary
J. Balázs
Affiliation:
cInstitute of Psychology, Eotvos Lorand University, Vadaskert Child Psychiatric Hospial and Outpatient Clinic, Budapest, Hungary
J. Thome
Affiliation:
SThome, Klinik und Poliklinik für Psychiatrie und Psychotherapie, Universitatsmedizin Rostock, Rostock, Germany
G. Dom
Affiliation:
XAntwerp University (UA, CAPRI), Boechout, Belgium
S. Kasper
Affiliation:
dMedical University Vienna, Department of Psychiatry and Psychotherapy, Vienna, Austria
C. Nunes Filipe
Affiliation:
Nova Medical School. Universidade NOVA Lisboa, Lisboa, Portugal
S. Stes
Affiliation:
eUniversity Psychiatric Center, KU Leuven, Kortenberg, Belgium
P. Mohr
Affiliation:
WNational Institute of Mental Health, Klecany, Czech Republic; Third Faculty of Medicine, Charles University Prague, Czech Republic
S. Leppämäki
Affiliation:
fHelsinki University Central Hospital, Department of Psychiatry, HUS, Finland
M. Casas
Affiliation:
gDepartment of Psychiatry, Hospital Universitari Vall d'Hebron, Barcelona, Catalonia, Spain; Psychiatric Genetics Unit, Vall d'Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain; Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Catalonia, Spain; Department of Psychiatry and Forensic Medicine, Universitat Autònoma de Barcelona, Barcelona, Catalonia, Spain
J. Bobes
Affiliation:
ODepartment of Psychiatry, School of Medicine, University of Oviedo - Centro de Investigación Biomédica and Red de Salud Mental, CIBERSAM, Oviedo, Spain
J.M. Mccarthy
Affiliation:
hVisiting senior lecturer, King’s College London, United Kingdom; Midland Regional Forensic Service, Hamilton, New Zealand
V. Richarte
Affiliation:
iDepartment of Psychiatry, Hospital Universitari Vall d’Hebron, Barcelona; Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona; Department of Psychiatry and Legal Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain
A. Kjems Philipsen
Affiliation:
jDPC Naestved, Ladby, Naestved, Region SjaellandDenmark
A. Pehlivanidis
Affiliation:
National and Kapodistrian University of Athens Medical School, Eginition Hospital, Department of Psychiatry, Athens, Greece
A. Niemela
Affiliation:
kWellmind Terveys Oy, Oulu, Finland
B. Styr
Affiliation:
lMccabi Health Services (H.M.O), Tel Aviv, Israel
B. Semerci
Affiliation:
Hasan Kalyoncu University, Poyracık Sokak, Istanbul, Turkey
B. Bolea-Alamanac
Affiliation:
mGeneral Systems Division, Centre for Addiction and Mental Health/ Dept. Of Psychiatry, University of Toronto, Toronto, Canada
D. Edvinsson
Affiliation:
nUppsala University, Uppsala University Hospital, Akademiska sjukhuset, Uppsala, Stockholm, Sweden
D. Baeyens
Affiliation:
oParenting and Special Education, KU Leuven, Leuven, Belgium
D. Wynchank
Affiliation:
aPsyQ Psycho-Medical Programs, Expertise Center Adult ADHD, Carel Reinierszkade 197, 2593 HRThe Hague, The Netherlands
E. Sobanski
Affiliation:
LCentral Institute of Mental Health, Mannheim; University Medical Center Mainz, Mainz, Germany
A. Philipsen
Affiliation:
pUniversity of Bonn, Department of Psychiatry and Psychotherapy, Bonn, Germany
F. McNicholas
Affiliation:
University College Dublin, Dublin, Republic of Ireland
H. Caci
Affiliation:
MHopitaux Pediatriques de Nice CHU Lenval, Nice, France
I. Mihailescu
Affiliation:
qAlexandru Obregia Clinical Hospital of Psychiatry, Bucharest, Romania
I. Manor
Affiliation:
Geha MHC, Petach-TikvaIsrael
I. Dobrescu
Affiliation:
rUniversity of Medicine and Pharmacy “Carol Davila”. Child and adolescent Psychiatry Department, Prof. Dr. Alex Obregia”Psychiatry Hospital, Bucharest, Romania
T. Saito
Affiliation:
HDepartment of Child and adolescent Psychiatry, Graduate School of Medicine, Hokkaido University, North 15,West 7, Kita-ku, Sapporo, 060-8638, Japan
J. Krause
Affiliation:
Outpatient Clinic, Ottobrunn, Germany
J. Fayyad
Affiliation:
sSt George Hospital University Medical Center, Balamand University Faculty of Medicine, Institute for Development, Research, Advocacy and Applied Care, Department of Psychiatry and Clinical Psychology, St George Hospital, Achrafieh, Beirut, Lebanon
J.A. Ramos-Quiroga
Affiliation:
NDepartment of Psychiatry, Hospital Universitari Vall d’Hebron, Barcelona, Catalonia, Spain; Psychiatric Genetics Unit, Vall d’Hebron Research Institute (VHIR), Barcelona, Catalonia, Spain; Biomedical Network Research Centre on Mental Health (CIBERSAM), Barcelona, Catalonia, Spain; Department of Psychiatry and Forensic Medicine, Universitat Autònoma de Barcelona, Barcelona, Catalonia, Spain
K. Foeken
Affiliation:
tVieux Chemin de Cagnes à La Gaude, la Gaude, France
F. Rad
Affiliation:
uUniversity of Medicine and Pharmacy “Carol Davila”; Child and adolescent Psychiatry Department, Prof. Dr. Alex Obregia”Psychiatry Hospital, Bucharest, Romania
M. Adamou
Affiliation:
vUniversity of Huddersfield and South West Yorkshire Partnership NHS, Manygates Clinic, Wakefield, England
M. Ohlmeier
Affiliation:
Klinikum Kassel, Department of Psychiatry and Psychotherapy, Kassel, Germany
M. Fitzgerald
Affiliation:
wTrinity College, Blanchardstown Village, Dublin, Republic of Ireland
M. Gill
Affiliation:
QDepartment of Psychiatry, Trinity College Dublin, School of Medicine, Dublin, Republic of Ireland
M. Lensing
Affiliation:
UOslo University Hospital, Department of Rare Disorders, NevSom - Norwegian Centre of Expertise for Neurodevelopmental Disorders and Hypersomnias, Oslo, Norway
N. Motavalli Mukaddes
Affiliation:
xIstanbul Institute of Child and Adolescent Psychiatry, Istanbul, Turkey
P. Brudkiewicz
Affiliation:
yCentrum Dobrej Terapii, Cracow, Poland
P. Gustafsson
Affiliation:
Lund University, Clinical Sciences Lund, Child and Adolescent Psychiatry, Lund, Sweden
P. Tani
Affiliation:
zDepartment of Psychiatry, Clinic for Neuropsychiatry, Helsinki University Central Hospital, HUS, Finland
P. Oswald
Affiliation:
High Security Hospital, CRP Les Marronniers, Tournai, Belgium
P.J. Carpentier
Affiliation:
AReinier van Arkel Mental Health Institute, ’s-Hertogenbosch, Netherlands
P. De Rossi
Affiliation:
YDepartment of Neurology and Psychiatry, Sapienza University of Rome, Rome; Department NSMOS, Faculty of Medicine and Psychology, University “Sapienza”of Rome, Rome, Italy
R. Delorme
Affiliation:
BChild and Adolescent Psychiatry Department, Robert Debré Hospital, Paris, France
S. Markovska Simoska
Affiliation:
CMacedonian Academy of Sciences and Arts, Skopje, Republic of Macedonia
S. Pallanti
Affiliation:
DStanford University Medical Center, University of Florence, INS Institute of Neuroscience, Florence, Italy
S. Young
Affiliation:
EPsychology Services Limited, Croydon, England
S. Bejerot
Affiliation:
VÖrebro Univerity, School of Medical Sciences, Campus USÖ, Örebro, Sweden
T. Lehtonen
Affiliation:
FNeuropsykologkonsult Taina Lehtonen, Hjärup, Sweden
J. Kustow
Affiliation:
GBarnet Adult ADHD Service, Barnet, Enfield and Haringey NHS Mental Health Trust, London; Barnet Adult ADHD Service, Springwell Centre, Barnet Hospital, Barnet, England
U. Müller-Sedgwick
Affiliation:
KAdult ADHD Service, Barnet, Enfield & Haringey NHS Mental Health Trust, North London & Department of Psychiatry, University of Cambridge; Adult ADHD Service, Springwell Centre / Barnet Hospital, Barnet, London, England
T. Hirvikoski
Affiliation:
ZCenter for Neurodevelopmental Disorders at Karolinska Institutet (KIND), CAP Research Center, Stockholm, Sweden
V. Pironti
Affiliation:
Cambridge Adult ADHD & ASD Clinic, Cambridge, England
Y. Ginsberg
Affiliation:
TStockholm Center for Eating Disorder R&D Unit, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden
Z. Félegyházy
Affiliation:
IADHD Központ(center) Budapest, Budapest, Hungary
M.P. Garcia-Portilla
Affiliation:
RDept. of Psychiatry, University of Oviedo, School of Medicine, Psychiatry, Oviedo, Spain
P. Asherson
Affiliation:
PSGDP Building, Institute of Psychiatry Psychology and Neuroscience, Kings' College London, London, England
Corresponding
E-mail address:

Abstract

Background Attention-deficit/hyperactivity disorder (ADHD) is among the most common psychiatric disorders of childhood that often persists into adulthood and old age. Yet ADHD is currently underdiagnosed and undertreated in many European countries, leading to chronicity of symptoms and impairment, due to lack of, or ineffective treatment, and higher costs of illness.

Methods The European Network Adult ADHD and the Section for Neurodevelopmental Disorders Across the Lifespan (NDAL) of the European Psychiatric Association (EPA), aim to increase awareness and knowledge of adult ADHD in and outside Europe. This Updated European Consensus Statement aims to support clinicians with research evidence and clinical experience from 63 experts of European and other countries in which ADHD in adults is recognized and treated.

Results Besides reviewing the latest research on prevalence, persistence, genetics and neurobiology of ADHD, three major questions are addressed: (1) What is the clinical picture of ADHD in adults? (2) How should ADHD be properly diagnosed in adults? (3) How should adult ADHDbe effectively treated?

Conclusions ADHD often presents as a lifelong impairing condition. The stigma surrounding ADHD, mainly due to lack of knowledge, increases the suffering of patients. Education on the lifespan perspective, diagnostic assessment, and treatment of ADHD must increase for students of general and mental health, and for psychiatry professionals. Instruments for screening and diagnosis of ADHD in adults are available, as are effective evidence-based treatments for ADHD and its negative outcomes. More research is needed on gender differences, and in older adults with ADHD.

Type
Original article
Creative Commons
This is an open access article under the CC BY-NC-ND license
Copyright
Copyright © European Psychiatric Association 2019

1. Introduction: the European Network Adult ADHD

The European Network Adult ADHD (ENAA) was founded in 2003 to help improve the diagnosis and treatment of ADHD in adults in Europe and beyond. ENAA represents mental health care professionals and researchers from 28 countries with expertise on ADHD in adults (www.eunetworkadultadhd.com). The Section Neurodevelopmental Disorders Across the Lifespan (NDAL) of the European Psychiatric Association (EPA) joined our effort to provide this update of our first Consensus Statement on adult ADHD published in 2010 [Reference Kooij, Bejerot, Blackwell, Caci, Casas-Brugue and Carpentier1].

1.1. Objectives of the updated consensus statement for clinicians

Despite strong evidence on the clinical presentation, genetics, neurobiology, the burden of the disorder, and on safe and effective treatment for ADHD in adults, many people are still underdiagnosed and undertreated. Specialized clinical services remain scarce in most parts of the world, including Europe [Reference Asherson, Buitelaar, Faraone and Rohde2, Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi3]. Our aim is to provide an update of the literature on assessment and treatment of adult ADHD to [Reference Kooij, Bejerot, Blackwell, Caci, Casas-Brugue and Carpentier1] increase awareness on ADHD as an impairing life-long neurodevelopmental condition up to old age [Reference Asherson, Buitelaar, Faraone and Rohde2]; update the assessment procedure for diagnosing ADHD in adults; and [Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi3] give updated recommendations for appropriate treatments.

1.2. Methodology

Creating a Consensus Statement does not follow the same procedure as required for the development of a guideline, such as systematic reviews using formal ratings of the evidence. Most of the authors participated in the development of a first Consensus Statement on adult ADHD in 2010, and were asked to provide an update of the previous text based on new findings in the literature since the time of publication. Subgroups dealing with different subjects were formed. The subgroups reached consensus on the text among themselves before sending it to the first author. The first author put all paragraphs together and edited the text with the help of a few other coauthors (DW, SY, PA, DB). This draft of the manuscript was send to all authors for their comments. The first author checked the comments and implemented adjustments into the text, and send the final version to all authors for agreement. All authors agreed with the final version.

2. Heritability and environment

Family, twin and adoption studies from the last 20 years show that ADHD is a familial disorder with high heritability, indicating that a significant genetic component influences risk for the disorder [Reference Faraone and Doyle4Reference Faraone, Perlis, Doyle, Smoller, Goralnick and Holmgren12]. Environmental factors such as severe institutional deprivation are also likely to play a role, either as main causal factors in a few cases [Reference Stevens, Sonuga-Barke, Kreppner, Beckett, Castle and Colvert13] or by interaction with genetic risks. Family studies indicate a risk to first-degree relatives of 4–5 fold the population rate or higher, with prevalence rates around 20% among first degree relatives [Reference Faraone, Biederman and Monuteaux14]. Data on ADHD in children and adolescents find average heritability of around 76% [Reference Faraone, Perlis, Doyle, Smoller, Goralnick and Holmgren12]. Studies in adult twins using self-rated ADHD symptoms consistently report lower estimates of heritability, around 30–40% [Reference Boomsma, Saviouk, Hottenga, Distel, de Moor and Vink15Reference Larsson, Asherson, Chang, Ljung, Friedrichs and Larsson17]. One reason for lower heritability of adult self-reported ADHD symptoms may be from the use of self-ratings. These lead to lower estimates of heritability compared to informant ratings regardless of age, perhaps due to variable levels of awareness among individuals rating their own ADHD symptoms [Reference Brikell, Kuja-Halkola and Larsson18, Reference Merwood, Greven, Price, Rijsdijk, Kuntsi and McLoughlin19]. Studies combining data across informants [Reference Chang, Lichtenstein, Asherson and Larsson20], or using clinical diagnostic information [Reference Larsson, Chang, D’Onofrio and Lichtenstein21] find heritability estimates for adult ADHD in the same range (70–80%) as for children [Reference Faraone and Larsson22].

2.1. Candidate genes

Early molecular genetic studies of ADHD in children reported genetic associations with several candidate genes. Genetic variants within or near the D4 and D5 dopamine receptor genes provided the most consistent findings supported by meta-analysis [Reference Li, Sham, Owen and He23]. Other specific candidate genes were implicated in the early studies [Reference Faraone, Perlis, Doyle, Smoller, Goralnick and Holmgren12, Reference Gizer, Ficks and Waldman24, Reference Kuntsi, Neale, Chen, Faraone and Asherson25], but none have provided consistent evidence or been replicated in more recent large-scale genome wide association studies. Taken together the traditional neurotransmitter system genes appear to explain only a small amount of the variance in ADHD [Reference Neale, Medland, Ripke, Asherson, Franke and Lesch26]. There is also some converging evidence for the role of genes that fit into a neurodevelopmental network involved in directed neurite outgrowth [Reference Poelmans, Pauls, Buitelaar and Franke27].

2.2. Genome wide association studies (GWAS)

More recent findings have emerged from genome-wide association studies [Reference Demontis, Walters, Martin, Mattheisen, Als and Agerbo28]. The most recent dataset reported included over 20,000 ADHD cases and 35,000 controls. These data were used to estimate that around 30% of the heritability of ADHD is explained by common genetic variation. In total, twelve loci achieved genome-wide significance, including FOXP2; notable because prior work had implicated it in adult ADHD [Reference Ribases, Sanchez-Mora, Ramos-Quiroga, Bosch, Gomez and Nogueira29]. These findings place ADHD firmly on the path to detecting very large numbers of associated common genetic variants as more samples are accrued.

LD regression analyses that estimate genetic correlations between disorders find strong genetic links between ADHD and a range of outcomes including educational performance, depression, obesity, smoking and lung cancer [Reference Demontis, Walters, Martin, Mattheisen, Als and Agerbo28]. A further finding is the very strong genetic correlation between the diagnosis of ADHD, and trait scores in general population samples, demonstrating that ADHD represent the extreme of a continuously distributed trait in the general population [Reference Middeldorp, Hammerschlag, Ouwens, Groen-Blokhuis, Pourcain and Greven30]. These finding confirm the polygenic nature of genetic liability to ADHD.

Rare copy number variants (CNVs) occurring on less than 1% of chromosomes are also known to play a role in a subset of individuals with ADHD [Reference Elia, Gai, Xie, Perin, Geiger and Glessner31, Reference Williams, Zaharieva, Martin, Langley, Mantripragada and Fossdal32]. CNVs were found to be 2-fold more common in children with ADHD within the normal IQ range, and 6-fold higher in those with IQs below 70 [Reference Williams, Zaharieva, Martin, Langley, Mantripragada and Fossdal32]. Specific genes suggested as CNVs linked to ADHD include the nicotinic alpha-7 acetylcholine receptor gene (e.g., [Reference Williams, Franke, Mick, Anney, Freitag and Gill33]), several glutamate receptor genes [Reference Elia, Glessner, Wang, Takahashi, Shtir and Hadley34] and neuropeptide-Y [Reference Lesch, Selch, Renner, Jacob, Nguyen and Hahn35], although these findings remain inconsistent and hard to verify due to low frequency in the population.

2.3. Molecular genetic studies of adult ADHD

Molecular genetic studies of adult ADHD are less advanced, but are expected to confirm some genetic associations identified in childhood and find other genetic associations related to persistence or remission of ADHD in adult life [Reference Chang, Lichtenstein, Asherson and Larsson20]. A preliminary report at the International Neuropsychology meeting (Washington, 2018) found the genetic correlation between child and adult ADHD to be greater than 80%. Most of the current research has been coordinated in Europe by Barbara Franke from the Netherlands for the International Multicentre Persistent ADHD Collaboration (IMPACT) group. This collaboration has successfully generated a multi-site sample of more than 3500 patients and continues to grow. To date several publications highlight potential associations with adult ADHD, some but not all of which are shared with genetic association findings in children [Reference Franke, Hoogman, Arias Vasquez, Heister, Savelkoul and Naber36Reference Sanchez-Mora, Ribases, Ramos-Quiroga, Casas, Bosch and Boreatti-Hummer42].

2.4. Environmental factors

It has been known for a long time that environmental factors are associated with ADHD [Reference Banerjee, Middleton and Faraone43], particularly prenatal risk factors such as exposure to alcohol and drugs, valproic acid, high blood pressure, maternal stress during pregnancy, as well as preterm birth and low birth weight [Reference Botting, Powls, Cooke and Marlow44Reference Cohen, Meador, Browning, May, Baker and Clayton-Smith46]. However sophisticated study designs are needed to clarify whether these association reflect direct effects of the environmental exposure or reflect genetically correlated risk measures. For example, although smoking during pregnancy is clearly associated with offspring ADHD, this association appears to be entirely accounted for by the genetic correlation between maternal smoking and offspring ADHD [Reference Gustavson, Ystrom, Stoltenberg, Susser, Suren and Magnus47]. In contrast, evidence from Romanian adoptees suggests that severe early deprivation is causally related to ADHD in a dose dependent way [Reference Stevens, Sonuga-Barke, Kreppner, Beckett, Castle and Colvert13]. Gene by environment interactions (G x E) have been proposed and may explain some of the missing heritability seen between heritability estimates derived from twin (0.76) and molecular genetic (0.22) data. However, to date no G x E effects have been clearly identified. The findings to date indicate that much more work is needed to understand the interplay between genetic and environmental risks.

3. Neurobiology of ADHD

3.1. Neuro-imaging: evidence for atypical gray and white matter areas

Structural brain scans of adults with ADHD showed grey matter abnormalities in several brain areas, including the right frontal and prefrontal areas [Reference Depue, Burgess, Bidwell, Willcutt and Banich48, Reference Pironti, Lai, Muller, Dodds, Suckling and Bullmore49], anterior cingulate [Reference Makris, Seidman, Valera, Biederman, Monuteaux and Kennedy50Reference Amico, Stauber, Koutsouleris and Frodl52], the basal ganglia and the cerebellum [Reference Seidman, Biederman, Liang, Valera, Monuteaux and Brown53Reference Proal, Reiss, Klein, Mannuzza, Gotimer and Ramos-Olazagasti56] with some preliminary research also showing abnormalities of the visual cortex [Reference Ahrendts, Rusch, Wilke, Philipsen, Eickhoff and Glauche57]. Additionally, cortical thickness was found to be reduced in adult ADHD [Reference Proal, Reiss, Klein, Mannuzza, Gotimer and Ramos-Olazagasti56, Reference Duerden, Tannock and Dockstader58, Reference Almeida, Ricardo-Garcell, Prado, Barajas, Fernandez-Bouzas and Avila59]. Some evidence suggests that grey matter abnormalities, in some subcortical regions, are more pronounced in children than adults. This might reflect the effects of age, medication, intrinsic heterogeneity of the ADHD syndrome, or a combination thereof [Reference Frodl and Skokauskas51, Reference Nakao, Radua, Rubia and Mataix-Cols60Reference Hoekzema, Carmona, Ramos-Quiroga, Richarte Fernandez, Picado and Bosch64].

Despite these reported findings the latest mega-analysis conducted by the Enigma consortium found no significant differences in brain structure between adult ADHD and controls; although, small but significant differences were found in children for subcortical regions including the accumbens, amygdala, caudate, hippocampus, putamen and intracranial volume with effects ranging from d =.10–.15 [Reference Hoogman, Buitelaar, Faraone, Shaw, Franke and group E-Aw65]. These findings indicate that while there are structural changes in subcortical brain regions in ADHD in children, these are relatively subtle effects that dissipate with increasing age.

Diffusion tensor imaging (DTI) highlighted that white matter tracts, including fronto-occipital, fronto-striatal, temporal and temporo-occipital fasciculi and part of the corpus callosum, bear microstructural abnormalities [Reference Dramsdahl, Westerhausen, Haavik, Hugdahl and Plessen6671]. Additionally, some findings also linked microstructure variability to symptomatology such that greater inattention but not hyperactivity-impulsivity was associated with significantly lower fractional anisotropy (that is lower microstructural integrity) in the left uncinate and inferior fronto-occipital fasciculi compared to controls [Reference Shaw, Sudre, Wharton, Weingart, Sharp and Sarlls70]. These results indicate that structural deficits in ADHD are not just confined to specific regions but involve interconnections among large scale brain networks [Reference Cortese, Imperati, Zhou, Proal, Klein and Mannuzza68, Reference Konrad, Dielentheis, El Masri, Bayerl, Fehr and Gesierich71Reference Liston, Cohen, Teslovich, Levenson and Casey73].

3.2. Functional neuroimaging

Regarding functional MRI (fMRI) studies, task-based and resting-state findings converge. Meta-analyses show that ADHD is associated with dysfunctions in several domain-specific fronto-striatal and fronto-cerebellar neural networks. Thus a meta-analysis of 39 child and 16 adult ADHD fMRI studies concluded that in ADHD there are significant dysfunctions in multiple neuronal systems involved in higher-level cognitive functions [Reference Cortese, Kelly, Chabernaud, Proal, Di Martino and Milham74]. These include hypoactivations in the frontoparietal executive control network, putamen, and ventral attention network, which is consistent with the classical model of ADHD as a disorder of deficient fronto-striatal activation.

Hyperactivations are also seen in regions of the default mode and visual networks, which support the contemporary view that ADHD is associated with faulty regulation of relationships between default mode and task positive networks. Similar findings come from meta-analyses, which show consistent underactivation in inferior fronto-striatal networks during cognitive tasks [Reference Hart, Radua, Nakao, Mataix-Cols and Rubia75], in dorsolateral fronto-striato-parietal networks during attention tasks [Reference Hart, Radua, Nakao, Mataix-Cols and Rubia75], and in fronto-cerebellar networks for timing functions [Reference Hart, Radua, Mataix-Cols and Rubia76]; in addition to abnormally enhanced activation in default mode regions [Reference Hart, Radua, Mataix-Cols and Rubia76].

The recent focus on resting state fMRI (RS-fMRI) identified multiple intrinsic neural circuits, reflecting functional connectivity within and between regions which is continuously encoded in the spontaneous activity of the brain [Reference Yeo, Krienen, Sepulcre, Sabuncu, Lashkari and Hollinshead77]. The intrinsic fronto-parietal, dorsal attentional, visual, motor and default mode networks all overlap with regions showing differential task activations during inhibition, attention, or working memory tasks in ADHD compared to controls [Reference Castellanos and Proal78]. Despite the wealth of established findings from fMRI and RS-fMRI studies of ADHD, cross-sectional neuroimaging data is correlational in nature and causal inferences cannot yet be made.

More recently outcome studies of children diagnosed with ADHD has been able to compare functional brain change in adults with persistent and remitted ADHD and compare these to age-matched controls. The largest such follow-up study to date, of 205 children with ADHD, found that persistence of ADHD was associated with loss of the balance of connections within the default mode network, and connections between the default mode and those supporting attention and cognitive control. In contrast there were no differences in these networks between those whose ADHD had remitted and non-ADHD controls [Reference Sudre, Szekely, Sharp, Kasparek and Shaw79].

Overall, despite the wealth of established findings from fMRI and RS-fMRI studies of ADHD, cross-sectional neuroimaging data is correlational in nature and causal inferences cannot yet be made. The finding that certain functional brain changes are seen to differ between persistent compared to remitted cases of childhood ADHD sheds some light on likely causal processes, but further longitudinal data is still required before firm conclusions can be drawn.

3.3. Neuropsychological and electrophysiological tests

As a group, individuals with ADHD are characterized by altered neuropsychological functioning across a variety of executive function (EF) measures. However, thus far there is neither a neurobiological nor a neuropsychological test (battery) for ADHD with sufficient positive predictive power to establish the diagnosis at the individual level [Reference Wasserman and Wasserman80]. In one study, the vast majority of neuropsychological instruments showed poor discriminative ability compared to clinical assessment measures such as the ASRS Screener v1.1 and the DIVA 2.0 Diagnostic Interview for ADHD in adults, with an overall classification accuracy ranging from 53% to 66% [Reference Pettersson, Soderstrom and Nilsson81]. Nevertheless, when used in combination with the DIVA 2.0, objective cognitive performance tests measuring omission and commission errors, and physical activity, were found to increase the correct classification of adult ADHD [Reference Pettersson, Soderstrom and Nilsson81]. There is currently insufficient evidence to warrant the use of neuropsychological testing to determine the diagnosis of ADHD [Reference Mostert, Onnink, Klein, Dammers, Harneit and Schulten82] or to predict impairment in major life domains [Reference Barkley and Fischer83].

Moreover, clinicians should also be aware of the possibility that a few individuals may feign ADHD symptoms to gain external incentives, like stimulant medication or special academic accommodations. There is some evidence supporting the effectiveness of performance validity tests (PVTs) in differentiating between genuine and feigned ADHD compared to rating scales [Reference Musso and Gouvier84].

Electrophysiological studies suggest that brain dysfunctions are involved in the central components of ADHD in both children and adults [Reference Bekker, Overtoom, Kenemans, Kooij, De Noord and Buitelaar85Reference Seidman, Valera and Makris89], although the finding of increased DAT density remains controversial [Reference Swanson, Elliott, Greenhill, Wigal, Arnold and Vitiello90, Reference Volkow, Wang, Newcorn, Fowler, Telang and Solanto91].

Data from Electro Encephalography (EEG) is relatively scarce in adult ADHD. Generally, EEG studies of ADHD find similar deficits in adults and children, while some findings change with age and might be sensitive to developmental changes [Reference Retz and Klein92]. Despite US Food and Drug Administration approval of an EEG device (2013) that assists in the diagnosis of ADHD subtypes [Reference Snyder, Rugino, Hornig and Stein93Reference Liechti, Valko, Muller, Dohnert, Drechsler and Steinhausen95], this remains controversial [Reference Arns, Loo, Sterman, Heinrich, Kuntsi and Asherson96]. EEG tests are not sufficiently accurate but could be useful to increase diagnostic certainty.

4. ICD and DSM criteria for ADHD

There are two diagnostic manuals used to diagnose ADHD: The Diagnostic and Statistical Manual of Mental Disorders (DSM) and the International Statistical Classification of Diseases and Related Health Problems (ICD). As ADHD has been recognized as a disorder affecting individuals across the lifespan, the diagnostic criteria for adolescents and adults have been adjusted in the DSM-5, published in May 2013:

  1. 1) ADHD is now in the chapter Neurodevelopmental Disorders, which includes conditions associated with factors affecting the brain development.

  2. 2) Diagnostic criteria have been adapted by adding some examples describing how ADHD symptoms are expressed across the lifespan.

  3. 3) The age of onset criteria has been changed requiring several symptoms to be present before age of 12 years, instead of some symptoms and impairment by age 7.

  4. 4) The term “subtype” has been replaced by “presentation”, reflecting the variation of ADHD symptoms within the same individual during the lifespan.

  5. 5) The symptom threshold required has been reduced to 5 symptoms instead of six for older adolescents and adults (>17 years) in either the inattention or hyperactive/impulsive domain.

  6. 6) Criteria requiring significant impairment has been modified to “clear evidence that symptoms interfere with or reduce the quality of social, academic and occupational functioning”, with specifiers regarding severity level.

  7. 7) The presence of Autism Spectrum Disorder (ASD) is no longer an exclusion criterion, consistent with evidence showing their frequent co-occurrence.

  8. 8) ADHD Not Otherwise Specified (NOS) has been changed into Other Specified ADHD and Unspecified ADHD.

The revision of ICD-10, ICD-11 has been published in June 2018. ICD-11, developed by the World Health Organization now refers to ADHD as Attention Deficit Hyperactivity Disorder, instead of previously Hyperkinetic Disorder (HKD) [Reference Faraone, Sergeant, Gillberg and Biederman97]. It now uses similar requirements as the DSM-5 regarding age of onset, and the same 3 presentation types. In Europe, ICD codes are often used for statistics on mortality, morbidity and by insurance agencies for health-related reimbursements [Reference Goodheart98], whereas DSM is primarily used in clinical practice by licensed mental health care professionals [Reference Kupfer, Kuhl and Wulsin99].

The diagnostic assessment starts by evaluation of self-reported symptomatology. The clinical interview is essential for diagnosing ADHD in adults, which investigates the characteristic symptoms and impairments of ADHD in both childhood and adulthood. In children and adolescents, informants’ ratings are higher correlated with heritability and cognitive and EEG findings than self-ratings [Reference Merwood, Greven, Price, Rijsdijk, Kuntsi and McLoughlin19]. Also prevalence and persistence rates increase when parent reports are used [Reference Merwood, Greven, Price, Rijsdijk, Kuntsi and McLoughlin19]. In adults this may be slightly different, as some research shows that the adult patient is the best informant [Reference Kooij, Boonstra, Swinkels, Bekker, de Noord and Buitelaar100]. The presence of a family member however (a parent and/or the partner) during the assessment can still provide valuable additional information, e.g. on severity and its translation into daily activities.

There is compelling evidence that a cut-off of four current symptoms is the most appropriate for an adult diagnosis [Reference Solanto, Wasserstein, Marks and Mitchell101, Reference Kooij, Buitelaar, van den Oord, Furer, Rijnders and Hodiamont102]. However, due to concern about the possibility of an artificial increase in the prevalence of the disorder, DSM-5 lowered the threshold for diagnosing ADHD from six to five symptoms for those older than 17 years of age. Several items have been expanded by some illustrative examples to facilitate the recognition of the disorder throughout development. Although not included in the criteria as such, behaviors reflecting executive dysfunction usually appear clearly during the assessment, when patients describe problems with organization, facing daily responsibilities, solving problems, managing time and self-regulating (inhibiting) behaviors.

DSM-5 also highlights the importance of mood lability and emotional dysregulation as “an associated feature that support the diagnosis”. Although emotional dysregulation may dominate the clinical presentation [Reference Barkley103Reference Brown105], it is not a criterion for classifying individuals as it lacks specificity, occurring in many other mental health conditions.

DSM-IV required that symptoms and impairment were present before age 7, but as research demonstrated no differences between children with an age of onset before and after age 7 [Reference Polanczyk, Laranjeira, Zaleski, Pinsky, Caetano and Rohde106] this criterion was changed to several symptoms by age 12. Similar findings have also been reported regarding adults reporting later-onset of symptoms [Reference Faraone, Kunwar, Adamson and Biederman107, Reference Chandra, Biederman and Faraone108], and there is disagreement both within and across sources concerning recall of symptom onset [Reference Moffitt, Houts, Asherson, Belsky, Corcoran and Hammerle109]. The fact that adults with ADHD frequently fail to recall childhood behavior led to the suggestion that clinicians take note that the onset of the disorder was during the developmental period, or they should use age 16 years as the upper age limit. Using this criteria captured all cases of childhood ADHD and 99% of adults with the disorder [Reference Kieling, Kieling, Rohde, Frick, Moffitt and Nigg110]. The decision of DSM-5 to extend the age of onset to 12 instead of 16 may have a negative impact on adults with ADHD who have difficulties with retrospective recall of childhood behaviors, and may not receive the diagnosis for this reason. This may be particularly true for those who had some compensation due to high intelligence, or lived in a highly structured or supported environment, or presented predominantly with inattentive symptoms. In such cases, the presence of a collateral informant (generally a parent or spouse) is of great value. Many adults with ADHD that are used to their lifelong symptoms, have limited awareness of how ADHD symptoms adversely impact their interpersonal relationships and affect their life; some reporting higher symptoms but lower impairments or vice versa.

Such inconsistency has been attributed to a lack of introspection and an incoherent self-view [Reference Morstedt, Corbisiero, Bitto and Stieglitz111, Reference Prevatt, Proctor, Best, Baker, Van Walker and Taylor112], and supports the utility of a collateral informant. If a significant other is not available, school reports or social care reports may be helpful.

4.1. Clinical picture

4.1.1. Inattention and hyperfocus

Patients with mainly inattention problems are often slow to think and formulate due to distractions. They may formulate things in a long-winded and tangential way, losing themselves in irrelevant details and having difficulty making decisions. A difficulty for the clinician is that this may hinder the diagnostic assessment. Patients may also over-concentrate or ‘hyperfocus’. This phenomenon most commonly occurs when engaged in activities that the patient finds very interesting and/or provide instant gratification, such as computer games or online chatting. For such activities, concentration may last for hours on end, in a very focused manner.

4.1.2. Hyperactivity

With respect to hyperactivity, adults do not present in the same way as children. Their hyperactivity usually manifests in a more subtle way. Clinicians need to assess their feelings of restlessness. A first impression of mobility is not definitive; sitting calmly during the diagnostic assessment does not exclude any ADHD. Hyperactivity in adults often manifests itself as feelings of continuous inner restlessness or agitation, talking too much, ceaseless mental activity, not being able to relax properly or needing alcohol or drugs to relax and/or sleep. Hyperactivity and/or restlessness may be temporarily relieved by the patient engaging in excessive sport activities, and in such cases the person may suffer physical ailments as the body may have insufficient time to recover and/or due to sustained injuries.

4.1.3. Impulsivity

Impulsive behavior and associated interpersonal conflicts often have consequences for relationships with family, friends, colleagues and employers. It may also seriously impact on personal finance when impulsive spending causes debt. Impulsive binge behaviors may also be present (e.g. binge eating), often to combat restlessness or due to a need for immediate gratification. Closely related to impulsivity are ‘sensation seeking’ behaviors when patients may seek out excitement from novel and thrilling stimuli. These often involve risk taking behaviors such as playing with fire, reckless driving, sexual risks, and provocative behavior leading to fights.

4.1.4. Emotional dysregulation

Emotional dysregulation is listed by DSM-5 as a characteristic feature of ADHD, supporting the diagnosis [113]. The type of emotional dysregulation seen in ADHD has been characterized as deficient self-regulation of emotional symptoms such as irritability, frustration and anger [Reference Skirrow and Asherson114], and low frustration tolerance, temper outbursts, emotional impulsivity, and mood lability [Reference Surman, Biederman, Spencer, Miller, McDermott and Faraone115]. Emotional dysregulation in ADHD is different from episodic symptoms such as marked sustained irritability occurring within the context of altered mood states, such as an episode of depression or mania. In ADHD, emotional symptoms tend to reflect short lived exaggerated changes, often in response to daily events, with rapid return to baseline within a few hours [Reference Skirrow and Asherson114]. Whether the type of emotional instability seen in ADHD is qualitatively different to that seen in other chronic conditions such as borderline personality disorder or post-traumatic stress remains unclear.

4.1.5. Excessive mind wandering

Another common feature of adult ADHD is excessive mind wandering, also referred to as mental restlessness [Reference Seli, Smallwood, Cheyne and Smilek116Reference Weyandt, Iwaszuk, Fulton, Ollerton, Beatty and Fouts118]. In DSM-5 mind wandering is briefly mentioned as the occurrence of unrelated thoughts. Although mind wandering is a universal experience, some forms of mind wandering are detrimental because they interfere with task performance. Adults with ADHD frequently report a distractible mental state with multiple unrelated thoughts that are constantly on the go and jump from one topic to another [Reference Asherson119, Reference Mowlem, Skirrow, Reid, Maltezos, Nijjar and Merwood120]. Mind wandering is also a feature of other mental health disorders such as depressive or obsessive disorders. However, in ADHD mind wandering is characterized by unfocused, short lived distractible thoughts with no pattern of repeated thoughts or abnormality of content. Research found that excessive mind wandering was strongly correlated with ADHD symptoms, was a strong predictor of the diagnosis (sensitivity and specificity around 90% for case-control differences), co-varied with ADHD symptoms over a 6-month period, and was a better predictor of ADHD-related impairments than the inattentive and hyperactive-impulsive symptoms of ADHD [Reference Mowlem, Skirrow, Reid, Maltezos, Nijjar and Merwood120]. In ADHD it can be measured using the Mind Excessively Wandering Scale [Reference Seli, Smallwood, Cheyne and Smilek116, Reference Weyandt, Iwaszuk, Fulton, Ollerton, Beatty and Fouts118, Reference Mowlem, Skirrow, Reid, Maltezos, Nijjar and Merwood120] (Table 1).

Table 1 Examples of ADHD-related symptoms.

4.1.6. Behavioral self-regulation (executive function deficits)

ADHD has been described as a disorder of executive functions such as inhibition and working memory. These include problems organizing, prioritizing and initiating work; focusing, sustaining and shifting attention to tasks; regulating alertness, sustaining effort and processing speed; managing frustration and regulating emotions; utilizing working memory and accessing recall; and monitoring and self-regulation of behavior [Reference Brown121, Reference Barkley122]. Although clinically these are good descriptions of the types of difficulties experienced by adults with ADHD, behavioral measures do not correlate well with cognitive or neuropsychological tests of executive control [Reference Brown121Reference Bijlenga, Jasperse, Gehlhaar and Sandra Kooij123]. A distinction needs to be made between rating scale measures of behaviours reflecting self-regulation of behavior referred to as EF (behavioral) deficits, and the results of neurocognitive tests of EFs such as working memory and inhibition. Neuropsychological test scores reflecting executive functioning lack ecological validity in that they have no significant relationship to behavioural rating scale measures of EF [Reference Toplak, West and Stanovich124]. The EF test scores also are very poor at predicting impairment in a variety of domains of major life activities, compared to EF behavioural rating scales [Reference Barkley and Fischer125].

4.1.7. Burden of ADHD

The impairments associated with ADHD across the lifespan are impressive. ADHD is associated with learning difficulties, school dropout, underachievement at work [Reference de Graaf, Kessler, Fayyad, ten Have, Alonso and Angermeyer126], frequent job changes [Reference Fredriksen, Dahl, Martinsen, Klungsoyr, Faraone and Peleikis127], chronic fatigue [Reference Rogers, Dittner, Rimes and Chalder128], financial problems, gambling and internet use [Reference Altszuler, Page, Gnagy, Coxe, Arrieta and Molina129, Reference Bielefeld, Drews, Putzig, Bottel, Steinbuchel and Dieris-Hirche130], home and traffic accidents leading to increased mortality rates [Reference Barkley and Cox131Reference Chang, Quinn, Hur, Gibbons, Sjolander and Larsson133], relationship difficulties and intimate partner violence [Reference Guendelman, Ahmad, Meza, Owens and Hinshaw134, Reference Buitelaar, Posthumus and Buitelaar135], early onset of addiction [Reference Kaye, Gilsenan, Young, Carruthers, Allsop and Degenhardt136], teenage pregnancies and sexual transmitted diseases [Reference Chang, Lichtenstein, D’Onofrio, Almqvist, Kuja-Halkola and Sjolander137, Reference Hosain, Berenson, Tennen, Bauer and Wu138], a two-fold increased smoking rate [Reference McClernon and Kollins139], an increased number of suicide attempts and self-harm in adolescents [Reference Furczyk and Thome140, Reference Swanson, Owens and Hinshaw141], and increased criminality [Reference Ginsberg, Hirvikoski and Lindefors142, Reference Young, Gudjonsson, Asherson, Theobald, Oliver and Scott143]. Moreover, physical disorders and ailments may become chronic due to forgetfulness, health problems induced by a negative lifestyle, poor eating and sleeping habits, and lack of health care follow-up [Reference Bijlenga, van der Heijden, Breuk, van Someren, Lie and Boonstra144Reference Instanes, Klungsoyr, Halmoy, Fasmer and Adult ADHD147]. ADHD has further been associated with auto-immune diseases [Reference Hegvik, Instanes, Haavik, Klungsoyr and Engeland148], obesity [Reference Cortese, Moreira-Maia, St Fleur, Morcillo-Penalver, Rohde and Faraone149], and physical multi-morbidity. In one large study, individuals with more than 4 diseases had over more than 3-fold higher odds of possible ADHD [Reference Stickley, Koyanagi, Takahashi, Ruchkin, Inoue and Kamio146]. The risk of diabetes, hypertension, cardiovascular disease and cancer, that are related to obesity, may be increased as well. An additional burden on family life may be the presence of one or more children with ADHD, which happens frequently due to the high familial risks of the disorder.

Clinicians should also be aware that high functioning adults with ADHD may not present with a typical pattern of functional impairments in their daily life. Adaptive or compensatory skills can develop that mask the more overt behavioral problems related to ADHD [Reference Asherson, Akehurst, Kooij, Huss, Beusterien and Sasane150]. Some may find work that is well suited to their symptom profile. Furthermore, in ADHD neurocognitive performance and inattentive symptoms are sensitive to the salience of task activities [Reference Tegelbeckers, Bunzeck, Duzel, Bonath, Flechtner and Krauel151, Reference Bozhilova, Michelini, Kuntsi and Asherson152]. Such people with ADHD may excel in certain aspects of their lives, but still be impaired in others, such as more routine and mundane tasks such as paying bills, looking after the house, or developing stable social relationships. Problems can include subjective distress from symptoms such as mental and physical restlessness, sleep problems, and emotional instability; and the use of drugs such as cannabis or alcohol to reduce these symptoms.

5. Prevalence of ADHD across the lifespan

In childhood, ADHD is among the most common psychiatric disorders with a prevalence rate of 3–5 % [Reference Polanczyk, Salum, Sugaya, Caye and Rohde153]. For this age group, well established diagnostic and treatment services are available throughout most of Europe. In the last four decades, a large body of evidence has accumulated, showing how in the majority of cases ADHD is a lifespan disorder, persisting as either the full blown disorder, or in ‘partial remission’ with persistence of some symptoms and continued clinical and psychosocial impairments [Reference Wood, Reimherr, Wender and Johnson154Reference Asherson, Chen, Craddock and Taylor161]. The prevalence of ADHD in adults across twenty countries was recently estimated at 2.8%, with a range between 1.4 - 3.6% [Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi3]. ADHD was also found in a Dutch population study to persist into old age (> 60 years) with a prevalence of 2.8–4.2% depending on cut-off (6 or 4 current symptoms respectively), and associated with impairment [Reference Michielsen, Semeijn, Comijs, van de Ven, Beekman and Deeg162Reference Torgersen, Gjervan, Lensing and Rasmussen166]. ADHD in older adults is accompanied by increased rates of mood and anxiety symptoms, general health problems, conflicts, divorce, loneliness, and a lower income, showing a similar pattern of problems as in younger age groups. Research exploring the needs for treatment of older adults with ADHD has commenced, and the first treatment protocol of older adults with ADHD has been published [Reference Kooij, Michielsen, Kruithof and Bijlenga167].

5.1. Sex issues

Sex differences in ADHD diagnosis are well documented, with girls being less likely to be diagnosed, and sex ratios ranging between 1:5 to 1:9 [Reference Rucklidge168]. Such discrepancy is less evident in epidemiological research in children where the sex ratio is 1:3, suggesting under recognition of ADHD in girls in the clinic. In both epidemiological and clinical studies of adult ADHD the sex ratio is closer to 1:1 [Reference Barkley, Murphy and Fischer169]. Several factors may explain the sex disparity during the lifespan. Girls with ADHD may have less hyperactive/impulsive symptoms than boys; because of higher disruptiveness, boys are more likely to be referred by parents and teachers, whereas girls remain undiagnosed [Reference Biederman, Mick, Faraone, Braaten, Doyle and Spencer170]. Missed diagnosis may be due to a lack of knowledge and recognition of ADHD in girls by health care professionals, and to the presence of other conditions: low self-esteem, anxiety as well affective disorders occur frequently in females with ADHD, and it is possible that ADHD symptoms may be mistakenly attributed to such comorbidities [Reference Vingilis, Erickson, Toplak, Kolla, Mann and Seeley171, Reference Quinn and Madhoo172]. Females with ADHD appear to develop better coping strategies than males, and are better able to mask symptoms of ADHD throughout childhood. However, this may no longer work well when they face salient life challenges, such as leaving school, attending college or university, commencing employment, managing intimate relationships, and taking responsibility for their own life decisions [Reference Ptacek, Kuzelova, Papezova and Stepankova173]. Different genetic liability between the sexes [Reference Arnett, Pennington, Willcutt, DeFries and Olson174], as well neuroendocrine factors affecting the dopaminergic system, such as thyroid and estrogen hormones [Reference Quinn and Madhoo172, Reference Argumedo, Sanz and Olguin175], have all been also suggested to play a role in the masking of ADHD in girls and women. In addition, girls and women with ADHD are less well studied than males.

Women with ADHD are particularly vulnerable to early adversities, health and mental health problems compared to controls [Reference Fuller-Thomson, Lewis and Agbeyaka176]. A higher prevalence of insomnia, chronic pain, suicidal ideation, generalized anxiety disorder, depressive disorders, a greater vulnerability to nicotine dependence [Reference Fuller-Thomson, Lewis and Agbeyaka176, Reference Van Voorhees, Mitchell, McClernon, Beckham and Kollins177] and an increased likelihood of risky sexual behaviors [Reference Hosain, Berenson, Tennen, Bauer and Wu138] has been reported in women with ADHD in comparison with controls.

5.2. Transition of adolescents to adult mental health services

As two-thirds or more of children with ADHD continue to have impairment into adulthood [Reference Faraone, Biederman and Mick178], many require the transition from child to adult mental health services. However, transition between services is generally difficult, placing youths with ADHD in an even more vulnerable position [Reference Casey and Jones179]. Research shows that disruption of care during transition adversely affects clinical outcome [Reference Singh180, Reference While, Forbes, Ullman, Lewis, Mathes and Griffiths181]. Clear recommendations have been formulated, mostly based on clinical experience, to facilitate successful transition of patients with ADHD from child to adult mental health services [Reference Kooij, Bejerot, Blackwell, Caci, Casas-Brugue and Carpentier1, Reference NICE182Reference Young, Adamou, Asherson, Coghill, Colley and Gudjonsson185]. These are a) transition should ideally be completed by the age of 18 years, b) transition should be planned in advance by both child and adult mental health services, c) young people with ADHD and their parents should have sufficient information regarding the transition process (e.g. psychoeducational material including available services), d) both continued parental care and child’s growing autonomy should be considered, e) if necessary a formal meeting involving child and adult mental health services (with specific knowledge on this age group) and patients and parents should be considered. All these can help to prevent the drop-out of young people with ADHD from services. However, the reality is quite different, as indicated by two reviews [Reference Singh, Paul, Ford, Kramer, Weaver and McLaren186, Reference Tatlow-Golden, Gavin, McNamara, Singh, Ford and Paul187]. Compared to other diagnostic groups, youth with ADHD were significantly less likely to be referred, they were more likely to refuse referral, and a significant number remained in child services well beyond their 18th year. Studies also have found transition policy deficits [Reference Singh, Paul, Ford, Kramer, Weaver and McLaren186, Reference McNamara, McNicholas, Ford, Paul, Gavin and Coyne188], suboptimal experience of transition when it does occur [Reference Singh, Paul, Ford, Kramer, Weaver and McLaren186, Reference Swift, Hall, Marimuttu, Redstone, Sayal and Hollis189], a dearth of adult ADHD services [Reference Hall, Newell, Taylor, Sayal and Hollis190], and a lack of expertise on ADHD amongst adult clinicians [Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi3, Reference Coghill191]. This suggests there is an urgent need for a multifaceted approach combining transition specific clinical guidelines, and funding for the training the training of clinicians, to ensure that those in need of ongoing intervention may successfully transition to adult services.

5.3. Late-onset ADHD?

Recent longitudinal studies have indicated that besides typical childhood onset ADHD, with the full diagnostic criteria being met before the age of 12 years, there may be later-onset cases with onset of the full diagnostic criteria beyond this age [Reference Skirrow and Asherson104, Reference Swift, Hall, Marimuttu, Redstone, Sayal and Hollis189, Reference Hall, Newell, Taylor, Sayal and Hollis190]. These findings have proven controversial due to severe methodological limitations [Reference Sibley, Rohde, Swanson, Hechtman, Molina and Mitchell192, Reference Faraone and Biederman193], however the large majority of later onset cases appear to meet the DSM-5 age of onset criteria of several symptoms by the age of 12 [113]. Late onset of symptoms was evaluated in the control arm of the long-term follow-up of the Multimodal Treatment study of ADHD (MTA). In most cases, other factors were present that could discount the late onset of ADHD symptoms and exclude the diagnosis of ADHD [Reference Caye, Sibley, Swanson and Rohde194], such as symptoms representing nonimpairing cognitive fluctuations, a comorbid disorder, or the cognitive effects of substance use [Reference Sibley, Rohde, Swanson, Hechtman, Molina and Mitchell192]. However, there remained a very small sample of adolescent onset cases. Another population cohort study found that the majority of those with apparent late-onset ADHD had high ADHD scores at least one point in childhood, suggesting that they may have been misclassified on the basis of their score at age 12 years [Reference Cooper, Hammerton, Collishaw, Langley, Thapar and Dalsgaard195]. These cases with high score before the age of 12 years might not have met full criteria before the age of 12 years, but would meet the current DSM-5 criteria for several symptoms in childhood. One conclusion is that clinicians should be aware that subthreshold cases of ADHD during childhood might go on to meet the full diagnostic criteria as older adolescents. Clinicians should take care to fully assess impairment, psychiatric history, and substance use when diagnosing and treating cases with apparent later-onset ADHD [Reference Sibley, Rohde, Swanson, Hechtman, Molina and Mitchell192].

6. Screening and diagnostic assessment

6.1. Screening

Several screening tools are available for ADHD in adults. The validated tool recognized by the World Health Organization (WHO) and updated for DSM-5 criteria is the Adult ADHD Self report Rating Scale (ASRS). This revised ASRS was studied in managed care, the general population and in a clinical group. The sensitivity was 91.4%; specificity 96.0%; AUC, 0.94; PPV, 67.3% [Reference Ustun, Adler, Rudin, Faraone, Spencer and Berglund196]. The previous version of the ASRS has been translated into many languages (see http://www.hcp.med.harvard.edu/ncs/asrs.php). The Wender Utah Rating Scale assesses besides ADHD a broader spectrum of symptoms that often accompany ADHD or are comorbid. Several other scales that ask about the 18 items as defined in the DSM-5 to classify ADHD are available, see Table 2.

A key question is who should be screened for ADHD. In general, since the hallmark of adult ADHD is a chronic trait-like condition that emerges out of childhood or early adolescence, anyone presenting with such a clinical picture should be screened [Reference Asherson, Buitelaar, Faraone and Rohde2]. This should include those with chronic histories of inattentive, restless or impulsive behaviors, as well as those with emotional instability. Targeted groups where rates of ADHD are significantly increased and should therefore be screened include family members of people with ADHD, and those with a history of behavioral problems, any chronic mental health disorder including anxiety, depression, cyclothymia, personality disorder, bipolar disorder, substance use disorders, those with multiple physical diseases [Reference Stickley, Koyanagi, Takahashi, Ruchkin, Inoue and Kamio146], and those within the criminal justice system [Reference NICE197].

6.2. Diagnostic assessment

For diagnostic assessment, the use of a semi-structured diagnostic interview is advised, such as the Diagnostic Interview for ADHD in adults, second edition (DIVA 2.0) [Reference Kooij198], based on the DSM-IV-TR criteria. DIVA 2.0 is available online without charge, currently in 19 languages (www.divacenter.eu). The Conner’s Adult ADHD Diagnostic Interview for DSM-IV (CAADID) has been validated in English and Spanish [Reference Ramos-Quiroga, Bosch, Richarte, Valero, Gomez-Barros and Nogueira199]. DIVA 2.0 has been validated in two European populations [Reference Pettersson, Soderstrom and Nilsson81, Reference Ramos-Quiroga, Bosch, Richarte, Valero, Gomez-Barros and Nogueira199], and is increasingly used in international research. A DIVA 2.0 app is available in the App and Google Play stores. The update of DIVA 2.0 for DSM-5 criteria into ‘DIVA-5’ in all languages is ongoing. DIVA-5-ID, for people with Intellectual Disability (ID) and Young DIVA, for children and adolescents, are new versions of DIVA-5. An alternative is ACE+ (http://www.psychology-services.uk.com/resources.htm), a semi-structured diagnostic interview to assess ADHD in adults (>16 years). ACE + assesses the core symptoms of ADHD in both adulthood and childhood, the extent to which they impair functioning, and the presence of co-existing conditions. ACE + is currently online available in 7 languages, with more translations underway. For these and other diagnostic tools, see Table 2.

6.3. The assessment process of ADHD and comorbidity

Diagnosis of ADHD is based on a careful and systematic assessment of a lifetime history of symptoms and impairment. Central to this process is the assessment of childhood-onset and current symptoms of ADHD, and the presence of symptoms and impairment in at least two domains (school, work, home, interpersonal contacts). For this lifetime assessment, collateral information from family members and spouse are useful. It is important to take a full medical history of psychiatric and somatic conditions, as well as a family history of psychiatric and neurological problems. High intelligence should be taken into account as a potential moderator in the diagnostic assessment, as ADHD is underdiagnosed in patients with high intelligence because they use more compensatory strategies [Reference Rommelse, van der Kruijs, Damhuis, Hoek, Smeets and Antshel200]. Clinicians should also be aware that high functioning adults with ADHD may not present with a typical pattern of functional impairments in their daily life. Adaptive or compensatory skills can develop that mask the more overt behavioral problems related to ADHD [Reference Asherson, Akehurst, Kooij, Huss, Beusterien and Sasane150]. Some may find work that is well suited to their symptom profile. Furthermore, in ADHD neurocognitive performance and inattentive symptoms are sensitive to the salience of task activities [Reference Tegelbeckers, Bunzeck, Duzel, Bonath, Flechtner and Krauel151, Reference Bozhilova, Michelini, Kuntsi and Asherson152]. Such people with ADHD may excel in certain aspects of their lives, but still be impaired in others, such as more routine and mundane tasks such as paying bills, looking after the house, or developing stable social relationships. Problems can include subjective distress from symptoms such as mental and physical restlessness, sleep problems, and emotional instability; and the use of drugs such as cannabis or alcohol to reduce these symptoms.

Table 2 Open access Scales and Interviews for Diagnostic Assessment of ADHD in adulthood.

a Other scales without open access are: Conners Adult ADHD Rating Scale (CAARS), and the Adult ADHD Investigator Rating Scale (AISRS).

b Other interviews without open access are: Conners Adult ADHD Diagnostic Interview (CAADID), Adult ADHD Clinical Diagnostic Scale (ACDS).

Adult diagnoses may be missed in clinical practice due to lack of knowledge about ADHD in adulthood among practitioners and due to the high frequency of comorbid psychiatric conditions [Reference Jacob, Romanos, Dempfle, Heine, Windemuth-Kieselbach and Kruse201]. The lifetime co-morbidity rate is 60–80%. Having three or more disorders was associated with a ten-fold increase of the chance of having ADHD in a population study in 20 countries [Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi3]. Before treatment start, all comorbidities must be established so that the best order of treatment can be determined together with the patient. In the study by Fayyad et al, data on ADHD and comorbidities was collected on 26,744 respondents [Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi202]. In adults with ADHD having one comorbidity was found in 23% of cases, two in 14% of cases and three in 14% of cases. Rates were particulary high for any mood disorder (22%), any anxiety disorder (34%), substance use disorders (11%) and any behavioural disorder (15%).

Psychiatric comorbidity is thus a clinically important dimension of ADHD heterogeneity and a factor that contributes to the persistence of ADHD in adulthood [Reference Faraone, Asherson, Banaschewski, Biederman, Buitelaar and Ramos-Quiroga203, Reference Roy, Hechtman, Arnold, Sibley, Molina and Swanson204]. It is important for the diagnosis of ADHD, as well as the correct targeting of treatments, to identify mood, anxiety, eating, sleep, somatic and substance use disorders, in addition to personality, tic and autistic spectrum disorders [Reference Instanes, Haavik and Halmoy205]. Because adults with ADHD often exhibit low self-esteem, low mood, mood lability and irritability, these symptoms may sometimes be confused with dysthymia, cyclothymia, bipolar disorder or borderline personality disorder. Furthermore, daily mood changes in ADHD are very common, and represent a poorly regulated but essentially normal range of moods, rather than the more severe extremes of depression and elation as seen in bipolar disorder. It has been argued that chronic mood instability should be considered part of the core syndrome of ADHD [Reference Skirrow, McLoughlin, Kuntsi and Asherson206, Reference Corbisiero, Morstedt, Bitto and Stieglitz207]. ADHD and borderline personality disorder share symptoms of impulsivity, mood instability, anger outbursts and feelings of boredom [Reference Wender, Wolf and Wasserstein158, Reference Ferrer, Andion, Matali, Valero, Navarro and Ramos-Quiroga208, Reference O’Malley, McHugh, Mac Giollabhui and Bramham209]. In the ADHD patient, impulsivity and anger are usually short-lived and thoughtless rather than driven. Conflicts in relationships, suicidal preoccupation, self-mutilation, identity disturbances and feelings of abandonment are usually less intense than in borderline personality disorder. However, the differences may not be clear-cut because these symptoms are chronic and trait-like in both conditions [Reference Van Dijk, Lappenschaar, Kan, Verkes and Buitelaar210].

ADHD in children is also associated with increased rates of neurodevelopmental disorders like autism spectrum disorder, dyslexia and impaired motor coordination which are thought to arise from overlapping genetic influences [Reference Gillberg211]. Such neurodevelopmental comorbidities are less well studied in adults, but they are commonly observed in clinical practice and may lead to continued impairments. As the order of treatment will depend on the presence and severity of comorbidities, evaluation of comorbid disorders is a key component of the ADHD assessment process, using appropriate clinical diagnostic approaches.

6.4. ADHD and criminality

The prevalence of ADHD is increased in forensic populations compared to the general population [Reference Foreman, Foreman, Prendergast and Minty212], and the risk of criminality is increased in individuals with ADHD, especially in those with comorbid oppositional defiant disorder, conduct disorder, substance misuse and antisocial personality disorder [Reference von Polier, Vloet and Herpertz-Dahlmann213]. A meta-analysis comprising 42 studies from 15 countries reported a 5-fold increased prevalence of ADHD in youth prison populations (30%) and a 10-fold increased prevalence in adult prison populations (26%) as compared to the general population [Reference Young, Moss, Sedgwick, Fridman and Hodgkins214]. When using diagnostic clinical interviews, the estimated ADHD prevalence in prisoners was 25.5%, without significant differences for gender and age [Reference Young, Moss, Sedgwick, Fridman and Hodgkins214]. Further, inmates with ADHD compared to those without are reported to have higher rates of psychiatric morbidity including substance misuse, an earlier onset of offending, more violent offences, criminal recidivism and more frequent and severe institutional aggression [Reference Young and Thome215, Reference Young and Goodwin216].

7. Treatment

7.1. Effective treatments

The treatment of adults with ADHD should follow a multimodal and multidisciplinary approach, which includes psychoeducation, pharmacotherapy, cognitive behavior therapy (CBT) and coaching for ADHD, which are all discussed in this article.

Ideally, the treatment plan also involves the adult’s partner, family or close relationships, and in some cases systemic (family) therapy may be required when gross disruption to family relationships and functioning is present.

7.2. Treatment focus in comorbid ADHD

In the most recent report of 20 nationally or regionally representative World Mental Health surveys, data on ADHD and comorbidities was collected on 26,744 respondents [Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi202]. In adults with ADHD having one comorbidity was found in 23% of cases, two in 14% of case and three in 14% of cases. Rates were particulary high for any mood disorder (22%), any anxiety disorder (34%), substance use disorders (11%) and any behavioural disorder (15%). Treatment of ADHD is therefore most often in the context of co-occuring disorders.

Before treatment starts, all comorbidities must be established so that the best order of treatment can be determined together with the patient. In general, the most severe disorder is prioritized. For instance, psychosis, bipolar disorder, substance abuse, severe depression and severe anxiety are usually treated first. Milder mood or anxiety disorders, and emotional instability, may respond to treatment of ADHD and can be treated at the same time as ADHD. Drug and alcohol abuse should be stabilized but can be treated at the same time as ADHD.

7.3. Psychoeducation on ADHD

According to consensus based on good clinical practice and the need to work on an informed consent basis within a multimodal treatment approach, psychoeducation should be the first step as a standard of care [Reference D’Amelio, Retz, Philipsen and Rösler217]. First evidence from an open trial and a randomized clinical trial shows, that patients and significant others who attend a structured psychoeducation program increase their knowledge about ADHD, and improve the quality of their relationships and psychological well-being [Reference Hirvikoski, Waaler, Lindstrom, Bolte and Jokinen218, Reference Hirvikoski, Lindström, Carlsson, Waaler, Jokinen and Bölte219].

7.4. Pharmacotherapy for ADHD

7.4.1. Introduction on pharmacotherapy

In the first European Consensus Statement [Reference Kooij, Bejerot, Blackwell, Caci, Casas-Brugue and Carpentier1] psychostimulants (methylphenidate and dexamphetamine) were recommended as the first-line pharmacotherapy for adult ADHD [Reference Kooij, Bejerot, Blackwell, Caci, Casas-Brugue and Carpentier1, Reference Bolea-Alamanac, Nutt, Adamou, Asherson, Bazire and Coghill184, Reference Volkow and Swanson220], as they exert moderate-to-high clinical effects, with average effects higher than atomoxetine (ATX) and other non-stimulant medications [Reference Asherson, Buitelaar, Faraone and Rohde2]. There were, however, no head-to-head studies providing robust comparative analysis of efficacy differences [Reference Bushe, Day, Reed, Karlsdotter, Berggren and Pitcher221]. Across most of Europe, lisdexamfetamine (LDX) has been introduced as a slow release formulation of dexamphetamine. The recent systematic review and network meta-analysis on the comparative efficacy and tolerability of medications for ADHD in children, adolescents and adults by Sam Cortese et al. showed, that the first pharmacological choice for ADHD in children and adolescents is methylphenidate, and amphetamines in adults [Reference Cortese, Adamo, Del Giovane, Mohr-Jensen, Hayes and Carucci222]. In fact in adults, amphetamines were not only the most efficacious compounds, as rated by clinicians and by self-report, but also as well tolerated as methylphenidate and the only compounds with better acceptability than placebo.

7.4.2. Licensing

Licensing of ADHD medications for adults is more diverse than in 2009 [Reference Kooij, Bejerot, Blackwell, Caci, Casas-Brugue and Carpentier1], reflecting greater understanding of ADHD, and efforts to market ADHD medications in Europe. In Denmark, Ireland, Norway, Sweden, Switzerland, the Netherlands and the United Kingdom, most ADHD medications can be prescribed, either with a full license (e.g. Medikinet®, Strattera®, Elvanse®) or transitional licenses (e.g. Concerta XL®) and off-label prescribing is endorsed by national guidelines and formularies. Dexmethylphenidate (Focalin XR®) is licensed in Switzerland only. In other countries, only a limited selection of medications is available for funding by the state sector, but off label prescribing is possible. In another group of countries (e.g. Greece, Slovenia, Poland), only very few ADHD medications are available, with off-label prescribing mostly in the private sector. The European Network on Adult ADHD (ENAA) and the Neurodevelopmental Disorders Across the Lifespan (NDAL) section at EPA strongly recommend that evidence-based treatments for adult ADHD are made more available and licensed across European countries.

7.4.3. Efficacy and adverse effects of stimulants

Meta-analyses of randomized controlled trials (RCTs) demonstrate the efficacy of stimulants and ATX in the reduction of ADHD symptoms in adults [Reference Koesters, Becker, Kilian, Fegert and Weinmann223Reference Cunill, Castells, Tobias and Capella227]. Standardized mean differences (SMDs) range from 0.4 to 0.7, with stimulants showing greater efficacy than ATX [Reference Faraone and Glatt224]. The longest RCT in adults still found significant effects of MPH after one year [Reference Philipsen, Jans, Graf, Matthies, Borel and Colla228]. National registry data also suggest long term benefits. Although these studies are not definitive due to lack of randomization and controls, they demonstrate ‘real-world’ societal benefits associated with the use of ADHD medications. These studies show that during periods of receiving medications for ADHD there are marked reductions in transport accidents and mortality rates [Reference Dalsgaard, Ostergaard, Leckman, Mortensen and Pedersen132, Reference Chang, Lichtenstein, D’Onofrio, Sjolander and Larsson229], criminal convictions [Reference Lichtenstein and Larsson230], suicidal behavior [Reference Chen, Sjolander, Runeson, D’Onofrio, Lichtenstein and Larsson231], violent reoffending [Reference Lichtenstein and Larsson230], depression [Reference Chang, D’Onofrio, Quinn, Lichtenstein and Larsson232] and substance misuse [Reference Chang, Lichtenstein, Halldner, D’Onofrio, Serlachius and Fazel233]. Similar analyses with antidepressants find no effects, suggesting the effects are specific to ADHD medications.

A 2011 meta-analysis [Reference Castells, Ramos-Quiroga, Rigau, Bosch, Nogueira and Vidal225] revealed that MPH (mean dose 41.2–82 mg/day) exerted a moderate effect on ADHD symptoms, with large effects observed at doses of >77.4 mg/day. Immediate release (IR) MPH has a short duration of action of maximum 4 h. Due to difficulties with compliance when needing to take medication up to several times a day, long-acting MPH preparations have been developed, with durations of action ranging between 6–12 h.

The recommended dose range of Immediate Release dexamphetamine (IR) is 5–60 mg/day [Reference Volkow and Swanson220]. Lisdexamfetamine (LDX) has a slow release profile giving the drug a relatively low abuse profile [Reference Sharman and Pennick234]. LDX is taken once daily with a mode of action of up to 14 h [Reference Setyawan, Hodgkins, Guerin, Gauthier, Cloutier and Wu235]. Three RCTs in adults indicate moderate to large effects on ADHD symptoms [Reference Adler, Goodman, Kollins, Weisler, Krishnan and Zhang236Reference Dupaul, Weyandt, Rossi, Vilardo, O’Dell and Carson238] (SMD = 0.97) [Reference Maneeton, Maneeton, Suttajit, Reungyos, Srisurapanont and Martin239], comparable to MPH. The safety and tolerability profile is similar to other stimulants [Reference Coghill, Caballero, Sorooshian and Civil240, Reference Adler, Dirks, Deas, Raychaudhuri, Dauphin and Lasser241].

The main adverse effects of stimulants are increased heart rate and blood pressure, and reduced appetite and sleep [Reference Epstein, Patsopoulos and Weiser242Reference Mick, McManus and Goldberg245]. Heart rate, blood pressure, sleep problems and weight are therefore assessed before, and monitored at least twice a year during treatment. Serious cardiac complications are rare [Reference Martinez-Raga, Knecht, Szerman and Martinez243, Reference Westover and Halm246, Reference Habel, Cooper, Sox, Chan, Fireman and Arbogast247] with reported risks for myocardial infarction, sudden cardiac death, ventricular arrhythmias or stroke no more than 0.2-0.4% higher in one study [Reference Schelleman, Bilker, Kimmel, Daniel, Newcomb and Guevara248]. MPH might trigger arrhythmias in patients with congenital heart diseases [Reference Shin, Roughead, Park and Pratt249]. The consensus is caution in patients with known cardiac defects, but risks are small.

7.4.4. Atomoxetine

ATX yields moderate efficacy in reducing ADHD symptoms (SMD: –0.33 to –0.40) [Reference Cunill, Castells, Tobias and Capella227]. Onset of action is 1–2 weeks, and full effects may take up to 6 months to develop [Reference Asherson, Bushe, Saylor, Tanaka, Deberdt and Upadhyaya250]. If rapid onset of effect is not essential, ATX may be a good choice for high risk patients who need stable control of ADHD symptoms [251].

The use of ATX as first line in drug abusers continues to be debated with other experts preferring stimulants due to rapid onset and potentially greater effects [Reference Ginsberg, Ahlqvist-Rastad, AM, Barroso, Bergquist and Brodd252]. Although in the past there were concerns that stimulants may increase the risk of substance use disorders (SUD), there is now a wealth of data demonstrating reductions in SUD during periods of treatment of ADHD with stimulants [Reference Chang, Lichtenstein, Halldner, D’Onofrio, Serlachius and Fazel233, Reference Quinn, Chang, Hur, Gibbons, Lahey and Rickert253].

ATX may be a good choice with co-occurring anxiety that might be exacerbated by stimulants, as a RCT of adults with comorbid ADHD and social anxiety disorder found improvements in both ADHD and social anxiety [Reference Adler, Liebowitz, Kronenberger, Qiao, Rubin and Hollandbeck254]. ATX does not appear to be effective in the treatment of comorbid depression in adolescents [Reference Bangs, Emslie, Spencer, Ramsey, Carlson and Bartky255].

7.4.5. Guanfacine and clonidine

In Europe, guanfacine extended-release (GXR), an alfa-2 adrenergic agonist, is licensed for the treatment of children and adolescents with ADHD for whom stimulants are not suitable, not tolerated or where shown to be ineffective [Reference Posey and McDougle256, Reference Huss, Chen and Ludolph257]. Notably, there are currently no RCTs in adult patients to support the use of GXR in this age group, only a study using GXR or placebo as an adjunct to stimulant treatment that had insufficient effect. Both treatments did not differ in efficacy [Reference Butterfield, Saal, Young and Young258].

Extended-release (ER) clonidine is approved in the US for treatment of ADHD in 6–17- year olds as monotherapy or an adjunct to stimulants. There are RCTs on both ER clonidine [Reference Kollins, Jain, Brams, Segal, Findling and Wigal259, Reference Jain, Segal, Kollins and Khayrallah260] and IR clonidine [Reference Palumbo, Sallee, Pelham, Bukstein, Daviss and McDermott261, Reference Hazell and Stuart262] in children and adolescents with ADHD, but no equivalent studies in adults.

7.4.6. Bupropion

There are conflicting findings for bupropion from a small number of adult studies. Positive results were reported with higher doses (400–450 mg per day) [Reference Maneeton, Maneeton, Intaprasert and Woottiluk263, Reference Hamedi, Mohammdi, Ghaleiha, Keshavarzi, Jafarnia and Keramatfar264]. Due to a limited evidence base, bupropion use should be restricted to cases who do not tolerate other ADHD medications.

7.4.7. Other medications

Selective noradrenaline reuptake inhibitors such as reboxetine may be an alternative to ATX [Reference Ghanizadeh265, Reference Riahi, Tehrani-Doost, Shahrivar and Alaghband-Rad266]. There is limited evidence for tricyclic antidepressants [Reference Otasowie, Castells, Ehimare and Smith267, Reference Prince, Wilens, Biederman, Spencer, Millstein and Polisner268]. Selective serotonin reuptake inhibitors (SSRIs) are not effective for the treatment of ADHD [Reference Chang, Lichtenstein, D’Onofrio, Sjolander and Larsson229, Reference Lichtenstein and Larsson230, Reference Weiss, Hechtman and Adult269]. Modafinil, a wakefulness-promoting agent used in the treatment of narcolepsy, has not been demonstrated as an effective treatment for adult ADHD in a phase 3 trial that had high rates of side effects (86%) and drop-out (47%) possibly resulting from excessive doses (210–510 mg/day) [Reference Arnold, Feifel, Earl, Yang and Adler270].

7.4.8. Long-term safety concerns

Currently there is no evidence of significant long-term risks using stimulants. Tomography scans find higher striatal dopamine transporter availability in ADHD patients treated with stimulants [Reference Wang, Volkow, Wigal, Kollins, Newcorn and Telang271]. The clinical implications of this up-regulation are not clear. Potential toxicity on heart valves of medications with an agonist effect on 5-HT2B receptors have been discussed [Reference Cavero and Guillon272], including MPH and guanfacine. Some argue that echocardiography should be routinely performed prior to treatment with potential valvulopathic drugs [Reference Droogmans, Kerkhove, Cosyns and Van Camp273]. This risk is not however established, and we and others do not recommend routine echocardiograms [Reference Bolea-Alamanac, Nutt, Adamou, Asherson, Bazire and Coghill184, Reference Ginsberg, Ahlqvist-Rastad, AM, Barroso, Bergquist and Brodd252, Reference Seixas, Weiss and Muller274], except in older adults (> age 50) [Reference Kooij, Michielsen, Kruithof and Bijlenga167].

7.4.9. Combined psychopharmacology

The high rate of psychiatric comorbidity in adult ADHD frequently necessitates combined psychopharmacology [Reference Sobanski, Bruggemann, Alm, Kern, Deschner and Schubert275]. Accordingly, the risk of possible drug-drug interactions when treating adults with ADHD must be considered. These include the following:

  1. Monoamine oxidase inhibitors are generally contraindicated due to the risk of hypertensive crisis.

  2. Although MPH is mainly metabolized in the liver, drug interactions via CYP enzymes are uncommon. Amphetamines, however, are metabolized primarily via the CYP 2D6 enzyme system making drug interactions possible (with inhibitors or inducers of this enzyme system, e.g. fluoxetine and paroxetine) [Reference Sharma and Couture276].

  3. Treatment with medications that act on the noradrenaline system, including certain antidepressants (e.g. duloxetine, venlafaxine), will have an additive effect and may increase the risk of hypertension and other adverse cardiovascular events.

  4. Due to its metabolism by the CYP 2D6 enzyme system, ATX levels can increase in combination with enzyme-inhibiting SSRIs (e.g. fluoxetine and paroxetine) [Reference Bazire277].

7.5. Considerations when treating special groups with pharmacotherapy

7.5.1. ADHD with comorbid bipolar disorder

A pharmaco-epidemiological study found that MPH monotherapy in patients with bipolar disorder increased the risk of switch to a manic episode (hazard ratio 6.7). However, when combined with a mood stabilizer, MPH reduced the risk of mania (hazard ratio 0.6) [Reference Viktorin, Ryden, Thase, Chang, Lundholm and D’Onofrio278]. This supports the current recommendation to treat ADHD in bipolar disorder patients with stimulants, so long as they are also taking mood stabilizers.

7.5.2. ADHD with comorbid substance use

Meta-analysis of RCTs in adults found that most ADHD medications reduce the core symptom severity of ADHD, but have limited effect on comorbid substance use [Reference Cunill, Castells, Tobias and Capella279]. However, a large Danish Registry study showed a decrease of substance use in ADHD patients when using MPH [Reference Steinhausen and Bisgaard280]. Recent RCTs using higher doses of ER Mixed Amphetamine Salts (Adderall XR®) or OROS MPH (Concerta®), combined with CBT found better effects on both ADHD and substance use, compared to studies using lower dosages [Reference Levin, Mariani, Specker, Mooney, Mahony and Brooks281, Reference Konstenius, Jayaram-Lindstrom, Guterstam, Beck, Philips and Franck282]. The relevance of higher doses is supported by a pharmaco-epidemiological study from Sweden showing that higher MPH dose was associated with long-term treatment adherence in patients with ADHD and substance use disorders (SUD) [Reference Skoglund, Brandt, Almqvist, D’Onofrio, Konstenius and Franck283]. Immediate-release stimulants should be avoided in patients with ADHD and SUD, whereas OROS-MPH and LDX have lower abuse potential [Reference Cobos, Sinol, Perez and Trujols284]. Further recommendations for treating comorbid substance use disorders can be found in Bolea-Alamanac et al. [Reference Bolea-Alamanac, Nutt, Adamou, Asherson, Bazire and Coghill184], and in the recently published international Consensus Statement on diagnosis and treatment of substance use disorders with comorbid ADHD [Reference Crunelle, van den Brink, Moggi, Konstenius, Franck and Levin285]. This Consensus Statement mentions that the use of stimulant treatment for ADHD does not precipitate the onset of SUD in adults without previous SUD [Reference Torgersen, Gjervan, Rasmussen, Vaaler and Nordahl286]; also that in SUD patients, treatment of ADHD can be useful to reduce ADHD symptoms without worsening the SUD, and should not be avoided [Reference Klassen, Bilkey, Katzman and Chokka287].

7.5.3. Cognitive enhancement in students

Another group where screening for ADHD is appropriate is the student population. This is because we know that ADHD specially interferes with educational attainment. Further, this has been highlighted be the finding that genetic risks for ADHD overlap with those for educational outcomes [Reference Demontis, Walters, Martin, Mattheisen, Als and Agerbo28]. Student groups with particularly high rates of ADHD include those presenting with specific learning difficulties [Reference Cheung, Frazier-Wood, Asherson, Rijsdijk and Kuntsi288] and mental health problems [Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi202]. Related to this, there are concerns, particularly in countries with a higher rate of stimulant prescriptions, that students may seek the diagnosis of ADHD to receive stimulants for cognitive enhancement. Some studies show that although most students use their ADHD medication as prescribed, misuse and diversion is not uncommon [Reference Rabiner, Anastopoulos, Costello, Hoyle, McCabe and Swartzwelder289]. Care must therefore be taken to ensure that students are diagnosed and treated for ADHD when appropriate, while minimising risks of diversion.

7.5.4. Pregnancy and breastfeeding

There is only limited information on the effects of ADHD medication on the fetus and new-born [Reference Besag290]. As suggested by population-based studies, MPH or amphetamine exposure during pregnancy is not related to higher rates of any congenital malformations [Reference Dideriksen, Pottegard, Hallas, Aagaard and Damkier291Reference Huybrechts, Broms, Christensen, Einarsdottir, Engeland and Furu293]. For cardiac malformations, MPH use was associated with a small increased risk (RR 1.28 (95% CI, 0.94–1.74), where amphetamines were not. There is some evidence suggesting that treatment with MPH or ATX might increase the risk of miscarriage [Reference Diav-Citrin, Shechtman, Arnon, Wajnberg, Borisch and Beck294, Reference Bro, Kjaersgaard, Parner, Sorensen, Olsen and Bech295], although there were several confounding factors such as younger age and social disadvantage, that could explain the association [Reference Haervig, Mortensen, Hansen and Strandberg-Larsen296]. Another study found that the use of stimulant medication during pregnancy is associated with miscarriage to the same degree as having ADHD itself [Reference Bro, Kjaersgaard, Parner, Sorensen, Olsen and Bech295], these findings need further investigation. Potential adverse effects on the fetus from intra placental exposure to medication in pregnancy should be considered against the possible adverse effects of interrupting treatment abruptly in women with ADHD [Reference Bolea-Alamanac, Nutt, Adamou, Asherson, Bazire and Coghill184, Reference McAllister-Williams, Baldwin, Cantwell, Easter, Gilvarry and Glover297, Reference Bolea-Alamanac, Green, Verma, Maxwell and Davies298]. Each case should be assessed individually taking into account possible risks of both treating and interrupting treatment.

Amphetamines may be given preference over other medications. Some authors do not consider Atomoxetine because of lack of safety data [Reference Larsen, Damkier, Pedersen, Fenger-Gron, Mikkelsen and Nielsen299, Reference Freeman300]. MPH seems to be safe during breastfeeding. The amounts of medication excreted in breast milk, and consumed by the infant, are very small (with the Relative Infant Dose (RID) (< 1%) [Reference Besag290, Reference Larsen, Damkier, Pedersen, Fenger-Gron, Mikkelsen and Nielsen299], and no drug-related side effects have been were reported. The impact of ATX, guanfacine, and clonidine on breastfeeding-related outcomes is largely unknown [301303], and they are not recommended [Reference Larsen, Damkier, Pedersen, Fenger-Gron, Mikkelsen and Nielsen299].

Until now no adverse reactions were reported among infants of mothers receiving LDX or dexamphetamine (RID: 4–10.6%). There are some preliminary reports suggesting that dexamphetamine treatment may lead to a suppression of prolactin secretion in postpartum women, though with unclear clinical implications [304]. Bupropion was found to produce low levels in milk, suggesting relative safety. Of note, there are two known cases of seizures developed by children breastfed by women receiving bupropion [305].

7.5.5. ADHD and sleep problems

In the majority of cases, ADHD in children and adults is associated with a circadian rhythm disorder with delayed sleep onset [Reference Van der Heijden, Smits, Van Someren and Gunning306Reference Kooij and Bijlenga308]. Meta-analysis of nine studies investigating the effects of stimulant medication on sleep in children and adolescents found that stimulants can lead to longer sleep latency, worse sleep efficiency, and shorter sleep duration [Reference Kidwell, Van Dyk, Lundahl and Nelson309]. Similar findings have been reported in adults [Reference Snitselaar, Smits, van der Heijden and Spijker310]. Careful titration of stimulants and psychoeducation around sleep optimization can improve the quality of sleep, possibly due to improved daytime structure, the maintenance of regular physical activity and improved mood [Reference Kooij198, Reference Kidwell, Van Dyk, Lundahl and Nelson309, Reference Barrett, Tracy and Giaroli311]. In children with ADHD and chronic insomnia, melatonin has been shown to advance the sleep onset, and increase sleep duration [Reference Van der Heijden, Smits, Van Someren, Ridderinkhof and Gunning312]. A trial targeting insomnia in adults with ADHD is ongoing, and clinical experience points in the same direction of possible efficacy of treatment with melatonin at night, and also of light therapy in the morning [Reference Kooij and Bijlenga308]. Treatment of insomnia should always start with sleep hygiene education and optimizing the stimulant or non-stimulant treatment of ADHD [Reference Barrett, Tracy and Giaroli311]. A low dose of IR MPH (usually 5 mg) taken at night time can reduce ceaseless mental activity to a degree that allows sleep in some cases.

7.6. Cognitive behavior therapy (CBT) and coaching for ADHD

Although pharmacological treatment of ADHD is very effective, many patients continue to experience significant symptoms and functional impairment in daily living. Empirical evidence from numerous uncontrolled studies, more than ten randomized controlled trials (RCTs) and a meta-analysis has shown that in group or individual settings, cognitive behavioral therapy (CBT) reduces ADHD-core symptoms, associated symptoms such as emotion dysregulation, anxiety and depression, and functional impairments across different areas of daily living in adults [Reference Philipsen, Jans, Graf, Matthies, Borel and Colla228, Reference Hirvikoski, Waaler, Alfredsson, Pihlgren, Holmstrom and Johnson313Reference Jensen, Amdisen, Jorgensen and Arnfred315]. CBT is best used within a multi-modal treatment approach and as an adjunct to medication as current research does not fully support the efficacy of CBT as a sole treatment for adult ADHD [Reference Seixas, Weiss and Muller274, Reference Arnold, Hodgkins, Caci, Kahle and Young316Reference Mongia and Hechtman318]. Most controlled studies have been conducted in patients taking ADHD medication and demonstrate an additional significant treatment effect [Reference Hirvikoski, Waaler, Alfredsson, Pihlgren, Holmstrom and Johnson313, Reference Mongia and Hechtman318Reference Emilsson, Gudjonsson, Sigurdsson, Baldursson, Einarsson and Olafsdottir322]. The largest controlled multi-center CBT-study to date has demonstrated that psychological interventions result in better outcomes when combined with MPH as compared to psychological interventions in unmedicated patients [Reference Philipsen, Jans, Graf, Matthies, Borel and Colla228]. In a systematic review of 51 pharmacological and non-pharmacological interventions [Reference Arnold, Hodgkins, Caci, Kahle and Young316], the highest proportion of improved outcomes (83%) was for patients receiving combination treatment. However, not all adults with ADHD desire or tolerate pharmacological treatment. In these cases CBT may be the best option.

Across all studies there are some consistent characteristics of CBT treatment, both in form and content. All approaches are highly structured. Most are manualized, and establish psychoeducation as the first step. Most programs are skills-based and focus on organizational and time management skills, emotional regulation/control, problem solving skills, prosocial competence and strategies to improve attention and impulsivity management. In addition to behavioral interventions that require patients to try out and rehearse in daily life techniques suggested in the therapy session, programs include cognitive strategies, such as the identification of negative automatic thoughts, methods to address ‘thinking errors’ and the introduction of cognitive restructuring techniques [Reference Young and Bramham323]. There is emerging evidence that cognitive distortions and dysfunctional cognitive schemes related to a biographic accumulation of negative experiences associated with ADHD-symptoms contribute to negative functional outcomes and lead to avoidance behavior, failure-orientation, reduced self-efficacy, procrastination, depressive symptoms and anxiety [Reference Knouse and Safren324Reference Torrente, Lopez, Alvarez Prado, Kichic, Cetkovich-Bakmas and Lischinsky326]. Furthermore, most programs highlight the importance of including significant others in the treatment process to reduce dysfunctional interactions and stigmatization associated with ADHD symptoms.

Coaching or mentoring is a derivative of the cognitive behavioral paradigm involving the development of a collaborative mentoring partnership. Coaching aims to provide structure, support and feedback for building life skills and changing negative outcomes related to ADHD in daily living [Reference D’Amelio, Retz, Philipsen and Rösler217, Reference Kubik327, Reference Prevatt and Yelland328]. However, there is no standard methodology and the coaching process varies considerably, including face-to-face contact, telephone calls and/or email contact. To date, there are no controlled studies assessing the efficacy of coaching as a therapeutic means in the treatment of adults with ADHD. Nevertheless there is some preliminary support for positive outcomes from uncontrolled studies [Reference Kubik327, Reference Prevatt and Yelland328]. Similarly there is some support for the effectiveness of mindfulness based cognitive therapy (MBCT) for adults with ADHD [Reference Hepark, Janssen, de Vries, Schoenberg, Donders and Kan329Reference Cairncross and Miller331].

8. Cost and cost effectiveness

Because of the broad impact of ADHD on general functioning, the disorder is likely to have serious economic implications for children, families, and society. The studies which calculate costs however are so far limited as they typically examine only one aspect of the costs, for example “from the perspective of a major German health insurance fund” [Reference Braun, Zeidler, Linder, Engel, Verheyen and Greiner332]. Particularly for adults with ADHD, estimates should include not only direct costs (the costs of labor, supplies, and equipment to provide direct patient care services) but also indirect costs (mainly related to the loss of productivity) such as costs to family, costs due to impairment in employment, costs due to accidents [Reference Swensen, Birnbaum, Ben Hamadi, Greenberg, Cremieux and Secnik333], smoking and substance misuse, and costs due to involvement with the criminal justice system.

Direct costs have been examined [Reference Birnbaum, Kessler, Lowe, Secnik, Greenberg and Leong334Reference Matza, Paramore and Prasad336], but are heavily depending on the healthcare system from which they are derived and the type of pathway/care package provided. These estimates therefore, although potentially useful for comparisons between disorders within the same healthcare system, should not be generalized to different contexts. The most comprehensive approach to calculate the total costs of ADHD in the Danish Psychiatric Central Register, showed that there is an economic burden of ADHD which is considerable and falls both on the individual and the state [Reference Daley, Jacobsen, Lange and Sørensen337].

Apart from the costs (either direct or indirect) of ADHD, there is also the question of cost benefit for treating ADHD. This first asks whether a treatment of a disorder is worthwhile when compared against alternatives in terms of allocation of healthcare funds, and second which ADHD intervention brings the most benefit at the lowest cost. For the former, an argument can be made that adult ADHD is a condition which is cost effective to treat from the societal perspective because of the efficacy and relatively low cost of the medicines used for its treatment [Reference Faraone and Glatt224, Reference Fredriksen, Halmoy, Faraone and Haavik338]. For the latter, among children and adolescents with ADHD, there is consistent evidence [Reference Gilmore and Milne339Reference Zupancic, Miller, Raina, Lee, Klassen, Olsen, Miller, Lee and Raina343] that pharmacotherapies are cost effective compared with no treatment or behavioral therapy [Reference Wu, Hodgkins, Ben-Hamadi, Setyawan, Xie and Sikirica344]. Unfortunately there is insufficient research to conclude the same for adults with ADHD (Table 3).

9. Stigma surrounding ADHD

Substantial stigmatization and myths continue to surround ADHD [Reference Lebowitz345]. A recent study on negative coverage of ADHD and autism in Flemish newspapers found a 2-fold more negative than neutral or positive coverage of ADHD than of autism [Reference Baeyens, Moniquet, Danckaerts and van der Oord346]. Stigma arises from lack of awareness, of prejudice about symptom etiology (e.g. poor parenting, lack of moral), incompetence (e.g. laziness) and perceived dangerousness (e.g. unpredictable and potentially violent behavior) [Reference Corrigan and Shapiro347]. Other variables contributing to stigma are doubts about the validity and reliability of an ADHD diagnosis, along with age, gender, ethnicity and the public's skepticism toward ADHD medication. Also, the restricted regulatory status for ADHD medications in many countries adds to the stigma within the mental health profession and the media. Public stigmatization of ADHD, and the following self-stigma and courtesy stigma are underestimated risk factors for treatment adherence, treatment efficacy, symptom aggravation, life satisfaction, and mental well-being of individuals affected by ADHD [Reference Mueller, Fuermaier, Koerts and Tucha348].

Table 3 Summary of key points.

Self-stigma has been studied in children and adolescents and is characterized by a sense of feeling different from peers, and negative self-evaluation as a consequence of that perception. However, some young people were prepared to challenge the stigma by self-disclosure and openness about their condition [Reference McKeague, Hennessy, O’Driscoll and Heary349]. Lower stigma in teachers towards adult ADHD seems to relate to greater knowledge about the condition [Reference Fuermaier, Tucha, Mueller, Koerts, Hauser and Lange350]. Among general practitioners (GPs) from the UK, Europe and Australia, there is mixed and often unhelpful attitudes regarding the validity of ADHD as a construct, the role of medication and how parenting contributes to the presentation [Reference Tatlow-Golden, Prihodova, Gavin, Cullen and McNicholas351]. A paucity of training was identified, alongside a reluctance of GPs to become involved in shared care practice. If access to services is to be improved for people with ADHD, there needs to be a focused and collaborative approach to training [Reference Tatlow-Golden, Prihodova, Gavin, Cullen and McNicholas351].

9.1. Combatting stigma

Disclosure of mental health problems can be a challenge [Reference Brohan, Henderson, Wheat, Malcolm, Clement and Barley352], but an increasing number of celebrities have cast aside stigma by revealing they had ADHD and, in some cases, have been pharmacologically treated for many years (https://www.additudemag.com/successful-people-with-adhd-learning-disabilities/). This is of course supportive for patients but it is strongly recommended that psychoeducation about ADHD should be included in anti-stigma programs [Reference Corrigan and Shapiro347]. Of note, adult ADHD is rarely included in college programs for medical and psychology students, or in the training of professionals working in adult mental health services. This contributes to misconceptions, underdiagnosis and undertreatment among professionals [Reference Asherson, Buitelaar, Faraone and Rohde2, Reference Fayyad, Sampson, Hwang, Adamowski, Aguilar-Gaxiola and Al-Hamzawi3]. Psychoeducation programs therefore need to target all clinical disciplines at all stages of professional development (e.g. from students through to primary and secondary care physicians, psychologists and nurses) to ensure that appropriate early recognition, diagnosis and treatment is provided.

Internationally recognized guidelines are available on the assessment, treatment and management of adults with ADHD, as well as the development and provision of clinical services [Reference NICE182, Reference Bolea-Alamanac, Nutt, Adamou, Asherson, Bazire and Coghill184, Reference Seixas, Weiss and Muller274, Reference CADDRA353]. The current lack of licensed indications for the use of stimulants in adults in most European countries (but not in the US or Canada) is not supported by available data, but rather results from the outdated focus that ADHD is a ‘child disorder’, caution from regulators regarding potential cardiovascular side effects, and commercial manipulation by the pharmaceutical industry. In Europe, this situation may change in the coming years as formulations of methylphenidate and dexamphetamine are being put forward for registration.

Stigma prevents patients to ask for help and increases their suffering and impairment. Hence the successful management of ADHD by prescribers will include an awareness of the potential stigma that may be perceived by the patient and its consequences on treatment initiation and maintenance. The only way to reduce stigma surrounding ADHD is community, health and education systems in Europe and beyond working together by education of professionals and the public, and by a unified licensing of medications for ADHD in adults.

10. Conclusions

This consensus statement reflects agreement on the state of ADHD, but by definition it is provisional. It does not negate the ongoing scientific debate in the field and the different opinions and hypotheses about adult ADHD among experts. Yet none of that undercuts the legitimacy or validity of the construct, or of the conclusions one can make about the current status of the consistency of the evidence. ADHD is a neurodevelopmental and heritable disorder with a lifespan perspective: starting in childhood, persisting in adulthood until old age, with significant psychosocial impairment, a high comorbidity rate and multi-morbidity. It is associated with high levels of personal distress, and a substantial economic burden for society if left unidentified and untreated. DSM-5 has changed some of the criteria that facilitate the diagnosis in adolescents and adults. Assessment should include a detailed account of the developmental history, of both current and retrospective ADHD symptoms and impairment, and associated comorbidities. To prevent under-reporting of symptoms, external validation is desirable by collateral information. Multimodal treatment is required, comprising of psychoeducation, pharmacotherapy, and cognitive behavior therapy and/or coaching. Psychoeducational European programs to combat stigma and to inform the public and (mental) health professionals about new knowledge on the lifespan perspective of ADHD are needed to improve and increase diagnostic and treatment services for adult ADHD. Research on the different presentation of ADHD in women, and on treatment of ADHD in old age should be further developed in order to improve their treatment options.

Conflicts of interest

Kooij, J.J.S.: No conflict of interest. Bijlenga, D.: No conflict of interest. Salerno, L.: No conflict of interest. Jaeschke, R.: No conflict of interest. Bitter I.: Honoraria or consultation fees from EGIS, EGRIS, Eli Lilly, Gedeon Richter, Janssen/Janssen-Cilag, Lundbeck, MedAvante, Pierre Fabre, PSI (CRO) and Servier. Balázs, J.: No conflict of interest. Thome, J.: No conflict of interest. Dom, G.: No conflict of interest. Kasper, S.: Grants/research support, consulting fees and/or honoraria within the last three years from Angelini, AOP Orphan Pharmaceuticals AG, AstraZeneca, Eli Lilly, Janssen, KRKAPharma, Lundbeck, Neuraxpharm, Pfizer, Pierre Fabre, Schwabe and Servier. Nunes Filipe, C.: No conflict of interest. Stes, S.: Principal Investigator before 2016 in studies funded by Janssen-Cilag, Lilly and Novartis; speaker fees and advisory board for Lilly, Novartis, Janssen-Cilag, and Shire. Since 2016 no conflicts of interest. Mohr. P.: consultant and speaker for Eli Lilly, Janssen-Cilag, and Lundbeck. Leppämäki, S.: No conflict of interest. Casas, M.: speaker fees from Janssen- Cilag, Bristol-Mayers Squibb, Ferrer-Brainfarma, Pfizer, Lundbeck, Otsuka, Servier, Lilly, Shire, GSK, Rovi and Adamed. Advisory board for Janssen-Cilag, Lilly, and Shire. Bobes, J.: research grants and/or consultant, advisor or speaker within de last 3 years for: AB-Biotics, Acadia Pharmaceuticals, Casen Recordati, D&A Pharma, Gilead, Ferrer, Hoffman La Roche, Indivior, Janssen-Cilag, Indivior, Lundbeck, Mundipharma, Otsuka, Pfizer, Reckitt-Benckiser, Servier and Shire, research funding from the Spanish Ministry of Economy and Competiveness – Centro de Investigación Biomedica en Red area de Salud Mental (CIBERSAM) and Instituto de Salud Carlos III, Spanish Ministry of Health, Social Services and Equality - Plan Nacional sobre Drogas- and the 7th Framework Program of the European Union. McCarthy, J.M.: No conflict of interest. Kjems Philipsen, A.: No conflict of interest. Pehlivanidis, A.: No conflict of interest. Niemela, A.: No conflict of interest. Bolea-Alamanac, B.: Honoraria on one occasion for an educational lecture for Janssen pharmaceuticals. Edvinsson, D.: No conflict of interest. Baeyens, D.: No conflict of interest. Wynchank, D.: Advisory boards of Janssen BV, Novartis and Eli Lilly for activities outside the scope of this paper (2009–2014). Sobanski, E.: lectures paid by Shire within the last two years. Philipsen, A.: Advisory boards, lectures, performed phase 5 studies, or travel grants within the last 5 years from Eli Lilly and Co, Janssen-Cilag, Lundbeck, MEDICE Arzneimittel, Pütter GmbH and Co KG, Novartis, Servier, and Shire; and has authored books and articles on ADHD published by Elsevier, Hogrefe, Oxford Press, Schattauer, Kohlhammer, Karger, and Springer. McNicholas, F.: Received an unrestricted educational grant from Shire Pharmaceuticals in 2016, and grant support for a UCD Newman Fellow 2014-2015. Caci, H.: No conflict of interest. Manor, I.: Honoraria, counseling and advisory boards for Jansen-Cilag, Israel, Teva Israel, Novartis Israel, Medison Israel. Asking for a research grant: Shire. Krause, J.: No conflict of interest. Fayyad, J.: No conflict of interest. Ramos-Quiroga, J.A.: speakers’ bureau and/or consultant for Eli-Lilly, Janssen-Cilag, Novartis, Shire, Lundbeck, Almirall, Braingaze, Sincrolab, and Rubió in the last 5 years. Travel awards (air tickets + hotel) for meetings from Janssen-Cilag, Rubió, Shire, and Eli- Lilly. The Department of Psychiatry chaired by him received unrestricted educational and research support in the last 5 years from: Eli-Lilly, Lundbeck, Janssen- Cilag, Actelion, Shire, Ferrer, and Rubió. Foeken, K.: No conflict of interest. Adamou, M.: No conflict of interest. Ohlmeier, M.: No conflict of interest. Fitzgerald, M.: No conflict of interest. Gill, M.: No conflict of interest. Lensing, M.: No conflict of interest. Motavalli Mukaddes, N.: advisor and speaker of Sanofi Drug Company. Brudkiewicz, P.: No conflict of interest. Gustafsson, P.: Former member of advisory board for Lilly, advisory board for Elvanse and Intunive (Shire). Tani, P.: No conflict of interest. Oswald, P.: No conflict of interest. Carpentier, P.J.: No conflict of interest. De Rossi, P.: No conflict of interest. Delorme, R.: No conflict of interest. Markovska Simoska, S.: No conflict of interest. Pallanti, S.: No conflict of interest. Young, S.: Honoraria for consultancy, travel, educational talks and/or research from Janssen, Eli Lilly, HB Pharma, and/or Shire. She is author of the Young-Bramham CBT Programme. Lehtonen, T. No conflict of interest. Hirvikoski, T.: no conflict of interest related to this article. Royalties for text books and manuals from Hogrefe. Pironti, V.: No conflict of interest. Ginsberg, Y.: Speaker fees, reimbursement for travel costs and/or consultant for Novartis, HB Pharma, Shire, Eli Lilly, Hogrefe, Broadman Clarke Partners, Medscape, Medibas and Natur & Kultur. Félegyházy, Z.: No conflict of interest. Richarte, V.: Speakers’ bureau for Eli-Lilly, Shire in the last 5 years. Travel awards (air tickets + hotel) for psychiatric meetings from Shire. The Department of Psychiatry received unrestricted educational and research support in the last 5 years from: Eli-Lilly, Lundbeck, Janssen- Cilag, Actelion, Shire, Ferrer, and Rubió. Kustow, J.: Consultancy services to Eli Lilly and Shire and speaker fees from Eli Lilly, Jansen Cilag and Shire. Müller, U.: Advisory board / consultancy fees or speaker honorarium from Eli Lilly, Heptares and Shire, Educational grants / travel expenses from Eli Lilly, Flynn Pharma / Medice, Janssen-Cilag, Lundbeck, Shire and Sunovion (all United Kingdom). Bejerot, S.: No conflict of interest. Semerci, B.: No conflict of interest. Dobrescu, I.: No conflict of interest. Styr, B.: No conflict of interest. Rad, F.: No conflict of interest. Mihailescu, I.: No conflict of interest. Garcia-Portilla, M.P.: No conflict of interest. Asherson, P.: Kings College London research support account for Asherson received honoraria for consultancy to Shire, Eli-Lilly and Novartis; educational/research awards from Shire, Lilly, Novartis, Vifor Pharma, GW Pharma and QbTech; speaker at sponsored events for Shire, Lilly and Novartis.

Acknowledgement

This project did not receive any financial support from funding agencies in the public, commercial, or not-for-profit sectors.

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