Guidelines for identification ad treatment of individuals with Attention Deficit/Hyperactivity Disorder and associated Fetal Alcohol Spectrum disorders based upon expert consensus
File(s)
Author(s)
Type
Journal Article
Abstract
Background: The association of attention deficit/hyperactivity disorder (ADHD) and fetal alcohol
spectrum disorders (FASD) results in a complex constellation of symptoms that complicates the
successful diagnosis and treatment of the affected individual. Current literature lacks formal guidelines,
randomized control trials, and evidence-based treatment plans for individuals with ADHD and associated
FASD. Therefore, a meeting of professional experts was organized with the aim of producing a
3
consensus on identification and treatment guidelines that will aid clinicians in caring for this unique
patient population.
Methods: Experts from multiple disciplines in the fields of ADHD and FASD convened in London, United
Kingdom, for a meeting hosted by the United Kingdom ADHD Partnership (UKAP; www.UKADHD.com) in
June 2015. The meeting provided the opportunity to address the complexities of ADHD and FASD from
different perspectives and included presentations, discussions, and group work. The attendees worked
towards producing a consensus for a unified approach to ADHD and associated FASD.
Results: The authors successfully came to consensus and produced recommended guidelines with
specific regards to identification and assessment, interventions and treatments, and multiagency
liaisons and care management, highlighting that a lifespan approach to treatment needs to be adopted
by all involved. Included in the guidelines are: 1) unique ‘red flags’, which when identified in the ADHD
population can lead to an accurate associated FASD diagnosis, 2) a treatment decision tree, and 3)
recommendations for multiagency care management.
Conclusions: While clinically useful guidelines were achieved, more research is still needed to contribute
to the knowledge base about the diagnosis, treatment, and management of those with ADHD and
associated FASD.
spectrum disorders (FASD) results in a complex constellation of symptoms that complicates the
successful diagnosis and treatment of the affected individual. Current literature lacks formal guidelines,
randomized control trials, and evidence-based treatment plans for individuals with ADHD and associated
FASD. Therefore, a meeting of professional experts was organized with the aim of producing a
3
consensus on identification and treatment guidelines that will aid clinicians in caring for this unique
patient population.
Methods: Experts from multiple disciplines in the fields of ADHD and FASD convened in London, United
Kingdom, for a meeting hosted by the United Kingdom ADHD Partnership (UKAP; www.UKADHD.com) in
June 2015. The meeting provided the opportunity to address the complexities of ADHD and FASD from
different perspectives and included presentations, discussions, and group work. The attendees worked
towards producing a consensus for a unified approach to ADHD and associated FASD.
Results: The authors successfully came to consensus and produced recommended guidelines with
specific regards to identification and assessment, interventions and treatments, and multiagency
liaisons and care management, highlighting that a lifespan approach to treatment needs to be adopted
by all involved. Included in the guidelines are: 1) unique ‘red flags’, which when identified in the ADHD
population can lead to an accurate associated FASD diagnosis, 2) a treatment decision tree, and 3)
recommendations for multiagency care management.
Conclusions: While clinically useful guidelines were achieved, more research is still needed to contribute
to the knowledge base about the diagnosis, treatment, and management of those with ADHD and
associated FASD.
Date Issued
2016-09-22
Date Acceptance
2016-08-24
Citation
BMC Psychiatry, 2016, 16
ISSN
1471-244X
Publisher
BioMed Central
Journal / Book Title
BMC Psychiatry
Volume
16
Copyright Statement
© 2016 The Author(s). Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver
(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver
(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
License URL
Sponsor
Shire Pharmaceuticals Development Ltd
Grant Number
RTJ6011480
Subjects
Psychiatry
1103 Clinical Sciences
Publication Status
Published
Article Number
324