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Appraisal of clinical practice guidelines for the management of attention deficit hyperactivity disorder (ADHD) using the AGREE II Instrument: A systematic review

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Background and objective High quality evidence-based clinical practice guidelines (CPGs) have a major impact on the appropriate diagnosis and management and positive outcomes. The evidence-based healthcare for patients with attention deficit hyperactive disorder (ADHD) is challenging. The objective of this study was to appraise the quality of published CPGs for ADHD. Methods A systematic review was conducted for ADHD CPGs using CPG databases, DynaMed, PubMed, and Google Scholar. The quality of each included CPG was appraised by three independent appraisers using the Appraisal of Guidelines for Research & Evaluation II (AGREE II) instrument. Results Six CPGs were critically reviewed. The AGREE II standardized domain scores revealed variation between the quality of these CPGs with the National Institute of Health and Care Excellence (NICE), University of Michigan Health System, and American Academy of Pediatrics CPGs as the top three. Overall, the recommendations for management of ADHD were similar in these CPGs. Conclusions Reporting of CPG development is often poorly documented. Guideline development groups should aim to follow the AGREE II criteria to improve the standards and quality of CPGs. The NICE CPG showed the best quality. Embedding the AGREE II appraisal of CPGs in the training and education of healthcare providers is recommended. The protocol for this study was published in PROSPERO (International prospective register of systematic reviews). Link: http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=CRD42017078712 and is additionally available from protocols.io. Link: https://dx.doi.org/10.17504/protocols.io.q27dyhn.
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RESEARCH ARTICLE
Appraisal of clinical practice guidelines for the
management of attention deficit hyperactivity
disorder (ADHD) using the AGREE II
Instrument: A systematic review
Yasser Sami AmerID
1,2,3,4
*, Haya Faisal Al-Joudi
5
, Jeremy L. VarnhamID
6,7
, Fahad
A. Bashiri
8
, Muddathir Hamad Hamad
8
, Saleh M. Al Salehi
9
, Hadeel Fakhri Daghash
10
,
Turki Homod Albatti
6,11
, on behalf of The Saudi ADHD Society
1CPG Unit, Quality Management Department, King Saud University Medical City, Riyadh, Saudi Arabia,
2Pediatrics Department, King Khalid University Hospital, King Saud University Medical City, Riyadh,
Saudi Arabia, 3Research Chair for Evidence-Based Health Care and Knowledge Translation, Deanship of
Scientific Research, King Saud University, Riyadh, Saudi Arabia, 4Alexandria Center for Evidence-Based
Clinical Practice Guidelines, Alexandria University, Alexandria, Egypt, 5Department of Neurosciences,
King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia, 6Saudi ADHD Society, Riyadh,
Saudi Arabia, 7School of Psychology, University of East London, London, United Kingdom, 8Division of
Neurology, Department of Pediatrics, College of Medicine, King Saud University Medical City, King Saud
University, Riyadh, Saudi Arabia, 9Child Development Center, King Abdullah Bin Abdulaziz University
Hospital, Princess Noura Bint AbdulRahman University, Riyadh, Saudi Arabia, 10 Ada’a Program, Assistant
Deputyship for Hospital Services, Ministry of Health, Riyadh, Saudi Arabia, 11 Department of Psychiatry,
King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia
Membership of the Saudi ADHD Society is provided in the Acknowledgments
*yassersamiamer@gmail.com
Abstract
Background and objective
High quality evidence-based clinical practice guidelines (CPGs) have a major impact on
the appropriate diagnosis and management and positive outcomes. The evidence-based
healthcare for patients with attention deficit hyperactive disorder (ADHD) is challenging. The
objective of this study was to appraise the quality of published CPGs for ADHD.
Methods
A systematic review was conducted for ADHD CPGs using CPG databases, DynaMed,
PubMed, and Google Scholar. The quality of each included CPG was appraised by three
independent appraisers using the Appraisal of Guidelines for Research & Evaluation II
(AGREE II) instrument.
Results
Six CPGs were critically reviewed. The AGREE II standardized domain scores revealed
variation between the quality of these CPGs with the National Institute of Health and Care
Excellence (NICE), University of Michigan Health System, and American Academy of
PLOS ONE | https://doi.org/10.1371/journal.pone.0219239 July 5, 2019 1 / 15
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OPEN ACCESS
Citation: Amer YS, Al-Joudi HF, Varnham JL,
Bashiri FA, Hamad MH, Al Salehi SM, et al. (2019)
Appraisal of clinical practice guidelines for the
management of attention deficit hyperactivity
disorder (ADHD) using the AGREE II Instrument: A
systematic review. PLoS ONE 14(7): e0219239.
https://doi.org/10.1371/journal.pone.0219239
Editor: Pan Lin, South-Central University for
Nationalities, CHINA
Received: July 21, 2018
Accepted: June 19, 2019
Published: July 5, 2019
Copyright: ©2019 Amer et al. This is an open
access article distributed under the terms of the
Creative Commons Attribution License, which
permits unrestricted use, distribution, and
reproduction in any medium, provided the original
author and source are credited.
Data Availability Statement: All relevant data are
within the paper and its Supporting Information
files.
Funding: This work was supported by Saudi ADHD
Society. URL: https://adhd.org.sa/. This is part of a
comprehensive project for adaptation of National
CPG for ADHD sponsored by the Saudi ADHD
Society. The funders had no role in study design,
data collection and analysis, decision to publish, or
preparation of the manuscript.
Pediatrics CPGs as the top three. Overall, the recommendations for management of ADHD
were similar in these CPGs.
Conclusions
Reporting of CPG development is often poorly documented. Guideline development groups
should aim to follow the AGREE II criteria to improve the standards and quality of CPGs.
The NICE CPG showed the best quality. Embedding the AGREE II appraisal of CPGs in the
training and education of healthcare providers is recommended.
The protocol for this study was published in PROSPERO (International prospective regis-
ter of systematic reviews). Link: http://www.crd.york.ac.uk/PROSPERO/display_record.
php?ID=CRD42017078712 and is additionally available from protocols.io. Link: https://dx.
doi.org/10.17504/protocols.io.q27dyhn.
Introduction
Attention deficit hyperactivity disorder [1,2] or Attention-Deficit/ Hyperactivity Disorder
[3,4] (ADHD), is a chronic neurodevelopmental disorder characterized by developmentally
inappropriate levels of hyperactivity-impulsivity and/or inattention [19]. ADHD is clinically
and genetically heterogeneous with multiple possible etiologies and frequent neuropsychiatric
comorbidities [10,11]. ADHD is highly prevalent in 5–6% of children and in 3.8–4.4% of adults
[12].
Clinical practice guidelines (CPGs) summarize the best available evidence and provide
guidance for healthcare providers during their daily practice. CPGs can support the knowl-
edge-to-action cycle effectively if they were developed using a systematic and rigorous meth-
odology. Published evidence has revealed that CPGs can improve patient outcomes, patient
experience, and quality and safety in healthcare [13].
In 2011, the Health and Medicine Division (HMD) of the American National Academies,
formerly the Institute of Medicine (IOM), published its eight criteria of trustworthy CPGs,
Clinical Practice Guidelines We Can Trust [14]. Since then, many sets of standards or criteria
for high quality CPGs have been published or updated, including the Guidelines International
Network’s [15], the GIN-McMaster Checklist [16], and the AGREE II Reporting Checklist
[17], based upon the AGREE II Instrument’s 23 criteria. These standards have helped in shap-
ing the development process and methodologies of CPGs worldwide [18].
Two systematic reviews of CPG appraisal tools have included a total of 64 tools [19,20];
these revealed that the AGREE II Instrument was the only tool that had a validated scoring sys-
tem, as well as already being widely adopted. It has proven to become the international gold
standard for quality assessment and development of CPGs, being cited more than 746 times
between 2013–2018 [21].
A brief review of literature on the utilization of AGREE II for ADHD CPGs revealed two
uses: One was restricted to psychopharmacological management of ADHD [22], and the other
was conducted as part of a Master’s thesis in Pediatrics at Alexandria University [23]. The pri-
mary objective of this study is to provide a comprehensive, easily accessible, and updated
assessment of the quality of available CPGs pertaining to ADHD diagnosis and management,
using the gold standard instrument, AGREE II; CPGs included were published between 2012
and 2019, following the publication of the HDM and G-I-N CPG standards. Earlier published
Quality of guidelines for attention deficit hyperactivity disorder
PLOS ONE | https://doi.org/10.1371/journal.pone.0219239 July 5, 2019 2 / 15
Competing interests: The authors have declared
that no competing interests exist.
CPGs in general were found to be of variable quality and poor compliance with available meth-
odological standards at that time [24,25]
Methods
The protocol for this study was published in PROSPERO (International prospective register of
systematic reviews). Link: http://www.crd.york.ac.uk/PROSPERO/display_record.php?ID=
CRD42017078712 [26] and is also available from Protocols.io. Link: https://dx.doi.org/10.
17504/protocols.io.q27dyhn [25].
Eligibility criteria
Criteria for including CPGs were: (1) Evidence-based CPGs (i.e. with a clear description of the
development methodology); (2) English language; (3) original source CPGs (de novo devel-
oped); (4) both national and international CPGs; (5) published between January 1, 2012 and
July 1, 2017 (the search was further extended till June 15, 2019); (6) published by an organiza-
tion or group authorship in a CPG database or peer-reviewed journal. Only the most current
version of each source CPG was included whether in the format of a full CPG document
retrieved from the developing organization’s official website or in the form of a full-text publi-
cation that was authored by the CPG development group.
We excluded CPGs that were published earlier than 2012, written in non-English language,
presented as consensus or expert-based statements or CPGs, adapted from other source CPG
(s), or that had single authorship. Relevant publications summarizing or reporting implemen-
tation of the included CPGs by different authors were not considered for this CPG appraisal.
Information resources (identification of ADHD CPGs)
We used literature searches of bibliographic databases (Medline/PubMed and Google Scholar),
EBSCO DynaMed Plus (US), and CPG databases: American Agency for Healthcare Research
and Quality’s (AHRQ) National Guideline Clearinghouse (US), Guidelines International Net-
work (GIN), Scottish Intercollegiate Guidelines Network (SIGN; UK), National Institute of
Health and Care Excellence (NICE; UK), and the Australian National Health and Medical
Research Council (NHMRC). We also searched databases of national and international socie-
ties specializing in fields related to ADHD (e.g. American Psychiatric Association, European
Psychiatric Association).
Search, Screen, and Study Selection
Keywords used included attention-deficit/hyperactivity disorder” or ADHD,” and guideline,”
practice guideline,” clinical practice guideline,” practice parameter,” guidance,” or recom-
mendations [2628].
The PubMed search strategy included "attention deficit hyperactivity disorder"[tiab] OR
"ADHD"[tiab]. Filters activated: Guideline, Publication date from 2012/01/01 to 2018/06/30
(extended to 2019/6/15), Humans.
Additionally, we used the PIPOH (Patient Population, Interventions, Professionals, Out-
comes, and Healthcare Setting) checklist [18,28] to further assist in the inclusion and exclusion
process. The following is a description of the characteristics derived from and used via PIPOH:
Our patient population (P) was children and adults being assessed for or with a diagnosis of
ADHD. Interventions (I) included diagnosis (complaints of the parent, teacher, or adolescent,
history and physical examination, psychological tools, investigations, comorbidities) and treat-
ment (pharmacological treatment, psychological and behavioral interventions, adverse effects
Quality of guidelines for attention deficit hyperactivity disorder
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of treatments, treatment of adverse effects, monitoring, special cases, complementary medi-
cine, and transition of care from childhood to adulthood). Type of professionals (P) included
physicians (e.g. psychiatrists, pediatricians, and neurologists), clinical psychologists, pharma-
cists, nurses, dieticians, occupational therapists, and social workers. Major outcomes (O)
included ADHD symptom severity, academic performance, functional status, side effects of
stimulant medications, and quality of life. Healthcare setting (H) included primary, secondary,
and tertiary care settings addressing assessment, treatment, and management of ADHD.
Two reviewers (YA, JV) independently screened titles and abstracts of retrieved CPGs and
articles meeting the inclusion criteria. The screening was rechecked by three other reviewers
(TA, FB, MH). Disagreements were resolved by further discussions with the entire group after
retrieval and review of the full CPG documents or full-text articles, including links to any avail-
able supplemental documents or web pages. We repeated our search before the final manu-
script re-submission in June 2019 based on the pre-publication peer review to identify any
new eligible CPGs.
Assessment of CPGs using the AGREE II Instrument
The AGREE II Instrument (www.agreetrust.org) consists of 23 items or questions organized in
six domains including scope and purpose (items 1–3), stakeholder involvement (items 4–6),
rigor of development (items 7–14), clarity of presentation (items 15–17), applicability (items
18–21), and editorial independence (items 22–23). Each item or question is scored on a Likert
scale from one to seven, where 1 = strongly disagree and 7 = strongly agree. The AGREE II
assessment was conducted by using the “My AGREE PLUS” online tool developed by the
AGREE Enterprise. My AGREE PLUS supports the AGREE II assessment process by creating
a CPG “appraisal group” for each CPG, compiling and calculating the items’ scores into
domain scores, and generating the final reports. My AGREE PLUS users are required to com-
plete a free registration process before starting the AGREE online assessment for a given CPG.
Each CPG appraisal group is handled by a “coordinator” who registers group’s details, invites
assessors, reviews data, and generates the final AGREE II reports. Two separate reports can be
generated from My AGREE PLUS once the CPG group assessment is completed: One for the
“ratings” (i.e. individual item scores and standardized domain scores) and another for the
“comments.” Additionally, the AGREE website provides online audiovisual training resources
for using the AGREE II Instrument, as well as videos describing different functionalities of the
My AGREE PLUS online platform.
Seven AGREE II assessors were selected with a wide range of clinical expertise (a child psy-
chiatrist, two pediatric neurologists, a developmental pediatrician, a clinical neuropsycholo-
gist, a clinical pharmacist, and a general pediatrician and CPGs methodologist). At the outset
of this project, AGREE II capacity building was conducted for the assessors by the expert
methodologist through training and hands-on sessions in the concepts and standards of CPGs,
and using the instrument. Each reviewer independently scored his/her assigned CPGs. Each
one of the included CPGs was independently appraised by three reviewers: two clinicians and
a methodologist.
All assessors reviewed the full CPG document, in addition to any supplementary docu-
ments or links to online pages related to the guideline’s methodology or implementation tools.
For each item, AGREE assessors were asked to record the rationale for their scores in the com-
ment section. Differences between assessors’ scores were resolved by asking those who had
provided outlying scores to re-assess after discussion with the group. The disagreements were
mainly observed in questions highly related to the CPG development methodology (i.e. ques-
tions 7–14 of domain 3) and implementation (especially question 18 of domain 5). The
Quality of guidelines for attention deficit hyperactivity disorder
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percentage of preliminary disagreements in some CPGs was 9 per 23 questions (39%) but were
less in subsequently appraised CPGs with the rising learning and understanding curve for uti-
lizing the AGREE II criteria for quality assessment. The standardized AGREE domain scores
(ranging from 0 to 100%) were automatically calculated by My AGREE PLUS following the
equations provided by the AGREE II User’s Manual.
A cut-off point of 60% for each AGREE standardized domain score was agreed upon by the
reviewers, with more weight emphasized on the scores of domains three and five to facilitate
the final assessment of the reporting quality of CPGs. Similar categorization of domains was
recently reported and published [13,29,30].
An additional validation of the six CPGs for inclusion of systematic reviews with or without
meta-analyses in their evidence-base and the frequency and percentage of Cochrane systematic
reviews among these reviews was conducted.
Moreover, we checked whether the Grading of Recommendations Assessment, Develop-
ment and Evaluation (short GRADE) methodology was utilized for the CPG development pro-
cess as several CPG developing organizations are increasingly shifting to using the GRADE
(e.g. World Health Organization, NICE, SIGN, NHMRC, etc.) [3134]. The GRADE is a
method of assessing the certainty in evidence (i.e. quality of evidence or confidence in effect
estimates) and the strength of recommendations in health care. It has important implications
for summarizing evidence for systematic reviews, health technology assessments, and CPGs as
well as other decision makers [35,36].
Results
Identification of ADHD CPGs
The results of the search were summarized in S1 Fig. The initial list of 30 retrieved CPGs was
reviewed, discussed and filtered by the assessors. Six recent ADHD CPGs complying with the
identified PIPOH and inclusion criteria were eligible. These CPGs were developed by the
American Academy of Pediatrics (AAP) in 2012, the University of Michigan Health System
(UMHS) in 2012, the National Institute of Health and Care Excellence (NICE) in 2016
(updated in 2018), the National Health Medical Research Center (NHMRC) in 2013, the Cana-
dian ADHD Resource Alliance (CADDRA) in 2014 (updated in 2018), and the Singapore Min-
istry of Health (SMOH) in 2014 [3742].
An updated search and screen was conducted for ADHD Source CPGs in June 2019 using
the same aforementioned information resources and criteria. This repeated search did not
reveal any eligible CPG that needed to be added to the previous AGREE appraisal. Though
excluded, several recent CPGs or relevant online material were worthwhile to mention due to
the national and/or international impact of their publishing organizations.
Examples of these (with reasons for exclusion) include (i) the Interdisciplinary Evidence-
and Consensus-based Guideline “ADHD in Children, Young People and Adults” June 2018 by
the Association of the Scientific Medical Societies in Germany (AWMF) Online (in German)
[43]; (ii) CPG on Therapeutic Interventions in ADHD 2017 by the Working group of the Clin-
ical Practice Guideline on Therapeutic Interventions in ADHD, Ministry of Health, Social
Services and Equality, Health Sciences Institute in Aragon (IACS) (in Spanish) [44]; (iii) the
Updated European Consensus Statement on diagnosis and treatment of adult ADHD 2019 by
the European Network Adult ADHD (ENAA) (Consensus statement) [45], (iv) British Associ-
ation for Psychopharmacology’s (BAP) CPG for the pharmacological management of ADHD
2014 (Consensus statement) [46], and (v) the Centers for Disease Control and Prevention
endorsed and posted the AAP treatment recommendations in their official website as of Sep-
tember 2018 (adopted AAP 2011 CPG) [47].
Quality of guidelines for attention deficit hyperactivity disorder
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A number of online resources for the professionals and public summarized and discussed
the recommendations of some these CPGs and relevant documents for example DynaMed
Plus (updated in May 2019) [48,49], the World Federation ADHD Guide (2019) [50], and the
ADHD Institute (updated in March 2019) [51] but without using a formal CPG appraisal tool
like the AGREE II Instrument [19,20].
Key characteristics of CPGs
Tables 1and 2demonstrate characteristics of all eligible CPGs. The eligible CPGs included
five national CPGs (AAP, NICE, NHMRC, CADDRA, and SMOH) and one local CPG
(UMHS). Two CPGs were developed by US-based organizations (n = 2, 33%), followed by one
CPG (n = 1, 17%) developed by each of a Canadian-based, UK-based, Australian-based, and
Singaporean-based organization respectively. The six included CPGs were developed by gov-
ernmental bodies (n = 3, 50%), medical specialty society (n = 2, 33%), and healthcare improve-
ment and CPG developer organizations (n = 2, 33%).
Table 1. Characteristics of the ADHD clinical practice guidelines (general).
Title Year of
publication
Country Level of
development
Organization
(short name)
Total number of
references
American Academy of Pediatrics (AAP) CPG on diagnosis, evaluation,
and treatment of ADHD in children and adolescents (37)
2012 United
States
National AAP 70
Canadian ADHD Resource Alliance (CADDRA)-Canadian ADHD CPGs
(CAP-Guidelines) 3
rd
Edition (updated in 4
th
edition). (39)
2015 (updated
2018)
Canada National CADDRA 264
National Health and Medical Research Council (NHMRC) Clinical
Practice Points on diagnosis, assessment, and management of ADHD in
children and adolescents (40)
2014 Australia National NHMRC 112
National Institute for Health and Care Excellence (NICE) ADHD CPG
(42)
2016 (updated
2018)
United
Kingdom
National NICE 2941
Singapore Ministry of Health (SMOH) Guideline on ADHD (41) 2013 Singapore National SMOH 250
University of Michigan Health System ADHD (UMHS) (38) 2013 USA Local UMHS 14
https://doi.org/10.1371/journal.pone.0219239.t001
Table 2. Characteristics of the ADHD clinical practice guidelines (clinical content/ options of care).
Clinical content/ Options of care AAP
(37)
CADDRA
(39)
NHMRC
(40)
NICE
(42)
SMOH
(41)
UMHS
(38)
Diagnosis and Assessment
1. Parent/ Teacher/ Patient (adolescent) complaints Y Y Y Y Y Y
2. Clinical picture Y N Y Y N Y
3. Psychological Tools Y Y N N N Y
4. Differential diagnosis Y Y N Y Y Y
5. Investigations N Y N N Y Y
6. Treatment
7. Psychological and Behavioral interventions (PBI) Y Y Y Y Y Y
8. Pharmacological treatment Y Y Y Y Y Y
9. Treatment of adverse effects of pharmacological treatment Y Y Y Y N Y
10. Comorbidities Y Y Y Y Y Y
11. Monitoring Y Y Y Y Y Y
12. Special cases Y N N N N Y
13. Complementary medicine Y N Y N Y Y
14. Transition of care from childhood to adulthood Y N Y Y Y N
Y = Yes (included); N = No (not included)
https://doi.org/10.1371/journal.pone.0219239.t002
Quality of guidelines for attention deficit hyperactivity disorder
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Reporting the quality of ADHD CPGs
The AGREE II standardized domain scores were summarized in Table 3.
Domain 1: Scope and purpose. The AGREE II standardized score for domain 1 ranged
from 37% to 100%. Scores of all CPGs were greater than 60% in domain 1 except the SMOH
CPG, in which the limited description of overall objectives, health questions, and patient
populations resulted in a lower score. The two CPGs scoring more than 90% were NICE and
UMHS.
Domain 2: Stakeholder involvement. The AGREE II standardized domain scores for
domain 2 ranged from 43% to 96%. Scores of all CPGs were greater than 60% in domain 1
except the SMOH, CADDRA, and UMHS CPGs. The lack of adequate descriptions of patient
preferences or target users resulted in the low scores for these CPGs. Only the NICE CPG
scored more than 90%.
Domain 3: Rigor of development. The AGREE II standardized scores for domain 3 ran-
ged from 35% to 93%. Three CPGs received scores greater than or equal to 60%: NICE (93%),
Table 3. AGREE II domain-standardized scores (ratings) for CPGs on management of ADHD.
ADHD CPGs (reference)/ AGREE II
Domains-standardized scores
AAP
(37)
CADDRA
(39)
NICE
(42)
NHMRC
(40)
SMOH
(41)
UMHS
(38)
Domain 1. Scope and Purpose
Items 1–3: Objectives; Health question(s);
Population (patients, public, etc.).
80% 74% 100% 72% 37% 91%
Domain 2. Stakeholder Involvement
Items 4–6: Group Membership; Target
population preferences and views; Target
users.
67% 50% 96% 76% 59% 43%
Domain 3. Rigour of development
Items 7–14: Search methods; Evidence
selection criteria; Strengths and limitations
of the evidence; Formulation of
recommendations; Consideration of benefits
and harms; Link between recommendations
and evidence; External review; Updating
procedure.
66% 35% 93% 53% 47% 60%
Domain 4. Clarity and presentation
Items 15–17: Specific and unambiguous
recommendations; Management options;
Identifiable key recommendations
76% 63% 89% 65% 83% 81%
Domain 5. Applicability
Items 18–21: Facilitators and barriers to
application; Implementation advice/ tools;
Resource implications; Monitoring/ auditing
criteria
64% 35% 92% 29% 69% 69%
Domain 6. Editorial independence
Items 22, 23: Funding body; Competing
interests
75% 78% 92% 67% 28% 69%
Overall Assessment 1
(Overall quality)
56% 67% 100% 56% 50% 72%
Overall Assessment 2
(Recommend the CPG for use)
Yes-1,Yes with
modifications-2,
No-0
Yes-1,Yes with
modifications-2,
No-0
Yes-1,Yes with
modifications-2,
No-0
Yes-0,Yes with
modifications-3,
No-0
Yes-0,Yes with
modifications-2,
No-1
Yes-2,Yes with
modifications-1,
No-0
AGREE II Assessors HA,TA,YA SA,TA,YA FB,MH,YA HD,TA,YA FB,HD,YA HA,SA,YA
American Academy of Pediatrics (AAP), the University of Michigan Health System (UMHS), National Institute of Health and Care Excellence (NICE), the National
Health Medical Research Center (NHMRC), the Canadian ADHD Resource Alliance (CADDRA), and the Singapore Ministry of Health (SMOH), Clinical Practice
Guidelines (CPGs), AGREE II (Appraisal of Guidelines for Research and Evaluation Instrument Version II)
https://doi.org/10.1371/journal.pone.0219239.t003
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AAP (66%), and UMHS (60%). The rest (NHMRC, CADDRA, and SMOH) received less than
60% in domain 3. Comprehensive search methods and strategy, evidence selection criteria,
strengths and limitations of the evidence (evidence tables), detailed process of formulation
of recommendations, discussion of the process of trade-off between risks and benefits, process
of external review, and details of the updating process were the most common weaknesses
among the NHMRC, CADDRA, and SMOH CPGs.
Domain 4: Clarity of presentation. The AGREE II standardized scores for domain 4 ran-
ged from 63% to 89%. Scores of all CPGs were greater than 60% in domain 4. This domain was
well-addressed in all included CPGs, where recommendations were specific, unambiguous, and
easily identifiable in all CPGs. Three CPGs scored more than 80% (NICE, SMOH, and UMHS).
Domain 5: Applicability. The AGREE II standardized scores for domain 5 ranged from
29% to 92%. Scores of all CPGs were greater than 60% in domain 5 except CPGs for CADDRA
and NHMRC, where facilitators, barriers, monitoring and auditing criteria, resource implica-
tions, and formal cost-analyses were not addressed. NICE CPG received the highest score,
being the only guideline that received a score above 90%.
Domain 6: Editorial independence. The AGREE II standardized scores for domain 6
ranged from 28% to 92%. Scores of all CPGs were greater than 60% except the SMOH CPG.
Overall assessment. The AGREE II standardized domain scores for overall assessment
ranged from 50% to 100%. All CPGs scored greater than 60% in the first overall assessment,
except AAP, NHMRC and SMOH. Overall the NICE CPG received the highest scores on all
six AGREE II domains, in addition to the highest score in the first overall assessment; it was
the only CPG that received a score of 100%.
Recommending the CPGs for use in practice. The second (overall) assessment, pertain-
ing to the overall recommendation for using the given CPG in clinical practice, revealed a vari-
ation between this score and the individual scores of domains in each CPG. This could be
illustrated in the NICE CPG where this second overall assessment did not reflect a similarly
high score as the scores received in the other six domains and the first overall assessment (i.e.
in it, two assessors recommended NICE CPG for use with modifications, and one recom-
mended it for use without modifications). A similar result was noted in the assessment of the
AAP and CADDRA despite lower scores in other domains. UMHS was recommended for use
by two appraisers. Nevertheless, there was an observed overall consistency in the recommen-
dations of ADHD management throughout the included CPGs despite the variable strengths
and weaknesses in each CPG according to the AGREE II criteria. This included diagnosing
ADHD using the DSM-5 criteria, identifying comorbidities, initiation of the psycho-social or
psycho-behavioral treatment, different management plans according to the age group, and
stepwise approach of the pharmacological treatment with psycho-stimulants as the first-line.
All included CPGs cited systematic reviews and meta-analyses in their references list. The
largest number of systematic reviews was observed in the evidence-base of the CPGs from
NICE (N = 67), SMOH (N = 17), NHMRC (N = 14), CADDRA (N = 7), AAP (N = 2), and
UMHS (N = 1) in descending order. Cochrane systematic reviews were only included in
three CPGs: NICE (n = 19, 28%), NHMRC (n = 5, 36%), and SMOH (4, 24%). Moreover, two
Cochrane systematic reviews were mentioned in the text of the UMHS CPG but were not cited
in the references section and henceforth were considered not reported (0) (S2 Table). Overall,
the lines of management of ADHD were similar in these CPGs (S3 Table).
Discussion
The aim of this systematic review was to explore the quality of and critically appraise recently
published evidence-based CPGs for the management of ADHD in all age groups [26]. An
Quality of guidelines for attention deficit hyperactivity disorder
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additional purpose was to assist clinicians and CPG groups in identifying high-quality and
trustworthy evidence-based CPGs for ADHD using the AGREE II criteria.
Internationally accepted standards and appraisal tools for evidence-based CPGs recom-
mend the transparent reporting of the CPG development process. This process includes; (i)
selection of the health topic, (ii) composition of the CPG development group, (iii) key health
questions, (iv) scope of the CPG, (v) systematic evidence review and decision-making process,
(vi) formulation and articulation of CPG recommendations, ratings of evidence and recom-
mendations, and evidence-to-recommendations links, (vii) implementation considerations
and tools, (viii) peer review and stakeholder consultations, (ix) CPG expiration and updating,
(x) financial support and sponsoring organization, and (xi) management of conflicts of inter-
est [1418]. Our appraisal, conducted using the AGREE II Instrument, highlighted several
areas for improvement in the methodological rigor of the ADHD CPGs included for critical
appraisal. The ADHD CPGs had several gaps in their Rigor of Development (Domain 3),
which is the largest (and the core) AGREE II domain and in their Applicability (Domain 5) as
well. Highlighting the importance of these two domains has been suggested [52]. There was
consistency in ADHD recommendations despite variable evidence-bases. This consistency
may reflect consensus in the healthcare community towards management of ADHD, despite
the absence of a strong evidence-base in some CPGs. The AGREE II instrument has under-
gone several updates and improvements. Some of the shortcomings of the AGREE II instru-
ment has been addressed in a recently developed tool entitled ‘AGREE-REX’
(Recommendation EXcellence) that addresses clinical credibility and implementability of the
CPG recommendations. This new tool has been validated and is currently being refined before
being shared publicly [53].
To the best of our knowledge, this is the first study to systematically evaluate the quality
of recently published CPGs for management of ADHD in all age groups using the complete
AGREE II instrument. The ADHD CPG review by the Canadian Agency for Drugs and Tech-
nologies in Health, even though limited to pharmacological treatment, is highly consistent with
our findings [19]. It listed the AAP, and SMOH as the most rigorous ADHD CPGs. The afore-
mentioned Alexandria University thesis reviewed 4 ADHD CPGs identified at the time of that
study (viz. NICE 2008, AAP 2011, SIGN 2009, and ICSI 2010), with similar findings for the
NICE and AAP CPGs as this appraisal [23]. Andrade et al systematically reviewed CPGs for the
assessment, prevention and treatment of disruptive behavior (including ADHD, oppositional
defiant disorder, conduct disorder and aggression) in children and youth using the AGREE II
Instrument. It priotitized three AGREE II domians, viz. domains 2,3, and 6, to classify CPGs
[54]. Despite being more broad in the scope of the review in terms of diagnosis (i.e. disruptive
behavior) and more specific in terms of the age group (i.e. children and youth), it revealed over-
all similar results including selecting domain 3(rigor of development) as a key domain for filter-
ing CPGs and displaying NICE as a superior ADHD CPG [54]. Moreover, Andrade chose to
use different cutoffs for quality ratings (viz. 50% for minimum and 70% for maximum) [54].
Our review showed that only one ADHD CPG applied the GRADE methodology to
appraise the quality of evidence (NICE) [31]. The NICE CPG development methodology is
based on internationally recognized CPG standards like the AGREE II criteria, the Guideline
Implementability Appraisal tool, in addition to primary methodological research and evalua-
tion conducted by NICE. It includes transparent and clear health questions, search strategy,
selection criteria for evidence, critical appraisal of clinical and economic evidence, consulta-
tion and validation process, and a noted component for implementation considerations and
tools [31]. The NHMRC announced on its website that it started developing CPGs using
GRADE in 2016 which followed the publication date of its most recent ADHD CPG (2012)
[33]. All six CPGs under study included cross-referenced systematic reviews but only three
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CPGs included Cochrane reviews (NICE, NHMRC, and SMOH) despite increased production
of Cochrane reviews. Currently, the total number of ADHD-related systematic review proto-
cols registered in the PROSPERO database is 417, which comprises 337 ongoing reviews, 35
completed but not published including this review under study, 39 completed and published,
one review is ongoing update, and two reviews that were discontinued [55]. Four Cochrane
reviews on; (i) cognitive-behavioral interventions for attention deficit hyperactivity disorder
(ADHD) in adults, (ii) methylphenidate for attention deficit hyperactivity disorder (ADHD)
in children and adolescents—assessment of adverse events in non-randomised studies; (iii)
Pharmacological treatment for attention deficit hyperactivity disorder (ADHD) in children
with comorbid tic disorders; and (iv) Amphetamines for attention deficit hyperactivity disor-
der (ADHD) in adults in addition to 9 protocols were published after the publication of the
NICE CPG in 16
th
of March 2018 [5659]. Despite the utilization of systematic reviews in the
included ADHD CPGs, an area for improvement remains regarding the utilization of high-
quality systematic reviews like Cochrane reviews in these CPGs. Similar recommendations
were reported by Vale et al [60].
Furthermore, other reviews were published for ADHD but none have utilized a validated
tool such as the AGREE II Instrument except the review by Siexas et al. that utilized the first
version of the AGREE Instrument [6164]. This appraisal was also conducted by a multidisci-
plinary team and an expert methodologist, which adds a layer of strength to the assessment.
Moreover, an additional implication for practice is to encourage healthcare providers car-
ing for patients with ADHD to adopt principles of ‘Evidence-Based’ rather than ‘Eminence-
Based’ Healthcare in their daily practice through training and education on CPG standards
and appraisal tools [6568]
One limitation to utilizing the AGREE II instrument is that it does not comprehensively
critically appraise other important items included in the GRADE methodology for CPG devel-
opment (e.g. risk of bias, precision, consistency, directness, and publication bias).The selection
of 60% as a cut-off point for standard domain scores is another potential limitation as the orig-
inal AGREE II does not mandate such a cut-off but similar studies have used it previously [13].
Other raters may choose different cut-offs [54]
Another limitation of our review was the exclusion of Non-English CPGs from our set of
appraised CPGs despite the existence of Dutch, Finnish, Norwegian, German, and Spanish
ADHD CPGs. Similar exclusion criteria were selected in published AGREE appraisals for
CPGs [64,69,70]
The results of this appraisal can be used as a main component of a CPG development or
adaptation project for the management of ADHD. Furthermore, it highlights the importance
of inclusion of the AGREE II Instrument as a part of the capacity building for clinicians to
guide them during the identification and adoption of CPGs for use in their daily practice.
In conclusion, The AGREE II assessment of the six included ADHD CPGs revealed meth-
odological shortcomings in several domains. We recommend several areas for improvement
for future CPGs, using the AGREE II criteria and the NICE CPG as a model. This critical
appraisal illustrates the importance of regular quality assessment of CPGs by clinicians to
ensure the transparency and rigor of the CPG development process and the evidence-base
management of patients with ADHD.
Supporting information
S1 Fig. PRISMA flow diagram. Systematically searching and selecting the clinical practice
guidelines for management of ADHD.
(DOC)
Quality of guidelines for attention deficit hyperactivity disorder
PLOS ONE | https://doi.org/10.1371/journal.pone.0219239 July 5, 2019 10 / 15
S1 Protocol.
(PDF)
S1 Table. PRISMA checklist.
(DOC)
S2 Table. Mapping of ADHD CPGs against systematic reviews, meta-analyses and the uti-
lization of the GRADE method.
(DOCX)
S3 Table. Key recommendations of included ADHD CPGs.
(DOCX)
Acknowledgments
The authors wish to thank Prof. Tarek Omar for sharing the AGREE II scores of ADHD CPGs
from the relevant Master thesis from Alexandria University.
The unified ADHD Clinical Practice Guidelines Project is the strategic project 7.2 of the
Saudi ADHD Society for the period 2017–2019. The Saudi ADHD Society is a registered non-
profit under license 474 from the Saudi Ministry of Labor and Social Development, and the
project received the Ministry approval (No. 52476) on 5/8/1438. The project is entirely funded
by the Saudi ADHD Society. No funding was received from any pharmaceutical or industrial
company.
¶Members of the Saudi ADHD Society include TA and JLV.
Author Contributions
Conceptualization: Yasser Sami Amer.
Data curation: Yasser Sami Amer, Jeremy L. Varnham, Fahad A. Bashiri, Muddathir Hamad
Hamad, Saleh M. Al Salehi, Hadeel Fakhri Daghash, Turki Homod Albatti.
Formal analysis: Yasser Sami Amer.
Investigation: Yasser Sami Amer, Haya Faisal Al-Joudi, Fahad A. Bashiri, Muddathir Hamad
Hamad, Hadeel Fakhri Daghash, Turki Homod Albatti.
Methodology: Yasser Sami Amer.
Project administration: Yasser Sami Amer, Jeremy L. Varnham.
Resources: Yasser Sami Amer, Haya Faisal Al-Joudi, Jeremy L. Varnham, Fahad A. Bashiri,
Muddathir Hamad Hamad, Hadeel Fakhri Daghash.
Supervision: Yasser Sami Amer.
Validation: Yasser Sami Amer.
Writing original draft: Yasser Sami Amer, Haya Faisal Al-Joudi, Jeremy L. Varnham.
Writing review & editing: Yasser Sami Amer, Haya Faisal Al-Joudi, Fahad A. Bashiri, Mud-
dathir Hamad Hamad, Saleh M. Al Salehi, Hadeel Fakhri Daghash, Turki Homod Albatti.
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Quality of guidelines for attention deficit hyperactivity disorder
PLOS ONE | https://doi.org/10.1371/journal.pone.0219239 July 5, 2019 15 / 15
... Reflecting the importance of neurobiological factors, the current standard of treatment is pharmacological (1). There are various national clinical guidelines for its assessment and management although most are from the Western countries (2)(3)(4)(5). A consensus report on diagnosis and management of ADHD among Turkish youth was prepared previously (6). ...
... Comorbid conditions are common among children with ADHD (1-6, 36, 37). The most common comorbid conditions include the Disruptive Behavior Disorders (30.0% to 80.0%), Learning Disorders (15.0% to 40.0%), Anxiety Disorder (25.0% to 35.0%), and Major Depressive Disorder (15.0% to 20.0%) (1)(2)(3)(4)(5)(6)(36)(37)(38). Also, ADHD may be accompanied by bipolar disorder, tic disorder, substance use disorders, specific speech disorders (particularly in girls), developmental coordination disorder, and sleep disorder (1-6, 36-38). ...
... Also, ADHD may be accompanied by bipolar disorder, tic disorder, substance use disorders, specific speech disorders (particularly in girls), developmental coordination disorder, and sleep disorder (1-6, 36-38). Symptoms of hyperactivity and impulsivity may increase the risk of behavioral problems, while concomitant diagnoses of inattention and learning disorder may reflect the shared genetic risk factors (1)(2)(3)(4)(5)(6)(36)(37)(38). In one study from our country, 41.3% of ADHD cases had one comorbid condition, while 12.0% and 30.0% ...
Article
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Attention Deficit/Hyperactivity Disorder (ADHD) is one of the most common and heritable neurodevelopmental disorders which may last through the life-span. A consensus report on diagnosis and management of ADHD among Turkish youth was prepared previously. However, the participants as well as the management options were rather limited and developments in the past decade necessitated a revision and update of the consensus. Therefore, this review aims to summarize the consensus among Child and Adolescent Psychiatrists from Türkiye on the nature and management of pediatric ADHD. For those aims, the etiology of ADHD, diagnostic and evaluation process, epidemiology, developmental presentations, differential diagnoses and comorbidities, course/outcome and pharmacological as well as non-pharmacological management options were reviewed and suggestions for clinical practice are presented. Since ADHD is a chronic disorder with wide-ranging effects on functionality that is frequently accompanied by other mental disorders, a multidimensional therapeutic approach is recommended. However, since the disorder has neurobiological basis, pharmacotherapy represents the mainstay of treatment. Additional therapies may include psychosocial therapy, behavioral therapy, school-based therapeutic approaches, and family education. This review provides recommendations for ADHD at the national and global levels. It contains information about ADHD that will contribute to and facilitate clinicians’ decision-making processes. It is advisable to consider this guideline in clinical practice.
... Numerous guidelines have been created for a broad range of professionals to inform the assessment and treatment of ADHD. Two recent reviews have been conducted examining ADHD clinical practice guidelines [27,28]; however, to our knowledge, no systematic review has explicitly focused on the ADHD differential assessment process recommended within clinical practice guidelines. Therefore, the current study sought to synthesise and evaluate recommendations provided in current ADHD guidelines to determine if they include standardised procedures for differential and co-occurring diagnosis during the ADHD assessment process. ...
... A percentage was then calculated by dividing the summed domain score by the total score possible [31]. Using these percentages, recommendations regarding guideline use were then made [27]. ...
... It is possible that the excluded guidelines provide insight into the gaps which this review has highlighted. Furthermore, the cut-off score used to distinguish the quality of guidelines was based on AGREE II interrater assessments conducted in two recently published guideline reviews [27,30]. Other guideline reviews may have determined a different cut-off score and therefore reached different conclusions regarding overall appraisals. ...
Article
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Objective: The current review sought to synthesise and evaluate ADHD guidelines to identify recommended procedures for co-occurring and differential diagnosis for ADHD assessments of school aged children. Method: A systematic literature review was conducted by searching PsycInfo, Medline, CINAHL and Web of Science. A grey literature search was also performed. ADHD guidelines that described a diagnostic process for school aged children, published between 2013 and 2021, by Government organisations or a national professional association, and written in English were included. Results: Each of the six included guidelines were produced by panels consisting primarily of paediatricians and psychiatrists. All guidelines recommended assessing for co-occurring conditions. Five of the guidelines recommended consideration of a differential diagnosis. Five guidelines also recommended referral to a specialist, mental health clinician or psychologist when diagnostic uncertainty exists. Conclusions: Guidelines to assist in the assessment of referred cases were not discovered. There is a need for recommendations to be developed to supplement existing guidelines to aid psychologists and mental health clinicians in a systematic ADHD assessment process, particularly in complex cases.
... Attention deficit hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders that affects cognitive, emotional, social, academic, and occupational functioning [1]. It is classified into three main presentations: predominantly inattentive, predominantly hyperactive/impulsive and combined presentation [2]. ...
... AGREE II is a valid and reliable instrument with 23 items organized into six domains and is considered the gold standard for quality assessment of CPGs [22]. A cutoff point of 60% for each AGREE II standardized domain score was agreed upon by the members of the GAG [1]. ...
... Based on the results of the AGREE II appraisal [1] and in-depth content review of the source CPG from NICE, there was a consensus among the members of the GAG that the recommendations were clear and were based on the most relevant scientific evidence, applicable to the local context, and acceptable to people with ADHD. ...
Article
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Background We recently adapted the published National Institute for Health and Care Excellence (NICE) Attention deficit hyperactivity disorder (ADHD) diagnosis and management guideline to the Saudi Arabian context. It has been postulated that adaptation of evidence-based clinical practice guidelines to the local healthcare context rather than de-novo development will improve their adoption and implementation without imposing a significant burden on resources. The objective of this paper is to describe the adaptation process methodology utilized for the generation of the first national guideline for management of people with ADHD in Saudi Arabia. Methods We used the KSU-Modified-ADAPTE methodology for the guideline adaptation process. We describe the full process in detail including the three phases of set-up, adaptation, and finalization. The process was conducted by a multidisciplinary guideline adaptation group in addition to an external review for the clinical content and methodology. Results The group adapted ten main categories of recommendations from one source CPG (NICE). The recommendations include: (i) service organisation and training, (ii) recognition, identification and referral, (iii) diagnosis, (iv) support, (v) managing ADHD, (vi) dietary advice, (vii) medication, (viii) maintenance and monitoring, (ix) adherence to treatment, and (x) review of medication and discontinuation. Several implementation tools were compiled and developed to enhance implementability including a clinical algorithm, quality measures, coding system, medication tables, translations, patient information, and online resources. Conclusions The finalized clinical practice guideline provides healthcare providers with applicable evidence-based guidance for the management of people with ADHD in Saudi Arabia. The project also demonstrated the effectiveness of KSU-Modified-ADAPTE, and emphasized the value of a collaborative clinical and methodological expert group for adaptation of national guidelines.
... Background Attention de cit hyperactivity disorder (ADHD) is one of the most common neurodevelopmental disorders that affects cognitive, emotional, social, academic, and occupational functioning [1]. It is classi ed into three main presentations: predominantly inattentive, predominantly hyperactive/impulsive and combined presentation [2]. ...
... AGREE II is a valid and reliable instrument with 23 items organized into six domains and is considered the gold standard for quality assessment of CPGs [22]. A cut-off point of 60% for each AGREE II standardized domain score was agreed upon by the members of the GAG [1]. ...
... Based on the results of the AGREE II appraisal [1] and in-depth content review of the source CPG from NICE, there was a consensus among the members of the GAG that the recommendations were clear and were based on the most relevant scienti c evidence, applicable to the local context, and acceptable to people with ADHD. ...
Preprint
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Background: We recently adapted the published National institute for Health and Care Excellence (NICE) Attention deficit hyperactivity disorder (ADHD) diagnosis and management guideline to the Saudi Arabian context. It has been postulated that adaptation of evidence-based clinical practice guidelines to the local healthcare context rather than de-novo development will improve their adoption and implementation without imposing a significant burden on resources. The objective of this paper is to describe the adaptation process methodology utilized for the generation of the first national guideline for management of people with ADHD in Saudi Arabia. Methods: We used the KSU-Modified-ADAPTE methodology for the guideline adaptation process. We describe the full process in detail including the three phases of set-up, adaptation, and finalization. The process was conducted by a multidisciplinary guideline adaptation group in addition to an external review for the clinical content and methodology. Results: The group adapted ten main categories of recommendations from one source CPG (NICE). The recommendations include; (i) service organisation and training, (ii) recognition, identification and referral, (iii) diagnosis, (iv) support, (v) managing ADHD, (vi) dietary advice, (vii) medication, (viii) maintenance and monitoring, (ix) adherence to treatment, and (x) review of medication and discontinuation. Several implementation tools were compiled and developed to enhance implementability including a clinical algorithm, quality measures, coding system, medication tables, translations, patient information, and online resources. Conclusions: The finalized clinical practice guideline provides healthcare providers with applicable evidence-based guidance for the management of people with ADHD in Saudi Arabia. The project also demonstrated the effectiveness of KSU-Modified-ADAPTE, and emphasized the value of a collaborative clinical and methodological expert group for adaptation of national guidelines.
... Domain scores were calculated by summing individual item scores allocated by both reviewers within each domain, and then scaling the total as a percentage of the maximum possible score (Brouwers et al., 2010). Finally, guidelines were categorised as "strongly recommend", "recommend with alterations" or "do not recommend" according to domain percentage scores, similar to other published appraisals of clinical practice guidelines (Amer, 2019;Bennett et al., 2018;Sekercioglu, 2017;Yan et al., 2013). ...
... There is also no validated cut-off score or pattern of domain scores established for the AGREE-II to differentiate between high and poor quality guidelines (Brouwers et al., 2010). As per the recommendation of the instrument developers, we interpreted scores using categorisation of domains similar to another recently published study (Amer et al., 2019). Other reviews may establish different parameters for cut-off scores, limiting the ability to make direct comparisons. ...
Article
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This review aimed to assess the quality and content of recommendations for delivering an autism diagnosis, published internationally within clinical practice guidelines. Seventeen relevant guidelines were identified. When methodological information was provided, recommendations for feedback were predominantly formed through consensus. Recommendations consistently included who should attend feedback, the timing and mode of delivery, the clinician’s manner, and what should be discussed and/or included in an accompanying report. Specific recommendations were not consistent however, and a number of gaps were identified, such as the inclusion of educators and educational specific recommendations. Although individual variation is necessary for autism diagnosis disclosure, agreement on minimum standards of practice is warranted. Further investigation is required to establish best practice.
Chapter
In this chapter, we provide an overview of clinical practice for treating attention deficit/hyperactivity disorder (ADHD) by comparing three highly evaluated clinical practice guidelines (CPGs) for ADHD. When a clinician considers a treatment policy for an individual patient, it is necessary to understand the target and purpose of the CPGs, to refer to the CPGs, and to examine the setting of treatment goals. In addition, it is necessary to take sufficient time for diagnosis, and to obtain information from multiple sources. Comprehensive treatment that combines drug therapy and nondrug therapy is recommended for ADHD. Pharmacotherapy has the strongest evidential basis but requires pretreatment screening. In addition to CPGs, it is necessary to confirm the insurance coverage in the patient’s country. Side effects and the need for continued treatment should be assessed on a regular basis. We hope that this chapter will be useful for readers and clinicians, and will benefit their patients.
Article
BACKGROUND: Clinical practice guidelines (CPGs) can act as a bridge between clinical research and everyday practice. CPGs have been generated to inform Fiberoptic Endoscopic Evaluation of Swallowing (FEES), but their quality is unclear. OBJECTIVE: This study aims to systematically evaluate the quality of FEES CPGs to identify their suitability for use in clinical practice. METHODS: A systematic review of the literature was conducted. A comprehensive search of four academic databases (Medline, Embase, CINAHL, Web of Science) and other sources was completed. Three independent researchers used the Appraisal of Guidelines for Research and Evaluation-II (AGREE-II) instrument to appraise the quality of included CPGs. CPGs were rated over 23 items across six domains. Intraclass correlation coefficients established agreement across raters. RESULTS: Four FEES CPGs were included. Individual CPG scores ranged from 0% to 89% across AGREE-II domains. Median domain scores were “Scope and Purpose” 66%; “Stakeholder Involvement” 47%; “Rigour of Development” 29%; “Clarity of Presentation” 60%; “Applicability” 13% and “Editorial Independence” 0% . None of the CPGs included sufficient detail regarding their development methodology and supporting evidence. No CPG was recommended to guide practice in their current state. Only 1 CPG was recommended for use, upon appropriate modifications. CONCLUSION: CPGs are highly influential tools that play a vital role in guiding clinical practice. Study findings highlight a scarcity of high-quality FEES CPGs to inform dysphagia practice. Superior FEES CPGs are required to ensure individuals with dysphagia are benefiting from high-quality research emerging internationally.
Article
Attention-Deficit/Hyperactivity Disorder (ADHD) is often misdiagnosed or mistreated in adults because it is often thought of as a childhood problem. If a child is diagnosed and treated for the disorder, it often persists into adulthood. In adult ADHD, the symptoms may be comorbid or mimic other conditions making diagnosis and treatment difficult. Adults with ADHD require an in-depth assessment for proper diagnosis and treatment. The presentation and treatment of adults with ADHD can be complex and often requires interdisciplinary care. Mental health and non-mental health providers often overlook the disorder or feel uncomfortable treating adults with ADHD. The purpose of this manuscript is to discuss the diagnosis and management of adults with ADHD.
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Clinical practice guidelines (CPG) provide a framework for evidence-based practice; however, few studies have assessed the methodological quality of CPGs relevant to child and youth mental health. This study was a systematic review of CPGs for the assessment, prevention and treatment of disruptive behavior, including attention-deficit hyperactivity disorder (ADHD), oppositional defiant disorder (ODD), conduct disorder (CD) and aggression in children and youth. Systematic review identified 29 CPGs meeting inclusion criteria that were appraised using the Appraisal of Guidelines for Research and Evaluation II (AGREE II) validated tool. Twenty-two guidelines addressed ADHD, 2 CD, 1 ODD, 2 for Behavior Disorders collectively and 2 for Aggression. Among the 29 guidelines, two that were developed for ADHD (NICE 2013a; Spanish Ministry of Health, 2010) and one practice guideline developed for CD (NICE 2013b) met high quality criteria; one guideline for behavior disorders (Gorman et al. 2015), two for ADHD (AAP 2011a, b; SIGN 2009a, b, c, d, e), and two for aggression (Knapp et al. 2012; Scotto Rosato et al. 2012a, b) met minimum quality criteria. Findings from this review provide important information for clinicians and organizations who want to utilize guidelines to implement best-practice clinical services for children and youth with disruptive behavior.
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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.
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Background: Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder in childhood. The psychostimulant methylphenidate is the most frequently used medication to treat it. Several studies have investigated the benefits of methylphenidate, showing possible favourable effects on ADHD symptoms, but the true magnitude of the effect is unknown. Concerning adverse events associated with the treatment, our systematic review of randomised clinical trials (RCTs) demonstrated no increase in serious adverse events, but a high proportion of participants suffered a range of non-serious adverse events. Objectives: To assess the adverse events associated with methylphenidate treatment for children and adolescents with ADHD in non-randomised studies. Search methods: In January 2016, we searched CENTRAL, MEDLINE, Embase, PsycINFO, CINAHL, 12 other databases and two trials registers. We also checked reference lists and contacted authors and pharmaceutical companies to identify additional studies. Selection criteria: We included non-randomised study designs. These comprised comparative and non-comparative cohort studies, patient-control studies, patient reports/series and cross-sectional studies of methylphenidate administered at any dosage or formulation. We also included methylphenidate groups from RCTs assessing methylphenidate versus other interventions for ADHD as well as data from follow-up periods in RCTs. Participants had to have an ADHD diagnosis (from the 3rd to the 5th edition of the Diagnostic and Statistical Manual of Mental Disorders or the 9th or 10th edition of theInternational Classification of Diseases, with or without comorbid diagnoses. We required that at least 75% of participants had a normal intellectual capacity (intelligence quotient of more than 70 points) and were aged below 20 years. We excluded studies that used another ADHD drug as a co-intervention. Data collection and analysis: Fourteen review authors selected studies independently. Two review authors assessed risk of bias independently using the ROBINS-I tool for assessing risk of bias in non-randomised studies of interventions. All review authors extracted data. We defined serious adverse events according to the International Committee of Harmonization as any lethal, life-threatening or life-changing event. We considered all other adverse events to be non-serious adverse events and conducted meta-analyses of data from comparative studies. We calculated meta-analytic estimates of prevalence from non-comparative cohorts studies and synthesised data from patient reports/series qualitatively. We investigated heterogeneity by conducting subgroup analyses, and we also conducted sensitivity analyses. Main results: We included a total of 260 studies: 7 comparative cohort studies, 6 of which compared 968 patients who were exposed to methylphenidate to 166 controls, and 1 which assessed 1224 patients that were exposed or not exposed to methylphenidate during different time periods; 4 patient-control studies (53,192 exposed to methylphenidate and 19,906 controls); 177 non-comparative cohort studies (2,207,751 participants); 2 cross-sectional studies (96 participants) and 70 patient reports/series (206 participants). Participants' ages ranged from 3 years to 20 years. Risk of bias in the included comparative studies ranged from moderate to critical, with most studies showing critical risk of bias. We evaluated all non-comparative studies at critical risk of bias. The GRADE quality rating of the evidence was very low.Primary outcomesIn the comparative studies, methylphenidate increased the risk ratio (RR) of serious adverse events (RR 1.36, 95% confidence interval (CI) 1.17 to 1.57; 2 studies, 72,005 participants); any psychotic disorder (RR 1.36, 95% CI 1.17 to 1.57; 1 study, 71,771 participants); and arrhythmia (RR 1.61, 95% CI 1.48 to 1.74; 1 study, 1224 participants) compared to no intervention.In the non-comparative cohort studies, the proportion of participants on methylphenidate experiencing any serious adverse event was 1.20% (95% CI 0.70% to 2.00%; 50 studies, 162,422 participants). Withdrawal from methylphenidate due to any serious adverse events occurred in 1.20% (95% CI 0.60% to 2.30%; 7 studies, 1173 participants) and adverse events of unknown severity led to withdrawal in 7.30% of participants (95% CI 5.30% to 10.0%; 22 studies, 3708 participants).Secondary outcomesIn the comparative studies, methylphenidate, compared to no intervention, increased the RR of insomnia and sleep problems (RR 2.58, 95% CI 1.24 to 5.34; 3 studies, 425 participants) and decreased appetite (RR 15.06, 95% CI 2.12 to 106.83; 1 study, 335 participants).With non-comparative cohort studies, the proportion of participants on methylphenidate with any non-serious adverse events was 51.2% (95% CI 41.2% to 61.1%; 49 studies, 13,978 participants). These included difficulty falling asleep, 17.9% (95% CI 14.7% to 21.6%; 82 studies, 11,507 participants); headache, 14.4% (95% CI 11.3% to 18.3%; 90 studies, 13,469 participants); abdominal pain, 10.7% (95% CI 8.60% to 13.3%; 79 studies, 11,750 participants); and decreased appetite, 31.1% (95% CI 26.5% to 36.2%; 84 studies, 11,594 participants). Withdrawal of methylphenidate due to non-serious adverse events occurred in 6.20% (95% CI 4.80% to 7.90%; 37 studies, 7142 participants), and 16.2% were withdrawn for unknown reasons (95% CI 13.0% to 19.9%; 57 studies, 8340 participants). Authors' conclusions: Our findings suggest that methylphenidate may be associated with a number of serious adverse events as well as a large number of non-serious adverse events in children and adolescents, which often lead to withdrawal of methylphenidate. Our certainty in the evidence is very low, and accordingly, it is not possible to accurately estimate the actual risk of adverse events. It might be higher than reported here.Given the possible association between methylphenidate and the adverse events identified, it may be important to identify people who are most susceptible to adverse events. To do this we must undertake large-scale, high-quality RCTs, along with studies aimed at identifying responders and non-responders.
Thesis
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The trend of the last decades has been to base clinical decision making more and more on sound scientific evidence, i.e. evidence based medicine, in practice, this has led medical specialists to develop evidence-based clinical practice guidelines (CPGs) for promoting standards of medical care. Worldwide, a number of organizations such as SIGN (Scottish Intercollegiate Guidelines Network) and CBO (Dutch Institute for Health Care Improvement).In 2002 the Guidelines International Network was founded to promote the systematic development of CPGs through international collaboration. Recently the AFM-CEBCPGs (Alexandria Universty Faculty of Medicine Center Evidence Based Clinical Practice Guidelines)in Egypt was founded in 2009 to proceed with the same endeavors in the field of guidelines and become a member of the G-I-N. One way to reduce the costs and time, avoid variations of institutions setting, such as the type of practice and location, considering the availability of resources, and respecting local policies and practice patterns is by relying on local adaptation of guidelines developed at the international level by expert groups. Therefore clinical guidelines developed by the government agencies or medical specialty organizations at the national level usually need to be adapted to fit the local practice before they can be actually used by clinicians at specific institutions and successful guideline implementation has to be supported by organizational efforts. The aim of work is to adapt international clinical practice guidelines in the treatment of ADHD. And to know the prevalence of ADHD among primary school children in Alexandria. A study was done on 200 children in primary schools either governmental or private schools, the range of age from 6-12 years, from primary one to primary six, Conners score for teachers was applied on them randomly to detect prevalence of ADHD among them The guideline is adapted specially to this group of children to avoid wide practice variation in the treatment of ADHD According to the results of our study sample, the prevalence of ADHD is 6%, and regarding treatment of ADHD medical, psychological and alternative medicine were all recommend in our study according to the grade of impairment of the child Our panel has used the ADAPTE process for guideline adaptation with its resource toolkit as their methodology. The process started by adapting 5 CPGs, one of them was excluded because it has the lowest AGREE score, and the selected 4 were processed throughout the ADAPTE process. A draft adapted CPG was produced and reviewed by the external review group from AUCH staff. Plans for updates were stated after 2 years, and implementation tools were stated in the adapted CPG.
Article
Clinical practice guidelines (CPGs) are systematically-developed statements aimed to assist decision-making relevant to the clinical encounter, to inform clinical policy, and to strengthen health care systems. The development of a CPG begins with the identification of a problem for which evidence-informed guidance is required. Interdisciplinary panels work to craft – and then execute - a protocol that will serve as a blueprint for the development process. It includes the scope of the project; who is involved and how they will function; the specific systematic review and consensus methods that will be used to ensure quality recommendations and to mitigate bias. CPGs should undergo a formal review of relevant stakeholders and results of this review, actions taken by the panel, and the final recommendations should be documented in the final CPG report. Dissemination activities, including the use of social media platforms, and more purposefully designed implementation activities are required to optimize the adoption of recommendations. Methods to keep recommendations current are required to ensure on-going validity and credibility of the recommendations. Two tools, AGREE II, and the AGREE REX, provide quality criteria related to the whole CPG development process and the CPG recommendations, respectively. The AGREE II is comprised of 23 items within 6 CPG quality domains: scope and purpose, stakeholder involvement, rigor, clarity of presentation, applicability, and editorial independence. The AGREE REX is comprised of 9 items within 3 CPG Recommendation quality domains: clinical applicability, values and preferences, and implementability. CPGs are important tools to an overall quality agenda.
Article
Background: Attention deficit hyperactivity disorder (ADHD) is a childhood-onset disorder characterised by inattention, hyperactivity, and impulsivity. ADHD can persist into adulthood and can affects individuals' social and occupational functioning, as well as their quality of life and health. ADHD is frequently associated with other mental disorders such as substance use disorders and anxiety and affective disorders. Amphetamines are used to treat adults with ADHD, but uncertainties about their efficacy and safety remain. Objectives: To examine the efficacy and safety of amphetamines for adults with ADHD. Search methods: In August 2017, we searched CENTRAL, MEDLINE, Embase, PsycINFO, 10 other databases, and two trials registers, and we ran citation searches for included studies. We also contacted the corresponding authors of all included studies, other experts in the field, and the pharmaceutical company, Shire, and we searched the reference lists of retrieved studies and reviews for other published, unpublished, or ongoing studies. For each included study, we performed a citation search in Web of Science to identify any later studies that may have cited it. Selection criteria: We searched for randomised controlled trials comparing the efficacy of amphetamines (at any dose) for ADHD in adults aged 18 years and over against placebo or an active intervention. Data collection and analysis: Two review authors extracted data from each included study. We used the standardised mean difference (SMD) and the risk ratio (RR) to assess continuous and dichotomous outcomes, respectively. We conducted a stratified analysis to determine the influence of moderating variables. We assessed trials for risk of bias and drew a funnel plot to investigate the possibility of publication bias. We rated the quality of the evidence using the GRADE approach, which yielded high, moderate, low, or very low quality ratings based on evaluation of within-trial risk of bias, directness of evidence, heterogeneity of data; precision of effect estimates, and risk of publication bias. Main results: We included 19 studies that investigated three types of amphetamines: dexamphetamine (10.2 mg/d to 21.8 mg/d), lisdexamfetamine (30 mg/d to 70 mg/d), and mixed amphetamine salts (MAS; 12.5 mg/d to 80 mg/d). These studies enrolled 2521 participants; most were middle-aged (35.3 years), Caucasian males (57.2%), with a combined type of ADHD (78.8%). Eighteen studies were conducted in the USA, and one study was conducted in both Canada and the USA. Ten were multi-site studies. All studies were placebo-controlled, and three also included an active comparator: guanfacine, modafinil, or paroxetine. Most studies had short-term follow-up and a mean study length of 5.3 weeks.We found no studies that had low risk of bias in all domains of the Cochrane 'Risk of bias' tool, mainly because amphetamines have powerful subjective effects that may reveal the assigned treatment, but also because we noted attrition bias, and because we could not rule out the possibility of a carry-over effect in studies that used a cross-over design.Sixteen studies were funded by the pharmaceutical industry, one study was publicly funded, and two studies did not report their funding sources.Amphetamines versus placeboSeverity of ADHD symptoms: we found low- to very low-quality evidence suggesting that amphetamines reduced the severity of ADHD symptoms as rated by clinicians (SMD -0.90, 95% confidence interval (CI) -1.04 to -0.75; 13 studies, 2028 participants) and patients (SMD -0.51, 95% CI -0.75 to -0.28; six studies, 120 participants).Retention: overall, we found low-quality evidence suggesting that amphetamines did not improve retention in treatment (risk ratio (RR) 1.06, 95% CI 0.99 to 1.13; 17 studies, 2323 participants).Adverse events: we found that amphetamines were associated with an increased proportion of patients who withdrew because of adverse events (RR 2.69, 95% CI 1.63 to 4.45; 17 studies, 2409 participants).Type of amphetamine: we found differences between amphetamines for the severity of ADHD symptoms as rated by clinicians. Both lisdexamfetamine (SMD -1.06, 95% CI -1.26 to -0.85; seven studies, 896 participants; low-quality evidence) and MAS (SMD -0.80, 95% CI -0.93 to -0.66; five studies, 1083 participants; low-quality evidence) reduced the severity of ADHD symptoms. In contrast, we found no evidence to suggest that dexamphetamine reduced the severity of ADHD symptoms (SMD -0.24, 95% CI -0.80 to 0.32; one study, 49 participants; very low-quality evidence). In addition, all amphetamines were efficacious in reducing the severity of ADHD symptoms as rated by patients (dexamphetamine: SMD -0.77, 95% CI -1.14 to -0.40; two studies, 35 participants; low-quality evidence; lisdexamfetamine: SMD -0.33, 95% CI -0.65 to -0.01; three studies, 67 participants; low-quality evidence; MAS: SMD -0.45, 95% CI -1.02 to 0.12; one study, 18 participants; very low-quality evidence).Dose at study completion: different doses of amphetamines did not appear to be associated with differences in efficacy.Type of drug-release formulation: we investigated immediate- and sustained-release formulations but found no differences between them for any outcome.Amphetamines versus other drugsWe found no evidence that amphetamines improved ADHD symptom severity compared to other drug interventions. Authors' conclusions: Amphetamines improved the severity of ADHD symptoms, as assessed by clinicians or patients, in the short term but did not improve retention to treatment. Amphetamines were associated with higher attrition due to adverse events. The short duration of studies coupled with their restrictive inclusion criteria limits the external validity of these findings. Furthermore, none of the included studies had an overall low risk of bias. Overall, the evidence generated by this review is of low or very low quality.
Article
Background: This is an update of the original Cochrane Review published in Issue 4, 2011.Attention deficit hyperactivity disorder (ADHD) is the most prevalent of the comorbid psychiatric disorders that complicate tic disorders. Medications commonly used to treat ADHD symptoms include stimulants such as methylphenidate and amphetamine; non-stimulants, such as atomoxetine; tricyclic antidepressants; and alpha agonists. Alpha agonists are also used as a treatment for tics. Due to the impact of ADHD symptoms on the child with tic disorder, treatment of ADHD is often of greater priority than the medical management of tics. However, for many decades, clinicians have been reluctant to use stimulants to treat children with ADHD and tics for fear of worsening their tics. OBJECTIVES: To assess the effects of pharmacological treatments for ADHD in children with comorbid tic disorders on symptoms of ADHD and tics. Search methods: In September 2017, we searched CENTRAL, MEDLINE, Embase, and 12 other databases. We also searched two trial registers and contacted experts in the field for any ongoing or unpublished studies. Selection criteria: We included randomized, double-blind, controlled trials of any pharmacological treatment for ADHD used specifically in children with comorbid tic disorders. We included both parallel-group and cross-over study designs. Data collection and analysis: We used standard methodological procedures of Cochrane, in that two review authors independently selected studies, extracted data using standardized forms, assessed risk of bias, and graded the overall quality of the evidence by using the GRADE approach. Main results: We included eight randomized controlled trials (four of which were cross-over trials) with 510 participants (443 boys, 67 girls) in this review. Participants in these studies were children with both ADHD and a chronic tic disorder. All studies took place in the USA and ranged from three to 22 weeks in duration. Five of the eight studies were funded by charitable organizations or government agencies, or both. One study was funded by the drug manufacturer. The other two studies did not specify the source of funding. Risk of bias of included studies was low for blinding; low or unclear for random sequence generation, allocation concealment, and attrition bias; and low or high for selective outcome reporting. We were unable to combine any of the studies in a meta-analysis due to important clinical heterogeneity and unit-of-analysis issues.Several of the trials assessed multiple agents. Medications assessed included methylphenidate, clonidine, desipramine, dextroamphetamine, guanfacine, atomoxetine, and deprenyl. There was low-quality evidence for methylphenidate, atomoxetine, and clonidine, and very low-quality evidence for desipramine, dextroamphetamine, guanfacine and deprenyl in the treatment of ADHD in children with tics. All studies, with the exception of a study using deprenyl, reported improvement in symptoms of ADHD. Tic symptoms also improved in children treated with guanfacine, desipramine, methylphenidate, clonidine, and a combination of methylphenidate and clonidine. In one study, tics limited further dosage increases of methylphenidate. High-dose dextroamphetamine appeared to worsen tics in one study, although the length of this study was limited to three weeks. There was appetite suppression or weight loss in association with methylphenidate, dextroamphetamine, atomoxetine, and desipramine. There was insomnia associated with methylphenidate and dextroamphetamine, and sedation associated with clonidine. Authors' conclusions: Following an updated search of potentially relevant studies, we found no new studies that matched our inclusion criteria and thus our conclusions have not changed.Methylphenidate, clonidine, guanfacine, desipramine, and atomoxetine appear to reduce ADHD symptoms in children with tics though the quality of the available evidence was low to very low. Although stimulants have not been shown to worsen tics in most people with tic disorders, they may, nonetheless, exacerbate tics in individual cases. In these instances, treatment with alpha agonists or atomoxetine may be an alternative. Although there is evidence that desipramine may improve tics and ADHD in children, safety concerns will likely continue to limit its use in this population.
Article
Background: Attention deficit hyperactivity disorder (ADHD) is a developmental condition characterised by symptoms of inattention, hyperactivity and impulsivity, along with deficits in executive function, emotional regulation and motivation. The persistence of ADHD in adulthood is a serious clinical problem.ADHD significantly affects social interactions, study and employment performance.Previous studies suggest that cognitive-behavioural therapy (CBT) could be effective in treating adults with ADHD, especially when combined with pharmacological treatment. CBT aims to change the thoughts and behaviours that reinforce harmful effects of the disorder by teaching people techniques to control the core symptoms. CBT also aims to help people cope with emotions, such as anxiety and depression, and to improve self-esteem. Objectives: To assess the effects of cognitive-behavioural-based therapy for ADHD in adults. Search methods: In June 2017, we searched CENTRAL, MEDLINE, Embase, seven other databases and three trials registries. We also checked reference lists, handsearched congress abstracts, and contacted experts and researchers in the field. Selection criteria: Randomised controlled trials (RCTs) evaluating any form of CBT for adults with ADHD, either as a monotherapy or in conjunction with another treatment, versus one of the following: unspecific control conditions (comprising supportive psychotherapies, no treatment or waiting list) or other specific interventions. Data collection and analysis: We used the standard methodological procedures suggested by Cochrane. Main results: We included 14 RCTs (700 participants), 13 of which were conducted in the northern hemisphere and 1 in Australia.Primary outcomes: ADHD symptomsCBT versus unspecific control conditions (supportive psychotherapies, waiting list or no treatment)- CBT versus supportive psychotherapies: CBT was more effective than supportive therapy for improving clinician-reported ADHD symptoms (1 study, 81 participants; low-quality evidence) but not for self-reported ADHD symptoms (SMD -0.16, 95% CI -0.52 to 0.19; 2 studies, 122 participants; low-quality evidence; small effect size).- CBT versus waiting list: CBT led to a larger benefit in clinician-reported ADHD symptoms (SMD -1.22, 95% CI -2.03 to -0.41; 2 studies, 126 participants; very low-quality evidence; large effect size). We also found significant differences in favour of CBT for self-reported ADHD symptoms (SMD -0.84, 95% CI -1.18 to -0.50; 5 studies, 251 participants; moderate-quality evidence; large effect size).CBT plus pharmacotherapy versus pharmacotherapy alone: CBT with pharmacotherapy was more effective than pharmacotherapy alone for clinician-reported core symptoms (SMD -0.80, 95% CI -1.31 to -0.30; 2 studies, 65 participants; very low-quality evidence; large effect size), self-reported core symptoms (MD -7.42 points, 95% CI -11.63 points to -3.22 points; 2 studies, 66 participants low-quality evidence) and self-reported inattention (1 study, 35 participants).CBT versus other interventions that included therapeutic ingredients specifically targeted to ADHD: we found a significant difference in favour of CBT for clinician-reported ADHD symptoms (SMD -0.58, 95% CI -0.98 to -0.17; 2 studies, 97 participants; low-quality evidence; moderate effect size) and for self-reported ADHD symptom severity (SMD -0.44, 95% CI -0.88 to -0.01; 4 studies, 156 participants; low-quality evidence; small effect size).Secondary outcomesCBT versus unspecific control conditions: we found differences in favour of CBT compared with waiting-list control for self-reported depression (SMD -0.36, 95% CI -0.60 to -0.11; 5 studies, 258 participants; small effect size) and for self-reported anxiety (SMD -0.45, 95% CI -0.71 to -0.19; 4 studies, 239 participants; small effect size). We also observed differences in favour of CBT for self-reported state anger (1 study, 43 participants) and self-reported self-esteem (1 study 43 participants) compared to waiting list. We found no differences between CBT and supportive therapy (1 study, 81 participants) for self-rated depression, clinician-rated anxiety or self-rated self-esteem. Additionally, there were no differences between CBT and the waiting list for self-reported trait anger (1 study, 43 participants) or self-reported quality of life (SMD 0.21, 95% CI -0.29 to 0.71; 2 studies, 64 participants; small effect size).CBT plus pharmacotherapy versus pharmacotherapy alone: we found differences in favour of CBT plus pharmacotherapy for the Clinical Global Impression score (MD -0.75 points, 95% CI -1.21 points to -0.30 points; 2 studies, 65 participants), self-reported depression (MD -6.09 points, 95% CI -9.55 points to -2.63 points; 2 studies, 66 participants) and self-reported anxiety (SMD -0.58, 95% CI -1.08 to -0.08; 2 studies, 66 participants; moderate effect size). We also observed differences favouring CBT plus pharmacotherapy (1 study, 31 participants) for clinician-reported depression and clinician-reported anxiety.CBT versus other specific interventions: we found no differences for any of the secondary outcomes, such as self-reported depression and anxiety, and findings on self-reported quality of life varied across different studies. Authors' conclusions: There is low-quality evidence that cognitive-behavioural-based treatments may be beneficial for treating adults with ADHD in the short term. Reductions in core symptoms of ADHD were fairly consistent across the different comparisons: in CBT plus pharmacotherapy versus pharmacotherapy alone and in CBT versus waiting list. There is low-quality evidence that CBT may also improve common secondary disturbances in adults with ADHD, such as depression and anxiety. However, the paucity of long-term follow-up data, the heterogeneous nature of the measured outcomes, and the limited geographical location (northern hemisphere and Australia) limit the generalisability of the results. None of the included studies reported severe adverse events, but five participants receiving different modalities of CBT described some type of adverse event, such as distress and anxiety.
Article
Rationale, aims and objectives: Type 2 diabetes mellitus (T2DM) is a worldwide and national public health problem that has a great impact on the population in Saudi Arabia. High-quality clinical practice guidelines (CPGs) are cornerstones in improving the health care provided for patients with diabetes. This study evaluated the methodological rigour, transparency, and applicability of recently published CPGs. Methods: Our group conducted a systematic search for recently published CPGs for T2DM. The searching and screening for Source CPGs were guided by tools from the ADAPTE methods with specific inclusion/exclusion criteria. Five reviewers using the second version of the Appraisal of Guidelines for Research and Evaluation (AGREE II) Instrument independently assessed the quality of the retrieved Source CPGs. Results: Domains of Scope and purpose and Clarity of presentation received the highest scores in all CPGs. Most of the assessed CPGs (86%) were considered with high overall quality and were recommended for use. Rigour of development and applicability domains were together highest in 3 CPGs (43%). The overall high quality of DM CPGs published in the last 3 years demonstrated the continuous development and improvement in CPG methodologies and standards. Conclusions: Health care professionals should consider the quality of any CPG for T2DM before deciding to use it in their daily clinical practice. Three CPGs have been identified, using the AGREE criteria, as high-quality and trustworthy. Ideally, the resources provided by the AGREE trust including the AGREE II Instrument should be used by a clinician to scan through the large number of published T2DM CPGs to identify the CPGs with high methodological quality and applicability.