International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND).

Consensus recommendations Education Mental health Neurodevelopmental disability Rare genetic disorders TAND Tuberous sclerosis complex

Journal

Journal of neurodevelopmental disorders
ISSN: 1866-1955
Titre abrégé: J Neurodev Disord
Pays: England
ID NLM: 101483832

Informations de publication

Date de publication:
14 09 2023
Historique:
received: 27 04 2023
accepted: 28 08 2023
medline: 18 9 2023
pubmed: 15 9 2023
entrez: 14 9 2023
Statut: epublish

Résumé

Tuberous sclerosis complex (TSC) is associated with a wide range of physical manifestations for which international clinical recommendations for diagnosis and management have been established. TSC is, however, also associated with a wide range of TSC-Associated Neuropsychiatric Disorders (TAND) that are typically under-identified and under-treated yet associated with a profound burden of disease. The contemporary evidence base for the identification and treatment of TAND is much more limited and, to date, consensus recommendations for the diagnosis and management of TAND have also been limited and non-specific. The TANDem project was launched with an international, interdisciplinary, and participatory consortium of 24 individuals, including TSC family representatives, from all World Health Organization (WHO) regions but one. One of the aims of the TANDem project was to generate consensus recommendations for the identification and treatment of TAND. At the time of this project, no internationally adopted standard methodology and methodological checklists existed for the generation of clinical practice recommendations. We therefore developed our own systematic procedure for evidence review and consensus-building to generate evidence-informed consensus recommendations of relevance to the global TSC community. At the heart of the consensus recommendations are ten core principles surrounded by cluster-specific recommendations for each of the seven natural TAND clusters identified in the literature (autism-like, dysregulated behavior, eat/sleep, mood/anxiety, neuropsychological, overactive/impulsive, and scholastic) and a set of wraparound psychosocial cluster recommendations. The overarching recommendation is to "screen" for TAND at least annually, to "act" using appropriate next steps for evaluation and treatment, and to "repeat" the process to ensure early identification and early intervention with the most appropriate biological, psychological, and social evidence-informed approaches to support individuals with TSC and their families. The consensus recommendations should provide a systematic framework to approach the identification and treatment of TAND for health, educational, social care teams and families who live with TSC. To ensure global dissemination and implementation of these recommendations, partnerships with the international TSC community will be important. One of these steps will include the generation of a "TAND toolkit" of "what to seek" and "what to do" when difficulties are identified in TAND clusters.

Sections du résumé

BACKGROUND
Tuberous sclerosis complex (TSC) is associated with a wide range of physical manifestations for which international clinical recommendations for diagnosis and management have been established. TSC is, however, also associated with a wide range of TSC-Associated Neuropsychiatric Disorders (TAND) that are typically under-identified and under-treated yet associated with a profound burden of disease. The contemporary evidence base for the identification and treatment of TAND is much more limited and, to date, consensus recommendations for the diagnosis and management of TAND have also been limited and non-specific.
METHODS
The TANDem project was launched with an international, interdisciplinary, and participatory consortium of 24 individuals, including TSC family representatives, from all World Health Organization (WHO) regions but one. One of the aims of the TANDem project was to generate consensus recommendations for the identification and treatment of TAND. At the time of this project, no internationally adopted standard methodology and methodological checklists existed for the generation of clinical practice recommendations. We therefore developed our own systematic procedure for evidence review and consensus-building to generate evidence-informed consensus recommendations of relevance to the global TSC community.
RESULTS
At the heart of the consensus recommendations are ten core principles surrounded by cluster-specific recommendations for each of the seven natural TAND clusters identified in the literature (autism-like, dysregulated behavior, eat/sleep, mood/anxiety, neuropsychological, overactive/impulsive, and scholastic) and a set of wraparound psychosocial cluster recommendations. The overarching recommendation is to "screen" for TAND at least annually, to "act" using appropriate next steps for evaluation and treatment, and to "repeat" the process to ensure early identification and early intervention with the most appropriate biological, psychological, and social evidence-informed approaches to support individuals with TSC and their families.
CONCLUSIONS
The consensus recommendations should provide a systematic framework to approach the identification and treatment of TAND for health, educational, social care teams and families who live with TSC. To ensure global dissemination and implementation of these recommendations, partnerships with the international TSC community will be important. One of these steps will include the generation of a "TAND toolkit" of "what to seek" and "what to do" when difficulties are identified in TAND clusters.

Identifiants

pubmed: 37710171
doi: 10.1186/s11689-023-09500-1
pii: 10.1186/s11689-023-09500-1
pmc: PMC10503032
doi:

Types de publication

Consensus Development Conference Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

32

Informations de copyright

© 2023. BioMed Central Ltd., part of Springer Nature.

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Auteurs

Petrus J de Vries (PJ)

Division of Child and Adolescent Psychiatry, Centre for Autism Research in Africa (CARA), University of Cape Town, 46 Sawkins Road, Rondebosch, Cape Town, 7700, South Africa. petrus.devries@uct.ac.za.

Tosca-Marie Heunis (TM)

Mental Health and Wellbeing Research Group, Department of Public Health, Vrije Universiteit Brussel, Brussels, Belgium.

Stephanie Vanclooster (S)

Mental Health and Wellbeing Research Group, Department of Public Health, Vrije Universiteit Brussel, Brussels, Belgium.

Nola Chambers (N)

Division of Child and Adolescent Psychiatry, Centre for Autism Research in Africa (CARA), University of Cape Town, 46 Sawkins Road, Rondebosch, Cape Town, 7700, South Africa.

Stacey Bissell (S)

School of Psychology, University of Birmingham, Birmingham, UK.

Anna W Byars (AW)

TSC Clinic Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Division of Neurology, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Jennifer Flinn (J)

TSC Canada, Mississauga, ON, Canada.

Tanjala T Gipson (TT)

Department of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN, USA.
Le Bonheur Children's Hospital and Boling Center for Developmental Disabilities, Memphis, TN, USA.

Agnies M van Eeghen (AM)

Emma Children's Hospital, Amsterdam University Medical Center, Amsterdam, Netherlands.
TAND Expert Centre, 'S Heeren Loo, Hoofddorp, Netherlands.

Robert Waltereit (R)

Child and Adolescent Psychiatry, University Medical Center Göttingen, Göttingen, Germany.

Jamie K Capal (JK)

Department of Neurology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Sebastián Cukier (S)

Department of Psychopathology and Mental Health, Pedro de Elizalde Hospital, Buenos Aires, Argentina.

Peter E Davis (PE)

Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Catherine Smith (C)

TSC Alliance, Silver Spring, MD, USA.

J Chris Kingswood (JC)

Department of Clinical Genetics, St George's University Hospitals, London, UK.
Sussex Renal Unit, The Royal Sussex County Hospital, Brighton, UK.

Eva Schoeters (E)

Be-TSC, Mortsel, Belgium.
TSCi, Mortsel, Belgium.

Shoba Srivastava (S)

Division of Child and Adolescent Psychiatry, Centre for Autism Research in Africa (CARA), University of Cape Town, 46 Sawkins Road, Rondebosch, Cape Town, 7700, South Africa.
Society of Parents of Children With Autistic Disorders (SOPAN), Mumbai, India.

Megumi Takei (M)

Japanese Society of Tuberous Sclerosis Complex, Family Network, Tokyo, Japan.

Sugnet Gardner-Lubbe (S)

MuViSU (Centre for Multi-Dimensional Data Visualisation), Department of Statistics and Actuarial Sciences, Stellenbosch University, Stellenbosch, South Africa.

Aubrey J Kumm (AJ)

Division of Child and Adolescent Psychiatry, Centre for Autism Research in Africa (CARA), University of Cape Town, 46 Sawkins Road, Rondebosch, Cape Town, 7700, South Africa.

Darcy A Krueger (DA)

TSC Clinic Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Division of Neurology, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Mustafa Sahin (M)

Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Rosamund Stone Zander Translational Neuroscience Center, Boston Children's Hospital, Boston, MA, USA.

Liesbeth De Waele (L)

Department of Paediatric Neurology, University Hospitals Leuven, Louvain, Belgium.
Department of Development and Regeneration, KU Leuven, Louvain, Belgium.

Anna C Jansen (AC)

Mental Health and Wellbeing Research Group, Department of Public Health, Vrije Universiteit Brussel, Brussels, Belgium.
Department of Pediatrics, Koningin Mathilde Moeder-en Kindcentrum, Antwerp University Hospital, Antwerp, Belgium.
Department of Translational Neurosciences, University of Antwerp, Antwerp, Belgium.

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