Epilepsy related multimorbidity, polypharmacy and risks in adults with intellectual disabilities: a national study.


Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
May 2022
Historique:
received: 05 11 2021
accepted: 11 12 2021
pubmed: 25 1 2022
medline: 23 4 2022
entrez: 24 1 2022
Statut: ppublish

Résumé

A quarter of people with Intellectual Disability (ID) in the UK have epilepsy compared to 0.6% in the general population and die much younger. Epilepsy is associated with two-fifths of all deaths with related polypharmacy and multi-morbidity. Epilepsy research on this population has been poor. This study describes real-world clinical and risk characteristics of a large cohort across England and Wales. A retrospective multi-centre cohort study was conducted. Information on seizure characteristics, ID severity, relevant co-morbidities, psychotropic and antiseizure drugs (ASDs), SUDEP and other risk factors was collected across a year. Of 904 adults across 10 centres (male:female, 1.5:1), 320 (35%) had mild ID and 584 (65%) moderate-profound (M/P) ID. The mean age was 39.9 years (SD 15.0). Seizures were more frequent in M/P ID (p < 0.001). Over 50% had physical health co-morbidities, more in mild ID (p < 0.01). A third had psychiatric co-morbidity and a fifth had an underlying genetic disorder. Autism Spectrum Disorder was seen in over a third (37%). Participants were on median two ASDs and overall, five medications. Over quarter were on anti-psychotics. Over 90% had an epilepsy review in the past year but 25% did not have an epilepsy care plan, particularly those with mild ID (p < 0.001). Only 61% had a documented discussion of SUDEP, again less likely with mild ID or their care stakeholders (p < 0.001). Significant levels of multi-morbidity, polypharmacy and a lack of systemised approach to treatment and risk exist. Addressing these concerns is essential to reduce premature mortality.

Sections du résumé

BACKGROUND BACKGROUND
A quarter of people with Intellectual Disability (ID) in the UK have epilepsy compared to 0.6% in the general population and die much younger. Epilepsy is associated with two-fifths of all deaths with related polypharmacy and multi-morbidity. Epilepsy research on this population has been poor. This study describes real-world clinical and risk characteristics of a large cohort across England and Wales.
METHODS METHODS
A retrospective multi-centre cohort study was conducted. Information on seizure characteristics, ID severity, relevant co-morbidities, psychotropic and antiseizure drugs (ASDs), SUDEP and other risk factors was collected across a year.
RESULTS RESULTS
Of 904 adults across 10 centres (male:female, 1.5:1), 320 (35%) had mild ID and 584 (65%) moderate-profound (M/P) ID. The mean age was 39.9 years (SD 15.0). Seizures were more frequent in M/P ID (p < 0.001). Over 50% had physical health co-morbidities, more in mild ID (p < 0.01). A third had psychiatric co-morbidity and a fifth had an underlying genetic disorder. Autism Spectrum Disorder was seen in over a third (37%). Participants were on median two ASDs and overall, five medications. Over quarter were on anti-psychotics. Over 90% had an epilepsy review in the past year but 25% did not have an epilepsy care plan, particularly those with mild ID (p < 0.001). Only 61% had a documented discussion of SUDEP, again less likely with mild ID or their care stakeholders (p < 0.001).
CONCLUSIONS CONCLUSIONS
Significant levels of multi-morbidity, polypharmacy and a lack of systemised approach to treatment and risk exist. Addressing these concerns is essential to reduce premature mortality.

Identifiants

pubmed: 35067759
doi: 10.1007/s00415-021-10938-3
pii: 10.1007/s00415-021-10938-3
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2750-2760

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

Références

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Auteurs

James J Sun (JJ)

Barnet, Enfield and Haringey Mental Health NHS Trust, London, UK.

Bhathika Perera (B)

Barnet, Enfield and Haringey Mental Health NHS Trust, London, UK.

William Henley (W)

University of Exeter Medical School, Exeter, UK.

Heather Angus-Leppan (H)

Royal Free London NHS Foundation Trust, London, UK.

Indermeet Sawhney (I)

Hertfordshire Partnership University NHS Foundation Trust, St Albans, UK.

Lance Watkins (L)

Swansea Bay University Health Board, Swansea, UK.

Kiran N Purandare (KN)

Central and North West London NHS Foundation Trust, London, UK.

Mogbeyiteren Eyeoyibo (M)

Kent and Medway NHS and Social Care Partnership Trust, Kent, UK.

Mark Scheepers (M)

Gloucestershire Health and Care NHS Foundation Trust, Gloucester, UK.

Geraldine Lines (G)

Oxleas NHS Foundation Trust, London, UK.

Robert Winterhalder (R)

Oxleas NHS Foundation Trust, London, UK.

Samantha Ashby (S)

SUDEP Action, Wantage, UK.

Ravi De Silva (R)

Barnet, Enfield and Haringey Mental Health NHS Trust, London, UK.

Jonjo Miller (J)

Barnet, Enfield and Haringey Mental Health NHS Trust, London, UK.

David E Philpott (DE)

Cornwall Partnership NHS Foundation Trust, Truro, TR4 9LD, UK.

Chris Ashwin (C)

Cornwall Partnership NHS Foundation Trust, Truro, TR4 9LD, UK.

Joshua Howkins (J)

Cornwall Partnership NHS Foundation Trust, Truro, TR4 9LD, UK.

Harriet Slater (H)

Swansea Bay University Health Board, Swansea, UK.

David Medhurst (D)

Swansea Bay University Health Board, Swansea, UK.

Rohit Shankar (R)

Cornwall Partnership NHS Foundation Trust, Truro, TR4 9LD, UK. Rohit.shankar@plymouth.ac.uk.
University of Plymouth Peninsula School of Medicine, Plymouth, UK. Rohit.shankar@plymouth.ac.uk.
Cornwall Intellectual Disability Equitable Research (CIDER), Threemilestone Industrial Estate, Cornwall, TR4 9LD, Truro, UK. Rohit.shankar@plymouth.ac.uk.

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