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Letter to the Editor

Published online by Cambridge University Press:  30 January 2017

V. Murphy
Affiliation:
St Stephen’s Hospital, Glanmire, Cork, Ireland (Email: valeriee.murphy@hse.ie)
G. Gulati
Affiliation:
University Hospital Limerick, Limerick, Ireland
S. Luppe
Affiliation:
Gloucestershire Royal Hospital, Gloucestershire, UK
E. Chaila
Affiliation:
University Hospital Limerick, Ireland
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Abstract

Type
Correspondence
Copyright
© College of Psychiatrists of Ireland 2017 

The prevalence of epilepsy in Ireland varies between 10/1000 for adults based on self-report and 9/1000 for those over the age of 5 years based on prescription data (Linehan et al. Reference Linehan, Walsh, Kerr, Brady and Kelleher2009). Epilepsy is frequently comorbid with psychiatric illness and over represented in people with learning disabilities.

Jones et al. (Reference Jones, Rickards and Cavanna2010) reviewing 13 methodologically robust studies, noted that in people with epilepsy, the prevalence of comorbid psychiatric disorders can be 24–75% for mood disorder, 10–25% for anxiety disorders and 2–7% for psychosis.

In the case of people with learning disabilities, Lhatoo & Sander (Reference Lhatoo and Sander2001) summarise community surveys citing prevalences between 6% of those with mild learning disabilities rising to 50% in those with profound learning disabilities. People with epilepsy and learning disabilities suffer with higher morbidity and indeed have higher mortality rates, particularly in those with recent seizures (Robertson et al. Reference Robertson, Hatton, Emerson and Baines2015).

A patient with epilepsy may present a challenge from a diagnostic, therapeutic and risk-related viewpoint for the psychiatrist. Diagnostically, there is a possibility that the seizure disorder could be presenting as mental illness such as in the psychoses of epilepsy (Kanner & Rivas-Grajales, Reference Kanner and Rivas-Grajales2016). Conversely, seizures could be mistaken as evidence of psychiatric illness (Mirsattari et al. Reference Mirsattari, Gofton and Chong2011). Therapeutically, medication used for seizure control may have psychiatric sequelae (Nadkarni & Devinsky, Reference Nadkarni and Devinsky2005) and psychiatric medication may interact with anti-epileptic drugs (Johannessen & Landmark Reference Johannessen and Landmark2010) or alter seizure threshold. From a risk-related viewpoint, those with comorbid epilepsy have specific risks to consider including but not limited to areas such as bathing and using electrical equipment (National Institute of Clinical Excellence, 2016).

Given the complexity cited above, it would follow that knowing seizure patterns, allowing for triangulation from a number of information sources, particularly close carers and specialists would be of significant diagnostic benefit as would a system to consider potential drug interactions and common risks. We therefore reviewed relevant guidance from the Epilepsy Society (epilspsysociety.org.uk) and the National Institute of Clinical Excellence, (2016) to operationalise key recommendations to develop a ‘yellow card’ for the patient record in approved centres. This would summarise key aspects of the patient’s epilepsy at a glance and serve as a useful aide-memoire to consider assessment and risks for people with epilepsy in a psychiatric setting. The document was compiled in consultation with an Epilepsy Nurse Specialist, an Occupational Therapist and Consultant Neurologists. The ‘yellow card’ with a distinctive colour, would be easy to identify in the patient record, and likely improve the reliability of information gathering, with potential positive diagnostic, therapeutic and risk management implications. We are presently arranging to pilot the ‘yellow card’ scheme in approved centres across six Irish counties, and would welcome collaboration from other approved centres nationwide. The ‘yellow card’ may be found as an appendix to this letter and is available for viewing online.

Supplementary material

To view supplementary material for this article, please visit https://doi.org/10.1017/ipm.2016.48

References

Johannessen, SI, Landmark, CJ (2010). Antiepileptic drug interactions – principles and clinical implications. Current Neuropharmacology 8, 254267.CrossRefGoogle ScholarPubMed
Jones, R, Rickards, H, Cavanna, AE (2010). The prevalence of psychiatric disorders in epilepsy: a critical review of the evidence. Functional Neurology 25, 191194.Google ScholarPubMed
Kanner, AM, Rivas-Grajales, AM (2016). Psychosis of epilepsy: a multifaceted neuropsychiatric disorder’. CNS Spectrums 21, 247257.CrossRefGoogle ScholarPubMed
Lhatoo, SD, Sander, JWAS (2001). The epidemiology of epilepsy and learning disability. Epilepsia 42, 69.CrossRefGoogle ScholarPubMed
Linehan, C, Walsh, P, Kerr, M, Brady, G, Kelleher, C (2009). The prevalence of epilepsy in Ireland: a summary report. Brainwave the Irish Epilepsy association, Dublin (http://www.epilepsy.ie/assets/16/BB1D6D7E-D941-18FF-F8010F269F3E5E29_document/Prevalence_Summary.pdf). Accessed 6 November 2016.Google Scholar
Mirsattari, SM, Gofton, TE, Chong, DJ (2011). Misdiagnosis of epileptic seizures as manifestations of psychiatric illnesses. Canadian Journal of Neurological Sciences 38 (3): 487493.CrossRefGoogle ScholarPubMed
Nadkarni, S, Devinsky, O (2005). Psychotropic effects of antiepileptic drugs. Epilepsy Currents 5, 176181.CrossRefGoogle ScholarPubMed
National Institute of Clinical Excellence (2016). Epilepsies: diagnoses and management: CR137 (https://www.nice.org.uk/guidance/CG137/chapter/Introduction.Google Scholar
Robertson, J, Hatton, C, Emerson, E, Baines, S (2015). Mortality in people with intellectual disabilities and epilepsy: a systematic review. Seizure 29, 123133.CrossRefGoogle ScholarPubMed
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Yellow Card

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