Hostname: page-component-7b9c58cd5d-6tpvb Total loading time: 0 Render date: 2025-03-15T02:24:46.073Z Has data issue: false hasContentIssue false

The neurology–psychiatry interface in epilepsy

Published online by Cambridge University Press:  19 December 2018

Valerie Murphy*
Affiliation:
Clinical Senior Lecturer, Department of Psychiatry, University College, Cork, Ireland
Brian Hallahan
Affiliation:
Senior Lecturer, Department of Psychiatry, National University of Ireland, Galway, Ireland
Henry O’ Connell
Affiliation:
Adjunct Associate Clinical Professor, Department of Psychiatry, University of Limerick, Limerick, Ireland
Brenda Wright
Affiliation:
Consultant Forensic Psychiatrist, Central Mental Hospital, Dublin, Ireland
Brendan D Kelly
Affiliation:
Professor of Psychiatry, Trinity College Dublin, Dublin, Ireland
Gautam Gulati
Affiliation:
Adjunct Clinical Senior Lecturer, Department of Psychiatry, University of Limerick, Limerick, Ireland
Rohit Shankar
Affiliation:
Honorary Associate Clinical Professor, Exeter Medical School, Exeter, Consultant Neuropsychiatrist Cornwall Partnership NHS Foundation Trust, United Kingdom
*
*Address for correspondence: Valerie Murphy PhD, University College, Cork, Ireland. (Email: valeriee.murphy@hse.ie)
Rights & Permissions [Opens in a new window]

Abstract

Epilepsy and mental illness have a bidirectional association. Psychiatrists are likely to encounter epilepsy as comorbidity. Seizures may present as mental illness. Equally, the management of psychiatric conditions has the potential to destabilise epilepsy. There is a need for structured epilepsy awareness and training amongst psychiatrists. This paper outlines key considerations around diagnosis, treatment and risk while suggesting practical recommendations.

Type
Perspective Piece
Copyright
© College of Psychiatrists of Ireland 2018

Introduction

Epilepsy is a common neurological disorder with a prevalence in Ireland of approximately 1% (Linehan et al., Reference Linehan, Walsh, Kerr, Brady and Kelleher2009). The definition of epilepsy has evolved over the last two decades and an internationally accepted clinical definition (Fisher et al., Reference Fisher, Acevedo, Arzimanoglou, Bogacz, Cross, Elger, Engel, Forsgren, French, Glynn, Hesdorffer, Lee, Mathern, Moshé, Perucca, Scheffer, Tomson, Watanabe and Wiebe2014) as adopted by the international league against epilepsy reflects clinical considerations, risk of further seizures as well as the issue of disease resolution. While epilepsy is a complex neurological condition and managed primarily by neurologists, in this paper we outline diagnostic, therapeutic and risk-related aspects that highlight the relevance of this neurological illness to the practising psychiatrist.

Epilepsy and mental health

Psychiatrists encounter epilepsy as both a comorbidity and a differential diagnosis. Olfactory hallucinations in a patient with psychosis may raise the possibility of temporal lobe epilepsy (TLE) (Flor-Henry, Reference Flor-Henry1969) or seizure activity may have a role in challenging behaviour in a person with an intellectual disability (Blickwedel et al., Reference Blickwedel, Ali and Hassiotis2017).

Encountering epilepsy in psychiatric patients is not uncommon as psychiatric morbidity is over-represented in individuals with epilepsy with increased rates of affective disorders (25–74%), anxiety disorders (10–25%) and psychosis (2–7%) (Jones et al., Reference Jones, Rickards and Cavanna2010). A recent Irish study (Murphy et al., Reference Murphy, Hallahan, Moloney, Smthwick, Costello and Gulati2018) noted the prevalence of epilepsy in general psychiatric inpatient settings to be over 3%; three times that of general population estimates. This is perhaps unsurprising as some of these illnesses, particularly psychotic illness are thought to have a neurodevelopmental origin (Murray & Lewis, Reference Murray and Lewis1987). Additionally, there is evidence of genetic overlap between psychosis and epilepsy (Clarke et al., Reference Clarke, Tanskanen, Huttunen, Clancy, Cotter and Cannon2012).

Epilepsy and psychiatric disorders are individually related to higher mortality rates. In epilepsy this is particularly true of those with uncontrolled seizures (Robertson et al., Reference Robertson, Hatton, Emerson and Baines2015). The two conditions are also associated with a higher risk of suicide and other physical comorbidities.

Epilepsy and people with intellectual disabilities

The prevalence of epilepsy in people with intellectual disabilities is significantly higher. A recent systematic review and meta-analysis (Robertson et al., Reference Robertson, Hatton, Emerson and Baines2015) showed a pooled epilepsy prevalence of 22.2% (95% confidence interval 19.6–25.1) in those with intellectual disabilities with prevalence increasing as the severity of disability increased. The Royal College of Psychiatrists has published recent guidance for the management of epilepsy in those with intellectual disabilities which recommends epilepsy training as part of higher specialist training (HST) for those psychiatrists who specialise in intellectual disabilities in the United Kingdom (Royal College of Psychiatrists, 2017b). In Ireland, people with intellectual disabilities often receive care in general adult psychiatric settings, particularly where individuals have a mild-to-moderate intellectual disability or additionally if individuals require involuntary treatment. Thus reasonable knowledge of epilepsy concerns in people with intellectual disability is important across the psychiatric specialism in Ireland.

Diagnostic issues

Seizures can present as symptoms of mental illness

Complex partial seizures can present as poor impulse control, ‘rage attacks’, suicide attempts, rapid mood swings, depression, psychotic episodes, bulimia, panic attacks, obsessive-compulsive symptoms and somatic complaints (Stern & Murray, Reference Stern and Murray1984). A patient may be treated with psychotropic medication for years before an organic cause is suspected. Herein lies the value of being alert to epilepsy as a differential diagnosis where there are atypical presentations, diagnostic overshadowing, treatment resistant illness, neurological signs, history of central nervous system illness such as encephalitis, a concerning medical history such as one involving unexplained loss of consciousness or a family history of seizures.

A particularly important type of seizure that may present as mental illness is TLE which can present as psychosis. Psychosis in TLE (Belletsky & Mirsattari, Reference Beletsky and Mirsattari2012) may have either a relapsing-remitting (concurrent with seizures) or chronic course (involving interictal phase) and preictal states may present with an altered sensorium, including a range of perceptual abnormalities including visual, auditory, olfactory or gustatory illusions or hallucinations.

Frontal lobe epilepsy can present with behavioural disturbance, psychiatric symptoms including depression or psychosis and cognitive changes (Braakman et al., Reference Braakman, Vaessen, Hofman, Debeij-van Hall, Backes, Vles and Aldenkamp2011; Gold et al., Reference Gold, Sher and Maldonado2016); it can be associated with attention deficit hyperactivity disorder (ADHD) in children (Braakman et al., Reference Braakman, Vaessen, Hofman, Debeij-van Hall, Backes, Vles and Aldenkamp2011).

There may be a relationship between seizure control and psychotic symptoms in some patients. The term ‘forced normalisation’ is used to describe psychotic episodes associated with the remission of seizures and disappearance of epileptiform activity on electro-encephalogram in individuals with epilepsy (Loganathan et al., Reference Loganathan, Enja and Lippmann2015). Further there could be psychotic activity associated with seizures during the pre-ictal, ictal or post-ictal stages. There could be identified changes in affect and mood associated with seizures (Kanner & Rivas-Grajales, Reference Kanner and Rivas-Grajales2016). The management of such psychoses require a careful balance between antiepileptic medications, antipsychotic or other psychotropic drugs, with close clinical monitoring and communication between the patient, their family, and involved specialities.

In people with intellectual disability presenting with challenging behaviour, it is important for the treating clinician to rule out seizure activity given the high rate of seizure disorder as a comorbidity in this group (Blickwedel et al., Reference Blickwedel, Ali and Hassiotis2017; Roberston et al., 2015). The assessing clinician may need to consider the role of factors such as seizure frequency, peri-ictal events and the role of anti-epileptic drugs (AEDs) additionally in their formulation (Kerr et al., Reference Kerr, Linehan, Brandt, Kanemoto, Kawasaki, Sugai, Tadokoro, Villanueva, Wilmshurst and Wilson2016).

The value of an Electro-Encephalogram (EEG)

An electro-encephalogram (EEG) may be helpful in the investigation of possible seizure disorder. However, caution is required in interpretation as either no abnormal activity or only minimal changes such as focal slowing or brief patterns of spikes and waves may be evident even in individuals with diagnosed epilepsy. The sensitivity of interictal EEG varies from 29–55% (Pillai & Sperling, Reference Pillai and Sperling2006) with higher estimates for repeat examinations and activation techniques whilst specificity is variable with estimates in excess of 90% for some epilepsy syndromes (Oliviera & Rosado, Reference Oliveira and Rosado2004). Video-EEGs have significantly greater diagnostic yield (Pillai & Sperling, Reference Pillai and Sperling2006). There needs to be specific caution in interpreting EEGs in people with intellectual disability as they may have abnormal brain wave patterns linked to a congenital brain defect or damage.

EEG departments helpfully use photic stimulation, hyperventilation or sleep deprivation (all of which lower the seizure threshold) to help evaluate cases where a referral clearly queries the diagnosis of epilepsy. Video-EEG is the only definite way to diagnose functional seizures and behavioural disturbance linked with epileptic activity. This is sometimes limited to tertiary centres but as an investigation this can be invaluable in providing diagnostic certainty.

Indications for Magnetic Resonance Imaging (MRI) of the Brain

Where an organic cause is suspected in individuals presenting with either behavioural disturbance or symptoms suggesting a mental illness and particularly where focal deficits are noted on neurological examination, magnetic resonance imaging (MRI) of the brain should be obtained. Brain MRIs are often superior to Computerised Tomography due to their higher resolution allowing them to identify smaller space occupying lesions and separate more clearly grey and white matter. Despite this, a normal MRI of the brain does not exclude a diagnosis of epilepsy. MRI abnormalities may be seen in 80% of patients with refractory focal epilepsy but estimates are four times lower in patients with a single unprovoked seizure or epilepsy in remission (Roy & Pandit, Reference Roy and Pandit2011).

Therapeutic issues

Psychotropics and seizure threshold

Seizure thresholds may be affected by the majority of psychotropic agents, although there is a large variance between psychotropic agents in relation to such an effect. As a basic tenet, psychotropic agents that have sedative effects have an increased likelihood to be associated with inducing seizures (Taylor et al., Reference Taylor, Paton and Kapur2015). This is important as even when prescribing antidepressants or antipsychotics in a patient with well controlled epilepsy, there is a potential for destabilisation which should be highlighted to the patient, his/her carer and clinical correspondence copied to the concerned neurologist or general practitioner. An effect on seizure threshold may have implications for driving and safety in other social situations.

Guidelines are constantly evolving in this area but the Maudsley Prescribing Guidelines 13th edition (Taylor et al., Reference Taylor, Barnes and Young2018) currently state that selective serotonin reuptake inhibitors (SSRIs) (except citalopram), the antidepressant mirtazapine and the antipsychotic agents risperidone, aripiprazole, haloperidol, amisulpiride and sulpiride are associated with a minimal impact on seizure thresholds and thus should be considered for the management of mood or psychotic disorders in individuals with epilepsy. Caution must also be exercised in discontinuing benzodiazepines, lamotrigine or sodium valproate (when used as mood stabilisers) as these may be masking latent seizures in a patient who has well controlled epilepsy.

ADHD is overrepresented in individuals with epilepsy (Williams et al., Reference Williams, Giust, Kronenberger and Dunn2016). Stimulant medication and potentially atomoxetine used in the treatment of ADHD have the potential to reduce seizure threshold (Harpin et al., Reference Harpin2008).

Anti-Epileptic Drugs (AEDs) and psychiatric/behavioural manifestations

There is increasing evidence of psychiatric disorders or behavioural disturbance arising due to treatment with AEDs. AEDs may be neutral, have positive effects on the management of mental illness or negative effects (Nadkarni & Devinsky, Reference Nadkarni and Devinsky2005; Royal College of Psychiatrists, 2017a). Positive effects of AEDs include, for example, the antidepressant effect of lamotrigine or mood stabilising effects of sodium valproate. Negative effects of AEDs include cognitive problems and dependence risk with barbiturates and the risk of psychosis and affective disorders with phenytoin and vigabatrin. Levetiracetam in particular has been associated with behavioural disturbance and affective adverse effects (Abou-Khalil, Reference Abou-Khalil2008). Such adverse effects have been associated with significant AED discontinuation rates (Stephen et al., Reference Stephen, Wishart and Brodie2017).

AED/Psychotropic interactions

Another area of caution when prescribing psychotropics is the potential for pharmacokinetic interactions through cytochrome P450 enzymes (Taylor et al., Reference Taylor, Barnes and Young2018). Some commonly prescribed antidepressants such as fluoxetine and sertraline at higher doses can increase anticonvulsant plasma levels. Some anticonvulsants such as phenytoin and carbamazepine can reduce plasma levels of psychotropics. Of note, recent guidance for AED prescribing (Royal College of Psychiatrists, 2017a) advocate against the first line use of older AEDs such as phenytoin and phenobarbitone in epilepsy.

Teratogenicity

Sodium valproate can be prescribed both for affective disorders and seizure control. The use of this medication is best avoided in women of child bearing age given its significant teratogenic potential (Ornoy, Reference Ornoy2009). Particular care must be taken with additional safeguards such as a clear discussion of risks and benefits as well as the use of contraception should its use be necessary, in keeping with recent regulations (Sisodiya, Reference Sisodiya2018).

Medication adherence

In patients with comorbid mental illness and epilepsy, non-adherence with prescribed medication has the potential to precipitate relapse in mental illness and destabilise seizure control. Both conditions are separately known to have limited adherence rates with one study citing that a third of those with epilepsy may not be adherent to prescribed medication (Getnet et al., Reference Getnet, Woldeyohannes, Bekana, Mekonen, Fekadu, Menberu, Yimer, Assaye, Belete and Belete2016). Up to 60% of those with psychosis may be non-adherent at some point over a 4 year follow up period (Valenstein et al., Reference Valenstein, Ganoczy, McCarthy, Myra Kim, Lee and Blow2006). Patients may therefore need suitable education, oversight and support for continuity with medication.

Specific considerations in people with intellectual disabilities

The prescription of psychotropic medication in people with intellectual disabilities requires care due to a lower threshold for side effects and an increased prevalence of physical comorbidities. Medication, when clearly indicated, should be used cautiously at lower doses with specific monitoring for outcomes and emergence of side effects. The prescription of antiepileptic medication in people with intellectual disabilities and epilepsy requires particular care in respect of issues around consent, capacity to consent, the involvement of carers, monitoring of outcomes and specific choice of medication (Royal College of Psychiatrists, 2017).

Areas of Risk

Given that psychiatric treatment can potentially destabilise seizure control, a clinician may need to be mindful of the social risk profile that this may create. Alcohol misuse, for example, is a significant comorbidity with mental illness (Regier et al., Reference Regier, Farmer, Rae, Locke, Keith, Judd and Goodwin1990) and carries the risk of destabilising seizure control (Hillbom et al., Reference Hillbom, Pieninkeroinen and Leone2003).

Driving

Experiencing a seizure whilst driving can risk injury to the person or other road users. In Ireland, regulations governing driving for those with epilepsy are published by the Road Safety Authority (RSA, 2016) and this makes an essential reference document for practitioners. They make different recommendations for those with daytime and nocturnal seizures as well as some specific aetiologies. The RSA recommends a 12-month seizure free period prior to recommencing driving for those with daytime seizures, alongside other stipulations such as compliance with treatment.

Activities of daily living

Guidance from the National Institute for Health and Care Excellence (NICE) (2018) highlights the need to be mindful of risks in those with seizures in activities of daily living. Such may extend to psychiatric inpatient settings. Examples would include situations such as operating electrical equipment and swimming if undertaken as part of occupational therapy. Bathing arrangements require special care and showers are safer than baths in those with seizures. Where the person wishes to bathe, continuous observation during that time would be the only measure that mitigates risk. Risks associated with activities of daily living require particular care and specialist care planning in people with intellectual disabilities who are more likely to have other physical comorbidities, a greater sensitivity to changes in medication and require assistance with communication (Royal College of Psychiatrists, 2017b).

SUDEP

The risk of sudden unexpected death in epilepsy (SUDEP) is 1 in 1000 person years but can be as high as 1 in 100 person years in those with treatment resistant epilepsy and uncontrolled seizures (Shankar et al., Reference Shankar, Elizabeth, McLean, Nashef and Tomson2017). There are potentially modifiable risk factors that mitigate this risk such as nocturnal monitoring, compliance and advice on sleeping position (Shankar et al., Reference Shankar, Walker, McLean, Laugharne, Ferrand, Hanna and Newman2016). For the psychiatrist an awareness of the impact of treatment adherence and co-morbid alcohol or psychoactive substance (ab)use are important due to them being modifiable risk factors for individuals with epilepsy. Some studies suggest that intellectual disabilities are a risk factor for SUDEP (Young et al., Reference Young, Shankar, Palmer, Craig, Hargreaves, McLean, Cox and Hillier2015). Specialist advice from a neurologist may be helpful when considering the prescription of new psychotropic in those with poorly controlled seizures and this is particularly important in those with comorbid intellectual disabilities. A good tool to inform patients of their risk of SUDEP is the SUDEP and Seizure Safety Checklist (SUDEP Action, 2017).

Management of prolonged seizures

Doctors working in psychiatry may find themselves responding to a prolonged seizure for an inpatient or working with patients who have a history of past status epilepticus. The management of such can often be foreseen and a history at the time of admission is often the best time to prescribe a ‘rescue medication’ on an ‘as required’ basis. Buccal midazolam may be safer and more acceptable to patients than other modalities of benzodiazepine use (Scott et al., Reference Scott, Besag and Neville1999). Training in administering midazolam and the other aspects of emergency care in status is invaluable for first responders.

Discussion

Epilepsy is a prevalent neurological disorder that is over-represented in patients in psychiatric services (Murphy et al., Reference Murphy, Hallahan, Moloney, Smthwick, Costello and Gulati2018). Patients with epilepsy report uncertainty for their future and describe the fear of having a seizure as the ‘worst thing about having epilepsy’ and as important as the limitations in lifestyle, school, driving and employment that may occur with this diagnosis (Fisher et al., Reference Fisher, Vickrey, Gibson, Hermann, Penovich, Scherer and Walker2000). Carers for those with epilepsy have a high level of knowledge (McEwan et al., Reference McEwan, Taylor, Caswell, Entwistle, Jacoby, Gorry, Jacoby and Baker2007) around epilepsy and can be an invaluable source of information when assessing a patient and this is particularly true for patients with an intellectual disability (Espie et al., Reference Espie, Watkins, Duncan, Sterrick, McDonach, Espie and McGarvey2003) where there may be special needs around communication. A diagnosis of epilepsy has been demonstrated to not alone reduce the quality of life of the patient but also adversely impact on the quality of life of the care-givers (Guti-Errez et al., Reference Gutierrez-Angel, Martinez-Juarez, Hernandez-Vanegas and Crail-Melendez2018).

A psychiatrist should be alert to the bi-directional impact of mental illness and physical illness on each other. The spectrum of physical illness that a psychiatrist particularly needs to be aware of includes endocrine, metabolic, cardiac and neurological disorders. Epilepsy is one such neurological disorder at the interface of medical specialities that requires particular care in view of its higher mortality and complex risk profile. Simple interventions and effective communication has the potential to offer incremental benefit for patients in diagnosis, therapeutics and risk management.

A useful aid for key aspects of history and management considerations for patients with epilepsy in psychiatric inpatient settings is presented as Table 1. This has been formalised into a diagnosis triggered tool which has been piloted in Irish settings (Murphy et al., Reference Murphy, Gulati, Luppe and Chaila2017; Moloney et al., Reference Moloney, Smithwick, Mullane, O’Sullivan and Gulati2017) and is attached as supplementary online material to this article. Additional sources of advice for psychiatrists when managing a patient with comorbid epilepsy are included as an online appendix.

Table 1 Information to be recorded in psychiatric inpatient notes

There is substantial training for neurologists in relation to epilepsy both in basic and HST schemes and this is a disorder managed primarily by consultant neurologists, often in tertiary centres. There is a need for increased awareness of this disorder as a comorbidity in the psychiatric setting (Murphy et al., Reference Murphy, Hallahan, Moloney, Smthwick, Costello and Gulati2018). With awareness and a systematic approach to assessment, this may be an area where psychiatric expertise can contribute to safer and better lives for people with epilepsy.

Supplementary materials

To view supplementary material for this article, please visit https://doi.org/10.1017/ipm.2018.49

Acknowledgements

None

Financial Support

This research received no specific grant from any funding agency, commercial or not-for-profit sectors.

Conflict of Interest

VM has no conflicts of interest to declare. BH has no conflicts of interest to declare. HOC has no conflicts of interest to declare. BDK has no conflicts of interest to declare. BW has no conflicts of interest to declare. GG has received honoraria from Jansen and Lundbeck unrelated to the submitted work. RS is a stakeholder of the ‘SUDEP and Seizure Safety Checklist’ and the mobile app based on the checklist – EpSMon. RS has received institutional and research support and personal fees from LivaNova, UCB, Eisai, Special Products, Bial and Desitin outside the submitted work.

Ethical Standards

The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committee on human experimentation with the Helsinki Declaration of 1975, as revised in 2008. The authors assert that ethical approval for publication of this paper was not required by their local REC.

References

Abou-Khalil, B (2008). Levetiracetam in the treatment of epilepsy. Neuropsychiatric Disease and Treatment 4, 507523.CrossRefGoogle ScholarPubMed
Beletsky, V, Mirsattari, SM (2012). Epilepsy, mental health disorder, or both? Epilepsy Research and Treatment, article ID 163731. https://doi.org/10.1155/2012/163731.CrossRefGoogle ScholarPubMed
Blickwedel, J, Ali, A, Hassiotis, A (2017). Epilepsy and challenging behaviour in adults with intellectual disability: a systematic review. Journal of Intellectual & Developmental Disability. https://doi.org/10.3109/13668250.2017.1327039.Google Scholar
Braakman, HM, Vaessen, MJ, Hofman, PA, Debeij-van Hall, MH, Backes, WH, Vles, JS, Aldenkamp, AP (2011). Cognitive and behavioral complications of frontal lobe epilepsy in children: a review of the literature. Epilepsia 52, 849856.CrossRefGoogle ScholarPubMed
Clarke, MC, Tanskanen, A, Huttunen, MO, Clancy, M, Cotter, DR, Cannon, M (2012). Evidence for shared susceptibility to epilepsy and psychosis: a population-based family study. Biological Psychiatry 71, 836839.CrossRefGoogle ScholarPubMed
Espie, CA, Watkins, J, Duncan, R, Sterrick, M, McDonach, E, Espie, E, McGarvey, C (2003). Perspectives on epilepsy in people with intellectual disabilities: comparison of family carer, staff carer and clinician score profiles on the Glasgow Epilepsy Outcome Scale (GEOS). Seizure 12, 195202.CrossRefGoogle Scholar
Fisher, RS, Acevedo, C, Arzimanoglou, A, Bogacz, A, Cross, JH, Elger, CE, Engel, J, Forsgren, L, French, JA, Glynn, M, Hesdorffer, DC, Lee, BI, Mathern, GW, Moshé, SL, Perucca, E, Scheffer, IE, Tomson, T, Watanabe, M, Wiebe, S (2014). ILAE official report: a practical clinical definition of epilepsy. Epilepsia 55, 475482.CrossRefGoogle ScholarPubMed
Fisher, RS, Vickrey, BG, Gibson, P, Hermann, B, Penovich, P, Scherer, A, Walker, S (2000). The impact of epilepsy from the patient’s perspective I. Descriptions and subjective perceptions. Epilepsy Research 41, 3951.CrossRefGoogle ScholarPubMed
Flor-Henry, P (1969). Psychosis and temporal lobe epilepsy: a controlled investigation. Epilepsia 10, 363395.CrossRefGoogle ScholarPubMed
Getnet, A, Woldeyohannes, SM, Bekana, L, Mekonen, T, Fekadu, W, Menberu, M, Yimer, S, Assaye, A, Belete, A, Belete, H (2016). Antiepileptic drug nonadherence and its predictors among people with epilepsy. Behavioural Neurology 2016, 16.CrossRefGoogle ScholarPubMed
Gold, JA, Sher, Y, Maldonado, JR (2016). Frontal lobe epilepsy: a primer for psychiatrists and a systematic review of psychiatric manifestations. Psychosomatics 57, 445464.CrossRefGoogle Scholar
Gutierrez-Angel, AM, Martinez-Juarez, IE, Hernandez-Vanegas, LE, Crail-Melendez, D (2018). Quality of life and level of burden in primary caregivers of patients with epilepsy: Effect of neuropsychiatric comorbidity. Epilepsy & Behavior 81, 1217.CrossRefGoogle ScholarPubMed
Harpin, VA (2008). Medication options when treating children and adolescents with ADHD: interpreting the NICE guidance 2006. Archives of Disease in Childhood – Education and Practice 93, 5865.CrossRefGoogle ScholarPubMed
Hillbom, M, Pieninkeroinen, I, Leone, M (2003). Seizures in alcohol-dependent patients: epidemiology, pathophysiology and management. CNS Drugs 17, 10131030.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 Scholar
Kanner, AM, Rivas-Grajales, AM (2016). Psychosis of epilepsy: a multifaceted neuropsychiatric disorder. CNS Spectrums 21, 247257.CrossRefGoogle ScholarPubMed
Kerr, M, Linehan, C, Brandt, C, Kanemoto, K, Kawasaki, J, Sugai, K, Tadokoro, Y, Villanueva, V, Wilmshurst, J, Wilson, S (2016). Behavioral disorder in people with an intellectual disability and epilepsy: a report of the Intellectual Disability Task Force of the Neuropsychiatric Commission of ILAE. Epilepsia Open 1, 102111.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 8 April 2018.Google Scholar
Loganathan, MA, Enja, M, Lippmann, S (2015). Forced normalisation: epilepsy and psychosis interaction. Innovations in Clinical Neuroscience 12, 3841.Google Scholar
McEwan, L, Taylor, J, Caswell, M, Entwistle, R, Jacoby, K, Gorry, J, Jacoby, A, Baker, GA (2007). Knowledge of and attitudes expressed toward epilepsy by carers of people with epilepsy: a UK perspective. Epilepsy & Behavior 11, 1319.CrossRefGoogle ScholarPubMed
Moloney, N, Smithwick, D, Mullane, N, O’Sullivan, D, Gulati, G (2017). Epilepsy in psychiatric inpatient settings: the “Yellow Card” initiative – a completed audit cycle from the Mid-West. Poster Presented at the Annual Psychiatry Study Day at the University of Limerick, December 2017.Google Scholar
Murray, RM, Lewis, SW (1987). Is schizophrenia a neurodevelopmental disorder? British Medical Journal 295, 681682.CrossRefGoogle ScholarPubMed
Murphy, V, Gulati, G, Luppe, S, Chaila, E (2017). Letter to the editor. Irish Journal of Psychological Medicine 34, 149149. https://doi.org/10.1017/ipm.2016.48.CrossRefGoogle ScholarPubMed
Murphy, V, Gulati, G, Luppe, S, Chaila, E (2017). Epilepsy care planning in psychiatric inpatient settings – the ‘Yellow Card’. International Journal of Integrated Care 17, A553.CrossRefGoogle Scholar
Murphy, V, Hallahan, B, Moloney, M, Smthwick, D, Costello, S, Gulati, G (2018). Epilepsy in Irish psychiatric inpatients settings. Irish Medical Journal 111, 809.Google Scholar
Nadkarni, S, Devinsky, O (2005). Psychotropic effects of antiepileptic drugs. Epilepsy Currents 5, 176181.CrossRefGoogle ScholarPubMed
NICE (2018). Epilepsies: diagnoses and management: CG137. (https://www.nice.org.uk/guidance/CG137). Accessed 28 April 2018.Google Scholar
Oliveira, SN, Rosado, P (2004). EEG interictal – sensitivity and specificity of the diagnosis of epilepsy. Acta Médica Portuguesa 17, 465470.Google Scholar
Ornoy, A (2009). Valproic acid in pregnancy: how much are we endangering the embryo and fetus? Reproductive Toxicology 28, 110.CrossRefGoogle ScholarPubMed
Pillai, J, Sperling, MR (2006). Interictal EEG and the diagnosis of epilepsy. Epilepsia 47, 1422. https://doi.org/10.1111/j.1528-1167.2006.00654.x.CrossRefGoogle Scholar
Regier, DA, Farmer, ME, Rae, DS, Locke, BZ, Keith, SJ, Judd, LL, Goodwin, FK (1990). Comorbidity of mental disorders with alcohol and other drug abuse. Results from the Epidemiologic Catchment Area (ECA) Study. JAMA 264, 25112518.CrossRefGoogle ScholarPubMed
Road Safety Authority (2016). Sláinte agus Tiomáint. Medical Fitness to Drive Guidelines (Group 1 and 2 Drivers), 5th edition, pp. 4347. RSA: Ireland. (http://www.rsa.ie/Documents/Licensed%20Drivers/Medical_Issues/Sláinte_agus_Tiomáint_Medical_Fitness_to_Drive_Guidelines.pdf). Accessed 8 April 2018.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
Roy, T, Pandit, A (2011). Neuroimaging in epilepsy. Annals of Indian Academy of Neurology 14, 7880.CrossRefGoogle ScholarPubMed
Royal College of Psychiatrists (2017a). CR206: prescribing anti-epileptic drugs for people with epilepsy and intellectual disability. (https://www.rcpsych.ac.uk/usefulresources/publications/collegereports/cr/cr206.aspx).Google Scholar
Royal College of Psychiatrists (2017b). CR203: management of epilepsy in adults with intellectual disability. (https://www.rcpsych.ac.uk/usefulresources/publications/collegereports/cr/cr203.aspx). Accessed 6 April 2018.Google Scholar
Scott, RC, Besag, FM, Neville, BG (1999). Buccal midazolam and rectal diazepam for treatment of prolonged seizures in childhood and adolescence: a randomised trial. Lancet 353, 623626.CrossRefGoogle ScholarPubMed
Shankar, R, Walker, M, McLean, B, Laugharne, R, Ferrand, F, Hanna, J, Newman, C (2016). Steps to prevent SUDEP: the validity of risk factors in the SUDEP and seizure safety checklist: a case control study. Journal of Neurology 263, 18401846.CrossRefGoogle ScholarPubMed
Shankar, R, Elizabeth, JD, McLean, B, Nashef, L, Tomson, T (2017). Sudden unexpected death in epilepsy (SUDEP): what every neurologist should know. Epileptic Disorders 19, 19. https://doi.org/10.1684/epd.2017.0891.Google ScholarPubMed
Sisodiya, SM (2018). Valproate and childbearing potential: new regulations. Practical Neurology. Published online April 2018. doi:10.1136/practneurol-2018-001955.CrossRefGoogle ScholarPubMed
Stephen, LJ, Wishart, A, Brodie, MJ (2017). Psychiatric side effects and antiepileptic drugs: observations from prospective audits. Epilepsy & Behavior 71, 7378.CrossRefGoogle ScholarPubMed
Stern, TA, Murray, GB (1984). Complex partial seizures presenting as a psychiatric illness. The Journal of Nervous and Mental Disease 172, 625627.CrossRefGoogle ScholarPubMed
SUDEP Action (2017). SUDEP and Seizure Safety Checklist Version 2. SUDEP Action, Wantage, UK. (https://sudep.org/checklist). Accessed 4 August 2018.Google Scholar
Taylor, DM, Barnes, TRE, Young, AH (2018). The Maudsley Prescribing Guidelines in Psychiatry, 13th edn. Wiley-Blackwell: London. ISBN 978-1-119-44260-8.Google Scholar
Taylor, DM, Paton, C, Kapur, S (2015). The Maudsley Prescribing Guidelines in Psychiatry, 12th edn. Wiley-Blackwell: London: ISBN: 978-1-118-75460-3.Google Scholar
Valenstein, M, Ganoczy, D, McCarthy, JF, Myra Kim, H, Lee, TA, Blow, FC (2006). Antipsychotic adherence over time among patients receiving treatment for schizophrenia: a retrospective review. Journal of Clinical Psychiatry 67, 15421550.CrossRefGoogle ScholarPubMed
Williams, AE, Giust, JM, Kronenberger, WG, Dunn, DW (2016). Epilepsy and attention-deficit hyperactivity disorder: links, risks, and challenges. Neuropsychiatric Disease and Treatment 12, 287296.Google ScholarPubMed
Young, C, Shankar, S, Palmer, J, Craig, J, Hargreaves, C, McLean, B, Cox, D, Hillier, R (2015). Does intellectual disability increase sudden unexpected death in epilepsy (SUDEP) risk? Seizure 25, 112116.CrossRefGoogle ScholarPubMed
Figure 0

Table 1 Information to be recorded in psychiatric inpatient notes

Supplementary material: File

Murphy et al. supplementary material

Murphy et al. supplementary material 1

Download Murphy et al. supplementary material(File)
File 355.9 KB