Evidence Based Guidelines Management of Epilepsy in Adults Evidence Based Guidelines recommended for use in The Royal Melbourne Hospital July 2002 Review Date: July 2004 Department of Neurology & Clinical Epidemiology and Health Service Evaluation Unit Supported by funding from the Department of Human Services 1 Table of Contents Introduction......................................................................................................................................................3 Multi-disciplinary Review Group ................................................................................................................3 Other Contributors .......................................................................................................................................3 Document Preparation..................................................................................................................................3 Intent of the guidelines.................................................................................................................................3 Process of Guidelines Development ............................................................................................................4 Levels of Evidence for Evaluating the Clinical Research data....................................................................4 Emergency Department management of First Seizure in adults – 1 Page Flow-Chart ..................................5 Emergency Department management of Status Epilepticus in adults – 1 Page Flow-Chart ..........................6 1. FIRST SEIZURE – click for evidence review.........................................................................................7 1.a Emergency department management of first seizure in adults ............................................................7 Table 1. Recommendations: Emergency Department management of first seizure ..............................7 1.b Decision to start an Antiepileptic Drug................................................................................................8 Table 2: Information to discuss with patient prior to commencing AED...............................................8 Table 3. Recommendations. Decision to start AED following first seizure ..........................................8 Table 4. Choice of antiepileptic drug for seizure type............................................................................9 2. ESTABLISHED EPILEPSY....................................................................................................................9 2.a Ongoing management of patients with Epilepsy .................................................................................9 Table 5: Recommendations: Ongoing management of patients with epilepsy......................................9 2.b Therapeutic dose & haematological monitoring for adverse effects - click for evidence review .......9 Table 6: Recommendations: Therapeutic dose & haematological monitoring for adverse effects ......10 2.c Treatment of refractory epilepsy........................................................................................................10 Table 7: Recommendations: Treatment of refractory epilepsy.............................................................10 3. STATUS EPILEPTICUS - click for evidence review ...........................................................................11 Table 8: Recommendations: Management of Convulsive Status Epilepticus .....................................11 4. VIDEO EEG MONITORING - click for evidence review....................................................................12 Table 9: Recommendation: Indications for Video EEG monitoring ...................................................12 5. SURGERY - click for evidence review .................................................................................................12 Table 10: Recommendations: Surgery for epilepsy.............................................................................12 6. WOMEN WITH EPILEPSY- click for evidence review.......................................................................13 Table 11: Recommendations. Management of women with epilepsy .................................................13 7. DRIVING GUIDELINES ......................................................................................................................14 Table 12. Recommendations: Driving guidelines................................................................................14 Appendix 1: International Classification of Epileptic Seizures (abbreviated)..............................................15 Appendix 2: Guidelines for fitness to drive following an epileptic seizure...................................................16 For non-commercial drivers.......................................................................................................................16 For Commercial licences ...........................................................................................................................16 Appendix 3: Emergency Department Discharge Pack - First Seizure ..........................................................17 Appendix 4: Letter to General Practitioner following a presumed seizure – First Seizure ..........................18 Appendix 5: Emergency Department Discharge Pack – Established Epilepsy ............................................19 Appendix 6: Letter to General Practitioner following a presumed seizure – Established Epilepsy .............20 References ......................................................................................................................................................21 2 Introduction Multi-disciplinary Review Group The guidelines were developed by Christine Kilpatrick, Donald Campbell, and Adrian Lowe. The following multi-disciplinary group reviewed and contributed to the guidelines. A/Prof Christine Kilpatrick Dr Alastair Meyer A/Prof David Russell A/Prof Donald Campbell Mr Andrew Van Slobbe A/Prof David Taylor Dr Cassandra Szoeke Dr Kasha Singh Dr Isabella Taylor Dr Anita Vinton Dr Mark Parsons Dr Mark Hew Dr Helmut Butzkueven Dr Peter Greenberg Dr Karen Honson Dr Ian Fraser Dr Heather Smith Mr Adrian Lowe Deputy Director Acting Director, Emergency Medicine Director Unit Head Nurse Unit Manager Director of Emergency Medicine Research Epilepsy Registrar Stroke Registrar Neurology Registrar Neurology Registrar Neurologist Senior Medical Registrar Neurologist Director of Evidence Based Medicine Neuroscience Pharmacist Director of Physician Training Medical Education Officer Epilepsy Project Officer Department of Neurology Emergency Department Department of General Medicine Clinical Epidemiology Ward 4 South Emergency Department Department of Neurology Department of Neurology Department of Neurology Department of Neurology Department of Neurology Department of General Medicine Department of Neurology Department of General Medicine Department of Pharmacy Department of Nephrology Medical Administration Department of Neurology Other Contributors Internal review of the guidelines was performed by A/Prof Terry O’Brien and Dr Zelko Matkovic, who are both epileptologists and work at The Royal Melbourne Hospital. Dr Raymond Martyres reviewed the guidelines from the perspective of a General Practitioner. Document Preparation This document was prepared by Adrian Lowe, and reviewed by all members of the multi-disciplinary reference group. Intent of the guidelines This document provides current evidence-based guidance about critical decisions in the management of adult patients with epilepsy and a first seizure attending Royal Melbourne Hospital. • • • These guidelines are not a prescriptive standard of medical care. Standards of medical care are determined on the basis of all clinical data available for an individual patient. This is a guide to evidence-based practice. Adherence to these guidelines will not ensure a successful outcome in every case. The guidelines may not include all proper methods of care or exclude other acceptable methods of care aimed at achieving the same results. The ultimate choice about clinical procedures and/or treatments are made by the patient (and/or carer) following recommendations from the treating medical practitioner based on the range of options available. 3 Process of Guidelines Development The development of these guidelines has been based on existing international and national guidelines for 12 3-13 the overall management of epilepsy and specific aspects of epilepsy . Further systematic searching of the literature has been undertaken to supplement the information presented in existing guidelines. Key articles referenced by existing guidelines were retrieved, and search strategies were devised around the Medical Subject Headings (MeSH) and key words that described these core papers. The reference list of each article retrieved was reviewed for articles relevant to the topic under review. These articles were obtained, checked, and summarised if appropriate. If the article was appropriate, but did not appear in the results from the original search strategy, the articles MESH headings were examined to determine why it was not identified previously, and the search strategy modified accordingly to determine if other articles had also been missed for the same reason. As such, a cascade approach was adopted. Individual searches were conducted on various topics (see http://www.mh.org.au/clinicalepidemiology/epreview.pdf) for full details of each search strategy’s results). The search strategy aimed to find the highest level of evidence possible for a particular question. If a high level of evidence was located, then the search ceased. If not, the search continued for lower levels of evidence. To view the evidence review on a particular topic, click on the heading of the topic in this document. This will open the evidence review document used to from this document. Two general search limits were applied to all strategies. Due to time and budget limitations, only articles in English were retrieved. As these guidelines are directed only at treatment of adult patients at Royal Melbourne Hospital, articles that only studied children were excluded, unless no other studies existed. The guidelines were developed through weekly focus group meetings conducted at The Royal Melbourne Hospital between Christine Kilpatrick, Donald Campbell, and Adrian Lowe. Please send any comments or recommendations concerning these guidelines please e-mail Christine.Kilpatrick@mh.org.au . Levels of Evidence for Evaluating the Clinical Research data The National Health and Medical Research Council’s (NH&MRC’s) levels of evidence when evaluating clinic research data have been used. 77el Type of Evidence Level I II III – 1 III – 2 III – 3 IV Type of Evidence. Evidence obtained from a systematic review of all relevant randomised controlled trials Evidence obtained from at least one properly designed randomised controlled trial Evidence obtained from well-designed controlled studies without randomisation Evidence obtained from well-designed cohort or case-control analytic studies preferably from more than one centre or research group Evidence obtained from multiple time series with or without the intervention. Dramatic results in uncontrolled experiments (such as the results of the introduction of penicillin treatment in the 1940s) are examples of this type of evidence Opinions of respected authorities, based on clinical experience, descriptive studies and/or reports of expert committees 4 Emergency Department management of First Seizure in adults – 1 Page Flow-Chart Confirm diagnosis and type of seizure Initial treatment to stop seizure activity if patient in Status or has multiple seizures. See Emergency Department Status Protocol If epileptic seizure not suspected refer if appropriate to General Medical Registrar Evaluate potential causes of Seizure Consider: Infection, provoked seizure (medication, alcohol, drug use or sleep deprivation), metabolic disturbance & non-epileptic seizure CT brain & contrast, ECG, FBE, U&E, LFT in Emergency Department Order outpatient EEG Abnormal test results If appropriate treat underlying cause. (eg CT lesion/tumour) Normal test results AED usually not commenced if single seizure and investigations normal Consider commencement of AED medication If definite Seizure & CT reveals an epileptogenic lesion or history of recent previous seizure Discuss with Neurology registrar Admit or Discharge? Admit if: Multiple Seizures or Status Prolonged post ictal confusion, or focal neurological deficit Investigations reveal underlying condition that requires treatment Discharge if: Patient has normal test results, and has fully recovered. Actions on Discharge Confirm EEG ordered Make appointment for First Seizure Clinic Give safety advice (no driving or operating heavy machinery, swimming alone, heights, or baths) Give patient discharge pack (see appendix 3 & 4) 5 Emergency Department management of Status Epilepticus in adults – 1 Page Flow-Chart 1. Secure airway 2. Commence oxygen 3. Assessment of cardiac and respiratory function 4. IV access 5. Draw blood for FBC, U&E, LFTs, Ca, Glucose, clotting, AED levels and storage for later analysis IMMEDIATE ACTIONS IV Diazepam (0.15mg/kg at 5mg/min). Repeat if status epilepticus continues Establish aetiology. 50ml 50% glucose IV if suggestion of hypoglycaemia; 250mg thiamine IV if suggestion of alcohol abuse or impaired nutritional status IV Phenytoin (18mg/kg at 50mg/min) FOLLOWED BY Resume or commence oral AED when patient is able IF STATUS / SEIZURES CONTINUE Transfer to ICU Call Neurology registrar for all cases of status epilepticus 6 1. FIRST SEIZURE – click for evidence review 1.a Emergency department management of first seizure in adults Seizures and seizure like events may be induced by a myriad of conditions. The role of the Emergency Department assessment of patients presenting with a seizure is to confirm that the patient is in no immediate danger, establish a probable cause for the seizure, and to refer the patient to appropriate followup services. Table 1. Recommendations: Emergency Department management of first seizure 1 3 14-19 Perform physical and neurologic examination, and take medical history that includes: - Provoking factors (sleep deprivation, medication, alcohol or drugs) - Type of seizure - Details of previous seizures Brain CT scan with contrast. This will help determine if there is an underlying cause for the 20-22 23-33 seizure and assist making a differential diagnosis . 20-22 34-39 Perform EEG within 48 hours of seizure if possible. If not, as soon as available MRI brain scan will be ordered through First Seizure clinic, if indicated 1 14 16 18 Consider differential diagnosis. Common conditions that should be considered are 1. Syncope 2. Migraine 3. TIA 4. Psychogenic seizures 5. Metabolic disturbances (eg. Na, Mg) An attempt to determine the seizure type, as per the International Classification of Seizures 1 14 18 40 (See appendix 1), should be made Discuss with Neurology registrar, including need for Anti-epileptic drug (AED) treatment if: - Multiple seizures - History of recent previous seizures - CT brain scan reveals an epileptogenic lesion See table 4 choice of AED drug 14 The decision to admit or discharge the patient should be made on the following grounds Discharge if Admit if - patient fully recovered - Prolonged postictal state - brain CT satisfactory and - Multiple seizures or status epilepticus - laboratory tests satisfactory - Focal signs on examination - Investigations reveal underlying condition that requires treatment If a patient is deemed appropriate for discharge, and an epileptic seizure is suspected, the 14 following actions should be taken: 1. Make appointment for First Seizure Clinic, and an outpatient EEG, or organise follow up as a private patient 2. Give advice that due to the risk of further seizures, patients should a. Not drive any form of motor vehicle (see appendix 2 for guidelines) b. Not swim alone c. Have a shower instead of a bath. Turn on the cold tap first. Lower the temperature on the hot water service. d. Avoid heights e. Avoid dangerous machinery 3. Give patient a copy of the First Seizure Discharge Pack (see appendix 3 & 4). Fill in details of the patient’s follow up appointments If the patient has an established diagnosis of epilepsy, give them the Established Epilepsy Discharge Pack (see appendix 5 & 6). Refer the patient to their GP, or to their specialist or the Epilepsy Clinic at the Royal Melbourne Hospital. Evidence grade IV III-2 III-2 IV IV IV IV IV IV IV 7 1.b Decision to start an Antiepileptic Drug There are a number of antiepileptic medications available. The possibility of commencing medication should be raised with the patient following a seizure. It is ultimately the patient’s decision as to whether or not to start this medication. The following information should be discussed with patients prior to deciding to take AED medication. Table 2: Information to discuss with patient prior to commencing AED 20-22 34-39 41-53 The overall risk of a second seizure over a 3-year period is 40 - 50% The risk of further seizures is highest in the first months following a seizure, and drops 20-22 34-39 41-53 quickly following this period An epileptic discharge on an EEG test increases the risk of recurrence, to approximately 20 21 34-39 80% 20An epileptogenic lesion on CT scan increases the risk of recurrence to approximately 80% Evidence grade III-2 III-2 III-2 III-2 22 39 51-53 AED medication lowers risk of a further seizure to 20 - 25% All AED medication can cause adverse reactions (such as somnolence and rash). If these do 54-69 occur, most effects are reversible simply by discontinuing the medication Very rarely, a patient may have severe or even fatal adverse reaction to AED. This will 70 normally occur in the first 6 months of treatment AEDs can cause reproductive difficulties and possibly have some teratogenic effects in some 6 11 72-74 women, and reduce the effectiveness of oral contraception Staff should consider discussing the risk of Sudden Unexplained Death in Epilepsy (SUDEP) with the patient. SUDEP is a rare event (0.5 to 2 per 1,000 patient years) where a patient 75-78 with epilepsy dies for no known reason. The causes of SUDEP are uncertain Patients should consider the benefit of this reduced risk of seizures, but also the lifestyle and 67 safety issues of taking AED II I Table 3. Recommendations. Decision to start AED following first seizure Evidence grade IV 1 Use of an AED following a single seizure is generally not recommended, if tests are normal III-3 III-3 IV IV 67 If epileptic discharge is detected on EEG, or neuroimaging reveals an epileptogenic lesion, or the patient has had one or more seizures in the recent past, then commencing an AED is 1 67 recommended If the patient elects to begin AED therapy, they should be warned that the AED may have adverse effects, and to seek medical attention for symptoms including rash, bruising or somnolence with vomiting especially if they occur in the first weeks of treatment. If a rash 1 67 develops the drug should be ceased IV IV 8 Table 4. Choice of antiepileptic drug for seizure type 2 Recommendations made by Therapeutic Guidelines Seizure Type Partial Seizures (simple or complex) Tonic-clonic seizures - generalised - secondarily generalised - undetermined if generalised or partial Absence seizures Myoclonic seizures Anti-epileptic drug Carbamazepine Sodium valproate Carbamazepine Carbamazepine, Sodium valproate Ethosuximide (absence only) Sodium valproate (absence and tonic-clonic) Sodium valproate For additional information on the use of AEDs, please refer to the ‘Clinician’s Health Channel’ and (http://www.clinicians.vic.gov.au/eleclib.htm) and click on the Neurology section of the ‘Therapeutic Guidelines’. 2. ESTABLISHED EPILEPSY 2.a Ongoing management of patients with Epilepsy Epilepsy is a chronic condition, with potentially complex management issues. Communication between hospital staff and the patient’s General Practitioner (GP) is essential to maintain a continuum of care for the patient. Unfortunately, patients with epilepsy often report feeling that care for their condition is not being shared properly between hospital staff and their GP. Table 5: Recommendations: Ongoing management of patients with epilepsy Staff from the First Seizure Clinic and Epilepsy Clinic should correspond with the patient’s GP concerning the diagnosis and management of the patient’s epilepsy Patients with epilepsy should be encouraged to visit their GP every 3 months, to review their condition GPs should be encouraged to refer patients with refractory epilepsy, or who require medication regime alterations, to the Epilepsy Clinic Staff should encourage patients to gain a greater understanding of their epilepsy. Patient information on various topics concerning epilepsy has been produced by the Epilepsy Foundation of Victoria, which can be contacted with the following details: Epilepsy Foundation of Victoria’s: http://www.epinet.org.au/, or by calling 1300 852 853 Evidence grade IV IV IV IV 2.b Therapeutic dose & haematological monitoring for adverse effects - click for evidence review All AEDs may cause adverse effects, with the majority being dose related. The effectiveness of AED medication is determined by the free plasma concentration of the active anti-epileptic drug. Routine plasma AED concentration measures total not free drug. This needs to be taken into consideration when interpreting levels. Each AED has a recommended dosage regime, and plasma concentration of the active drug (see http://www.amh.hcn.net.au/). There is no evidence that routine AED level monitoring increases seizure control, when compared to clinical management of dosage level based on seizure frequency and signs of toxicity. However, there are instances where AED level monitoring is appropriate (see table 6). 9 Due to the potential for serious adverse effects, haematological monitoring for liver function and blood cell count has been proposed. There is however, no evidence that such monitoring reduces the risk of such events, due to the enormous sample sizes required to form a definitive answer to this question. Table 6: Recommendations: Therapeutic dose & haematological monitoring for adverse effects 79-87 Routine AED plasma level monitoring should not be undertaken 84 Measurement of plasma AED levels should be taken only for one of the following purposes Evidence grade III-2 IV 88 89 1. Establishing compliance 2. Establishing ‘baseline’ effective concentrations 3. Evaluating potential cause for lack of efficacy 4. Evaluation potential cause for toxicity 5. Evaluating potential cause for loss of efficacy 6. Judging ‘room to move’ or when to change AEDs 7. Patients who are pregnant There is no conclusive evidence to support or refute the use of haematological monitoring 90 91 for serious adverse effects Many however, recommend FBE, U&E and LFT be performed on initiation of AED therapy 92-95 and every 6 months thereafter 2.c III-2 IV Treatment of refractory epilepsy In approximately 30% of patients, the initial AED will not prevent all seizures. The patient has a number of options in this situation. Table 7: Recommendations: Treatment of refractory epilepsy Patients with refractory epilepsy should be referred to the epilepsy clinic If seizures continue following initiation of AED medication at an appropriate dose, the patient should be presented with the following options 54 56-59 64 96 1. If reasonable response to initial AED, add another AED 2. If limited response to initial AED, replace with another AED 2 97 Evidence grade IV I IV 10 3. STATUS EPILEPTICUS - click for evidence review Status epilepticus is defined as epileptic activity lasting longer than 30 minutes. Generalised convulsive status epilepticus is a medical emergency, and is associated with high levels of morbidity and mortality. Frequent recurrence seizures should also be treated in this manner. Table 8: Recommendations: Management of Convulsive Status Epilepticus Immediate measures: Secure airway; commence oxygen; assessment of cardiac and respiratory function; IV access; draw blood for FBC, U&E, LFTs, Ca, Glucose, clotting, 1 15 98 AED levels and storage for later analysis 99 100 IV Diazepam (0.15mg/kg at 5mg/min). Repeat if status epilepticus/seizures continue Establish aetiology. Give 50ml 50% glucose IV if any suggestion of hypoglycaemia; IV 15 98 thiamine 250mg if any suggestion of alcohol abuse or impaired nutritional status 100 Followed by: IV Phenytoin (18mg/kg at 50mg/min). When the patient is able, long term oral AED medication should be initiated as indicated by 2 seizure type 101 If status continues or seizures recur: Transfer the patient to ICU The Neurology registrar should be informed of all cases of status epilepticus Evidence grade IV II IV II IV III - 3 IV 11 4. VIDEO EEG MONITORING - click for evidence review Video EEG monitoring involves the simultaneous recording of a patient’s EEG pattern and a video recording of the patient’s behaviour. Epileptic seizures are defined by abnormal electrical patterns in the brain. An interictal EEG is conducted between seizures, and aims to detect epileptiform activity not associated with a seizure. However, not all patients with epilepsy will have epileptiform EEG activity between seizures. The aim of video-EEG is to record a patient’s EEG activity whilst having a seizure, and correlate this with their behaviour. To do this, patients are recorded for extended periods of time. Due to the time and the intensive nature of Video EEG, indications for its use are limited. Table 9: Recommendation: Indications for Video EEG monitoring 4 7 102-106 Indications for Video-EEG monitoring 1. Diagnosis of non-epileptic attacks Evidence grade IV 2. Classification of seizure types (eg complex partial and atypical absence seizure), particularly where seizures are refractory to AED therapy 3. Localisation of epileptogenic region in preparation for epilepsy surgery 5. SURGERY - click for evidence review Surgery can be performed in some patients to remove the region of the brain responsible for the epileptic activity. However, only a small group of patients are suitable for this form of therapy. Patients with Temporal Lobe Epilepsy caused by hippocampal sclerosis are the most common surgical candidates. Such patients normally undergo a temporal lobectomy. Surgery for epilepsy is invasive, and is associated with some risk of adverse effects. Table 10: Recommendations: Surgery for epilepsy Patients who have intractable epilepsy, despite appropriate use of AEDs, should be referred 14 for surgical evaluation Approximately 63% of patients with temporal lobe epilepsy who undergo surgery will be seizure free at twelve months following the operation, compared to only 8% of patients 107 treated medically 70-80% of patients with well lateralised temporal lobe seizure focus due to hippocampal sclerosis, have an excellent outcome. AED medication should be continued following 108 surgery Approximately 5% of patients will have a major complication associated with surgery for epilepsy (such as infarct, infection, and decline in memory), while approximately 10% will 108 have minor and resolvable complications Evidence grade IV II III - 1 III - 2 12 6. WOMEN WITH EPILEPSY- click for evidence review Women with epilepsy face a number of potential problems, particularly concerning child-bearing. These problems include decreased effectiveness of oral contraception whilst taking AED medications, increased risk of adverse outcomes associated with pregnancy and other health related issues. Table 11: Recommendations. Management of women with epilepsy Contraception. Due to their liver enzyme inducing properties, the following AEDs are associated with decreased effectiveness of oral contraception: carbamazepine, phenytoin, phenobarbitone, primidone, and possibly topiramate. A high dose contraceptive formulations may provide some protection, but women should be warned that there is still an 109-120 increased risk of conception whilst taking these AEDs Referral for women considering pregnancy. Any woman with epilepsy who is considering a pregnancy should be referred to a Neurologist/Epileptologist or a physician with particular knowledge of this topic Pre-pregnancy. To reduce risk of neural tube defects in the foetus, all women of child121-124 bearing age on an AED should take a folate supplement (5mg/day). However, women should also be warned that folate supplementation may be associated with 125 126 an increased incidence of multiple births Risk of seizures during pregnancy. Women should be warned that there maybe an increased risk of seizures during pregnancy, although the majority of patients remain 127-138 stable AED treatment practice during pregnancy. Women with epilepsy should be treated with the lowest effective dose of AED. Where possible, monotherapy should be used. The need for AED medication should be re-evaluated prior to a woman becoming pregnant, to ensure 73 139 the medication is truly needed AED serum monitoring during pregnancy. The pharmacokinetics of AEDs change during pregnancy, resulting in reduced serum levels. Serum AED levels may need to be monitored more closely during pregnancy and post partum. Ideally, the free level of the AED should be 10 72 73 139 140 measured, due to decreased protein binding during pregnancy Risk of foetal malformation. Women on AEDs should be warned that the risk of major malformations in their foetus is twice to three times that of the general population, and is probably between 4-9%. This risk increases with the number of AEDs used, and higher 11 72 73 139 140 doses of AEDs during the pregnancy At birth. Vitamin K supplement should be administered, to reduce the risks of cerebral haemorrhage in the neonate, due to the inhibitory actions of AEDs on vitamin K 141-145 production. Following birth. Close attention should be paid to the mother following delivery. AED 10 72 73 139 levels can rise rapidly, as the pharmacokinetics of the AEDs return to normal state Evidence grade IV IV IV III-2 IV IV III-2 III-2 IV 140 Breast-feeding. All AEDs are excreted in breast milk. The rates of transfer vary between AEDs. If it is decided to breast feed, attention should be paid to ensure that the infant is not sedated by the AEDs. Breast-feeding is contraindicated if the patient is taking 146 147 benzodiazepines or barbiturates Other health issues. AEDs may be associated with dyslipidemia and accelerated 11 osteoporosis IV III-3 13 7. DRIVING GUIDELINES The effect of having an epileptic seizure whilst driving a car, or other vehicle, can be devastating for both the patient and the public. To balance the needs of the individual and the public, and maintain fairness and a uniform approach, guidelines have been produced by Austroads and National Road Transport Commission (NRTC). These should be used to assess a patient’s fitness to drive. The Medical Advisory Board of VicRoads may be contacted to clarify recommendations for specific patients. Table 12. Recommendations: Driving guidelines What to tell the patient: Advice must be given to patients concerning their fitness to drive 12 following a seizure. The guidelines formulated by Austroads (non-commercial licences) & 13 NRTC (commercial licences) should be utilised (see appendix 2) Where to go if the guidelines are unclear: If the Austroads or NRTC guidelines are unclear on their recommendations for a particular patient’s circumstances, or there is some dispute over the recommended seizure free time, the Medical Advisory Board from VicRoads should be contacted (Medical Review, VicRoads Registration and Licensing, PO Box 2504, Kew 3101) Evidence grade IV IV 14 Graphic Appendix 1: International Classification of Epileptic Seizures (abbreviated) I Partial (arising from a focal or local cortical lesion, most commonly the temporal lobe) A Simple partial (no loss of consciousness) B Complex partial (loss of consciousness; may start with loss of awareness or may follow a simple partial seizure; may be with or without automatisms, e.g. lipsmacking, rubbing hands, walking, running with no recollection) C Partial evolving to secondarily generalised seizure with tonic, tonic-clonic or clonic features II Generalised (with bilateral discharges involving subcortical structures -convulsive or nonconvulsive; EEG shows bilateral discharges; consciousness is lost at the onset except in myoclonus; motor features bilateral) A Absence (previously called ‘petit mal’; last seconds; +/- minor automatisms) B Myoclonic (may be simple or multiple jerks, often upper limbs) C, D, E Tonic, Tonic-clonic or Clonic (previously called ‘grand mal’) F Atonic (a form of ‘drop attack’; sudden loss of posture of head, limbs or body) III Unclassified (usually used when an adequate description is not available, e.g. often in seizures from sleep) Adapted from Commission of Classification and Terminology of the International League against Epilepsy. 148 Epilepsia 1981; 22:489-501. 15 Appendix 2: Guidelines for fitness to drive following an epileptic seizure For non-commercial drivers Excerpt from Austroads (2001). Assessing fitness to drive: Guidelines and standards for health 12 professionals in Australia. Austroads: Sydney. pp 27-29 . Also located at http://www.austroads.com.au/austroads/Others/ftd2001(sec).pdf. Please see this document for a discussion of the principles behind these recommendations. The Medical Advisory Board of VicRoads may be contacted to clarify recommendations for specific patients. MEDICAL STANDARDS – EPILEPSY (recommended seizure-free periods) Condition Drivers of cars and light trucks, motorcycle riders Chronic Epilepsy Generally 2 years. A shorter period only on (history of previously uncontrolled recommendation of an experienced consultant where seizures) there is clear evidence of seizure control (eg. following adjustment and stabilisation of anti-epileptic drug treatment) Isolated Seizure 3-6 months. Consultant opinion recommended Recently Diagnosed Epilepsy 3-6 months. Consultant opinion recommended Recurrent Seizure in a Person Previously 3 months from last seizure, if fulfilling all other Seizure Free due to Identifiable criteria as set out in these guidelines. Provocation may Provocation include illness, drug interaction, sleep deprivation Recurrent Seizure on Withdrawal of 1 month after resuming previously effective Medication on Medical Advice medication or 2 years if refusing to resume medication Seizure Causing Accident Minimum of 1 year. Consultant opinion essential Seizures only in Sleep 12 months from the last seizure whilst awake Surgery for Epilepsy 12 months Withdrawal of Anti-Epileptic Drug The full period of withdrawal and at least 3 months Therapy where there is significant risk of thereafter. Consultant opinion is recommended to recurrent seizure determine if there is a significant level of risk or otherwise. For Commercial licences Excerpt from National Road Transport Commission (1994). Medical Guidelines for Commercial Vehicle 13 Drivers . NRTC. Located at http://www.nrtc.gov.au/publications/med-e.asp?lo=public. Please see this document for a discussion of the principles behind these recommendations. Criteria The criteria are NOT met: ∙ if epilepsy is confirmed. A conditional licence may be considered: ∙ if the person has - a past history of febrile convulsions; or - a past history of epilepsy with seizure free period of 5 years whilst not on any anticonvulsant medication; or - had a past single seizure, or cluster of seizures, due to exceptional and nonrepeatable circumstances; or ∙ if the person has epilepsy which is so well controlled as to reduce the risk of a convulsion to that of any member of the general population, noting the inherent features of the individual’s job. 16 Appendix 3: Emergency Department Discharge Pack First Seizure Appointments You have experienced what is suspected to be a seizure. To investigate the cause of this seizure the following appointments have been made for you. First Seizure Clinic appointment: Date: ____________________ Location: Royal Melbourne Hospital, 1st Floor Main Block, Ambulatory Care Centre Contact Number: 9342 7393 EEG appointment Date: Location: Contact Number: ____________________ Royal Melbourne Hospital, 4th Floor, Ward 4 North, Main Block. 9342 7583 Safety information As you have had one seizure, there is a risk you may have another, particularly in the next few months. To avoid injuring yourself, and others, please observe these safety precautions. • Do not drive a motor vehicle or operate dangerous machinery until advised otherwise by a doctor. • Have a shower instead of a bath. Run the cold water first, then the hot. Lower the temperature setting on your hot water service. • Do not go swimming alone. • Avoid heights (eg. walking on roofs). • Please consider and avoid any other activities that could cause serious harm to yourself or others in the event of another seizure. Discuss with your doctor if you are uncertain. • Avoid consuming excess alcohol, sleep deprivation and flashing lights. These may trigger seizures in some people. In the event of another seizure, an observer should • Clear the area around the person so that they do not injure themselves. • Do not place anything in the person’s mouth, or try to restrain them. • If possible, place a pillow or soft item under their head. • When the seizure finishes, place the person into the recovery position, lying them on their side. • Arrange for the patient to return to hospital as soon as possible. If needed call an ambulance on 000, and say “epileptic seizure” If you need further information about seizures or epilepsy If you wish to talk to a doctor at the Royal Melbourne Hospital, please ring the • Royal Melbourne Hospital Switch: 9342-7000 or • Neurology Department: 9342 7722 and ask to speak to the Neurology or Epilepsy registrar Alternatively, you can contact your local General Practitioner (GP). Also, if you would like to talk to someone about your experience, you can contact the Epilepsy Foundation of Victoria. The contact details for the Epilepsy Foundation of Victoria’s are as follows: http://www.epinet.org.au/, or by calling 1300 852 853 17 Appendix 4: Letter to General Practitioner following a presumed seizure – First Seizure Dear Dr _____________________________ Your patient, __________________________(patient name), attended the emergency department at the Royal Melbourne Hospital following a presumed first seizure. Whilst in the emergency department they received a CT brain scan. This scan revealed Insert Details An outpatient EEG appointment has been made for __________________(insert date), and an appointment has been made for the First Seizure Clinic for __________________(insert date). The doctor at the First Seizure Clinic will write to you to inform you of the results of these further investigations. Your patient has been discharged, but due to the risk of further seizures, I have warned him/her of a number of safety issues. Specifically, the patient should not drive or operate heavy machinery, should avoid heights, have a shower instead of a bath, and avoid any other situations where a seizure may cause themselves or others harm. I have prescribed the following medication Medication Indication Dose Plan Royal Melbourne Hospital contact details If you wish to talk to a doctor at the Royal Melbourne Hospital with regards to this patient, please ring the • Royal Melbourne Hospital Switch: 9342-7000 or • Neurology Department: 9342 7722 and ask to speak to the Neurology or Epilepsy registrar (Insert any other comments) Yours sincerely, Insert ED doctor’s name. 18 Appendix 5: Emergency Department Discharge Pack – Established Epilepsy Safety information You have experienced what is suspected to be another epileptic seizure. As you will be aware, you have previously been diagnosed with epilepsy. To avoid injuring yourself, and others, please observe these safety precautions. • • • • • • Do not drive a motor vehicle or operate dangerous machinery until advised otherwise by a doctor. Have a shower instead of a bath. Run the cold water first, then the hot. Lower the temperature setting on your hot water service. Do not go swimming alone. Avoid heights (eg. walking on roofs). Please consider and avoid any other activities that could cause serious harm to yourself or others in the event of another seizure. Discuss with your doctor if you are uncertain. Avoid consuming excess alcohol, sleep deprivation and flashing lights. These may trigger seizures in some people. In the event of another seizure, an observer should • Clear the area around the person so that they do not injure themselves. • Do not place anything in the person’s mouth, or try to restrain them. • If possible, place a pillow or soft item under their head. • When the seizure finishes, place the person into the recovery position, lying them on their side. • If needed, take the patient to hospital, or call an ambulance on 000, and say “epileptic seizure”. If you need further information about seizures or epilepsy If you wish to talk to a doctor at the Royal Melbourne Hospital, please ring the • Royal Melbourne Hospital Switch: 9342-7000 or • Neurology Department: 9342 7722 and ask to speak to the Neurology or Epilepsy registrar Alternatively, you can contact your local General Practitioner (GP). Also, if you would like to talk to someone about your experience, you can contact the Epilepsy Foundation of Victoria. The contact details for the Epilepsy Foundation of Victoria’s are as follows: http://www.epinet.org.au/, or by calling 1300 852 853 19 Appendix 6: Letter to General Practitioner following a presumed seizure – Established Epilepsy Dear Dr _____________________________ Your patient, __________________________(patient name), attended the emergency department at the Royal Melbourne Hospital following a presumed seizure. As you will be aware, this patient has been diagnosed with epilepsy. Your patient has been discharged, but due to the risk of further seizures, I have warned him/her of a number of safety issues. Specifically, the patient should not drive or operate heavy machinery, should avoid heights, have a shower instead of a bath, and avoid any other situations where a seizure may cause themselves or others harm. This patient is on the following medications. Medication Indication Dose Plan Follow up arrangements I have made the following follow up arrangements for this patient. ❐ Referred to General Practitioner or current specialist. ❐ Referred to Royal Melbourne Hospital Epilepsy Clinic. 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