Children’s Health – Suspected seizure
Guidance and Resources – Suspected seizure
Case Introduction – Suspected seizure
Further Case Information – Suspected seizure
Background Science – Suspected seizure
Case Conclusion – Suspected seizure
Formative Assessment – Suspected seizure
Luke is a 2 year old with developmental delay, presenting to A&E with an unresponsive shaking episode.
Guidance and Resources – Suspected seizure
In case Children’s Health – Suspected seizure
Guidance
This case initiates the theme of recognizing and managing a child with altered consciousness and with a suspected seizure. As you work through the case, you need to learn:
· Patient with altered consciousness
· How to evaluate of a patient with altered consciousness
· What is the difference in a children’s Glasgow Coma Score
· Seizure and epilepsy
· To give a definition for a seizure and epilepsy and how to diagnose epilepsy.
· How to take a relevant history for a child with a seizure.
· To interpret relevant examination and investigative results to consider the differential causes for a young child with a seizure
· Treatment of epilepsy.
· Developmental delay
· How to take a history relevant to a child with developmental delay
· To provide a differential diagnosis for gross motor delay in children
· To give a definition for cerebral palsy and list possible etiological causes.
eBooks
Illustrated Textbook of Paediatrics 4th edition. Lissauer (Mosby Elsevier)
Textbooks
Advanced Paediatric Life Support: the practical approach to emergencies. Martin Samuels & Susan Wieteska (Chapters 8 & 9)
Nelson Essentials of Pediatrics:, Karen Marcdante MD, Robert M. Kliegman MD
Web Links
Fits, faints and funny turns in children – Australian Family Physician Vol. 34, No. 12, December 2005
Epilepsies: diagnosis and management – Clinical guideline [CG137]
The management of children and young people with an acute decrease in conscious level – RCPCH
Status Epilepticus – APLS
International League Against Epilepsy
British Paediatric Neurology Association
CASE COMPONENT
Case Introduction – Suspected seizure
Luke is a 2 year old who was generally well the day of attendance to A&E. He has a viral upper respiratory illness and was sat waiting for his breakfast when mum noticed he looked odd, turning his head to one side and suddenly became stiff, jerking his limbs and turning blue. Mum panicked and called 999. The paramedics found Luke to be in a convulsive seizure and gave rectal diazepam, which stopped the seizure. Temperature recorded by the paramedics was 37.3C. His BM was 6. Luke was taken to the local A&E by ambulance.
Example algorithm from Australian APLS is similar to the UK:
· Status Epilepticus – APLS
You are the Foundation Year Doctor who is asked to assess Luke in A&E. Luke is unconscious.
What is your approach to this case in A&E?
You have asked to get help! You have adopted an ‘ABCDE’ approach and have checked that Luke is not in a seizure.
What are you assessing for in each letter of the ABCDE approach?
Here is what was found for Luke:
A - Airways maintained
B - Breathing spontaneous, snoring/stertor slow but good air entry bilaterally, Respiratory Rate 23, Satn 99% in air
C - Circulation Pink colour, warm peripheries, CRT<2seconds, pulse normal volume and character, rate 96, BP88/55
D - ‘Don’t forget glucose’ Spot Glucose 7.0 and Disability (AVPU, GCS 8, posture normal but floppy, Pupils equal & reactive, fundoscopy- limited view but optic discs visualised, no nuchal rigidity)
Luke is unconscious. How do you score a child’s Glasgow Coma Scale compared to an adult?
Eye opening, verbal, motor
Further information:
What are the possible conditions with Luke?
· Febrile seizure - Unlikely as temperature at time of seizure by paramedics was under 38C .
· Encephalopathy - Yes, possibly- altered consciousness/awareness that last persists/fluctuates
· Encephalitis/meningitis - Possible, but no fever so if he wakes up himself fully, this condition is unlikely
· Post-ictal - Yes, ONLY if Luke wakes up, returns to himself (usually within an hour of a seizure)
· Sepsis/shock - Less likely, as ‘Circulation’ parameters were all intact and lack of illness prodrome
· Brain tumour - Fairly unlikely, as this is acute, providing Luke wakes fully without focal neurology
· Epilepsy - Possible if Luke had multiple separate afebrile seizures
· Metabolic disorder - The younger the unconscious child, the higher the possibility of a metabolic cause for being persistently unconscious/encephalopathic or intractable seizures. Family history of infant deaths.
· Poisoning/intoxication - Similarly, should be actively ruled out in any patient, if persistent encephalopathic
Other conditions to consider in an unconscious child include: Trauma/ head injury, hypertension, hydrocephalus
Please take time to read this National guideline developed in Nottingham on managing an unconscious child (2008):
· The Management of a Child (aged 0-18 years) with a Decreased Conscious Level – The Paediatric Accident and Emergency Research Group
RCPCH national guideline on the management of children and young people with an acute decreased conscious level (2015) is an indepth review of the original guideline:
· The management of children and young people with an acute decrease in conscious level – RCPCH
History from a reliable witness is the key to diagnosis of a child with seizure (and altered consciousness).
What do you ask in parents regarding the suspected seizure? Group your responses using the headings below.
Hre are the questions to ask for a child with seizure:
Further Case Information – Suspected seizure
In case Children’s Health – Suspected seizure
Here is what you found out about Luke that you presented to Dr James ST4:
He was well recently and was himself. He has a viral cold but no fever. There was no history of head injury, ingestion, vomiting or choking. He was sat on a baby high chair waiting his breakfast when his mum witnessed Luke suddenly looking up and towards his left side. His body stiffened asymmetrically with extension of his left arm and legs before his whole body and 4 limbs jerked rhythmically. During this event Luke’s face twitched with the body. He had blue lips and abnormal gurgling breathing efforts. His eyes rolled upwards and he was not responsive. The Jerking continued for 7 minutes but stopped gradually after 2minutes of receiving rectal diazepam by the paramedics. Luke then fell into a deep sleep-like state afterwards and did not flinch when a finger prick sugar test was carried out. He remained is this state until he woke up during the consultation in A&E. He was upset and disorientated initially but within 15 minutes was back to himself fully. He did not have urinary incontinence and has no injuries.
Relevant Background history
Luke was born by emergency caesarean section at 37+2 for foetal distress.
Luke had a left focal febrile seizure 12 months ago. It was with a definite febrile respiratory illness. Lasting 10 minutes, it stopped before paramedics arrived.
What is the definition of a febrile seizure and what is the difference between a simple and a complex febrile seizure?
Read this short but comprehensive review article:
· Recommendations for the management of “febrile seizures” Ad hoc Task Force of LICE Guidelines Commission - Capovilla et al (2009)
Do you think neuroimaging is indicated for Luke with an afebrile seizure? Please justify your reason.
Indications for urgent head CT or MRI:
· Encephalopathic or coma
· Suspected raised intracranial pressure
· Progressive neurological deficit
Indications for elective head MRI:
· In a child under 2 year of age at onset
· hard focal neurological signs
· a focal epilepsy
· associated significant learning difficulties
· an epilepsy resistant to full doses of 2 appropriate drugs
Do you think an EEG is indicated for Luke with an afebrile seizure? Please justify your reason.
Please read the NICE Guidelines:
Investigations: Epilepsies: diagnosis and management - Clinical guideline [CG137]
EEG is fraught with danger. It can show epileptic activity in normal population but can be normal in a large number of children with epilepsy. The principle of EEG requesting is summarised as follows:
Urgent Indications:
· suspected non-convulsive status
· Non traumatic encephalopathy
· Coma of unknown cause
Elective standard EEG if:
· strong suspicion of epilepsy (to support classification)
· developmental or language regression
NOT generally after a first afebrile seizure or febrile seizures
What is a seizure? What is epilepsy?
An epileptic seizure is a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.
Regarding Luke’s seizure and drowsy state, he recovered fully an hour after the seizure and was observed overnight. His observations overnight were stable. He woke up himself and had breakfast. The parents were visibly upset about the events they witnessed.
What aspects of Luke’s seizure do you think the parents would need to be counselled on?
1. Counselling on recurrence risk of fever related seizures and risk of epilepsy.
2. Parents need first aid training and what not to do in a convulsive seizure (especially not to put something into the child’s mouth or do chest compressions)
3. They maybe considered for training to administer rescue medication, buccal midazolam for example, at 5 minutes.
4. They need to be aware of when to call an ambulance (e.g. after 5 minutes of a convulsive seizure, or if rescue medication was ineffective after 5 minutes)
5. Follow up arrangements, by either their Consultant, or a referral to an epilepsy specialist
Regarding Luke’s background, you took a detailed developmental history and found that Luke started to sit unsupported by 9 months, got up to standing at 20 months, walking independently at 22 months. He cannot climb stairs. He had early right hand dominance at 6 months. He talked since his first birthday and speaks in sentences. He uses a fork and spoon to self-feed and is dry in the days. He can scribble circles. He knows some body parts and can help to get undressed.
What do you think of his development?
Children who show an early hand preference before 12 months have a higher risk of hemiplegia of the non-dominant side. Luke shows gross motor delay in his milestones.
Please read this RCPCH summary of developmental assessment:
List the possible causes of delayed walking.
Central causes: delayed maturation (constitutional); global developmental causes (e.g. genetic/chromosomal disorders with often hypotonia or dysmorphism); all causes of hemiplegia often with hypertonia including cerebral palsy
Peripheral: spinabifida
Muscular and neuromuscular diseases: such as Duchenne Muscular dystrophy
Enviromental: bottom shufflers, institutionalised (chronically ill, prematurity, gross pycho-social deprivation)
Orthopaedic: developmental dysplasia of the hip
Metabolic/hormonal: Hypothyroidism, rickets, mucopolysaccharidosis
You examined Luke as he is fully awake and recovered from his seizure. You found that he has more brisk tendon reflexes to his left knee and ankle. He has up going plantar reflex with some ankle clonus of the left foot. He had similar antigravity movements of his legs and gait.
What could be the possible causes of this?
Regarding Luke’s background, you took a detailed developmental history and found that Luke started to sit unsupported by 9 months, got up to standing at 20 months, walking independently at 22 months. He cannot climb stairs. He had early right hand dominance at 6 months. He talked since his first birthday and speaks in sentences. He uses a fork and spoon to self-feed and is dry in the days. He can scribble circles. He knows some body parts and can help to get undressed.
What do you think of his development?
Children who show an early hand preference before 12 months have a higher risk of hemiplegia of the non-dominant side. Luke shows gross motor delay in his milestones.
Please read this RCPCH summary of developmental assessment:
· Developmental assessment in children - Dr Vanessa Rippon
List the possible causes of delayed walking.
Central causes: delayed maturation (constitutional); global developmental causes (e.g. genetic/chromosomal disorders with often hypotonia or dysmorphism); all causes of hemiplegia often with hypertonia including cerebral palsy
Peripheral: spinabifida
Muscular and neuromuscular diseases: such as Duchenne Muscular dystrophy
Enviromental: bottom shufflers, institutionalised (chronically ill, prematurity, gross pycho-social deprivation)
Orthopaedic: developmental dysplasia of the hip
Metabolic/hormonal: Hypothyroidism, rickets, mucopolysaccharidosis
You examined Luke as he is fully awake and recovered from his seizure. You found that he has more brisk tendon reflexes to his left knee and ankle. He has up going plantar reflex with some ankle clonus of the left foot. He had similar antigravity movements of his legs and gait.
What could be the possible causes of this?
· Stroke
· Intraventricular haemorrhage (IVH)
· Venous sinus thrombosis
· Complicated migraine syndrome
· Head Trauma: brain contusion, subdural hematoma or epidural hematoma
· Sturge-Weber Syndrome
· Todd’s Paralysis
· Brain tumor (Primary or metastatic disease)
· Infection: brain abscess, encephalitis, subdural empyema or meningitis
· Vasculitis
· Demyelinating disease
· Hereditary disease: leukodystrophies
· Congenital or perinatal injury
· Arteriovenous malformations
· Other congenital malformations
Luke has left sided upper motor neurone lesion signs. This might correspond to his afebrile seizure, which had some possible left sided focal features. This would also match his previous left sided febrile seizure. You query if there is structural brain abnormality as an underlying cause for this. You have discussed with Dr James your findings and this information was shared the next day at the Consultant ward round. The Consultant, Dr Ward, found the same neurology signs. Luke seemed to have very mild left sided out swinging of his leg and toe strike when he ran. This is therefore not just a post-seizural phenomenon. This focal neurology is likely longstanding. The diagnosis is likely cerebral palsy.
What neuroimaging would you ask for and why?
CT brain scans have a very high radiation dosage and should be avoided for elective imaging, unless an MRI is not available. An elective brain MRI scan is also preferred as it would detect subtle changes a CT might miss. As a two year old will not lie still for neuroimaging and an MRI brain scan takes longer than a CT scan, then it needs to be done under sedation or even sometimes under general anaesthetic.
CT MRI
very high radiation dosage and should be avoided
for elective imaging, unless an MRI is not available
takes longer than a CT scan, then it needs to be done under sedation or even sometimes under general anaesthetic.
An elective brain MRI scan is also preferred as it would detect subtle changes a CT might miss
Background Science – Suspected seizure
In case Children’s Health – Suspected seizure
What is cerebral palsy?
Cerebral palsy is the name for a group of lifelong conditions that affect movement and co-ordination, caused by a problem with the brain that occurs before, during or soon after birth.
Further information:
Here is some useful background on the pathophysiology of seizures:
CASE COMPONENT
Case Conclusion – Suspected seizure
In case Children’s Health – Suspected seizure
Luke had an MRI brain scan 2 weeks later:
The report was shared with the family in the clinic. It showed right encephalomalacia with evidence of an old cerebral infarction to the distribution of the right middle cerebral artery with right sided cerebral atrophy and ventriculomegaly present. The family was counselled on the diagnosis that Luke has mild cerebral palsy due to this brain injury that had occurred, most likely in-utero. Often a stroke before birth, does not reccur and further investigation will very unlikely yield a causation.
The family were further counselled that:
Luke’s mild weakness should not worsen.
A referral to community paediatric team to further assess and manage Luke is required.
A referral to the physiotherapist was also made.
They were also counselled regarding epilepsy risk, which is a significantly higher with these MRI changes and given Luke’s focal febrile and then afebrile seizure.
Equipped with the prognosis, the family choose to ‘wait and see’ and this is supported by their Consultant. A plan of ‘what if’ Luke had another afrebile seizure was made. An EEG was not requested at this stage. Their Consultant arranged for a second opinion regarding the neuroimaging and clinical situation with a local pediatric neurologist and follow-up.
Formative Assessment – Suspected seizure
Choose the most generally acceptable regime of rescue medication for prolonged seizures, 10 minutes apart:
· PR diazepam, IV lorazepam, IV lorazepam, IV phenytoin
· Buccal midazolam, IV lorazepam, IV phenytoin
· PR diazepam, IV lorazepam, PR paraldehyde, IV phenytoin
· IV lorazepam, IV lorazepam, IV phenobarbital, IV phenytoin
· Buccal midazolam, PR paraldehyde, IV lorazepam, IV phenytoin
Buccal midazolam, IV lorazepam, IV phenytoin
.Correct answer.
Never give three lots of benzodiazepines as it has a high risk of respiratory depression. Phenytoin follows benzodiazepines except in infants.
Which of the following would be regarded as a complex febrile seizure (FS)?
· Focal FS lasting 5 minutes
· Generalised seizure lasting 2 minutes
· Generalised seizure 10 minutes long, recur within 24 hours
· Generalised seizure lasting over 20 minutes
· Generalised Seizure, lasting 10 minutes
· Focal FS lasting 5 minutes
.Correct answer.
· Generalised seizure lasting 2 minutes
· Generalised seizure 10 minutes long, recur within 24 hours
.Correct answer.
· Generalised seizure lasting over 20 minutes
.Correct answer.
The diagnosis of epilepsy should be based on:
· History from patient and a reliable witness
· History from a reliable witness and EEG
· EEG alone
· EEG and an abnormal brain MRI
· The presence of tongue-biting during seizure.
· History from patient and a reliable witness
Epilepsy is a clinical diagnosis from history (and videos). EEG may be requested to classify the epilepsy. This classification can guide prognosis and treatment. It is possible to have a normal resting EEG and still have epilepsy (we sometimes do sleep EEGs and 24 hour EEGS).
What is cerebral palsy?
· Acquired evolving brain condition occurring pre or post birth with motor and sensory dysfunction, with neuroimaging changes
· Static brain injury pre or shortly post birth, causing a motor and coordination dysfunction, usually with neuroimaging changes
.Correct answer.
· Static brain injury pre or shortly post birth causing a motor and balance dysfunction, without neuroimaging changes
· Acquired evolving brain condition at birth, affecting motor and sensory function, usually without neuroimaging changes
· None of the above
Static brain injury pre or shortly post birth, causing a motor and coordination dysfunction, usually with neuroimaging changes
An 8 year old previously fit & well child is brought to A&E with reduced consciousness. He is saying occasional words which do not make sense and does not answer any questions or obey commands. When his mother squeezes his hand he withdraws his arm and opens his eyes.
What is his GCS?
· 12
· 11
· 10
· 9
· 8
9
.Correct answer.