Neurological Problems Flashcards

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1
Q

What are the different types of neurological problems

A
  • Epilepsy
  • Migraines and headaches
  • Multiple sclerosis
  • Myasthenia Gravis
  • Myotonic dystrophy
  • Idiopathic intracranial hypertension (idiopathic)
  • Stroke
  • Bell’s palsy
  • Subarachnoid haemorrhage
  • Cerebral vein thrombosis
  • Posterior reversible encephalopathy syndrome
  • Entrapment neuropathies
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2
Q

What is epilepsy?

A
  • seizure (neurons synchronously active) disorder
  • A neurological condition characterised by recurrent seizures
  • Seizure are due to brief distributions in the electrical functions of the brain
  • Caused by abnormal electrical discharge of cortical neurones (nerve cells)
  • During a seizure clusters of neurons in the brain become temporarily impaired and starts to suddenly send excitatory signals over and over- paroxysmal.
  • This occurs due to either too much excitation or too little inhibition.
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3
Q

Why do epileptic fits happen?

A
  • Idiopathic
  • Physical causes: head injury, cerebral tumours, stroke, hypertension, infection
  • Metabolic causes: hyperglycaemia, hypoxia, uraemia, fluid and electrolyte imbalance, hyper or hyponatraemia
    o Metabolic anomalies: Alteration in cell membrane properties due to abnormal blood concentrations on various ions/electrolytes
  • Syndromes: Antiphospholipid, Alzheimer’s, Wernicke-Karsakoff (thiamine B1 deficiency), Wilson’s disease
  • Congenital defects: cerebral palsy, intracranial cysts
  • Infection
  • Postdural puncture
  • Gestational epilepsy (idiopathic)
  • Pseydoepilepsy/ non-epileptic seizure disorder
  • Eclampsia
  • Cerebral Vein thrombosis
  • Thrombotic Thrombocytopenic purpura (TTP)
  • Stroke
  • Subarachnoid haemorrhage
  • Drugs and alcohol (withdrawal)
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4
Q

What are the different types of fits?

A

Partial fits

  • Simple partial
  • Complex partial
  • Secondary generalised

Generalised seizures: whole brain

  • Absence
  • Myoclonic
  • Tonic
  • Atonic
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5
Q

What are the partial fits?

A

commonly affects temporal lobe
o Simple partial: remain conscious, experience and aura, change in the way things look, smell, taste or sound, pins and needles in the arm, déjà vu.
o Complex partial: change in awareness, loses memory of the event, rubbing of hands, smacking of lips: chewing, fiddling with objects.
o Secondary generalised: partial seizures begin in one part of the brain and spread to the whole brain and tonic clonic seizures occur.

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6
Q

What are the generalised seizures?

A

o Absence: staring and blinking, daydreaming, mainly affects children and lose awareness for 5-20 seconds
o Myoclonic: brief muscle jerking or one or both arms and legs. Last a fraction of a second and remains conscious.
o Tonic: all muscles of the body contract causing falling but with convulsions. Lasts <20 seconds
o Tonic clonic: most common seizures with two stages: whole body convulse/twitch. Lasts 1-2 minutes with possible incontinence
o Atonic: all muscle tone lost very briefly; fall limpy to the ground. Head injury likely to occur. No confusion likely to get up after

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7
Q

What are the precipitating factors for seizures?

A
  • Sleep deprivation/physical exhaustion
  • Emotional stress
  • Increased body temperature
  • Environmental factors: flashing lights
  • Menstruation
  • Metabolic disturbances
  • Excessive alcohol/drug misuse
  • Certain medication
  • Non-compliance with drug therapy
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8
Q

What are the key investigations?

A
  • Clear history & eyewitness accounts of seizures (Most already with
  • known history of epilepsy)
  • Blood pressure measurement +obs, urinalysis
  • Blood tests
    o Haematology (FBC, platelets, coagulation screen, blood fil, thrombophilia screen)
    o Biochemistry (U&Es, urate, glucose, serum calcium and sodium, LFTs)
    o Toxicology screening
  • Computerised tomography scan (CT scan)
    o Look for evidence of cerebral structural damage
  • Magnetic resonance imaging (MRI)
    o More detailed view of brain structural changes
  • Electroencephalogram (EEG)
    o Classifies seizure type by identifying origin of abnormal electrical discharge
    o Gives you the diagnosis- tells you where the seizure is
  • Telemetry
    o Uses video & EEG in order to observe & identify seizure type
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9
Q

What are the managements of epilepsy?

A
  • Aims to identify cause of seizures & prevent recurrence (if possible)
  • Usually requires anti-epileptic drugs (AED) which may be lifelong; complete control gained in 70%+ of cases
  • Majority treated with monotherapy; 5-10% require polytherapy; a few will require surgery
  • Aim of therapy is to use lowest possible dose of AEDs in order to control seizures, as all drugs have side effects
  • Dosage needs to be adjusted during weight gain (pregnancy) and weight loss (illness)
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10
Q

What do you do when someone is having an epileptic fit?

A
  • A –Assess the situation – are they in danger of injuring themselves? Remove any nearby objects that could cause injury
  • C -Cushion their head (with a jumper, for example) to protect them from head injury
  • T – Time, Check the time – if the seizure lasts longer than five minutes you should call an ambulance
  • I – Identity, Look for a medical bracelet or ID card – it may give you information about the person’s seizures and what to do
  • O –Over, Once the seizure is over, put them on their side (in the recovery position). Stay with them and reassure them as they come round
  • N – Never restrain the person, put something in their mouth or try to give them food or drink
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11
Q

What are anti-epileptic drugs?

A
  • These are anticonvulsant drugs
  • Usually they act by suppressing the hyperexcitability of neurons in the cerebral cortex
  • Some act by enhancing the activity of the inhibitory neurotransmitter, GABA (gamma aminobutyric acid)
  • Common side-effects of AEDs (dose-related)
  • Drowsiness, irritability, vertigo, double vision, poor memory, loss of concentration, weight gain/loss
  • Most people with epilepsy (70-85%) can control recurrent seizures adequately with these drugs
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12
Q

Enzyme-inducing dugs

A
  • Drugs that cause the liver to increase its production of certain enzymes
    o Can result in increased rate of breakdown of drugs
    o Can reduce effectiveness of oral contraceptive pill
    Examples:
  • Carbamazepine (“Tegretol”)
  • Phenytoin (“Epanutin”)
  • Topiramate (“Topamax”)
  • Primidone (“Mysoline”)
  • Oxcarbazepine (“Trileptal”)
  • Phenobarbitone
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13
Q

Non-enzyme inducing drugs

A
- These drugs do not have the same effect on liver enzymes and are not thought to interfere with effectiveness of oral contraceptive pill
Examples:
- Sodium valproate (“Epilim”)
- Gabapentin (“Neurontin”)
- Clonazepam (“Rivotril”)
- Vigabatrin (“Sabril”)
- Zonisamide (“Zonegran”)
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14
Q

What are the complications of epilepsy?

A
  • Status epilepticus – repeated seizures without any recovery of consciousness
  • Trauma – occurring at the time of the convulsion i.e. tongue biting, head trauma, hot water burns
  • Cardio-respiratory failure – arising from status epilepticus where treatment was delayed
  • Sudden Adult Death – Phenomenon whereby patient dies suddenly and no toxicological or anatomic cause of death is apparent
    o Sudden unexpected death in epilepsy (SUDEP)
    o High seizure frequency
    o Polytherapy to control condition (> 3 drugs)
    o Early-onset epilepsy
    o Poor compliance/concordance with medication regime
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15
Q

What is the pre-conception issues and care?

A
  • All women should be offered preconception counselling
  • Pregnancy deferred until seizure control is optimal
  • Current medication should be reviewed and changed if necessary
  • AEDs: Increased risk of folate deficiency and therefore neural tube defects= 5mg folic acid before and up to 12/40
  • Women who have been seizure free for a minimum of 5yrs may consider withdrawing AEDs
  • AEDs should be used at the lowest number and dose of drugs possible as polytherapy = ↑Major Congenital Malformations
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16
Q

What are the effects of pregnancy on epilepsy?

A
  • Usually, no effect on frequency of seizures
  • If seizure free for many years → unlikely in pregnancy if good meds compliance
  • Poorly controlled epilepsy → higher risk of deterioration
  • If seizures of multiple types ↑ increase of frequency
  • ↑ risk postpartum (3.5 % intrapartum)
17
Q

What are the possible reasons for perinatal deterioration?

A
  • Hormonal changes of pregnancy
  • Decreased plasma drug levels (pharmacokinetics and pharmacodynamics altered in pregnancy)
  • Lack of sleep (end of pregnancy, during labour, postpartum)
  • Lack of absorption of AEDs from the GI tract during labour
  • Hyperventilation and stress
  • Poor compliance with AED
  • Change to less effective drugs because of the perceived lower risk of teratogenicity
  • Decreased drug levels related to nausea and vomiting
  • Pharmacokinetic changes with decreased plasma antiepileptic drug levels, particularly lamotrigine
  • ↓ gastrointestinal absorption and ↑hepatic and renal clearance resulting in insufficient drug levels
18
Q

Effects on epilepsy on pregnancy

A
  • Short episodes of hypoxia appear to be tolerable by the fetus (possible bradycardia, but no long-term effects)
  • No increased risk of miscarriage or obstetric complications (unless trauma)
  • Status epilepticus is rare, but dangerous for both mother and baby (1-2.5% of all pregnancies of WWE)
  • ↑ of child to develop epilepsy, too
    If another sibling is affected, the risk is 10%
    o If both parents epileptic, the risk is 15-20%
    o If mother with idiopathic epilepsy with early onset (less than 10y old), ↑ of child to develop epilepsy
  • ↑ of congenital anomalies due to meds
19
Q

Teratogenicity

A
  • All cross the placenta and teratogenic
  • Carbamazepine (2.2%), phenobarbitone, phenytoin (3.7%), sodium valproate (6.2% risk)
  • The effects of newer anticonvulsants are not known as fully as for other medications - vigabatrin, gabapentin, lamotrigine (3% risk)
  • Dose dependant teratogenic effects for SV and Lamotrigine
  • Higher risk with polytherapy
20
Q

Complications in pregnancy

A
  • Aetiology unclear - ?genetics, ? Seizures, ? AEDs
  • Fetal abnormalities
  • Spontaneous abortion
  • Stillbirth
  • Placental defects
  • Placental abruption
  • Pre-term labour
  • Hypertensive disorders
  • Haemorrhage
21
Q

What is the role as a MW

A
  • Detailed history taking with emphasis on current drug therapy
  • Referral to specialist care- consultant led
  • Ongoing support
  • Advice on safe self care and safe baby care
  • Liaison with multidisciplinary team
  • Foster positive partnership
  • Be informed (CPD) and use evidence based approach
22
Q

Antenatal care

A
  • 5mg folic acid up to 12/40 if not already
  • Women taking sodium valporate should continue with 5mg FA for the remainder of the pregnancy
  • Serum screening with AFP for neural tube defects
  • Detailed USS at 18-22 weeks to screen for anomalies
  • Women taking AEDs should receive 10mg Vit K PO from 36/40 or 4 weeks before delivery
  • Adviced not to have a bath alone
  • Encourage to register with UK Epilepsy and Pregnancy Register
  • MDT care – obstetrician, neurologist, midwife
  • Advise against hot baths and steamy environments
  • Ascertain expectations and educate re potentially dangerous plans i.e. water births
23
Q

Intrapartum care

A
  • Risk of seizures increase around the time of delivery
  • Increased stress, lack of sleep, over breathing, pain, dehydration
  • 2-3% will have a grand mal seizure
  • Prolonged or repeated seizures = fetal hypoxia
  • Pethidine is metabolised to norpethidine and may induce a seizure therefore its use should be avoided in labour
  • Epidural (early)
  • One to one care should be provided, do not leave alone in a single room
  • Most women with epilepsy have normal vaginal deliveries and CS is only required if there are recurrent generalized seizures in late pregnancy or labour.
24
Q

What is the management of status epilepticus?

A
  • Senior obstetric and anaesthetic staff to be present
  • Maintain airway – recovery position, do not restrain
  • Ensure safe environment
  • Oxygen therapy – 6-10L/min via face mask
  • Initial Rx magnesium sulphate (just in case eclampsia)
  • Prolonged seizures – lorazepam 4mg (less sedative and longer acting than diazepam)
  • Seek advise from neurologist if not effective
  • Consider IV phenytoin with continuous EEG monitoring
  • If not successful paralyse and sedate woman, ventilate mechanically
  • Consider delivery of fetus at this point
  • If CTG undertaken will initially be bradycardic, reduced baseline variability and decelerations for up to 30mins post seizure
25
Q

Postnatal care

A
  • During the 1st 24hrs 1-2% chance of grand mal seizures
  • Physiological changes of pregnancy reversed = ↑AED levels
  • AEDs interfere with Vit K metabolism in the neonate = possible haemorrhagic disease = 1mg Vit K IM at delivery
  • Encourage BF: AEDs are secreted but less than therapeutic level for neonates and less that that received in utero
  • Sedation, poor feeding, hypotonia and respiratory distress occasionally seen in neonates with increased AED levels
  • Advise women how to minimise risks when caring for the baby in case of seizure; risk assessment