Neurology Flashcards

(39 cards)

1
Q

Define epileptic seizure

A

Sudden synchronous discharge of cerebral neurons causing symptoms or signs that are apparent either to patient or observer.

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2
Q

Classification of seizures

A

General:
- Absence seizures with 3Hz spike-and-wave discharge (petit mal)
- Generalised tonic-clonic seizures (grand mal)
- Myoclonic seizures
- Tonic and Atonic seizures
Partial seizures or Focal seizures (location related epilepsy)
- Simple partial seizures (without impaired awareness e.g. Jacksonian seizures)
- Complex partial seizures (with impaired awareness e.g. temporal lobe seizures)
- Partial seizures with secondary generalisation
Unclassified seizures: any that don’t fit in the above categories.

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3
Q

What is syncope?

A

Transient loss of consciousness due to transient global cerebral hypoperfusion. Rapid onset, short duration and spontaneous complete recovery.

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4
Q

Causes of syncope

A
  1. Neurally mediated: vasovagal, carotid sinus, situational
  2. Orthostatic: drug induced, ANS failure
  3. Cardiac Arrhythmia: Brady(sick sinus) tachy(VT/SVT) Long QT
  4. Structural cardio-pulmonary: aortic stenosis, HOCUM
  5. Non-cardiovascular: psychogenic, metabolic, neurological
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5
Q

Red flag signs for pathological cause of syncope

A

ECG abnormalities
Heart failure or previous MI
TLoC during exercise
Family history of sudden cardiac death

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6
Q

Dangerous ECG signs

A
Long or short QTc
Pre-excited QRS complex
Brugada syndrome: RBBB with ST elevation V1-V3
Abnormal T wave inversion
Negative T waves in right precordial leads, epsilon waves suggest ARVC
Pathological Q waves
Conduction abnormality
Inappropriate persistent bradycardia
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7
Q

What is an epsilon wave on ECG?

A

Small positive deflection ‘blip’ buried in end of QRS
Characteristic of ARVD- arrhythmogenic right ventricular dysplasia. (Seen often with T wave inversion in ; prolonged S wave upstroke (55ms); local QRS widening 110ms; all in V1-V3)

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8
Q

Classification of cardiovascular causes of syncope

A

Vascular
Obstructive
Arrhythmias

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9
Q

Vascular causes of syncope

A

AKA neurally mediated reflex syncope (NMS)
Neurocardiogenic (vasovagal: if no features of other diagnosis and features suggesting uncomplicated faint)
Postural hypotension
Postprandial hypotension
Micturition syncope
Carotid sinus syndrome
Situational syncope

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10
Q

Structural cardiovascular causes of syncope

A
Ventricular arrhythmia 2a to structural disease
- HCM
- DCM
- ARVD (arrhythmogenic right ventricular cardiomyopathy)
- Ischaemic cardiomyopathy
Obstructive
- HOCM (hypertrophic obstructive cardiomyopathy)
- Severe AS (aortic stenosis)
- Atrial myxoma or thrombus
- Pulmonary hypertension/emboli
- defective prosthetic valve
- Pulmonary stenosis
- Tetralogy of Fallot
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11
Q

Arrhythmic causes of syncope

A

Brady:
- sinus arrest, exit block (significant pauses)
- high grade or acute complete AV block e.g. Stoke-Adams attacks
- artificial pacemaker failure
Tachy (rarely due to SVT)
- ventricular: VT and VF

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12
Q

How useful is EEG to investigate seizures

A

Single awake EEG -> 29-56% show changes

Repeat inc sleep EEG -> 59-92% show changes

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13
Q

Types of epilepsy

A

Provoked seizure

Unprovoked seizure: generalised or focal… Etc

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14
Q

Provocation of seizures

A

In those not prone to epilepsy: drug OD, hypoglycaemia

In epileptics: sleep deprivation; stress; alcohol; TV/strobe lighting; menstruation.

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15
Q

Common types of epilepsy in childhood

A

Absence seizures ‘petit mal’
Febrile convulsions
Infantile spasms
Juvenile myoclonic epilepsy

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16
Q

Common causes of epilepsy in neonates and childhood

A

Neonatal:
- hypoxia: perinatal hypoxic ischaemic encephalopathy (HIE)
- vascular insufficiency (or intracranial haemorrhage)
- birth trauma;
- acute infection
- metabolic
- congenital malformation
- genetic
Childhood: (most idiopathic)
- acute infection
- trauma
- febrile convulsion
OR: congenital abnormality; tuberous sclerosis; metabolic storage disorders
Any age: Metabolic; infection; tumour; AVM; Inflammation.

17
Q

Secondary causes of epilepsy in adulthood/elderly

A

Any age: metabolic, infection, tumour, AVM, inflammation.
Adult:
- head injury
- drug and/or alcohol intoxication/withdrawal
Elderly:
- cerebrovascular disease
- degenerative disease e.g. Alzheimer’s, huntington’s

18
Q

Secondary causes of epilepsy in any age

A
  • Metabolic e.g. Hypoglycaemia, hypocalcaemia, hyponatraemia
  • Cerebral infection e.g. Meningitis, encephalitis, abscess
  • cerebral tumour or AVM
  • Inflammation e.g. Vasculitis, SLE, rarely demyelination.
19
Q

Differential diagnoses for epilepsy

A
  • syncope e.g. Vasovagal, micturition, cough
  • cerebrovascular disease e.g. Transient ischaemic attack; critical carotid artery stenosis; vertebrobasilar ischaemia
  • vestibular disorders
  • low cardiac output states
  • metabolic e.g. Hypoglycaemia
  • postural hypotension
  • narcolepsy
  • psychiatric disorders e.g. Conversion hysteria
20
Q

Characteristics of infantile spasms

A
  • brief shock-like spasms, flexion of arms, head and neck, drawing up knees
  • asn with progressive learning difficulties
  • causes: perinatal asphyxia/metabolic disorders/encephalitis/cerebral malformations
21
Q

Prognosis of absence seizures and febrile convulsions

A

Absence seizures: (4-10y, F>M) no post-ictal period; few continue after puberty, 5-10% have adult seizures

Febrile convulsions (

22
Q

Common causes of adolescent seizures

A
Teenage:
- Idiopathic
- Trauma
- drug/EtOH withdrawal
- Arteriovenous malformation
Young adult 18-35
- trauma
- alcoholism
- brain tumour
23
Q

Common causes of seizure in >35

A
  • tumour
  • stroke
  • Metabolic: ureamia; liver failure; electrolyte disturbance; hypoglycaemia
  • alcohol
24
Q

Teenage onset infrequent general seizure and daytime absences

A

=juvenile myoclonic epilepsy

- asn with myoclonus

25
Common Types of epilepsy seen in adults
1. Primary generalised epilepsy (tonic-clonic/grand mal) Prodrome/aura of dizziness/irritable/etc -> LoC ->tonic phase (generalised muscle spasms clonic phase (sharp repetitive muscular jerks in all limbs) ->unconscious for about 30min and Post-ictal for hours Asn with tongue biting/involuntary micturition 2. Temporal lobe epilepsy Typical aura of fear/deja-vu/hallucinations(visual/olfactory/gustatory)/rising sensation in epigastrium Confusion and anxiety (+automatism/organised stereotyped movements e.g. Chew/lip smacking) 3. Jacksonian (focal) epilepsy (parallel to sensory epilepsy) From 1 area of motor cortex= 1 body part-> entire side->whole body Temporary paresis of originally affected limb post-attack (Todd's paresis)
26
Define status epilepticus and management
Recurring or continuous seizures without regaining consciousness between attacks. Medical emergency. - basic life support/resus - seizure control - ID and correct predisposing cause Nursed in HDU/ICU (+restart anticonvulsant meds ASAP if known epilepsy)
27
Drugs used for partial seizures (+/- secondary generalisation)
``` 1st line: Carbamazepine Lamotrigine Oxcarbazepine Sodium valproate 2nd line Clobazam Gabapentin Levetiracetam Pregabalin Topiramate ```
28
Drugs for generalised tonic-clonic epilepsy
``` 1st line Carbamazepine Lamotrigine Sodium valproate 2nd line Clobazam Levetiracetam Phenytoin Topiramate ```
29
Drugs for absence seizure epilepsy
``` 1st line: Ethosuximide Sodium valproate Alternatives: Clonazepam Lamotrigine ```
30
Drugs used for myoclonic epilepsy
1st line: sodium valproate | 2nd line: clonazepam, levetiracetam, Topiramate
31
Drugs used for status epilepticus
- IV lorazepam 4mg (or clonazepam, diazepam). Can repeat dose after 10mins if seizures recur/continue - IV phenytoin 15mg/kg, max: 50mg/min (or fosphenytoin- prodrug). Both need ECG monitoring. OR phenobarbitone 10mg/kg, max 100mg/min, when established status epilepticus - IV thiopentone, bolus then infusion, AND ventilation/NMJ block = if seizures >30-60min. OR midazolam and propofol. EEG monitoring to confirm termination of seizure.
32
Problems of epilepsy in pregnancy
Uncontrolled seizures: risk to mother and foetus Sodium valproate/carbamazepine: screen for neural tube defects and folic acid supplements (preconception and pregnancy) Carbamazepine/phenobarbitone/phenytoin- Vit K before delivery and for newborn (due to enzyme induction- hepatic microsomal enzymes increasing metabolism of oestrogens/progestagens = OC pill ineffective!)
33
Signs of optic neuropathy?
``` Pale disc Loss of visual acuity Loss of red colour vision Central Scotsman Afferent pupillary defect: pupil dilates to light in swinging torch test (Marcus Gunn pupil) ```
34
Signs of background diabetic retinopathy
Microaneurysms and hard exudates
35
What is maculopathy? Differentials? Causes?
Reduction in visual acuity either due to cataracts or maculopathy. Check visual acuity. Commonly due to diabetes (macular oedema
36
Features of pre-proliferative diabetic retinopathy?
Cotton wool spots (infarct of nerve cell layer on retina); venous beeding and looping; intra-retinal microvascular abnormalities
37
Features of proliferative diabetic retinopathy?
New vessels
38
Features of end stage diabetic retinopathy?
Scarring with white bands of scar tissue and retinal traction
39
Management of status?
``` Oh My Lord Fetch the Anaesthetist! Oxygen Midazolam buccal Lorazepam IV Phenytoin Get the anaesthetist for Rapid sequence induction ```