Title: Phase 2
1 Neurology Part 2
- Phase 2
- Kaveesha Rajapaksa
- Ryad Chebbout
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2Aims
- Pathology, Aetiology, Clinical Symptoms and
Signs, Investigations and Management of - Epilepsy
- Multiple Sclerosis
- Guillain-Barre Syndrome
- Motor Neuron Disease
- Parkinson's Disease
- Dementia
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3Epilepsy
- Definition
- Recurrent tendency to have spontaneous,
intermittent and abnormal electrical activity in
a part of the brain or generalised across the
brain. Leading to seizures.
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4Epilepsy
- Aetiology
- Idopathic (2/3rds)
- Structural (Trauma, SOL, Developmental, Stroke)
- Metabolic (hypoglycaemia, hypocalcemia,
hyponatraemia)
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5Epilepsy
- Partial focal onset (localising features!)
- Generalised no localising features!
- Simple aware
- Complex impaired awareness
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6Epilepsy
- Partial Seizures
- Commonly caused by structural pathology.
- Simple Partial (Jacksonian March)
- Complex Partial classically temporal lobe!
- Partial Secondary Generalisation
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7Epilepsy
- Generalised Seizures
- Commonly idiopathic.
- Absence lt/ 10sec, childhood
- Tonic-Clonic complex, stiff-gtjerk, post-ictal
confusion drowsiness - Myoclonic sudden limb/face/trunk jerk
- Atonic loss of tone-gtfall, no LOC
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8Epilepsy
- Prodrome Aura Ictal Post-Ictal
- Prodrome
- Mood/Behaviour Change
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9Epilepsy
- Aura
- Strange Smell, Flashing Lights, Déjà vu/Jamais vu
- Post-Ictal
- Headache, Confusion, Myalgia, Sore Tongue, Todds
Palsy (hemiplegia), Dysphasia
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10Epilepsy
- Ictal Localising Features
- Temporal Lobe Automatisms (lip
smacking/fiddling), Visceral Aura (abdominal
rising sensation), Dysphasia, Déjà vu/Jamais Vu,
Hallucinations - Frontal Lobe Jacksonian March (tingling/muscle
contractions from fingers to ipsilateral face),
Todds Palsy
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11Epilepsy
- Parietal Lobe Tingling Numbness
- Occipital Visual Phenomena (spots/lines/flashes)
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12Epilepsy
- Investigations
- EEG (classification)
- MRI (structural lesions)
- MEG/PET/SPECT ictal (localise epileptogenic focus
for surgery)
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13Epilepsy
- Management
- Partial Carbamazepine
- Generalised Sodium Valproate OR Lamotrigine
- Neurosurgical Resection
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14Epilepsy
- Management
- Counselling employment, insurance, driving (1yr
seizure free) - Contraception and pregnancy
- Epilepsy Nurse Specialist
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15Epilepsy
- Complications
- Sudden Unexpected Death in Epilepsy (SUDEP)
- Status Epilepticus
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16Multiple Sclerosis
- Discrete Plaques of Demyelination in Central
Nervous System - T-cell Mediated
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17Multiple Sclerosis
- Risk Factors Women, Temperate Areas
- 30yrs
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18Multiple Sclerosis
- Demyelination Plaque (commonly periventricular,
cervical spine, brain stem) - Heals Incompletely
- Prolonged Demyelination
- Axonal Loss
- Clinically Progressive Symptoms
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19Multiple Sclerosis
- Clinical Courses
- Benign
- Relapsing Remitting
- Secondary Progressive
- Primary Progressive
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20Multiple Sclerosis
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21Multiple Sclerosis
- Symptoms
- Monosymptomatic!
- Disseminated in Time and Space
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22Multiple Sclerosis
- Optic Neuritis Decreased Visual Acuity, Pain on
Eye Movement, Dyschromatopsia - Sensory Lhermittes Sign, Limb Numbness/Tingling
- Motor Transverse Myelitis, UMN Weakness,
Uhthoffs Phenomenon
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23Multiple Sclerosis
- Other Ataxia, Erectile Dysfunction, Urinary
retention -
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24Multiple Sclerosis
- Investigation
- Dissemination in Time and Space!
- Clinically (attacks clinical lesions, 22, 21,
11) - /- Aid of MRI
- CSF (Oligoclonal Bands)
- Evoked Potentials
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25Multiple Sclerosis
- Management
- Acute Methylprednisolone IV
- Chronic Interferon/Glatiramer, Natalizumab
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26Guillain-Barre Syndrome
- Acute AUI Inflammatory Demyelinating
Polyneuropathy - Triggers Campylobacter jejuni, CMV, Mycoplasma
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27Guillain-Barre Syndrome
- Symptoms
- 4 wk peak!
- Weakness Leg, Trunk, Respiratory. Proximal,
Distal. Symmetrical. - Back/Limb Pain
- Autonomic Features seating, tachycardia,
arrhythmias.
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28Guillain-Barre Syndrome
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29Guillain-Barre Syndrome
- Investigations
- Nerve Conduction Studies slow conduction
- Regular FVC
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30Guillain-Barre Syndrome
- Management
- IV Immunoglobin or Plasma Exchange
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31Motor Neuron Disease
- Selective loss of motor neurons in Motor Cortex
(UMN), Cranial Nerve Nuclei (UMN/LMN) and
Anterior Horn Cells (LMN). - gt40yrs.
- lt/10 Familial. 20 SOD1 mutation.
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32Motor Neuron Disease
- Key Features
- UMN LMN Signs
- No Sensory Loss/Sphincter Disturbance
- No Eye Involvement
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33Motor Neuron Disease
- Clinical Patterns
- Amyotrophic Lateral Sclerosis
- Progressive Bulbar Signs CN IX-XII,
bulbar/pseudobulbar palsy - Progressive Muscular Atrophy no UMN signs
- Primary Lateral Sclerosis mainly UMN
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34Motor Neuron Disease
- Associations
- Fronto-Temporal Dementia (10-35)!
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35Motor Neuron Disease
- Signs
- Stumbling Spastic Gait
- Foot Drop /- Proximal Myopathy
- Weak Grip
- Spasticity/Hypereflexia/Upwards Plantars
Wasting/Fasciculations
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36Motor Neuron Disease
- Investigations
- MRI/LP/Neurophysiology exclude other causes
- Management
- Riluzole prolong life by 3months
- Symptomatic MDT (Ventilation, PEG)
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37Parkinson's Disease
- Decreased Dopaminergic Neurons in Substantia
Nigra (Pars Compacta) - Decreased Striatum Dopamine Levels
- Decreased Basal Ganglia Cortex Communication
- Decreased Movement
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38Parkinson's Disease
- 65yrs. Associated with Lewy Bodies
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39Parkinson's Disease
- Classic Triad
- Tremor resting, pill-rolling
- Rigidity increased tone, cogwheel rigidity,
leadpipe rigidity - Bradykinesia slowness of movement initiation
- Expressionless Face, Monotonous Hypophonic
Speech, Micrographia - Gait Festinant, Reduced Arm Swing
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40Parkinson's Disease
- Other Symptoms
- Anosmia
- Depression
- Sleep disturbances
- Visual Hallucinations (animals,
children)Dementia (late stage)
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41Parkinson's Disease
- Management
- L-Dopa Dopa-Decarboxylase Inhibitor (e.g.
Madopar) - Efficacy reduces with time Increased Dose
- Dyskinesias, Off Freezing, End-of-Dose Reduced
Relapse
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42Parkinson's Disease
- Management
- Dopamine Agonist Ropinirole/Pramipexole
- Apomorphine potent DA agonist, acute
- Anticholinergics tremor
- Deep brain stimulation
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43Dementia
- Syndrome of progressive deficits in 2 or more
higher cognitive domains. (Memory, language,
apraxia, agnosia, visuospatial function,
personality) - Interferes with social functioning.
- Occurs in clear consciousness.
- gt80yrs20, gt100yrs70
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44Dementia
- Types
- Alzheimer's Disease
- Vascular Dementia
- Lewry Body Dementia
- Fronto-Temperal Dementia
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45Alzheimer's Dementia
- Increased Beta-Amyloid Peptide Progressive
Neuronal Damage (hippocampus, amygdala, temporal
neocortex) - Neurofibillary Tangles
- Amyloid Plaques
- Decreased Ach
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46Alzheimer's Dementia
- Risk Factors
- Family History, Downs Syndrome, Homzygosity for
ApoE e4 Allele, DM/HTN/AF - Protective Factors
- Smoking, Oestrogen
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47Alzheimer's Dementia
- Symptoms
- Progressive Global Cognitive Impairment
- Aphasia
- Anosognosia (lack of insight)
- Irritability
- Mood Disturbance Depression, Euphoria
- Behavioural Change Wandering, Aggression
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48Alzheimer's Dementia
- Investigations
- MMSE or Addenbrooks Cognitive Exam
- CT temporal/parietal atrophy, ventricular
enlargement - MRI hippocampus/amygdala/medial temporal lobe
grey matter atrophyCSF phosphorylated tau
protein
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49Alzheimer's Dementia
- Management
- Acetylcholinesterase Inhibitors (Donepezil,
Rivastigmine, Galantamine) help lay down new
memories - Memantine (Antiglutamatergic)
- BP Control
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50Vascular Dementia
- Cumulative effect of many small strokes.
- Vascular RFs Stroke Hx, HTN
- Sudden Onset Stepwise Deterioration
- Emotional/Personality Changes
- Cognitive Defecits
- Depression/Labile Mood
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51Lewy Body Dementia
- Fluctuating Cognitive Impairment
- Visual Hallucinations (animals/children) /-
Parkinsonism - Repeated Falls/Syncope
- CT/MRI relative sparing of medial temporal lobe
- Histology Lewy Bodies in Brainstem/Neocortex
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52Fronto-Temporal Dementia
- Frontal Temporal Atrophy. AD Histology.
- Early, 45-65yrs
- Behavioural/Personality Change
- Disinhibition
- Change in Diet (sweets, overeating)
- Emotional Blunting
- Pick bodies on histology
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53Dementia
- Management
- Care Coordinator
- Capacity
- Develop Routines, Plan Ahead
- Challenging Behaviour Lorazepam, Risperidone
(not Lewy Body!) - Depression - Citalopram
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54- A 65 year old man with walking difficulties
presented to his general practitioner. He
complained of worsening tremor in the right arm
with stiffness, which he said on occasion spread
to his right leg. He said that the tremor was
much worse when he was stressed, or in public.
Examination revealed a man with a resting tremor,
marked cogwheeling rigidity of the right side and
an inability to perform repetitive tasks with the
right arm. His gait was not normal and he had a
reduced arm swing on the right.
55- A 36 year old male patient presents with
increasing unsteadiness which started two days
ago. Two years ago he had blurred vision in his
left eye which improved considerably within a few
weeks, but left him with some minor deficit.
Eight years ago he had a 3 week episode of
numbness in his left arm.