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334 Cards in this Set
- Front
- Back
What is Amaurosis Fugax? |
Temporary occlusion of the RETINAL artery "feels like curtain descending" |
|
3 most common causes of TIA? |
Atherothromboembolism from Carotid
Cardioembolism = Mural thrombus post MI / AF/ Valve Disease/ Prosthetic Valve
Hyperviscosity = Polycythaemia / Sickle Cell / Myeloma |
|
3 most common differential diagnosis for a TIA? |
Hypoglycaemia Migraine Aura Focal seizure |
|
Investigations for a TIA? |
Blood glucose FBC ECG Carotid Doppler + MRI/Angiography |
|
What is the risk of stroke after TIA criteria called? |
ABCD2
Age > 60 Blood pressure (Systolic >140 or Diastolic >90) Clinical Features Duration (10-59 or 60>) Diabetes
Greater than 4 points = referral in 24 hours |
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Management of TIA |
1) Control CV risk factors (BP/Cholesterol/Smoking/DM)
2) Anti-Platelets = Aspirin / Dipyridamole (ONLY FOR TIA/ POST MI)
3) Warfarin = IF cardiac embolic - AF/mitral stenosis/ septal MI)
4) Carotid Endarterectomy |
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What is the different types of stroke classification? |
Bamford Classification / Oxford Stroke Classiciation |
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What are the four types of strokes |
TACS PACS POCS LACS |
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What is TACS |
Total Anterior Circulation Stroke All 3 1) Unilateral Weakness of Face + Arm+ Leg (+/- sensory deficit) 2) Homonymous Hemianopia 3) Higher cerebral dysfunction (Dysphasia/Visualspatial disorder)
|
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What is PACS |
Partial Anterior Circulation Stroke 2/3 of
1) Unilateral Weakness of Face + Arm + Leg (+/- sensory deficit) 2) Homonymous Hemianopia 3) Higher cerebral dysfunction (Dysphasia/Visuosparial disorder) |
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What is POCS? |
Posterior Circulation Syndrome 1/3 of
1) Cerebellar of Brainstem Syndrome 2) Loss of consciousness 3) Isolated Homonymous Hemianopia |
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What is LACS |
Lacunar Syndrome (Basal Ganglia/ Internal Capsule/ Thalamus/ Pons)
CS-PAP
1) Clumsy hand dysarthria 2) Sensorimotor stroke 3) Pure Motor stroke 4) Ataxic hemiparesis 5) Pure sensory stroke |
|
4 Most common causes of a stroke? |
1) Small Vessel Occlusion / Cerebral Microangiopathy 2) Cardiac Emboli 3) Atherothromboembolism 4) CNS bleeds (Increased BP/Trauma/Aneurysm Rupture/Anti-Coagulants) |
|
Other rarer causes of stroke |
Watershed stroke (BP drop by >40 mmHg) Carotid Artery Dissection Vasculitis Subarachnoid Haemorrhage Venous Sinus Thrombosis Antiphospholipid Syndrome Paradoxial Emboli (ASD/VSD) |
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What stroke symptoms would make you think of a haemorrhagic stroke? |
Meningism Severe headache coma
|
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3 types of stroke |
Cerebral Infarct Brain stem infarct Lacunar Infarct |
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What happens in a cerebral infarct |
Contralateral sensory loss OR hemiplegia - initially FLACCID (about 1 hour) before SPASTIC (UMN lesion)
Dysphasia/Homonymous hemianopia/ Visuo-spatial deficit |
|
What happens in a brain stem infarct |
QUADRIPLEGIA / Disturbance of gaze and vision / Locked-In Syndrome
Pseudo-bulbar palsy = CN9-12 affected due to stroke |
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What happens in a lacunar infarct? |
Affects the: Pons/Basal Ganglia/ Thalamus/ Internal Capsule CS-PAP 1) Clumsy Hand Dysarthria 2) Sensorimotor Stroke 3) Pure motor stroke 4) Ataxic Hemiplegia 5) Pure sensory stroke |
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4 differential diagnosis for a stroke? |
Head injury Hypoglycaemia Subdural haemorrhage Hemiplegic Migraine |
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What is the first hour management plan for stroke? |
Protect Airway Blood Glucose Urgent CT Head IV Alteplase (once haemorrhagic is ruled out) within 4.5 hours of a stroke Nil by mouth Aspirin (After haemorrhagic ruled out)
|
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Contraindications of IV Alteplase
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Previous CNS bleed AVM Aneurysm Varices Portal hypertension |
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If a patient has prosthetic valves, what must you give them as primary prevention for a stroke? |
Warfarin |
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What is the name of the scoring system used to predict whether AF will cause a stroke? |
CHA2DS2-VASc Score |
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If the CHA2DS2-VASc score is 0 or >1 what do you give as prophylaxis? |
0 = Aspirin/ Nothing >1 = Warfarin |
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7 cardiac causes of a stroke? |
1) Non valvular AF 2) Prosthetic Valve 3) Post MI 4) External cardioversion 5) Cardiac Surgery - e.g. bypass graft 6) Paradoxical systemic emboli 7) Valve vegetation from Subacute Bacterial Endocarditis/IE |
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What is the secondary prevention for a stroke? (After adjusting modifiable risk factors) |
1) Copidogrel ONLY (P2Y12 inhibitor) 2) Warfarin (if indicated - e.g. prosthetic valve / CHA2D2-VASc >1) |
|
Investigations for causes of a stroke? |
1) Hypertension? - retinopathy/nephropathy/CXR 2) Cardiac source? - 24 hour ECG/ECHO 3) Carotid Artery Stenosis? Carotid Doppler USS + CT/MRI Angiography 4) Hypo/hyperglycaemia - Dyslipidaemia - Hyperhomocyteinaemia 5) Vasculitis? ESR/ANA 6) Prothrombic state? Thrombophilia / Antiphospholipid syndrome 7) Hyperviscosity = Polycythaemia / Sickle Cell Disease 8) Genetic Tests = CADASIL/Fabry's Disease |
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4 complications of a stroke |
Aspiration Pneumonia Pressure sores Constipation Depression |
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How do you manage a patient non-medically after a stroke? |
BARTHEL'S index of activities of daily living
- Enablement Approach = Agree to tasks/ plan steps - agree to goals/ review goals
- Make physio fun - swimming/music/videogames |
|
2 most common causes of Sub-Arachnoid Haemorrhage? |
1) Rupture of a Saccular Aneurysm (80%) 2) Arterio-venous malformations |
|
5 risk factors of an SAH |
Hypertension Smoking Alcohol misuse Bleeding disorders Microcytic Aneurysm |
|
3 most common sites for a saccular aneurysm |
JUNCTION of ANTERIOR communicating artery and ANTERIOR cerebral artery
JUNCTION of POSTERIOR communicating artery and internal carotid
BIFURCATION of the MIDDLE cerebral artery |
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3 causes of saccular aneurysms ? |
ADPKD Ehlers- Danlos Coarctation of the aorta |
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Symptoms of SAH? |
Sudden occipital headache (thunderclap - hit in the back of the head) Vomiting Collapse Seizures Coma/Drowsiness Neck stiffness Kernig's Sign |
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What is TERSON'S Syndrome? |
Retinal/Subhyaloid/Vitreous bleeds |
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What may a person with an SAH feel before the headache |
Sentinel headache = warning headache a few days before |
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Investigations for an SAH |
1) CT scan within 48 hours 2) Lumbar puncture = IF CT is negative and NO contraindications AFTER 12 hours x 3 times = should see XANTHOCHROMIA (yellow due to bilirubin) |
|
Management of SAH? |
If proven = Immediate Neurosurgery Re-examine CNS / Keep Hydrated
NIMODIPINE (Ca2+ antagonists - reduced vasospasm in coronary arteries)
CT Angiography --> Endovascular coiling / Surgical clipping / Intracranial stents |
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4 complications of SAH |
Rebleed Hyponatraemia Hydrocephalus Cerebral ischaemia |
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Subdural Haemorrhage - what blood vessels/ what shape on CT/ where? |
Bridging veins between cortex and venous sinuses Sickle/Crescent Shape (S=S) Haematoma between DURA and ARACHNOID |
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What happens in a subdural haemorrhage? |
Gradual rise in ICP Shifts mid-line structures AWAY from the side of the clot = eventual tentorial herniation & coning |
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Risk Factors for a SUB-DURAL haemorrhage? |
Elderly (brain atrophy makes bridging veins more vulnerable) Falls (Alcoholics/ Epileptics) Anticoagulation |
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Symptoms of Subdural haemorrhage |
Fluctuating levels of consciousness Physical or intellectual slowing Sleepiness Headache Personality Change
Raised ICP Seizures |
|
Investigations for a subdural haemorrage? |
CT scan = Clot (Sickle/Crescent shaped) + midline shift |
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Management of Subdural Haemorrhage? |
Irrigation via Burr Twist Drill & Burr Hole Craniostomy |
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Where does an extra-dural haemorrhage occur? What blood vessel? |
Between the dura and skull Middle meningeal artery AND vein
|
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Most common cause of an extra-dural haemorrhage |
Fractured Temporal or Parietal Bone - typically after trauma |
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Clinical Features of an ExtraDural Haemorrhage |
After head injury - conscious level falls LUCID INTERVAL - may last up to days before a decrease in the GCS due to a raised ICP
Severe headache / vomiting / confusion / fits Hemiparesis with brisk reflexes + upgoing plantar |
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What are the complications of an extra-dural haemorrhage if the bleeding continues? |
Ipsilateral pupil dilatation Coma Bilateral limb weakness Death |
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Investigations for an extra-dural haemorrhage |
CT = Biconvex/Lens-shaped haematome |
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Management of Extra-Dural Haemorrhage |
Clot Evacuation + Ligation of Bleeding Vessel Mannitol (Do decrease raised ICP) |
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Define a seizure? |
Recurrent tendency to spontaneous/intermittent/abnormal electrical activities in parts of the brain = SEIZURES |
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What are the 3 elements of a seizure? |
1) Prodrome 2) Aura = part of the seizure when the patient is aware (Deja-Vu/Jamais-Vu/Strange smells/Flashing lights) - implies a FOCAL seizure 3) Post-Ictally Headache/confusion/myalgia/sore tongue Temporary weakness after a focal seizure in the motor cortex (Todd's Palsy) Dysphasia following focal seizure in temporal lobe |
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What are the three types of partial seizures? |
Partial Seizure = Focal onset with features referable to part of one section
1) Simple Partial Seizure 2) Complex Partial Seizure 3) Partial Seizures with secondary generalisation |
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What happens in a simple partial seizure? |
UNIMPAIRED awareness Focal/motor/sensory/autonomic/psychic disturbance NO post-ictal seizures |
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What happens in a complex partial seizure? |
IMPAIRED awareness Most common from the temporal lobe = Post Ictal Confusion Rapid recovery after seizures = Frontal Lobe |
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What happens in partial seizures with secondary generalisation? |
Electrical disturbance = focal --> wide = secondary generalised |
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What are the classical symptoms of a TEMPORAL LOBE partial seizure? |
1) Automatisms (Lip-smacking / singing / kissing) 2) Abdominal rising sensation / pain 3) Dysphasia 4) Deja-vu/Jamais vu 5) Hippocampal involvement = Emotional disturbances (terror/panic/anger) 6) Uncal involvement = Auditory/Smell/Taste hallucinations |
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What are the classical symptoms of a FRONTAL LOBE partial seizure? |
1) Motor Features = Peddling legs / posturing 2) Jacksonian March --> Todd's Paralysis 3) Motor Arrest 4) Subtle behaviour disturbances 5) Dysphasia or speech arrest |
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What are the classical symptoms of a PARIETAL LOBE partial seizure? |
1) Sensory disturbances = tingling / numbness 2) Motor symptoms = due to spread to pre-central gyrus |
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What are the classical symptoms of an OCCIPITAL LOBE partial seizure? |
Visual phenomena / Spots - Lines - Flashes |
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5 types of primary generalised seizures? |
1) Absence (usually children) 2) Tonic-Clonic Seizures 3) Myoclonic Seizures 5) Atonic (akinetic) seizures 5) Infantile Spasms (Associated with tuberous sclerosis) |
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What are absence seizures (Petit mal)? |
Usually last for under 10 seconds - usually children Child suddenly PAUSE - stops mid-sentence - then carries on |
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What are Tonic-Clonic Seizures (Grand-mal)? |
Loss of awareness Limbs stiffen (TONIC) --> Jerk (CLONIC) May have one without the other Post-ictal confusion and drowsiness |
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What are MYOCLONIC seizures |
Sudden JERK of a limb/face or trunk Either patient suddenly is thrown onto the ground or has a VIOLENTLY DISOBEDIENT limb |
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What is an Atonic (akinetic) seizure? |
Sudden loss of muscle tone = FALL (no lose of consciousness) |
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If you're diagnosed with epilepsy - what do you have to tell the DVLA? |
Cannot drive until seizure free for >1 year |
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Causes of Epilepsy? |
Idiopathic Cortical scarring Space-occupying lesions Stroke Vascular malformations Tuberous sclerosis SLE Sarcoidosis |
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Non-epileptic causes of seizures? |
Alcohol Trauma Stroke Haemorrhage Raised ICP |
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Metabolic disturbance causes of seizures? |
Hypoxia Liver Disease Infection (Meningitis / Encephalitis/ Syphilis / HIV) Fever Drugs (Cocaine / Tramadol) |
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Management of primary generalised seizures? |
1) Generalised Tonic-Clonic Seizures = Sodium Valporate - Lamotrigine - Toprimate
2) Absence Seizures = Sodium Valporate - Lamotrigine - Ethosuximide
3) Tonic/Atonic/Myoclonic Sodium Valporate - Lamotrigine - Toprimate
|
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Management of partial seizures? |
CARBAMAZEPINE Sodium Valporate/ Lamotrigine / Topiramate |
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Side effects of Sodium Valporate |
Nausea + VALPORATE Appetite increase - weight gain Liver failure Pancreatitis Oedema Reversible hair loss Ataxia Teratogenic (Neural Tube Defects) / Tremor Encephalopathy |
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Side effects of LAMOTRIGINE |
Maculopapular rash (STEVENS-JOHNSON syndrome) Hypersensitivity (Fever/DIC) Vomiting Diplopia Blurred Vision Photosensitivity Tremor |
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Side effects of CARBAMAZEPINE? |
Leucopenia Diplopia Blurred Vision Impaired balance Drowsiness |
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Side effects of Phenytoin? |
Nystagmus Diplopia Depression Decreased intellect Acne Gum hypertrophy |
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What is non-epileptic attack disorder? |
Uncontrollable symptoms No learning disabilities CT/MRI/EEG = All normal |
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How do you investigate Seizures? |
Bloods/LP EEG (Normal between attacks) CT + Enhancement MEG PET Ictal SPECT |
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How do you manage epilepsy if an epileptogenic focus can be identified? (e.g. hippocampal sclerosis or small low grade tumour?) |
Neurosurgical resection Vagal nerve stimulation |
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What is Status Epilepticus? |
Seizure lasting >30 minutes OR repeated seizures without intervening consciousness |
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Name 2 percipitating factors for status epilepticus? |
Alcohol Stopping medication Pre-Eclampsia (If pregnant)
|
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How do you treat Status epilepticus? |
100% Oxygen IV Lorazepam x 2 Rectal Diazepam Buccal Midazolam Phenytoin/Diazepam infusion Dexamethason |
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3 Cardinal Symptoms of PARKINSONISM |
(RAT) Rigidity/ Tone = "Cog-Wheel" / "Lead-Pipe" Rigidity - Increase in tone in limbs + trunk Limb resists THROUGHOUT movement
Bradykinesia / Hypokinesia = Slow to initiate movement / Stoop / Micrographia/ Lessened Arm swing/ FESTINANCE (shuffling steps) / Freezing at obstacles/ HYPOMIMIA
Tremor = 4-7Hz RESTING - "pill-rolling" thumb & fingers - IMPROVED by voluntary movement/ worse by anxiety |
|
5 Causes of Parkinsonism |
1) Idiopathic Parkinson's Disease (Mutation in Fbx07) (Fbitches x 07) 2) Drugs (Neuroleptics / Metoclopramide) 3) Wilson's 4) HIV 5) Trauma |
|
Non motor features of Parkinson's Disease? |
REM sleep disorders Prosody Constipation Frequency Dementia Decreased sense of smell Visual Hallucinations Depression |
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Pathology behind IPD? |
Mitochondrial DNA dysfunction causes a degeneration of the dopaminergic neurones in the substantia nigra pars compacta (associated with Lewy Bodies) = Lowered striatal dopamine levels |
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Management of IPD? |
MDT Meeting Involvement = GP Neurologist PD Nurse Social Worker Carers Physiotherapist Occupational therapist |
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Management of IPD?
|
1) LevoDopa + Benserazide (Dopa-decarboxylase inhibitor) = CO-BENELDOPA
SE = Nausea and Vomiting (Give Domperidone) Efficacy reduced with time/psychosis/visual hallucinations/painful dystonias Carbedopa + LevoDopa 2) Dopamine Agonists (ROPINOROLE) SE = Pathological gambling / compulsive shopping 3) MAO-B Inhibitors (SELEGILINE) SE = Postural Hypotension 4) COMT Inhibitors (TOLCAPONE) SE = Severe hepatic complications |
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Other management ideas for PD? |
1) Anticholinergics - for tremor = BENZHEXOL 2) APOMORPHINE (DA agonist - rescue pen) 3) Depression? SSRI 4) Disease Psychosis? OLANZAPINE 5) Respite Care 6) Deep brain stimulation 7) Surgical ablation of overactive subthalamic nuclei |
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Mneumonic for remembering 5 key symptoms of IPD? |
SMART Shuffling Gate Mask-like facies Akinesia Rigidity Tremor |
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5 Parkinson's Plus Syndrome |
Parkinsonism + Evidence of separate pathology PMLVC (Parkinson's Makes Life Very Crap)
Progressive Supranuclear Palsy Multiple System Atrophy (Shy-Drager) Lewey Body Dementia Vascular Parkinsonism Cortico-Basal Degeneration |
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5 Parkinson's Plus Syndrome plus VIVID signs |
VIVID Progressive supranuclear palsy = Vertical gaze palsy Multiple System Atrophy = Impotence / Incontinence Lewey Body Dementia = Visual Hallucinations Cortico-Basal Degeneration = Autonomous Interfering Activity Vascular Dementia = In Diabetics |
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Define Huntington's Disease? |
Autosomal DOMINANT condition affecting the corpus striatum and cortex = incurable/progressive/neurodegenerative disorder |
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Pathology behind Huntington's Disease |
Atrophy and Neuronal Loss of CORPUS STRIATUM AND CORTEX Expansion of CAG repeats on Ch4
= Depletion of GABA and Acetylcholine BUT SPARES DOPAMINE |
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Clinical Features of Huntington's? |
Irritability/Depression/Incoordination --> Chorea --> Dementia + Fits ---> Death |
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What is Chorea? |
Continuous flow of jerky, quasi-purposive movement Fleeting from one part of the body to the other |
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Investigation and Management for Huntingtons? |
MRI = Ventricularmegaly NO CURE - only symptomatic
Chorea = Neuroleptics Depression = Seroxate Aggression = Haloperidol |
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7 Classical Features of DEMENTIA |
MAHAWAM MEMORY LOSS Agitation Hallucinations Aggression Wandering Apathy Mood Disturbances |
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2 Diagnostic Tests for Dementia? |
AMT Addenbrooke's Cognitive Examination
|
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4 Main Types of Dementia? |
A VERY LOVELY FRIEND
Alzheimer's Vascular Dementia Lewey Body Dementia Fronto-Temporal Dementia |
|
Describe Vascular Dementia |
Cumulative effects of MANY small strokes Thus - SUDDEN ONSET and STEP-WISE deterioration is characteristic
Look for evidence of vascular pathology = HTN/Past strokes/ Focal CNS signs |
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Describe Lewy Body Dementia |
Typically FLUCTUATING cognitive impairment Detailed Visual Hallucinations - Small Animals / Children
Histologically = Lewy Bodies in BRAINSTEM & Neocortex |
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Decribe Fronto-Temporal Dementia |
Contains PICK inclusion bodies Executive impairment Behavioural/Personality Change Disinhibition Hypeorality Emotional Unconcern |
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5 other causes of dementia? |
HIV HD IPD Whipple's Repeated Head Trauma |
|
Clinical Features of Alzheimer's |
MAVEV ---> BIMAL
Memory loss Anosognosia Verbal Abilities Executive Function Visuo-spatial skills
Behavioural Change (aggression/wandering) Irritability Mood disturbance (depression) Agnosia Hallucinations/Dellusions (Psychosis) |
|
Pathogenesis behind Alzheimer's disease? |
Accumulation of B-amyloid peptide --> Progressive Neuronal Damage
NEUROFIBRILLARY TRIANGLES B-AMYLOID PLAQUES TAU PROTEINS Decreased Acetylcholine
Neuronal Loss is Selective = Hippocampus/Amygdala/Temporal neocortex |
|
RISK Factors of Alzheimer's |
Down's Syndrome 1st Degree Relative Depression Loneliness |
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Management of Alzheimers Disease
|
1) Referral to memory service
2) Acetylcholinesterase inhibitors = RIVASTIGMINE SE = D&V/Cramps/Headache/Insomnia 3) NMDA inhibitor= MEMANTINE SE = Hallucinations / Confusion / Hypertonia 4) Sensation stimulation/ CBT/Cognitive stimulation programmes/ Massage/ Dance therapies |
|
8 Issues in managing someone with dementia? |
1) Care Coordinator? Laundry/DayCare/Priority Parking 2) Capacity to make decisions? 3) MUST develop a routine 4) PLAN AHEAD - DO NOT MOVE HOUSE 5) Day Care 6) Care for the carers? 7) Challenging Behaviour? Lorazepam 8) Depression? Citalopram |
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What is the difference between common and classic migraines? |
Common = Migraine WITHOUT aura Classic = Migraine WITH aura |
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Define migraine |
Episodic severe headaches with/without aura Often prementrual Usually Unilateral with NAUSEA/VOMITING +/- Photo/phonophobia |
|
What 4 auras can occur in migraine? |
Visual = Chaotic cascading / Distorting / Dots / Zigzags / Scotomata hemianopia
Somatosensory = Paraesthesiae = fingers -->face
Motor = Dysarthria / Ataxia/ Opthalmoplegia / Hemiparesis
Speech = Dysphasia / Paraphasia |
|
Pathophysiology of Migraine? |
Cortical spreading depression Altered modulation of normal sensory stimuli + trigeminal nerve dysfunction |
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What is the diagnostic criteria for a NON-migraine aura? |
>5 Headaches (Lasting 4-72 hours + N&V (or Photo/phonophobia) AND 2 of : Unilateral - Pulsating - Worsened by routine activity |
|
Triggers of a migraine? |
CHOCOLATE
Caffeine Hangovers Orgasms Cheese Oral contraception Lie-In Alcohol Tireness Exercise/Emotions
|
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Management of a migraine? |
1) NSAIDS (Ketoprofen) 2) Oral 5HT Agonists (Sumatriptan) CI = IHD/Coronary Spasm 3) Ergotamine SE = Gangrene 4) 12-weekly Botulinim Toxin Type A 5) Warm/Cold Packs |
|
Prophylaxis for Migraine? |
Avoid Triggers IF over 2x per month AND not responding to treatment =
1) Propanolol 2) Amitriptyline 3) Topiramate 4) Valporate |
|
What facial pain has post-nasal drip/ dull constant ache over the face / worse pain on bending over? |
SINUSITIS |
|
What happens in acute glaucoma? |
Occurs in the elderly/long-sighted Constant aching pain - develops around one eye - radiates to forehead CF = Cloudy cornea/decreased acuity/red eye/N&V/ haloes Percipitating Factors = Dilating Eye drops/ emotional upset/ sitting in the dark
Rx = IV ACETAZOLAMIDE |
|
Describe a tension headache? |
Tight band around the head BILATERAL Non-pulsatile headache + scalp muscle tenderness
Rx = Explanation/Reassurance/ Withdraw analgesics / Massage/ AMITRIPTYLINE |
|
4 things that make raised intracranial pressure headaches worse? |
Walking Lying Bending forward Coughing |
|
4 symptoms associated with raised intracranial pressure? |
Vomitting Papilloedema Seizures Odd behaviour Alleviated by standing |
|
Investigations for suspected raised intracranial pressure? |
CT Head = EXCLUDE space occupying lesion Consider idiopathic intracranial hypertension
NO NO NO LUMBAR PUNCTURE |
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Management for raised ICP |
Lose Weight Mannitol |
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Tell me a bit about medication overuse (analgesic rebound) headache? |
Causes by mixed analgesics usually (paracetamol + codeine / opiates) Also Ergotamine/ triptans
|
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Management of medication overuse headache? |
Withdraw analgesia + aspirin After = Valporate/Gabapentin
Inform them - no more than 6 painkillers a month |
|
Causes of Cluster Headache? |
Superficial temporal artery smooth muscle hyper-reactivity to 5HT ALSO hypothalamic grey matter abnormalities |
|
Clinical Features of Cluster Headaches? |
Rapid-onset of EXCRUCIATING pain around one eye Watery & Bloodshot / Lid swelling/ Lacrimation/ Facial Flushing/ Rhinorrhoea / Miosis + Ptosis
STRICTLY unilateral
|
|
Management of Cluster Headaches? |
100% OXYGEN SC Sumatriptan / ZOLMITRIPTAN nasal spray |
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2 preventative treatments for cluster headache? |
Sub-occipital steroid injections Verapamil Lithium |
|
What is Trigeminal Neuralgia? Where do you most often get it? |
Paroxysms of intense STABBING pain - lasting seconds in trigeminal nerve distribution MOSTLY Mandibular & Maxillary
- Face screws up with pain (Tic Doloureux) |
|
5 Triggers for Trigeminal Neuralgia |
WASTED
WAshing Shaving Talking Eating Dental prostheses |
|
Causes of Trigerminal Neuralgia |
1) Compression of nerve root = Anomalous or Aneurysmal intracranial vessels/tumour
2) Chronic meningeal inflammation
3) MS
4) Skull base malformation
|
|
Management of Trigerminal Neuralgia? |
CARBAMAZEPINE Lamotrigine
Surgical = Microvascular Decompression / Thermocoagulation of trigeminal ganglion |
|
What age group does GCA normally affect? |
OVER 60 If under 55 - think Takayasu's Arteritis d |
|
Define Giant Cell Arteritis |
Granulomatous arteritis of unknown aetiology - associated with Polymyalgia Rheumatica |
|
Clinical Features of GCA |
Headache Temporal artery & scalp tenderness (when combing hair) Jaw Claudication Amaurosis Fugax OR sudden blindness (central retinal artery) |
|
Extracranial symptoms of GCA? |
Dyspnoea Morning Stiffness Unequal or weak pulses Weight loss Malaise Fever |
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What do you see on examination of the superficial temporal artery in GCA? |
Tender Firm Pulseless |
|
Investigations for GCA |
ESR&CRP UP UP UP UP Raised Platelets and Alk Phos
TEMPORAL ARTERY BIOPSY within 7 days of steroids |
|
Management of GCA |
PREDNISOLONE RIGHT AWAY Also: PPI's Bisphosphonates |
|
What is Polymyalgia Rheumatica? |
>50 years old Subacute onset (<2 weeks) Bilateral aching tenderness Morning stiffness in SHOULDERS and PROXIMAL LIMB MUSCLES (Pelvic Girdle?)
Also: Mild polyarthritis / Tensosynovitis / Carpal Tunnel Syndrome Fatigue / Fever/ Weight loss/ Anorexia |
|
Investigations for PMR |
Raised ESR/CRP/ALP |
|
Management of PMR? |
PREDNISOLONE = Dramatic response within 1 week |
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Where is the lesion if there is paraplegia? Hemiplegia? |
Paraplegia = Cord compression Hemiplegia = Brain lesion |
|
Clinical Features of Spinal Cord Compression? |
Spinal/Nerve root dull ache pain Leg weakness/sensory loss Arm weakness (suggests cervical cord lesion) Bladder and anal sphincter involvement = LATE symptom |
|
What are typical LMN signs? |
Decreased tone Decreased reflexes Wasting Fasciculations |
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What are typical UMN signs? |
Increased tone Brisk reflexes Weakness in EXTENSORS (bent arm post stroke) |
|
Cord compression will produce UMN or LMN? |
LMN at the level of the lesion UMN signs below |
|
7 Causes of Spinal Cord compression |
1) SECONDARY MALIGNANCY (BBTKP) 2) Infection (Epidural Abscess) 3) Cervical Disc prolapse 4) Haematoma (warfarin?) 5) Intrinsic cord tumour 6) Myeloma 7) Spinal TB (Pott's Disease) |
|
Differential Diagnosis for spinal cord compression? |
Transverse myelitis MS Cord vasculitis Trauma Dissecting Aneurysm |
|
Investigations for spinal cord compresssion? |
IMMEDIATE MRI |
|
Management of Spinal Cord Compression? |
If secondary to a malignancy?
Epidural abscess? Decompression + Antibiotics
Decompressive Laminectomy |
|
Causes of Unilateral Food Drop |
DM Common Peroneal Nerve Palsy Stroke Prolapsed Disc MS |
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Causes of weak legs with NO sensory loss |
MND Polio
|
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Causes of chronic spastic paraparesis |
MS Cord tumour (astrocytoma) Cord metastases MND
|
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Causes of chronic flaccid paraparesis? |
Peripheral Neuropathy Myopathy |
|
Cauda Equina Syndrome - 4 CLASSIC symptoms |
1) Bowel/Bladder Dysfunction 2) Decreased sensation in SADDLE area (Perineal) 3) Sexual Dysfunction 4) Neurological deficit in the lower limb = Motor/sensory loss/ reflex change |
|
Causes of Cauda Equina? |
L4/L5 --> L5/S1= LUMBAR DISC HERNIATION Tumours Epidural Abscess Congenital (Spina bifida) Sponylolisthesis Late stage AS |
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Other symptoms of cauda equina syndrome? |
Lower back / leg pain / motor or sensory deficits Urinary retention Saddle & Perineal Anaesthesia Bowel/Bladder Dysfunction Asymmetrical weakness with loss of reflexes Sexual dysfunction |
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Investigations for Cauda Equina? |
MRI MRI MRI MRI MRI |
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What is the difference between cauda equina and conus medullaris syndrome? |
Conus medullaris is located at T12-L2 Associated with urinary retention and constipation LESS PAINFUL |
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Management of cauda equina syndrome? |
URGENT SURGICAL DECOMPRESSION |
|
Define Multiple Sclerosis? |
Discrete PLAQUES of demyelination at multiple CNS sites from T-cell mediated immune response
RELAPSING AND REMITTING DISSEMINATED IN TIME AND SPACE |
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What happens after prolonged demyelination? |
Axonal Loss Clinically progressive symptoms |
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Eye Signs in Multiple Sclerosis |
Unilateral Optic neuritis (Pain on eye movement + rapid decreased in central vision) Diplopia / Hemianopia BILATERAL INTERNUCLEAR OPTHALMOPLEGIA
Charles Bonnet Syndrome = Decreased Visual Acuity + Hallucinations Uhthoff's Phenomenon = Decreased vision on exercise/hot meals/ hot bath. Phosphenes (flashed) on eye movement Pulrich Effect = Unequal Eye Latencies Argyle Robertson Type Pupil
|
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Sensory Signs in MS? |
Lhermitte's Sign = Neck Flexion causes "electric shock in trunk and limbs
Numbness/tingling in limbs Decreased vibration sense Trigeminal neuralgia |
|
Motor Signs in MS? |
Spastic Weakness (Les?) Transverse Myelitis = Loss of motor/sensory/autonomic/reflex and sphincter function BELOW the level of the lesion
Devic's Syndrome = Neuromyelitis Optics = Transverse myelitis + Optic atrophy + NMO-IgG antibodies |
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GI Signs in MS? |
Swallowing Disorders Constipation |
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Cerebellum Signs in MS? |
Trunk and limb ataxia Intention tremor Scanning speech Falls |
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Sexual/GU signs in MS? |
Erectile Dysfunction Urinary retention Incontinence |
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Cognitive / Visuospatial Signs in MS? |
Amnesia Decreased executive functioning Change in mood |
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5 signs of POOR prognosis in MS? |
Increased AGE Motor signs at onset Many relapses early Axonal loss Increased MRI lesions |
|
Diagnosis of MS? |
Clinical = Lesions Disseminated in TIME&SPACE - with no other viable causes MRI of brain and spinal cord CSF = Oligoclonal bands of IgG on electrophoresis NOT present in the serum Evoked potentials = Delayed visual/auditory/somatosensory |
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What is the criteria required to diagnose MS? |
McDONALD CRITERIA
Attacks must be >1 hour - with 30 days in between |
|
MRI abnormalities seen in MS? |
3/4 needed
Gadolinum enhancing OR >9 T2 hyperintense lesions
>1 infratentorial lsions >1 juxtacortical leions >3 periventricualr lesions |
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3 antibodies in MS? |
NMO-IgG (Devic's Syndrome) MOG MBP |
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Management of MS |
MINGA - White Trash 30 year old
Methylprednisolone Interferon 1-B & Interferon-IA x = Abortion/ Depression Natalizumab (Acts against VLA-4 Receptors) Glatiramer Acetate (Doxorubicin Analogue) Azathioprine
|
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Palliative Treatment? |
Spasticity? Diazepam Tremor? Botulinum Toxin Type A Urgency/Frequency? Intermittend Self-Catheterisation |
|
What is Myasthenia Gravis? |
Autoimmune disease mediated by ANTIBODIES to nicotinic AchR - interfering with neuromuscular transmission VIA a depletion of post-synaptic receptor sites
MAY BE ASSOCIATED WITH THYMOMA |
|
Pathophysiology in MG? |
Antibodies BLOCK the postsynaptic ACh receptors = prevent end plate potential from triggering muscle contraction = MUSCLE WEAKNESS
Acetylcholinesterase then BREAKS down ACh = takes it away |
|
Clinical Features of MG |
Increasing muscular fatigue - Extra-ocular (Ptosis / Diplopia / Peek sign) - Bulbar - Face (Myasthenic snarl / Dysphonia / Chewing or Talking difficulties) - Neck - Limb girdle
IMPROVES AFTER REST |
|
6 things that worsens weakness in MG? |
1) Pregnancy 2) Hypokalaemia 3) Gentamicin 4) Opiates 5) Emotion 6) Exercise 7) Infection 8) Over treatment |
|
Aetiology of MG? |
<50 years old = Female/Other AI Diseases/ THYMIC HYPERPLASIA >50 years old = Male / Thymic Atrophy or Tumour I |
|
Investigations for MG? |
Anti-AChR antibody OR MUSK Antibody Neurophysiology (Evoked Potentials) CT of Thymus ICE PACK TEST -ptosis improves by >2mm after Ice pack for >2 minutes Tensilon Test |
|
Management of MG? |
Acetylcholinesterase Inhibitor = PYRIDOSTIGMINE SE = Lacrimation / Sweats / Vomiting / Diarrhoea
Immunosuppression = PREDNISOLONE + AZATHIOPRINE
THYMECTOMY - Consider if <50 OR not controlled by Pyridostigmine |
|
What happens during a Myasthenic Crisis? |
WEAKNESS OF THE RESPIRATORY MUSCLES during a relapse - can be life threatening
Must must monitor FVC + Give Ventilatory Support |
|
Management of Myasthenic Crisis? |
Plasmapheresis IV Immunoglobulin |
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Causes of Lambert-Eaton Myasthenic Syndreom |
Paraneoplastic (Small Cell Lung Ca) Autoimmune |
|
3 clinical signs of LEMS |
Gait difficulty FIRST - before eye signs
Autonomic involvement = Dry mouth / constipation / Impotence
Hyporeflexia & Weakness = Improves AFTER exercise
|
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Management of LEMS |
IV Immunoglobulin |
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MND affects which neurones? |
MOTOR CORTEX CRANIAL NERVE NUCLEI ANTERIOR HORN CELLS |
|
What does MND spare? |
Affects BOTH LMN and UMN BUT
1) No Sensory loss or sphincter disturbance (Distinguishes from MS/Polyneuropathies)
2) NEVER affects eye movements (Distinguishes from MG) |
|
Genetics behind MND? |
ALS-FTD locus at Ch9
Or
Autosomal Dominant D90A SOD1 Mutation |
|
4 Clinical Patterns of MND |
All Bald Men Shine (ABML)
ALS (Amyotrophic Lateral Sclerosis) Progressive Bulbar Palsy Progressive Muscular Atrophy Primary Lateral Sclerosis |
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What happens in ALS (Amyotrophic Lateral Sclerosis) |
Loss of motor neurones in the MOTOR CORTEX and in the ANTERIOR HORN
Weakness UMN Signs (Increase Tone/Increased Reflexes/ Upgoing Plantars) LMN Signs (Wasting / Fasciculation)
Worse prognosis if: Older/Decreased FVC/Bulbar onset |
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What happens in Progressive Bulbar Palsy? |
Only affects CN9-12 See LATERP |
|
What happens in Progressive Muscular Atrophy |
ANTERIOR HORN CELL ONLY = No UMN signs Affects DISTAL muscle groups before proximal
Weakness/Wasting/Fasciulations |
|
What happens in Primary Lateral Sclerosis? |
Loss of BETZ cells in motor cortex UMN signs + Marked Spastic Weakness + Pseudobulbar Palsy |
|
When to think of MND? |
>40 Stumbling/Spastic gait Foot drop + Proximal Myopathy Weak grip & shoulder abduction Aspiration pneumonia |
|
How do you diagnose MND? |
EL ESCORIAL CRITERIA |
|
Most likely cause of death in MND? |
Respiratory Failure due to bulbar palsy + pneumonia |
|
MDT involvement in MND? |
Neurologist Palliative Nurse Hospice Physiotherapy OT Speech and Language Therapist Dietician Social Services |
|
Management for MND |
1) Antiglutamateric Drugs (Sodium Channel Blocker) = RILUZOLE
2) Drooling? = PROPANTHELINE + AMITRIPTYLINE
3) Dysphagia? Blended food/ Ng tube
4) Non-invasive ventilation / NSAIDs/ Opiods |
|
What is Bulbar Palsy? |
Disease of the NUCLEI of CN9-12 in the medulla |
|
Signs of Bulbar Palsy? |
LMN lesions of the tongue and muscles of talking/swallowing = Flaccid / Fasciculating tongue/ Jaw Jerk Decreased/ Dysphonia / Drooling |
|
Causes of Bulbar Palsy |
MND GBS Polio MG |
|
What is Psudobulbar palsy (Corticubulbar palsy)? |
More common than Bulbar UMN lesions of the muscles of swallowing & talking due to BILATERAL lesions above the mid-pons e.g. Corticobulbar tracts (MS/MND/STROKE) |
|
Signs of Corticobulbar palsy? |
Slow tongue movements with slow deliberate speech Increased Jaw Jerk Increased Pharyngeal & Palatal Reflexes Emotional incontinence = uncontrolled weeping/giggling Palatal movements absent Persistent dribbling |
|
Define a TIA |
Sudden onset of a focal neurological deficit lasting for less than 24 hours due to an occlusion of part of the cerebral circulation |
|
Define Gullian-Barre Syndrome |
Acute inflammatory demyelinating polyneuropathy = symmetrical ascending muscle weakness starts |
|
4 things that can trigger GBS? |
Campylobacter Jejuni CMV HIV EBV
= Leads to autoantibody mediated nerve cell damage |
|
Clinical Features of GBS |
Progressive onset of LIMB weakness = 4 WEEKS -----> Recovery - Proximal muscles affected more (e.g. Trunk/Respiratory/Cranial Nerves CN7) - Pain in back/limbs
DIAGNOSTIC = PROGRESSIVE WEAKNESS OF ALL 4 LIMBS AREFLEXIA
Supporting symptoms = Progression over days / symmetrical / CN involvement
|
|
What is the main DD for GBS? |
MG Botulism Poliomyelitis Chronic Inflammatory Demyelinating Radiculopathy = Slower onset & recovery |
|
What is Miller Fisher Syndrome? |
Associated with Anti- GQ1b antibodies in serum
1) Opthalmoplegia 2) Ataxia 3) Areflexia |
|
Investigations for GBS? |
1) Nerve Conduction Studies = Slow motor conduction 2) CSF = Increased protein 3) Respiratory Involvement = FVC check every 4 hours 4) Spine MRI |
|
Management of GBS |
IV Immunoglobulin /// CI = in IgA deficiency
Plasma Exchange
Supportive Treatment (Heparin / Physiotherapy / NG Tube) |
|
Causes of Mononeuropathies |
Trauma Entrapment (e.g. tumour) Acute compression (e.g. common peroneal nerve) |
|
Define Mononeuritis Multiplex |
When 2 or more peripheral nerves affects --> tends to be systemic |
|
Causes of Mononeuritis Multiplex |
WARDS PLC
Wegener's Aids Rheumatoid DM Sarcoidosis
PAN Leprosy Carcinomatosis |
|
Median Nerve (C6-T1) - Which muscles does it innervate? |
LOAF Lumbricals Opponens Pollicis Abducter Pollicis Brevis Flexor Pollicis Brevis |
|
Hand Examination = Thumb abduction and opposition = which nerve? |
Median Nerve |
|
Ulnar Nerve C6-T1 - Most common cause of damage? |
Elbow Trauma (Cubital Tunnel / Epicondylar Groove) |
|
5 Signs of Ulnar Nerve Damage |
Weakness/wasting of : 1) Medial wrist flexors (ulnar side) 2) Interossi (Cannot cross fingers) 3) Medial two lumbricals (claw hand) 4) Hypothenar eminence
5) Also sensory loss in ulnar distribution |
|
4 ways to treat ulnar nerve damage? |
Rest/Avoid pressure Night time soft elbow splint Decompression in situ Medial epicondylectomies |
|
Where does damage to the radial nerve (C5-T1) happen? |
Compression against the humerus |
|
Signs of Radial Nerve Damage |
SATURDAY NIGHT PALSY Wrist/Finger drop Sensory loss at snuff box |
|
What 4 muscles are innervated by the radial nerve? |
BEST
Brachoradialis Extensors Supinator Triceps |
|
Clinical features of brachial plexus damage? |
Pain/paraesthesiase and weakness in affected arm |
|
Causes of Brachial Plexus damage? |
Trauma Radiotherapy (e.g. for Breast Ca) Pancoasts Tumour Cervical Rub |
|
What two clinical features will present with phrenic nerve palsy |
C3,4,5 keeps the diaphragm alive
Orthropnoea Raised hemidiaphragm on CXR |
|
Causes of Phrenic Nerve palsy |
Lung carcinoma Myeloma Thymoma Cervical spondylosis HIV Lyme disease TB |
|
What symptoms do you get from damage to the LATERAL cutaneous nerve of the thigh (L2-L3) |
Meralgia Paraesthesia Burning pain on the anterolateral part of the thigh due to entrapment of the nerve under the inguinal ligament |
|
Sciatic Nerve (L4-S3) - Damage from where? |
Pelvic tumours or fractures to the pelvis/femur Lesions affect the hamstrings and all muscles below the kneed (e.g. foot drop) Loss of sensation below the knee (laterally) |
|
Common Peroneal Nerve Damage (L4-S1) - What happens? |
Originates from the SCIATIC nerve just above the knee Damage is from the FIBULAR head (trauma/sitting cross legged)
FOOT DROP FOOT DROP FOOT DROP Weak ankle dorsiflexion/eversion Sensory loss over the dorsum of the foot |
|
What happens in Tibial Nerve Damage |
Loss of plantar flexion of the foot (tip toe) Loss of inversion/flex toes Sensory loss over the sole |
|
Carpal Tunnel Syndrome affects WHAT nerve? |
MEDIAN NERVE - WAKE AND SHAKE WAKE AND SHAKE |
|
Clinical Features of Carpal Tunnel Syndrome? |
Aching pain (typically at night) Paraesthesiae in the thumb / index / middle fingers (relieved by hand shake) Sensory loss and weakness of Abducter Pollicis ?brevis
Loss of light touch / 2-point discrimination / sweating |
|
Causes of Carpal Tunnel Syndrome |
MEDIAN TRAPS
Myxoedema (Hypothyroid) Enforced flexion Diabetic neuropathy Idiopathic Acromegaly Neoplasm (Myeloma)
Tumour - Benign (Lipoma) RA Amyloidosis Pregnancy Sarcoidosis |
|
Investigations for Carpal Tunnel Syndrome? |
Neurophysiology Tinnel's test Phalen's test |
|
Management of Carpal Tunnel Syndrome? |
Splinting Local Steroid Injection Decompression Surgery |
|
Classical features of polyneuropathy? |
Symmetrical & widespread distribution - distal weakness and sensory loss (glove&stocking) |
|
3 ways to classify polyneuropathy? |
Course (acute or chonic - e.g. GBS?) Function (Sensory/Motor/Autonomic) Pathology (Demyelination / Axonal degeneration/ Both)
|
|
3 causes of MOTOR polyneuropathies |
GBS Charcot-Marie Tooth (Distal wasting below the knees - inverted champagne bottles) Lead Poisoning |
|
3 causes of SENSORY polyneuropathies |
DM Renal Failure Leprosy |
|
Causes of Polyneuropathies in general |
Metabolic = DM/Renal Failure/ Hypo/Hyper Thyroidism / Hypoglycaemia
Vasculitides: PAN/RA/Wegner's
Malignancy: Polycythaemia Rubra Vera
Inflammatory: GBS/Sarcoidosis
Infections: Syphillis / HIV
Nutritional: Deficiency in Vitamin B1 & B12 Too much OR Too little Vit B6
Drugs: Alcohol/ Isoniazid / Phenytoin |
|
Symptoms of Peripheral Neuropathy? |
Sensory = Numbness/ Pins&Needles - glove and stocking/ Trauma or Burns
Motor = Progression/ Weak or clumsy hands / Difficulty in walking/ Breathing difficulty = LMN lesion symptoms / Decreased FVC |
|
Autonomic Neuropathy Symptoms? |
SEE NEXT FEW CARDS |
|
Investigations for polyneuropathy |
Nerve Conduction Studies (Demyelinating v axonal causes) BLOODS - CXR - URINALYSIS - LP + specific genetic tests (PMP22 for charcot) |
|
Management of polyneuropathy |
Treat the cause Involve physiotherapy / OT Foot care / shoes Neuropathic Pain? Amitriptyline / Gabapentin |
|
6 causes of autonomic neuropathy |
GDL is ASS
GBS DM Leprosy
Amyloidosis Sjogren's SLE |
|
Clinical features of SYMPATHETIC autonomic neuropathy? |
Postural Hypotension Decreased sweating Constipation Horner's |
|
Clinical Features of PARASYMPATHETIC autonomic neuropathy? |
Constipation Nocturnal Diarrhoea Urine retention Holmes- Adie pupil |
|
Penis and autonomic neuropathy? |
POINT & SHOOT
Parasympathetic = Erectile Dysfunction
Sympathetic = Ejaculatory Failure |
|
Investigations for autonomic neuropathy |
BP standing and lying - DROP of >20/10 is abnormal ECG Cystometry Pupils Paraneoplastic antibodies (Anti-Hu/Anti-Yo/Anti-Ri) |
|
What does Vitamin B1 (THIAMINE) deficiency cause |
WERNICKE'S ENCEPHALOPATHY Classical Triad: 1) Confusion 2) Ataxia 3) Opthalmoplegia (Nystagmus/Lateral Rectus palsy) |
|
Pathology of B1 deficiency |
Periaqueductal punctate haemorrhages & focal damage |
|
Causes of Vitamin B1 deficiency? |
Chronic Alcoholism Eating Disorders Malnutrition |
|
Management of Vitamin B1 deficiency |
Can lead Korsakoff's syndrome IV/IM THIAMINE |
|
What is Vitamin B6? |
PYRIDOXINE |
|
What causes Vitamin B6 deficiency? What symptoms can this cause? |
Mainly isoniazid therapy for TB - SENSORY NEUROPATHY MOSTLY
Management= PYRIDOXINE |
|
What can Vitamin B12 deficiency cause? |
Subacute combined degeneration of the spinal cord = Insidious onset with peripheral neuropathy |
|
Vitamin B12 deficiency clinical symptoms? |
Symmetrical Dorsal Column Loss = Touch/ Propioception/ Vibration & LMN signs
Symmetrical Corticospinal tract loss = Motor & UMN signs
Joint position/Vibration --> Ataxia --> Stiffness --> Weakness |
|
Triad of symptoms in Vitamin B12 deficiency |
1) Extensor Plantars (UMN) 2) Absence Knee Jerks (LMN) 3) Absent Ankle Jerks (LMN)
Pain and Temperature IN TACT |
|
Management of Vitamin B12 deficiency? |
IM HYDROXOCOBALAMIN |
|
What happens in Brown-Sequard Syndrome? |
Hemisection or unilateral cord lesion
|
|
Clinical Features of Brown-Sequard? |
1) IPSILATERAL UMN weakness below the lesion ** Severed corticospinal tract** = Spastic paraparesis = Brisk reflexes = Extensor plantars
2) IPSILATERAL loss of propioception and vibration **Severed dorsal column**
3) CONTRALATERAL loss of pain and temperature **Severed spinothalamic tract that has crossed** |
|
Causes of Brown-Sequard? |
Bullet Tumour Disc Hernia Cervical Spondylosis MS Myelitis Septic Emboli
MRI MRI MRI MRI MRI MRI MRI MRI MRI MRI |
|
What is a pontine lesion? What does it cause? |
Pons lies above the decussation of the posterior columns
Pontine lesion causes LOSS of ALL forms of sensation on the OPPOSITE side of the lesion |
|
Causes of Cranial Neve Lesions? |
DM Stroke MS Tumours Sarcoidosis Vasculitis = PAN/SLE Syphillis |
|
Loss of sense of smell? |
CN1 - OLFACTORY NERVE Causes = Trauma / Respiratory Tract Infection / Meningitis |
|
Loss of Vision? |
CN2 - OPTIC NERVE
1) Monocular Blindness = MS/GCA 2) Bilateral Blindness = DM/MS/Neurosyphillis 3) Bitemporal Hemianopia = Optic chiasm compression (Pituitary adenoma/craniopharyngioma/internal carotid aneurysm) 4) Homonymous hemianopia = Stroke/Abscess/Tumour 5) Optic neuritis = Pain on moving eye / loss of central vision / relative afferent pupillary defect/ Disc swelling 6) Papilloedema Bilateral swollen discs = RAISED ICP / Retro-orbital lesion (e.g. cavernous sinus thrombosis) 7) Optic Atrophy = Pale optic disc/Reduced Acuity = MS/Frontal Tumours 8) Ischaemic Papillopathy = Swelling of disc due to stenosis of posterior ciliary artery = GCA |
|
Causes of raised ICP |
Tumour Abscess Encephalitis Hydrocephalus Idiopathic intracranial hypertension |
|
Optic Nerve Tract Lesions? |
|
|
Cranial Nerve 3 (Occulomotor Lesion) causes? |
PCA aneurysm Raised ICP GCA DM HTN |
|
What muscles does the occulomotor nerve supply? |
Superior Rectus Inferior Rectus Medial Rectus
Inferior Oblique Sphincter Pupillae Levator Palpebrae Superioris |
|
What do you see in a patient with CN3 palsy? |
Eye is DOWN and OUT DILATED PUPILS Ptosis |
|
Most common symptoms of a brainstem infarct? |
Lateral Medullary Syndrome = Occlusions of one vertebral artery / posterior inferior cerebellar artery = Vertigo / Vomiting/ Dysphagia / Nystagmus / Ipsilateral ataxia / Ipsilateral Horner's Syndrome |
|
What muscle does CN4 supply? |
TROCHLEAR NERVE SO4? = Superior Oblique |
|
Clinical Features of CN4 palsy? |
Diplopia on looking down and in Head tilting compensation (OCULAR TORTICOLLIS) |
|
CN6 (Abducens) Which Muscle? |
Lateral Recturs Eye cannot be abducted beyond the midline Horizontal diplopia on looking outwards |
|
CN 5 - What Nerve? What lost first? What does it supply? |
Trigeminal Nerve 3 Branches = Opthalmic/Maxillary/Mandibular Supplies sensation to these three areas CORNEAL reflex is lost first
Motor = Travels with Mandibular - supplies muscles of mastication = JAW deviates TOWARDS the side of the lesion
|
|
Causes of CN5 palsy |
Sensory? = Trigeminal Neuralgia / Herpes Motor? (Rare) = Nasopharyngeal Carcinoma / Acoustic Neuroma |
|
What is CN7? |
Facial Nerve Supplies muscles of expression in the face Two major branches 1) Chorda tympani 2) Stapedius |
|
What causes a CN7 lesion? |
Fracture affecting the PETROUS bone |
|
What happens in an LMN CN7 lesion |
Ipsilateral weakness of the facial expression muscles commonest = BELLS PALSY |
|
What is Bell's Palsy |
Sudden onset unilateral facial weakness Ipsilateral numbness/pain around the ear Hypersensitive to sounds
Drooling Frontalis weakness Eyes can't close |
|
Investigation's of Bell's Palsy |
ESR Glucose Increase in Borrelia Antibodies in Lyme Disease MRI |
|
Complications of Bell's Palsy |
Synkinesis Crocodile Tears |
|
Management of Bell's Palsy? |
Prednisolone Protect Eyes = Dark glasses / Lateral Tarsorrhaphy / Artificial Tears |
|
Causes of Bell's Palsy |
HSV HIV EBV CMV Sarcoidosis Lyme Disease |
|
Other causes of LMN lesions? |
Polio Otitis Media Acoustic Neuroma Malignant parotid tumours Herpes Zoster = RAMSAY HUNT SYNDROME |
|
What is Ramsay Hunt Syndrome? |
LATENT VARICELLA ZOSTER VIRUS reactivates in the geniculate ganglion
= Painful vesicular rash on auditory canal = Loss of taste in anterior 2/3rd of tongue
Rx = ACICLOVIR / PREDNISOLONE |
|
UMN Lesion of the facial nerve? |
Weakness in the lower part of the face Upper facial muscles are SPARED (Can still lift eyebrows) Cause = Stroke / Tumour |
|
CN8 palsy- clinical features? |
Vestibulocochlear nerve
Vetibular = Equilibrium Cochlear = Hearing
Sensorineural Deafness and tinnitus Vertigo (Illusion of movement) Vomiting Nysatgmus (Pendular = poor visual fixation - Jerk Horizontal = Middle Ear - Jerk Vertical = Brain stem/Cerebellum) Ataxia C |
|
Causes of CN8 Palsy |
ACOUSTIC NEUROMA Paget's Gentamicin Meniere's disease |
|
CN9-12? |
Glossopharyngeal Vagus Accessory Hypoglossal
All usually affected together (Bulbar palsy) |
|
CN9-11 lesion causes? |
Trauma / Jugular Foramen Lesion |
|
Groups of CN's affected? |
CN8 ---> 5/6/9/10 = Cerebellopontine angle tumours (Acoustic Neuroma)
CN3/4/6 = Stroke/MS
CN3/4/5(a)/6 = Cavernous Sinus thrombosis
CN9/10/11 = Jugular Foramen Lesion |
|
5 clinical features of a space occupying lesion? |
1) RAISED ICP - Worse on walking/lying/bending forward/coughing - Vomiting / Papilloedema - As tumour grows = downward displacement of brain + pressure on stem = drowsiness/respiratory depression/coma
2) SEIZURES 3) EVOLVING FOCAL NEUROLOGY 6th nerve / 3rd nerve palsy 4) SUBTLE PERSONALITY CHANGE Irritable/Apathy/Socially inappropriate behaviourC |
|
Causes of a space occupying lesion? |
Tumour Abscess Aneurysms Chronic subdural haematoma Tuberculos |
|
5 primary brain tumours |
Astrocytoma Glioblastoma Multiforme Oligodenroglioma Ependymoma Meningioma |
|
Investigations for an SOL? |
CT/MRI
NO NO NO LP = Cerebellar tonsils will hermiate through the foramen magnum = death |
|
What is the management for an SOL? |
1) Excision + Carmustine wafers 2) Hydrocephalus? Ventriculo-peritoneal shunt 3) Glioblastoma? TEMOZOLOMIDE 4) Cerebral Oedema? Dexamethasone / Mannitol |
|
Clinical Features of a frontal lobe SOL? |
Hemiparesis Personality Change Grasp Reflex Brocca's Dysphasia Unilateral anosmia |
|
Clinical Features of a PARIETAL lobe SOL? |
Hemisensory loss Decreases 2 point discrimination Astereognosis Sensory inattention Dysphasia |
|
Clinical Features of a TEMPORAL lobe SOL? |
Dysphasia Contralateral homonymous hemianopia Amnesia |
|
Clinical Features of an OCCIPITAL lobe defect? |
Contralateral visual field defects Palinopsia Polyopia |
|
Symptoms of a Cerebellopontine angle lesion? |
Acoustic Neruoma / Vestibular Schwannoma Ipsilateral deafness Nystagmus Decreased corneal reflex Facial weakness IPSILATERAL cerebellar signs Papilloedema 6th nerve palsy |
|
What is the classic symptom of a mid-brain infarction (pineal tumour) |
Failure of up or down gaze |
|
3 ways in which micro-organisms can reach the meninges? |
Ears Nasopharynx Bloodstream |
|
5 causes of meningitis |
NHS
Neisseria Meningitides Haemophilus Influenzae Streptococcus Pneumoniae Listeria monocytogenes Cryptococcus TB (If immunocompromised) |
|
Clinical Features of Meningitis |
Initially = Headache/ Leg Pains/ Cold Hands & Feet Later= MENINGISM = Neck stiffness / Photophobia / Kernig's Sign Decreased conscious level / coma / seizures/ focal CNS signs |
|
What would you suspect if you saw a petechial rash that is NON-BLANCHING on a patient with meningitis? |
MENINGOCOCCAL SEPTICAEMIA |
|
Complications of Meningitis |
Venous Sinus Thrombosis Severe cerebral oedema Cerebral abscess |
|
Causes of VIRAL Meningitis |
Coxsackie A Coxsacke B Echovirus HSV2
Rx = Aciclovir - usually self limiting |
|
Management of Meningitis? |
At GP before hospital = BEN PEN At hospital <55 years old = IV CEFOTAXIME >55 years old = IV CEFOTAXIME + AMPICILLIN (for Listeria) |
|
Prophylaxis for meningitis? |
Rifampicin |
|
Investigations for Meningitis? |
HEAD CT SCAN U&E/FBC/LFT/ Blood Culture
|
|
If the patient is immunocompromised with meningitis, what stains do you use? |
Auramine stain = TB India ink stain = Cryptococcus |
|
What would you see in the CSF of a patient with meningitis? |
1) Bacterial? Low glucose/ Neutrophilia 2) TB = Low glucose / Lymphocytosis 3) Viral = High protein/ Lymphocytosis
4) SAH = High RBC |
|
What is encephalitis? |
Inflammation of the brain parenchyma |
|
Symptoms of encephalitis? |
Odd behaviour Headache/Fever Reduced consciousness Focal neurological deficit / Seizure Coma |
|
What is the difference between encephalopathy and encephalitis? |
Encephalopathy = NO PRODROME Encephalitis = Prodome (Fever/Rash/Lymphadenopathy) |
|
Causes of Encephalopathy |
Hypoglycaemia Hepatic encephalopathy DKA SLE |
|
Viral (most common) causes of encephalitis |
HSV1 HSV2 CMV EBV HIV Varicella-Zoster Virus
ALSO = Japanese B Encephalitis / West Nile VirusN |
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Non viral causes of encephalitis |
Any bacterial meningitis TB Malaria Listeria Lyme disease Schistosomiasis Legionella I |
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Investigations for Encephalitis? |
1) Bloods - Blood Culture / Serum for viral PCR /Malaria FIlm 2) Contrast enhanced CT 3) LP 4) EEG |
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Management for Encephalitis? |
IV ACICLOVIR |
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What causes shingles? |
After an infection with varicella zoster (chicken pox) - the virus remains dormant in: 1) DORSAL ROOT GANGLION 2) CRANIAL NERVE GANGLIA
Reactivation of the infection = Shingles |
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Clinical Features of Shingles |
Pain + Tingling in dermatomal distribution RASH = Lower thoracic region / Opthalmic division of the trigeminal Fever Malaise M |
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Management of shingles? |
IV ACICLOVIR |
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Compleciation of Shingles and Management? |
Post-Herpetic Neuralgia
Amitriptyline + Carbamazepine (or topical lidocaine patches / gabapentine)
Last resort = Ganglion ablation |