Core Knowledge Flashcards
(34 cards)
What are the key common features of Stroke?
Vision loss or visual field defect
Weakness
Aphasia
Impaired Co-Ordination (ataxia)
What are the first investigations to order in Stroke?
Non-contrast CT scan
MRI Brain
Serum Glucose - exclude hypoglycaemia
UEC - Rule out renal failure and metabolic causes
Cardiac Enzymes and ECG - exclude arrhythmia or ischaemia
FBC - Excludes anaemia or thrombocytopenia prior to possible initiation of thrombolytics, anticoagulants, or antithrombotics.
DDX of ischaemic stoke
Intracerebral haemorrhage
TIA
Hypoglycaemia
Seizure
Brain tumour
Management of Ischaemic stroke
Intravenous thrombolysis
Aspirin
What are the key features of a TIA?
By definition TIA symptoms are brief and the majority will resolve within the first hour.
Patient/caregiver report of focal neurological deficit
What are strong risk factors for TIA? (5)
AF
Valvular disease
Carotid stenosis
Congestive heart failure
Hypertension
Diabetes mellitus
Cigarette smoking
Alcohol abuse
Advanced age
How is TIA managed?
Similar to MI
Anticoagulation
Antiplatlet
Lipid Lowering Agent
Lifestyle Modification (Weight loss, smoking cess, alcohol reduction, regular exercise)
What are the key diagnostic factors of Parkinson’s disease? (5)
Presence of risk factors (advancing age, fam hx)
Bradykinesia
Resting tremour
Cogwheel Rigidity
Postural Instability
Masked facies
Hypophonia
What are the ddxs for Parkinson’s disease? (5)
Progressive supranuclear palsy (PSP)
Multiple system atrophy (MSA; formerly Shy-Drager syndrome)
Lewy body dementia
Corticobasal degeneration
Alzheimer’s disease with parkinsonism
Drug-induced parkinsonism
Metabolic abnormalities
Normal pressure hydrocephalus
How is Parkinson’s disease managed?
Levodopa (L-DOPA) mainstay therapy
Dopamine Agonists – Bromocriptine, Pergolide
Anticholinergics for tremor – Benztropine, Benzhexol
Complimentary drugs to enhance L-DOPA:
Carbidopa/Benserazide (DOPA decarboxylase inhibitor)
Tolcapone/Entacapone (COMT Inhibitor)
Selegeline – MAO-B Inhibitor
What is Progressive Supranuclear Palsy?
Parkinsonian sx and vertical gaze palsy
Tremor might not be as prominent.
Parkinsonian Symptoms. Strong sx of autonomic dysfunction especially orthostatic hypotension; UMN sx: hyperreflexia, primitive reflexes; cerebellar sx; nystagmus
Shy-Drager Syndrome
AKA Multiple Systems Atrophy
What are the Lung causes of Dyspnoea? (7)
Pneumonia
Pneumothorax
Pulmonary Embolism
Pleural Effusion
Pulmonary Cancer
Obstructive Lung Disease
COPD and Asthema
Restrictive Lung Disease
Alveolar Haemorrhage
What are the cardiac causes of Dyspnoea?
- MI
- CHF
- SYS or DIA
- Ischemic or Non-Ischemic
- All cardiomyopathies
- Pericardial tamponade
- Valve issues
- Arrhythmia
What are the cardinal features of Guillian-barre?
Preceding viral illness
Progressive symmetrical muscle weakness usually affecting lower extremities before upper extremities and proximal muscles before distal muscles accompanied by paraesthesias in the feet and hands.
Respiratory distress
Speech problems
Paraesthesia
Areflexia / Hyporeflexia
What are the investigations for Gullian Barre?
Nerve conduction studies
Lumbar puncture (LP) - elevated CSF protein with normal cell count
LFTs (AST and ALT)
Spirometry (may show reduced vital capacity)
What are the ddxs for Guillain-Barre syndrome?
Myasthenia gravis
Lambert-Eaton myasthenic syndrome (LEMS)
Botulism
Polymyositis
What is the difference between LEMS and Myasthinia Gravis?
Lambert–Eaton myasthenic syndrome is caused by autoantibodies to the presynaptic membrane.
Myasthenia gravis is caused by autoantibodies to the postsynaptic acetylcholine receptors.
LEMS improves over time.
Myasthinia Gravis fatigues.
How is Guillian-Barre treated?
IVIG
What are the cardinal features of MS?
Visual disturbance in one eye
Peculiar sensory phenomena
Female
Age 20 to 40 years
Fatigue
Urinary frequency
Bowel dysfunction
Spasticity/increased muscle tone
Increased deep tendon reflexes
What are the ddxs for MS?
Vitamin B12 deficiency
Ischaemic stroke
Guillain-Barre syndrome
Amyotrophic lateral sclerosis (ALS)
Systemic lupus erythematosus
How is MS treated? (5)
Methylprednisolone
Interferon Beta 1a/1b
Glatiramer
Fingolimod
Natalizumab
What is the pathophys of MS?
Immune-mediated inflammatory disease that attacks myelinated axons in the central nervous system, destroying the myelin and the axon in variable degrees.
Thought to be linked to T-cells crossing the BBB
What are the types of headache?
Migraine
Cluster
Tension
SAH