NEUROLOGY (ADULT) Flashcards

(230 cards)

1
Q

WHAT ARE THE CAUSES OF UNILATERAL VISUAL LOSS

A

VASCULA

OPTIC NEURITIS OR PAPILLITIS

RETINAL DETACHEMENT

VITREOUS HAEMORRAGE

RETINOPATHY AND MACULAR DEGENERATION

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2
Q

WHAT ARE SOME EXAMPLES OF VASCULAR CAUSES OF UNILATERAL VISUAL LOSS

A

OCCLUSION OF CENTRAL RETINAL ARTERY

OCCLUSION OF CENTRAL RETINAL VEIN

TEMPORAAL ARTERITIS (GIANT CELL)

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3
Q

WHAT IS ANTERIOS ISCHEMIC OPTIC NEUOPATHY

A

OCCLUSION OF POSTERIOS CILLARY ARTERY SUPPLYING THE OPTIC NERVE HEAD

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4
Q

WHAT IS ANTERIOS ISCHEMIC OPTIC NEUOPATHY ASSOCIATED WITH

A

GIANT CELL ARTERITIS

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5
Q

WHAT WOULD YOU FIND ON FUNDOSCOPY FOR ANTERIOR ISCHEMIC OPTIC NEUOPATHY

A

SWOLLEN OPTIC DISK

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6
Q

WHAT ARE THE FINDINGS ON FUNDOSCOPY OF CENTRAL RETINAL ARTERY OCCLUSION

A

A PALE RETINAL DISK W CHERRY SPOTS ON THE MACULA

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7
Q

WHAT DOES THE CENTRAL RETINAL ARTERY SUPPLY

A

THE WHOLE RETINA

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8
Q

WHAT WOULD YOU FIND ON FUNDOSCOPY OF CENTRAL RETINAL VEIN OCCLUSION

A

DILATATION OF BRANCH VEINS

COTTON WOOL PATCHES

MULTIPLE HAEMORRAGES

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9
Q

WHAT TESTS WOULD YOU USE TO DIAGNOSE UNILATERAL VISUAL LOSS

A

MRI

VISUAL EVOKED POTENTIAL

FLUORESCEIN ANGIOGRAPHY

TONOMETRY

USS

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10
Q

WHAT WOULD YOU USE TO DIAGNOSE OPTIC NEURITIS

A

MRI

VISUAL EVOKED POTENTIAL

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11
Q

WHAT WOULD YOU USE TO DIAGNOSE CENTRAL RETINAL VEIN/ARTERY OCCLUSION

A

FLUORESCEIN ANGIOGRAPHY

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12
Q

WHAT WOULD YOU USE TO MEASURE INTRAOCCULAR PRESSURE FOR GLAUCOMA

A

TONOMETRY

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13
Q

WHAT WOULD YOU USE USS TO DIAGNOSE FOR

A

VITREOUS HAEMORRAGES

RETINAL DETACHEMENT

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14
Q

WHAT IS OPTIC NEURITIS

A

INFLAMMATION OF THE OPTIC NERVE CAUSING DAMAGE AND SUBSEQUENT VISUAL LOSS

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15
Q

WHAT IS OPTIC NEURITIS ASSOCIATED WITH

A

MS

TEMPORAL ARTERITIS

SLE

LYME

SYPHILLIS

B12 DEFICIENCE

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16
Q

HOW DOES OPTIC NEURITIS PRESENT

A

DECREASED VISUAL ACUITY OVER DAYS

PAIN MOVING EYE

VISION LOSS EXACERBATED BY HEAT OR EXCERSISE

AFFERENT PUPILLARY DEFECT

INABILITY TO DISTINGUISH COULOR HUES (DYSCHROMATOPSIA)

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17
Q

HOW WOULD YOU MANAGE OPTIC NEURITIS

A

STEROIDS TO SPEED UP RECOVERY

RESOLVES ON ITS OVER AFTER AOUND 6W

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18
Q

WHAT IS OPTIC NEURITIS OFTEN A FIRST PRESENTATION FOR

A

MULTIPLE SCLEROSIS

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19
Q

WHAT IS MULTIPLE SCLEROSIS

A

A CHRONIC DEMYLENATING DISEASE WHICH IS AUTOIMMUNE AND MAY CAUSE NEURODEGENERATIVE AXONIAL LOSS

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20
Q

WHERE DO MULTIPLE SCLEROSIS LESIONS OFTEN OCCUR

A

OPTIC NERVE

BRAIN STEM

BASAL GANGLIA

SPINAL CORD

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21
Q

WHAT ARE THE OPTIC NERVE SYMPTOMS OF MULTIPLE SCLEROSIS

A

REDUCED VISUAL ACUITY OVER DAYS

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22
Q

WHAT ARE THE BASAL GANGLIA SYMPTOMS OF MULTIPLE SCLEROSIS

A

NYSTAGMUS (OFTEN CONTRALATERAL TO AFFECTED EYE)

TREMOUR

SLOWED MOVEMENTS

ATAXIA

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23
Q

WHAT ARE THE SPINAL CORD SYMPTOMS OF MULTIPLE SCLEROSIS

A

PINS AND NEEDLES

MUSCLE SPASM AND MUSCLE WEAKNESS

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24
Q

WHAT ARE THE BRAIN STEM SYMPTOMS OF MULTIPLE SCLEROSIS

A

PYRAMIDAL WEAKNESS ie muscle weakness and spastic parapesis

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25
WHAT ARE SIGNS THAT ARE ASSOCIATED W MULTIPLE SCLEROSIS
UMN LESION SIGNS * BRISK REFLEXES * SPASTIC HYPERTONIA * MUSCLE WEAKNESS * BABINKKI SIGN AND OTHER PRIMATIVE SIGNS ALSO OPTIC ATROPHY AND CEREBELLAR SIGNS IE ATAXIA AND NYSTAGMUS
26
WHAT ARE THE CRITERIA REQUIRED TO DIAGNOSE MULTIPLE SCLEROSIS
MULTIPLE CNS LESIONS PLUS 1. LESIONS ARE DISSEMINATED IN SPACE EITHER CLINICALLY OR ON MRI 2. ARE DISSEMINATED IN TIME (OVER 1 MONTHS) 3. SYMPTOMS LAST LONGER THAN 24HRS
27
WHAT IS THE INVESTIGATION OF MULTIPLE SCLEROSIS
MRI LP EVOKED POTENTIALS (VISUAL)
28
IN MULTIPLE SCLEROSIS WHAT WOULD YOU FIND ON LP
OLIGOCLONAL BANDS
29
WHAT ARE THEY TYPES OF MULTIPLE SCLEROSIS
1. BENIGN 2. RELAPSING REMITTING 3. SECONDARY CHRONIC PROGRESSIVE 4. PRIMARY PROGRESSIVE
30
DESCRIBE BENIGN MULTIPLE SCLEROSIS COURSE
NOT NEURODEGENERATIVE. HAS FLARES BUT THEN THERE WILL BE FULL RECOVERY BACK TO NORMAL LEVELS OF ABILITY
31
DESCRIBE RELAPSING REMITTING CAUSE OF MULTIPLE SCLEROSIS
SLOW STEPWISE DECLINE IN ABILITY WITH EACH FLARE. THERE IS PARTIAL RECOVERY AFTER EACH FLARE
32
DESCRIBE SECONDARY PROGRESSIVE COURSE OF MULTIPLE SCLEROSIS
AT THE START THERE IS STEPWISE DECLINE OF ABILITY WITH PARTIAL RECOVERY AFTER EACH FLARE. LATER IN THE DISEASE CAURSE THERE IS A STEADY PROGRESSIVE DECLINE IN ABILITY WITHOUT FLARES
33
DESCRIBE PRIMARY PROGRESSIVE COURSE OF MULTIPLE SCLEROSIS
A SLOW AND STEADY DECLINE IN ABILITY WITHOUT FLARES
34
WHAT IS GIANT CELL ARTERITIS
IN INFLAMMATORY DISEASE OF THE LARGE BLOOD VESSELS OF THE HEAD
35
WHAT IS THE PRESENTATION OF GIANT CELL ARTERITIS
HEADACHE JAW AND TONGUE CLAUDICATION (+POSSIBLE TONGUE NECROSIS) DECREASED VISUAL ACUITY (OPTIC NEURITIS) SUDDEN VISUAL LOSS (OPTHALMIC ARTERY OCCLUSION) PAIN AND TENDERNESS BRUSHING HAIR OR TOUCHING SCALP
36
WHAT IS GIANT CELL ARTERITIS ASSOCIATED WITH
SLE POLYMYALGIA RHEUMATICS VARICELLA RHEUMATOID ARTERITIS
37
WHAT IS THE DIAGNOSIS OF GIANT CELL ARTERITIS
BRUITS BLOODS: INCREASE IN - CRP - ALP - ESR BIOPSY OF TEMORAL ARTERY = GOLD STANDARD
38
HOW DO YOU TREAT GIANT CELL ARTERITIS
PREDNISOLONE ASAP TO AVOID BLINDNESS ALSO CAN ADD IMMUNOSUPPRESSIVE TOCILIZUMAB
39
what is the Px of proximal myopathy
struggle going up and down stairs/hills crabman syndrome proximal muscle weakness
40
what is the commonest causes of proximal myopathy
steriods in inflammatory diseases (SLE) alcohol renal/liver failure bone marrow transplants/chemo/resp diseases
41
Myesthic syndromes presentation
repeated movements causing fatigueability partial ptosis
42
treatment of myesthenic syndromes
Pyridostigmine an acetylcolinesterase inhibitor
43
what do mononeuropathies commonly affect
upper limbs
44
what is a mononeuropathy
a disease process of a named nerve
45
what are common mononeuropathies
carpel tunnel syndrome ulnar nerve palsey
46
pt reports having pain in their thumb,index and middle finger. The pain radiates down to the wrist, worse in the morning struggles to open jars, texting/taking selfies what is the diagnosis
carpel tunnel syndrome
47
what is the presentation of an ulnar nerve palsey
trouble with fine movements doing up buttons paying with coins makeup
48
what does the ulnar nerve supply
small muscles of the hands
49
how do oyu check the axillary nerve
deltoid for sensation and movement
50
when does the radial nerve usually get damaged
humerous fracture
51
what is the function of the radial nerve
flexion of the wrist
52
what nerve causes foot drop
common perineal nerve
53
what pathology usually causes a foot drop
rediculopathy
54
what are common causes of peripheral neuropathies
diabetes leprosy
55
what is the difference between ridiculopathy and neuropathy
rediculopathy is a pinched nerve. Neuropathy is a damaged nerve for whatever reason and can present similarly to a rediculopathy
56
what are the two types of symptom groups of periferal neuropathy
small fibre (C fibre) early onset symptomsburning pain, numbness Large fibres (A fibres) loss of motor function
57
what is a classic presentation of a diabeteic neuropathies
thin, dry, shiny skin, pigmented skin hair loss callusus+ulcers aka trophic changes
58
what is the presentation of vertebral pain syndrome
pain in neck, radiating to shoulder ache and discomfort decreased ROM no sensory loss or muscle weakness
59
what is vertebral pain syndrome
a myelopathy commonly caused by osteoarthritis of the neck
60
what would vertebral pain syndrome in the thoracic spine be indicative of
cancer mets wedge fracture RED FLAG!
61
what is the presentation of a rediculopathy
sharp shooting painful joins in dermatomal pattern worse on coughing or sneezing sudden onset usually after doing something manual not many neurological symptoms
62
what rediculopathy would cause bicep, thumb and index finger presentations of pins and needles, weakness
6 (biceps has 6 letters, thumb is sixth finger )
63
what nerve root would cause tricep and middle finger weakness
C7 tricep has 7 letters middle finger (8th finger) = fuck you = 8 letters
64
what rediculopathy would cause foot drop
L5 for dorsi flexion (nnervates dorsum of food)
65
what rediculopathy would cause innability to raise on tip toes
s1 innability to plantar flex s1 innervates, small toes, side of foot sole of foot
66
what normally causes rediculopathies
disc prolapse
67
what would occipital lobe disorder present as
contralateral visual disturbances
68
what would parietal lobe disorder present as
contralateral disturded sensations (not pain) impared higher sensory processes ie dysgarthia, feeling 3D of objects Dyslexia (reading)
69
what would frontal (back of) lobe disorder present as
hemiparesis
70
what would frontal (front) lobe disorder present as
personality and executive function disorders must be bilateral for Sx
71
what would basal ganglia disorders cause
if decreased Dopamine (paskinsonianism) there too high control = ridgidity if increased dopamine = dereased control causing chorea + dystonia (ie hontingtons)
72
what can cause meningism
blood (subarachnoid haemorrage) pus (infection0
73
what is the Px of meningism
headaches, photophobia, neck stiffness, N+V, systemic Sx
74
What are causes of raised IC pressure
headaches worse in morning, decreased conciousness, N+V,blurred vision (papilloedema), Double visison (paralytic squint). just not quite right
75
what can the presentation of pituitary tumour be in males
bilateral hemienopia ED less body hair gynecomastia fatgiue
76
what can the presentation of pituitary tumour be in females
bilateral hemienopia irregular periods fatigue
77
what is a migrane
a headache causing moderate to svere pain lasting from hours to days and if often preceeded by an 'aura'
78
what is the pain description of a migrane
moderate/severe throbbing + pulsating worse on moving, photophobia and aversion to sound
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what causes an aura
unregulated neuron (electic) activity on surface on the brain causing altered perceptions of sensation often lasting less than an hour
80
what associated symptoms are there with migranes
N+V tingling in arm or face speech difficulties difficulty moving limbs
81
triggers for migranes
bright lights strong smells weather changes stress lack of sleep missed meals alcohol
82
what parts of a migrain history would you ask
date of attach severiy duration treatment used deatils of associated sx
83
Ix fir migranes
MRI/CT
84
Mx of migranes
PROFYLAXIS: propranolol topiramate (antiepileptic) Amitriptyline (TCA) ACUTE: analgesia : paracetamol/aprin/ibruprofen triptans: sumatriptan (taken at onset) anti emetics: metoclopramide
85
what is a cluster headache
a severe headache which occurs on one side of the head typically around the eye. PAin lasting for 15mins to 3hrs pain tends to occur daily for a few weeks then there will be a pain free period
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sympoms of cluster headache
severely paunful one sided headache with pain ususally behind one eye/temple lasting form 15min-3hrs cranial autonomic sx agitation and restlessness 1-4 attacks every day pain usually at same times daily
87
what are cranial autonomic Sx
reddening and tearing of eye drooping of eyelid smaller pupil o one eye blocking/running on nose facial sweating or flushing
88
who typically gets cluster headaches
male 20-40 smoker/drinkier
89
what are RF for cluster headaches
poor sleep smoking alcohol
90
what causes cluster heaaches
abnormal activity of the hypothalamus
91
Mx of cluster headaches
oxygen (12-15l/min) for 15-20 min sumatriptan injections sumptriptan nasal spray
92
profylactic Mx of cluster headaches
verapamil (CCB) lithium corticosteroids GABApentin
93
what is a tension headache
constant ache that affects both sides of the head mild/moderate pain usually lasts for 30 minutes to several hours, but can last for several days.
94
triggers for tension headaches
stress and anxiety squinting poor posture tiredness dehydration missing meals lack of physical activity bright sunlight noise certain smells
95
Mx of tension headaches
Painkillers such as paracetamol or ibuprofen can be used
96
profylactic Mx of tension headaches
Regular exercise and relaxation Maintaining good posture hydrated good sleep up to 10 sessions of acupuncture over a 5- to 8-week period amitriptyline
97
what is medication overuse headache
one of the most common daily headache disorders in the world taking painkillers or triptans for as little as for 10 consecutive days a month can cause it
98
what medicines can cause MOH
caffiene paracetamol codiene triptans (eg. sumatriptan) ibruprofen and other NSAID
99
who is at risk of MOH
those with preexisting headaches such as tension/migraine
100
what are the Sx of MOH
stopping painkillers and getting headaches + poor sleep anxiety nausea
101
what is a subarachnoid haemorrhage
an uncommon type of stroke caused by bleed under the arachnoid mater (surface of the brain)
102
what is the Px of a subarachnoid haemorrhage
a sudden severe headache unlike anything you’ve experienced before a stiff neck N+V photophobia blurred vision/diplopia stroke-like symptoms * such as slurred speech and weakness on one side of the body loss of consciousness convulsions
103
what can osnet a subaracnoid haemorrage
physical effort or straining * coughing, * going to the toilet, * lifting something heavy * or having sex.
104
Ix of subarachnoid haemorrage
CT + CTA (computed tomography angiography) LP (RBC)
105
RF for subarachnoid haemorrages
known brain aneurysm smoking high blood pressure excessive alcohol consumption Severe head injurys (traumatic subarachnoid haemorrhage)
106
what is the cause of most subarachnoid haemorrages
a ruptured brain aneurysm
107
Mx of Subarachoid haemorrage
nimodipine (reduces risk of ischemia, taken for 3 weeks) morphine + combination of codeine and paracetamol. +/- anticonvulsants(phenytoin) and antiemetics (promethazine) **surgery**
108
Side effects of Nimodipine
flushing feeling sick increased heart rate headaches a rash
109
what complications can occur due to SAH
Hydrocephalus ischemia (leading to cog impairement)
110
what is myesthenia gravis
a muscular disease ausing fatiguability due to the immune system attacking neuromuscular junctions
111
Px of Myesthenia gravis
ptosis impaired swallow slurred speech (dysarthia) repetative movements causing fatiguability SOB
112
what is the staging of Myesthenia gravis
1. occular muscle weakness 2. difficulty talking + swallowing 3. resp difficulties
113
how do you Ix Myesthenia gravis
nerve conduction studies anti Ach receptor antibodies
114
how do you Mx Myesthenia gravis
galantamine (anticholinesterases) pyridostigmine (cholinesterase inhibitor) Methotrexate, rutiximab (immunosuppressants) Prednisolone (corticosteroids) Plasmaphoresis - IVIg Thyrectomy (removal of thymus)
115
what is motor neurone disease
a neurodegenerative disorder affecting motor neurons
116
name the types of MND
* ALS * amyotropic lateral sclerosis * PBP * progressive bulbar palsey * PP * pseudobulbar palsey * PMA * progressibe muscular atrophy * PLS * primary lateralising sclerosis * MMA * Monomelic amyotrophy
117
what is the pathophysiology of ALS
death of voluntary muscle neurons
118
what is the pathophysiology of PBP
neurone death of bulbar muscles (head and neck)
119
what is the pathophysiology of PP
no neuronal death but inability to control facial muscles
120
what are Sx of ALS
spastic tetraparesis wasting fasiculations muscle weakness - trouble swallowing/speakingbeing dexterous
121
what is the common cause of mortality of ALS
death usually after 3 years due to resp failure, bulbar Sx and pneumonai
122
how do you Ix MND/ALS
clinical EMG supporting evidence
123
How do you manage MND/ALS
Riluzole * inhibits glutamate release and slows progression
124
what is Guillian-Barre syndrome
an acute neuropathy
125
what is the cause of Guillian-Barre syndrome
post infections with EBV, campylobacter jejuni, CMV
126
what is the pathophysiology of Guillian-Barre syndrome
demyelination causing resp failure via molecular mimicary
127
what is the Px/natural progression of Guillian-Barre syndrome
START * numbness and tingling in arms and legs * arm and leg weakness * ptosis and swallowing difficulties * muscle pain * resp failure (1/4 of cases) END
128
how do yox Ix Guillian-Barre syndrome
LP * ++proteins nerve conduction studies serium antibodies Bloods * -Na -K (due to innapropriate secretion of antidiuretic hormone MRI
129
how do you treat Guillian-Barre syndrome
IvIg plasmaphoresis intubation daltaparin rehab phisio
130
what does the cerebellum do
controls coordination and movement
131
what can cause cerebellar disorders
Tumours / Space occupying lesions genetic disorders such as wilsons disease ataxias: * genetic/alcohol/periferal neuropathies/ gluten/ vitamin D deficiency/ auoimmune degeneration disorders ie parkinsons
132
what is the presentation of cerebellar disorders
dysdidokinesis ataxia nystagmus intention tremour scanning and speech (dysarthia) hypotonia
133
what Ix are required ffor cerebellum disorders
Bloods Mri
134
What is the management of cerbellar disorders
underlying cause : lifestyle or medication changes vit D, thymine, B12 supplments rutiximab if autoimmune
135
what is Parkinsons Disease
a common neurodegenerative disease most commonly in the elderly
136
what is the pathophysiology of Parkinsons Disease
depletion of dopamine secreting cells in substancia nigra leading to altered neural networks and +++ control from basal ganglia
137
what is the Px of Parkinsons Disease
tremour - pill rolling resting tremour ridgidity - + tone in limbs and trunk akinesia (difficulty tsarting movement) expressionless + unblinking, slow monotenous speech, micrographia postural changes - stooped gait, shuffling gait, poor blaance
138
what is the natural progression of Parkinsons Disease
neuropsychiatric Sx sleep disorders XS saliva and sweat and GI disturbances Fatigue and weightloss death (bronchopneumonia)
139
how do you Ix parkinsons disease
clinical absence of disease on MRI
140
how do you Mx Parkinsons Disease
levodopa (dopamine precurser) Ropinirole (Dopamine agonists) Seleqine (monoamine oxidase B inhibitor) Physio SSRI stereotatic neurosurgery
141
what are SE of dopamine agonists
-- impulse control
142
how do monoamine oxidase B inhibiors work
inhibit catacbolism of dopamine in brain
143
what is narcolepsy
Narcolepsy is a rare long-term brain condition that causes a person to suddenly fall asleep at inappropriate times. The brain is unable to regulate sleeping and waking patterns normally
144
what is the Px of Narcolepsy
excessive daytime sleepiness – feeling very drowsy throughout the day and finding it difficult to concentrate and stay awake sleep attacks – falling asleep suddenly and without warning cataplexy – temporary loss of muscle control, often in response to emotions such as laughter and anger sleep paralysis – a temporary inability to move or speak when waking up or falling asleep excessive dreaming and waking in the night
145
what are the DD of narcolepsy
sleep apnoea epilepsy depression hypothyroidism a previous head injury
146
how do you Dx Narcolepsy
eliminate other DD (MRI, EEG) sleep analysis Epworth sleepiness scale Polysomnography multiple sleep latency tests
147
what is polysomnography
electroencephalography (EEG), which monitors brain waves electrooculography, which monitors eye movements EMG recordings of movements in your chest and abdomen recordings of airflow through your mouth and nose pulse oximetry, ECG
148
what is the The Epworth sleepiness scale
The Epworth sleepiness scale is a questionnaire used to assess how likely it is you'll fall asleep while doing different activities. undertaken by GP to see if refferal to specialist services is necessary
149
Mx of Narcolepsy
sleep hygiene stimulants: dexamphetamine Sodium oxybate (helps control loss of muscle control) antidepressants
150
what is wernicke encephalitis
presence of neurological symptoms caused by depletion of B-vitamin reserves, in particular thiamine (vitamin B1)
151
what is the presentation of wernicke encephalitis
triad of * ophthalmoplegia usually lateral rectus palsy * ataxia * confusion
152
causes of wernecke encephalitis
alcoholics but it is also in chronically malnusrished
153
Mx of werneckes
Thiamine IM/IV until clinically better then suppliment further PO (+ B12 and other B vitamins)
154
what is korsicoff syndrome
wernicke's encephalopathy if untreated is followed by Korsakoff's syndrome.
155
what is the Px of Korsicoff
permanent: ## Footnote disorientation, confusion or mild memory loss undernutrition - for example, the person is very underweight involuntary, jerky eye movements or paralysis of the muscles that move the eyes poor balance or unsteadiness, or other signs of damage to a part of the brain called the
156
what would an MRI show of Korsicoff
shrunken cerebellum
157
What is the Mx of Korsicoff
stop alcohol intake support and care
158
what is huntingtons
is an inherited disorder that results in the death of brain cells. causing too little control over movement coordination causing hyperkinesis
159
Sx of Hyntingtons
Chorea :jerky, random, and uncontrollable movements also causing stumbling and clumsiness (this will then progess to rigidity, writhing motions or abnormal posturing) difficulty concentrating and memory lapses depression/ mood swings and personality changes / progressive cognitive impairement problems swallowing, speaking and breathing difficulty moving
160
When does Huntingotns present
25's-50's
161
what genetic mutation causes Huntingtons
Repetition of the CAG gene
162
how do you diagnose huntingtons
genetic testing
163
what is the Mx of Huntingtons
Chlorpromazine /benzos/antipsychotics (chorea- antidopaminergic/ D2 antagosist) SSRI
164
What drugs induce parkinsonism
antipsychotics (neuroleptic drugs) CCB namely cinnarizine
165
What is Trigeminal Neuralgia
Compression of CN V (trigeminal) by loops of blood vessels (rarely by tumours or MS)
166
what is the Px of Trigeminal neuralgia
function, sensation and touch affected - usually unilateral Usually caused by triggers in the trigeminal area ie shaving beards, brushing teeth Severe pain from face, teeth and mouth - feels like electric shock pain lasting around 2 minutes with a dull ache afterwards theres increased production fo saliva and tears
167
how would you investigate trigeminal neuralgia
MRI if the patient is young or the cause/presentation is unclear (patients affected are usually older women)
168
What is the managment of trigeminal neuralgia
carbamazipine glucerol injections deep brain stimulation surgical deconpression
169
What is epilepsy
recurrent tendancy to have spontaneous, intermittent and abnormal electrical ativity in a part of the brain/generalised accross the brain leading to seizures
170
what are causes of epilepsy
idiopathic stroke trauma malignancy
171
what is the presentation of temporal seizures
smell/taste abnormalities auditory phenomena lip smacking walking w/o purpose deja-vu
172
what is the Px of Frontal seizures
motor phenomena, repeated movements may lead to jacksonian march
173
what is the Px of occipital seixures
visual phenomena
174
what is the Px of parietal seizures
sensory disurbances ie tingling and numbness
175
what is the presentation of an Absence seizure
transient LoC \<10s with abrupt onset and termination kind of like daydreaming/phasing out
176
what is the Px of a myoclonic seizure
sudden brief jerking of limb/face/trunk
177
what is the Px of a Tonic seizure
sudden increase in tone often causing fall
178
what is the Px of a tonic -clonic seizure
tonic phase: LoC + increased tone clonic phase : rythmic jerking of limbs
179
what is the Px of an Atonic Seizure
no LoC sudden loss of muscle tone ie drop of hand or fall
180
how do you Ix Epilepsy
Video EEG test lactate to differentiate non - epileptic attacks
181
what is the management of a partial seizure
carbamezipine lamotragine
182
what is the management of a tonic seizure
sodiu valproate carbamezipine is wanting children
183
what is the management of an atonic seizure
sodium valproate
184
what is the management of a myoclonic seizure
sodium valproate
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what is a simple seizure
aware of what happened
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what is a complex seizure
impaired awareness of what happened
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what is status epilipticus
a medical emergency seizures lasting \>5min
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what is the managment of satus epilipticus
open and maintain airway, gain IV access Buccal midlazapam/rectal diazapam (community) IV lorazapam (hospital) phenytoin if prolonged
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what are the types of parkinsonism plus
a progressivee supranuclear palsy corticobasal degeneration multiple system atrophy dementia with lewi bodies
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what is the Px of parkinsons + progressive supranuclear palsy
parkinsonism + postural instability and falls with vertical gaze palsy. Is of a symmetrical onset and has truncal rigidity
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what is the Px of parkinsons + corticobasal degeneration
parkinsons + aparxia, aphasia and asterognosis
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what is the Px of parkinsons + multiple system atrophy
aka Shy-drager syndrome parkinsonism + autonomic dysfunction (postural hypotension, bladder dysfunction) and cerebellar signs
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what is the Px of parkinsons + dementia w lewi bodies
commonest form of parkinsons plus parkinson + variation in cognition, visual hallucination, REM sleep disturbance, orthostatic hypotension
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what is the pathophysiologies of the 4 types of parkinsonism +
progressibe supranuclear: tau tangles cotricobasal degeneration: tau tangles multiple system atrophy: cell loss w sunsequent gliosis lewi body dementia: alpha-synucelin and ubiquitin (lewi bodies)
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What is Hydrocephalus
abnormal accumulation of CSF in ventricles
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what are the types of hydrocephalus
obstructive non-obstructibe normal pressure
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describe the pathophysiology of obstructive Hydrocephalus
Impaired outflow due to lesion or stenosis causing acute drop in conciousness
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describe the pathophysiology of non-obstructive Hydrocephalus
Impaired reabsorbtion due to tumour or meningitis
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describe the pathophysiology of normal pressure Hydrocephalus
isopathic chronic ventricular enlargement with damage of long tracts (UMN lesion) spasticity, hyperreflexia, and abnormal reflexes usually in elderly
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what is the Mx of Hydrocephalus
drain peritoneal shunt
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What are causes of meningitis in neonates
GBS E COLI
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What are causes of meningitis in children
Haemophylis influenza neisseria meningitidis strep pneumoniae
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what are causes of meningitis in adults
neisseria meningitidis strep pneumoniae
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what are causes of meningitis in OAP
strep pneumoniae
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what are viral causes of meningitis
HIV enterovirus
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what are fungal causes of meningitis
candida albicans cryptococcus
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what is the Px of meningitis
headache + neckstiffness photophobia and fever if bacterial - intense malaise and fever +/- petechial rash if meningococcal
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what Ix would you perform for meningitis
blood and urine cultures LP Blood: lactate
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what is encephalitis
inflammation of the brain
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what causes encephalitis
mainly viral Mumps HSV (most commonly) Enterovirus Rabies
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How do you Ix encephalitis
MRI LP (monocytes, lymphocytes, protein)
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What is Horners syndrome
damage to Sympathetic nerves trunk that supplies face
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what causes horners syndrome
Glioma infarction neurofibromatosis T1 brachial nerve lesion Dissected internal carotid artery
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what is the presentation of horners syndrome
miosis ptosis anhydrosis (on half of face)
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Pt cant Abduct eye (lateral rectus) what Cranial nerve is involved
CN VI
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Pt cantdepress, rotate or adduct eye (superior oblique) what Cranial nerve is involved
CN IV
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Pt has deviated jaw and tongue what Cranial nerve is involved
trigeminal (deviate towards lesion)
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Pt cant open eye lid fully (ptosis) One eye always depressed and abducted (down and out) with reactive pupil what Cranial nerve is involved
CN III
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Describe Bells Palsey and the nerve its caused by
forhead, half unresponive to movement (so LMN because UMN are unaffected) CN VII
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What is LEMS = Lambert- Eaton Myasthenic syndrome
neuromuscular junctions affected Where functions of pre synaptic voltage gated Ca2+ channels is impaired by autontibodies resulting in impaired ACh release Similar to MG but with slighly different presentations
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what is the difference in presentation between MS and LEMS
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How do yo mx a myaesthenic crisis
Intubation IVIg plasma exchange
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What is a rediculopathy
mechanical compression of a nerve as it leaves the spinal cord
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What are causes of Rediculopathy
Osteopathic growth disc degeneration and lateral protrusion verebral collapse tumour growth
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what is the px of rediculopathyPa
Pain!! sensory disturbances loss of reflexes tingling and numbness in dermatomal / myotomal distribution
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what is the Ix of rediculopathy
clinical unless considering surgery then MRI
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what is the Mx of rediculopathy
Rest and analgesia surgical decompression
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what is a myelopathy
Trauma or compression of the spinal cord causing 'muscle problems'
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what are the symptoms of myelopathy
depends on tracts affected but loss of fine otor skills tingling not associated with nerve like pain back may hurt
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what are the differences between a subdural and extradural haemorrage
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