Get Ahead Flashcards

1
Q

Vasovagal syncope

A

Occurs when there is excessive activation of PNS in response to certain stimuli such as heat fear stress. PNS activity causes systemic vasodilation and bradycardia- causes hypotension and cerebral hypoperfusion.

Collapse is often preceded by nausea faintness sweating ringing in ears. May have twitching/ uriary incontinence.
Recovery rapid.

Always ask about before during after- sob dizziness chest pain tongue biting incontinence postictal paralysis parestesia.

Investigation ecg glucose by lying and standing

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2
Q

Wolf Parkinson white syndrom

A

Abnormal accessory conduction pathway that connects atria to ventricles known as bundle of Kent. Extra pathway is able to conduct atrial depolarisation of ventricle faster than av node. May trigger dangerous arrhythmias SVT, VT,VF. Patients may be a symptomatic or suffer from dizziness palpitations, chest pain, syncope and sudden cardiac death. ECG changes in WPW include a shortened PR interval wide QRS complex slurred upstroke of r wave.

Radio ablation of the accessory pathway.

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3
Q

Erbs palsy

A

Damage to upper brachial plexus involves c5 c6 nerve roots. Commonly caused by traction injuries RTA.- motorcycle.
Flaccid paralyissi of arm abductors , lateral orators of shoulder and supinators- affected arm hangs limp and is medically rotated , extended at elbow and pronanted. WAITERS TIP. Loss of sensation over the lateral arm and forearm.

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4
Q

Long thoracic nerve

A

Supplies the serrated anteror- helps to stabilise the scapula. Nerve can be damaged during breast and axillary surgery. Lesions of nerve result in winging of scapula

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5
Q

Radial nerve

A

Supplies extensor of forearm and wrist. Damage will causes an inability to extend the wrist or MCP joints- risk drop. Loss of sensation in the snuff box

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6
Q

Accessory nerve

A

Shrug shoulders- supplies traps and scm. Can be damage during dissections of the neck.

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7
Q

Axillary nerve

A

Wraps around the surgical neck of the humerus. Damaged in 5-10% of anterior dislocations and also in fractures of the numeral neck. Supplies the deltoid muscle. Damage causes regimental badge sensory loss and loss of abduction from deltoid.if lifted above 90 degrees will stay there because of supraspinous.

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8
Q

Carpal tunnel syndrome

A

Compression of the distal median nerve in carpal tunnel as it passses behind flexor retinaculum.
More common in women- pregnancy, RA and hypothyroidism.
Numbness and tingling in radial 3 1/2 digits which may be followed by wasting of the air muscles.
Titles test- taspping over median nerve at wrist- bring symptoms
Phalens test- symptoms are produced when wrist is palmerflexed fro 1 min.

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9
Q

Neuropathic ulcer

A

Small, punched out well circumscribed and painless.
Patient usually has glove and stocking syndrome- diabetes complication.

Complications; superficial infection, abscess formation and osteomyelitis

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10
Q

Autonomic neuropathy

A

In diabetes in can cause postural hypotension- cant compensate for transient drop in by on standing- cerebral hypoperfusiin and collapse.

Auto also causes erectile dysfunction, gastroparesis, urinary retention and nocturnal diarrhoea

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11
Q

Charcots joint

A

Neuropathic joint disease.
Destruction of weight bearing joints secondary to sensory neuropathy.
Ankles and knees are most commonly affected.
Repeated unnoticed trauma and abnormal stress result in cartilage, ligament synovium and bone damage- grossly deformed and unstable but painless joint.

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12
Q

Nephropathy

A

30% can develop renal failure during lifetime
Glomerular involvement ischaemia and infection
Earliest detectable sign is microalbuminuria.
ACEi and ARBs are shown to reduce the progression and contribute to be control.

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13
Q

NECROBIOSIS LIPOIDICA

A

Rare 1% patients.
Anterolateral aspect of the lower limb
Usually begins as a red small nodule that increases in size and flattens over time. Eventually it becomes depressed irregular scaly waxy and develops brownish yellowish discolouration.

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14
Q

small cell lung tumour

A

Incidence 20%
Squamous 35%
ADENO 30%
Large cell 15%

Cause horners
Ectopic ADH secretion
Ectopic adrencorticotrophic hormone 
Ectopic PTH- squamous cell
Carcinoid syndrome- right sided murmur, cutaneous flushes, apparent cyanosis, hepatomegaly, cough wheeze dyspnea, diarrhoea, cramps n.v 
Gynecomastia
EL syndrome
Clubbing
HPOA
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15
Q

CF

A

Incidence is 1 in 1500, in Ireland
Defective gene carried by 1 in 19
Caused by an abnormal CFTR located on chromo 7
Most common mutation is delta f 508
G551d mutation
Neonatal- jaundice, bowel obs or rectal prolapse
Mgmt involves physio antibiotics pancreatic enzyme supplements newer drugs eg lumacaftir/ ivacaftir
Complications; diebaetes mellitus, hepatic cirrhosis, infertility in males, servers pul htn, cor pulmonale and chronic lung infection- pseudomonas aeruginosa

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16
Q

Mesothelioma

A

Malignant Timor of the pleura.
Asbestos is the most potent cause.
20 year lag time between contact and development.
Present with chest pain and symptoms of a pleural effusion.
The effusion tends to be blood stained.
Definitive diagnosis is made by pleural biopsy.
No curative tx, radio may slow growth

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17
Q

Asbestos related lung disease

A

Asbestos can cause pleural plaque- asymptomatic calcified pleural thickening resembling holly leaves.
Asbestosis is a diffuse fibrosis of the lungs and pleura.
Develops in people who have been exposed to large amounts over years
Clinical ft clubbing progressive dyspnoea and lower zone onspiratory creeps.
No specific mgmt, steroids don’t work

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18
Q

Minimal change gloperulonephritis

A

Type of nephrotic syndrome - loss of large amounts of protein in the urine due to a leaky glomerular BM.
Fts include; proteinura, peripheral oedema, hypoalbuminemai, hypertension, hyperlipidaemia hypercoag and increased risk of infection.

In children main cause of nephrotic syndrome is minimal change glomerulnephritis >90% of cases.

On biopsy histology is normal. Tx involves steroid therapy, fluid restriction, low salt, penicillin prophylaxis and ace inhibitors to reduce proteinuri ADN STATINS.

19
Q

Membranous glomerulonephritis

A

Most common cause of nephrotic syndrome in adults.
Immune complexes are formed when circulation Ab bind to BM antigens. Immune complexes activate an IR that involves the complement cascade. Response damages the BM making it more permeable.

Usually idiopathic but may be secondary to SLE, hep , systemic infection and drugs.
Tx is same as for minimal change disease.
Prognois is variable- 1/3 recover spontaneously. 1/3 respond to IS. 1/3 end stage renal failure.

20
Q

Good pastures syndrome

A

Rare condition where autoAb are formed against the BM and the alveolar membrane.
Ab trigger a type II rxn that causes renal failure pulmonary haemorrhage and haemoptysis.
Condition is usually detected by anti glomerular BM ab in the serumand via renal biopsy.
Biopsy often shows focal or diffuse crescent Iv.
Tx witth plasmapheresis, steroids and immunosuppression.

21
Q

IgA nephropathy

A

Most common cause of primary glomerular nephritis.
IgA Ab are deposited within the mesangium and trigger an immune response via activation of the complement cascade.
IgA nephropathy maybe asymptomatic fro many years and may be discovered incidentally when dipstick showed microscopic haematuria and proteinuria.
May also present as haematura usually within 2days of an upper RTI.
Renal biopsy required for diagnosis
30% people will develop end stage renal failure.

22
Q

Post strep glomerulonephritis

A

Seen 1-2 weeks after a group A beta haemolytic strep- tonsilitis/ cellulitis.
Immune complex deposition in BM
Patients present with acute nephrotic syndrome- fluid retention, peripheral oedema ,HTN, protein and blood in ursine. Unwind is dark In colour- Pepsi urine

Management is supportive with fluid restriction and antihypertesnive meds.

23
Q

CSF Results in Cryptoccus neoformans

A

Clear fluid, low abc, neutrophils, low glucose, high protein, positive India ink stain

24
Q

CSF results in mumps

A

No organisms present, high wbc

25
Q

CSF results MS

A

No organisms, oligoclonal bands

26
Q

CSF results n meningitis

A

High neutrophils, cloudy fluid, gram neg diplodocus

27
Q

CSF results TB

A

High wbc, positive Ziegler Nielsen stain

28
Q

De quervians thyroiditis

A
Hyperthyroid initially then hypothyroid
Inflammation of the thyroid secondary to a viral infection
S&S; goitre tenderness fever flu like symptoms
Blood tests; elevated esr and crp 
TFT;  high T4, TSH suppression 
Hyper in acute
Then they become hypo
4-6 months back to euthyroid state
No tx just anti-inflammatory for pain
29
Q

Graves’ disease

A

Autoimmune IgG ab bind and stimulate TSH receptor and cause release of T4.
Graves is the only cause of thyroid eye disease
AutoAb directed against retro orb structures cause proptosis ophthalmeplegia and periobital oedema.

Heat intolerance, weight loss, anxiety, diarrhoea, tremor and palpitations.
TFT; elevated t4 and suppressed TSH , may also have a normocytic anaemia, elevated esr and deranged liver tests .

Tx; beta blockers for symptom control
Block slowly by titrating carbimazole against blood tests until enthyroid
Block fully with carbimazole and add synthetic t4

Tx withdrawn after 6months

30
Q

Hypothyroidism secondary to lithium therapy

A

Lithium used to treat bipolar disorder and affects the thyroid
Can cause goitre to from and inhibit T3 and T4.
Prior to starting Li need to exam the neck and do TFTs, majority become sub clinically hypothyroid, unless unwell tx with T4 and do TFTs every 6/12

31
Q

Hashimoto’s thyroiditis

A

Autoimmune in which thyroid gland becomes infiltrated with plasma cells and lymphocytes.

Leads to development of goitre and thyroid dysfunction.

At presentation majority are euthyroid some are hypo and minority are hyper. Up to 50% will eventually become hypo.

Serology often reveals autoab to thyroid peroxidase and thyroglobulin. Tx is with T4

32
Q

Sick euthyroid syndrome

A

Abnormal thyroid function in the presence of systemic disease.
Everything is low usually , as patient recovers TFTs usually become normal

33
Q

Hyperkalemia during blood transfusion

A

Complications include hypothermia, thrombocytopenia, hypocalcaemia, deranged clotting and hyperkalamia.

Hyperkalamia on ecg- wide qrs and peaked t waves
Give calcium gluconate as it protects the myocardium from the actions of potassium. Insulinand glucose should be prescribed to drive potassium in to the intracellular compartment.

34
Q

Lewy body dementia

A

Second most common dementia after ALzheimers.
Characteristic features include day to day fluctuating levels of cog fx, visual hallucinations, sleep disturbance and transient loss of consciousness, recurring falls and parkinsonain features (tremor hypokinesia rigidity and postural instability) .
Are Prone or hallucinations, anti psychotics should be avoided as they precipitate severe Parkinsonism in 60%.

35
Q

CJD

A

Rapidly progressive dementia caused by prions- infectious agents composed of only protein.
Features include rapid cognitive impairment which may be preceded by anxiety depression.
Later physical features become prominent including muscle disturbance- rigidity tremor wasting spasticity fasiculations cyclonic jerks and choreoathetoid movements.
Convulsions may also occur
Death occurs in 6-8month.

36
Q

New variant CJD

A

occurs secondary to ingestion of bovine spongiform encephalopathy bse infected beef.
More common in younger adults
Features are same as cjd but decline is slower
Death occurs in 18Months.
MRI pulvinar sign.

37
Q

Vascular dementia

A

Ischemic disorder characterised by multiple small cerebral infarcts in the cortex and white matter.
Beings in 60 with a stepwise deterioration of cognitive function
Focal neurology fits nocturnal confusion
Risk factors are same for any atherosclerotic disease.
Death often occurs in 5 years due to ischemic heart disease or stroke

38
Q

Frontotemporal dementia (picks)

A

Disinhibition inattention antisocial behaviour and personality changes.
Later apathy akinesia and withdrawal
Memory loss and disorientation occur only late

39
Q

Normal pressure hydrocephalus

A

Triad of dementia, gait disturbance and urinary incontinence
Caused by increase in volume of CSF with only a small change in pressure as the ventricles dilate to compensate.
There is an underlying obstruction in the sub arachnoid space that prevent CSF from being reabsorbed but allows it to flow from the ventricular system into the SAS. Diagnosis is by LP.
Treatment is with VP shunting.

40
Q

Takayasu arteritis

A

Rare granulomatojs inflammation of the aorta and its major branches
Results in poor supply to peripheries and lack of pulses.
Common in Japanese women
Systemic illness on presentation- malaise fever weight loss and arm claudication
1/3 vision disturbance
Diagnosis by angiography
Tx with steroids

41
Q

Churg Strauss syndrome

A

Rare systemic vasculitis associated with eosinophilia and asthma
Disease may be triphasic- prod Roma ladies period with rhinitis and allergies
Eosinophilia asthma / gastroenteritis
Systemic vasculitis

Associated with pANCA

Tx with steroids

42
Q

Behcets

A

Chronic vasculitis common in med and turkey
Associated with Hal b5, worse in males
Characterised by occlusive vasculitis and venulitis
Clinical diagnosis recurrent oral and genital ulceration recurrent iritis skin lesions and thrombophlebitis

Pathergy reaction

43
Q

Polymyalgia rheumatica

A

Common females over 50
Abrupt onset proximal muscle pain shoulders and hips and stiffness without weakness
Symptoms worse in morning
Tx rapid improvement with steroids

Giant cell arteritis

44
Q

Granulomatosis polyangitis

A
Wagners disease 
Classic triad of upper airway pathology - epitaxis, saddle Jose, deformity, rhinitis, deafness, proptosis 
Respiratory and renal disease 
cANCAs in 90%?
Tx with steroids and immunosuppressant