Misc Flashcards

1
Q

thumb printing on AXR

A

intestinal oedema/ haemorrhage

– ischaemic colitis

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2
Q

Cinchonism

A

Quinine toxicity
Quinine is an antimalarial drug also used for leg cramps

features of toxicity: cardiac arrhythmias, nausea, vomiting and tinnitus, VISUAL disturbance

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3
Q

drugs that can be cleared by haemodialysis

A

Drugs that can be cleared with haemodialysis - mnemonic: BLAST
Barbiturate
Lithium
Alcohol (inc methanol, ethylene glycol)
Salicylates
Theophyllines (charcoal haemoperfusion is preferable)

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4
Q

what is a normal ABPI value and what value suggests arterial disease?

A

a ‘normal’ ABPI may be regarded as between 0.9 - 1.2. Values below 0.9 indicate arterial disease.

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5
Q

what do ABPI values above 1.3 suggest?

A

values above 1.3 may also indicate arterial disease, in the form of false-negative results secondary to arterial calcification

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6
Q

Proteasome function

A

Along with the lysosome pathway involved in degradation of protein molecules that have been tagged with ubiquitin

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7
Q

Peroxisome function

A

Catabolism of very long chain fatty acids and amino acids
Results in the formation of hydrogen peroxide

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8
Q

Li-Fraumeni syndrome

A

A mutation in the P53 gene can cause Li-Fraumeni syndrome which can present with soft tissue sarcomas, breast carcinoma, glioblastoma, lymphoma and leukaemia. It is a rare autosomal dominant disorder.

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9
Q

stopping of anti-epileptic drugs (AED)

A

Can be considered if seizure free for > 2 years, with AEDs being stopped over 2-3 months
37%

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10
Q

Paget’s disease urine test

A
  • increased serum and urine levels of hydroxyproline
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11
Q

what CD marker Found on cytotoxic T cells is a Co-receptor for MHC class I

A

CD8

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12
Q

The main ECG abnormality seen with hypercalcaemia is

A

shortening of the QT interval

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13
Q

large volumes of 0.9% Sodium Chloride for fluid therapy risks what metabolic change?

A

hyperchloraemic metabolic acidosis

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14
Q

Motion sickness treatment

A

hyoscine > cyclizine > promethazine

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15
Q

Hepatorenal syndrome is primarily caused by

A

splanchnic vasodilation

This occurs due to the release of vasodilatory substances such as nitric oxide and prostaglandins in response to portal hypertension.

The resultant splanchnic vasodilation leads to a decrease in effective arterial blood volume, which in turn triggers activation of the renin-angiotensin-aldosterone system (RAAS) and antidiuretic hormone (ADH) secretion. These compensatory mechanisms cause renal vasoconstriction and sodium retention, leading to worsening renal function.

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16
Q

Behcet’s syndrome, HLA association

A

HLA B51

17
Q

biochemical changes with adrenaline infusion

A

Adrenaline induces hyperglycemia, hyperlactatemia and hypokalaemia

18
Q

treatment of choice for essential tremor

A

Propranolol

19
Q

Marfan’s syndrome + lower back pain associated with neurological problems such as bladder and bowel dysfunction - what manifetation?

A

dural ectasia (ballooning of the dural sac at the lumbosacral level)

20
Q

the most appropriate test to check for latent tuberculosis?

A

Mantoux test

  1. interferon gamma
21
Q

Which blood marker is first to appear during acute hepatitis B infection?

A

HBsAg

22
Q

rascburicase vs allopurinol mechanism of action

A

Rasburicase - a recombinant version of urate oxidase, an enzyme that metabolizes uric acid to allantoin

allopurinol - xanthine oxidase inhibitor so less uric acid formed

23
Q

urine dip, UTI and bacteria link

A

Gram negative organisms test positive on the nitrite test as they convert nitrates to nitrites for energy. Gram positive organisms are unable to reduce nitrate to nitrite and therefore, test negative.

24
Q

examples of live attenuated vaccines

A

BCG
measles, mumps, rubella (MMR)
influenza (intranasal)
oral rotavirus
oral polio
yellow fever
oral typhoid

do not give to immunocompromised

25
Q

Infertility in PCOS

A
  • clomifene is typically used first-line

metformin is second line

26
Q

Down’s syndrome risk

A

1/1,000 at 30 years then divide by 3 for every 5 years

27
Q

adrenaline doses

A

anaphylaxis: 0.5mg - 0.5ml 1:1,000 IM

cardiac arrest: 1mg - 10ml 1:10,000 IV
or 1ml of 1:1000 IV

28
Q

mitochondrial disease unifying finding on muscle biopsy

A

muscle biopsy classically shows ‘red, ragged fibres’ due to increased number of mitochondria

29
Q

muscle biopsy classically shows ‘red, ragged fibres’ due to increased number of mitochondria

A

mitochondrial disease

30
Q

Bisphosphonates MOA

A

inhibit osteoclasts

31
Q

the most common bacterial cause of pharyngitis (sore throat) in children and young adults.

A

Streptococcus pyogenes. This organism, also known as Group A Streptococcus (GAS), is

32
Q

people who are allergic to latex can also be allergic to which fruits

A

Latex-fruit syndrome

banana, pineapple, avocado, chestnut, kiwi fruit, mango, passion fruit and strawberry.

33
Q

vitamin B and C deficiency

A

Vitamin B1(thiamine) deficiency can cause Wernicke-Korsakoff syndrome, cardiomyopathy and peripheral neuropathy. It is not particularly associated with angular cheilitis.

Vitamin B3(niacin) deficiency causes pellagra. This constitutes diarrhoea, dermatitis and dementia. While dermatitis may manifest as angular cheilitis, there is no mention of diarrhoea in the question stem so this answer is incorrect.

Vitamin B6(pyridoxine) deficiency causes sideroblastic anaemia and peripheral neuropathy. It is mainly caused by medications such as isoniazid.

Vitamin C(ascorbic acid) deficiency causes gingivitis, bruising and poor wound healing.

34
Q

which phase determine the length of the cell cycle:

A

G1

35
Q

Yellow nail syndrome (YNS)

A
  1. yellow discolouration of the nails
  2. lymphoedema
  3. respiratory manifestations.
36
Q

A common complication of plasma exchange is

A

hypocalcaemia

which occurs as calcium is chelated by sodium citrate, the agent used as an anticoagulant during the procedure.

37
Q

Torticollis is caused by

A

contracture of the ipsilateral sternocleidomastoid muscle which leads to the chin being pushed to the opposite side.

38
Q

wilsons disease
inheritance and pathogenesis

A

Autosomal recessive
abnormal copper accumulation
low caeruloplasmin

Wilson’s disease, absence of ATP7B, also known as the Wilson’s disease protein, means caeruloplasmin cannot be correctly synthesised in hepatocytes, resulting in an effective absence in serum. copper accumulates in tissues