Passmed round 2 Flashcards

1
Q

What newborn complication can occur if phenytoin is given in pregnancy?

A

Phenytoin induces vitamin K metabolism, which can cause a relative vitamin K deficiency, creating the potential for hemorrhagic disease of the newborn. The most common sites of bleeding are the umbilicus, mucous membranes, gastrointestinal tract, and venepunctures.

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2
Q

What is the mechanism of action of bosentan?

A

Bosentan is a non-selective endothelin antagonist. Endothelin causes pulmonary vasoconstriction and therefore antagonists can be used to treat pulmonary hypertension. It can be associated with abnormalities in liver function tests (LFTs) and so regular LFTs are needed during treatment.

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3
Q

How is cryptosporidium diagnosed?

A

Modified Ziehl-Neelsen stain (acid-fast stain) of the stool may reveal the characteristic red cysts of Cryptosporidium

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4
Q

How can Addison’s disease cause features of androgen deficiency such as loss of pubic hair and reduced libido?

A

Dehydroepiandrosterone is the most abundant circulating adrenal steroid. Adrenal glands are the main source of dehydroepiandrosterone in females - loss of functioning adrenal tissue as in Addison’s disease may result in symptoms secondary to androgen deficiency, such as loss of libido. Research is ongoing as to whether routine replacement of DHEA is beneficial

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5
Q

Patients with allergy to sulphasalazine may also be allergic to what?

A

Aspirin

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6
Q

What supplementation should occur in bariatric bypass surgeries?

A

The duodenum is the primary site of absorption for both iron and calcium. All gastric bypass operations bypass the duodenum. Nearly all menstruating women will therefore require iron supplementation.

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7
Q

What is the mechanism of action of doxazosin?

A

Tamsulosin is alpha-1a (mainly acts on urinary tract)

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8
Q

Bombesin is a tumour marker in which malignancies?

A

Small cell lung carcinoma, gastric cancer, neuroblastoma

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9
Q

S-100 is a tumour marker in which malignancies?

A

Melanoma, schwannomas

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10
Q

What are the complications of RTA type 1?

A

nephrocalcinosis and renal stones

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11
Q

Which drugs cause drug induced acne?

A

This patient has drug-induced acne is most commonly caused by glucocorticoids and androgens but can also be precipitated by azathioprine, phenytoin, antipsychotics, and isoniazid

This typically presents as monomorphic papules and pustules with no comedones, cysts or nodules within 2 weeks of starting medication. This subset of patients will not respond to standard acne treatment, discontinuation of offending agents typically clears up the rash.

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12
Q

What is the mechanism of action of ocreotide?

A

somatostatin analogue
directly inhibits the release of growth hormone

effective in 50-70% of patients

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13
Q

What tests are used to diagnose HIV during seroconversion?

A

antibodies to HIV may not be present

HIV PCR and p24 antigen tests can confirm diagnosis

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14
Q

What are the rules about driving following syncope?

A

simple faint: no restriction
single episode, explained and treated: 4 weeks off
single episode, unexplained: 6 months off
two or more episodes: 12 months off

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15
Q

What are the rules regarding driving post stroke?

A

stroke or TIA: 1 month off driving, may not need to inform DVLA if no residual neurological deficit

multiple TIAs over short period of times: 3 months off driving and inform DVLA

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16
Q

Which HIV medication is associated with pancreatitis?

A

Purine nucleoside analogue and reverse transcriptase inhibitor

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17
Q

What is the strongest independent prognostic factor in CLL?

A

Deletion of 17p13 is the strongest independent prognostic factor for CLL. The disease progresses more rapidly and tends to be refractory to many conventional treatments.

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18
Q

What is the most common genetic aberration in CLL?

A

The most common genetic aberration in CLL is deletion of 13q. It is associated with a more indolent course of the disease improving the prognosis.

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19
Q

What is the treatment for cyanide poisoning?

A

sodium thiosulfate, hydroxocobalamin or dicobalt edetate

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20
Q

What is the treatment for myoclonic seizures?

A

sodium valproate
second line: clonazepam, lamotrigine
——————————
Carbamazepine may worsen myoclonic seizures

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21
Q

What is used for screening in latent TB

A

The Mantoux test is the main technique used to screen for latent tuberculosis.

In recent years the interferon-gamma blood test has also been introduced. It is used in a number of specific situations such as:

  • The Mantoux test is positive or equivocal
  • People where a tuberculin test may be falsely negative
  • -miliary TB
  • -sarcoidosis
  • -HIV
  • -lymphoma
  • -very young age (e.g. < 6 months)
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22
Q

What factors increase the risk of pulmonary haemorrhage in Goodpastures syndrome (anti-GBM disease)?

A
smoking
lower respiratory tract infection
pulmonary oedema
inhalation of hydrocarbons
young males
-----------------------------
In contrast dehydration actually reduces risk of pulmonary haemorrhage
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23
Q

What are the features of villous adenoma?

A

Villous adenomas are colonic polyps with the potential for malignant transformation. They characteristically secrete large amounts of mucous, potentially resulting in electrolyte disturbances.

The vast majority are asymptomatic. Possible features:

  • non-specific lower gastrointestinal symptoms
  • secretory diarrhoea may occur
  • microcytic anaemia
  • hypokalaemia
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24
Q

CA15-3 is a tumour marker in which malignancy?

A

breast

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25
Q

How do you differentiate lymphogranuloma venereum?

A

The presence of ulcers and significant rectal symptoms in a sexually active man raises the question of lymphogranuloma venereum, which is caused by a type of Chlamydia trachomatis.

Rectal infection with gonorrhoea could cause similar symptoms but would not be expected to cause ulcers.

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26
Q

Which valvular abnormality is associated with pulmonary hypertension?

A
Functional tricuspid regurgitation
----------------------------
Signs are
-pan-systolic murmur
-prominent/giant V waves in JVP
-pulsatile hepatomegaly
-left parasternal heave
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27
Q

What test can be used to test pancreatic function in suspected chronic pancreatitis?

A

Secreted by S cells in upper small intestine
Stimulated by Acidic chyme, fatty acids

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28
Q

What is fanconi syndrome?

A

Fanconi syndrome describes a generalised reabsorptive disorder of renal tubular transport in the proximal convoluted tubule resulting in:

  • type 2 (proximal) renal tubular acidosis
  • polyuria
  • aminoaciduria
  • glycosuria
  • phosphaturia
  • osteomalacia
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29
Q

What is the mechanism of action of sitagliptin?

A

Sitagliptin is an inhibitor of the enzyme dipeptidyl-peptidase 4 (DPP-4). As such, it prevents DPP-4 from catalysing the breakdown of naturally occurring incretins, potentiating their ability to stimulate insulin release.

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30
Q

What is the mechanism of pioglitazone?

A

A type of thiazolidinediones.

Activate peroxisome proliferator-activated receptor gamma (PPAR-γ) to increase insulin sensitivity

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31
Q

What is the mechanism of action of dapagliflozin?

A

Decrease blood glucose by inhibiting renal glucose re-uptake via sodium-glucose co-transporter 2 (SGLT2)

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32
Q

What is the mechanism of action of exanatide?

A

Mimic incretins by binding to GLP-1 receptors and stimulating insulin release

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33
Q

What is the treatment for face, flexural and genital psoriasis?

A

NICE recommend offering a mild or moderate potency corticosteroid applied once or twice daily for a maximum of 2 weeks

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34
Q

What is the mechanism of action of ondansetron?

A

5-HT3 antagonist

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35
Q

What is the treatment for invasive amoebiasis?

A

Treatment for invasive amoebiasis should be followed by a luminal amoebicide to eradicate the cystic stage which is resistant to metronidazole and tinidazole (which are used against the invasive stage)

e.g. 7 days of metronidazole followed by 10 days of diloxanide furoate

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36
Q

What investigation is useful in clinically unstable suspected aortic dissection?

A

Transoesophageal echocardiography (TOE) may be a useful investigation in clinically unstable patients with a suspected aortic dissection

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37
Q

When is dexamethasone used in meningitis?

A

Intravenous dexamethasone should be given prior to or with the first dose of antibiotic to reduce the risk of neurological sequelae by reducing cerebrospinal inflammation.

If pneumococcal meningitis is suspected or confirmed from clinical features, cerebrospinal fluid parameters or culture results, then dexamethasone should be continued for 4 days. It should be stopped if another causative organism is strongly suspected or confirmed

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38
Q

What is the management of hypertension in pheochromocytoma?

A

Phenoxybenzamine is a non-selective alpha-adrenoceptor antagonist and should be started before a beta-blocker is introduced

There is ongoing debate about the optimal medical management of phaeochromocytoma, with the suggestion that antihypertensive treatment regimes other than non specific alpha-blockade are just as effective and safe. There are however no trials to provide an answer to this question yet

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39
Q

What is Wellen’s Syndrome?

A

Wellens’ syndrome is an ECG manifestation of critical proximal left anterior descending (LAD) coronary artery stenosis in patients with unstable angina. It is characterized by symmetrical, often deep (>2 mm), T wave inversions in the anterior precordial leads.

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40
Q

When do patients with aortic stenosis warrant aortic valve replacement?

A

Aortic valve replacement if symptomatic, otherwise cut-off is gradient of 40 mmHg mean

Also consider if AS and reduced LVEF

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41
Q

What is Fabry Disease?

A

Fabry disease is a rare genetic disorder that prevents the body from making an enzyme called alpha-galactosidase A. Alpha-galactosidase A normally breaks down a fatty substance called globotriaosylceramide. As a result, this fatty substance builds up in the cells of your body particularly cells lining blood vessels in the skin and cells in the kidneys, heart, and nervous system.

Characteristic features of Fabry disease include episodes of pain in the hands and feet (acroparesthesia); clusters of small, dark red spots on the skin called angiokeratomas; a decreased ability to sweat (hypohidrosis); cloudiness or streaks in the front part of the eye (corneal opacity or corneal verticillata); problems with the gastrointestinal system; ringing in the ears (tinnitus) and hearing loss.

X-linked recessive

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42
Q

What is the advantage of capecitabine over flurouracil?

A

Pyrimidine analogue inducing cell cycle arrest and apoptosis by blocking thymidylate synthase (works during S phase)

Adverse effects: Myelosuppression, mucositis, dermatitis

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43
Q

What rheumatoid arthritis drugs are proven to be safe in pregnancy?

A

There is some evidence that TNF-a inhibitors may be afe but studies are poor

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44
Q

Which drug is contraindicated in ventricular tachycardia?

A

Verapamil is contraindicated in VT as intravenous administration of a calcium channel blocker can precipitate cardiac arrest.

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45
Q

What receptor type does insulin bind to?

A

Insulin binds to tyrosine kinase, a type of enzyme receptor in the cell membrane, resulting in a signal transduction cascade, activating enzymes and transcription factors within the cell that mediates the intracellular effects of insulin.

Other tyrosine kinase receptors include insulin-like growth factor (IGF) and epidermal growth factor (EGF).

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46
Q

How do you differentiate systemic mastocytosis and carcinoid syndrome?

A

Given the history of diarrhoea and flushing a diagnosis of carcinoid syndrome should be considered, which would be investigated with urinary 5-HIAA levels. This would not however explain the urticarial skin lesions. In a young person a diagnosis of systemic mastocytosis should be considered. Another factor against carcinoid syndrome is the age of the patient - the average age of a patient with a carcinoid tumour is 61 years

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47
Q

What is the mechanism of action of memantine?

A

NMDA antagonist

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48
Q

What is the strongest risk factor for cervical cancer and why?

A

Having multiple sexual partners is the strongest risk factor for the development of cervical carcinoma. This is because having multiple sexual partners greatly increases the chance of being infected with the human papilloma virus.

The 16 and 18 viral strain then triggers the carcinogenesis by inhibiting the tumor suppressor gene p53 and RB.

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49
Q

Why should allopurinol and rasburicase not be given together in tumour lysis syndrome?

A

Rasburicase is the preferred treatment choice for patients at high risk of tumour lysis syndrome.

Rasburicase is a recombinant form of urate oxidase which catalyzes the oxidation of existing uric acid to allantoin. Allantoin is more soluble than uric acid and is therefore excreted in the kidneys.

Allopurinol stops new uric acid being made by blocking the conversion of xanthines to uric acid. If less uric acid is made, this will reduce the substrate available for rasburicase to work. They should not be given together.

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50
Q

What is the mechanism of action of macrolides?

A

Erythromycin is a macrolide, which works by inhibiting the 50S subunit of ribosomes. This prevents the production of proteins from bacteria.

Macrolides are commonly confused with tetracyclines, which inhibit the 30S subunit of ribosomes

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51
Q

What are the causes of onycholysis?

A

idiopathic
trauma e.g. Excessive manicuring
infection: especially fungal
skin disease: psoriasis, dermatitis
impaired peripheral circulation e.g. Raynaud’s
systemic disease: hyper- and hypothyroidism

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52
Q

What are the contraindications to liver biopsy?

A
deranged clotting (e.g. INR > 1.4)
low platelets (e.g. < 60 * 109/l)
anaemia
extrahepatic biliary obstruction
hydatid cyst
haemoangioma
uncooperative patient
ascites
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53
Q

CCK is released by which cells?

What does it result in?

A

CCK is a peptide hormone that increases the digestion of fats and proteins. It is synthesized and released from I cells in the upper small intestine in response to increased detection of partially digested proteins and fats.

CCK results in several processes including the secretion of digestion enzymes from the pancreas, contraction of the gallbladder, relaxation of the sphincter of Oddi, decreased gastric emptying, and a trophic effect on pancreatic acinar cells all of which result in fat and protein breakdown as well as hunger suppression.

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54
Q

What drugs should be avoided in breast feeding?

A
Antibiotics: ciprofloxacin, tetracycline, chloramphenicol, Sulphonamides
Psychiatric drugs: lithium, benzodiazepines
Aspirin
Carbimazole
Methotrexate
Sulfonylureas
Cytotoxic drugs
Amiodarone
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55
Q

What are the stages of CKD?

A

1 = Greater than 90 ml/min, with some sign of kidney damage on other tests (if all the kidney tests* are normal, there is no CKD)

2 = 60-90 ml/min with some sign of kidney damage (if kidney tests* are normal, there is no CKD)

3a = 45-59 ml/min, a moderate reduction in kidney function

3b = 30-44 ml/min, a moderate reduction in kidney function

4 = 15-29 ml/min, a severe reduction in kidney function

5 = Less than 15 ml/min, established kidney failure - dialysis or a kidney transplant may be needed

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56
Q

How do you calculate the Mentzer index?

A

Mentzer index :

The index is calculated from the results of a complete blood count. If the quotient of the mean corpuscular volume (MCV, in fL) divided by the red blood cell count (RBC, in Millions per microLiter) is less than 13, thalassemia is said to be more likely. If the result is greater than 13, then iron-deficiency anemia is said to be more likely

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57
Q

What is the mechanism of pilocarpine?

A

a direct parasympathomimetic (e.g. pilocarpine, causes contraction of the ciliary muscle → opening the trabecular meshwork → increased outflow of the aqueous humour)

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58
Q

What is the management of stress urinary incontinence?

A

pelvic floor muscle training
-NICE recommend at least 8 contractions performed 3 times per day for a minimum of 3 months

surgical procedures: e.g. retropubic mid-urethral tape procedures

duloxetine may be offered to women if they decline surgical procedures

  • a combined noradrenaline and serotonin reuptake inhibitor
  • mechanism of action: increased synaptic concentration of noradrenaline and serotonin within the pudendal nerve → increased stimulation of urethral striated muscles within the sphincter → enhanced
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59
Q

What is the treatment for chlamydia?

A

Doxycycline (7 day course) if first-line

  • This is now preferred to azithromycin due to concerns about Mycoplasma genitalium.
  • This infection is often coexistant in patients with Chlamydia and there is evidence of rising levels of macrolide resistance, hence why doxycycline is preferred

If doxycycline is contraindicated / not tolerated then either azithromycin (1g od for one day, then 500mg od for two days) should be used

If pregnant then azithromycin, erythromycin or amoxicillin may be used. The SIGN guidelines suggest azithromycin 1g stat is the drug of choice ‘following discussion of the balance of benefits and risks with the patient’

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60
Q

What is the safest TCA in overdose?

A

Lofepramine

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61
Q

What are the features of Lesch-Nyhan syndrome?

A

This disease, also known as juvenile gout, is characterized by hyperuricemia. It is a genetic condition with an X-linked pattern of inheritance. It is caused by a defect in the purine salvage pathway due to the absence of the hypoxanthine-guanine phosphoribosyltransferase (HGPRT) enzyme which catalyzes the conversion of hypoxanthine to inosine monophosphate (IMP) and guanine to guanosine monophosphate (GMP). The consequence is an accumulation of uric acid. The typical findings supporting this diagnosis in this patient is the aggressive behavior, self-mutilation, intellectual impairment as well as laboratory finding of hyperuricemia

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62
Q

What is the Simon Broome criteria for diagnosis of familial hypercholesterolaemia?

A

In adults total cholesterol (TC) > 7.5 mmol/l and LDL-C > 4.9 mmol/l or children TC > 6.7 mmol/l and LDL-C > 4.0 mmol/l, plus:

  • for definite FH: tendon xanthoma in patients or 1st or 2nd degree relatives or DNA-based evidence of FH
  • for possible FH: family history of myocardial infarction below age 50 years in 2nd degree relative, below age 60 in 1st degree relative, or a family history of raised cholesterol levels
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63
Q

What finding is usually seen on ECG in myotonic dystrophy?

A

A prolonged PR interval is seen in around 20-40% of patients

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64
Q

How does peptic ulceration occur in primary hyperparathyroidism?

A

Peptic ulceration caused by hypercalcaemia which stimulate Gastrin secretion

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65
Q

What are the features of zinc deficiency?

A
perioral dermatitis: red, crusted lesions
acrodermatitis
alopecia
short stature
hypogonadism
hepatosplenomegaly
geophagia (ingesting clay/soil)
cognitive impairment
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66
Q

Coarctation of the aorta is associated with which conditions?

A

Turner’s syndrome
bicuspid aortic valve
berry aneurysms
neurofibromatosis

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67
Q

What drugs cause drug induced lupus?

A

Most common causes

  • procainamide
  • hydralazine

Less common causes

  • isoniazid
  • minocycline
  • phenytoin

Anti-histone antibodies are in 80-90%

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68
Q

How often should lithium levels be checked once established?

A

Lithium levels should be checked every 3 months once a stable dose has been achieved

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69
Q

What are the ECG features of Wolff-Parkinson White?

A

short PR interval
wide QRS complexes with a slurred upstroke - ‘delta wave’
left axis deviation if right-sided accessory pathway*
right axis deviation if left-sided accessory pathway*

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70
Q

What are the risk factors for pseudogout?

A

Patients who develop pseudogout at a younger age (e.g. < 60 years) usually have some underlying risk factor, such as:

  • haemochromatosis
  • hyperparathyroidism
  • low magnesium, low phosphate
  • acromegaly, Wilson’s disease
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71
Q

What is the treatment of discoid lupus erythematosis?

A

Discoid lupus erythematous - topical steroids → oral hydroxychloroquine

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72
Q

What is the mechanism of action of botulism?

A

Botulinum toxin inhibits the release of acetylcholine at synapses

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73
Q

What are the indications for dialysis in salicylate overdose?

A
serum concentration > 700mg/L
metabolic acidosis resistant to treatment
acute renal failure
pulmonary oedema
seizures
coma
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74
Q

Why is silica a risk factor for TB?

A

Toxic to macrophages

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75
Q

What are the causes of a normal anion gap metabolic acidosis?

A

Normal anion gap ( = hyperchloraemic metabolic acidosis)

  • gastrointestinal bicarbonate loss: diarrhoea, ureterosigmoidostomy, fistula
  • renal tubular acidosis
  • drugs: e.g. acetazolamide
  • ammonium chloride injection
  • Addison’s disease
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76
Q

What are the causes of a raised anion gap metabolic acidosis?

A

Raised anion gap

  • lactate: shock, sepsis, hypoxia
  • ketones: diabetic ketoacidosis, alcohol
  • urate: renal failure
  • acid poisoning: salicylates, methanol
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77
Q

What is the pathophysiology of methaemoglobinuria?

A

Methaemaglobinaemia is an underlying problem of EXCESSIVE oxidation of Fe2+ to Fe3+, rendering RBCs unable to bind O2.

Methaemaglobin reductase reduces methaemoglobin to haemoglobin (Fe3+ to Fe2+) by transferring electrons from NADH to methaemoglobin. Therefore congenital deficiency will cause methaemoglobinaemia.

(OIL RIG - Oxidation is loss, Reduction is gain)

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78
Q

What are the characteristic side effects of indinavir?

A

renal stones, asymptomatic hyperbilirubinaemia

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79
Q

t(14:18) is associated with which malignancy?

A

The t(14;18) translocation causes increased BCL-2 transcription and causes follicular lymphoma

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80
Q

What translocation occurs in Ewing’s sarcoma?

A

t(11;22) is a translocation which occurs in Ewing sarcoma. This is a malignant bone tumour which often occurs in individuals under 15 years of age. The disease is known to be very aggressive and is associated with the development of early metastases

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81
Q

t(12;15) is associated with which cancer?

A

t(12;15) is associated with the development of breast cancer, more specifically secretory breast carcinoma. This type of breast cancer is known to be rare and the clinical outcome following is usually good.

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82
Q

What is the conversion of codeine to oral morphine?

A

Divide by 10

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83
Q

What drugs should be avoided in WPW and AF?

A

Wpw with Afib: Avoid drugs which prolong av delay

e.g V BAD: Verapamil, B-blocker Adenosine, Digoxin

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84
Q

What is the mechanism of action of digoxin?

A

inhibits the Na+/K+ ATPase pump

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85
Q

How does ticagrelor cause breathlessness?

A

Dyspnoea is a common side effect of ticagrelor and is estimated to occur in up to 15% of patients started on this medication. It is hypothesised that the sensation of dyspnoea in ticagrelor-treated patients is triggered by adenosine, because ticagrelor inhibits its clearance (by inhibiting the enzyme adenosine deaminase), thereby increasing its concentration in the circulation. It is important to be aware of this side effect in order to avoid unnecessary treatment and/or investigation, as it is easily remedied by switching the patient to clopidogrel

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86
Q

What electrolyte abnormalities are seen in Addison’s disease?

A

hyperkalaemia
hyponatraemia
hypoglycaemia
metabolic acidosis

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87
Q

What are the causes of Chorea?

A
Huntington's disease, Wilson's disease, ataxic telangiectasia
SLE, anti-phospholipid syndrome
rheumatic fever: Sydenham's chorea
drugs: oral contraceptive pill, L-dopa, antipsychotics
neuroacanthocytosis
pregnancy: chorea gravidarum
thyrotoxicosis
polycythaemia rubra vera
carbon monoxide poisoning
cerebrovascular disease
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88
Q

What is the treatment of Thrombotic Thrombocytopenic Purpura?

A

no antibiotics - may worsen outcome
plasma exchange is the treatment of choice
steroids, immunosuppressants
vincristine

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89
Q

What is the pathogenesis of homocystinuria?

A

Homocystinuria is caused by a deficiency of cystathionine beta synthase

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90
Q

What is the most sensitive clinical sign in hypocalcaemia?

A

Hypocalcaemia: Trousseau’s sign is more sensitive and specific than Chvostek’s sign

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91
Q

What is the management of Guttate psoriasis?

A

Most cases resolve spontaneously within 2-3 months
(there is no firm evidence to support the use of antibiotics to eradicate streptococcal infection)

Topical agents as per psoriasis

UVB phototherapy

Tonsillectomy may be necessary with recurrent episodes

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92
Q

What are the British Journal of Haematology Guidelines in patients on warfarin having emergency surgery:

A
  • If surgery can wait for 6-8 hours - give 5 mg vitamin K IV

- If surgery can’t wait - 25-50 units/kg four-factor prothrombin complex

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93
Q

What conditions cause a false positive VRDL/RPR?

A

False positive VDRL/RPR: ‘SomeTimes Mistakes Happen’ (SLE, TB, malaria, HIV)

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94
Q

What is the prevalence of rheumatoid arthritis in the UK?

A

1%

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95
Q

What are the causes of papillary necrosis?

A
chronic analgesia use
sickle cell disease
TB
acute pyelonephritis
diabetes mellitus
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96
Q

What are the side effects of checkpoint inhibitors?

A

Novel immunotherapy drugs that target checkpoint inhibitors leads to reduced checkpoint inhibition. This keeps the immune system activated and thus potentiating anti-tumour effects. However, it is important to realise, as a consequence, there is reduced self-tolerance and auto-immune side effects occur. Prominently
- Thyroiditis
- Hypophysitis
- Adrenalitis
- Brittle diabetes (T1)

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97
Q

What is the genetics of alport syndrome?

A

X-linked dominant

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98
Q

What antibody is a marker of development of ILD in polymyositis?

A

The anti-Jo-1 antibody is a predictor of the presence of ILD at diagnosis, with up to 70% of patients with the antibody having concurrent ILD. The 5-year survival rate is between 60 and 80%.

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99
Q

What motor neurone disease carries the worst prognosis?

A

Progressive bulbar palsy?

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100
Q

What are the features of Pseudoxanthoma elasticum?

A

Pseudoxanthoma elasticum is an inherited condition (usually autosomal recessive*) characterised by an abnormality in elastic fibres.

  • retinal angioid streaks
  • ‘plucked chicken skin’ appearance - small yellow -papules on the neck, antecubital fossa and axillae
  • cardiac: mitral valve prolapse, increased risk of -ischaemic heart disease
  • gastrointestinal haemorrhage
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101
Q

How do you determine the cause of a lesion in bitemporal hemianopia?

A

upper quadrant defect > lower quadrant defect = inferior chiasmal compression, commonly a pituitary tumour

lower quadrant defect > upper quadrant defect = superior chiasmal compression, commonly a craniopharyngioma

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102
Q

What are the common causes of environmental asthma?

A

GF works at PEPSI factory and comes home every day with asthma symptoms:

-GF— Glutaraldehyede. Flour

PEPSi :

  • Platinum salt
  • Epoxy resins
  • Proteiolytic enzymes
  • Soldering flux resins
  • Isocynayes
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103
Q

What is the treatment of hiccups in palliative care?

A

chlorpromazine or haloperidol

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104
Q

What is the difference in side effects for sulphasalazine and mesalazine?

A

Sulphasalazine

  • A combination of sulphapyridine (a sulphonamide) and 5-ASA
  • Many side-effects are due to the sulphapyridine moiety: rashes, oligospermia, headache, Heinz body anaemia, megaloblastic anaemia, lung fibrosis
  • Other side-effects are common to 5-ASA drugs (see mesalazine)

Mesalazine
-A delayed release form of 5-ASA
-Sulphapyridine side-effects seen in patients taking sulphasalazine are avoided
————————–
Common to both 5-ASA
-GI upset, headache, agranulocytosis, pancreatitis*, interstitial nephritis

*Pancreatitis is 7 times more common in patients taking mesalazine than sulfasalazine

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105
Q

How do you differentiate radial tunnel syndrome from lateral epicondylitis?

A

Radial tunnel syndrome presents similarly to lateral epicondylitis however pain is typically distal to the epicondyle and worse on elbow extension/forearm pronation

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106
Q

What are the criteria for gestational diabetes?

A

“5678”

Either:

  • fasting glucose is >= 5.6 mmol/L
  • 2-hour glucose is >= 7.8 mmol/L
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107
Q

What starting insulin regimens are recommended by NICE for type 1 and type 2 DM?

A

Type 1 - try basal bolus first. 2nd line twice daily ‘mixed’.

Type 2 - Start with isophane once or twice daily

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108
Q

What is the pathophysiology of hepatorenal syndrome?

A

Hepatorenal syndrome is primarily caused by splanchnic vasodilation

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109
Q

What are the cut-offs for bariatric surgery under NICE?

A

Obesity - NICE bariatric referral cut-offs

  • with risk factors (T2DM, BP etc): > 35 kg/m^2
  • no risk factors: > 40 kg/m^2
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110
Q

What is the management of methaemoglobinuria?

A

NADH - methaemoglobinaemia reductase deficiency: ascorbic acid

IV methylthioninium chloride (methylene blue) if acquired

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111
Q

In general what are the 2 causes of nephrotic syndrome in adults?

A

FSGS

Membranous glomerulosclerosis

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112
Q

What are the guidelines for controlling high INR on warfarin?

A

Major bleed: stop warfarin.
Give prothrombin complex . give vit k

Minor bleeding : stop warfarin
. Give vitamin k

No bleeding : manage according to INR

5:8 …..hold 2 doses &reduce dose
8:12 …. hold warfarin & give vit k 2.5 mg
More than 12 …..hold warfarin & give vitk 5 mg

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113
Q

Donepazil is relatively contraindicated in what?

A

Bradycardia

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114
Q

What antibiotics increase the risk of acquisition of MRSA?

A

Although ciprofloxacin is not a beta-lactam antibiotic, its use is strongly linked to the acquisition of MRSA as with all quinolone antibiotics.

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115
Q

What MRI finding can be seen in Wernicke’s encephalopathy?

A

The MRI finding of enhancement of the mamillary bodies due to petechial haemorrhages is specific for Wernicke’s encephalopathy, although sensitivity is only 50%.

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116
Q

How do you calculate the standard error of the mean?

A

Standard error of the mean = standard deviation / square root (number of patients)

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117
Q

Which anti-epileptic is contraindicated in absence seizures?

A

Carbamazepine is contraindicated and can worsen absence seizures (along with phenytoin, vigabatrin and gabapentin)

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118
Q

What drugs should be avoided in HOCM?

A

nitrates
ACE-inhibitors
inotropes

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119
Q

What test do you use to ensure eradication in H. Pylori infection?

A

Urea breath test is the only test recommended for H. pylori post-eradication therapy

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120
Q

What are the poor prognostic factors Guillain-Barre syndrome?

A
age > 40 years
poor upper extremity muscle strength
previous history of a diarrhoeal illness (specifically Campylobacter jejuni)
high anti-GM1 antibody titre
need for ventilatory support
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121
Q

What are the causes of pseudohyperkalaemia?

A

Haemolysis during venipuncture (excessive vacuum of Blood drawing, prolonged tourniquet use or too fine a needle gauge)

Delay in the processing of the blood specimen

Abnormally high numbers of platelets, leukocytes, or erythrocytes (such as myeloproliferative disorders)

Familial causes

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122
Q

What are the features of Tay-Sachs Disease?

A

Tay-Sachs disease typically presents with developmental delay and cherry red spot on the macula, without hepatomegaly or splenomegaly.

This can present after 3 months of age as hypotonia, muscle weakness and myoclonic jerks and then progress to psychomotor retardation and regression, muscle spasticity, recurrent seizures, dementia and eventual death in early childhood. The cherry red spot in the macular is present in 90%.

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123
Q

What are the features of Dural Ectasia?

A

Dural ectasia affects around 60% of patients with Marfan’s syndrome. It may cause lower back pain associated with neurological problems such as bladder and bowel dysfunction.

124
Q

What are the investigations in lead poisoning?

A

The blood lead level is usually used for diagnosis. Levels greater than 10 mcg/dl are considered significant

Full blood count: microcytic anaemia. Blood film shows red cell abnormalities including basophilic stippling and clover-leaf morphology

Raised serum and urine levels of delta aminolaevulinic acid may be seen making it sometimes difficult to differentiate from acute intermittent porphyria

Urinary coproporphyrin is also increased (urinary porphobilinogen and uroporphyrin levels are normal to slightly increased)

125
Q

What is the difference in potency between clobetasone butyrate 0.05% and clobetasol propionate 0.05%?

A

Clobetasone butyrate 0.05% (moderate) and Clobetasol propionate 0.05% (very potent)

126
Q

What is the mechanism of action of orlistat?

A

Orlistat works by inhibiting gastric and pancreatic lipase to reduce the digestion of fat

127
Q

What are the circumstances under which parathyroidectomy should be considered in primary hyperparathyroidism?

A

Age under 50 years.

Adjusted serum calcium concentration that is 0.25 mmol/L or more above the upper end of the reference range.

Estimated glomerular filtration rate (eGFR) less than 60 mL/min/1.73 m2 although this threshold depends on other factors, such as age.

Renal stones or presence of nephrocalcinosis on ultrasound or CT.

Presence of osteoporosis or osteoporotic fracture.

Symptomatic disease

128
Q

What are the Keith-Wagener stages of hypertensive retinopathy?

A

I = Arteriolar narrowing and tortuosity
Increased light reflex -silver wiring

II = Arteriovenous nipping

III = Cotton-wool exudates
Flame and blot haemorrhages

IV = Papilloedema

129
Q

What are the features of Anti-synthetase syndrome?

A

Anti-synthetase syndrome is related to dermatomyositis/polymyositis.

Findings include relatively acute disease onset, constitutional symptoms (eg, fever and weight loss), myositis, the Raynaud phenomenon, mechanic’s hands, arthritis that is generally nonerosive, and interstitial lung disease. Patients have antibodies towards tRNA synthetase.

Consider the diagnosis if antisynthetase Ab positive PLUS 2 of the following: ILD, inflammatory myopathy, inflammatory polyarthritis.

130
Q

What is the treatment for keloid scars?

A

early keloids may be treated with intra-lesional steroids e.g. triamcinolone
excision is sometimes required

131
Q

S4 coincides with which part of the ECG

A

An S4 heart sound occurs in late diastole where there is active left ventricular filling when atrial contraction forces blood into a noncompliant left ventricle. The P wave represents the depolarization of the left and right atrium, which results in atrial contraction. Hence, S4 coincides with the P wave of the ECG.

132
Q

What is the equation for variance?

A

Variance = square of standard deviation

Therefore Standard deviation = square root variance

133
Q

What is the treatment for inducing remission in crohns disease?

A

1) Glucocorticoid/Budesonide to induce remission
1b) 5-ASA (Mesalazine) is second in line to induce remission

2) Azathioprine/Methotrexate/Mercaptopurine can be used as add on to steroid (not monotheraphy)
3) Infliximab finally

134
Q

Which drugs cause drug induced thrombocytopenia?

A

Quinine

Abciximab

NSAIDs

Diuretics: furosemide

Antibiotics: penicillins, sulphonamides, rifampicin

Anticonvulsants: carbamazepine, valproate
heparin

135
Q

What are the genetics of CADASIL?

A

It is, as implied by the name, an autosomal dominant condition caused by a NOTCH3 mutation on chromosome 19.

CADASIL (also known as cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) is the most common cause of hereditary cerebral small-vessel disease and vascular cognitive impairment in young adults.

Characteristically, this presents with a migraine with aura, and a family history of such, which can ultimately lead to stroke-like features and is a recognised important cause of stroke in the young. Brain imaging will reveal multiple subcortical white matter lesions, particularly in the anterior temporal lobes and basal ganglia, out of keeping with the patient’s age.

136
Q

What is the treatment for melioidosis?

A

IV ceftazidime.

Melioidosis is a severe, bacterial infection caused by Burkholderia pseudomallei and is common in East Asia and Northern Australia.

It can present with localised or septicaemic disease with the lung being the most common site of localised disease. Diabetes is a strong risk factor both for acquiring melioidosis and for developing severe disease.

The bacteria is inherently resistant to many antibiotics and for severe disease ceftazidime or a carbapenem should be used. Intravenous treatment should last for at least 10 days and should be followed by an oral maintenance phase of at least 20 weeks to reduce the risk of relapse.

137
Q

Where do thiazide diuretics have their effect?

A

inhibiting sodium reabsorption at the beginning of the distal convoluted tubule (DCT) by blocking the thiazide-sensitive Na+-Cl− symporter.

138
Q

What are the features of acute interstitial nephritis?

A

Acute interstitial nephritis (AIN) typically arises following drug therapy in the majority of cases (~75%), with infections and systemic vasculitides forming the rest. The most common drug causes include: non steroidal anti-inflammatories (NSAIDs), penicillins, sulphur-based medications, proton pump inhibitors (PPIs), ciprofloxacin and allopurinol.

Definitive diagnosis is done by renal biopsy, which is typically reserved for when the diagnosis is unclear or if another aetiology is suspected to occur concurrently/in equal likelihood. Management involves stopping the offending agent, with severe cases requiring steroids and potentially dialysis.

139
Q

What are the x-ray features of ankylosing spondylitis?

A

Subchondral erosions, sclerosis

and squaring of lumbar vertebrae

140
Q

How do you manage hypothyroidism in pregnancy?

A

Increase thyroid hormone replacement dose by up to 50% as early as 4-6 weeks of pregnancy.

141
Q

What is the treatment of prinzmetal angina?

A

Dihydropyridine calcium channel blocker

142
Q

What biochemical abnormalities cause acute pancreatitis?

A

Hypertriglyceridaemia, Hyperchylomicronaemia, Hypercalcaemia

143
Q

What is the current first line treatment in HIV?

A

The current BHIVA (British HIV Association) guidelines recommend bictegravir/tenofovir–alafenamide/emtricitabine - ‘Biktarvy’ - as first-line treatment for HIV in the absence of contraindications and drug-drug interactions. This regimen has a high barrier to resistance and is the optimal choice during the coronavirus pandemic where access to baseline testing for resistance may be less than normal. This patient has normal renal and hepatic function and is not on any other medications. Therefore, this combination is the typical initial choice.

144
Q

What are the indications for total parathyroidectomy in primary hyperparathyroidism?

A

Refer for surgery if primary hyperparathyroidism is confirmed and the patient has:
• Polydipsia, polyuria or constipation.
• Osteoporosis, fragility fracture or nephrolithiasis.
• Albumin-adjusted serum calcium is ≥ 2.85 mmol/L.

145
Q

What are the features of Kearns-Sayre syndrome?

A

Mitochondrial inheritance
Onset < 20-years-old
External ophthalmoplegia
Retinitis pigmentosa

146
Q

How do you treat mycobacterium avium complex?

A

rifampicin + ethambutol + clarithromycin

147
Q

What organs are retro-peritoneal?

A
Suprarenal (adrenal glands)
Aorta
Duodenum
Pancreas
Ureters
Colon
Kidneys
Esophagus
Rectum
148
Q

What are the features of Neuromyelitis optica?

A

Neuromyelitis optica which is also known as Devic’s disease is an autoimmune disorder in which immune system cells and antibodies attack the optic nerves and the spinal cord. The pathophysiology is still however completely unclear. The diagnosis of neuromyelitis optica is determined as follows:

Absolute criteria:

  • Optic neuritis
  • Acute myelitis

Supportive criteria:

  • Brain MRI not meeting criteria for MS at disease onset
  • Spinal cord MRI with contiguous T2-weighted signal abnormality extending over three or more vertebral segments
  • NMO-IgG seropositive status (The NMO-IgG test checks the existence of antibodies against the aquaporin 4 antigen.)

Compared to multiple sclerosis, the acute episodes are not understood to be triggered by the immune system’s T cells, but rather by antibodies called NMO-IgG.

149
Q

What are the differences between Pemphigus Vulgaris and Bullous Pemphigoid?

A

Pemphigus Vulgaris:
Rare and life threatening
IgG Autoantibodies to Desmoglein (Dsg3)
Dsg3 is an adhesion molecule between epidermal cells
Antibodies disrupt adhesion causing INTRA-epidermal blistering
Affects mucosa and skin

Bullous Pemphigoid:
More common than Pemphigus Vulgaris
Less aggressive and generally not life threatening
IgG antibodies to BP180 and/or BP 230, components of hemidesmosomes
BP180 anchors hemidesmosomes to lamina densa of basement membrane
Blistering is SUB-epidermal

Investigation for Both:
Skin Punch Biopsy
ELISA in specialist setting/centres

Management:
Pemphigoid Vulgaris: Oral Steroids
Bullous Pemphigoid: Topical Steroids
In both further treatments –> Immunosuppression / Plasmapheresis

150
Q

What are the 2 main parts of antibodies (immunoglobulins)?

A

Fab region: antigen-binding fragment - the region that binds to antigens

Fc region: fragment crystallizable region - the tail region of an antibody that interacts with cell surface receptors

151
Q

How does pulmonary capillary wedge pressure work?

A

Pulmonary capillary wedge pressure (PCWP) is measured using a balloon tipped Swan-Ganz catheter which is inserted into the pulmonary artery. The pressure measured is similar to that of the left atrium (normally 6-12 mmHg).

One of the main uses of measuring the PCWP is determining whether pulmonary oedema is caused by either heart failure or acute respiratory distress syndrome.

In many modern ITU departments PCWP measurement has been replaced by non-invasive techniques.

152
Q

Where is the medial longitudinal fasciculus located?

A

Internuclear ophthalmoplegia is a disorder of conjugate gaze with the failure of adduction seen on the affected eye. This is caused by injury on the medial longitudinal fasciculus, located along the paramedian area of the midbrain and pons. In younger patients, lesions can be caused by multiple sclerosis but older populations can get this due to strokes. Convergence is maintained as this does not involve the medial longitudinal fasciculus. Convergence is mediated by the oculomotor nerve and the Edinger-Westphal nucleus.

153
Q

What are the features of relapsing polychondritis?

A

Relapsing polychondritis is a rare autoimmune disorder characterised by recurrent episodes of inflammation and destruction of cartilaginous tissues resulting in widespread chondritis of the auricular, nasal, and tracheal cartilages as described in this case. Clinical features can include recurrent chondritis of the laryngotracheobronchitis tree and potentially end up with life-threatening laryngotracheal stenosis.

154
Q

Cat scratch disease is confirmed by which methods?

A

Bartonella henselae causes cat scratch disease. Patients typically develop low-grade fever, fatigue and malaise and regional ipsilateral lymphadenopathy. Diagnosis can be confirmed by microbiology through serology or culture, or histopathology through visualisation of bacilli in Warthin-Starry staining.

155
Q

What are the mitochondrial inherited diseases?

A

Leber’s optic atrophy

MELAS syndrome: mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes

MERRF syndrome: myoclonus epilepsy with ragged-red fibres

Kearns-Sayre syndrome: onset in patients < 20 years old, external ophthalmoplegia, retinitis pigmentosa. Ptosis may be seen

sensorineural hearing loss

156
Q

What organism causes granuloma inguinale?

A

Klebsiella granulomatis (previously called Calymmatobacterium granulomatis)

157
Q

What are the genetics of Neurofibromatosis?

A

NF1: chromosome 17 - as neurofibromatosis has 17 characters

NF2: chromosome 22 - all the 2’s

158
Q

What electrolyte abnormality does copious NaCl 0.9% cause?

A

Large volume resuscitation with normal saline leads to an overload of chloride ions into the blood. The increased chloride ions, force bicarbonate into the cells and in doing so reduce the available bicarbonate for the pH buffering system.

The result is a hyperchloraemic metabolic acidosis.

159
Q

How do your divide the causes of peripheral neuropathy?

A

Predominately motor loss

  • Guillain-Barre syndrome
  • porphyria
  • lead poisoning
  • hereditary sensorimotor neuropathies (HSMN) (Charcot-Marie-Tooth)
  • chronic inflammatory demyelinating polyneuropathy (CIDP)
  • diphtheria

Predominately sensory loss

  • diabetes
  • uraemia
  • leprosy
  • alcoholism
  • vitamin B12 deficiency
  • amyloidosis
160
Q

How do you treat hereditary angiodema?

A

IV C1-inhibitor concentrate, fresh frozen plasma (FFP) if this is not available

prophylaxis: anabolic steroid Danazol may help

161
Q

What are the diabetic nephropathy stages?

A

Stage 1: Hyperfiltration
Stage 2: Silent
Stage 3: Microalbuminuria
Stage 4: Proteinuria

162
Q

What antibiotic is used in cholera?

A

Doxycycline

163
Q

What are the cut offs for impaired fasting glucose and impaired glucose tolerance?

A

A fasting glucose greater than or equal to 6.1 but less than 7.0 mmol/l implies impaired fasting glucose (IFG)

Impaired glucose tolerance (IGT) is defined as fasting plasma glucose less than 7.0 mmol/l and OGTT 2-hour value greater than or equal to 7.8 mmol/l but less than 11.1 mmol/l

164
Q

What are the clinical features of varient Creutzfeldt-Jakob disease (vCJD)?

A

The typical presentation is that of a younger patient with progressive dementia (less rapid the sporadic CJD) with myoclonus and, in the later stages, mutism and vertical upgaze palsy (found in 50%). An MRI brain reveals a characteristic ‘hockey stick sign’ where the pulvinar region and dorsomedial thalamus are hyperintense on T2-weighted imaging (or pulvinar sign where the pulvinar region is hyperintense only). CSF protein for 14-3-3 and periodic sharp wave complexes on the EEG are more commonly seen in sporadic CJD.

165
Q

What B vitamin is niacin?

A

B3

166
Q

What are the diagnostic criteria for ARDS?

A

Criteria (American-European Consensus Conference)

  • acute onset (within 1 week of a known risk factor)
  • pulmonary oedema: bilateral infiltrates on chest x-ray (‘not fully explained by effusions, lobar/lung collapse or nodules)
  • non-cardiogenic (pulmonary artery wedge pressure needed if doubt)
  • pO2/FiO2 < 40kPa (200 mmHg)
167
Q

What is the mechanism of action of Dipyridamole?

A

generally described as a non-specific phosphodiesterase (PDE) inhibitor but it is known to be particularly active against PDE5 (like sildenafil) and PDE6.

168
Q

What are the functions of the different interleukins?

A

HOT T-BONE stEAk BiN IT Now.

HOT (IL1 - fever)
T (IL2 T cell stim)
BONE (IL3 stimulates bone marrow)
E (IL4 - IgE and B cell stim)
A (IL5 - IgA and eosinophils)

B (IL6 - B cell stim)
N (IL8 - Neutrophil chemotaxis)
IT (IL10 - Inhibs Th1 cells)
N - (IL12 - NK stim + T0 -> Th1)

169
Q

What are the features of Fabry’s disease?

A
FABRY'C disease:
F - foggy lens
A - angiokeratomas
B - burning pain
R - renal failure
Y - youth death
C - CV malformation
170
Q

How is lassa fever spread?

A

Ribavarin is used to treat

171
Q

What immunological changes are seen in progressive HIV?

A

Reduction in CD4 count

Increase B2-microglobulin

Decreased IL-2 production

Polyclonal B-cell activation

Decrease NK cell function

Reduced delayed hypersensitivity responses

172
Q

Give examples of type II hypersensitivity reaction

A
  • Autoimmune haemolytic anaemia
  • ITP
  • Goodpasture’s syndrome
  • Pernicious anaemia
  • Acute haemolytic transfusion reactions
  • Rheumatic fever
  • Pemphigus vulgaris / bullous pemphigoid
173
Q

Give examples of type III hypersensitivity reaction

A
  • Serum sickness
  • Systemic lupus erythematosus
  • Post-streptococcal glomerulonephritis
  • Extrinsic allergic alveolitis (especially acute phase)
174
Q

Give examples of type IV hypersensitivity reaction

A
  • Tuberculosis / tuberculin skin reaction
  • Graft versus host disease
  • Allergic contact dermatitis
  • Scabies
  • Extrinsic allergic alveolitis (especially chronic phase)
  • Multiple sclerosis
  • Guillain-Barre syndrome
175
Q

Give examples of type V hypersensitivity reaction

A
  • Graves’ disease

* Myasthenia gravis

176
Q

Give some examples of extracellular signals which work on G protein-coupled receptors

A

activated by a wide variety of extracellular signals e.g. Peptide hormones, biogenic amines (e.g. adrenaline), lipophilic hormones, light

177
Q

What is the pathophysiology of clostridium tetani?

A

Produces an exotoxin (tetanospasmin) that prevents the release of glycine from Renshaw cells in the spinal cord causing a spastic paralysis

178
Q

What is the pathophysiology of clostridium perfringes?

A

produces α-toxin, a lecithinase, which causes gas gangrene (myonecrosis) and haemolysis

features include tender, oedematous skin with haemorrhagic blebs and bullae. Crepitus may present on palpation

179
Q

Why has the use of B-blockers for hypertension declined in the last 5 years?

A

Less likely to prevent stroke and potential impairment of glucose tolerance.

This was demonstrated in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA).

180
Q

What are the features of pseudohypoparathyroidism?

A

-Target cells being insensitive to PTH
-Due to abnormality in a G protein
-Associated with low IQ, short stature, shortened 4th and 5th metacarpals
-Low calcium, high phosphate, high PTH
diagnosis is made by measuring urinary cAMP and phosphate levels following an infusion of PTH.
—In hypoparathyroidism this will cause an increase in both cAMP and phosphate levels.
—In pseudohypoparathyroidism type I neither cAMP nor phosphate levels are increased whilst in pseudohypoparathyroidism type II only cAMP rises.
—————————–
Pseudopseudohypoparathyroidism has features of pseudohypoparathyroidism but normal biochemistry

181
Q

What percentage of values lie in the SD of a normal distribution (up to 3 SD)?

A
  1. 3% of values lie within 1 SD of the mean
  2. 4% of values lie within 2 SD of the mean
  3. 7% of values lie within 3 SD of the mean
182
Q

What are the rotator cuff muscle?

A

SItS (small t for teres minor)

Supraspinatus - aBDucts arm before deltoid
Infraspinatus - Rotates arm laterally
teres minor - aDDucts & rotates arm laterally
Subscapularis - aDDuct & rotates arm medially

183
Q

What is the mechanisms of action of amiloride?

A

Amiloride is a potassium-sparing diuretic. Specifically, it inhibits the epithelial sodium channels found in the distal convoluted tubule

184
Q

What specific feature can indicate hypertrophic olivary degeneration?

A

Palatal myoclonus is a specific feature of hypertrophic olivary degeneration. This is caused by a lesion in the triangle of Guillain and Mollaret (triangle linking the inferior olivary nucleus, red nucleus and the contralateral dentate nucleus). An MRI brain is the gold standard imaging for this lesion.

185
Q

What is the mechanism of action of hydralazine?

A

Increases cGMP leading to smooth muscle relaxation. This relaxation occurs to a greater extent in the arterioles rather than the veins

186
Q

What is the first line investigation in suspected Cushing’s?

A

There is some debate as to whether a 24 hour urinary free cortisol or an overnight dexamethasone suppression test should be used to screen patients for Cushing’s.

The overnight (not high-dose) dexamethasone suppression test has however been shown to be more sensitive and is now much more commonly used in clinical practice.

187
Q

What is the least sedating antihistamine?

A

Loratidine (LORRYtadine for lorry drivers)

Cetirizine is also relatively non sedating but loratadine is best.

188
Q

What are the features of Parinaud syndrome?

A

This patient has Parinaud syndrome as a result of a lesion at the dorsal midbrain.

Rostral interstitial nucleus of medial longitudinal fasciculus lies at the dorsal midbrain and control vertical gaze. They project to the vestibular nuclei. It results in the following symptoms:

Upward gaze palsy, often manifesting as diplopia
Pupillary light-near dissociation (Pseudo-Argyll Robertson pupils)
Convergence-retraction nystagmus

It’s aetiology include:

Brain tumours in the midbrain or pineal gland (pinealoma)
Multiple sclerosis
Midbrain stroke

189
Q

What advice do you need to give patients taking phosphodiesterase type V inhibitors and alpha blockers?

A

The BNF recommends avoiding alpha-blockers for 4 hours after sildenafil

190
Q

What drugs cause dyspepsia?

A

Causes

  • NSAIDs
  • bisphosphonates
  • steroids

The following drugs may cause reflux by reducing lower oesophageal sphincter (LOS) pressure

  • calcium channel blockers*
  • nitrates*
  • theophyllines
  • calcium channel blockers and nitrates are occasionally used in the management of achalasia, itself a cause of dyspepsia, because of their effect on the LOS.
191
Q

What is the mechanism of action of tolvaptan?

A

Tolvaptan blocks the action of vasopressin at the V2 receptor. This receptor is found on the basolateral membrane of the principal cells in the collecting ducts of the kidney. This reduces water absorption (through decreased aquaporin 2) and increases aquaresis without sodium loss. Desmopressin is a synthetic analogue of vasopressin that exerts agonism at the V2 receptor.

192
Q

What are the features of Raloxifene treatment in osteoporosis?

A

Has been shown to prevent bone loss and to reduce the risk of vertebral fractures, but has not yet been shown to reduce the risk of non-vertebral fractures

Has been shown to increase bone density in the spine and proximal femur

May worsen menopausal symptoms

Increased risk of thromboembolic events

May decrease risk of breast cancer

193
Q

What is the strongest risk factor for cervical cancer?

A

Human papillomavirus infection (particularly 16, 18 & 33) is by far the most important risk factor

194
Q

What is the prevalence of Factor V Leiden?

A

5%

195
Q

What are the most sensitive and the most specific antibodies in pernicious anaemia?

A

So the most common antibodies are parietal cells antibodies and the most specific antibodies are intrinsic factor antibodies

196
Q

Give 2 mixed alpha and beta antagonists

A

Carvedilol and labetalol are mixed alpha and beta antagonists

197
Q

How do you differentiate aortic regurgitation and mitral stenosis?

A

e(AR)ly diastolic -> Aortic Regurgiation (AR)

(M)id Diastolic -> (M)itral stenosis

198
Q

What are the differences between MODY 3, 2 and 5?

A

MODY 3

  • 60% of cases
  • due to a defect in the HNF-1 alpha gene
  • is associated with an increased risk of HCC

MODY 2

  • 20% of cases
  • due to a defect in the glucokinase gene

MODY 5

  • rare
  • due to a defect in the HNF-1 beta gene
  • liver and renal cysts
199
Q

What are the causes of jejunal villous atrophy?

A
COELIAC DISEASE
tropical sprue
hypogammaglobulinaemia
gastrointestinal lymphoma
Whipple's disease
cow's milk intolerance
200
Q

What are the good prognostic features in MS?

A
female sex
age: young age of onset (i.e. 20s or 30s)
relapsing-remitting disease
sensory symptoms only
long interval between first two relapses
complete recovery between relapses
201
Q

What are the causes of hypokalaemia with hypertension?

A

Hypokalaemia with hypertension

  • Cushing’s syndrome
  • Conn’s syndrome (primary hyperaldosteronism)
  • Liddle’s syndrome
  • 11-beta hydroxylase deficiency*

Carbenoxolone, an anti-ulcer drug, and liquorice excess can potentially cause hypokalaemia associated with hypertension

*21-hydroxylase deficiency, which accounts for 90% of congenital adrenal hyperplasia cases, is not associated with hypertension

202
Q

Fanconi, Barter’s, Gittleman and Liddle syndromes effect which parts of the kidney?

A

PCT= Fanconi
Ascending loop= Barter
DCT= Gitlmn
Collecting tubule= Liddle

203
Q

What drug is used for prophylaxis in cluster headache?

A

Verapamil

204
Q

What are the diagnostic criteria for ARDS?

A

Acute onset (within 1 week of a known risk factor)

Pulmonary oedema: bilateral infiltrates on chest x-ray (‘not fully explained by effusions, lobar/lung collapse or nodules)

Non-cardiogenic (pulmonary artery wedge pressure needed if doubt)

pO2/FiO2 < 40kPa (200 mmHg)

205
Q

Give 3 centrally acting antihypertensives

A

methyldopa: used in the management of hypertension during pregnancy
moxonidine: used in the management of essential hypertension when conventional antihypertensives have failed to control blood pressure
clonidine: the antihypertensive effect is mediated through stimulating alpha-2 adrenoceptors in the vasomotor centre

206
Q

How do SGLT-2 inhibitors affect cholesterol?

A

SGLT-2 inhibitors are recognised to increased total cholesterol, (both HDL and LDL), although cardiovascular outcome studies as yet do not suggest this translates into increased risk of MACE events. In fact, the EMPA-reg study with empagliflozin demonstrated a reduction in overall mortality.

SGLT-2 inhibitors like dapagliflozin promote increased glucose excretion because they inhibit glucose reabsorption in the kidney. This corresponds to a calorie load of 200-400 kcal per day. In some patients, this results in dramatic weight loss, although on average this equates to 1-2% reduction in weight over 6 months.

207
Q

What are the features of pendred syndrome?

A

Pendred is an autosomal recessive genetic disorder that is characterised by bilateral sensorineural deafness, with mild hypothyroidism and a goitre. The patients tend to present with progressive hearing loss and delay in academic progression. Often head trauma tends to make the sensorineural deafness worse, leading to patients having to avoid contact sports.

In Pendred syndrome there is a defect in the organification of iodine, leading to dyshormonogenesis. However thyroid symptoms in pendred syndrome are often mild and patients are often clinically euthyroid, presenting only with a goitre. Thyroid function tests are also often normal, requiring the perchlorate discharge test to aid diagnosis.

The syndrome can be diagnosed via genetic testing (Pendred syndrome (PDS) gene, chromosome 7), audiometry and MRI imaging to look for characteristic one and a half turns in the cochlea, compared to the normal two and a half turns.

Treatment is with thyroid hormone replacement and cochlear implants.

208
Q

What are the rules for treating tetanus prone wounds?

A

Full course 5 vaccines, last within 10 years: No Ig or booster (regardless of wound)

Full course 5 vaccines, last >10 years:

  • Tetanus-prone wound: Booster dose + further doses to complete
  • High risk wound: Booster dose + Tetanus Ig

Incompletely immunised/not known: Booster dose regardless of clean, if tetanus prone/high risk: booster + Ig

209
Q

What are the 5 layers of skin and their features?

A

Come lets go sun bathe

Stratum corneum - Flat, dead, scale-like cells filled with keratin. Continually shed

Stratum lucidum - Clear layer - present in thick skin only

Stratum granulosum - Cells form links with neighbours

Stratum spinosum - Squamous cells begin keratin synthesis. Thickest layer of epidermis

Stratum (basale) germinativum - The basement membrane - single layer of columnar epithelial cells

  • Gives rise to keratinocytes
  • Contains melanocytes
210
Q

What agents can be used for SVT prophylaxis in pregnancy?

A

For pregnant lady with SVT prophylaxis - Metoprolol

otherwise - flecainide given there is no structural heart disease .

211
Q

How does nephrotic syndrome predominantly result in a hypercoagulable state?

A

Nephrotic syndrome is associated with a hypercoagulable state due to loss of antithrombin III via the kidneys

212
Q

When do you perform AVR in aortic stenosis?

A

if asymptomatic then observe the patient is a general rule
if symptomatic then valve replacement

if asymptomatic but valvular gradient > 40 mmHg and with features such as left ventricular systolic dysfunction then consider surgery

213
Q

What is Stauffer’s syndrome?

A

Paraneoplastic Hepatic dysfunction syndrome = Stauffer’s syndrome

Stauffer’s syndrome is a group of signs/symptoms indicative of liver dysfunction arising due to underlying renal cell carcinoma. Biochemically, there is can be an elevated alkaline phosphatase (ALP), γ-glutamyl transferase (GGT), platelets; prolonged prothrombin time (PT) with hepatosplenomegaly without hepatic metastasis or jaundice.

Paraneoplastic syndromes commonly occurring with renal cell carcinoma can be constitutional symptoms such as fever, cachexia, and weight loss, ranging to more specific metabolic and biochemical disturbances like hypercalcemia, non-metastatic liver dysfunction, amyloidosis etc.

214
Q

What is the criteria for beta interferon use in MS?

A

relapsing-remitting disease + 2 relapses in past 2 years + able to walk 100m unaided

secondary progressive disease + 2 relapses in past 2 years + able to walk 10m (aided or unaided)

215
Q

What is the mechanism of action of natalizumab in MS?

A

a recombinant monoclonal antibody that antagonises Alpha-4 Beta-1-integrin found on the surface of leucocytes, thus inhibiting migration of leucocytes across the endothelium across the blood-brain barrier

216
Q

What is the mechanism of action of fingolimod in MS?

A

sphingosine 1-phosphate receptor modulator, prevents lymphocytes from leaving lymph nodes. An oral formulation is available

217
Q

Describe the choice of biologic therapy for asthma.

A

NICE currently advises 5 different monoclonal antibodies in the treatment of uncontrolled severe asthma. These target various aspects of the underlying inflammatory pathway and the choice of antibody depends on whether or not there is a strong association with allergy. The choice for the specialist clinician is whether or not to target IgE (in the allergic phenotype) or to target eosinophil maturation via IL-4/5/13 (in the eosinophilic phenotype). There is a clear overlap between IgE and eosinophilia, therefore classifying the asthma phenotype is complex and requires measurement of serum IgE and serum eosinophil counts.

In this scenario, the patient is stated to have severe allergic asthma. NICE, therefore, recommends IgE monoclonal antibody therapy after 4 or more trials of oral corticosteroids have been completed in the previous year with optimised standard therapy. This is in the form of omalizumab (Xolair).

In the instance of uncontrolled severe eosinophilic asthma, NICE recommends various IL-5 antibody therapies in the form of mepolizumab, reslizumab and benralizumab or IL-4/13 antibody therapy in the form of dupilumab.

Plasma cells are responsible for producing IgE. After IgE is released, it binds to the Fc domain on the IgE receptor found on mast cells and basophils. In response to an allergen, this receptor-bound IgE causes degranulation and release of allergic mediators including histamine that form the allergy cascade. Omalizumab is a monoclonal antibody that selectively binds to the domain at which IgE normally does, preventing interaction with its receptor.

218
Q

What is the most common cause of biliary disease in HIV?

A

The most common cause of biliary disease in patients with HIV is sclerosing cholangitis due to infections such as CMV, Cryptosporidium and Microsporidia

219
Q

What antibiotics classically lower the seizure threshhold?

A

Quinolones (levofloxacin, ciprofloxacin)

220
Q

What laxative does NICE recommend you avoid in IBS?

A

Lactulose (worsens bloating symptoms)

221
Q

What is the most common biochemical abnormality in plasma exchange and why?

A

One of the commonest adverse effects of this treatment process is hypocalcaemia which occurs as calcium is chelated by sodium citrate, the agent used as an anticoagulant during the procedure. Patients undergoing plasma exchange are therefore required to have their blood tests monitored closely.

222
Q

What are the different types of second heart sound and the most common causes?

A

loud: hypertension
soft: AS
fixed split: ASD
reversed split: LBBB

223
Q

HLA antigens are coded for on what chromosome?

A

6

224
Q

Where does insulin resistance occur in impaired fasting glucose and impaired glucose tolerance?

A

There are two main types of IGR:
impaired fasting glucose (IFG) - due to hepatic insulin resistance
impaired glucose tolerance (IGT) - due to muscle insulin resistance

patients with IGT are more likely to develop T2DM and cardiovascular disease than patients with IFG

225
Q

How does metformin cause macrocytic anaemia?

A

Long-term therapy with metformin is known to reduce intestinal absorption of vitamin B12, specifically on calcium-dependent membrane action responsible for vitamin B12-intrinsic factor absorption in the terminal ileum. One study reports a highly significant inverse correlation between the dose and duration of metformin treatment and reduced serum levels of vitamin B12, with 33% of study participants affected.

226
Q

How does ethanol result in polyuria?

A

Ethanol reduces the calcium-dependent secretion of anti-diuretic hormone (ADH) by blocking channels in the neurohypophyseal nerve terminal.

227
Q

Renal angiomyolipoma is associated with which condition?

A

Around 1 in 10 people who are diagnosed with a renal angiomyolipoma have underlying tuberous sclerosis. Conversely, most patients with tuberous sclerosis will have several renal angiomyolipomata affecting both kidneys.

228
Q

What is the aetiology of pitiryasis rosea?

A

The aetiology is not fully understood but is thought that herpes hominis virus 7 (HHV-7) may play a role.

229
Q

How do you differentiate HELLP and Acute fatty liver of pregnancy (AFLP)?

A

Hypertension is present in essentially 100 percent of patients with preeclampsia, 85 percent of patients with HELLP, and up to about 50 percent of patients with AFLP. Severe symptoms and signs of hepatic insufficiency such as hypoglycemia, encephalopathy, ascites and coagulopathy are more consistent with AFLP than HELLP or severe preeclampsia. Multi-organ involvement is also more common with AFLP, especially renal failure. Hypertension and proteinuria are often more severe in HELLP and severe preeclampsia

230
Q

Bisphosphonate infusions can cause which electrolyte abnormality?

A

Bisphosphonate infusions can lead to hypocalcaemia although it is more common when using larger doses in malignancy induced hypercalcaemia as oppose to the smaller dose used in osteoporosis.

231
Q

What are the indications for surgery in infective endocarditits?

A

Severe valvular incompetence

Aortic abscess (often indicated by a lengthening PR interval)

Infections resistant to antibiotics/fungal infections

Cardiac failure refractory to standard medical treatment

Recurrent emboli after antibiotic therapy

232
Q

What drugs cause SIADH?

A
sulfonylureas*
SSRIs, tricyclics
carbamazepine
vincristine
cyclophosphamide
233
Q

What conditions are associated with raised lymphocytes in CSF?

A
viral meningitis/encephalitis
TB meningitis
partially treated bacterial meningitis
Lyme disease
Behcet's, SLE
lymphoma, leukaemia
234
Q

What is the most common cause of visceral larva migrans?

A

commonly acquired by ingesting eggs from soil contaminated by dog faeces
commonest cause of visceral larva migrans
other features: eye granulomas, liver/lung involvement

235
Q

What eye conditions are associated with acute angle closure glaucoma and primary open-angle glaucoma?

A

Acute angle closure glaucoma= Hypermetropia (hyper and acute both crazy)

priMarY OPen-angle glaucoma= MYOPia

236
Q

What hyperthyroid features are specific to graves disease?

A

1) Ex“opathalmo”s+“ Opthalmo”plegia [ NOT lid lag]
2) Pretibial myxedema
3) Thyroid acropachy (clubbing)

237
Q

What technique is used to detect mutated oncogenes?

A

Polymerase chain reactions are used to detect mutated oncogenes

238
Q

How can iron/ calcium carbonate affect levothyroxine?

A

Iron / calcium carbonate tablets can reduce the absorption of levothyroxine - should be given 4 hours apart

239
Q

What is the treatment for Chlamydia psittaci?

A

1st-line: tetracyclines e.g. doxycycline

2nd-line: macrolides e.g. erythromycin

240
Q

What valve abnormality is seen in Takayasu Arteritis?

A

The early diastolic murmur is caused by aortic regurgitation, which is seen in around 20% of patients with Takayasu’s arteritis.

241
Q

Alpha thalassaemia mutation is on which chromosome?

A

16

242
Q

What is catecholaminergic polymorphic VT?

A

It is a catecholaminergic polymorphic VT. This basically means that the arrhythmia is catecholamine i.e. adrenaline driven. So more the adrenaline release/ emotional stress/exercise, higher chances of VT or other life threatening arrhythmias.

Why do we get arrhythmia with adrenaline in CPVT? Dysfunctional calcium regulation within cells resulting in calcium sparks during cardiac muscle contraction due to a genetic defect in Ryanodine receptor. These calcium sparks are triggered by adrenaline hence leading to excessive action potentials and contraction of cardiac muscles resulting in bidirectional adrenaline triggered VTs.

Diagnosis? Challenging! Symptoms of syncope in young. ECG is mostly normal and routine cardiac investigations are also normal. Stress test ECG however picks ventricular ectopics due to adrenaline release.

Treatment options are beta blockers, flecainide, sympathetic denervation, ICD. Research ongoing.

243
Q

Bronchiectasis is associated with which HLA?

A

HLA-DR1

244
Q

Can you breastfeed in HIV?

A

No

245
Q

What is the mechanism of action of rifampicin?

A

Rifampicin is an RNA synthesis inhibitor. It specifically inhibits bacterial DNA-dependent RNA polymerase. In doing so, elongation is physically blocked and so, without adequate RNA, bacteria cannot translate proteins.

246
Q

What are the side effects of the progesterone only pill.

A

Head pops (headache), breasts pop (breast tenderness), Tummy pops (weight gain) and skin pops (acne), endometrium pops (irregular periods)

247
Q

What conditions cause a 3rd heart sound?

A

heard in left ventricular failure (e.g. dilated cardiomyopathy), constrictive pericarditis (called a pericardial knock) and mitral regurgitation

248
Q

How do you calculate average blood sugar from HbA1c?

A

31mmol is 5%. add 11mmol for every 1% thereon

249
Q

PT and APTT measure which components of the clotting cascade?

A

APTT measures intrinsic pathway (appointments happen inside)
PT measures extrinsic pathway (playtime happens outside)
—————————–
And APTT evaluates factors VIII to XII
While PT evaluates factor VII
And both evaluate the common pathway (factors X –> V –> II –> I)

To narrow down where the problem is!

250
Q

How do you differentiate the congenital causes of long QT syndrome?

A

Jervell-Lange-Nielsen syndrome (includes deafness and is due to an abnormal potassium channel)

Romano-Ward syndrome (no deafness)

251
Q

What are the features of Bardet-Biedl syndrome?

A

Bardet-Biedl syndrome is a rare autosomal recessive condition that gives retinitis pigmentosa, but also presents with obesity, polydactyly and frequently mental retardation.

252
Q

What is the mechanism of action of metformin?

A

Metformin acts by activation of the AMP-activated protein kinase (AMPK)

253
Q

When is hazard ratio used?

A

The hazard ratio (HR) is similar to relative risk but is used when risk is not constant to time. It is typically used when analysing survival over time

254
Q

What is the best immunosuppressant for SLE in pregnancy?

A

A large body of evidence from the use of azathioprine in pregnancy for the treatment of both rheumatological conditions and inflammatory bowel disease, supports its use. Although it is less effective in the management of SLE with renal disease versus other options, balance of benefit risk makes it the preferred intervention.

255
Q

What are the relative glucocorticoid and mineralocorticoid effects of fludrocortisone, hydrocortisone, prednisolone and dexamethasone?

A

Minimal glucocorticoid activity, very high mineralocorticoid activity,
-Fludrocortisone

Glucocorticoid activity, high mineralocorticoid activity,
-Hydrocortisone

Predominant glucocorticoid activity, low mineralocorticoid activity
-Prednisolone

Very high glucocorticoid activity, minimal mineralocorticoid activity
-Dexamethasone/ Betamethasone

This is clinically relevant as there are some situations where it is important to combine high glucocorticoid (anti-inflammatory) activity with minimal mineralocorticoid (fluid-retention) effects. A good example is the use of dexamethsone for patients with raised intracranial pressure secondary to brain tumours.

256
Q

What are the key investigations in determining who gets cardiac resynchronisation therapy?

A

The key diagnostic tests used to identify patients likely to benefit from cardiac resynchronization therapy is the transthoracic echocardiogram and ECG.

Those with left ventricular ejection fractions of <35% and a LBBB (QRS duration greater than 120 ms) on ECG are excellent candidates for CRT (biventricular pacing). The echo will show asynchronous contraction of the LV and RV and subsequently reduced ejection fraction. A transoesophageal echo is not required.

Biventricular pacing improves quality of life and exercise tolerance amongst other endpoints, and does so by ensuring that the ventricles contract at the same time (resynchronization) due to asynchronous stimulation (LBBB causing asynchronous activation) via the conduction system.

257
Q

What is Froin Syndrome?

A

Froin syndrome is characterized by xanthochromia and hypercoagulability of the cerebrospinal fluid (CSF) due to elevated protein levels. This entity results from blockage of the spinal canal by a mass lesion leading to an isolated caudal CSF space.

258
Q

What is the breakdown of the ECOG scoring system?

A

0 Fully active, able to carry on all pre-disease performance without restriction

1 Restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature, e.g., light house work, office work

2 Ambulatory and capable of all selfcare but unable to carry out any work activities; up and about more than 50% of waking hours

3 Capable of only limited selfcare; confined to bed or chair more than 50% of waking hours

4 Completely disabled; cannot carry on any selfcare; totally confined to bed or chair

5 Dead

259
Q

What is the mechanism of action of Meglitinides (e.g. repaglinide, nateglinide)?

A

increase pancreatic insulin secretion
like sulfonylureas they bind to an ATP-dependent K+(KATP) channel on the cell membrane of pancreatic beta cells
often used for patients with an erratic lifestyle
adverse effects include weight gain and hypoglycaemia (less so than sulfonylureas)

260
Q

How do you differentiate polymorphic eruption of pregnancy and pemphigoid gestationis?

A

Polymorphic eruption of pregnancy

  • Pruritic condition associated with last trimester
  • Lesions often first appear in abdominal striae
  • Management depends on severity: emollients, mild potency topical steroids and oral steroids may be used

Pemphigoid gestationis

  • Pruritic blistering lesions
  • Often develop in peri-umbilical region, later spreading to the trunk, back, buttocks and arms
  • Usually presents 2nd or 3rd trimester and is rarely seen in the first pregnancy
  • Oral corticosteroids are usually required
261
Q

Which immunoglobulin is involved in activating B cells?

A

IgD

262
Q

What drugs cause acute angle closure glaucoma?

A

Drugs which may precipitate acute glaucoma include anticholinergics and tricyclic antidepressants

(any drugs which dilate the pupil)

263
Q

What is the insulin stress test used to investigate?

A

Basics
-used in investigation of hypopituitarism
-IV insulin given, GH and cortisol levels measured
with normal pituitary function GH and cortisol should rise

Contraindications

  • epilepsy
  • ischaemic heart disease
  • adrenal insufficiency
264
Q

What are the side effects of sodium valproate?

A

VALPROATE

Vomiting
Alopecia
Liver toxicity
Pancreatitis/ Pancytopenia
Retention of fats (weight gain)
Oedema (peripheral oedema)
Anorexia
Tremor
Enzyme inhibition
265
Q

What are the EEG features of the different stages of sleep?

A

N1 → N2 → N3 → REM

Theta → Sleep spindles/K-complexes → Delta → Beta

The Sleep Doctor’s Brain

266
Q

How do you manage Hep B in pregnancy?

A

All pregnant women are offered screening for hepatitis B
babies born to mothers who are chronically infected with hepatitis B or to mothers who’ve had acute hepatitis B

During pregnancy should receive a complete course of vaccination + hepatitis B immunoglobulin

Studies are currently evaluating the role of oral antiviral treatment (e.g. Lamivudine) in the latter part of pregnancy

There is little evidence to suggest caesarean section reduces vertical transmission rates

Hepatitis B cannot be transmitted via breastfeeding (in contrast to HIV)

267
Q

What antibiotics treat liver abscess?

A

Amoxicillin + Ciprofloxacin + Metronidazole

268
Q

What is the gold standard for investigating cerebral metastases?

A

MRI with contrast enhancement

269
Q

What is the mechanism of varenicline and bupropion?

A

Varenicline is a nicotinic receptor partial agonist

Bupropion is a norepinephrine and dopamine reuptake inhibitor, and nicotinic antagonist

270
Q

What is the treatment for larva migrans?

A

larva migrans: there are two disease entities:
cutaneous (caused by Ancylostoma) and visceral (cause by toxocara).

  • cutaneous larva migrans: IVERMECTIN or THIABENDAZOLE.
  • visceral larva migrants: self limited. steroids if severe. ALEBENDAZOLE for eradication
271
Q

What stain is applied to bronchoalveolar lavage in pneumocystis carinii pneumonia?

A

Silver Stain

272
Q

What test remains positive in a patient with syphilis despite treatment?

A

Treponema pallidum haemagglutination test (TPHA)

273
Q

What is the treatment for epididymo-orchitis?

A

ABCD = Achey balls? cef and doxy

ceftriaxone 500mg intramuscularly single dose, plus doxycycline 100mg by mouth twice daily for 10-14 days

274
Q

Which vaccines are contraindicated in HIV patients?

A

Contraindicated

  • Cholera CVD103-HgR
  • Influenza-intranasal
  • Poliomyelitis-oral (OPV)
  • Tuberculosis (BCG)

Can be used if CD4 >200

  • MMR
  • Varicella
  • Yellow fever
275
Q

What is the treatment for generalised tonic-clonic seizures?

A

sodium valproate

second line: lamotrigine, carbamazepine

276
Q

What is the treatment of absence seizures?

A

sodium valproate particularly effective if co-existent tonic-clonic seizures in primary generalised epilepsy

*carbamazepine may exacerbate absence seizures

277
Q

What is the treatment of Myoclonic seizures?

A

sodium valproate

carbamazepine may exacerbate myoclonic seizures

278
Q

What is the treatment of focal seizures?

A

carbamazepine or lamotrigine

second line: levetiracetam, oxcarbazepine or sodium valproate

279
Q

What is the mechanism of action of unfractionated heparin?

A

Unfractionated heparin activates antithrombin III which in turn inhibits thrombin and factors Xa, Ixa, XIa and XIIa. This stops fibrin formation and thrombin from activating factors V, VIII, and XI. This process can be reversed with protamine sulphate.

280
Q

New Delhi metallo-beta-lactamase 1 mutation causes carbapenem resistance in which bacteriae?

A

New Delhi metallo-beta-lactamase 1 is the mutation that leads to carbapenem resistance. Typically found in Klebsiella pneumoniae, Escherichia Coli (E. Coli), Enterobacter cloacae and others. First line of management is the old antibiotic colistin and second line may be tigecycline.

281
Q

What is the mechanism of vancomycin resistant enterococci?

A

D-alanyl-D-lactate variation leading to loss of affinity to antibiotics is the mechanism of VRE (vancomycin resistant enterococci). Vancomycin binds D-ala-D-ala.

282
Q

What common mechanism does pseudomonas use to gain resistance to many antibiotics?

A

The presence of MexAB-OprM efflux pumps is one of the mechanisms by which pseudomonas aeruginosa is resistant to -lactams, chloramphenicol, fluoroquinolones, macrolides, novobiocin, sulfonamides, tetracycline, and trimethoprim.

283
Q

How does MRSA develop?

A

Alteration to the penicillin binding protein 2 is the mechanism behind methicillin-resistant staphylococcus aureus. Mutations in the MEC gene which codes the penicillin binding proteins give staphylococcus aureus its resistance.

284
Q

What is the most common side effect of ivabradine?

A

The commonest side effect caused by ivabradine is transient luminous phenomenon (reported by up to 15% of patients), such as bright spots appearing in their field of vision. Less commonly blurred vision is reported. Patients should be informed of this common side effect before starting the medication. The visual side effects of ivabradine are likely to be mediated by inhibition of a channel similar to the If channel found in the retina called the Ih channel. The h = hyperpolarisation-activated, these channels were formerly called IQ channels, Q = queer, again for their unusual characteristics.

285
Q

Why does trimethoprim cause a rise in creatinine?

A

Competitively inhibits the tubular secretion of creatinine

286
Q

What is the most important medication to stop when screening for primary aldosteronism?

A

ACEi, ARBs, thiazides, aldosterone antagonists, and dihydropyridine CCBs all cause falsely negative aldosterone renin ratio, whereas BBlockers cause ARR to be falsely positive. He distinctly said that stopping BBlockers was most important for screening for primary aldosteronism

287
Q

What is the pathophysiology of Gitelman’s syndrome?

A
Gitelman's syndrome is due to a reabsorptive defect of the NaCl symporter in the DCT
----------------
NORMOTENSION
hypokalaemia
hypocalciuria
hypomagnesaemia
metabolic alkalosis
---------------------------
Gitelman Na-Cl symporter not working
Bartter Na-K-Cl co-transporter; you can Barter with 3 things better than 2
288
Q

What are the indications for dialysis in salicylate overdose?

A
serum concentration > 700mg/L
metabolic acidosis resistant to treatment
acute renal failure
pulmonary oedema
seizures
coma
289
Q

What are the 3 types of troponin and their function in cardiac muscle contraction?

A

troponin C: binds to calcium ions
-Calcium ions are bound to by troponin C, playing the main role in Ca2+-dependent regulation of muscle contraction

troponin T: binds to tropomyosin, forming a troponin-tropomyosin complex

troponin I: binds to actin
-Actin holds the troponin-tropomyosin complex in place which regulates muscle contraction

290
Q

What test is used to assess exocrine function in chronic pancreatitis?

A

faecal elastase

291
Q

What is the minimum steroid intake a patient should be taking before they are offered osteoporosis prophylaxis?

A

Equivalent of 7.5 mg oral prednisolone each day for 3 months.

292
Q

What is the most common cause of erythema multiforme?

A

Herpes simplex

293
Q

What are the indications for urgent ophthalmology referral in graves disease?

A
  • Unexplained deterioration in vision
  • Awareness of change in intensity or quality of colour vision in one or both eyes
  • History of eye suddenly ‘popping out’ (globe subluxation)
  • Obvious corneal opacity
  • Cornea still visible when the eyelids are closed
  • Disc swelling
294
Q

What population is paroxetine the best SSRI?

A

Pregnancy/ Post natal = Paroxetine
-Less secreted in milk
———————————–
Highest incidence of discontinuation syndrome

295
Q

What is the diagnostic difference between MGUS, smoldering multiple myeloma and myeloma?

A

Monoclonal Gammopathy of Uncertain Significance (MGUS):
▪︎M protein <30 g/l
▪︎BM plasma cells <10%
▪︎No CRAB features

Smoldering Multiple Myeloma:
▪︎M protein > 30 g/l
▪︎BM plasma cells 10-60%
▪︎No CRAB features
▪︎Rx: Observe + monitor

Multiple myeloma:
▪︎M protein >30g/l
▪︎BM plasma cells >10%
▪︎CRAB features

296
Q

How do you confirm Gilbert’s syndrome?

A

rise in bilirubin following prolonged fasting or IV nicotinic acid

297
Q

When can you stop anti-epileptic drugs?

A

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

298
Q

What are the inducers of P450 system?

A
Antiepileptics: phenytoin, carbamazepine
Barbiturates: phenobarbitone
Rifampicin
St John's Wort
Chronic alcohol intake
Griseofulvin
Smoking (affects CYP1A2, reason why smokers require more aminophylline)
299
Q

How do you differentiate between leptospirosis and Tularaemia?

A

Tularaemia is a zoonotic infection involving the microorganism F. tularensis commonly transmitted through lagomorphs such as rabbits, hares and pikas but also in aquatic rodents - beavers and muskrat - and ticks. It can present in a variety of forms. Commonly, it produces an erythematous papulo-ulcerative lesion at the site of the bite with reactive and ulcerating regional lymphadenopathy. It is treated with antibiotics such as doxycycline.

300
Q

Which drugs cause a prolonged QTc?

A
THE MASCOTS:
• Terfenadine
• Haloperidol
• Erythromycin
• Methadone
• Amiodarone
• Sotalol
• Chloroquine
• Ondansetron
• TCAs
• SSRIs
301
Q

What is the mechanism of action of docetaxel?

A

Taxanes such as docetaxel - prevents microtubule depolymerisation & disassembly, decreasing free tubulin

302
Q

How do you differentiate TACO from TRALI?

A
  • TACO usually occurs in elderly patients with a decreased cardiovascular reserve and ability to compensate for an increase in fluid volume.
  • TACO is more likely in rapid/substantial transfusions, whereby receiving more units increase the likelihood of overload.
  • TACO presents with hypertension due to volume excess, whereas TRALI presents with hypotension due to ARDS and the resultant hypovolaemic shock.
  • TRALI is likely to be associated with fever and leukopenia, whereas TACO usually has neither.
303
Q

Which type of collagen is affected by Ehlers-Danlos syndrome?

A

Ehlers-Danlos syndrome is primarily caused by a genetic defect in collagen type III. Collagen Type V is affected in a less common variant of Ehlers-Danlos syndrome.

304
Q

Which antibiotic is used for acne in pregnancy?

A

Erythromycin

305
Q

What length of time do you need to leave between multiple live vaccines?

A

Live vaccines can be given on the same day. If not given on the same day, then there must be a 4 week interval between further live vaccinations to prevent the risk of immunological interference.