Passmed Flashcards

1
Q

If a patient with AF has a stroke or TIA, the anticoagulant of choice should be?

A

Warfarin or a direct thrombin or factor Xa inhibitor

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2
Q

What can cause gingival hyperplasia?

A

Phenytoin, ciclosporin, calcium channel blockers and AML

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3
Q

Hypokalaemia on an ECG?

A

Prolonged PR interval, inverted T waves, and prominent U waves

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4
Q

What may be seen on the full blood count as a long-term result of COPD?

A

Polycythaemia; inc. conc of haematocrit

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5
Q

Holmes ADIe pupil

A

DIlated pupil, females, absent leg reflexes

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6
Q

What is the purpose of studies where they focus on testing patients with the condition for which the drug is intended to treat?

A

The purpose of phase 2 studies is to assess the efficacy of drugs or devices

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7
Q

What is the most appropriate initial investigation to confirm a diagnosis of ankylosing spondylitis?

A

Plain radiography of pelvis: sacro-ilitis

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8
Q

What’s first-line for knee osteoarthritis?

A

Topical NSAIDs e.g. diclofenac

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9
Q

If renin is high then is it primary or secondary aldosteronism?

A

Secondary e.g. renal artery stenosis

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10
Q

A blood film shows crescent-shaped red blood cells and schistocytes.

A

Sickle cell

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11
Q

Bg of sickle cell.

Acutely painful right arm
Vomiting
Can’t eat or drink.
Apyrexial.
Anaemic, normal platelets.

DDx?

A

Thrombotic crises in sickle cell can be precipitated by infection, dehydration or deoxygenation

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12
Q

In X-linked recessive conditions, if there is an affected male then can he pass the condition onto a son?

A

No, but daughters may be carriers

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13
Q

How to calculate likelihood ratio for a positive test result?

A

Sensitivity / (1 - specificity)

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14
Q

Pt has first VTE and diagnosed with antiphospholipid syndrome. What’s the most appropriate long-term anticoagulation strategy?

A

Lifelong warfarin.

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15
Q

High-risk paracetamol overdose because of what factors?

A

Chronic alcohol, HIV, anorexia, P450 inducers

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16
Q

Proteinuric CKD and no diabetes. what drug to give?

A

Dapagliflozin (SGLT2 inhibitors) even if not diabetic

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17
Q

Ptosis + dilated pupil =

A

CNIII palsy

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18
Q

Ptosis + constricted pupil =

A

Horner’s

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19
Q

Persistent ST elevation in precordial leads after MI. Bibasal crackles, S3 and S4.

A

Left ventricular aneurysm

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20
Q

Post MI - 2 days - mitral regurgitation, hypotensive, pulmonary oedema.

A

Papillary muscle rupture.

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21
Q

Post MI - 24 hrs - Chest pain worse on lying flat

A

Pericarditis

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22
Q

What is brugada syndrome?

A

Genetic mutation

ST elevation in some leads, inverted T waves
Documented VF episode
Sudden cardiac death in relative
Nocturnal agonal breathing

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23
Q

Tear drop poikilocytes on blood film indicate:

A

Myelofibrosis

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24
Q

Abdominal pain + ascites + tender hepatomegaly =?

A

Budd-Chiari syndrome

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25
Q

Renal impairment, resp symptoms, joint pain, systemic features:

A

ANCA associated vasculitis

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26
Q

When to give platelet transfusion:
Bleeding + 29 platelet count

A

Give (under 30)

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27
Q

When to give platelet transfusion:
Not bleeding + 11 platelet count

A

No (under 10)

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28
Q

Ciclosporin side effects:

A

Everything increased - fluid, BP, K+, hairy, gums, glucose

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29
Q

What anaesthetic should be used in caution with a pneumothorax?

A

Nitrous oxide

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30
Q

SIADH treatment?

A

Fluid restriction

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31
Q

SACD presentation:

A

Distal sensory loss
Tingling
Absent ankle jerks
Extensor plantars
Romberg’s positive

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32
Q

Widened QRS?

A

> 100ms –> inc. risk seizures
160ms –> inc. risk ventricular arrhythmias

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33
Q

Secondary prevention for MI?

A

ACEi + beta-blocker + statin + aspirin + ticagrelor

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34
Q

Animal bite abx?

A

Co-amoxiclav

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35
Q

Photosensitivity, macular rash, heliotrope rash, Gottron’s papules, Raynaud’s

Diagnosis and antibody?

A

Dermatomyositis is associated with the anti-Jo-1 antibody

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36
Q

Hartmann’s is what

A

Sigmoid colectomy + formation of end colostomy

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37
Q

Which meds should be avoided in myasthenia gravis?

A

Beta-blockers

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38
Q

High pulmonary capillary wedge pressure means:

A

Backlog into the veins –> cardiac failure

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39
Q

TRALI vs ARDS

A

TRALI is ARDS within 6 hours of transfusion

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40
Q

A patient presents with numbness and tingling along the ulnar border of his wrist and forearm. On examination you also note weak flexion of all the digits including the thumb.

A

C8 radiculopathy

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41
Q

AF + QRS 130ms

A

AF with bundle branch block

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42
Q

Post MI - 1 week - acute heart failure, cardiac tamponade

A

Left ventricular free wall rupture

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43
Q

MMSE score of below 26 indicates?

A

Cognitive impairment –> complete blood screen

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44
Q

If G6PD deficiency, which antibiotic is contraindicated?

A

Ciprofloxacin

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45
Q

Highly specific test for SLE?

A

Anti-dsDNA

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46
Q

Management of Perthes’ disease

A

Reassurance and follow-up

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47
Q

HIV, neuro symptoms, multiple brain lesions with ring enhancement

A

Toxoplasmosis

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48
Q

Rheumatoid arthritis, splenomegaly, low WCC

A

Felty’s syndrome

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49
Q

What is a type II error?

A

Failure to reject the null hypothesis (that there is no difference between mindfulness and no intervention) when it is false.

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50
Q

Lithium toxicity can be precipitated by…

A

Dehydration
Renal failure
Diuretics
ACEi/ARBs
NSAIDs
Metronidazole

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51
Q

20M with acute swelling and tense knee joint. No other features and no signs of injury, plain X-R show no fracture.

Likely explanation?

A

Haemophilia A or B

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52
Q

First line for neuropathic pain?

A

amitriptyline, duloxetine, gabapentin or pregabalin

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53
Q

Pincer grip?

A

12 months

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54
Q

Corneal abrasion management?

A

Topical antibiotics should be given to prevent secondary bacterial infection

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55
Q

A patient develops acute heart failure 5 days after a myocardial infarction. A new pan-systolic murmur is noted on examination

A

Ventricular septal defect

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56
Q

Switching from fluoxetine to another SSRI

A

withdraw then leave a gap of 4-7 days (as it has a long half-life) before starting a low dose of the alternative SSRI

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57
Q

Stereotypical features of Legionella

A

flu-like symptoms and a dry cough, relative bradycardia and confusion. Blood tests may show hyponatraemia

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58
Q

Acute heart failure not responding to treatment. What should we consider?

A

Consider CPAP

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59
Q

ADPKD is a risk factor for SAH or bacterial meningitis?

A

SAH

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60
Q

What is the most common presentation of ALS?

A

Asymmetric limb weakness

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61
Q

First-line treatment for most patients with a pituitary tumour causing acromegaly

A

Trans-sphenoidal surgery

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62
Q

Increased risk of placental abruption is associated with

A

increasing maternal age, multiparity and maternal trauma

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63
Q

potential complication of panretinal photocoagulation

A

A decrease in night vision

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64
Q

Horner’s syndrome

A

miosis + ptosis + enophthalmos +/- anhydrosis

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65
Q

Notching of the inferior border of the ribs indicates what condition?

A

Notching of the inferior border of the ribs is present in around 70% of adults with coarctation of the aorta

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66
Q

What is management ofintracapsular (subcapital) and displaced hip injury?

A

Total hip replacement

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67
Q

What is management ofextracapsular (trochanteric or subtrochanteric) hip injury?

A
  • intertrochanteric → dynamic hip screw
  • subtrochanteric → intramedullary nail
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68
Q

What is management ofintracapsular (subcapital) and NOT displaced hip injury?

A

internal fixation (cannulated hip screw) (fit)
- hemiarthroplasty (unfit)

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69
Q

Pregnancy-induced HTN does not happen before what gestational age?

A

20 weeks

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70
Q

Patients with NHPCC (Lynch syndrome) are at a high risk of developing which cancers:

A

Inherited colon cancer (mostly proximal)

Endometrial cancer

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71
Q

Which inheritance pattern has no male-to-male transmission?

A

X-linked recessive or dominant

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72
Q

Which type of inheritance is not typically seen in every generation of an affected family?

A

Autosomal recessive

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73
Q

Which inheritance pattern causes all offspring to be carriers if one affected and one unaffected reproduce?

A

Autosomal recessive

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74
Q

Acute graft rejection

A

within months, is usually asymptomatic and is picked up by a rising creatinine, pyuria and proteinuria

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75
Q

Monteggia fracture

A

A Monteggia fracture involves dislocation of the proximal radioulnar joint in association with an ulnar fracture

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76
Q

Loss of corneal reflex with vertigo, tinnitus and unilateral sensorineural hearing loss

A

Acoustic neuroma

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77
Q

Conductive hearing loss in the affected ear. Disturbance in balance and vertigo.

A

Cholesteatoma

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78
Q

Acute vertigo, prolonged in the first few days and then eases.

A

Viral labyrinthitis

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79
Q

Tinnitus, vertigo and sensorineural hearing loss. Relapsing and remitting vertigo.

A

Meniere’s disease

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80
Q

Progressive, bilateral conductive hearing loss.

A

Otosclerosis

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81
Q

What is a normal anion gap?

A

10-18 mmol

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82
Q

What kind of anion gap does diarrhoea cause?

A

Normal anion gap (loss of bicarbs but inc. Cl- in the kidney compensates)

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83
Q

What kind of anion gap does DKA cause?

A

Raised anion gap (accumulation of ketotic acid)

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84
Q

What kind of anion gap does renal failure cause?

A

Raised anion gap (accumulation of uric acid)

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85
Q

What kind of anion gap does salicylate poisoning cause?

A

Raised anion gap (accumulation of salicylic acid)

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86
Q

What kind of anion gap does septic shock cause?

A

Raised anion gap (accumulation of lactic acid)

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87
Q

Which drugs can cause pancreatitis?

A

Azathioprine
Mesalazine
Didanosine
Bendroflumethiazide
Furosemide
Pentamidine
Steroids
Sodium valproate

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88
Q

Contralateral hemiparesis and sensory loss, lower extremity > upper

A

Anterior cerebral artery

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89
Q

Contralateral hemiparesis and sensory loss, upper extremity > lower
Contralateral homonymous hemianopia
Aphasia

A

Middle cerebral artery

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90
Q

Contralateral homonymous hemianopia with macular sparing
Visual agnosia

A

Posterior cerebral artery

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91
Q

Ipsilateral CN III palsy
Contralateral weakness of upper and lower extremity

A

Weber’s syndrome (branches of the posterior cerebral artery that supply the midbrain)

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92
Q

Ipsilateral: facial pain and temperature loss, cranial nerve palsy e.g. Horner’s
Contralateral: limb/torso pain and temperature loss
Ataxia, nystagmus

A

Posterior inferior cerebellar artery (lateral medullary syndrome, Wallenberg syndrome)

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93
Q

Symptoms are similar to Wallenberg’s (see above), but:
Ipsilateral: facial paralysis and deafness

A

Anterior inferior cerebellar artery (lateral pontine syndrome)

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94
Q

Sudden, painless vision loss in one eye that lasts seconds to minutes, often described as a “shade” or “curtain” descending over the visual field.

A

Amaurosis fugax due to retinal/ophthalmic artery

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95
Q

‘Locked-in’ syndrome

A

Basilar artery

96
Q

This condition presents with either isolated hemiparesis, hemisensory loss or hemiparesis with limb ataxia

PMHx HTN

A

Lacunar stroke

97
Q

Impairment of vertical gaze (down gaze worse than up gaze - patients may complain of difficulty reading or descending stairs)
Parkinsonism
Falls
Slurring of speech
Cognitive impairment

98
Q

What’s long-term prevention for cluster headaches?

99
Q

Wet, wacky, wobbly

i.e. urinary incontinence, dementia, gait disturbance

A

Normal pressure hydrocephalus

100
Q

Combo of UMN + LMN
Limb-onset or bulbar-onset

101
Q

PLS is upper or lower?

102
Q

PMA is upper or lower?

103
Q

Normal power on resisted movements of shoulder and hip
Morning stiffness
Severe tiredness
Shoulder and hip muscle pain

A

Polymyalgia rheumatica

104
Q

Multiple myeloma without metastasis bone profile results?

A

High calcium
Normal phosphate
Normal ALP

105
Q

All invasive diarrhoeas are treated with ciprofloxacin, except __ which is treated with ___

A

Campylobacter treated with clarithromycin

106
Q

Slow growing, painless, mobile lump in parotid gland of older female

A

Pleomorphic adenoma

107
Q

Otitis externa in diabetics. What Mx?

A

Ciprofloxacin to cover Pseudomonas

108
Q

MEN type I

A

3Ps

Parathyroid (95%): hyperparathyroidism due to parathyroid hyperplasia
Pituitary (70%)
Pancreas (50%): e.g. insulinoma, gastrinoma (leading to recurrent peptic ulceration)

Also: adrenal and thyroid

MEN1 gene

Most common presentation = hypercalcaemia

109
Q

MEN type IIa

A

Medullary thyroid cancer (70%)

2 P’s
Parathyroid (60%)
Phaeochromocytoma

RET oncogene

110
Q

MEN type IIb

A

Medullary thyroid cancer

1 P
Phaeochromocytoma

Marfanoid body habitus
Neuromas

111
Q

Cutaneous features
depigmented ‘ash-leaf’ spots which fluoresce under UV light
roughened patches of skin over lumbar spine (Shagreen patches)
adenoma sebaceum (angiofibromas): butterfly distribution over nose
fibromata beneath nails (subungual fibromata)
cafe-au-lait spots* may be seen

Neurological features
developmental delay
epilepsy (infantile spasms or partial)
intellectual impairment

Also
retinal hamartomas: dense white areas on retina (phakomata)
rhabdomyomas of the heart
gliomatous changes can occur in the brain lesions
polycystic kidneys, renal angiomyolipomata
lymphangioleiomyomatosis: multiple lung cysts

A

Tuberous sclerosis

112
Q

Cafe-au-lait spots (>= 6, 15 mm in diameter)
Axillary/groin freckles
Peripheral neurofibromas
Iris hamatomas (Lisch nodules) in > 90%
Scoliosis
Pheochromocytomas

A

Neurofibromatosis I

113
Q

Bilateral vestibular schwannomas
Multiple intracranial schwannomas, meningiomas and ependymomas

A

Neurofibromatosis II

114
Q

What investigation is most useful in investigating multiple myeloma?

A

Serum protein electrophoresis

115
Q

Tetracycline side effects

A

Photosensitivity
Discolouration of teeth in children and during pregnancy
Hepatotoxicity
Renal impairment

116
Q

What is an important cause of visual impairment in babies born before 32 weeks gestation?

A

Retinopathy of prematurity

117
Q

Chronic insomnia diagnostic criteria

A

may be diagnosed after three months, if a person has trouble falling asleep or staying asleep at least three nights per week

118
Q

AKI diagnostic criteria in adults

A

↑ creatinine > 26µmol/L in 48 hours
↑ creatinine > 50% in 7 days
↓ urine output < 0.5ml/kg/hr for more than 6 hours

119
Q

Tender, purple/red raised lesions with a pale centre. These lesions occur as a result of immune complex deposition.

A

Osler nodes

120
Q

Patients typically present with hard, painless nodules at the DIP joints. These nodes can be bilateral and may lead to decreased range of motion and functional impairment over time.

A

Heberdens nodes

121
Q

17M
Soft, fluctuant swelling on the dorsal aspect of the hand, it is most obvious on making a fist.

122
Q

Non-functioning pituitary tumours present with…?

A

hypopituitarism and pressure effects

123
Q

Marfan’s syndrome is caused by a mutation in what?

A

Fibrillin-1

124
Q

Types of nephrotic syndromes

A

Focal segmental glomerulosclerosis
Minimal change disease
Membranous nephropathy
Diabetic nephropathy

125
Q

Major bleeding (e.g. variceal haemorrhage, intracranial haemorrhage)

A

Stop warfarin
Give intravenous vitamin K 5mg
Prothrombin complex concentrate - if not available then FFP*

126
Q

INR > 8.0
Minor bleeding

A

Stop warfarin
Give intravenous vitamin K 1-3mg
Repeat dose of vitamin K if INR still too high after 24 hours
Restart warfarin when INR < 5.0

127
Q

INR > 8.0
No bleeding

A

Stop warfarin
Give vitamin K 1-5mg by mouth, using the intravenous preparation orally
Repeat dose of vitamin K if INR still too high after 24 hours
Restart when INR < 5.0

128
Q

INR 5.0-8.0
Minor bleeding

A

Stop warfarin
Give intravenous vitamin K 1-3mg
Restart when INR < 5.0

129
Q

INR 5.0-8.0
No bleeding

A

Withhold 1 or 2 doses of warfarin
Reduce subsequent maintenance dose

130
Q

Posterior Mi presents with what on ECG

A

Tall R waves V1-V2

131
Q

Types of nephritic syndrome?

A

IgA nephropathy
Membranoproliferative glomerulonephritis
Rapidly progressive glomerulonephritis

132
Q

Transudative causes of pleural effusions?

A

Transudate (< 30g/L protein)
heart failure (most common transudate cause)
hypoalbuminaemia
liver disease
nephrotic syndrome
malabsorption
hypothyroidism
Meigs’ syndrome

133
Q

Exudative causes of pleural effusions?

A

Exudate (> 30g/L protein)
infection
pneumonia (most common exudate cause),
tuberculosis
subphrenic abscess
connective tissue disease
rheumatoid arthritis
systemic lupus erythematosus
neoplasia
lung cancer
mesothelioma
metastases
pancreatitis
pulmonary embolism
Dressler’s syndrome
yellow nail syndrome

134
Q

Acute pancreatitis can cause what kind of mineral imbalance?

A

Hypocalcaemia

135
Q

Which two drugs together may cause bone marrow suppression and severe or fatal pancytopaenia?

A

Methotrexate and trimethoprim

136
Q

CN I

137
Q

CN II

138
Q

CN III

A

Oculomotor

139
Q

CN IV

140
Q

CN V

A

Trigeminal

141
Q

CN VI

142
Q

CN VII

143
Q

CN VIII

A

Vestibulocochlear

144
Q

CN IX

A

Glossopharyngeal

145
Q

CN X

146
Q

CN XI

147
Q

CN XII

A

Hypoglossal

148
Q

Function of CN I

149
Q

Function of CN II

150
Q

Function of CN III

A

Eye movement and blinking

151
Q

Function of CN IV

A

Superior oblique muscle –>
Up and down and back and forth eye movements

152
Q

Function of CN V

A

Facial sensations, muscles of mastication

153
Q

Function of CN VI

A

Lateral rectus muscle –>
Eye movements

154
Q

Function of CN VII

A

Expression and sense of taste

155
Q

Function of CN VIII

A

Hearing and balance

156
Q

Function of CN IX

A

Taste and swallowing

157
Q

Function of CN X

A

Heart rate and digestion

158
Q

Function of CN XI

A

Neck and shoulder movement

159
Q

Function of CN XII

A

Tongue movement

160
Q

First line for primary biliary cholangitis?

A

Ursodeoxycholic acid

160
Q

Management of bilateral adrenocortical hyperplasia

A

Primary hyperaldosteronism: Spironolactone

161
Q

All patients with PAD should take what?

A

Clopidogrel and atorvastatin

162
Q

Rheumatoid arthritis x-ray changes

A

loss of joint space
juxta-articular osteoporosis
soft-tissue swelling
periarticular erosions
subluxation

163
Q

Heberden’s nodes and Bouchard’s nodes for what?

A

Osteoarthritis

164
Q

First-line management in patients with hypercalcaemia

165
Q

If known COPD pt has a normal CO2 on ABG, what’s their target O2 sat?

166
Q

Paracetamol poisoning Mx?

A

activated charcoal if ingested < 1 hour ago
N-acetylcysteine (NAC)
liver transplantation

167
Q

Salicylate poisoning Mx?

A

Urinary alkalinization with IV bicarbonate
haemodialysis

168
Q

Opioid/opiates poisoning Mx?

169
Q

Benzodiazepine poisoning Mx?

A

Flumazenil
The majority of overdoses are managed with supportive care only due to the risk of seizures with flumazenil. It is generally only used with severe or iatrogenic overdoses.

170
Q

Tricyclic antidepressants overdose Mx?

A

IV bicarbonate may reduce the risk of seizures and arrhythmias in severe toxicity
arrhythmias: class 1a (e.g. Quinidine) and class Ic antiarrhythmics (e.g. Flecainide) are contraindicated as they prolong depolarisation. Class III drugs such as amiodarone should also be avoided as they prolong the QT interval. Response to lignocaine is variable and it should be emphasized that correction of acidosis is the first line in management of tricyclic induced arrhythmias
dialysis is ineffective in removing tricyclics

171
Q

Lithium poisoning Mx?

A

mild-moderate toxicity may respond to volume resuscitation with normal saline
haemodialysis may be needed in severe toxicity
sodium bicarbonate is sometimes used but there is limited evidence to support this. By increasing the alkalinity of the urine it promotes lithium excretion

172
Q

Warfarin poisoning Mx?

A

Vitamin K, prothrombin complex

173
Q

Heparin poisoning Mx?

A

Protamine sulphate

174
Q

Beta-blockers overdose Mx?

A

if bradycardic then atropine
in resistant cases glucagon may be used

175
Q

Ethylene glycol overdose Mx?

A

ethanol has been used for many years
works by competing with ethylene glycol for the enzyme alcohol dehydrogenase
this limits the formation of toxic metabolites (e.g. Glycoaldehyde and glycolic acid) which are responsible for the haemodynamic/metabolic features of poisoning
fomepizole, an inhibitor of alcohol dehydrogenase, is now used first-line in preference to ethanol
haemodialysis also has a role in refractory cases

176
Q

Methanol poisoning Mx?

A

fomepizole or ethanol
haemodialysis

177
Q

Organophosphate insecticides poisoning Mx?

A

atropine
the role of pralidoxime is still unclear - meta-analyses to date have failed to show any clear benefit

178
Q

Digoxin poisoning Mx?

A

Digoxin-specific antibody fragments

179
Q

Iron overdose Mx?

A

Desferrioxamine

180
Q

Lead poisoning Mx?

A

Dimercaprol, calcium edetate

181
Q

Carbon monoxide poisoning Mx?

A

Management
100% oxygen
hyperbaric oxygen

182
Q

Cyanide poisoning Mx?

A

Hydroxocobalamin; also combination of amyl nitrite, sodium nitrite, and sodium thiosulfate

183
Q

Scarlet fever school exclusion?

A

24 hours after starting Abx

184
Q

Whooping cough school exclusion?

A

2 days after starting Abx
or 21 days after Sx onset if no Abx

185
Q

Measles school exclusion?

A

4 days after rash

186
Q

Rubella school exclusion?

A

5 days after rash

187
Q

Chickenpox school exclusion?

A

Until lesions crusted over

188
Q

Mumps school exclusion?

A

5 days from onset of swollen glands

189
Q

D+V school exclusion?

A

Until settled for 48hrs

190
Q

Impetigo school exclusion?

A

Until lesions are crusted and healed, or 48 hours after commencing antibiotic treatment

191
Q

Scabies school exclusion?

A

Until treated

192
Q

Influenza school exclusion?

A

Until recovered

193
Q

Which drugs are contraindicated in aortic stenosis?

194
Q

Abdominal pain, diarrhoea and flushing triad is?

A

Carcinoid syndrome

195
Q

Likelihood ratio of a positive test result

A

Sensitivity/(1-Specificity)

196
Q

Likelihood ratio of a negative test result

A

(1-Sensitivity)/Specificity

197
Q

Over-replacement with thyroxine causes what

A

Osteoporosis

198
Q
  • Raynaud’s may be the first sign
  • Scleroderma affects face and distal limbs predominately
  • Associated with anti-centromere antibodies
  • A subtype of it is CREST syndrome.
  • Anti-centromere antibodies
A

Limited cutaneous systemic sclerosis

199
Q

Scleroderma affects trunk and proximal limbs predominately
associated with anti scl-70 antibodies
the most common cause of death is now respiratory involvement, which is seen in around 80%: interstitial lung disease (ILD) and pulmonary arterial hypertension (PAH)
other complications include renal disease and hypertension
patients with renal disease should be started on an ACE inhibitor - captopril is typically used due to its rapid onset and short half-life, allowing for dose titration
ACE inhibitors target the underlying mechanism by reducing efferent arteriolar vasoconstriction and limiting renin-angiotensin system activation
poor prognosis

Anti-Scl-70 antibodies

A

Diffuse cutaneous systemic sclerosis

200
Q

tightening and fibrosis of skin
may be manifest as plaques (morphoea) or linear

A

Scleroderma without organ involvement

201
Q

CREST syndrome stands for…

A

Calcinosis, Raynaud’s phenomenon, oEsophageal dysmotility, Sclerodactyly, Telangiectasia

202
Q

After an initial negative result when testing for HIV in an asymptomatic patient, offer a repeat test at…

203
Q

AML is characterised by…?

A

Neutropaenia and thrombocytopaenia

204
Q

Guttate psoriasis Mx?

A

Reassurance + topical treatment if lesions are symptomatic

205
Q
  • asthma
  • blood eosinophilia (e.g. > 10%)
  • paranasal sinusitis
  • mononeuritis multiplex
  • renal involvement occurs in around 20%
  • pANCA positive in 60%
A

Eosinophilic granulomatosis with polyangiitis

206
Q

What is the most common cause of traveller’s diarrhoea? (non-bloody)

207
Q

If you are waiting for a phaeochromocytoma surgery, what medical management do you give first?

A

Phenoxybenzamine

208
Q

What’s the RRR equation?

A

(Treatment rate - Control rate) / Control rate

209
Q

Pain at rest in leg for greater than 2 weeks, often at night, not helped by analgesia

A

Critical limb ischaemia

210
Q

Premenstrual syndrome Mx?

A

Drospirenone-containing COC taken continuously

211
Q

RBC transfusion threshold for patients with ACS is what

212
Q

Which meds can cause SJS?

A

* Carbamezapine
* Lamotrigine
* Allopurinol
* Sulfonamide
* Phenobarbital

* Phenytoin
* Salicylates
* Sertraline
* Imidazole antifungal agents
* Nevirapine

213
Q

What should we give a lady with a fibroids who is waiting for surgery?

A

GnRH agonist e.g. Goserelin

214
Q

If UTI + catheter, no symptoms, what Mx?

A

NOTHING; DON’T DO ANYTHING.

215
Q

Which cranial nerves are affected in vestibular schwannomas?

A

V, VII, VIII

216
Q

PID + RUQ pain =

A

Fitz-Hugh-Curtis Syndrome

217
Q

Type I SH fracture

A

Fracture through physis (x-r may be normal)

Transverse

218
Q

Type II SH Fracture

A

Physis and metaphysis

—/

219
Q

Type III SH Fracture

A

Physis, epiphysis, include joint

|—

220
Q

Type IV SH Fracture

A

Physis, metaphysis, epiphysis

|

221
Q

Initial Mx for Graves’ disease?

A

Propanolol

222
Q

Rovsings sign in…

A

Appendicitis

223
Q

Boas sign in…

A

Cholecystitis

224
Q

Murphy’s sign in…

A

Cholecystitis

225
Q

Cullens sign in…

A

Pancreatitis

226
Q

Grey-Turners sign in…

A

Pancreatitis

227
Q

Cardiac tamponade triad

A

Elevated JVP, hypotension, muffled heart sounds

228
Q

CT within an hour indications?

A
  • GCS <13 now
  • <15 after
  • Vomiting > 1
  • Skull fracture
  • Seizures
229
Q

CT within 8 hours

A
  • > = 65
  • Anticoagulants
  • Dangerous mechanism of injury
230
Q

Tell me pneumothorax guidelines

231
Q

What do you not give in a variceal bleed?

232
Q

In patients with nephrotic syndrome, you give prednisolone and furosemide. What next?

A

Prophylactic LMWH e.g. enoxaparin due to inc. risk of VTE

233
Q

What are the contraindications for suxamethonium?

A
  • Penetrating eye injuries
  • Acute glaucoma

Because it inc. IOP