QuQuick recall 3 Flashcards

1
Q

Pathways!

Warfarin:
Heparin:
LMWH:

A

Warfarin: Extrinsic pathway –> prothrombin time

Heparin: Intrinsic pathway –> APTT

LMWH: enoXaparin - anti-factor Xa levels

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2
Q

Septic arthritis requires prolonged antibiotic therapy of at least

A

4-6 weeks

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3
Q

Standard heparin vs LMWH

A

Adverse effects of heparin:
–> bleeding
–> thrombocytopenia
–> osteoporosis (increased risk of fractures|0
–> hyperkalaemia

Heparin over dose: reversed by protamine sulphate

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4
Q

IgG,A,M,D,E

A

IgG: G for gestational - only Ig that can cross the placenta
IgA: A being the first letter, is the first Ig to be given to baby thru breastfeeding
IgM: M is a simp for the body (M’lady i’ll be the Main protector from pathogens)
IgD: D is like unsolicited dick pics, nobody knows what they’re good for
IgE: E is for Eosinophiles, which are also associated with the allergic response

IgM - pentamer
IgA - monomer / dimer
Rest monomer

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5
Q

The diagnostic criteria for HHS include

A
  • hypovolaemia
  • hyperglycaemia (BM > 30mmol)
  • serum osmolality (320 mosmol/kg)

Clinical features
- fatigue
- lethargy
- altered consciousness
- hypotension
- tachycardia

monitor SERUM OSMOLALITY

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6
Q

Carcinoid syndrome: investigation and management

A

Investigation
–> Urinary 5-HIAA
–> plasma chromogranin A y

Management
–> somatostatin analogues e.g. octreotide
–> diarrhoea: CRYPTOHEPATIDINE

Features
- flushing
- diarrhoea
- bronchospasm
- hypotension
- right heart valvular stenosis
- rare: pellagra

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7
Q

Hyperkalaemia management

mild: 5.5-5.9mmol/l
moderate: 6-6.4 mmol/l
severe: > 6.5mmol/l

A
  1. stabilisation of cardiac membrane: IV calcium gluconate
  2. Short term shift i K+ from ECF to intracellular fluid compartment
    –> combined insulin / dextrose infusion
    –> nebulused salbutamol
  3. Potassium removal from body
    –> calcium resonium (enema&raquo_space; oral)
    –> loop diuretics
    –> dialysis (w/ AKI

ECG: QRS widening and peaked T waves

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8
Q

TIA: assessment and referral

A
  1. ABCDE prognostic score
  2. Immediate antithrombotic therapy
    –> aspirin 300mg
    –> UNLESS: bleeding disorder, already on low dose aspirin or contraindicated
  3. Specialist review
    –> in last 7 days: arrange urgent assessment w/i 24 hrs
    –> post 7 days: asap w/i 7 days

INVESTIGATION:
1. MRI (diffusion-weighted and blood-sensitive sequences)
2. Carotid imaging: urgent carotid dopller

Further management
1. Secondary prevention: clopidogel 1st line
–> OR aspirin + dipyridamole
2. Statin
3. carotid stenosis > 70% –> CAROTID A. ENDARECTOMY (on side contralateral to symptoms)

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9
Q

Episodic, intense, unilateral eye pain, lacrimation, restless →

A

cluster headache
–> high flow oxygen + subcutaneous sumatriptan

Prophylaxis
- verampil

Paroxysmal hemicrania responds well to indomethacin

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10
Q

mnemonic for raised anion gap based on symptoms

In acidosis –> kussmaul breathing

A

K - ketones
u - uraemia
s - sepsis
s - salicylate
m - methanol
a - aldehyde
l - lactic acidosis

OR

MUDPILES for high anion gap

Methanol
Uraemia
DKA
Paracetamol/Paraldehyde
Iron
Lactate
Ethanol
Salicylates/Sepsis

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11
Q

Normal ion gap metabolic acidosis:

normal anion gap (6 - 16 mmol/L)

A

HARD ASS
Hyperalimentation
Addison’s
RTA
Diarrhoea

Acetazolamide
Spironolactone
Saline

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12
Q

Triad of sudden onset abdominal pain, ascites, and tender hepatomegaly: seen in

A

BUDD CHIARI SYNDROME (hepatic vein thrombosis)

  • raised SAAG >11 indicates portal HTN caused the ascites

IX - USS w/ doppler flow studies

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13
Q

Variceal haemorrhage: management

A

ABCDE
1. correct clotting: FFP, vit K
Before endoscopy
2. Vasoactive: terlipressin (or octreotide?)
3. prophylactic IV Abx (quinolones?)
4. Endoscopic varcieal band ligation

UNCONTROLLED HAEMORRHAGE
–> SENGSTAKEN-BLAKEMORE TUBE

TIPS if all else failed!

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14
Q

Prophylaxis of variceal haemorrhage

A
  1. Propranolol
  2. Endoscopic variceal band ligation (at 2 weekly intervals until eradication) + PPI
  3. TIPS if unsuccessful
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15
Q

DVLA: neurological disorders

A

Epilepsy
–> unprovoked: 6 months off IF no abnormalities on EEG (increased to 12 months)
–> established: driving licence if seizure free 12 months, no seizure for 5 years
–> withdrawal of AED: 6 months after last dose

Syncope
–> faint: no restriction!
–> single, explained, treated –> 4 WEEKS OFF
–> single, unexplained –> 6 MONTHS off
–> 2 or more –> 12 months off

Stroke / TIA
–> 1 month off, no need to inform DVLA if no neurological deficiit
–> multiple TIAs: 3 months off driving and inform DVLA

Craniotomy
–> 1 year off driving

Pituitary tumour
–> 6 months

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16
Q

Statin doses for primary and secondary prevention

A
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17
Q

Retro-orbital headache, fever, facial flushing, rash, thrombocytopenia in returning traveller →

A

DENGUE fever
–> maculopapular after 3-4 days after onset of illness
–> thrombocytopenia

18
Q

Recent sore throat, rash, arthritis, murmur →

A

rheumatic fever
- following streptococcus pyogenes infection

19
Q

Hyperosmolar hyperglycaemia state: Pathophysiology

A

hyperglycaemia → ↑ serum osmolality → osmotic diuresis → severe volume depletion

Managment:
1. IV fluid replacement (0.5-1L/hr) , monitor K+
2. Insulin (not until BG stops falling while giving IV Fluids)
3. VTE prophylaxis

20
Q

The anion gap is calculated by:

A

(sodium + potassium) - (bicarbonate + chloride). A normal anion gap is 10-18 mmol/L.

21
Q

Paget’s disease of the nipple:

A

Diagnosis made via punch biopsy, mammography and USS of breast

Needs breast clinic referral urgent!

22
Q

THESE are typically spared in motor neurone disease

A

Eye movements

23
Q

CT shows:

A

**Aortic dissection **
- intraluminal tear formed a ‘flap’ in the ascending aorta
- Stanford TYPE A DISSECTION

HTN common in AD aar cathecholamine surge

24
Q

Hoffman’s sign

A

Involuntary flexion movement of the thumb and or index finger when the examiner flicks the fingernail down.

Degenerative cervical myelopathy.

25
typically presents with abdominal, neurological and psychiatric symptoms
acute intermittent porphyria - autosomal dominant - enzyme involved in biosynthesis of haem - leads to toxic accumulation of delta aminolaevulinic acid and porphobilinogen
26
1st line treatment for chronic myeloid leukaemia
Imantinib - tyrosine kinase inhibitor Philadelphia chromosome ! | - high white cell - blast cells would indicate acute anaemia
27
P450 enzyme inducers
PC BRATS- inducers Phenytoin Carbamazepine Barbiturates Rifampicin Alcohol Topiramate Sulfonylureas
28
Tracheal deviation, resonant to percussion and absent breath sounds in the context of respiratory distress and shock -
TENSION PNEUMOTHORAX MX: immediate decompression via needle thoracostomy Causes: 1. Traumatic: blunt / penetrating chest trauma 2. Iatrogenic: thoracentesis, central venous catheter placement, positive pressure mechanical ventilation 3. Spontaneous: COPD / CF, lung blebs may rupture
29
A 25-year-old lady presents with an swelling located at the anterior border of the sternocleidomastoid muscle. The swelling is intermittent and on examination it is soft and fluctuant.
Branchial cysts are remnants of the branchial cleft. They may become infected.
30
Differentiating posterior vitreous detachment, retinal detachment and vitreous haemorrhage: POSTERIOR VITREOUS DETACHMENT
1. Flashes of light (photopsia) in peripheral field of vision 2. Floaters (often temporal side of central vision)
31
Differentiating posterior vitreous detachment, retinal detachment and vitreous haemorrhage: - dense shadow starting peripherally moving towards central vision - a veil or curtain over field of vision - straight lines appear curved - central vision loss
RETINAL DETACHMENT
32
Large bleeds cause sudden visual loss Moderate bleeds may be described as numerous dark spots Small bleeds may cause floaters
Vitreous haemorrhage
33
Anti-GBM disease typically presents with:
Haemoptysis + AKI/proteinuria/haematuria Small vessel vasculitis associated with both pulmonary haemorrhage and rapidly progressive glomerulonephritis. --> may be exacerbated by cold IX: renal biopsy showing linear IgG deposits Mx: --> plasma excahnge --> steroids --> cyclophosphamide key complication is pulmonary haemorrhage!
34
ASA gradings
35
Osteomalacia
Causes: Vit D deficiency, CKD, Liver disease, coeliacs Feature: bone pain, muscle tenderness, fractures, proximal myopathy (waddling gait) IX: Bloods : vit D, raised ALP X-RAY: translucent bands (looser's zones or psuedofractures) Tx: 1. Vit D supplementation (loading dose needed) 2. calcium supplementation if dietary calcium inadequate | Softening of bones secondary to low vitamin D levels
36
Causes of respiratory alkalosis:
Respiratory Alkalosis PAST PH Panic attacks Anxiety attacks Salicylates Tumour Pulmonary embolism Hypoxaemia ## Footnote Note: salicylate overdose can cause mixed primary resp alkalosis and metabolic acidosis
37
first-line treatment for magnesium sulphate induced respiratory depression.
Calcium gluconate
38
This woman has a symptomatic megaloblastic anaemia associated with glossitis. This is likely due to
Pernicious anaemia: B12 deficiency Intrinsic factor antibodies Mx: Vit B12 injections, 3 injections weekly for 2 weeks followed by 3 monthly treatment of vitamin b12 injections --> folic acid supplementation? ## Footnote B12 important for RBC production and myelination of nerves
39
Different type of cysts
Epidermoid cyst - 'Blackhead' Sebaceous cyst - 'Whitehead' Dermoid cyst - Can contain hair (or teeth/other abnormal growths within -dependent on the location [ovaries]) Desmoid tumours are benign tumours of connective tissue
40
What does the following show:
- papilloedema - lurring of the optic disc edges - enlargement of the surrounding veins. - small haemorrahges surrounding optic disc
41