Miscellaneous Flashcards

(29 cards)

1
Q

Treatment for Paracetamol overdose

A

IV N-acetylcysteine

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2
Q

Treatment for Opiate overdose

A

Naloxone

IM if non-medical
Intravenous injection if medical/post-op respiratory depression

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3
Q

Treatment for Aspirin overdose

A

Sodium Bicarbonate

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4
Q

Treatment for Benzodiazepine overdose

A

Flumezanil

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5
Q

Treatment for organophosphate poisoning

A

Atropine

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6
Q

Management of STEMI (Acute)

A

Aim is to relieve pain, promote re-perfusion and reduce mortality:

Morphine 2-4mg IV every 15 minutes 
Metoclopramide 10mg IV
Oxygen 15L/min non-rebreather mask
Nitrates (GTN)
Anti-platelet (Aspirin and Clopidogrel 300mg oral)
Beta-blockers
ACEi
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7
Q

Management of STEMI (long-term)

A
Aspirin 75mg oral
Beta-blocker (metoprolol, propanolol, timolol)
CCB if BB CI (verapamil)
ACEi
Nitrates
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8
Q

Hereditary pattern: Polycystic kidney disease

A

Autosomal Dominant

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9
Q

Hereditary pattern: Cystic Fibrosis

A

Autosomal Recessive

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10
Q

Hereditary pattern: Haemophilia

A

X-linked recessive

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11
Q

Hereditary pattern: Thalassaemia

A

Autosomal Recessive

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12
Q

Hereditary pattern: Huntingdon’s disease

A

Autosomal Dominant

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13
Q

Hereditary pattern: Marfan’s Syndrome

A

Autosomal Dominant

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14
Q

Hereditary pattern: Sickle Cell Disease

A

Autosomall Recessive

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15
Q

Hereditary pattern: Hereditary Haemorrhagic Telangiectasia

A

Autosomal Dominant

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16
Q

Hereditary pattern: Peutz-Jeghers Syndrome

A

Autosomal Dominant

17
Q

Hereditary pattern: G6PD Deficiency

A

X-linked Recessive

18
Q

Hereditary pattern: Red-Green Colour blindness

A

X-linked recessive

19
Q

Hereditary pattern: Von Willebrand Disease I, II, III

A

I: Autosomal Dominant
II: Autosomal Dominant
III: Autosomal Recessive

20
Q

Hereditary pattern: Ehler’s Danlos

A

Autosomal Dominant

21
Q

Hereditary pattern: Glanzann’s Thrombasthenia

A

Lack of GIp IIb/IIIa -> no platelet aggregation (via fibrinogen)

Autosomal Recessive

22
Q

Hereditary pattern: Bernard Soulier Syndrome

A

Lack of GIp Ib -> no platelet adhesion (via vWF)

Autosomal Recessive

23
Q

Hodgkin’s Lymphoma is associated with: (multiple)

a. Reed Sternberg Cells
b. CMV
c. EBV
d. Tender lymphadenopathy
e. Non-tender lymphadenopathy
f. Pruritis
g. Bone pain
h. jaundice
i. HIV
j. B symptoms
k. Fewer Constitutional symptoms
l. Commin in Men
m. Extranodal spread
n. Localised group of nodes
o. B or T cells
p. Bimodal age distribution (young and old)
q. 20-40 year olds

A
Reed-Sternberg Cells
EBV
Non-tender lymphadenopathy (pain with alcohol drinking)
Pruritis
B symptoms
Common in Men
Localised node spread
Bimodal age distribution
24
Q

Non-Hodgkin’s Lymphoma is associated with: (multiple)

a. Reed Sternberg Cells
b. CMV
c. EBV
d. Tender lymphadenopathy
e. Non-tender lymphadenopathy
f. Pruritis
g. Bone pain
h. jaundice
i. HIV
j. B symptoms
k. Fewer Constitutional symptoms
l. Commin in Men
m. Extranodal spread
n. Localised group of nodes
o. B or T cells
p. Bimodal age distribution (young and old)
q. 20-40 year olds

A
Non-Tender lymphadenoapthy 
Fewer constitutinal symptoms
Extranodal spread (other organs e.g. bone, spleen)
B or T cells
20-40 year olds
25
Cough productive of large volumes and can be rusty-coloured. Recurrent infections with other symptoms such as haemoptysis, dyspnoea, chest pain, weight loss. On auscultation it is coarse crepitations and wheeze
Bronchiectasis
26
SLE is a multisystem autoimmune disease where there are varieties of antibodies against self-antigens, resulting in wide-spread tissue damage. SLE is diagnosed if 4 of 11 of which criteria are met?
SOAP BRAIN MD Serositis (pleuritis, paricarditis) Oral Arthritis (non-erosive) Photosensitivity Blood disorders (Haemolytic anaemia, leukopenia, thrombocytopenia) Renal disorders (proteinuria, red cell casts) ANA Immunological disorders (anti-dsDNA/phospholipid antibodies) Neuro disease (psychosis, seizures) Malar rash Discoid rash
27
Three organisms that cause a cavitating lesion in the lungs with background history of cough, fever, SoB
Staphylococcus aureus, Klebsiella pneumoniae | TB
28
Name the four histopathological types of malignant melanoma
1. Superficial spreading (arises from naevi already there. Darkening of area and spread radially as supposed to vertically. 'Slowly changing mole' 2. Nodular (rapidly grows out of skin from no previous naevi and grow vertically as blue-black or blue-red mole) 3. Acral Lentiginous (Brown-black macules confined in the soles and palms of feet and hands. Irregular borders) 4. Lentigo (arises from sun-exposed skin. Large, dark and can be nodular
29
Cardiac Tamponade is characterised by Beck's Triad, which is;
1. Muffled heart sounds 2. Raised JVP 3. HYPOtension