Randop Flashcards

1
Q

aptt

A

lab test used to evaluate the clotting ability of blood by measuring the time it takes for a clot to form in a plasma sample after adding an activator, phospholipid, and calcium

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2
Q

isolated prolonged aptt

A

(aPTT) means that the aPTT is longer than normal, but other coagulation tests (such as prothrombin time [PT] and platelet count) are within the normal range.

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3
Q

prothrombin time

A

how long it takes for blood to clot

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4
Q

joint symptoms and hyper pigmented appearance

A

iron overload

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5
Q

risk of regular transfusions

A

iron overload

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6
Q

hbh disease

A

1/4 functioning alpha genes

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7
Q

frontal bossing sign of

A

beta thalaessemia major

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8
Q

vwf assoc

A

bleeding time prolonged
factor viii decreased
aptt increased ]

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9
Q

joint bleeding

A

haemophilia

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10
Q

nose bleeds, gum bleeding etc

A

vwd

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11
Q

MOA of doacs

A

inhibtio of factor xa

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12
Q

MOA of warfarin

A

vit k antagonist

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13
Q

blood film finding on DIC

A

schisocytes

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13
Q

what factor def is haemophilia b

A

factor IX

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14
Q

what factor def do patients with haemo[hilia a have

A

factor viii

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15
Q

foetal complication alpha thalassaemia

A

barts hydrops fetalis

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16
Q

treatment of dvt for active cancer

A

doac for at least 3 months

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17
Q

pt and aptt in ttp

A

normal

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18
Q

pt and aptt in dic

A

prolonge d

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19
Q

what does giving lmwh increase risk of immediately post op

20
Q

what causes an elevated A2 level

A

beta thalaessmia trait

21
Q

who does non hodgkins usually present in

A

older people

22
Q

who does hodgkins usually present in

23
Q

pentad of symptoms of thrombotic thrombocytopenic purpura

A

acute kidney injury, fever, low platelets, neurological features , microangiopathic anaemia

24
Q

what organisms are those with sickle cell disease susceptible to

A

strep penumo, haemophilus influenza, pseudomonas aurginosa

25
Q

myeloid lineage

A

innate response

platelets
rbcs
granulocytes
macrophages
monocytes
dendritic

26
Q

lymphoid lineage

A

adaptive response

b cellls
t cells
nk cells

27
Q

What technique reliably identifies the cell-type (lineage)?

A

immunophenotyping

28
Q

what suppresses erythopoieses in polycythaemia vera

A

hydroxycarbamide

29
Q

essential thrombosis age relation

A

women in their 50-70s

30
Q

where do drugs inhibitng dna synthesis target

31
Q

leukoeryythroblastic

A

immature wbcs and rbcs in peripheral blood

32
Q

polycythaemia treatment

A

aspirin 75mg and venesection <45%

33
Q

treatment for essential thrombocythaemia if cant have aspirin aka if have asthma etc

A

hydroxyurea

34
Q

what might anabolic steroid use cause

A

secondry polycythaemia

35
Q

aplastic crisis

A

low retic count and severe anaemia due to paravirus b19

36
Q

low platelet count, prolonged bleeding time and mucosal bleeding

A

immune thrombocytopenic purpura

37
Q

first line treatment for immune thrombocytopenic purpura

A

steroids to suppress immune system to stop attacking platelets

38
Q

risk with heparin

A

heparin induced thrombocytopenia

39
Q

how to confirm hereditary spheroytosis

A

Eosin-5′-maleimide (EMA) binding test

40
Q

what might methotrexate cause

A

folate deficiency so must be co prescirbed

41
Q

first line treatment for chronic myeloid leukaemia

42
Q

fatigue, pallor, dizzy, tingling

43
Q

g6pd inheritance

A

x linked recessive

44
Q

drug which suppresses erythrpoietin

A

hydroxycarbamide

45
Q

cause of aplastic crisis

A

parvovrius b19

46
Q

first line dvt

A

rivaroxaba - any doac