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
what organisms are those with sickle cell disease susceptible to
strep penumo, haemophilus influenza, pseudomonas aurginosa
25
myeloid lineage
innate response platelets rbcs granulocytes macrophages monocytes dendritic
26
lymphoid lineage
adaptive response b cellls t cells nk cells
27
What technique reliably identifies the cell-type (lineage)?
immunophenotyping
28
what suppresses erythopoieses in polycythaemia vera
hydroxycarbamide
29
essential thrombosis age relation
women in their 50-70s
30
where do drugs inhibitng dna synthesis target
s phase
31
leukoeryythroblastic
immature wbcs and rbcs in peripheral blood
32
polycythaemia treatment
aspirin 75mg and venesection <45%
33
treatment for essential thrombocythaemia if cant have aspirin aka if have asthma etc
hydroxyurea
34
what might anabolic steroid use cause
secondry polycythaemia
35
aplastic crisis
low retic count and severe anaemia due to paravirus b19
36
low platelet count, prolonged bleeding time and mucosal bleeding
immune thrombocytopenic purpura
37
first line treatment for immune thrombocytopenic purpura
steroids to suppress immune system to stop attacking platelets
38
risk with heparin
heparin induced thrombocytopenia
39
how to confirm hereditary spheroytosis
Eosin-5′-maleimide (EMA) binding test
40
what might methotrexate cause
folate deficiency so must be co prescirbed
41
first line treatment for chronic myeloid leukaemia
Imatinib
42
fatigue, pallor, dizzy, tingling
b12 def
43
g6pd inheritance
x linked recessive
44
drug which suppresses erythrpoietin
hydroxycarbamide
45
cause of aplastic crisis
parvovrius b19
46
first line dvt
rivaroxaba - any doac
47