haem Flashcards

(39 cards)

1
Q

mx of post-thrombotic syndrome

A

compression stockings

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2
Q

when does post-thrombotic syndrome occur

A

6 months to 2 years after a DVT

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3
Q

causes of petechiae in adults

A
ITP
bone marrow failure (secondary to leukaemias, myelodysplasia or bone mets)
senile purpura
drugs
nutritional deficiencies
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4
Q

non-emergency mx of ITP in adults

A

platelet count >30 - observe

platelet count <30 - oral prednisolone

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5
Q

ix for polycythaemia vera (after FBC)

A

JAK2 mutation screen

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6
Q

sickle cell with high reticulocyte

A

sequestration crisis

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7
Q

sickle cell with low reticulocytes

A

aplastic anaemia caused by Parvovirus

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8
Q

diagnostic criteria for tumour lysis syndrome (TLS)

A

positive laboratory TLS (raised uric acid, hyperkalaemia, hyperphosphataemia or hypocalcaemia)
AND
positive clinical TLS (increased creatinine, cardiac arrhythmia or seizure)

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9
Q

ABX for neutropenic sepsis

A

IV Tazobactam and Piperacillan (Tazocin)

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10
Q

what can myelodysplasia transform into?

A

AML

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11
Q

what can CML transform into?

A

AML or ALL

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12
Q

what can CLL transform into?

A

non-Hodgkin’s lymphoma (Richter’s transformation)

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13
Q

CML bloods

A

increase in granulocytes at different stages of maturation

anaemia

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14
Q

CLL bloods

A

lymphocytosis
anaemia
smudge cells

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15
Q

transfusion threshold NO ACS

A

70 g/L

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16
Q

transfusion threshold ACS

17
Q

features of TTP (thrombotic thrombocytopenic purpura)

A
FAT RN 
Fever
Anaemia
Thrombocytopenia
Renal failure
Neuro features
18
Q

myeloma bloods

A

raised Ca
normal/high phosphate
normal ALP

19
Q

mx of antiphospholipid syndrome

A

primary thromboprophylaxis - low dose aspirin
secondary thromboprophylaxis - lifelong warfarin
- initial VTE - target INR of 2-3
- recurrent VTE - target INR of 3-4 (if occurred whilst taking warfarin then consider adding low-dose aspirin)
- arterial thrombosis - target INR 2-3

20
Q

features of multiple myeloma

CRABBI

A
Calcium raised
Renal failure
Anaemia
Bone lesions
Bleeding (thrombocytopenia)
Infection
21
Q

FBC in beta thalassaemia trait

A

Microcytosis disproportionate to anaemia

22
Q

what are acute haemolytic transfusion reactions the result of

A

RBC destruction by IgM antibodies

23
Q

features of tumour lysis syndrome

A

hyperkalaemia
hyperphosphataemia
hypocalcaemia

24
Q

mx of tumour lysis syndrome

25
which leukaemia may polycythaemia rubra vera transform into
AML
26
ITP in adults
thrombocytopenia | any of: purpura, epistaxis or major haemorrhage (e.g. intracranial)
27
universal donor of fresh frozen plasma
AB RhD negative blood
28
inheritance pattern of G6PD deficiency
X-linked
29
direct Coombs test
autoimmune haemolytic anaemia
30
blood film findings in AML
Auer rods
31
dx for painful vaso-occlusive crisis in sickle cell
clinical - no additional tests will confirm this
32
when to think about autoimmune haemolytic anaemia
anaemia in Mycoplasma infection with raised LDH and raised unconjugated bilirubin
33
antibodies to measure in macrocytic anaemia
INTRINSIC FACTOR
34
blood film findings of G6PD deficiency
bite and blister cells
35
bloods in DIC
low platelets and fibrinogen | prolonged PT, APTT and bleeding time
36
bloods in alcoholic liver disease
macrocytic anaemia | thrombocytopenia
37
when to transfuse platelets
platelet count <30x10^9 and clinically significant bleeding | platelet count <10x10^9 if no active bleeding
38
bloods in von Willebrand disease
normal platelets prolonged bleeding time prolonged APTT
39
bloods in anaemia of chronic disease
normocytic anaemia low serum iron low TIBC raised ferritin