Haem Flashcards

1
Q

What antibiotic is contraindicated in G6PD deficiency

A

ciprofloxacin

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2
Q

how does factor v leiden increase risk of VTE

A

factor V is a clotting agent
protein c inactivates it 10 times slower

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3
Q

Role of von willibrand factor

A

large glycoprotein that triggers platelet adhesion to damaged endothelium
Normal platelets, raised APTT, raised bleeding time

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4
Q

What is used to monitor heparin

A

APTT
Activates antithrombin III. Forms a complex that inhibits thrombin, factors Xa, IXa, Xia and XIIa

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5
Q

What is used to monitor LMWH

A

Factor Xa
Activates antithrombin III. Forms a complex that inhibits factor Xa

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6
Q

polycythaemia vera long term management

A

aspirin

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7
Q

what factors does warfarin affect?

A

2,7,9,10

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8
Q

treatment of von willibrand

A

desmopressin

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9
Q

TTP deficiency

A

ADAMTS13 which breaks down large clumps of von willebrand factor

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10
Q

polycythaemia vera complications

A

AML or myelofibrosis

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11
Q

trasnfusion thresholds

A

normally 70g/L but 80g/L if ACS

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12
Q

drugs contraindicated in G6PD

A

sulph- drugs: sulphonamides, sulphasalazine and sulfonylureas can trigger haemolysis
anti-malarials: primaquine
ciprofloxacin

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13
Q

first line investigation for PRC

A

JAK2 mutation

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14
Q

AIHA treatment

A

steroids + rituximab

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15
Q

secondary cause of PRV

A

copd: hypoxia leads to increased EPO

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16
Q

Wide distribution of red blood cells/High RDW

A

mixed anaemia e.g. iron deficiency with b12.

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17
Q

Blister cells

A

G6PD

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18
Q

electrolyte abnormality with packed red blood cells

A

hyperkalemia

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19
Q

what viral infection causes facial flushing

A

dengue fever

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20
Q

waldenstroms macroglobulinaemia

A

secretion of a monoclonal IgM paraprotein

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21
Q

platelet transfusion before invasive procedure

A

must be above 50

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22
Q

1st line imaging for multiple myeloma

A

whole body MRI

23
Q

acute haemolytic transfusion reaction patho

A

Binding of IgM-type antibodies to red blood cells causing haemolysis
39%

24
Q

how to differentiate AML and CML

A

AML: neutropenia
CML: neutrophillia

25
atypical lymphocytes
glandular fever
26
richters transformation
CLL -> non-hodgkins (DLBCL)
27
reverseal of dabigatran
idarucizumab
28
Reversal of other doacs
andexanet alfa
29
why are irradiated blood products used
avoid transfusion-associated graft versus host disease e.g. hodgkins lymphoma
30
most common type of hodgkins lymphoma
nodular scelrosing
31
painful when drinking alcohol
hodgkins
32
clinical TLS signs
increased serum creatinine (1.5 times upper limit of normal) cardiac arrhythmia or sudden death seizure
33
gastric malt lymphoma association
h.pylori (non-hodgkin's)
34
G6PD diagnosis
enzyme assay at the time and in 3 months
35
what effect can p450 inducers have on warfarin
increased clearance
36
cause of acute haemolytic febrile reaction
ABO incompatible blood
37
Name 2 immediate steps that need to be taken after a acute haemolytic reaction
Stop blood transfusion & inform the hospital Transfusion Laboratory Take a post transfusion sample from patient & send to Transfusion Laboratory for direct Coombs test, repeat typing and cross-matching
38
What can cause TACO
Excessive rate of transfusion, pre-existing heart failure
39
what causes minor allergic reaction in transfusions?
reaction to foreign plasma proteins
40
cause of non-haem febrile reaction
antibodies reacting with white cell fragments in the blood product and cytokines that have leaked from the blood cell during storage
41
sickle cell management
pneumococcal polysaccharide vaccine every 5 years
42
HbH vs Barts
HbH: beta chains form tetrameres (splenomegaly, hypochromic, microcytic anaemia) Barts: gamma chains form tetramers (hydrops fetalis)
43
How can warfarin lead to skin necrosis
when warfarin is first started biosynthesis of protein C is reduced this results in a temporary procoagulant state after initially starting warfarin, normally avoided by concurrent heparin administration thrombosis may occur in venules leading to skin necrosis
44
features of haemochromatosis
fatigue, erectile dysfunction and arthralgia (often of the hands) 'bronze' skin pigmentation diabetes mellitus
45
vitamin k dependent clotting factors
2,7,9,10
46
blood products
Fresh frozen plasma (FFP) - universal donor of FFP is AB blood because it lacks any anti-A or anti-B antibodies Cryoprecipitate - contains concentrated Factor VIII:C, von Willebrand factor, fibrinogen, Factor XIII and fibronectin - fibrinogen concentration < 1.5 g/L Prothrombin complex concentrate - emergency reversal of anticoagulation in patients with either severe bleeding or a head injury with suspected intracerebral haemorrhage
47
factors to reduce risk of sickle cell crisis
avoid dehydration/cold/exhaustion smoking + alcohol
48
neutropenic sepsis organism
staph epidermis
49
target cells 'pencil' poikilocytes
iron deficiency
50
most common type of non-hodgkins lymphoma
diffuse large b cell
51
contraindications to platelet transfusion
Chronic bone marrow failure Autoimmune thrombocytopenia Heparin-induced thrombocytopenia, or Thrombotic thrombocytopenic purpura.
52
complication of myelodysplasia
AML
53
transformations
Myelodysplasia --> AML CML --> ALL or AML CLL --> NHL