Haematology Flashcards

(61 cards)

1
Q

What does APTT measure?

A

Time taken for a blood clot as a function of the intrinsic and common pathways

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2
Q

What causes Haemophilia A?

A

Factor VIII deficiency

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3
Q

What causes Haemophilia B?

A

Factor IX deficency

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4
Q

What factors deficiencies will prolong APTT?

A

I, II, V, VIII, IX, XII

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5
Q

What does PT measure?

A

Time taken for blood to clot as a function on the extrinsic and common pathways

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6
Q

What would PT and APTT results be for Haemophilia A and B?

A

APTT prolonged

Normal PT

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7
Q

Which lymphomas are associated with EBV?

A

Hodgkin
Burkitt
AIDS-associated

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8
Q

What is Lymhoma?

A

Tumour derived from lymphocytes
Can be Hodgkin or non-Hodgkin
NHL has many subtypes

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9
Q

What are symptoms of lymphoma?

A

FLAWS
Lymphadenopathy
Pruritus
Fatigue

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10
Q

What causes chronic myeloid leukaemia?

A

Chromosomal translocation

Produces a fusion protein

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11
Q

What is the main use of anti-coagulants?

A

Prevent thrombus formation
(thrombus comprising of fibrin web, platelets and RBCs)
Mainly venous

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12
Q

What class of drug is Warfarin?

A

Vitamin K antagonist

Affect reversible by giving Vit K (phytomenadione)

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13
Q

What drug is more appropriate for arterial occlusion?

A

Aspirin

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14
Q

What needs to be monitored in patients on warfarin?

A

INR

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15
Q

What is the main adverse effect of oral anticoagulants?

A

Haemorrhage

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16
Q

What are some DOACs?

A

Apixaban
Rivaroxiban
Used in prevention of strokes in AF and 2ry prevention of DVT/PE

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17
Q

What is the advantages of DOACs?

A

Do not need to be monitored

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18
Q

What can reverse apixaban/rivaroxiban?

A

Andexanet alfa

Used for uncontrolled/life threatening bleeding

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19
Q

When must a patient taking Warfarin inform their GP for possible dose adjustment?

A

symptoms of, or confirmed, COVID-19 infection

are otherwise unwell with sickness or diarrhoea, or have lost their appetite

changes to diet, smoking, or alcohol

taking any new medicines or supplements;
are unable to attend their next scheduled blood test

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20
Q

What does anti-platelet therapy do?

A

Decreased platelet aggregation and inhibits thrombus formation in the arterial circulation

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21
Q

What are some anti-platelet therapies?

A

Asprin

Clopidogrel

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22
Q

What are the main indications for anti-platelets?

A

Prevention of atherothrombotic events
Prevention of cardiovascular events for high risk
Prior to PCI

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23
Q

What is 1st line anti-platelet for ACS?

A

Lifelong Asprin and 12 months ticagrelor

Same for PCI

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24
Q

What is 1st line anti-platelet for TIA, Ischaemic stroke and PAD?

A

Clopidogrel

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25
What score is used to calculate risk of bleeding?
HAS-BLED
26
What score is used to AF stroke risk?
CHA2DS2VASc ``` CHF HTN >75 years DM Stroke Vascular Age 65-74 Sex (female) ```
27
What CHA2DS2VASc score suggests oral anticoagulation?
>2
28
What HAS-BLED score suggests oral anticoagulation?
>3
29
What is disseminated intravascular coagulation?
Dysregulation of coagulation and fibrinolysis Results in widespread clotting and resultant bleeding Mediated by Tissue Factor
30
What are causes of DIC?
sepsis trauma obstetric complications malignancy
31
What would blood look like in DIC?
``` ↓ platelets ↓ fibrinogen ↑ PT & APTT ↑ fibrinogen degradation products schistocytes (haemolytic anaemia) ```
32
What would blood looks like on a patient taking warfarin?
PT prolonged APTT normal Platelet count normal
33
What would blood looks like on a patient taking asprin?
PT normal APTT normal Bleeding time prolonged Platelet count normal
34
What are some presenting features of DIC?
``` Petechiae Haematuria Epistaxis Gangrene Mental disorientation ```
35
What investigations should be done in DIC?
``` Platelet count PT Fibrinogen D-dimer APTT ```
36
What is the treatment for DIC?
Treat underlying cause If high bleeding risk or active bleeding: Platelet transfusion FFP for coagulation factors If chronic: Heparin Antifibrinolytic agents e.g. tranexeamic acid
37
What can produce lower than expected HbA1c?
Sickle cell GP6D deficiency Hereditary spherocytosis (decreased red cell lifespan)
38
What can produce higher than expected HbA1c?
Vitamin B12/folic acid deficiency Iron-deficiency anaemia Splenectomy (increased red cell lifespan)
39
Why is CO poisoning dangerous?
High affinity for haemoglobin Left-shit of O2 dissociation curve Tissue hypoxia Pulse Ox might be falsely high
40
What is ferritin?
Intracellular protein that binds iron and stores it
41
What are some myeloproliferative disorders?
CML Polycythaemia vera Essential Thrombocythaemia Primary myelofibrosis
42
What are myeloproliferative disorders?
Rare disorders of the bone marrow that cause an increase in the number of blood cells
43
What are some symptoms of MPDs?
``` asympto headaches tiredness bruising or unusual bleeding blurred vision ringing in your ears getting more infections than usual ```
44
What is essential thrombocytosis?
myeloproliferative disorder associated with an increase in number and size of circulating platelets
45
What would investigations show in essential thrombocytosis?
Platelet count >450x10^9/L Large platelets seen on peripheral blood smear Howell-Jolly bodies
46
What is the treatment for essential thrombocytosis if thrombosis or bleeding are evident?
Plateletpheresis Removing blood, separating it, removing platelets before returning
47
What is pancytopenia?
reduction in the number of red blood cells, white blood cells, and platelets
48
What are some differentials for pancytopenia?
``` Chemo Radio B12 def Folic acid def Non-hodgkins ```
49
What are the three categories of polycythaemia?
Relative - dehydration - stress Primary - vera Secondary - COPD - altitude - OSA - excess erythropoietin
50
What is Polycythaemia vera?
myeloproliferative disorder caused by clonal proliferation of a marrow stem cell leading to an increase in red cell volume
51
What re the presenting features of polycythaemia vera?
``` hyperviscosity pruritus, typically after a hot bath splenomegaly haemorrhage (secondary to abnormal platelet function) plethoric appearance hypertension in a third of patients low ESR ```
52
What investigations are done for polycythaemia vera?
full blood count/film (raised haematocrit; neutrophils, basophils, platelets raised in half of patients) JAK2 mutation serum ferritin renal and liver function tests
53
What is the diagnostic criteria for polycythaemia vera?
``` If JAK2 mutation present: High haematocrit (>0.52 in men, >0.48 in women) OR raised red cell mass ``` No JAK2 mutation: Raised red cell mass (>25% above predicted) OR haematocrit >0.60 in men, >0.56 in women + Splenomegaly/Thrombocytosis etc.
54
How is polycythemia vera managed?
Asprin Phlebotomy Cytoreductive therapy (Chemo)
55
What is ecchymosis?
Bruise
56
What are some differentials for easy bruising?
``` Anticoagulant use, NSAIDs, corticosteroids Heavy alcohol use Drug induced thrombocytopenia Von Willebrand disease Cushings Abuse Bone marrow malignancy ```
57
What are some causes of splenomegaly?
``` Myelofibrosis CML Malaria Haemolytic anaemia Infection e.g. hepatitis, EBV Sickle cell but can also be atrophied Infective endocarditis RA ```
58
What are common causes of hepatomegaly?
Cirrhosis Malignancy Right sided HF
59
What is a petechial rash?
Red or purple non-blanching macules smaller than 2 mm in diameter
60
What is a purpuric rash?
spots larger than 2 mm in diameter | non-blanching
61
What might purpura indicate?
Meningococcal sepsis Acute Leukaemia Von Willebrand disease Immune thrombocytopenic purpura