Haem Flashcards

1
Q

What causes high ferritin with iron overload?

A

Haemochromatosis

Repeated transfusions

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2
Q

If eGFR<15, what anticoagulant?

A

LMWH

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3
Q

Monitoring of heparin?

A

aPTT

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4
Q

Rx for polycythaemia?

A

Aspirin
Venesection
Hydroxyurea (slight risk of CML)

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5
Q

Diagnosis of G6PD?

Diagnosis of spherocytosis?

A

G6PD - enzyme assay at time and after 3 months

Sphero - EMA binding test

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6
Q

Extrinsic pathway?

A

TF/VII activate X

Measurement: PTT

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7
Q

Intrinsic pathway?

A

9a/8a activate factor X

Measurement: aPTT

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8
Q

Common pathway?

A

Xa binds Va and activates prothrombin to thrombin

This converts fibrinogen to fibrin

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9
Q

TTP?

A

MAHA and thrombocytopaenia

ADAMTS-13 gene

Fever, bleeding, AKI, drowsy, seizure

NORMAL COAGULATION

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10
Q

Management of essential thrombocytosis?

A

Hydroxyurea

Interferon alpha if young

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11
Q

When to stop heparin before surgery

A

Day before

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12
Q

When to stop warfarin before surgery?

A

5 days before

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13
Q

What can potentiate warfarin?

A

Liver disease
Cranberry juice
P450 inhibitors (cipro, amiodarone, valproate)

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14
Q

What drug can cause neutrophilic?

A

Steroids

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15
Q

Platelet transfusion limit in active bleeding?

A

30 in most cases

100 in CNS

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16
Q

Platelet transfusion limit prior to planned procedure?

A

50 for most

75 if high risk

100 if surgery at critical site

17
Q

Platelet transfusion limit if no bleeding or planned procedure?

A

10

18
Q

What to prescribe if HF patient receiving packed red cells?

A

Furosemide STAT

Even if already on regular furosemide

19
Q

How long is elective RBC transfusion done over?

A

90-120 mins

20
Q

DIC what is given?

A

FFP or cryoprecipitate

21
Q

What DOAC to AVOID if renal failure?

What one should be used?

A

AVOID Dabigatran

USE apixaban

22
Q

Major constituent of cryoprecipitate?

A

Factor VIII

used in haemophilia

23
Q

ALL?

A

Kids
Low everything
Bone pain, testicular etc

24
Q

AML?

A

Anaemia
WCC high but neutropenia
Thrombocytopaenia

AUER RODS
Mostly blasts

25
Q

CLL?

A

Asymptomatic, picked up randomly
May have lymphadenopathy

Lymphocytosis and anaemia
SMUDGE cells

Immunophenotyping Ix

Warm haemolytic anaemia
Richters transformation

26
Q

CML?

A
60-70 y/o
PHILADELPHIA CHROMOSOME
Decreased ALP
Increase in different stages of maturation
Thrombocytosis and anaemia

Imatinib

Can undergo blast transformation

27
Q

Myelofibrosis?

A

Pancytopaenia
Tear drop poikilocytes
Dry tap
High urate and LDH