Haem Flashcards

(27 cards)

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?

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?

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
CLL?
Asymptomatic, picked up randomly May have lymphadenopathy Lymphocytosis and anaemia SMUDGE cells Immunophenotyping Ix Warm haemolytic anaemia Richters transformation
26
CML?
``` 60-70 y/o PHILADELPHIA CHROMOSOME Decreased ALP Increase in different stages of maturation Thrombocytosis and anaemia ``` Imatinib Can undergo blast transformation
27
Myelofibrosis?
Pancytopaenia Tear drop poikilocytes Dry tap High urate and LDH