Haem Flashcards

(43 cards)

1
Q

What are the causes of raised APTT?

A

Haemophilia
vWD
DIC
Use of heparin

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2
Q

What are the causes of raised PT?

A

Severe liver disease
Vit K deficiency
DIC
Sepsis

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3
Q

What blood test abnormalities are seen in vWD?

A

Increased APTT

Decreased factor VIII and vW factor

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4
Q

What tx can be given for mild vWd?

A

Desmopressin

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5
Q

Which clotting factors are deficient in haemophilia A and B?

A
A = VIII
B = IX
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6
Q

What are the three main causes of DIC?

A

Sepsis
Malignancy
Obstetric

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7
Q

What are the three tests you would conduct to investigate for haemolytic anaemia?

A

Reticulocyte count
LDH level
Haptoglobin

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8
Q

Which tests if positive will tell you that haemolytic anaemia is caused by an immune cause?

A

Coombs test

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9
Q

Blood test abnormality seen in DIC

A

Low platelets
Increased PT and APTT
Low fibrinogen

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10
Q

Which test is diagnostic of polycythaemia rubra vera?

A

JAK 2 mutation

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11
Q

What are the secondary causes of polycythaemia?

A

COPD
Sleep apnoea
hypoxia (high altitude, smoking)
Increased EPO - renal cell carcinoma and hepatocellular carcinoma

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12
Q

What is the main complication of polycythaemia vera?

A

Thrombosis

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13
Q

What is the tx for polycythaemia vera?

A

Venesection or (hydroxycarbamide if high risk thrombosis)
+
daily ASPIRIN

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14
Q

What conditions may polycythaemia vera progress to?

A

Myelofibrosis

Acute leukaemia

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15
Q

What is a sign on blood film of G6PD deficiency?

A

Heinz bodies

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16
Q

What’s the only tx for TTP?

A

Plasma exchange

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17
Q

How do you distinguish AML from ALL on bone marrow biopsy?

A

Presence of AUER rods in AML

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18
Q

In which condition is the Philadelphia chromosome found?

19
Q

What would the FBC show in CML?

A

Increased myeloid cells (e.g. eosinophils, neutrophils, monocytes, basophils)

20
Q

What drugs can be used to tx CML?

A

Tyrosine kinase inhibitors (e.g. imatinib)

21
Q

What are the comps of CLL?

A

1) autoimmune haemolysis
2) Infection (hypogammaglobulinaemia)
3) Marrow failure

22
Q

How is Hodgkin’s lymphoma staged?

A

Ann Arbor system

23
Q

What two abnormalities are seen on FBC with alcohol misuse?

A

Thrombocytopenia
Raised MCV
Anaemia

24
Q

Two signs of thalassaemia

A

Skull bossing

Hepatosplenomegaly

25
What sign on blood film indicates thalassaemia?
Target cells | Microcytic hypochromic RBCs
26
Dx for thalassaemia
Hb electrophoresis
27
Which types of immunoglobulin cause warm and cold autoimmune haemolytic anaemia?
``` Warm = IgG Cold = IgM ```
28
What are seen on blood film in G6PD?
Heinz bodies
29
What findings suggest intravascular haemolytic anaemia?
Increased free plasma Hb decreased haptoglobin Increased haemoglobinuria
30
What practical measures would you instigate in a neutropenic patient?
Full barrier nursing Avoid IM injections Vitals 4 hourly (screen for infection, check bloods and cultures)
31
What drug can help stimulate neutrophil production?
G-CSF
32
What Ix for pernicious anaemia?
Parietal cell antibodies IF antibodies Schilling test
33
What blood film features are consistent with AML?
Blast cells | AUER RODS
34
How is CML treated?
Tyrosine kinase inhibitors
35
What factor favours a more favourable prognosis in CML?
Presence of Philadelphia chromosome
36
What is the main comp of CML?
Blast crisis (leads to AML and pancytopenia)
37
Comps of CLL
1) autoimmune haemolysis 2) Infection due to hypogammaglobulinaemia 3) Marrow failure
38
What staging system is used for CLL?
Binet
39
What could cause a cough in NHL?
Mediastinal mass | Pneumonia
40
ddx for NHL?
HL ALL Infectious mononucleosis
41
How is lymphoma staged?
Ann-Arbor system
42
Symptoms of hyperviscosity?
Headache, tinnitus. dizziness, visual disturbance, Plethoric appearance
43
Which type of leukaemia are patients with myelodysplastic syndrome at risk of?
AML