Haematology HL

Question 1

Approach to anaemia

Question 2

Causes of microcytic, disease pathophysiology, FBC, film and other findings

Question 3

Causes of normocytic, disease pathophysiology, FBC, film and other findings

Question 4

Causes of macrocytic, disease pathophysiology, FBC, film and other findings

Question 5

cAUSES of PT, APTT, bleed time, fibrinogen, D dimer and common associated disease

Question 6

Markers of ahemolusis

Question 7

Causesof haemolysis

Question 8

Describe the components and significance of FBC

Question 9

Provide overview of aematopoiesis, cells and sites; lifecycles and functions

Question 10

Describe the in vivo model of coagulation

Question 11

Describe the in vitro model of coagulation

Question 12

Describe the moa of common anticoags

Question 13

Describe the moa of common Describe the moa of common anticoags
“ antiplatelets

Question 14

Describe common adverse reactions associated with anticoags and antiplatelets

Question 15

Describe coulter principle

Question 16

Describe how FBc parametesrs are measured

Question 17

Which coags are made by liver, which neeed K and which ahas shortes t t1/2

Question 18

List three (min) chronic diseases and explain how they cayse anaemia

Question 19

Provide overview of et, MF and PV

Question 20

Describe the underlying genetics and mainfestiation of cml

Question 21

Discuss dx and comps of cml

Question 22

Describe how abo and rh work

Question 23

Describe aiha and manifestations and dx/mx. Disntiguish with delayed

Question 24

Describe rh disease and manifestations and dx/mx

Question 25

Whats a massive transfusion and what are the complicatiosn

Question 26

Describe direct combs and indirect

Question 27

* Describe Patho-physiology * Clinical features, and * Basic laboratory diagnosis of: i) Thalassaemia major ii) Sickle cell disease iii) Hereditary spherocytosis iv) G6PD deficiency

Question 28

Describing staging for lymphomas and broad amangemt

Question 29

What are some causes of aplasia

Question 30

Describe causes and presenataiton of aa

Question 31

How to manage aa and issues

Question 32

What is MDS, geatuers

Question 33

Describe MDS management

Question 34

Describe thrombocytopenia issues

Question 35

Dsescribe work up for purpura and ppissble causes

Question 36

Describe ITP

Question 37

Describe hit

Question 38

Describe DIC

Question 39

Describe FACTOR V

Question 40

Describe cancer and lupus in thrombocutosis

Question 41

Describe diagnostic appraich to thrombocytosis

Question 42

Whena re blodod product indicated

Question 43

Describe haemophilai and vqf

Question 44

Describe bloods of liver, hiv, mal, chronic

Question 45

Distinguish between MGUS, MM, smoudlering and approach to treat MM

Question 46

Describe Virchow and distinguish between arterial and venous thrombo

Question 47

How ti investigate tphilia

Question 48

Role of serum protein ephoresis and proteins measured

Question 49

Interpret ephoresis and immunofiation, role og these

Question 50

Ddx for acute haemolutics

Question 51

What is massive tfusionand comps