Haematology I - Lecture 8 Flashcards

1
Q

What is the average blood volume of an adult?

A

5L

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2
Q

What are the main components of blood?

A

○ 55% = Plasma [normal range 46-63%]
○ 45% = Red blood cells
○ <1% = White blood cells and platelets

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3
Q

What are the components of plasma?

A

○ Water = 92%
○ Plasma Proteins = 7% (Albumin, globulin, fibrinogen, regulatory proteins)
○ Other Solutes = 1% (Electrolytes, organic nutrients and waste)

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4
Q

What are the main functions of blood?

A

Transport of:
○ O2 and CO2
○ Nutrients
○ Waste
○ Temperature
○ Hormones
Defenese:
○ Antibodies, WBCs
○ Clotting factors

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5
Q

What is haematopoiesis?

A

Process by which blood cells are formed from hemocytoblast

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6
Q

What happens during erythropoiesis?

A

○ Stem cell = hemocytoblast
○ Committed cell = proerythroblast
Phase 1: Ribsome synthesis (decreases)
○ Early erythroblast -> Late erythroblast
Phase 2: Haemoglobin accumulation (increases)
○ Late erythroblast -> Normoblast
Phase 3: Ejection of nucelus
○ Normoblast (ejected nucleus) -> Reticulocyte -> Erythrocyte

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7
Q

What are the requirements for erythropoiesis?

A

○ Erythropoietin (EPO) = Growth factor
○ Iron
○ Vitamins B12 & folic acid (B9)
○ Intrinsic factor = Absorbs Vitamin B12
○ Amino acids = Used to make globin in haemaglobin

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8
Q

Where does erythropoiesis occur?

A

○ Foetus: yolk sac, then liver & spleen, later in bone marrow
○ Infant: all bone marrow
○ Adult: red bone marrow (ribs, vertebrae, skull, upper ends of long bones)
Rate: 2-3 million red blood cells per second

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9
Q

What is the structure of a red blood cell?

A

○ Biconcave disc
○ Highly flexible and readily deformed
○ Contains haemoglobin
○ Average size is 7.2-8.4 um
○ Lifespan ~ 120 days

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10
Q

What cell breaks down aged or damaged RBCs?

A

○ Macrophage

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11
Q

Which organs are macrophages found?

A

○ Liver
○ Spleen (main)
○ Lymph node

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12
Q

What is haemaglobin broken down into?

A

Heme -> bilirubin and iron
Globin -> amino acids

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13
Q

What happens to the broken down iron?

A

Transferrin (transport protein) stores it in the spleen or stores it as ferritin in the liver

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14
Q

What happens to the broken down bilirubin?

A

○ Taken to the liver by serum albumin
○ Bilirubin is secreted into the bile
○ Excreted as urine or feces

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15
Q

What happens in erythrocyte homeostasis?

A

○ Low O2 blood level detected
○ Kidneys increase production of erythropoietin
○ Stem cells increase RBC production
○ O2 blood levels return to normal

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16
Q

What are the causes of hypoxia?

A

○ Increase in exercise
○ High altitude
○ Smoking
○ Bleeding

17
Q

How many haemoglobin molecules are there per red blood cell?

A

~280 million

18
Q

When does synthesis of haemoglobin begin?

A

Begins in proerythroblast
○ 65% at erythroblast stage
○ 35% at reticulocyte stage

19
Q

How much haemoglobin is there in males and females?

A

○ Females: 12-16g/dL
○ Males: 13.5-17.5g/dL

20
Q

What is the structure of Haemoglobin adult (HbA)?

A

○ 4 subunits: 2 alpha and 2 beta
○ Each subunit consists of: Haem bound to long polypeptide chain (globin)
○ Fe2+ in the centre

21
Q

What is anaemia?

A

○ Haemoglobin concentration in whole blood below the accepted normal range
○ Less than 13.5g/dL for men and less than 12.0g/dL for women
○ Common problem affecting 1/3 of the world population

22
Q

What are the causes of anaemia?

A

○ Decreased RBC production
○ Increased RBC destruction
○ Blood loss

23
Q

What are the characteristics of iron deficiency anaemia?

A

○ Most common anaemia
○ Hypochromic (pale RBCs)
○ Microcytic (small) RBCs
○ Decreased mean cell volume

24
Q

What are the causes of iron deficiency anaemia?

A

○ Pregnanacy
○ Bleeding from GI tract
○ Malabsorption
○ Menorrhagia
○ Malnutrition

25
Q

What are the characteristics of megaloblastic anaemia?

A

○ Abnormal RBC
○ Reduced Haemoglobin concentration
○ Macrocytic (large)
○ Increased mean cell volume

26
Q

What causes megaloblastic anaemia due to folate deficiency?

A

Get macrocytic anaemia
○ Pregnancy
○ Elderly
○ Dietary deficiency

27
Q

What causes megaloblastic anaemia due to Vitamin B12 deficiency?

A

Unable to absorb vitamin B12
○ Lack of Intrinsic Factor needed to absorb vitamin B12 (pernicious anaemia)
○ Chrohn’s, coeliac disease

28
Q

What are the characteristics of sickle cell anaemia?

A

○ Hereditary: African or West Indian descent
○ Abnormal haemoglobin structure
○ Sickle-shaped red blood cells, which can get stuck in blood vessels

29
Q

What are the characteristics of thalassaemias?

A

○ Hereditary: Mediterranean, Middle Eastern or Far Eastern descent
○ Abnormal haemoglobin production (alpha and beta thalassaemias)