Red Blood Cells Flashcards

1
Q

What is anaerobic glycolysis

A

Metabolic activity- to maintain Haem Fe in reduced state by NADPH.

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2
Q

What is erythropoesis

A

A part of the process of haemopoeisis

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3
Q

Where does erythropoesis occur

A

In adults mainly in the narrow spaces of the sternum, pelvis and long bones

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4
Q

What does erythropoietin do

A

Act on committed erythroid precursors to increase cell division and therefore rbc numbers

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5
Q

What is a rbc lifespan

A

Around 120 days

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6
Q

What is haemolysis

A

A shortening of the rbc lifespan

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7
Q

Where are rbc destroyed

A

In the spleen by macrophages if defective

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8
Q

What is the function of hb

A

To transport o2 from the lungs to respiratory tissues

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9
Q

What is 02 affinity

A

The relationship between hb 02 saturation and p02

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10
Q

What is anaemia

A

Reduced hb in blood

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11
Q

What is anaemia

A

Low hb in blood

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12
Q

What are physical symptoms of anaemia

A
  • shortness of breath
  • weakness
  • pallor =pale skin
  • lethargy =tired
  • headaches
  • heart failure
  • palpitations
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13
Q

What are clinical signs of anaemia

A
  • pallor of nail beds
  • concave nails
  • jaundice
  • leg ulcers
  • bone deformities
  • recurrent infection or bruising
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14
Q

What rbc features show normocytic, normochromic anaemia

A
  • Mcv is normal
  • MCH is normal
  • MCHB is normal
  • rbc count is reduced
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15
Q

What rbc features show microcytic, hyperchromic anaemia

A
  • rbc volume is reduced
  • low mcv
  • low mch
  • low mchc
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16
Q

What rbc features shows macrocytic, normochromic anaemia

A
  • rbc count is low
  • rbc volume is increased
  • hb have a normal concentration
  • mcv is up
  • mchc is normal
  • mch is up
17
Q

What causes microcytic, hypochromic anameia

A
  • poor diet
  • poor malabsorption
  • chronic blood loss
18
Q

How is IDA anaemia treated

A

Iron supplements

19
Q

What is hereditary elliptocytosis

A

An inherited disorder that makes the rbc elliptical shaped

20
Q

What is acquired haemolytic anaemia

A

Anaemia gained from drugs or autoimmune diseases

21
Q

What is sickle cell

A

The most commonly inherited blood disease that causes sickle shaped rbcs

22
Q

What is the structure of hb

A

2 a-globin chains, 2 b-globin chains
Fe atom
Porphyrin rings

23
Q

What are the 2 categories of haemoglobinopathy

A

1- structural variations- where hb is made in normal amounts but the structure is abnormal.
2- thalassemia- where there is a loss of ability to produce a type of globin chain

24
Q

What is a-thalassemia

A

The impaired ability to synthesise a globin chains

25
Q

What does a-thalassemia cause

A

Mild microcytic hypochromic anaemia due to excess b chains

26
Q

What is b-thalassemia

A

Impaired ability to synthesise b globin chains

27
Q

What does b- thalassemia cause

A

Excess a chains bind to the rbc membrane reducing its survival

28
Q

What is heterozygous b-thalassemia

A

Mild microcytic hypochromic anaemia and they are a carrier

29
Q

What is homozygous b-thalassemia

A

Severe anaemia usually fatal in infancy or childhood without intervention

30
Q

How is b-thalassemia treated

A

Transfusion, fe chelation therapy or in extreme cases bone marrow transplant