Blood and Haemostasis Flashcards

1
Q

What is left shift?

A

Left shift or blood shift is an increase in the number of immature leukocytes in the peripheral blood, particularly neutrophil band cells.

Left shift may also refer to a similar phenomenon in severe erythroanemia, when reticulocytes and immature erythrocyte precursors appear in the peripheral circulation

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2
Q

What is the tissue O2 delivery equation and what is its significance?

A

Tissue O2 delivery: CO x Hb x O2 Sat x 1.34

Don’t only look at Hb levels, Ability of cardiac system to compensate for loss in Hb can still preserve O2 delivery, HR is a good guide to assess anaemic patients and ability to compensate is dependent on time (i.e. SV can increase if anaemia happens slowly overtime)

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3
Q

What are the classifications of anaemia?

A
  • Regenerative (susceptible to haemolysis, quick drop in Hb or O2 delivery, very dangerous)
  • Aregenerative (compensate better, more time)

-Microcytic, normocytic, macrocytic

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4
Q

What are the increased signs of production, destruction and loss of RBC?

A
Signs of increased production
-reticulocytes, polychromasia (blue tinge due to Hb formation)
Signs if increased destruction
-Jaundice (increased serum bilirubin)
-haptoglobins
LDH
Blood Loss
-overt (see it)/covert (ask about it)
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5
Q

What are the 6 things to know about how blood is made?

A
  1. How much is enough
    • RBC 3-5 x 1012 /L, replace every 120 days
    • WBC 2-6 x 109 /L, replace every 3-5 days
    • Platelets 150-400 x 109 /L, replace every 10 days
    1. Where is it made
      - Yolk sac - first few weeks
      - Liver and spleen - 6wks-7months (can be enlarged by re-recruiting liver and/or spleen in diseases of the blood to make more blood cells)
      - Bone marrow - 7 months-whole life (bone marrow sampling from the pelvis)
    2. Pluripotent stem cell
      - Capable of self renewal
      - Differentiate into all haemopoietic cell lines
      - Give rise to lymphocytes and osteoclasts
      - Exist in small numbers in marrow
    3. Bone marrow stroma
      - Provides specific environment for BM to grow, complex
      - Change in adhesion molecules mark progression of cells through the stroma
      - Bone marrow in continuity with blood circulation - can find its way back to BM when injected into veins
    4. Haemopoietic Growth factors
      - Glycoprotein hormones
      - Local and circulating action
      - Multiple effects mediated through specific receptors, Conformational change when binding to receptor
    5. Haematinic
      - Iron: in Hb carries O2, need adequate levels in diet
      - B1: animal products,
      - Folate: green leafy vegetables
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6
Q

What is Virchow’s triad?

A

Abnormalities in:

  1. Vessel Walls
  2. Blood flow
  3. Blood composition

can all lead to thrombosis!

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7
Q

What is the principle of coagulation testing and what does it tell us?

A

Take patient sample, spin it and separate plasma from cells, only do tests on plasma (no endothelium, platelets or cells) and add activation factors which activate cascade at a certain point and measure time until clot formation

  • artificial construct, not a true measure of physiology, can only predict clinical behaviour and integrity of factors within the cascade.
  • must maintain sample integrity and undertake duplicate testing!
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8
Q

What are the consequences of abnormal levels of thrombin?

A

Insufficient Thrombin = bleeding

Excessive thrombin = thrombosis

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9
Q

What is subunit co-operativity and how does it explain sigmoidal O2 binding?

A

Co‐operativity
1. Haemoglobin needs to have high “ affinity ” to bind O2 in the lungs. (Hb is ~90% saturated)

  1. Once the Hb‐O2 complex reaches the tissue thatconsumes oxygen, the O2 needs to be transferred to myoglobin. (Hb in venous blood is 64% saturated)
  2. Sigmoidal curve: represents weak‐binding state at low P02 and strong binding state at high P02
    - conformational change at one subunit induces increased O2 binding affinity in adjacent subunit in a co-operative manner (progressive stabilisation of tense state with increased O2 binding and vice versa)
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10
Q

Hb makes up …% of RBC dry content?

A

97%

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11
Q

How is CO2 transported by Hb?

A

@ tissues: 15% of CO2 formed is carried on amino terminal of deoxy-Hb as carbamate

@ lungs: O2-Hb binds CO2 less readily than deoxy-Hb, so CO2 is released in lungs

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12
Q

What are the effects of allosteric effectors to achieve variable sigmoid binding of oxygen?

A

2,3‐BPG: binding decreases Hb affinity for O2 => helps release O2 in the tissues

The Bohr effect: Acid is produced in the tissues
‐ The binding of protons to Hb lowers its affinity
for O2

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13
Q

How does foetal Hb differ from adult and what is the significance?

A

‐ HbF (containing 2 gamma subunits instead of beta) binds O2 with greater affinity than the mother’s HbA (adult form of Hb) because HbF binds 2,3‐BPG less avidly than HbA.

‐ this gives the foetus access to oxygen carried by the mother’s HbA.

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14
Q

What is mutation causes sickle cell anaemia (HbS) and what are the consequences?

A

Mutation is a one base change from Glutamate to Valine

HbSS => susceptible to sickle‐cell crisis (e.g vaso‐occlusion)
‐ HbSA => no symptoms = sickle‐cell trait; some protection from malaria

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