Haematology Flashcards

1
Q

Outline some features present in blood

A
  • Many RBC
  • Few WBC
  • Platelets
  • Plasma- water electrolytes (K+), glucose, lipids, metabolites, gases, hormones, drugs, plasma proteins albumins (transport and colonial osmotic pressure allowing fluid to be sucked back into capillary at venous side), globulins (transport, clotting, precursors to hormones- angiotensinogen so help regulate blood pressure, defence), fibrinogen (clotting)
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2
Q

Outline difference between plasma and serum

A
  • Serum- coagulated blood so no clotting factors- expose to foreign surface
    Plasma- uncoagulated blood- often need to add anticoagulation factors: watery substance with many other factors
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3
Q

Outline key facts on RBC

A
discoid (large SA: volume)
8 micrometres in diameter 
No nucleus 
Haemoglobin for O2 and CO2 transport 
120 day lifespan
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4
Q

Can RBC be a good measure of glucose intake over last 3 months

A

Hb1Ac- glycosylated haemoglobin- value increases with more glucose as proteins becomes glycosylated- therefore good measure of glucose intake in last 3 months
can be measures in a blood test

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5
Q

Outline some key WBC

A
  • Neutrophils (60-70%)
  • Eosinophils- parasite (worm/ helmet) killing and inflammation (allergic asthma)
  • Basophils- release histamine in hypersensitivity reactions
  • Monocytes- phagocytic- leave blood to be come macrophages
    Lymphocytes- produce antibodies
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6
Q

Explain groupings of cells into phagocytes and immunocytes

A

Phagocytes- granulocytes (neutrophils, eosinophils, basophils) and monocytes
Immunocytes- lymphocytes

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7
Q

Explain appearance and significance of platelets/ thrombocytes

A
  • Cellular fragments
  • Non-nucleated
  • Fragments stick together–> Clot formation
  • Gives rise to many forms of strokes
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8
Q

Explain where blood clots are formed (haematopoiesis)

A
  • Foetus+ neonate- liver and spleen

- Neonate+child+adult- bone marrow

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9
Q

Explain name of some myeloid and lymphoid stem cells

A
  • Myeloid stem cells form megakaryocytes -> platelets, RBC, Granulocytes (eosinophils, basophils, neutrophils), monocytes
    Lymphoid stem cells- B and T lymphocytes
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10
Q

name of regulator of platelet levels and why this has to be controlled so tightly

A

Thrombopoietin- glycoprotein: produced by liver and kidney

  • tightly regulates platelet level
  • Thrombosis- clotting can occur if too high no. platelets
  • Bleeding- if platelet levels too low
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11
Q

Name of regulator of RBC levels and why this gas to be controlled so tightly

A

EPO- erythropoietin- natural hormone produced by the kidney
- juxtaglomerular cell in kidney: sense O2 levels too low (hypoxia)
- kidney produces EPO
goes to the bone marrow- so more RBC produced

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12
Q

How do we control WBC production

A
  • Interleukins- type of cytokine controlling proliferation of other WBC
  • Colony- stimulating factors (CSF)- stimulated by infections and released by endothelial and other cells
    e.g. ‘granulocyte CSF- stimulate neutrophil cell line
    Cytotoxic anti-cancer chemotherapy can lead to the destruction of bone marrow cells (as fast growing)- hence often treat with CSF in between 21 day cycle of treatments to help recovery of WBC
  • However, can in leukaemia (myeloid proliferation)- can lead to greater production of abnormal cells
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13
Q

Explain different ways of recognising no/ amounts of RBS within the blood and why this is clinically important

A
  • Cells per volume- counted by machine or manually per 1L of blood
    (used to count RBC or neutrophils)
  • Haematocrit- centrifuge cells down and see % of RBC (about 45%)
  • Haemoglobin- amount (g) per L
  • Used to recognise anaemias
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14
Q

How do you work out the mean corpuscular volume of an individual RBC? What does this figure mean?

A

haematocrit (as decimal)/ no. of RBC per L
This tells you the size of each cell, and is measured in fl
Where each fl is 10^-15

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15
Q

How can the MCV be used to identify certain diseases

A
  • Microcytic anaemia: if patient has anaemia and RBC too small- consistent with deficiency in iron
  • Macrocytic anaemia: too large RBC
  • If not anaemic but RBC too large- can indicate that patient drunk too much alcohol in last 3 months
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16
Q

Be aware of following terms found on full blood count (FBC)

  • Haemoglobin
  • WBC
  • Platelets
  • MCV
  • MCH
  • RBC
  • HCT
  • MPV
A
  • haemoglobin
  • White blood cells
  • Platelets
  • MCV= mean corpuscular volume (size of RBC)
  • MCH= mean cell haemoglobin (average mass of haemoglobin per RBC in blood) bigger cells tend to have more haemoglobin so related to MCV
  • RBC
  • HCT- haematocrit test- % RBC
  • MPV- mean platelet volume (average size of platelets calculated)
17
Q

What does -philia, -penia, and -cytosis mean

e.g. pancytopenia- what does this mean and what can cause this

A
  • philia/ -cytosis- increased cell count
  • penia- decreased cell count
  • Pancytopenia= reduction in all cell counts due to anti-cancer chemotherapy
18
Q

Briefly explain what high/ low amounts of platelets, leukocytes, neutrophils, eosinophils, monocytes and lymphocytes can mean

A
  • Platelets- thrombocytosis (increased thrombosis/ clotting risk) or thrombocytopenia (caused as side effect drugs or idiopathic- no idea!)
  • Leucocytes- leucocytosis or leukopenia
  • Neutrophils- neutrophilia (caused by bacterial/ fungal infection, trauma or inflammation) or neutropenia (infection- viral or drugs)
  • Eosinophils- eosinophilia (allergy/ atopy associated with hay fever, asthma and eczema)
  • Monocytes (monocytosis- due to infection can be chronic e.g. TB)
  • Lymphocytes- Lymphocytosis (infection- bacterial/ viral or lymphoma- cancer lymphoid tissue) or lymphopenia (inflammation, lymphoma- again can increase or decrease no. lymphocytes or steroids)
19
Q

Explain some important markers of infection

A

Change in temperature
Delirium in older individuals
Neutrophilia
C reactive protein (released from the liver upon infection)

20
Q

Outline different blood groups

A

Over 400 blood groups yet ABO and rhesus are clinically important ones

ABO blood groups
REM: A has a antigens present on RBC so will produce B antibodies if foreign B antigen present
B- opposite
AB- both A and B antigens so no antibodies
O- has no A or B antigens o both antibodies

Rhesus
Important rhesus D antigen (RhD)
Referred to as +ve or -ve
If +ve D antigens present so no D antibodies

If in doubt O -ve- has A, B or D antigens so lack of immune response

21
Q

Why is it important to test if rhesus D +ve or -ve in pregnancy

A
  • Vast majority (85%) rhesus +ve
    If mother rhesus -ve, statistically likely that foetus rhesus +ve as likely that father rhesus +ve
    • Not a problem in first birth as no mix of foetal/ maternal blood until pregnancy
    • After birth or miscarriage foetal blood from placenta mixes with maternal blood so produces D antibodies
    • Affects 2nd pregnancy as haemolytic disease of new-born
    • Therefore given anti- D immunoglobulin- Mop up any D-antigens that get into maternal blood and prevent production of D- antibodies
      Obstetricians much cleverer than this and monitor if mother rhesus -ve even during 1st pregnancy