Blood Flashcards
stats for:
how much rbc?
how effective?
how large
shape?
lifespan?
f?
- 4.4 -5.9x10^12/L
- Hb = 13.5-16.7 g/dL
- MCV mean corpuscular volume) 80-100fl
- biconcave flexible disc -~8microm diameter
- 120 days
- deliver oxygen to tissues , carry Hb, maintain Hb in its ferrous (reduced state), maintain osmotic equlibirum and generate energy
what causes RBC shape changes? and what does this causes?
name 1 condition
- changes to the components of the membrane
- causes them to become more fragile and less deformable, so spleen recognises them as abnormal and takesn them up, which cancause haemolytic anemia
- spherocytosis
what is the structure of erythrocyte structure?
- Ankyrin ; spectrin, band 3 and 4.2
What are the instruments, and turn over time for UHL haem labs?
- 9 FBC analysers , 6 coagulation analysers
- URGENT (A&E) 1 hour
- Non-urgent (ward patients)
normal vs abnormal results
what affect normal results
- normal ranges = 95% of healthy population levels, but not everyones falls into the catergory, what you do is multiple tests and see if theres a drop, that would be abnormal
- gender, sex, ethnicity, co-morbidities
why do we get abnormal b results?
- due to issue or reactionof the blood (EDTA)
what errors can occur in;
- specimen collection
- delivery of specimen to lab
- specimen analysis and result reporting
- responsive action
- specimen mix up/ Wrong blood in tube(WBIT) / pooling of sample (combinined fluids like urine and blood) / poor technique
- delayed specimen/not delievered/wrong delivery method
- specimen mix up/ incorrect clinical details/wrong test performed/inherent test variability/technical error
- result not reviewed/reflex tests not carried out(reflex tests =additional tests)/right result applied to wrong patient
what are essential parameters of FBC?
what analysis techniques used?
- platelets / RBC /Hb/ WBC
- spectrophotometry ; (amount of light abosred by sample proportional to amount of absorbant compount within ite.g used to meaure Hb. it isues hypotonic solution to lysis cells and release Hb, then use light as the wavelength and use calibration curve to determine the sample concentration)
- Flow Cytometry ; involves cells in single line and light baem passing through, forward scatterng = size. and side scatter =whether mono/polymorphonuclear, or inreaceullar complexities like granules) can check myeloperoxidase activity = important in inflammation detection
PCV?
why used?
why shouldnt you always trust polycythenia results?
- packed cell volume aka haematocrit (L) allows you to see what proportion of blood allows visualisation
- used to assess anaemia and polycythemia
- pseudo polycythenia due to less water = less plasma so higher haematocrit
hb levels for
men
women
children 3-puberty
newborns
>135g/L
>115g/L
>110g/L
>150g/L
whats in vitro vs in vivo haemolysis?
what do they cause
- in vitro= haemolysis due to cellulr damage
- in vivo = RBC haemolysis due to increase in erythrocyte destruction rate or decreased erythrocyte life span
- reduced Hb
why do a RBC specifically? RCC of examples fo each
to test for anaemia and erythrocytosis (body makes ^RBC which can rsult in polycythesia)
- microcytic anaemia (RBCunsually small) ; iron deficiency anaemia = lower RBC because smaller RBC less Hb so less iron // thalassemia triat = higher RCC because lots of RBC but have defective hb
how do we measure size of RBC?
lighter scattered as they pass in a single fine past a laser
causes of anaemia
- megalablastic anaemia (vitB12, folate) = iron deficeny anaemia
- liver disease
what’s increased mean cell haemoglobin conc (g/L)
and why do we do it?
^ = spherocytosis (mishaped RBC si bone marrow makes more ‘normal’RBCsooverall higher PCV and higher MCHC
- most important test to identify of cold aggultinins (antibodies produced by body that target RBC and aggregate them together increasing risk of them being destroyed so increased number od cold aggulins = decreased RBC = decreased MCHC) caused by viral/mycoplasma infections