Blood smears Flashcards
How can you assess for analytical errors?
Quality control
Plausibility evaluation
Techincal and medical review
method of obtaining results from a sample
What can excitement (epinephrine) do to a haematology sample?
Lymphocytosis
Are band cells part of a stress leukogram?
No
What makes a good blood smear?
3/4 length of the slide
Well defined monolayer
Well defined feathered edge
No holes
WBCs not at feathered edge
Evenly distributed WBCs/ platelets
Well stained with good contrast and colour
No stain precipitate or other artifacts
What can a moderate to marked leukocytosis affect on haematology?
Hb
Platelet count
MCV
What can a microcytosis do to a haematology results
May cause errors in RBC, platelet numbers, and MCV, as they are confused for platelets
What can a lipaemia/ chylomicrons do to a haematology sample?
Cause errors in WBCs, platelets and eosinophils due to an affect on the light reflection that the measurements use
How do you do a WBC measurement on a smear?
Average WBCs per 40 field x 2000
How do you do a platelet measurement on a smear and how do values suggest the levels are?
Average per 100x field x 20,000
<2 per hpf - v low 2-5 low 5-25 adequate 25-50 high >50 v high
How do you differentiate between band and segmented neutrophils?
bands have parrallel sides
Segmented when any indentation of the nucleus is >25% of the nucleus
What is the rule of thumb with reticulocytes and polychromatophils
All polychromatophils are reticulocytes, but not all reticulocytes are polychromatophils
Which stain is good for parasites?
new methylene blue
What is the rule of 3 for checking if results are plausible?
Hct +/-3 = Hb x 3
What should you do if MCHC is high
Not physiologically possible
Look for signs of haemolysis
What are Howell-Jolly bodies?
small but prominent dark inclusions which are remnants of nuclear material
Sign of regeneration