Clinical pathology Flashcards
What is clinical pathology
Development, application & interpretation of laboratory procedures for:
- establishing diagnosis &/or prognosis
- monitoring of treatment in sick animals
- monitoring animal health
What is the purpose of clinical pathology analysis in healthy animals?
Monitoring of production/performance (e.g. metabolic profile in dairy herd)
Monitoring during critical periods (e.g. for anaemia in piglets)
Special purposes (e.g. transport/export)
What tests does clinical pathology involve?
Haematology
Clinical Biochemistry
Cytology
What fluids can be used in clinical pathology?
blood (blood, serum, plasma)
urine
fine needle aspirates (FNAs)
effusions
cerebrospinal fluid
lavages (e.g., BAL)
synovial fluid
What anticoagulant blood tubes are there and what are they used for?
Haematology:
- EDTA
Clinical Chemistry:
- Serum or
- (Li-heparin) plasma
- EDTA plasma
Glucose:
- Fluoride-oxalate
Haemostasis/Coagulation:
- Citrate
What type of blood tube should be used for measuring Ca2+?
Heparinised plasma
No other anticoagulants as they cause Ca+ levels to decrease
What factors should be considered when deciding in what order to fill blood tubes?
can’t risk bacterial contamination from other tubes for blood culture
can’t delay citrate sample for coagulation because can’t risk coagulation starting before sample hits citrate
don’t want to risk contaminating our chemistry samples with EDTA
Label these plasma colours in cattle
label these plasma colours in dogs
How can you prevent haemolysis in blood samples?
Choose appropriate gauge needle
Never dispense blood sample through needle
What are the effects of haemolysis in blood samples?
Increases in plasma/serum values of some compounds/enzymes due to higher concentration in RBC
Interferes determinations by colorimetry or interference in chemical interactions
How can lipaemia risk be decreased when taking blood samples?
Fast patients appropriately
What are the effects of lipaemia on blood samples?
Increases or decreases values of some compounds in plasma/serum due to:
- presence of extra lipid fractions
- turbidity caused by lipids interfering in light detection methods (colorimetry)
Main changes:
- increase in total lipid, triglycerides & cholesterol
- many determinations can’t be carried out or results significantly affected
What are some pre-analytical sources of variation/errors in lab results?
patient prep
sample prep (e.g. choice of collection tube)
shipping
What are some analytical sources of variation/errors in lab results?
Appropriate equipments/reagents
Quality control (e.g., equipment working?)