Intro to Clinical pathology Flashcards

1
Q

What is Clinical Pathology

A

Development, application and interpretation of laboratory procedure for:
establishing a diagnosis and/or prognosis
monitoring of treatment in sick animals
monitoring animal health

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2
Q

Clinical vs Anatomical Pathology

A

Clinical- related to care of live patient
Anatomical-
surgical- looking at biopsies of tissues
Necropsy

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3
Q

Anticoagulant used for haematology

A

EDTA

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4
Q

Anticoagulants used for clinical chemistry

A

Serum or
Li-heparin plasma or EDTA Plasma

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5
Q

Anticoagulant used for glucose

A

Fluoride-oxalate

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6
Q

Anticoagulant used for haemostasis/coagulation

A

Citrate (reversible)

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7
Q

Serum vs Plasma

A

serum has been allowed to clot, plasma has not

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8
Q

Effects of anticoagulants on K and ionised Ca

A

Heparinised- correct measuremenats
K- EDTA- false high K and low Ca

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9
Q

Effect of EDTAK- on alkaline phosphatase

A

Will be false low in sample as it depends on metallic cofactors

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10
Q

Importance of Draw/fill order

A

Preventing combination of chemistry samples with EDTA

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11
Q

What does icteric mean

A

Blood sample with high bilirubin
Plasma will be yellow, interferes with colorimetry

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12
Q

How to avoid haemolysis in blood samples

A

Choose appropriate gauge needle
Never dispense blood sample through needle

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13
Q

Effect of haemolysis on blood results

A

INCREASES in plasma/serum value of some compounds/enzymes due to their high conc. in the RBC
INTERFERES with determinations by colorimetry or with chemical reactions

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14
Q

How to avoid lipaemia in blood samples

A

Fast patient appropriately

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15
Q

Effect of lipemia in blood sample

A

Increase in total lipid, triglycerides and cholesterol
many determinations cannot be carried out or are significantly affected
Changes values of compounds in plasma/serum as:
presence of extra lipid fractions -> will be less aqueous -> false low readings of aqueous compounds such as electrolytes
turbidity caused by the lipids interfering in light detection methods (colorimetry)

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16
Q

Examples of pre analytical sources of variation and errors in lab results

A

Patient prep
Sample prep- e.g. choice of tube
Shipping

17
Q

Examples of analytical sources of variation and errors in lab results

A

Appropriate equipment/reagents (validated)
still working (QC)

18
Q

Examples of post analytical sources of variation and errors in lab results

A

Results to the right place for the right patient
appropriate interpretation
Diagnostic sensitivity and specificity

19
Q

how to control analytical variation

A

Techniques must be validated before analysis starts
Quality control must be performed regularly before and/or during routine anaylsis

20
Q

PASS validation of analytical technique

A

Precision - Repeatability/reproducibility
Accuracy- Measuring the right thing correctly
Specificity (analytical)- Different from «diagnostic specificity»
Sensitivity (analytical) and range (linearity)- When do we need to dilute a sample