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High diagnostic sensitivity
What is the most desirable form of screening test due to minimal false negatives
Increase specificity and decrease sensitivity
What does raising a cutoff value do in a screening test
Two consecutive controls greater than ± 2 SD
What starts the cause for rejecting an analytical run
Analyte concentrations that reflect the analytic measurement range and match patient samples
What makes a good QC material
Delta check
Used to investigate differences between two results from the same patient on the same day to catch preanalytical errors
Colligative properties
Freezing point depression, boiling point elevation, vapor pressure depression, osmotic pressure that depend on the number of dissolved particles
Precision
Reproducibility evaluated with CV and F-test
Accuracy
Closeness to the true value evaluated by t-test
Sensitivity/screening
Ability to detect disease and minimize false negatives
Specificity/confirmation
Ability to identify absence of disease and minimize false positives
Positive prediction value
Probability that a positive test means you actually have the disease
Negative predictive value
Probability that a negative test means you actually do not have the disease
Transfer/verify a reference interval
Requires 20 healthy patients and passes if 10% or less fall outside of the range.
Obtain 20 additional samples and pass if two or less fall outside the range
What to do if RI verification fails
Establish a new reference interval
Requires 120 healthy patients using 2.5th-97.5th percentiles due to natural skew
Proficiency testing
Blind external validation tested like patient samples to compare analyzers twice a year
All proficiency testing failures must be resolved in 30 days
What is the rule of PT
1_2s warning
One point outside ± 2SD
1_3s reject
1 point outside 3± SD to indicate random error
2_2s reject
2 consecutive points outside the same ± 2SD limit to indicate systematic error
R_4s reject
Range between consecutive runs exceeds 4 SD to indicate random error
4_1s reject
4 consecutive points exceed the same ± 1 SD to indicate systematic error
10_x reject
10 consecutive points fall on the same side of the Mean to indicate systematic error
Trend
Gradual deviation in one direction for 6 runs
Shift
Abrupt change establishing a new pattern for 6 runs
Analysis of control serum over 20 days
How to prepare a new Levey-Jennings chart
Constant error
Shift stays the same regardless of concentration (inference studies)
Proportional error
Shift gets worse as concentration increases (recovery studies)
Hemolysis
Intracellular components of burst RBCs leak into serum
Icterus
Caused by high bilirubin
Lipemia
Caused by high triglycerides and fats in the blood sample
Ammonia and Arterial Blood Gas
What types of analytes need to be kept on ice
Serum
No anticoagulant and is allowed to clot due to the lack of fibrinogen
Plasma
Contains anticoagulant and fibrinogen, and WBCs, platelets, and RBCs when spun
Arterial blood
Blood drawn from the radial artery
High K+ and low Ca2+
What signs suggest EDTA contamination
Diluted analytes with sugar and electrolyte spike
What signs suggest IV fluid contamination
Chlorhexidine
What should you use instead of alcohol wipes for Blood Alcohol tests
Fist pumping
What causes falsely elevated potassium and lactic acid levels
Prolonged tourniquet
What causes hemoconcentration and elevated analyte levels
Light
What must bilirubin be protected from
Beer’s law
Absorbance is directly proportional to concentration
Transmittance has a logarithmic inverse relationship to concentration
Absorbance and Transmitting relationship
Stock volume/Total volume
Dilution fraction
Normality
One gram equivalent weight of solute per liter of solution
Molarity
Moles of solute per 1 L of solution