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25 Cards in this Set
- Front
- Back
wellness screening tests
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things that we screen for that are very common in the pop, not $$, and there is a treatment for; ex. PSA’s (for older men), total cholesterol, lead level; done as a baseline for their particular age, gener etc.
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disease screening tests
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when you have something in mind; ex. They have the ssx for pneumonia (will do most of the time)
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how do i know what tests to order
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1. reccomendatiosn
2. require evaluation and revision 3. availability 4. cost 5. ethical and legal implications 6. techinical validity: acuracy and precision 6. diagnostic value: sensititivty, specificity, positive-predictive value, negative predictive value |
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accuracy
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o How close the test result is to the true value (to the target) of the substance being measured
o Routinely monitored with a “control specimen” (control-substance that is man made and has a certain amt of substances in it) |
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precision
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o How close together repeat measurements of a substance are in the same sample
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true and false positives, true and false negatives
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TP: with disease test +
TN: without disease test - FP: without disease test + FN: with disease test - |
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sensitivity
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-Proportion of those with disease that test positive
-Ability of a test to correctly identify an individual who truly have a disease; ability of a test to show true positives -sensitivity = TP / (TP + FN) x 100 (higher the numerator, higher the sensitivity) |
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SNOUT
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-When using a test with a high sensitivity, a NEGATIVE result rules OUT the diagnosis
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specificity
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-Proportion of those without disease that test negative (have true negatives)
-o In a test with a high specificity you have a low false positive rate so you can trust that your negative is a negative -specificity = TN / (TN + FP) x 100 |
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SPIN
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-When using a test with high specificity, a POSITIVE result rules IN the diagnosis
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positive predictive value (PPV)
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-Dependant on prevalence (more people with a disease in a particular population) of disease in the population or community
-varies with age, gender, geographic location -*the higher the sen the higher the spe the higher the prevalen the higher the PPV will be! |
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negative predictive value
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-Probability of a disease being absent if the test is negative
-Dependant on prevalence of disease in the population or community -The more rare a disease, the higher the NPV -varies with age, gender, location |
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quantitative
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-present or absent
-reported as positive or negative -no number ex. preg test |
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quantitative
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-a.Specific concentration of analyte is measured and reported with reference range
b.Results reported as a numerical value c.Result may indicate severity or stage of condition |
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semi-quantitative
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-results reported as number but not exact concentration (ex 1+)
-ex. urine dipsticks |
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stat
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results needed immediately
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profile/panel
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a.Multi-test measurements
b.Organ specific or instrument specific battery of tests i.Liver function profile ii.SMA 18 iii.Chem profile c.Complete blood count (CBC) d.Good concept but be weary of content (don’t order a panel if you don’t need it) |
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point of care testing
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- bring lab testing to the pt
-results quick |
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reference range
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-took a lot of people and did a test on them and come up with a mean number and if you go 2 standard deviations out
-not all created equal -"normal range" - established for most analytes used for clinical interpretation -results that fall within 2 standard deviations of the mean for sample population |
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panic or critical values
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oTest results significantly below or above reference range
oIndicates potential life threatening conditions oImmediate verbal notification to health care provider |
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pre-analytical factors
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-most common
-occurs between the time test was order and time specimen was collected -ex: completeness of pt info, ordering process, pt prep, physiologic variation, collection procedure, speicimen quality, specimen transport, handling and storage, speed of delivery |
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analytical factors
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- occur during testing of the specimen
ex: instrumentation mantenance and operation, test reagents and supplies, specimen error,type of method etc. |
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post analytical factors
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-b/t time of testing and reporting of results
-o Calculation, report timeliness, written/oral communication, reference range, method of reporting, transcription, confidentiality |
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serum
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oYellow portion of blood at top of clotted and centrifuged plain red top or SST tube
oDOES NOT contain fibrinogen, factor V or VIII and prothrombin (clotting factors) oNo anticoagulant in specimen |
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plasma
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oYellow portion of blood at top of centrifuged anticoagulated whole blood
oCONTAINS fibrinogen and other clotting factors |