SPSC Screening Test flashcards
SPSC Screening Test · Build recall with a focused review session.
32 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Sensitivity
- Proportion of people who truly have the condition and are correctly flagged by the test: TP / (TP + FN). High sensitivity means few false negatives, so a negative result is reassuring.
- Specificity
- Proportion of people without the condition who are correctly classified as negative: TN / (TN + FP). High specificity means few false positives, so a positive result is more trustworthy.
- Positive predictive value
- Probability that a person with a positive result actually has the condition: TP / (TP + FP). It rises with prevalence and falls when the same test is applied to a lower-risk population.
- Negative predictive value
- Probability that a person with a negative result truly lacks the condition: TN / (TN + FN). It is high when prevalence is low, which is why negative screens reassure more in rare disease.
- Likelihood ratio positive
- Sensitivity divided by (1 - specificity). It states how much a positive result multiplies the pre-test odds; values above 10 usually shift a diagnosis substantially.
- Likelihood ratio negative
- (1 - sensitivity) divided by specificity. It states how much a negative result multiplies the pre-test odds; values below 0.1 usually exclude the condition in practice.
- Receiver operating characteristic curve
- A plot of sensitivity against one minus specificity at every possible cut-off. It shows the trade-off available from a test and the thresholds that maximize either measure.
- Area under the curve
- Summary of ROC performance ranging from 0.5 (no discrimination, equivalent to chance) to 1.0 (perfect separation). It equals the probability a random case scores above a random non-case.
- Cut-off threshold
- The fixed value separating screen-positive from screen-negative. Lowering it raises sensitivity and false positives; raising it raises specificity and false negatives.
- Prevalence
- Proportion of the screened population that has the condition at the time of testing. It drives predictive values but does not change sensitivity or specificity of the assay.
- Number needed to screen
- The reciprocal of the absolute risk reduction attributable to screening: how many people must be screened to prevent one adverse outcome. It grows large when events are rare.
- Cohen's kappa
- Agreement beyond chance between two raters or two tests: (observed agreement minus chance agreement) divided by (1 minus chance agreement). Values near zero indicate chance-level agreement.
- Reliability versus validity
- Reliability is consistency of repeated measurements; validity is agreement with the true condition or reference standard. A test can repeat the same wrong answer reliably.
- Reference standard
- The best available method for establishing whether the condition is truly present, such as biopsy or definitive imaging. Screening results are judged against it.
- Lead-time bias
- Earlier diagnosis lengthens the interval from diagnosis to death without postponing death. Survival measured from diagnosis therefore looks better even when screening saves no lives.
- Length bias
- Slow-growing disease remains detectable for longer, so screening disproportionately finds indolent cases. This inflates apparent survival benefit relative to aggressive disease.
- Selection bias in screening
- People who volunteer for screening often differ in health and risk from those who do not. Comparing volunteers with non-volunteers overstates benefit unless groups are randomized.
- Verification bias
- Occurs when patients with positive screens receive more thorough confirmatory testing than those with negative screens, so missed disease among negatives goes uncounted.
- Spectrum bias
- Test accuracy measured in severely ill, referred patients overstates performance in the mild, early, asymptomatic population for which screening is actually intended.
- Overdiagnosis
- Detection of a condition that would never have caused symptoms or death during the person's lifetime. It produces treatment without benefit and is a core harm of screening.
- False positive result
- A screen-positive result in a person who does not have the condition. It triggers anxiety, further testing, cost, and occasionally procedural complications.
- False negative result
- A screen-negative result in a person who does have the condition. It delays diagnosis and is the main harm when sensitivity is low.
- Intention-to-screen analysis
- Analyzing participants by randomized allocation regardless of whether they attended screening. It preserves randomization and avoids healthy-adherer bias.
- Randomized screening trial
- The reference design: participants are randomly assigned to invitation or usual care, and condition-specific mortality is compared. It controls selection and lead-time bias.
- Wilson-Jungner criteria
- Classic conditions for a screening program: important health problem, accepted treatment, detectable latent stage, suitable test, agreed treatment policy, and cost-effectiveness.
- Absolute risk reduction
- Difference in event rates between screened and unscreened groups. It conveys real benefit size, unlike relative reduction, which can appear large on a tiny baseline.
- Cost-effectiveness threshold
- The maximum acceptable cost per quality-adjusted life-year a health system will pay. Screening programs exceeding it are usually not adopted despite clinical benefit.
- Informed consent for screening
- Disclosure that a screen may yield false positives, false negatives, and overdiagnosis, plus the follow-up pathway, before the person agrees to be tested.
- Confirmatory diagnostic test
- The test performed after a positive screen to establish diagnosis. It is usually more invasive or costly, so a low positive predictive value multiplies work-up burden.
- Blinding in test accuracy
- Readers of the screening test and of the reference standard must be unaware of each other's results. Blinding prevents review bias from inflating measured accuracy.
- Pre-test probability
- Estimated likelihood of disease before the screen, from prevalence or clinical features. Combined with likelihood ratios it yields the post-test probability.
- Screening versus diagnostic testing
- Screening tests asymptomatic people to estimate risk in a population; diagnostic tests confirm or exclude disease in individuals. They face different accuracy demands.