High sensitivity
Explore a test designed to miss fewer cases.
Enter a 2×2 table to get diagnostic accuracy with confidence intervals and a Fagan nomogram.
Load a scenario and adjust the numbers for your study.
Explore a test designed to miss fewer cases.
See how fewer false positives affect predictive values.
Compare predictive values across prevalence levels.
Calculate predictive values from sensitivity and specificity without counts.
View estimates side by side and select a test for the chart.
Inspect a table with no false positives.
Enter your data, examine the estimates, and take the results with you.
Enter a 2×2 table or reported sensitivity and specificity.
Use the study prevalence or enter an external estimate.
Read the confidence intervals and choose a chart.
Download a figure or export the results table.
The reference standard identifies disease status; the test produces positive or negative results. Positive predictive value (PPV) is TP / (TP + FP). The specificity formula is TN / (TN + FP). Predictive values depend on prevalence as well as sensitivity and specificity.
| Test | Disease + | Disease − |
|---|---|---|
| Positive test | TP | FP |
| Negative test | FN | TN |
References: Mercaldo et al. (2007) Newcombe (1998) Simel et al. (1991) STARD 2015
Combine a pre-test probability with a likelihood ratio to find a post-test probability.
References: Fagan (1975)
Sensitivity is the proportion of people with disease who test positive; specificity is the proportion without disease who test negative.
PPV is the proportion of positive results with disease, and NPV is the proportion of negative results without disease.
When disease is less common, false positives can make up a larger share of positive results even if sensitivity and specificity stay fixed.
Likelihood ratios compare the probability of a test result in people with and without disease; they update pre-test odds to post-test odds.
Draw a straight line from pre-test probability through the likelihood ratio and read post-test probability where it meets the right axis.
Study-based proportions use Clopper–Pearson or Wilson intervals. External-prevalence predictive values use Mercaldo logit intervals, and likelihood ratios use log intervals.
A 0.5 correction is added to every cell for LR+ if TP or FP is zero, for LR− if FN or TN is zero, and for DOR if any cell is zero. Other estimates use the original counts.
The point estimates and several intervals agree, but study-based predictive-value intervals use the selected binomial method here; MedCalc uses a fixed-prevalence logit method. External-prevalence accuracy intervals also use different methods.
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No. This tool is for research and education and does not provide a diagnosis or medical advice.
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