No test separates the sick from the healthy perfectly — the cutoff decides which errors you would rather accept.
What is this about?
A screening test is supposed to detect children with ADHD. But the test scores of affected and unaffected children overlap. Wherever you set the threshold (cut-off), errors arise: lowering it detects more affected children (high sensitivity) but also raises a false alarm for more healthy ones (low specificity) — and vice versa. How informative a positive result really is also depends on how common the disorder is at all. In the tool you compare a parent questionnaire with the clinical ADHD diagnosis as gold standard.
How to proceed
1. Distributions & cut-off — set location, spread and size of both groups and move the threshold (①). 2. Fourfold table & indices (②) — correctly detected, false alarm, missed, correctly ruled out. 3. ROC analysis (③) — all possible thresholds at a glance. 4. Concepts — trade-off, predictive values and prevalence.
What to watch for
Sensitivity and specificity are properties of the test — independent of how common the disorder is. PPV and NPV, in contrast, depend strongly on prevalence and answer the question for the individual person: how reliable is a positive or negative finding? There is no single right cut-off: it follows from the goal — e.g. the Youden index (both error types weighted equally) or a cost-benefit comparison when one error type is more expensive. Likelihood ratios (LR+ and LR−) measure discrimination independently of prevalence.
Things to try
Move the cut-off and watch sensitivity and specificity react in opposite directions. Then change the group sizes (and with them the prevalence) and see how strongly the PPV varies although the test stays the same.
What's next?
How the correlation between test and criterion affects these hits and errors is shown by Diagnostic Validity.
ADHD+ (Affected)
μ₊109
σ₊5
n₊100
ADHD− (Unaffected)
μ₋90
σ₋15
n₋200
Cut-Off
Threshold102.5
Prevalence
—
Display
Running Example
TGold standard: ADHD diagnosis by clinical interview (DSM-5)XTest: score on a parent-report screening instrumentcCut-off: test-score threshold for the screening decisionADHD+Affected: slightly elevated test scoresADHD−Unaffected: unremarkable test scores
At what test score should a screening be considered positive — and how many children does that miss (FN) versus how many are needlessly referred on (FP)? Distribution overlap, prevalence, and the cost of errors determine the optimal cut-off.
Sensitivity (SE) = TP / (TP + FN) — the proportion of affected people correctly identified as positive (few missed cases, FN). Specificity (SP) = TN / (TN + FP) — the proportion of unaffected people correctly excluded (few false alarms, FP). With overlapping distributions, both cannot be maximized at once: a lower cut-off raises SE and lowers SP — and vice versa. Which side matters more is decided by the clinical consequences.
The ROC curve plots sensitivity against 1−specificity for all cut-offs. A perfect test runs through the top-left corner (0,1); pure guessing corresponds to the diagonal. The AUC summarizes discriminative power, independent of any cut-off, in a single number (0.5 = chance, 1.0 = perfect). The farther apart and narrower the distributions, the higher the AUC.
Predictive Values & Prevalence
PPV = TP / (TP + FP) and NPV = TN / (TN + FN) answer the question for the specific person: how reliable is a positive or negative finding? Unlike SE and SP, they depend strongly on prevalence: for a rare condition, PPV drops low even with a good test, because among many unaffected people even a small percentage of false alarms (FP) outnumbers the few true cases. Prevalence form: PPV = (SE·prev) / (SE·prev + (1−SP)·(1−prev)).
Likelihood Ratios
LR+ = SE/(1−SP) and LR− = SP/(1−SE) are prevalence-independent measures of discriminative power. They are deliberately defined here so that for both, higher is better: LR+ supports the diagnosis given a positive finding, LR− rules it out given a negative finding. The variant common in many sources, LR− = (1−SE)/SP, is the reciprocal — needed for converting to odds (post-odds = pre-odds · LR), but less intuitive to interpret (there, "smaller is better"). Always pay attention to which definition is being used.
Choosing the Cut-Off
There is no single correct cut-off — it follows from the goal: Youden index (max SE+SP−1, equally weighted), cost-benefit (one error type is costlier → shift the cut-off), misclassification cost (prevalence-weighted total error), or predictive (max PPV/NPV). Try out the methods in the ROC panel and adopt the cut-off.
Property vs. Utility
SE and SP are properties of the test — prevalence-independent and transferable to other populations. PPV/NPV, by contrast, are situation-dependent. In selection contexts, PPV is called the success rate — the same quantity, a different field of application. → Diagnostic Validity · → Taylor-Russell Tables
Sensitivity & Specificity — Help
Example
A parent-report screening instrument should distinguish children with ADHD from unaffected children. We first want to examine the test — the location and spread of the distributions are initially unknown and are explored via the sliders. A clinical interview based on DSM-5 serves as the gold standard. Sought: the optimal cut-off c for the test decision.
The distributions overlap — no cut-off is error-free. At c=105: children with a test score ≥ 105 are screened positive (T=1), all others negative (T=0).
Sensitivity (SE) = the proportion of truly ADHD+ children correctly identified as positive (TP rate). High SE → few missed diagnoses (FN). Lowering the cut-off raises SE, lowers specificity.
SE = TP / (TP + FN)
Specificity (SP) = the proportion of truly ADHD− children correctly excluded (TN rate). High SP → few false alarms (FP). Raising the cut-off increases SP, lowers sensitivity.
SP = TN / (TN + FP)
In the example: with overlapping distributions, a perfect separation is impossible — the trade-off is unavoidable and depends on clinical priorities.
PPV (positive predictive value) = P(ADHD+ | test+): how likely is the diagnosis given a positive test? Strongly prevalence-dependent: for rare ADHD (5% prevalence), PPV drops sharply — many FP among few true positives.
NPV = P(ADHD− | test−): how certain is a negative finding? In the example: with high sensitivity and moderate ADHD prevalence, a negative result is very reliable.
Likelihood ratios:LR+ = SE/(1−SP) — how much more likely is a positive result given ADHD+ than given ADHD−? LR− = SP/(1−SE) — how much more likely is a negative result given ADHD− than given ADHD+? (Deliberately defined this way round so that, as with LR+, "higher is better"; the standard variant (1−SE)/SP is the reciprocal.) LRs are prevalence-independent.
The ROC curve shows sensitivity against 1−specificity for all possible cut-offs. A perfect test runs through the point (0,1): SE=1, 1−SP=0. A diagonal curve corresponds to guessing.
The AUC (Area Under the Curve) summarizes overall discriminative power in a single number (0.5=chance, 1.0=perfect). AUC is independent of the chosen cut-off — the farther apart and narrower the distributions, the higher the AUC.
Optimal Cut-Off Methods
Youden index (Youden, 1950): maximizes SE + SP − 1. The default choice with no specific assumptions, treats FP and FN as equally weighted, no prevalence influence. For normally distributed groups, the optimal cut-off sits midway between the distribution means — adjustable via the sliders.
Cost-benefit: sensible when one error type is clearly costlier. In the screening example: a missed ADHD diagnosis (FN) can be costly in the long run — a lower cut-off, favoring higher SE. The factor c = cost(FP)/cost(FN) controls this directly: c<1 → FN costlier → cut-off decreases.
Misclassification cost: incorporates prevalence — population-weighted total error. For rare ADHD (5%), FP errors occur more often; the model shifts the cut-off upward (more SP).
Prevalence-adjusted (PPV/NPV): when communicability is decisive. Maximizing PPV: for an invasive follow-up examination, a positive finding should be reliable. Maximizing NPV: for a serious condition, a negative result should reliably rule it out.