Likelihood ratios and the Fagan nomogram

A positive result carries more weight coming from some tests than from others, and the likelihood ratio is the number that says exactly how much. It asks one blunt question about a result: how many times more often does it show up in people who have the condition than in people who don't? A reactive 4th-generation HIV test is roughly 200 times more common in someone who has HIV than in someone who doesn't, so it should move your estimate a long way. A positive low-dose CT for lung cancer is only about four times more common in disease than in health, so it should move your estimate far less. Same kind of tool, very different pull — and the likelihood ratio is what lets you put both on one scale.

Every test yields two of these ratios. The positive likelihood ratio, LR+, grades a positive result; the negative likelihood ratio, LR−, grades a negative one. Both are built straight out of sensitivity and specificity:

Read the numerator as "how often this result happens in the sick" and the denominator as "how often the same result happens in the healthy." A ratio of 1 means the result is equally common in both groups, so it tells you nothing. The further above 1 an LR+ climbs, the harder a positive pushes toward disease; the closer to 0 an LR− falls, the harder a negative pushes away from it.

Reading two real tests off their accuracy

Take the two tests above and turn the crank. The 4th-generation HIV assay runs about 99.8% sensitive and 99.5% specific — the low ends of the ranges the U.S. Preventive Services Task Force reports for antigen/antibody tests:

A reactive result is about 200 times more likely in someone with HIV; a non-reactive result is about 500 times more likely in someone without it (1 ÷ 0.002 ≈ 500). Either result, on its own, is close to decisive. (The confirmatory algorithm that follows a reactive screen is worked through in HIV testing, by the numbers.)

Try it

Load a near-perfect test: the 4th-generation HIV assay, 99.8% sensitive and 99.5% specific, at 0.4% population prevalence across 100,000 people — an LR+ close to 200, with the true and false positives now large enough to count. Treatment settings are generic teaching inputs, not estimates for this test.

Open this scenario in the calculator →

Low-dose CT is a different animal — about 93.1% sensitive but only 76.5% specific:

A positive scan multiplies the odds of lung cancer by only about four; a negative scan divides them by about eleven (1 ÷ 0.09 ≈ 11). Notice the asymmetry — this test rules out better than it rules in. What separates it from the HIV assay is almost entirely specificity: 76.5% versus 99.5%. A 23.5% false-positive rate is a large denominator under LR+, and it drags the ratio down toward the unhelpful end.

Try it

Now load a modest one: low-dose CT for lung cancer, 93.1% sensitive and 76.5% specific, at a 1.1% pre-test probability drawn from the first screening round of the National Lung Screening Trial — where a positive multiplies the odds only about four-fold (LR+ ≈ 4).

Open this scenario in the calculator →

Why prevalence barely moves the ratio

Nothing in LR+ or LR− mentions how common the disease is — the ratios are assembled entirely from sensitivity and specificity. That is what makes them portable: the same LR+ ≈ 200 applies whether HIV turns up in 1 person per 1,000 or 1 per 20. Predictive value behaves the opposite way. PPV and NPV fold prevalence in through Bayes' theorem, so the identical test reads very differently in a low-risk population than a high-risk one — the engine behind the base-rate fallacy. A likelihood ratio deliberately strips prevalence out and describes the test's discriminating power on its own.

That portability comes with a hedge. Sensitivity and specificity are not carved in stone; they shift with the mix of patients actually tested, an effect called spectrum bias. A test measured on advanced, unmistakable disease looks more sensitive than the same test used to catch early disease, and referral patterns can push specificity around too. Even within one trial the figures move: the National Lung Screening Trial's report on its first screening round alone gave low-dose CT 93.8% sensitivity and 73.4% specificity — an LR+ nearer 3.5 than 4. So a likelihood ratio measured in one population is a well-travelled estimate, not a universal constant. Use published LRs freely, but hold them a little loosely.

Odds, and one turn of the crank

Likelihood ratios multiply odds, not probabilities, so the arithmetic has to run in odds. Converting is quick in both directions: odds = p ÷ (1 − p), and back again p = odds ÷ (1 + odds). A pre-test probability of 1.1% becomes pre-test odds of 0.011 ÷ 0.989 ≈ 0.01112 — roughly 1 to 90.

From there, Bayes' theorem collapses to a single multiplication:

pre-test odds × LR = post-test odds

That 1.1% comes from the low-dose CT scenario above. In the National Lung Screening Trial (NLST), whose participants were aged 55 to 74 with at least 30 pack-years of smoking, lung cancer was diagnosed in 1.1% of the low-dose CT group after the first screening round. Run a positive scan through the crank with the LR+ of 0.931 ÷ 0.235 ≈ 3.962:

0.01112 × 3.962 ≈ 0.0441 post-test odds, and 0.0441 ÷ 1.0441 ≈ 0.042 — about a 4.2% chance of lung cancer.

A positive scan roughly quadruples the odds and still leaves the probability under 5%, because the starting odds were long. A plain count agrees: among 1,000 such people, 11 have lung cancer; the scan flags about 10 of them plus about 232 of the 989 without it, so roughly 10 of 242 positives — again about 4% — are cancer. The calculator's Fagan nomogram shows the same update as one straight line, and the full step-by-step lives on pre-test to post-test probability. For the opposite extreme — an LR+ near 200 that, from a 0.4% start, still lands at only about 44% — see HIV testing, by the numbers.

How strong is strong?

A rough convention, set out in the JAMA Users' Guides to the Medical Literature and later distilled by McGee, sorts the ratios into bands. An LR+ above 10 drives a large, often decisive rise in probability; 5 to 10 is moderate; 2 to 5 is small; anything between 1 and 2 barely registers. The negatives mirror it: an LR− below 0.1 is a strong rule-out, 0.1 to 0.2 is moderate, 0.2 to 0.5 is small, and near 1 is useless. By that ruler the HIV assay is off the scale at both ends (≈ 200 and ≈ 0.002), while low-dose CT sits in the "small" band for a positive (≈ 4) and only just crosses into strong rule-out territory for a negative (≈ 0.09).

McGee also offered a bedside shortcut that skips the odds algebra entirely: across the middle range of pre-test probability, likelihood ratios of 2, 5, and 10 add roughly 15, 30, and 45 percentage points, and ratios of 0.5, 0.2, and 0.1 subtract about the same. It drifts near the extremes — the low starting probabilities on this page, 1.1% and 0.4%, are exactly where it breaks down — but for everyday numbers it is close enough to reason with out loud.

The Fagan nomogram

Thomas Fagan compressed that one multiplication into a picture in a one-paragraph 1975 letter to the New England Journal of Medicine. It is three parallel scales: pre-test probability on the left, likelihood ratio down the middle, post-test probability on the right. Lay a straightedge on your pre-test probability, pivot it through the test's likelihood ratio, and read the answer where the line meets the right-hand scale. The scales are logarithmic — that is the trick that quietly turns "multiply the odds" into "draw a straight line." One chart handles any test at any starting probability, no calculator required.

This tool draws that nomogram live for a positive result: move the prevalence, sensitivity, or specificity sliders and the line and its endpoints follow. Open either scenario above and read it in the calculator's Fagan nomogram. The HIV line pivots through an LR near 200 yet, starting from 0.4%, lands at only about 44%; the low-dose-CT line pivots through an LR near 4 and carries 1.1% to about 4%.

Correction, September 2026. The 1.1% lung-cancer starting point is now attributed to the first screening round of the National Lung Screening Trial (2013 report), and the description of the HIV example on the nomogram was corrected: from a 0.4% starting point a positive lands at about 44%, not near the top of the scale. The corrections log lists every change.

References

  1. Fagan TJ. Nomogram for Bayes's theorem (letter). New England Journal of Medicine, 1975.
  2. McGee S. Simplifying likelihood ratios. Journal of General Internal Medicine, 2002.
  3. Jaeschke R, Guyatt GH, Sackett DL. Users' guides to the medical literature. III. How to use an article about a diagnostic test. JAMA, 1994.
  4. U.S. Preventive Services Task Force. HIV Infection: Screening (reported sensitivity 99.76%–100% and specificity 99.50%–100% for antigen/antibody tests). USPSTF, 2019.
  5. Pinsky PF, et al. ROC curves for low-dose CT in the National Lung Screening Trial (sensitivity 93.1%, specificity 76.5%). Journal of Medical Screening, 2013.
  6. National Lung Screening Trial Research Team; Church TR, Black WC, Aberle DR, et al. Results of initial low-dose computed tomographic screening for lung cancer (first screening round: lung cancer diagnosed in 292 participants, 1.1%, of the low-dose CT group; sensitivity 93.8%, specificity 73.4%). New England Journal of Medicine, 2013;368(21):1980–91.

Educational model — not medical advice. It illustrates the statistics of testing and treatment; it does not describe any specific real-world test.