Glossary
Every term used across PrevIQ, defined in one place.
Prevalence rate—percentage— The fraction of tested specimens in which an organism was detected, within a single syndrome and panel.detected / tested.Tested—count— The number of specimens actually tested for an organism in a given panel — the denominator. Excludes "not tested" (N/A) and invalid results.Detected—count— The number of tested specimens in which the organism was found — the numerator.Specimen—entity— A single patient sample. One specimen typically generates many organism-result cells (one per organism on its panel).Organism-result cell—entity— A single organism's result on a single specimen. PrevIQ stores these as normalized records; they are not the same as specimens.Specimen count (estimate)—count— An estimate of distinct specimens for a syndrome, computed as the sum of the maximum tested count within each panel. Used so headline numbers reflect specimens, not raw cells.Syndrome—bucket— A clinical-area grouping of panels — RESPIRATORY, UTI, STI, VAGINOSIS, WOUND, GI, GBS_PRENATAL. See Syndromes & panels.Panel—entity— A specific test panel (e.g. "UTI with AMR"). Prevalence is computed at the panel level first.Combo panel—entity— A panel spanning multiple clinical areas (e.g. "Female STI + Vaginosis"). Its organisms are routed to their constituent syndromes.Vendor (vendor ID)—entity— A laboratory, identified by a short code such asAFCorOBG-YN.Sample-size tier—A | B | C— A quality grade for a rate based on its tested count: A (n ≥ 100), B (30–99), C (< 30, not reportable). See Sample-size tiers.Clinically reportable—boolean—truefor Tier A and B;falsefor Tier C. Indicates whether a rate is solid enough to act on.Confidence interval (95%)—range— The plausible range for the true rate, computed with the Wilson score method. Reported as[lower – upper].Classification—INCLUDE | WATCH | RARE— The panel-design verdict for an organism. See Panel classifications.Result status—positive | negative | skip | exclude— How a raw result cell is interpreted. Skip and exclude leave the math entirely. See Result statuses.Methodology footnote—text— The standard note attached to every report stating that prevalence uses an all-tested-specimens denominator.Grouping level—vendor | syndrome | cross_vendor— How prevalence rows are rolled up: per lab, pooled within a syndrome, or pooled across all labs.Ingestion run—event— A single load of a data file, with row counts and QA flags. Visible in ingestion history.QA flag—label— A data-quality marker on an ingestion run, e.g.UNKNOWN_RESULTorALL_NA_ROW.RESP-NET—external dataset— Public CDC respiratory hospitalization surveillance (COVID-NET, FluSurv-NET, RSV-NET), shown as context only — never blended into prevalence. See Geo.