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| Μελέτη Περίπτωσης-Ελέγχου Πραγματολογικής Προσέγγισης× | Μελέτη Περίπτωσης-Ελέγχου (Case-Control Study) Αναδρομικού Τύπου× | |
|---|---|---|
| Πεδίο | Επιδημιολογία | Επιδημιολογία |
| Οικογένεια | Process / pipeline | Process / pipeline |
| Έτος προέλευσης≠ | 1950s–1960s (classical); pragmatic framing 1967–2000s | 1950s–1960s (formal methodology) |
| Δημιουργός≠ | Evolved from classical case-control methodology (Dorn, 1954; Cornfield, 1956); pragmatic framing formalized by Schwartz & Lellouch (1967) | Jerome Cornfield; formalized by Brian MacMahon and others in mid-20th-century epidemiology |
| Τύπος≠ | Observational epidemiological study design | Observational analytical study |
| Θεμελιώδης πηγή≠ | Rothman, K. J., Greenland, S., & Lash, T. L. (2008). Modern Epidemiology (3rd ed.). Lippincott Williams & Wilkins. ISBN: 978-0781755641 | Schlesselman, J. J. (1982). Case-Control Studies: Design, Conduct, Analysis. Oxford University Press. ISBN: 978-0195029338 |
| Εναλλακτικές ονομασίες | real-world case-control study, pragmatic case-control design, effectiveness case-control study, PCCS | case-control study, retrospective case-referent study, case-referent design, trohoc study |
| Συναφείς≠ | 6 | 5 |
| Σύνοψη≠ | A pragmatic case-control study is an observational design that compares individuals who have developed a disease or outcome (cases) with those who have not (controls), using data collected under routine real-world conditions rather than strictly controlled experimental settings. Exposure histories are reconstructed from clinical records, registries, or administrative databases. The design is chosen when a conventional explanatory case-control study would be impractical, unethical, or too narrow to inform actual clinical or public-health decisions. | A retrospective case-control study identifies individuals who already have an outcome of interest (cases) and a comparable group without it (controls), then looks backward in time using existing records to determine prior exposure to a suspected risk factor. The primary measure of association is the odds ratio. This design is especially efficient for studying rare diseases or outcomes with long latency periods, since the outcome has already occurred before the study begins. |
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