So sánh phương pháp

	Nghiên cứu bệnh-chứng thực dụng	Nghiên cứu bệnh chứng hồi cứu
Lĩnh vực	Dịch tễ học	Dịch tễ học
Họ	Process / pipeline	Process / pipeline
Năm ra đời	1950s–1960s (classical); pragmatic framing 1967–2000s	1950s–1960s (formal methodology)
Người khởi xướng	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
Loại	Observational epidemiological study design	Observational analytical study
Công trình gốc	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
Tên gọi khác	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
Liên quan	6	5
Tóm tắt	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.