Table 1.
Level | Therapy/prevention, etiology/harm | Prognosis |
1a | SR (with homogeneity1) of RCTs | SR (with homogeneity1) of inception cohort studies; CDR2 validated in different populations |
1b | Individual RCT (with narrow Confidence Interval2) | Individual inception cohort study with > 80% follow-up; CDR2 validated in a single population |
1c | All or none3 | All or none case-series |
2a | SR (with homogeneity1) of cohort studies | SR (with homogeneity1) of either retrospective cohort studies or untreated control groups in RCTs |
2b | Individual cohort study (including low quality RCT; e.g., < 80% follow-up) | Retrospective cohort study or follow-up of untreated control patients in an RCT; Derivation of CDR2 or validated on split-sample4 only |
2c | "Outcomes" Research; Ecological studies | "Outcomes" research |
3a | SR (with homogeneity1) of case-control studies | |
3b | Individual case-control study |
A systematic review (SR) that is free of worrisome variations (heterogeneity) in the directions and degrees of results between individual studies. Studies displaying worrisome heterogeneity should be tagged with a “-” at the end of their designated level;
Clinical decision rule (CDR) (These are algorithms or scoring systems that lead to a prognostic estimation or a diagnostic category);
Met when all patients died before the Rx became available, but some now survive on it; or when some patients died before the Rx became available, but now none die on it;
Split-sample validation is achieved by collecting all the information in a single tranche, and subsequently artificially dividing this into “derivation” and “validation” samples. RCTs: Randomized control trials.