Levels of evidence | |
I | Evidence from at least one large randomised, controlled trial of good methodological quality (low potential for bias) or meta-analyses of well-conducted randomised trials without heterogeneity |
II | Small randomised trials or large randomised trials with a suspicion of bias (lower methodological quality) or meta-analyses of such trials or of trials with demonstrated heterogeneity |
III | Prospective cohort studies |
IV | Retrospective cohort studies or case–control studies |
V | Studies without control group, case reports, expert opinions |
Grades of recommendation | |
A | Strong evidence for efficacy with a substantial clinical benefit, strongly recommended |
B | Strong or moderate evidence for efficacy but with a limited clinical benefit, generally recommended |
C | Insufficient evidence for efficacy or benefit does not outweigh the risk or the disadvantages (adverse events, costs, etc), optional |
D | Moderate evidence against efficacy or for adverse outcome, generally not recommended |
E | Strong evidence against efficacy or for adverse outcome, never recommended |
*By permission of the Infectious Diseases Society of America.2