Table 4.
Quality assessment for nonrandomized trials | Kohler et al. (7) |
---|---|
A clearly stated aim | 2 |
Inclusion of consecutive patients | 2 |
Prospective data collection | 0 |
Endpoints appropriate to the aim of the study | 2 |
Unbiased assessment of the study endpoint | 0 |
A follow-up period appropriate to the aims of study | 0 |
Less than 5% loss to follow-up | 0 |
Prospective calculation of the sample size | 0 |
An adequate control group | 1 |
Contemporary groups | 0 |
Baseline equivalence of groups | 1 |
Adequate statistical analyses | 2 |
Total score | 10 |
The items are scored 0 (not reported), 1 (reported but inadequate) or 2 (reported and adequate). The global ideal score being 16 for non-comparative studies and 24 for comparative studies.