Table 5.
Item |
Zablocki et al.2 |
Wilmes et al.32 |
Lai et al.40 |
Lee et al.36 |
Borsos et al.38 |
Kuroda et al.11 |
1. A clear stated aim | 2 | 2 | 2 | 2 | 2 | 1 |
2. Inclusion of consecutive patients | 1 | 1 | 1 | 2 | 1 | 0 |
3. Prospective collection of data | 2 | 2 | 2 | 2 | 2 | 1 |
4. Endpoints appropriate to the aim of the study | 2 | 2 | 2 | 2 | 2 | 2 |
5. Unbiased assessment of the study endpoint | 2 | 1 | 2 | 1 | 1 | 0 |
6. Follow-up period appropriate to the aim of the study | 2 | 2 | 2 | 2 | 2 | 2 |
7. Loss to follow up less than 5% | 1 | 1 | 1 | 2 | 1 | 0 |
8. Prospective calculation of the study size | 1 | 0 | 1 | 0 | 0 | 0 |
9. An adequate control group | 2 | 2 | 2 | 2 | 2 | 2 |
10. Contemporary groups | 1 | 2 | 1 | 2 | 1 | 2 |
11. Baseline equivalence of groups | 2 | 2 | 1 | 1 | 2 | 1 |
12. Adequate statistical analyses | 2 | 2 | 2 | 2 | 2 | 2 |
Total | 20 | 19 | 19 | 20 | 18 | 13 |
The items are scored 0 (not reported), 1 (reported but inadequate), or 2 (reported and adequate), with the global ideal score being 16 for noncomparative studies and 24 for comparative studies.14