Table 2.
Quality assessment of the included non-randomised controlled trials using the Methodological Index for Non-randomised Studies
| Assessment | Efrati 2015 et al 39 | Guggino et al 202034 | Curtis et al 202132 | Casal et al 201935 | Bosco et al 201936 | Atzeni et al 201937 |
| 1. A clearly stated aim | 2 | 2 | 2 | 2 | 2 | 2 |
| 2. Inclusion of consecutive patients | 2 | 2 | 2 | 2 | 2 | 2 |
| 3. Prospective collection of data | 2 | 2 | 2 | 2 | 2 | 2 |
| 4. Endpoints appropriate to the aim of the study | 2 | 2 | 2 | 2 | 2 | 2 |
| 5. Unbiased assessment of the study endpoint | 2 | 0 | 1 | 1 | 0 | 0 |
| 6. Follow-up period appropriate to the aim of the study | 0 | 0 | 2 | 0 | 2 | 0 |
| 7. Lost to follow-up less than 5% | 0 | 0 | 2 | 0 | 0 | 0 |
| 8. Prospective calculation of the study size | 2 | 2 | 0 | 0 | 0 | 2 |
| 9. An adequate control group | 2 | 2 | 2 | – | – | – |
| 10. Contemporary groups | 2 | 2 | 2 | – | – | – |
| 11. Baseline equivalence of groups | 2 | 2 | 2 | – | – | – |
| 12. Adequate statistical analyses | 2 | 2 | 2 | – | – | – |
| Total score | 20 | 18 | 21 | 9 | 10 | 10 |