Skip to main content

Table 4 Summary of findings table according to the GRADE approach for the comparison of bone-borne versus tooth-borne rapid maxillary expansion

From: Are there benefits from using bone-borne maxillary expansion instead of tooth-borne maxillary expansion? A systematic review with meta-analysis

 

Anticipated absolute effectsa (95% CI)

Outcome

Trials (patients)

Tooth-borne RMEb

Bone-borne RME

Difference

Quality of the

evidence (GRADE)c

What happens

Suture opening at 1st premolar

Post-retention

40 patients (1 trial)

1.3 mm

2.3 mm more

(1.7 to 2.9 more)

moderated

due to imprecision

Probably greater sutural opening with bone-borne RME

Suture opening at 1st molar

Post-retention

40 patients (1 trial)

1.1 mm

2.0 mm more

(1.4 to 2.6 more)

⃝ moderated

due to imprecision

Probably greater sutural opening with bone-borne RME

Buccal tipping of 1st premolar

Post-retention

73 patients (2 trials)

3.9°

2.4° less

(9.5 less to 4.8 more)

⃝⃝⃝ very lowd, e, f

due to bias, inconsistency, imprecision

Little to no difference in premolar buccal tipping

Buccal tipping of 1st molar

Post-retention

73 patients (2 trials)

5.7°

1.9° less

(9.5 less to 5.7 more)

⃝⃝⃝ very lowd, e, f

due to bias, inconsistency, imprecision

Little to no difference in molar buccal tipping

Nasal cavity width at 1st premolar/orbita$

Post-retention

81 patients (2 trials)

1.8 mm$

0.7 mm more(0.1 less to 1.4 more)

⃝⃝ lowd, e

due to bias, imprecision

Little to no difference in nasal cavity width

Root resorption volume at 1st molar

Post-retention

41 patients (1 trial)

49.3 mm3

17.8 mm3 less

(46.0 to 10.4 more)

⃝⃝ lowd, e

due to bias, imprecision

Little to no difference in root resorption volume

  1. Bone-borne versus tooth-borne rapid maxillary expansion
  2. Population and intervention: adolescent or adult patients with skeletal maxillary deficit
  3. Settings: university clinics, private practices, and clinics (Canada, Netherlands, Sweden, Turkey)
  4. CI confidence interval, GRADE Grading of Recommendations Assessment, Development and Evaluation
  5. aThe basis for the risk in the control group (e.g., the median control group risk across studies) is provided in footnotes. The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI)
  6. bResponse in the control group is based on average response of included trials
  7. cStarts from “high,” due to the inclusion of randomized studies
  8. dDowngraded by one point due to imprecision, as the optimal information size was judged not to be met
  9. eDowngraded by one point for risk of bias (lack of blind outcome assessment)
  10. fDowngraded one for inconsistency (I2 > 75%)
  11. $Standardized mean difference was used for the meta-analysis and was back-translated to natural units based on the data from the Celenk-Koca 2018 [30] trial