Removable splintage versus below‐elbow cast for buckle or minimally displaced fracture in children | ||||||
Patient or population: children with stable wrist fracture, predominantly buckle (torus) fracturesa Settings: hospital clinic Intervention: Removable splintb for 2 to 6 weeks Comparison: Below‐elbow cast for 2 to 6 weeks | ||||||
Outcomes | Illustrative comparative risks* (95% CI) | Relative effect (95% CI) | No of Participants (studies) | Quality of the evidence (GRADE) | Comments | |
Assumed risk | Corresponding risk | |||||
Below‐elbow cast | Removable splint | |||||
Pain VAS (0 to 10; worst pain) during device use (4 ‐ 6 weeks follow‐up) |
The mean score in the study control group was 2.92 | The mean score in the intervention group was 0.20 higher (1.10 lower to 1.50 higher) | ‐ | 50 children (1 study) | ⊕⊝⊝⊝ very lowc | A 0.2 difference is minute and clinically unimportant. Overall, 5 trials provided data on pain, using different measures and timings. The 2 trials (161 children) reporting pain at 1 week found higher median pain scores in the splint group but neither of the differences between the 2 groups reached statistical significance; moreover, the difference in 1 trial was also unlikely to be clinically important. Most children in these 2 trials had no or very little pain by the end of 2 or 3 weeks immobilisation |
Discomfort during use of device | See comment | See comment | Not estimable | ‐ | See comment | This outcome was not reported |
Participant satisfaction: child and/or parent preference for same device in future (3 to 6 weeks follow‐up) | See comment | See comment | Not estimable | 178 children (2 studies) | See comment | Results (1 indicating no difference, 1 favouring the splint) not pooled: clinically (e.g. different types of splint) and statistically heterogeneous (I2 = 83%)d |
Time to return to former activities | See comment | See comment | Not estimable | ‐ | See comment | This outcome was not reportede |
Skin problems (rash) (3 weeks follow‐up) | See comment | See comment | Not estimable | ‐ | See comment | 1 study reported 11 cases of rash (17% of 64) in the splint group but none in the cast group (73 children). Conversely it reported 5 cases of oedema (7% of 73) in the cast group. The severity of both complications was not stated and the trial also made a contradictory statement that there were no adverse events or skin problems |
Serious adverse events: refracture (6 months follow‐up) |
See comment | See comment | Not estimable | 87 children (1 study) | See comment | This study reported there had been no refractures |
Health‐related quality of life Modified Activities Scale for Kids ‐ performance version (0 to 100; best function; no disability) (4 weeks follow‐up) | See comment. The median score in the study control group was 99.11 (IQR 96.42 to 100.00) | See comment. The median score in the intervention group was 99.04 (IQR 95.29 to 100.00) | ‐ | 65 children (1 study) | ⊕⊝⊝⊝ very lowf | This outcome assesses physical function rather than quality of life but has been used as a basis for cost‐effectiveness analysis in Boutis 2010. The data for the final scores are shown here for illustrative purposes; with no evidence of a clinically important difference between the two groups (MCID set at 15 in the study for sample size calculation). |
Cast changes & number of outpatient visits (3 to 6 weeks follow‐up) | See comment | See comment | Not estimable | ‐ | See comment | Data for this outcome, which serves primarily as an indication of health care resource utilisation, were not available. |
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (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). CI: Confidence interval; RR: Risk Ratio; VAS: visual analogue scale | ||||||
GRADE Working Group grades of evidence High quality: Further research is very unlikely to change our confidence in the estimate of effect. Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality: We are very uncertain about the estimate. |