Rowland 2007.
Study characteristics | ||
Methods | 2‐arm parallel RCT | |
Participants |
Number recruited: 397 Sex (M:F): 156:241 Mean age: group 1: 14.8 years (SD 1 year 8 months), group 2: 15 years (SD 1 year 5 months) Inclusion criteria: all participants had preadjusted edgewise fixed appliances, with pretreatment records, treatment plan and study models available, and were willing to wear maxillary and mandibular retainers Exclusion criteria: single arch or sectional fixed appliance treatment; hypodontia requiring tooth replacement on the retainer; poor periodontal status; early debonding; transfer patients; learning difficulties; cleft lip or palate Setting: NHS specialist practice in Bristol, UK, treatment free of charge by 1 operator |
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Interventions |
Two types of removable retainers
Data collected after 6 months of retention |
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Outcomes | Stability: measured using: LII, intercanine width, intermolar width. Authors reported that tooth rotations, overjet and overbite analysis were measured, but no data were provided in the paper. Patient satisfaction assessed by questionnaire. Results of the most relevant questions provided in the paper Survival of retainers ‐ number of broken retainers recorded for each type of retainer Cost‐effectiveness was also reported, but was not one of the outcomes for our review. Time points: measured at 6‐month period of retention |
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Notes | Assessment of stability data provided as medians and IQRs. This could not be analysed using Review Manager 5 statistical software (Review Manager 2020), so we requested the raw data, which the study authors provided. Helen Worthington (author of this review) then converted these into data that could be put into Review Manager 5. Patient satisfaction data were dichotomised for full analysis as follows:
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Used block randomisation (taken from "www.randomisation.com") |
Allocation concealment (selection bias) | Low risk | Concealment done by ensuring randomisation was performed after consent was obtained, using the computer program www.randomisation.com, so the clinician and participant could not know what intervention would be generated |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Outcome assessor blinded to the type of retainer used |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Number of dropouts clearly reported and described |
Selective reporting (reporting bias) | High risk | Tooth rotations, overjet and overbite data measured but not reported. The authors also only reported the "most relevant" questions on the patient satisfaction questionnaire. |
Other bias | Low risk | Pretreatment equivalence shown for both groups and no other apparent bias present |