Risk factors and multiple failures in posterior resin-bonded bridges in a 5-year multi-practice clinical trial

Objectives: A randomized controlled clinical trial was undertaken, to study the influence of some patient- and operator-dependent variables on the survival of posterior resin-bonded bridges (PRBBs) and to assess the survival of ‘replacement’ PRBBs. This report contains some of the results of the 5-year analysis. Methods: Survival was defined at three levels: (1) complete survival (without any debonding), (2) functional survival (i.e. survival after one loss of retention) and (3) replacement survival (survival of ‘replacement’ PRBBs, inserted after rebonded bridges suffered a second dislodgement). Potential risk factors were analysed with Coxʹs proportional hazards model and differences were tested for significance with the Breslow test. Observed effects are expressed as conditional-relative-risk (CRR). Survival of ‘replacement’ PRBBs was assessed with the Kaplan-Meier method. Results: Factors showing significant influences on complete survival were: ‘location’ (highest risk for mandibular PRBBs: CRR = 2.2), ‘aetiology’ (higher risk in treatment of aplasia: CRR = 2.9), and ‘time of existence’ (open spaces existing less than 2 years before insertion of PRBB: CRR: 2.0). The factor ‘large open spaces in the mandible’ was a risk for both complete and functional survival (CCR values 3.1 and 3.5, respectively). The survival of mandibular and maxillary ‘replacement’ PRBBs after 5 years was 19 ± 7% and 31 ± 18%, respectively. Conclusions: Risk factors for PRBBs were: ‘location’, ‘aetiology’, ‘time of existence’, ‘isolation method’ and ‘large open spaces in the mandible’. Mandibular ‘replacement’ PRBBs showed such an unacceptably low survival rate that fabrication is not recommended.