Immediate functional loading of Branemark single tooth implants - An 18 months' clinical pilot follow-up study

A clinical and radiographical study was performed to evaluate the treatment outcome of single tooth replacements with artificial crowns retained to implants installed according to a 1-stage surgical procedure and immediate loading (Experimental Group=EG) in comparison to the original 2-stage concept (Control Group=CG). The EG comprised 14 patients (=14 implants) and the CG comprised 8 patients (= 8 implants), all with single tooth losses anterior to the molars. Beyond the non-smoking criterion the following criteria were adopted: i) the amount of bone had to allow for installation of a fixture with a minimum length of 13 mm and diameter = 3.75 mm, ii) the jaw relationship had to allow for bilateral occlusal stability, iii) the patients should be judged to be non-bruxers, and iv) the patients had to be available for the follow-up and maintenance programme. In the EG a temporary crown was connected to the implant within 24 h following fixture installation. Six months later this crown was replaced with a permanent one. In the CG the surgical and prosthetic treatment followed the standard protocol. Out of the 14 fixtures in the EG 2 were lost up to 5 months in function and were subsequently removed. All remaining 12 implants were stable at every subsequent follow-up examination. No fixture losses were recorded in the CG and all implants in this group were stable at the follow-ups. At the 6-month observation interval all the participating 20 patients were radiographically examined, an examination that was repeated at the 18-month follow-up. The analysis of the radiographs from the EG as well as from the CG disclosed that during the Ii-month observation period the mean change of bone support was about 0.1 mm. Further studies, designed as controlled multicenter ones, have to be performed before the results of this pilot study can be recommended for more general use.