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Implant overdentures become thinner and weaker after direct transfer of implant attachment housings. While much has been published on denture repair, these data do not directly apply to implant overdentures because the introduction of a metal housing changes the character of the repair. It is desirable to make a strong repair to avoid prosthesis fracture.The purpose of this study was to compare the flexural strengths of 4 different methods for chairside direct transfer of implant attachment housings.Eighty 11.5 × 9.1 × 39 mm heat-polymerized acrylic resin blocks were processed, assessed for porosities, and polished. An 8.5 mm diameter hole was drilled to a depth of 5 mm in the center of each block. Attachment housings were set into the bases with 4 different repair materials: autopolymerized acrylic resin (APAR), light-polymerized acrylic resin (LPAR), autopolymerized acrylic resin with silanated attachment housings (APSAH), and light-polymerized acrylic resin with silanated attachment housings (LPSAH). Blocks were immersed in water for 30 days in an incubator. A 3-point bend test was done in a universal testing machine, and load to fracture was recorded (MPa). Results were compared with 2-way ANOVA (α=.05).APSAH had the highest mean flexural strength at fracture (863.1 ±87 MPa) as compared to APAR (678.4 ±72.4 MPa), LPAR (550.9 ±119.3 MPa), and LPSAH (543.2 ±100.8 MPa). A comparison among the 4 groups showed that there were significant differences in maximum flexural strength (P<.001). The mean maximum strength of autopolymerized acrylic resin groups was significantly higher than light-polymerized acrylic resin groups. Silanation increased strength significantly compared to nonsilanated groups.The flexural strength of autopolymerized acrylic resin with silanated attachment housings was significantly higher than autopolymerized acrylic resin alone, light-polymerized acrylic resin alone, or light-polymerized acrylic resin with silanated attachment housings. Autopolymerized acrylic resin produced stronger constructs than light-polymerized materials.