[Dupuytren's contracture and trauma].
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Biomedical subjects
Publications and source records attributed to A Kirsch.
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A 77-year-old woman presents with a seven-year history of an isolated slowly progressive esotropia with bilateral abduction defects. The only potential cause discovered was dolichoectasia of the intracavernous carotid arteries.
Numerous problems have been reported following various therapies used to attach natural teeth to implants beneath a fixed prosthesis. This study documents the results of 843 consecutive patients treated with 1,206 natural tooth/implant-supported prostheses utilizing 3,096 screw-fixed attachments. After 3 to 14 years in function, only 9 intrusion problems were noted. All problems were associated with fractured or lost screws. This report demonstrates the efficacy of such a treatment approach when a natural tooth/implant-supported fixed prosthesis is contemplated.
Four types of implant superstructures were screwed onto implant bodies, and the strains created around the implant bodies were compared and analyzed within the IMZ Implant System. Three IMZ implants were embedded in the center of a polyurethane block (30 x 40 x 30 mm), and a total of 16 superstructures was fabricated by 4 methods: 1-piece cast, 1-piece cast/split soldering, soldering, and passive fit. Six strain gauges were placed on the surface of the block 1 mm apart. Three embedded implants were numbered, and a fixed partial denture was placed on these implants and screwed by a torque wrench using 14.5 Ncm torque. This procedure was repeated 7 times for each fixed partial denture, and each created strain was measured when the last screw was tightened. In all fixed partial dentures, strains were produced around the implant bodies when screws retaining the prosthesis were tightened, and the strain was relieved with unscrewing. The magnitude of strain was greater with the 1-piece cast method or the section/solder method than with the soldering and passive-fit methods. Of the 2 soldering methods, when the screw on the middle implant was tightened before those on the terminal 2 implants, the magnitude of strain was lower with the soldering method than with the 1-piece cast/split soldering method. When the order of screw tightening was changed, there were significant differences in the magnitude of strain at each gauge with the soldering method. With the passive-fit method, no differences in the magnitude of strain attributable to the order of screw tightening could be detected. The magnitude of strain produced around a screw-retained implant prosthesis was significantly lower with the passive-fit method when compared to the other 3 fabricating methods. Furthermore, the implants prepared by the passive-fit method were not affected by the order of screw tightening.
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The aim of this investigation was to determine the long-term clinical outcome and predictability of the maxillary sinus augmentation procedure utilizing a variety of bone augmentation materials. The augmentation materials evaluated were a xenograft alone (Bio-Oss), an alloplast alone (Interpore), a xenograft-alloplast combination (Bio-Oss mixed with Interpore in a 1:1 ratio), an alloplast (Interpore) mixed with autogenous bone from the iliac crest (in a 1:3 ratio), and an alloplast (Interpore) mixed with autogenous bone from the chin (in a 1:1 ratio). A total of 340 plasma-sprayed cylinder implants (IMZ) were placed, either simultaneously with the sinus augmentation procedure (235 implants), or 6 months after the procedure (105 implants) in 133 patients with insufficient bone volume in the posterior maxilla. The implants were restored with a total of 151 fixed detachable ceramometal prostheses and evaluated up to a 5-year period. Clinical evaluations included yearly assessments of peri-implant inflammation, implant mobility, and clinical attachment levels. Radiographs were also taken prior to sinus augmentation surgery, at abutment connection, at completion of the restoration, and thereafter at yearly intervals. All of the implants placed into the augmented sinuses achieved osseointegration. Only four implants (1.2%) failed to maintain osseointegration after prosthesis placement, yielding an implant survival rate of 98.8% during the entire course of the study. Of the 340 implants, 307 (90.3%) were considered successful according to the success criteria used. Gender, implant length and location, remaining bone height, and type of bone augmentation material had no effect on implant success. None of the 151 prostheses was lost during the observation period. The results of this study support the long-term clinical predictability of maxillary sinus augmentation procedures for the rehabilitation of the edentulous posterior maxilla with implant-supported prostheses.