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The distal extension fixed implant supported prosthesis is now available as an alternative to a partial denture. However, not all patients will be suitable for such treatment. Limitations imposed on fixture length, the effect of gape upon instrumentation, the size of abutment components and the design of the superstructure are discussed in this article, to assist the general practitioner in case referral.
OBJECTIVES: This article presents a review of published literature examining fibre-based endodontic post systems. DATA SOURCES: A MEDLINE search was carried out for any articles in dental journals pertaining to fibre-based post systems. Wherever possible articles cited were obtained from the journals and where this was not possible abstracts were obtained. Where no abstract was available the article was not considered for evaluation. DATA EXTRACTION: Articles were reviewed by a single observer and subject to meeting inclusion criteria were included in the review. Fifty-nine articles were considered suitable for inclusion. DATA SYNTHESIS: Articles were divided into categories and a subjective description of the articles was made. CONCLUSIONS: Review indicated that (1) most published literature on fibre-based posts took the form of laboratory analyses; (2) evidence for carbon-fibre posts far exceeds that for quartz-fibre posts; (3) laboratory evidence was contradictory and could not be used to inform practice reliably; (4) few clinical studies have been carried out though these have suggested fibre based posts may be clinically appropriate for restoration of the endodontically treated tooth; and (5) controlled prospective clinical trials evaluating fibre-based posts should be undertaken to inform use for clinical practice.
Prevention for patients requiring rehabilitation with oral implants is about preventing implant failure and biomechanical complications. This paper describes preventative strategies for the planning stage for implant treatment and the later maintenance period and indicates the level of scientific evidence supporting these strategies.
Failure of root canal treatment and/or post crowns can be avoided in many cases if appropriate tooth preparation is carried out. This paper discusses the rationale for the timing of post placement following root canal treatment and appropriate methods for removal of gutta-percha prior to post space preparation. The basic principles of post space preparation are described, which should reduce the risk of weakening the root unnecessarily, causing damage to the periodontium and post perforation.
The purpose of this study was to compare the anchorage effects of different palatal osseointegrated implants using a finite element analysis. Three types of cylinder implants (simple implant, step implant, screw implant) were investigated. Three finite element models were constructed. Each consisted of two maxillary second premolars, their associated periodontal ligament (PDL) and alveolar bones, palatal bone, palatal implant, and a transpalatal arch. Another model without an implant was used for comparison. The horizontal force (mesial 5N, palatal 1N) was loaded at the buccal bracket of each second premolar, and the stress in the PDL, implant, and implant surrounding bone was calculated. The results showed that the palatal implant could significantly reduce von Mises stress in the PDL (maximum von Mises stress was reduced 24.3-27.7%). The von Mises stress magnitude in the PDL was almost same in the three models with implants. The stress in the implant surrounding bone was very low. These results suggested that the implant is a useful tool for increasing anchorage. Adding a step is useful to lower the stress in the implant and surrounding bone, but adding a screw to a cylinder implant had little advantage in increasing the anchorage effect.
The purpose of this study was to evaluate the influence of titanium surface characteristics on bone integration of implants, and to describe the pattern of peri-implant tissue healing after simultaneous implant placement and guided bone regeneration. In four healthy mongrel dogs mandibular premolars were extracted. Two weeks following full mouth prophylaxis and 4 months after extractions, simultaneous membrane and implant surgeries were performed. Efforts were made to produce bony defects with dimensions of 7 x 7 x 7 mm. Into these, 24 standard ITI implants (diameter = 4.1 mm; length = 8 mm) with either a titanium plasma-sprayed (TPS) or a machined surface (MS) were placed. Although implants were inserted 4 mm into cancellous bone, difficulties in achieving optimal primary stability were encountered. All dogs were maintained on a soft diet. Chlorhexidine rinses were performed three times a week. Full mouth prophylaxis was performed every 2 weeks. In the case of membrane exposure, the membranes were removed prematurely (4-6 or 14-15 weeks after surgery). Two dogs were sacrificed at 16 weeks and two at 24 weeks after surgery. Nondecalcified histologic sections were processed and histometric analyses were carried out. When membranes were removed after 4-6 weeks, a vertical bone growth (VB) of 45-61% of the original defect was noted. After membrane removal at 14-15 weeks, similar VB was observed. However, if membranes were left in situ for 24 weeks, VB was between 79% and 96%. In this group of sites, the VB was 66% at 16 weeks and 86% at 24 weeks. Osseointegration in the regenerated bone area ranged from 12% to 32% for the TPS and from 0.0% to 3.6% for the MS implants at 16 and 24 weeks combined. Osseointegration in the pristine host bone area ranged from 16% to 35% for the TPS and from 0.0% to 11% for the MS sites at 16 and 24 weeks. In conclusion, the fraction of implant-bone integration was much higher in the pristine bone compared to that in the regenerated bone. TPS surfaces positively influenced the fraction of osseointegration in comparison to MS surfaces for both regenerated and pristine bone. Furthermore, early membrane removal negatively affected the fraction of bone defect fill.
The aim of this review was to offer a critical evaluation of the literature and to provide the clinician with scientifically-based diagnostic criteria for monitoring the implant condition. The review presents the current opinions on definitions of osseointegration and implant failure. Further, distinctions between failed and failing implants are discussed together with the presently used parameters to assess the implant status. Radiographic examinations together with implant mobility tests seem to be the most reliable parameters in the assessment of the prognosis for osseointegrated implants. On the basis of 73 published articles, the rates of early and late failures of Brånemark implants, used in various anatomical locations and clinical situations, were analyzed using a metanalytic approach. Biologically related implant failures calculated on a sample of 2,812 implants were relatively rare: 7.7% over a 5-year period (bone graft excluded). The predictability of implant treatment was remarkable, particularly for partially edentulous patients, who showed failure rates about half those of totally edentulous subjects. Our analysis also confirmed (for both early and late failures) the general trend of maxillas, having almost 3 times more implant losses than mandibles, with the exception of the partially edentulous situation which displayed similar failure rates both in upper and lower jaws. Surgical trauma together with anatomical conditions are believed to be the most important etiological factors for early implant losses (3.60% of 16,935 implants). The low prevalence of failures attributable to peri-implantitis found in the literature together with the fact that, in general, partially edentulous patients have less resorbed jaws, speak in favour of jaw volume, bone quality, and overload as the three major determinants for late implant failures in the Brånemark system. Conversely, the ITI system seemed to be characterized by a higher prevalence of losses due to peri-implantitis. These differences may be attributed to the different implant designs and surface characteristics. On the basis of the published literature, there appears to be a number of scientific issues which are yet not fully understood. Therefore, it is concluded that further clinical follow-up and retrieval studies are required in order to achieve a better understanding of the mechanisms for failure of osseointegrated implants.
Recently, an elastomeric polyethyleneoxide polybutylene-terephthalate (PEO:PBT) copolymer (Polyactive) was introduced, which exhibits bone-bonding characteristics. In contrast to ceramics, bioglass, titanium and other metals, PEO:PBT copolymers are flexible materials that could reduce undesirable peak stresses along the neck of a permucosal implant. The application of three types of Polyactive permucosal dental implants (one dense and two porous types) and one dense hydroxylapatite (HA) implant were clinically tested and compared during 30 weeks of loading in a dog experiment. With respect to the porous Polyactive implants, it was observed that the pore diameter had decreased to such an extent that optimal bone ingrowth was not achieved. Polyactive is known to expand due to water uptake, and, as a consequence, the sizes of the pores of the press-fit inserted implants had decreased to a large extent. This feature explained the high loss of the implants with the porous outer layer (6 out of 22). None of the dense Polyactive implants and only one of the HA implants were lost. Statistical analysis was performed solely on the dense Polyactive and the HA implants. At the lingual sites, plaque scores, gingiva indices, bleeding indices and corresponding pocket depths were statistically significantly lower for both implant types, when compared to the corresponding values at the buccal, mesial and distal sites, irrespective of the observation period. Differences between the dense Polyactive and the HA implants were not observed. A considerable difference in mobility was registered between the Polyactive and the hydroxylapatite implants, as measured by the Periotest. The dense Polyactive implants functioned adequately and had mobility resembling natural teeth. As such, these dense flexible materials showed a favourable clinical function and they seem promising for reducing undesired peak stresses when applied as a dental implant.
Measurements of the damping behaviour of dental implants with the Periotest device are considered to be an objective means to assess the mobility of implants. The effects of the position of an implant in the maxilla or mandible, the period of time passing between the measurements and implant placement and the height at which the Periotest measurements are performed on the damping behaviour of implants have been discussed controversially. This experimental study examined the influence of the use of different measuring devices, the measuring height and the embedding depth on the damping behaviour of IMZ implants. The implants were embedded in resin at different depths and damping measurements were carried out at different measuring heights. It was found that the values rose with an increasing measuring height and a decreasing embedding depth. Analysis of variance was used to assess the influence of the embedding depth and revealed that the embedding depth had a significant impact on the measuring values at each measuring height, above 6 mm. Moreover, it was found that the higher the measuring height, the higher the measured values and the greater the differences between the values obtained at the individual depths. The different measuring devices had no influence on the measuring results (P = 0.79). The results of this study suggest that a longitudinal follow-up of the peri-implant residual bone height around individual implants is possible. Single measuring values by themselves do not allow any conclusions about the prognosis of an implant. The assessment of the peri-implant bone height through Periotest measurements is conceivable only when a table of damping values taking into account the physical length of the implant, the embedding depth and the measuring height for the examined implant system is available. In cylindrical implants, the head of the available prefabricated measuring post can be recommended as a constant measuring point for further studies, especially when the results are to be compared with those obtained by other study groups.
To prevent loosening or fracture of screws retaining the prosthesis to the implants in the posterior partially edentulous region, the use of staggered buccal and lingual offset placement or wide implants is suggested. However, it is not known how this usage compensates for the torque produced by lateral occlusal forces. This study evaluated the effectiveness of offset placement of three implants and a wide implant placement at the most posterior site. Three-dimensional geometric analysis was used to calculate the tensile force applied to gold screws in clinical situations with buccal or lingual loading perpendicular to cuspal inclination (10 or 20 degrees ). Four variations of the placement of three implants (3.75 mm) are: (1) straight; (2) buccal offset of the second implant; (3) lingual offset of the second implant; (4) a wide implant (5 mm) placement at most posterior site. The offset placement did not always decrease tensile force at the gold screw, but wide implant placement and decrease in cuspal inclination did.
The aim of the present study was to show the dimensions and the amount of stresses caused by pins on dentin. Mathematically modelled stainless steel and titanium pins were applied to mandibular first molar teeth with extensive crown destruction. The stress caused by the pins was examined with the finite elements method (FEM). In both types of pin, the maximum diffuse and the dense stress areas were located at the bottom of the pin channel. It is believed that these stresses should be taken into consideration when evaluating the advantages and disadvantages of pin application to teeth with destroyed crowns.
STATEMENT OF PROBLEM: Teeth and implants have different mobility patterns. Thus, it has been believed that implant-supported restorations should not be connected to natural teeth. However, this is not always the case. PURPOSE: This article presents guidelines for connection of restorative components when implant abutments and natural teeth are involved. METHODS: Methods of connection are discussed. CONCLUSION: This article presents options for splinting of prosthetic components.
The 1-piece, implant-supported abutment and crown, colloquially described as the UCLA abutment, commonly is used to fabricate single, screw-retained crowns. This abutment was designed to allow attachment of the crown directly to the implant and requires a waxing and casting procedure by a laboratory technician. A new prefabricated abutment has been developed that uses a similar approach but does not require the waxing and casting process. The PDQ abutment is made from a metal-ceramic alloy that is custom contoured by grinding to support a porcelain veneer. Porcelain then is fired to the contoured abutment to develop the 1-piece artificial crown. This article describes the use of the PDQ abutment.
STATEMENT OF PROBLEM: Clinical loading may result in micromotion and metal fatigue in apparently stable implant screw joints. This micromotion may contribute to tissue inflammation and prosthesis failure. PURPOSE: This study investigated dental implant screw joint micromotion and dynamic fatigue as a function of varied preload torque applied to abutment screws when tested under simulated clinical loading. MATERIAL AND METHODS: Fifteen noble alloy single-tooth implant restorations, each containing a hexed UCLA-style gold cylinder, were randomly assigned to 3 preload groups (16, 32, and 48 N.cm). Each group consisted of 5 implants (each 3.75 x 15 mm) and 5 square gold alloy abutment screws. A mechanical testing machine applied a compressive cyclic sine wave load between 20 and 130 N at 6 Hz to a contact point on each implant crown. A liquid metal strain gauge recorded the micromotion of the screw joint interface after 100, 500, 1,000, 5,000, 10,000, 50,000, and 100,000 cycles. Baseline data at 0 N.cm were collected before the application of the specified preload torque. RESULTS: The 16 N.cm group exhibited greater micromotion (P<.001) than both the 32 and 48 N.cm groups at all cycle intervals (2-way ANOVA, Tukey HSD). Micromotion of the implant-abutment interface remained constant (P=.99) for each of the preload groups through 105 cycles. CONCLUSION: Under the loading parameters of this study, no measurable fatigue of the implant-abutment interface occurred. However, dental implant screw joints tightened to lower preload values exhibited significantly greater micromotion at the implant-abutment interface.
PURPOSE: This study examined potential differences in detorque values of abutment screws after fatigue testing when the dimensions between external implant hexagon and internal abutment hexagon were altered or the implant external hexagonal shape was eliminated. MATERIAL AND METHODS: Three subsets (N = 10) of NobelBiocare implants were assessed: (1) standard external hexagon (R), (2) modified hexagon (M), and (3) circular (C) platform geometry. Thirty Procera machined abutments with 25-degree angulated loading platforms were manufactured. Abutments were retained with gold Unigrip abutment screws tightened to 32 N/cm with an electronic torque controller. Vertical scribes across the implant-abutment interface allowed longitudinal displacement evaluation. A carousel-type fatigue testing device delivered dynamic loading forces between 20 and 200 N for 5,000,000 cycles, or the approximate equivalent of 5 years in vivo mastication, through a piston to the abutment platform. Macroscopic and radiographic examination of the implant/abutment specimens was performed. The abutment screws were removed and the detorque values recorded. Bearing surfaces were examined microscopically. RESULTS: No abutment looseness or longitudinal displacements at the implant-abutment interface were noted. Radiographic examination demonstrated no indication of screw bending or displacement. The mean detorque values for R, M, and C were 14.40 +/- 1.84 N/cm, 14.70 +/- 1.89 N/cm, and 16.40 +/- 2.17 N/cm, respectively. The analysis of variance demonstrated significant differences between only designs R and C (P=.031). CONCLUSION: Increasing the vertical height, or degree of fit tolerance, between the implant external hexagon and the abutment internal hexagon or completely eliminating the implant external hexagon did not produce a significant effect on the detorque values of the abutment screws after 5,000,000 cycles in fatigue testing, or the equivalent of 5 years' of mastication for the implant/abutment specimens evaluated.
Many factors affect the survival rate of osseointegrated implants placed in grafted maxillary sinuses. This clinical report describes the retrospective evaluation of 60 patients with 228 implants placed in 84 grafted maxillary sinuses at the Loma Linda University School of Dentistry. The factors used to determine the survival rates of these implants were implant type, simultaneous/delayed implant placement, pretreatment bone height, oral hygiene, and cigarette smoking habits. Out of the total 228 implants, 205 (89.9%) remained in function after a mean follow-up period of 41.6 months (range 0 to 60 months). A higher failure rate was associated with the use of non-threaded implants, poor oral hygiene, and smoking. This information may facilitate treatment planning and enhance communication between the dentist and patient regarding the risk/benefit ratio and outcomes of implants placed in grafted maxillary sinuses.
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STATEMENT OF PROBLEM: Screw loosening and/or fracture is common and has been attributed to many factors, including improper torque and preload. Purpose. This study evaluated the effect of repeated preload torque and salivary contamination on the preload of the slotted gold implant prosthetic screw. MATERIAL AND METHODS: Fifteen slotted gold prosthetic screws were tested in an unused stack of components consisting of an implant, an abutment cylinder, and a screw and gold cylinder. A custom load frame and load cell and associated electronics were used. The component stack was lubricated with human saliva. Each screw was tightened to 10 Ncm with a hand-held torque wrench fitted with strain gauge electronics and then removed 10 times. Preload values at the first (Group 1X), fifth (Group 5X), and tenth (Group 10X) repetition were measured. Repeated-measures 1-way analysis of variance (P<.05) and paired comparisons were used to analyze the data. RESULTS: The mean preload value increased from Group 1X (184.3 N +/- 28.9) to Group 5X (202.5 N +/- 27.7) to Group 10X (220.2 N +/- 29.0). The differences among these groups were significant (P=.004). CONCLUSION: Within the limitations of this study, higher preload was achieved after the repeated use of a saliva-lubricated gold prosthetic retaining screw.