Abstract:Objective:An appliance was designed to increase the cortical bone surface contact area of miniscrew implants (MSIs). The purpose of this in vitro study was to evaluate the effects of this appliance on the anchorage force resistance and the stability of orthodontic MSIs.Materials and Methods:A total of 48 MSIs were placed into bone specimens prepared from the ilium of bovines. Half were placed with the newly designed apparatus and half were placed conventionally. All the specimens were subjected to tangential f… Show more
“…Other considerations for these devices include the use of biological adhesive, a greater device diameter, a surface treatment or the combined insertion of mini-implant and auxiliary accessories with indentations facing the cortical bone 3 12 , 22 The application of small amounts of the adhesive lateral to the device 23 should be evaluated for primary stability in patients with thin cortical bone.…”
Objective: The objective of the present study was to perform a histological evaluation of a titanium mini-implant for orthodontic anchorage. Shear strength and fracture patterns that occurred immediately, 30 and 60 days after insertion with or without N-2-butyl-cyanoacrylate adhesive were evaluated. Methods: Ninety-six mini-implants (Arrow, Peclab, Brazil) were placed in the tibia of 9 male rabbits, with or without an adhesive (Vetbond™, 3M, USA). Histological evaluation was done by optical light microscope. Shear strength testing was performed, followed by fracture analysis with visual inspection. Results: Close contact between the newly formed bone and the device was evidenced in the group without adhesive, whereas gaps in the group with adhesive were found. Tukey test showed similar values in both groups at the immediate time point (20.70 N without adhesive and 24.69 N with adhesive), and higher values for the non-adhesive group, after 30 and 60 days (43.98 N and 78.55 N, respectively). The values for the adhesive group were similar for the immediate time point (24.69 N), 30 days (18.23 N) and 60 days (31.98 N). The fractures were adhesive for both groups at the immediate time point. The fractures were cohesive in bone for the non-adhesive group after 30 and 60 days. Conclusions: The mini-implants showed close bone contact and required higher shear strength for removal at 30 and 60 days for the non-adhesive group. Further studies are needed to assess the proper way to remove the orthodontic anchorage without cohesive fractures in bone.
“…Other considerations for these devices include the use of biological adhesive, a greater device diameter, a surface treatment or the combined insertion of mini-implant and auxiliary accessories with indentations facing the cortical bone 3 12 , 22 The application of small amounts of the adhesive lateral to the device 23 should be evaluated for primary stability in patients with thin cortical bone.…”
Objective: The objective of the present study was to perform a histological evaluation of a titanium mini-implant for orthodontic anchorage. Shear strength and fracture patterns that occurred immediately, 30 and 60 days after insertion with or without N-2-butyl-cyanoacrylate adhesive were evaluated. Methods: Ninety-six mini-implants (Arrow, Peclab, Brazil) were placed in the tibia of 9 male rabbits, with or without an adhesive (Vetbond™, 3M, USA). Histological evaluation was done by optical light microscope. Shear strength testing was performed, followed by fracture analysis with visual inspection. Results: Close contact between the newly formed bone and the device was evidenced in the group without adhesive, whereas gaps in the group with adhesive were found. Tukey test showed similar values in both groups at the immediate time point (20.70 N without adhesive and 24.69 N with adhesive), and higher values for the non-adhesive group, after 30 and 60 days (43.98 N and 78.55 N, respectively). The values for the adhesive group were similar for the immediate time point (24.69 N), 30 days (18.23 N) and 60 days (31.98 N). The fractures were adhesive for both groups at the immediate time point. The fractures were cohesive in bone for the non-adhesive group after 30 and 60 days. Conclusions: The mini-implants showed close bone contact and required higher shear strength for removal at 30 and 60 days for the non-adhesive group. Further studies are needed to assess the proper way to remove the orthodontic anchorage without cohesive fractures in bone.
“…In the present study, to evaluate the mechanical retention force of the miniscrews with and without the auxiliary device, the lateral displacement test was used. 12,22 Several studies have evaluated the stability of the implant by measuring insertion torque, removal torque, and pull-out strength. 5,25 However, measuring the insertion and removal torques cannot confirm the movement of the miniscrew during loading.…”
Section: Discussionmentioning
confidence: 99%
“…The mechanical retention force was evaluated by measuring the displacement of the miniscrew head. 12,22 The specimens were embedded into the plaster cube such that the long axis of the miniscrew was perpendicular to the bottom of the cube and the long axis of the femur was perpendicular to the side of the cube. Twelve hours after embedding the specimens into the cubes (Figure 3A), the displacement of the miniscrew head was measured after bidirectional loading using a compression test machine (TGE-5kN; Minebea, Nagano, Japan) set at a load of 5.0 kN and a compression velocity of 0.5 mm/min ( Figure 3B).…”
Section: Methodsmentioning
confidence: 99%
“…To date, several new designs of skeletal anchorage devices have been introduced to increase miniscrew stability, including the washer, 10,11 mini-implant ring, 12 and spiky miniplate. 13 However, the development of a clinically reliable skeletal anchorage device is still pending.…”
The auxiliary device improved the mechanical retention force without the need to increase miniscrew length or diameter. This may enable the safe use of miniscrews in difficult areas.
“…The present study represents an innovated design for skeletal anchorage devices without any intervention to the miniscrew designed by the manufacturer. Tozlu et al ( 28 ), has created an apparatus (a miniscrew ring) which was placed at the neck of the screw. The mentioned study claimed that this ring is able to increase stability due to increasing surface contact of bone with miniscrew.…”
BackgroundStability is determined as one of the requirements in use of Temporary Anchorage Devices (TAD) in orthodontics. Miniscrew has been a widely used Bone Anchor. Compared with mini-implant that necessitates osseointegration; mechanical retention is a determining factor for primary stability of miniscrew. Studies investigated various ways to increase primary stability. The aim of this study is to introduce a new configuration of miniscrew system which is believed to obtain more primary stability.Material and MethodsFreshly ovine mandibles were cut in blocks. Twenty-seven miniscrews (diameter 1.6 × 8 mm; G2, Dual Top Anchor System, Jeil Medical, Seoul, Korea) were inserted in the blocks and divided in 2 experimental groups: single miniscrew and the innovated design “Seifi Twin Screw (STS)”. Primary stability was evaluated by Periotest “M”® device.ResultsIndependent t-test showed a significant difference between 2 experimental groups in periotest evaluation (p< 0.05). STS demonstrated higher primary stability due to its mechanical configuration and design.ConclusionsThe STS provides higher primary stability and was found to be effective in increased success rate of miniscrew systems from the standpoint of primary stability.
Key words:Anchorage procedures, anchorage techniques, orthodontic anchorage procedures, miniscrews, temporary anchorage device.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.