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Osseointegration derives from the Greek osteon, bone, and the Latin integrare, to make whole. The term refers to the direct structural and functional connection between living bone and the surface of a load-bearing artificial implant. Osseointegration has enhanced the science of medical bone and joint replacement techniques as well as dental implants and improving prosthetics for amputees.
Osseointegration is also defined as : "the formation of a direct interface between an implant and bone, without intervening soft tissue". Osseointegrated implant is a type of implant defined as "an endosteal implant containing pores into which osteoblasts and supporting connective tissue can migrate". Applied to oral implantology, this thus refers to bone grown right up to the implant surface without interposed soft tissue layer. No scar tissue, cartilage or ligament fibers are present between the bone and implant surface. The direct contact of bone and implant surface can be verified microscopically.
Osseointegration may also be defined as :
In 1952, Per-Ingvar Brånemark of Sweden conducted an experiment where he utilized a titanium implant chamber to study blood flow in rabbit bone. At the conclusion of the experiment, when it became time to remove the titanium chambers from the bone, he discovered that the bone had integrated so completely with the implant that the chamber could not be removed. Brånemark called the discovery "osseointegration," and saw the possibilities for human use.
In dental medicine the implementation of osseointegration started in the mid-1960s as a result of Brånemark's work. In 1965 Brånemark, who was at the time Professor of Anatomy at the University of Gothenburg, placed dental implants into the first human patient - Gösta Larsson. This patient had a cleft palate defect and required implants to support a palatal obturator. Gosta Larsson died in 2005, with the original implants still in place after 40 years of function.
In the mid-1970s Brånemark entered into a commercial partnership with the Swedish defense company Bofors to manufacture dental implants and the instrumentation required for their placement. Eventually an offshoot of Bofors, Nobel Pharma, was created to concentrate on this product line. Nobel Pharma subsequently became Nobel Biocare.
Brånemark spent almost 30 years fighting the scientific community for acceptance of osseointegration as a viable treatment. In Sweden he was often openly ridiculed at scientific conferences. His university stopped funding for his research, forcing him to open a private clinic to continue the treatment of patients. Eventually an emerging breed of young academics started to notice the work being performed in Sweden. Toronto's Professor Zarb, a Maltese dentist working in Canada, was instrumental in bringing the concept of osseointegration to the wider world. The 1983 Toronto Conference is generally considered to be the turning point, when finally the worldwide scientific community accepted Brånemark's work. Today osseointegration is a highly predictable and commonplace treatment modality.
Two theories regarding the chemical mechanism by which endosteal implants integrate with bone have been proposed. Osseointegration, as defined above, contrasts with fibrosseous integration, in which soft tissues such as fibers and/or cells are interposed between the two surfaces.
Brånemark proposed that implants integrate such that the bone is laid very close to the implant without any intervening connective tissue. The titanium oxide permanently fuses with the bone, as Brånemark showed in 1950s.
Weiss' theory states that there is a fibro-osseous ligament formed between the implant and the bone and this ligament can be considered as the equivalent of the periodontal ligament found in the gomphosis. He defends the presence of collagen fibres at the bone-implant interface. He interpreted it as the peri-implantal ligament with an osteogenic effect. He advocates the early loading of the implant.
In 1985, Dr. C. de Putter proposed two ways of implant anchorage or retention as mechanical and bioactive. Mechanical retention can be achieved in cases where the implant material is a metal, for example, commercially pure titanium and titanium alloys. In these cases, topological features like vents, slots, dimples, threads (screws), etc. aid in the retention of the implant. There is no chemical bonding and the retention depends on the surface area: the greater the surface area, the greater the contact.
Bioactive retention can be achieved in cases where the implant is coated with bioactive materials such as hydroxyapatite. These bioactive materials stimulate bone formation leading to a physico-chemical bond. The implant is ankylosed with the bone.
For osseointegrated dental implants, metallic, ceramic, and polymeric materials have been used, in particular titanium. To be termed osseointegration the connection between the os and the implant need not be 100 percent, and the essence of osseointegration derives more from the stability of the fixation than the degree of contact in histologic terms. In short it represents a process whereby clinically asymptomatic rigid fixation of alloplastic materials is achieved, and maintained, in bone during functional loading. When osseointegration occurs, the implant is tightly held in place by the bone. The process typically takes several weeks or months to occur which is well enough for the implant dentist to complete the restorations. The fact is that the degree of osseointegration of implants is a matter of time. First evidence of integration occurs after a few weeks, while more robust connection is progressively effected over the next months or years. Though the osseointegrated interface becomes resistant to external shocks over time, it may be damaged by prolonged adverse stimuli and overload, which may result in implant failure. In studies performed using 3M™ ESPE™ MDI (Mini dental implants), it was noted that the absence of micromotion at the bone-implant interface was necessary to enable proper osseointegration. Further, it was noted that there is a critical threshold of micromotion above which a fibrous encapsulation process occurs, rather than osseointegration. Already Brånemark stated that the implant should not be loaded and left out of function during the healing period for osseous integration to occur.
Other complications may arise even in the absence of external impact. One issue is the growing of cement. In normal cases, the absence of cementum on the implant surface prevents the attachment of collagen fibers. This is normally the case due to the absence of cementum progenitor cells in the area receiving the implant. However, when such cells are present, cement may form on or around the implant surface, and a functional collagen attachment may attach to it.
Since 2005, a number of orthopedic device manufacturers have introduced products that feature porous metal construction. Clinical studies on mammals have shown that porous metals, such as titanium foam, may allow the formation of vascular systems within the porous area. For orthopedic uses, metals such as tantalum or titanium are often used, as these metals exhibit high tensile strength and corrosion resistance with excellent biocompatibility.
The process of osseointegration in metal foams is similar to that in bone grafts. The porous bone-like properties of the metal foam contribute to extensive bone infiltration, allowing osteoblast activity to take place. In addition, the porous structure allows for soft tissue adherence and vascularization within the implant. These materials are currently deployed in hip replacement, knee replacement and dental implant surgeries.
23. Trabecular Metal Material: The Next Best Thing to BoneTM: http://www.trabecularmetal.zimmerdental.com/Implant/imp_home.aspx