Nobel Biocare NEWS
Transcription
Nobel Biocare NEWS
Nobel Biocare NEWS Information for the Osseointegration Specialist Issue 1/2012 Designing for Life By Richard Laube, CEO Living the Endless Summer Nobel Biocare implant-based solutions provide longevity and exceptional quality of life. Implants from Nobel Biocare provide the foundation for a third dentition that can last to the end of life. By Frederic Love F or the past years, dentists all over the world have made a strong case for the importance of keeping one’s teeth. They have successfully argued this case in both the popular media and the dental office alike. Maintaining good, healthy teeth is certainly a worthy goal, but given current demographic trends, keeping them for a lifetime is not always possible, despite the impressive achievements of preventative dentistry and the best efforts of the patient. Trauma, systemic disease and even normal wear are just a few of the reasons a tooth may begin to fail. Conscientious brushing, flossing and regular checkups may delay the advent of serious problems, but there is likely to come a day—well before the tooth falls out of the mouth on its own—when replacement with a bone-anchored solution from Nobel Biocare will prove to be a prudent, positively life-changing decision for the patient. After half a century of gradual discovery, the many benefits of osseointegrated implants are now wellknown. Implants solve real, widespread problems. Not only do they provide stable, secure solutions that allow patients to eat virtually anything they want, they preserve the patient’s facial appearance and prevent bone loss, which provides enormous social and emotional benefits in addition to the purely physiological ones. nate lifetime solution—dentures for instance—should be taken into account when considering implant costs. “While it’s true that implant-based therapy generally represents a greater initial investment in treatment time and money than traditional prosthetic solutions,” he said recently, “traditional solutions such as dentures and bridges have recurring costs in terms of maintenance and the often-times deleterious effect they have on the adjoining dentition and bone.” When asked about the deeper value of longevity, he added simply, “From the earliest days, back in the sixties, life-long solutions were always what we aimed for—and time has shown that life-long solutions are also what we achieved.” Of all the companies active in the field of implant-based prosthetic dentistry, none has more experience or a longer patient follow-up data set than Nobel Biocare. Because the company understands that an implant doesn’t just serve as the foundation of a prosthetic solution—it also serves to restore or maintain the patient’s self-esteem— you can count on Nobel Biocare for promising life-long solutions. < Longevity just makes sense What is less well-known is that implants usually make great comparative economic sense as well, partly because remaining healthy teeth do not need to be compromised, but even more so because of the characteristic longevity of implants from Nobel Biocare. According to Professor Tomas Albrektsson of the University of Gothenburg in Sweden, the maintenance and replacement costs for an alter- In this Issue At Nobel Biocare, we are committed to improving the quality of life of every patient treated with our innovative products. Our customers—and their patients—can be confident that the solutions we promote for the restoration of lost teeth have been designed with the objective of providing fully functional, natural-looking results to last a lifetime. “Designing for Life” is an ambition that covers much more than product design and treatment innovation, however. It is a concise expression of the principle upon which we have established our business. It permeates everything we do, from scientific discovery and clinical trials to product information and customer relations. We have assisted our customers in the treatment of millions of patients. This experience has shown that a better smile, better speech, better oral health—not to mention the ability to eat normally again—dramatically improve a person’s life. Providing this level of care enhances both the quality of life of the patient and the professional reputation of the clinician. For Nobel Biocare, such improvements represent a long-term commitment to both our customer and the patient. Our dedication to improving patients’ quality of life grows from unparalleled experience. Building on the past years of pioneering scientific research and innovation in the field of implant-based restorative dentistry, Nobel Biocare will continue designing for life. Moving forward together 2 Brånemark’s 2nd patient. His implants are still working 45 years later. 8 TiUnite® Quite simply the gold standard. 7 Gunshot victim made whole with custom care. 10 Statistical presentations can be misleading. Reading critically helps. On the pages to follow, you’ll find thought-provoking reading on recent scientific findings, practical techniques to facilitate treatment, and the living history of osseointegration. Join us as we move the noble practice of implant dentistry forward together, one patient at a time. < 2 From the Editor Nobel Biocare NEWS Issue 1/2012 A 44-year Success Story Sven Johansson has had oral implants longer than anyone else on Earth. Nicolas Weidmann Senior VP Global Communications In the most recent issue of Nobel Biocare News, I wrote that we want this publication to be your newsletter as well as ours. From the enormous outpouring of good wishes and substantive ideas for new content that the editors have received since then, you are obviously of the same mind. Thank you for your kind words and encouraging suggestions! The third dentition When long-term, predictably positive prognoses are paramount, there is really no substitute for extensive, well-documented experience, which applies to suppliers, as well as the surgical and prosthetic teams. At Nobel Biocare, we’re prepared to share our experience to support your team at every stage of treatment. When you speak to your patient about a new set of tissue-integrated teeth, you can speak with authority, confident in the knowledge that Nobel Biocare stands behind you. Our wide range of TiUnite surface implants remain at the outer edge of the envelope for highest initial stability and enduring strength. Our company is a lot like that too—pioneering, stable and reliable—a partner you can trust. < Nobel Biocare NEWS Published regularly by Nobel Biocare Services AG Vol. 14, No. 1, 2012 Editor-in-chief Nicolas Weidmann Managing Editor Frederic Love Assistant Editor Jim Mack Editorial offices Nobel Biocare News Herdevägen 11 702 17 Örebro, Sweden Telephone: +46 19-330680 Telefax: +46 19-330681 email: [email protected] web: nobelbiocare.com/newsletter The contents of contributors’ articles do not necessarily express the opinions of Nobel Biocare. © Nobel Biocare Services AG, 2012. All rights reserved. Longevity comes from careful planning, quality products and treatment, and conscientious follow-up. By Dr. Christer Dagnelid G östa Larsson of Gothenburg, Sweden, was the first patient to be treated with implants by Professor Per-Ingvar Brånemark. That was in . When Larsson passed away in , he had had his implants—still in place and fully functioning—for more than forty years. Brånemark’s second patient, Sven Johansson, also of Gothenburg, received his implants in . This year will mark the th anniversary of his treatment, which makes him a part of living history in the field of osseointegration. Sven’s missing dentition was restored with two full-arch gold/ acrylic bridges supported by a total of Brånemark System implants in the upper and lower jaw. Further developed by Nobel Biocare, this signature system is still widely used and much appreciated today. All too common story Like so many other members of his generation, Sven had had problems with his teeth from an early age. Born in , by the time he was in his s, he was completely edentulous. The usual prosthetic solution at that time—the s—was treatment with full dentures. Dentures didn’t suit Sven well, however, and he experienced major problems in his relationships to other people as a result. As with so many other denture wearers, he had difficulty eating and he felt insecure in many common social situations. At the time, Sven was a cab owner and driver in Mölndal, a small town on the outskirts of Gothenburg. One day he received a call to drive a patient to the Brånemark Clinic, which was located there, and the passenger turned out to be none other than Gösta Larsson—Patient No. —who had not only been the first to be treated with Brånemark System implants, but had also been treated in both jaws. Gösta Larsson spoke highly of the professionalism of the people he had met at the clinic, the care he had received there, and the dramatic change he had seen in his life because of the results. His driver, Sven Johansson, decided immediately to book a consultation. After careful X-ray examinations, a thorough evaluation of the amount of remaining jawbone and a psychological exam, Sven was deemed suitable for treatment. A bold decision paid off Sven, by nature, is a brave soul. When he decided to subject himself to implant surgery, it had only been carried out once before, after all. When I asked him at a routine check-up this December if he hadn’t been anxious about submitting to the procedure, he simply shook his head and replied, “Not at all!” As it turned out, he had no reason to worry, of course. Always a man of few words, he explained succinctly, “The surgeries went very well. I had no problems.” Before came to an end, Sven felt secure once again in social situations that he had tried to avoid ever since becoming edentulous. His diet improved too. Sven had dreamed for years of once again being able to take a bite out of a large green apple, and that dream came true before the new year as well. In Sven’s own words, “Everything worked perfectly from the first moment.” In , I took over Professor Brånemark’s dental practice in Mölndal, and thus inherited Sven Johansson as a patient. A good patient, Sven has rarely missed a regularly scheduled dental check-up throughout the + years his implants have been in place. He has practiced good oral hygiene and problems such as peri-implantitis have never been a concern. Sven Johansson of Gothenburg, Sweden, was the second patient to ever receive Brånemark System implants. They have been serving him well since 1967. patient in an individualized recall program. In as much as the implant treatment amounts to a major investment for the patient, our objective is uncompromising: “Life-long service.” Over the last years, I have participated in and performed thousands of Brånemark System dental implant cases. High-quality products, skilled clinicians, good teamwork and an individualized recall system have led to great success and implant longevity for me, my colleagues and— most importantly—for our patients. The experience we have gained since Gösta Larsson and Sven Jo- hansson were first treated by Professor Brånemark has taught us that good implant-related dental care must be based on a long-standing relationship between the patient and dentist, where the number and frequency of return visits are tailored to the different stages of life. I take my hat off to Sven Johansson, who is rapidly approaching , and Professor Per-Ingvar Brånemark. Through a combination of boldness and insight they have helped millions of orally handicapped people return to a life of dignity over the last half-acentury. < Prerequisites for longevity From our side, as dentists, it is essential to create the conditions for good oral hygiene through the proper design of bone-anchored prosthetic reconstructions. Well-designed occlusion and articulation are also important prerequisites for optimal loading of the implants and essential for implant longevity. Sven, and thousands of other patients since Sven was first treated, have received instructions in good oral hygiene practices by my wife, Dental Hygienist Eva Dagnelid. From the moment he first received his Brånemark System implants, Sven has never missed a booked recall visit and he has conscientiously followed the oral hygiene advice that we’ve given him. To ensure longevity, it is also a good idea to follow up every implant These eleven implants were placed by Professor Per-Ingvar Brånemark himself and are still fully functional for Sven Johansson. Issue 1/2012 3 Nobel Biocare NEWS In Brief Landmark Science Nobel Biocare has the longest, most extensive follow-up data set. There’s an app for that A free app, not surprisingly called “Nobel Biocare News” now makes it possible for you to stay up-to-date with the latest edition of this newsletter on your iPad, iPhone or iPod Touch. Without two pioneering studies from 1981 and 1990, implant dentistry might still be in its infancy today. By Frederic Love M Just visit the App Store on your Apple mobile device and search for “Nobel Biocare News” to download the most appropriate app for your device. Naturally, it’s free of charge. Prefer to read Nobel Biocare News online? If you would rather catch up on Nobel Biocare News on your office computer or a laptop—of any brand and with any browser—there are several options open to you. You can read individual articles on our newsletter home page, nobelbiocare.com/newsletter, which also serves as a digital hub. Here you can do word searches or browse subject categories to find any studies have been carried out on the procedures and consequences of osseointegration since Per-Ingvar Brånemark treated his first implant patient, Gösta Larsson, years ago in . Perhaps none has been more widely read than “A year study of osseointegrated implants in the treatment of the edentulous jaw” by Ragnar Adell et al, which was published in the International Journal of Oral Surgery in . In this groundbreaking work, and the follow-up study published in , Adell and his colleagues meticulously documented the high success rates generated by implant treatment ad modum Brånemark and produced an impressive yardstick against which all subsequent studies would be measured. Dr. Adell, formerly head of the Department of Oral and Maxillofacial Surgery at the Örebro University Hospital in Sweden, recently commented, “When we started our work in the s, the possibility of the body permanently retaining a titanium fixture was not widely accepted. By the time our second report on this study was published in , the process of osseointegration had become accepted science.” Thanks in large part to the pioneering work of Adell and his colleagues, the viability of the routine placement of endosseous implants became wellknown among readers of dental literature in the s and s—and the rest, as they say, is history. < Dr. Ragnar Adell established a tradition for conscientious follow-up study that lives on today at Nobel Biocare. More to explore: Adell R, Eriksson B, Lekholm U, Brånemark PI, and Jemt T, “Longterm follow-up study of osseointegrated implants in the treatment of totally edentulous jaws.” Int J Oral Maxillofac Implants, 1990. 5(4): p. 347–359. Maintenance of Marginal Bone Ask questions of the expert panel – in person or in advance. individual articles on specific topics. Via links located at this site, you can also download entire issues as PDF files, view the current edition in PageFlip format, and/or sign-up for email delivery of our e-newsletters. Later in the year, every issue of Nobelpharma News and Nobel Biocare Global Forum—our current newsletter’s direct antecedents— will be available as PDF files going all the way back (14 volumes!) to the very first edition in 1987. Impressive snapshots Dr. Scott MacLean of Halifax, Nova Scotia, Canada, recently wrote to the editors about a NobelActive case and sent the following images. Last September, Nobel Biocare brought together a group of internationally acknowledged experts to reach agreement on the subject of marginal bone management. Held at Karolinska Institutet in Stockholm, it has became known as the “Consensus Meeting.” On June 8, they will be reconvening at Europerio 7 to publically discuss their findings. O Dr. Scott MacLean: “The molar was placed 5 years ago (one of the first placed in Canada during the initial pre-launch study). The premolar was immediately placed during study club in Feb 2011. Look at the bone between the implants ... This implant rocks!” n June , , Nobel Biocare will be hosting a public forum at Europerio in Vienna, Austria, on the subject of “Maintenance of Marginal Bone around Implants”. The panel will be made up of such well-known authorities as Drs. Marco Esposito, Björn Klinge, Jörg Meyle, Andrea Mombelli, Eric Rompen, Tom Van Dyke, Hom-Lay Wang, Arie-Jan van Winkelhoff, and Moderator, Daniel van Steenberghe. These experts were invited by Nobel Biocare on the basis of their interest in the subject and publication record. Since tens of millions of Before restoration and more than a decade later. Eleven years separate these two radiographs of an implant with a TiUnite surface from Nobel Biocare. Images courtesy of Dr. Giovanni Polizzi. patients now have oral implants, there is an increasing awareness of the need to ensure their longevity by maintaining stable marginal bone. A hot subject today, this issue is much discussed in the world of dental implants. After circulating their review papers among themselves, and then meeting for two days of candid exchanges at Karolinska Institutet in Stockholm last fall, the group formulated a set of consensus guidelines, both preventive and therapeutic. They updated their manuscripts and the papers have now been published as a special supplement to the European Journal of Oral Implantology. This Europerio will allow you to hear what the working group has to say about the key clinical issues. Questions will be entertained from the audience as well as via online submission. < More to explore Read the special supplement to the March issue of the European Journal of Oral Implantology. To pose advance questions to the Europerio 7 panel, please go to nobelbiocare.com/europerio2012 4 Nobel Biocare NEWS Issue 1/2012 Managing Soft Tissues by Design Longevity has many aspects. Good management of the soft tissue/implant interface is one of them. Creating an effective and stable soft tissue barrier around the abutment is essential for the esthetic and functional longevity of implant-supported restorations. By Hans Geiselhöringer I mplant treatment has proven to be a highly predictable and extremely reliable option for today’s patients. With sixty years of continuous research, innovation and clinical follow-up behind its implants and related components, Nobel Biocare continues today to provide optimal solutions for the patient, both in terms of functional and esthetically pleasing outcomes. Nobel Biocare designs products for solutions in harmony with the adjacent dentition—and ideally invisible to the human eye. Never complacent Despite the extremely high success rates that have resulted from treatment optimization over the years, Nobel Biocare continues to actively pursue scientific research with probable clinical consequences. The maintenance and stability of the peri-implant tissue architecture is currently a key area of enquiry. While pathways and cellular responses during the osseointegration of an implant have been described in detail, questions related to soft tissue stability and ideal treatment protocols are also being explored [Cairo et al, ]. Clinicians naturally want to create an effective barrier protecting the underlying bone from intraoral microorganisms and their by-products [Rompen et al, ]. In this context, it is generally accepted that the tight and stable soft tissue integration of an implant-based restoration means a great deal for long-term success. Although clinical protocols have been developed to maintain or improve soft tissue quality and quantity at implant recipient sites [Thoma et al., ], it is important to understand that the interaction and interdependencies of the tissue surrounding restorative components play as vital a role as the general anatomic situation at the implant site. Nobel Biocare has been among the first manufacturers to take this critical interface between the oral cavity and the body seriously in every as- pect of product development. To ensure safe, reliable and long-lasting implant outcomes, Nobel Biocare emphasizes four product characteristics that complement patient-related factors and the selection of appropriate treatment protocols in the quest for such outcomes. These are: r UIF EFTJHO BOE DPOUPVS PG UIF implant-abutment interface r UIFGJUPGNBUJOHDPNQPOFOUTBOE quality of the screw joint r UIF BCVUNFOU NPSQIPMPHZ BOE choice of materials and r FBTZBEBQUBUJPOUPBOZHJWFODMJOJcal situation (e.g. via tactile feedback). Meeting clinical needs and personal preferences Every patient is unique, as is every clinical situation. In terms of personal confidence and professional preferences for protocols and components, every dentist is also unique. Recognizing diverse needs and preferences, Nobel Biocare provides a wide variety of implant platform configurations. With recent NobelReplace line extensions featuring conical connection and platform shifting interfaces, Nobel Biocare has once again proven its commitment to meeting every clinician’s needs. Nobel Biocare incorporated new connections into the world’s most versatile and widely used implant system in order to facilitate the use of a variety of established and highly predictable treatment protocols. To put it another way, Nobel Biocare developed and launched implants with conical connection and platform shifting in order to provide new tools for soft tissue management erned by an apparent paradox: On the one hand, precision is paramount, on the other, acceptable tolerances make the seating of prosthetic components possible. In defining acceptable tolerances, Nobel Biocare has specified figures that facilitate passive fit yet remain well below the critical threshold limits that would lead to micromotion and ultimately to loosening of the implant-abutment joint. (Read more about micromotion in Professor John Brunski’s article on page .) An inconspicuous hero: the TorqTite™ screw The NobelActive conical connection is exceptionally strong, making for a tight seal achieved by the use of a special grade of commercially pure titanium and the radial design of the connection, which distributes the forces deep within the robust core of the implant. and the preservation of the crestal bone. Platform shifting provides a narrower diameter prosthetic component on a wider diameter implant platform (see figure on the next page and the accompanying case study by Dr. David Lustbader). This creates an exposed ridge on the implant platform where the soft tissue can develop. Implants with platform shifting increase the interface between biological width and retention and may act as a “stop” preventing tissue recession. Literature shows that utilizing platform shifting results in both significantly less radiographically detectable bone loss in humans and better soft tissue support and maintenance in the esthetic zone [Atieh MA et al, ; Canullo et al, ; López-Mari et al, ]. Decisive design features The back-tapered collar of the NobelActive regular platform implant has been designed to maximize the volume of bone at the alveolar crest and to improve soft tissue support. Tissue management is further supported by the built-in platform shift and the internal conical connection. The expanding tapered NobelActive implant body with doublelead thread is designed to condense bone gradually to provide high initial stability and support for immediate loading. The results of a multi-center study—encompassing partially or fully edentulous patients receiving NobelActive implants in centers—show that the marginal bone level as well as the soft tissue level is stable two years after implant insertion. The study demonstrates that NobelActive can be placed under demanding immediate loading conditions as it provides stable bone and soft tissue levels after two years of function [Martinez-de Fuentes et al, ]. The perfect balance NobelReplace Tapered NobelReplace Platform Shift NobelReplace Conical Connection The newly launched NobelReplace Platform Shift and NobelReplace Conical Connection demonstrate strength values in the same range as NobelReplace Tapered Groovy when evaluated mechanically using ISO tests. While the implant platform-abutment interface design plays a significant role in a stable and lasting connection, other design considerations have also been taken to reduce detrimental effects on the peri-implant tissues. Bona fide precision fit and the ingenious design of the Nobel Biocare abutment screw minimize micromotion, for example. The achievement of proper fit between mating components is gov- In the early days of implant dentistry, one of the most commonly reported maintenance needs for implant restorations was retightening or changing the abutment screws [Goodacre et al, ]. Nobel Biocare’s engineers solved the problem by developing a screw with features outclassing any other retaining screw. Other implant systems have tried to introduce similar screws, but the features of Nobel Biocare’s TorqTite screws remain unique. To keep the implant and abutment interface connected and to prevent any rotational movement upon load application, special features have been integrated into its design. For one thing, the screw is manufactured from a specific titanium alloy and coated with a carbon layer that reduces friction between the internal screw-threads of the implant and the threads of the retaining screw. A reduction of friction is namely needed to reach the pre-torque values required to create pre-tension in the screw shank. (See the Tips and Techniques article by Dr. Chandur Wadhwani on page .) Nobel Biocare’s TorqTite screws have been designed and tested to occupy the center of the proper torque zone. If screw threads ran all the way up to the head of the screw—as they do in many other implant systems—the shaft could not act as the pre-load spring necessary to ensure the longevity of the screw-joint. < There’s more to this story! For a longer version of this article, including a discussion of optimal material choices and the full list of references, please continue reading in our enhanced digital edition at: nobelbiocare.com/newsletter Issue 1/2012 Popular, Well-proven Concept Experience NobelReplace® Platform Shift from the clinical point of view. Platform shifting, or platform switching, is a concept that has come into the mainstream as it has become an integral feature of some of Nobel Biocare’s most popular implants. O 2012 IDEM Singapore 20–22 April Singapore Dental Salon Moscow 23–26 April Moscow, Russia Fig. 1. Platform shifting has been designed to maximize soft tissue volume. overcoming any negative tissue influences from a large maxillary frenum. The tooth was atraumatically removed and a surgical guide was fabricated to assist with depth placement of the implant. The osteotomy was started with twist drills, but finished with osteotomes to preserve the buccal plate. A x mm NobelReplace Platform Shift implant was placed using the . mm implant driver, placing the implant to just below the facial height Scandefa 26–28 April Copenhagen, Denmark ODA Spring Meeting 10–12 May Toronto, Canada Fig. 2. NobelReplace Platform Shift. The ease of use of the internal tri-channel connection combined with built-in platform shifting. Fig. 3. NobelReplace Conical Connection. The original tapered implant body combined with the tight conical connection and built-in platform shifting. of the crestal bone to take full advantage of the platform shift. A x mm healing abutment, . series was placed on the implant (fig- ure ), and the patient was then seen by his restorative dentist for immediate temporization (figure ). The patient functioned on the immediate temporary for weeks, at which time the final impression was taken (figure ). Note that at all times the integrity of the marginal bone was preserved. A CAD/CAM custom abutment was fabricated using the NobelProcera Scanner and Software (figure ). The final crown was inserted at weeks (figure ). As can be seen in the final restoration (figure ), tissue level integrity is preserved. Our practice has acquired a great deal of experience with NobelReplace Platform Shift and Conical Connection implants over the past year. We have seen superior esthetic results with excellent preservation of soft tissue and crestal bone. Although the follow-up period is relatively short, preliminary results are very encouraging. This is an excellent addition to the Nobel family of implant products. < Fig. 4–5. Pre-op clinical and radiographic views. Fig. 6–7. Extraction site and implant with healing abutment. Temporary and final crowns courtesy of Dr. Craig M. Allen. Fig. 8. Temporary crown at six weeks post-op. Fig. 9. Impression appointment 12 weeks post-op. EAED Spring Meeting 24–26 May Izmir, Turkey 62. Kongress der Deutschen Gesellschaft für Mund-, Kiefer- und Gesichtschirurgie 31 May – 2 June Freiburg, Germany Nobel Biocare Symposium 1–2 June Avignon, France Europerio 7 6–9 June Vienna, Austria Nobel Biocare Symposium 9–11 June Odessa, Ukraine Sino Dental 9–12 June Bejing, China Nobel Biocare Symposium 15–16 June Hamburg, Germany IADR General Session 20–23 June Iguaçú Falls, Brazil FDI Annual World Dental Conference 29 August – 1 September Hong Kong, China AAOMS Annual Meeting 10–15 September San Diego, USA EACMFS Congress 11–15 September Dubrovnik, Croatia ICOI World Congress 20–22 September Orlando, USA AAP Annual Meeting 29 September – 2 October Los Angeles, USA Platform shifting in practice The case illustrated in this page is of a -year-old man who had a vertical and horizontal fracture through tooth # (FDI ), evident clinically and on the pre-op film (figures and ). The treatment plan was to remove # and to immediately place a NobelReplace Platform Shift with immediate load. This implant was chosen to maximize soft tissue volume in hopes of Upcoming Events Visit Nobel Biocare at events around the world. They provide a great opportunity for observing the latest innovations and scientific research. By Dr. David Lustbader riginally described by Dr. Lazzara, platform shifting is a concept that involves an inward horizontal repositioning of the implant-abutment interface (figure ). This connection shifts the perimeter of the implant-abutment junction towards the center of the implant, creating a horizontal component for the total linear distance between the abutment and crestal bone required for biologic width. This allows for higher tissue volume and vascularization, ultimately leading to more stable crestal bone heights and interdental papilla. Most studies show that a horizontal component of about . mm results in significantly less radiographically detectable crestal bone loss and better soft tissue support in the esthetic zone. Platform shifting can be accomplished with the NobelReplace Platform Shift tri-channel (figure ) or NobelReplace Conical Connection (figure ), which is identical to the NobelActive configuration. I have had the good fortune to be able to place both the NobelReplace Platform Shift and Conical Connection implants during the pre-launch and evaluation stages. To date, our practice has placed over one hundred of these implants and have found the marginal bone levels and soft tissue esthetics to be excellent. The surgical placement and instrumentation is virtually identical to the standard NobelReplace system, making it ideal from a staff training and surgical armamentarium standpoint. A simple case illustration will demonstrate the ease of use and predictability. 5 Nobel Biocare NEWS Nobel Biocare Symposium 19–20 October Rimini, Italy Nobel Biocare Symposium 19–20 October Toronto, Canada Fig. 10. CAD/CAM abutment fabrication using NobelProcera Software. Fig. 11. Final crown insertion at 14 weeks. Note continued excellent bone level preservation. Fig. 12. The final restoration from the clinician’s perspective. To find out more, visit nobelbiocare.com/events | 6 Nobel Biocare NEWS Issue 1/2012 Meeting One-of-a-kind Patient Needs Custom-made devices from Nobel Biocare can make a decisive difference when no one else has a solution to offer. For over 20 years, Nobel Biocare has been offering a unique service to its worldwide customer base that you may not be aware of. A special custom-made device service exists in Sweden that makes it possible to create a one-time solution for a one-time patient need. By Jim Mack N o matter how far technology may advance your favorite products, you will always be left wanting more. But when it comes to a special patient need, or even an emergency, you may not be able to find your “dream product” in the marketplace. With Nobel Biocare’s custommade device service, all you have to do is ask. Your custom-made device can be created in a matter of weeks— or even less in cases of extreme medical emergency. Not your normal solution Custom-made solutions are tailored to fit a unique and one-time patient need. These special solutions extend beyond the typical esthetic circumstances and can also be used to assist trauma victims, including those recovering from such serious injuries as gunshot wounds. (See article on the facing page.) One caveat may be in order: This service is not meant to provide indi- “restorative auxiliary”, “surgery components” and “miscellaneous” (which includes maxillofacial surgical components). Attention to detail The production process typically takes around five weeks, unless an- “I have used the custom device workshop at Nobel Biocare for many years to provide me and my patients with bespoke parts to solve large and small problems alike.” — Dr. Andrew Dawood, London, United Kingdom tions, Nobel Biocare takes the responsibility of its heritage very seriously. The experience and production capability reflected in Dahlmo’s department put the company in a unique position to support clinicians worldwide in their efforts to improve their patients’ quality of life. In addition to simply recreating discontinued products, Nobel Biocare can further cater to needs beyond its core assortment. In many circumstances, clinical indications may be so complex that only sophisticated custom-made solutions are the right answer. < There’s more to this story! For a longer version of this article, vidually designed products for doctors to have in stock for similar indications. There are no catalogs, nor are there any product lists. While each item is reviewed by the Nobel Biocare regulatory department, custom devices are not CE marked as they are intended for specific patients and not for a general market release. For regulatory reasons, an order is based on a prescription filled out for a named patient only. Each device is classified into one of product categories, under the headings of “abutment components”, other timeline is decided upon. Each case that comes in requires great attention to detail and must be assessed individually according to Karin Dahlmo, who manages the Custom Devices and Replacement Parts department at Nobel Biocare in Gothenburg, Sweden. “We must look closely at all the circumstances of each case. Decisions are made based upon medical, legal and regulatory requirements.” As the founder of modern implant dentistry, with more than years at the forefront of implant-based restora- please continue the story in our enhanced digital edition at: nobelbiocare.com/newsletter Is a custom-made device the right solution for your patient? First contact your Nobel Biocare sales office to decide whether a custom-made device is required. If yes, fill in the online prescription form and follow the instructions on how to proceed at: nobelbiocare.com/ custom Unique service for unique circumstances. Nobel Biocare customized devices can solve those difficult, one-time surgical and prosthetic challenges for you and your patient. The Freedom to Choose and an Upgrade, too NobelClinician™ – for the Mac®, for Windows®, for you! Think of diagnostics and treatment planning software and your first association is probably “Windows!” No need for that any longer. Nobel Biocare gives you choices. By Jim Mack N obelClinician Software is now available for both Mac and Windows, and for the first time in the dental industry, clinicians can decide which platform is best for them. With an increasing number of dental professionals moving towards Apple products, that’s a very nice choice to have. “The look and feel of a treatment planning software is very important as it is often used to explain the treatment directly to the patient,” says Dr. Pascal Kunz, who leads the guided NobelClinician Software version 1.5 is now available as an upgrade for current users or for purchase as new. See more: Streak artifacts are gone and tooth roots are now shown in 3D. surgery solutions team at Nobel Biocare. “A clinician using a software like NobelClinician projects a modern image which can help build up additional confidence with the patient that this is the most favorable treatment for him or her.” Making a good impression Nothing says “cutting edge” like demonstrating a treatment plan to a patient on a sleek-looking MacBook Pro, but it’s important to note that the software has the same look and feel on Windows as well. On either OS, NobelClinician allows you to easily and impressively move between workspaces and display both the thought and process behind the plan. This provides the assurance a patient needs in order to select a safer, more predictable solution. < There’s more to this story! Please continue reading in our enhanced digital edition at: nobelbiocare.com/newsletter H ere’s some good news: opening up for other implant systems, NobelClinician v. includes Straumann® implants fully integrated into the system for planning for the first time. What’s more, reports in the new version contain more clinical information than ever before. The OPG cross-sectional X-ray views are included for each implant planned. You can create reports automatically in just a few seconds and use them with both free-hand and guided surgery. One of the things users asked most for in this version of NobelClinician was the removal of streak artifacts in the D model. Caused by metal fillings in remaining teeth, these artifacts are now history, leaving a clean D bone model that makes for faster planning, good-looking lecture pictures and easier-to-understand patient presentations. In version ., tooth roots can now be visualized in the D scene. This feature makes it easier to ensure than implants won’t collide with natural roots. NobelClinician now even provides an option to simulate tooth extraction in the D scene so the extraction socket can be visualized. New clinical warnings have also been added. You will now get a planning warning when an implant is either too close to a nerve or a root, which makes it easier to complete a plan. Minimum distances to trigger the warning—you’ll be glad to know—are customizable. < Issue 1/2012 7 Nobel Biocare NEWS Cross-border Cooperation Solves Case Solution for gunshot victim made possible by custom-made devices and 3D software from Nobel Biocare Reconstruction of 3D defects in the anterior maxilla are challenging in terms of both restored function and esthetics. The Chairman of the Department of Oral & Maxillofacial Surgery at Umeå University in Sweden sends us the following treatment report. By Professor Stefan Lundgren A -year-old female was wounded by a gunshot during a robbery in a store. The mm bullet, fired from the distance of a few meters, resulted in a significant D-defect in the left upper lip and maxilla. The bullet penetrated the throat and was stopped by the cervical vertebrae a few mm from the spinal cord. The -year-old Estonian female was seen in a consultation visit in Tallin by Dr. Juha Peltola, an oral & maxillofacial surgeon in private practice in Helsinki, who referred the patient for treatment planning—and if possible, treatment—to the Department of Oral & Maxillofacial Surgery, Umeå University Hospital. The initial treatment planning was done by Dr. Peltola together with me and Dr. Hans Nilson, the planned restorative dentist from the Department of Prostetic Dentistry at Umeå. The first step was a contact with Nobel Biocare to help with the funding of travel expenses, laboratory costs and components. Financial negotiatons were carried out with the University Hospital and The Dental Fig. 1. Patient with a significant defect in the left maxilla. The patient was injured from a gun shot. School in order for us to be able to complete the planned treatment at no cost to the patient, who was unable to otherwise finance it. Bone graft first Under general anesthesia, a bone graft was harvested from the anterior left iliac crest and placed in the defect in order to provide good bone architecture for the later placement of implants. Three months later, a CT with a radiological guide was performed in Helsinki and the implant placement was virtually planned with NobelGuide treatment planning software in collaboration with Matts Andersson and Andreas Pettersson at the Nobel Biocare office in Gothenburg. We placed the implants in the office of Dr. Peltola in Salora, Finland, with help from the surgical guide derived from the preoperative NobelGuide planning. At this point, the implants were placed in good bone, with a nice bone architecture, yet remote from the planned bridge! Placement of the implants—as well as the planned final navigation of the anterior maxillary segment, including the grafted bone and the three implants—was all performed in the virtual D environment. The implants were allowed to heal for two months before the distraction surgery was initiated. The external distraction device was custom-designed by the Department of Early Development, Nobel Biocare in Gothenburg. A distraction device Fig. 2. Predominantly cortical bone graft was harvested from the iliac crest, seen here in place in the defect for a 3D reconstruction of the bone that will later host three implants. Fig. 5. Segmental anterior maxillary osteotomy with the bone block including the three implants. A custom-designed distraction device acted also as a temporary bridge during active distraction and the consolidation period. Fig. 3. Implants, placed with the aid of the NobelGuide concept. Fig. 4. Virtual computerized planning showing the three planned implants in correct interrelated positions, but in a remote site. The custom designed distraction device was divided in two parts. A small Procera bridge connected the three implants in order to create a system of two rods which were parallel and in the direction of the planned vector. The second part of the distraction device was incorporated in the temporary bridge, which was retained with temporary cement, as a splint, on the posterior dentition. The third surgical phase was performed in Umeå under local anesthesia and I.V. sedation. The anterior maxillary segment was osteotomized and the bone segment, including the three implants, was mobilized. Then the different parts of the distraction device were assembled, the temporary bridge was cemented to the posterior maxillary teeth, and the surgical wound was closed with sutures. The patient went home to Tallinn the day after surgery and the active distraction was started ten days after Fig. 6. Left: Before the treatment. Right: After completed bone grafting, implant insertion and distraction osteotomy. Fig. 7. Permanent zirconium/ceramic bridge in place. Fig. 8. Bridge delivery followed by lip correction. the surgical intervention. The active distraction over ten days was assisted by the patient’s dentist in Tallin and was followed by two months of consolidation before the distraction device was removed, and the patient could receive a temporary bridge in Tallin. Then the patient came to Umeå for the processing of the final bridge, which was temporarily provided. After another few weeks, she returned again for the final adjustment of the bridge. After delivery of the corrected bridge we did the final surgical correction of the upper lip. requires treatment planning performed in a virtual D environment. The sequence of treatment provides a number of benefits. The distraction device, retained by the implants, can be removed in a noninvasive way as the device is extra-mucosally positioned. The distraction technique increases not only bone tissue but also mucosal volume. With the correct technique, the width of the keratinized mucosa can be increased both on the newly formed alveolar process and around the implants. < Note on technique Breine U, Brånemark P-I. According to this treatment protocol, we place the implants in the bone graft to allow optimal placement in the bone regardless of the final implant position. If the implants are correctly positioned in relation to each other, the bone segment (including the implants) can later be transported to the final correct position for the temporary bridge. This “Reconstruction of alveolar jaw More to explore: bone.” Scand J Plast Reconstr Surg 1980: 14: 23–48. Lundgren S, Sennerby L (eds). Bone Reformation: Contemporary Bone Augmentation Procedures in Oral and Maxillofacial Implant Surgery. Quintessence, Berlin, 2008. 8 Nobel Biocare NEWS Issue 1/2012 TiUnite – A Unique Biomaterial ® A remarkable set of images displays the process of osseointegration as it’s never been revealed before. Implant surface properties are of key importance for initial tissue interactions, the acceleration of bone healing and osseointegration. TiUnite is titanium oxide rendered into an osteoconductive biomaterial through spark anodization. New insights explain how TiUnite interacts with tissue and why it remains the osteoconductive surface of choice. By Drs. Peter Schüpbach and Roland Glauser N obel Biocare first introduced TiUnite to the market in on its Brånemark System implants, and then applied it to Replace Select in . Today, TiUnite is available on all Nobel Biocare implants, including those with machined collars. Unlike implants with machined surfaces, TiUnite has clinically demonstrated the ability to increase the predictability and speed at which dental implants osseointegrate through osteoconductive bone formation (Glauser et al, ). TiUnite is formed by spark anodization in an electrolytic solution containing phosphoric acid. This results in a thickened titanium oxide layer (up to microns) and a moderately rough porous surface topography (Ra .). TiUnite contains anatase and rutile, the most important Platelet activation: Immediately following implant insertion, blood proteins and platelets are attracted by the negatively charged TiUnite surface. The activated platelets form pseudopodia and clump together to form aggregates. titanium oxides, and is thereby a highly crystalline biomaterial. Studies have also shown the presence of phosphorus in the oxide layer (Lausmaa & Hall, ; Schüpbach et al, ). Thus, TiUnite may have both a topography-related as well as a chemistry-related effect on osseointegration. This article explains how TiUnite interacts with living tissue and accelerates wound healing. S&E Safety and Efficacy An inevitable chronology Wound healing comprises a cascade of events that the body brings into play to resolve injury. Nature’s first priorities are to stop bleeding, restore function and to prevent infection. Generally, the wound-healing events are grouped into four phases: hemostasis, inflammatory, proliferative/repair, and remodeling. Hemostasis (0 to 10 minutes following implant placement) TiUnite shows its strength already at the time of placement of an implant: Within seconds, blood proteins and platelets are attracted to the negatively charged TiUnite surface and become immediately activated. This first step is crucial for the wound healing. Their activation is followed by the release of growth factors, such as platelet-derived growth factor (PDGF) and transforming growth factor beta (TGF-b). These factors play a crucial role in the regulation of the wound-healing cascade (Park JY et al, ; Marx RE, ). During the first ten minutes, fibrin—the reaction product of thrombin and fibrinogen—will be released at the wound site. The resulting stabilized blood clot reveals improved adherence to the moderately rough TiUnite surface when compared to smooth surface implants. Day 1 to 2 The inflammatory phase The inflammatory phase begins minutes following the implant insertion and continues for approximately two days. Neutrophils are the first cells attracted by chemical signals released by the platelets, followed by macrophages. Both cell types will phagocytize small bone debris. The fibrin will be broken down by the enzyme plasmin and the debris will also be removed by the leukocytes. Fibrinolysis starts already during hemostasis but is slower and thereby contributes to its regulation. The breakdown of the fibrin clot creates the room in the wound site needed for the invasion of fibroblast and thereby the forming of the provisional matrix (Schüpbach et al, in preparation). Day 3 to 5 The proliferative/repair phase The proliferative phase is characterized by granulation tissue formation, angiogenesis, collagen deposition, and wound contraction. In granulation tissue formation, fibroblasts invade the wound and form a more on following page Hemostasis: Blood clot formation will be accomplished by the formation of the fibrin matrix. Activated platelets (arrows) become embedded in the matrix. Eventually, the platelets start to release granules containing full batteries of enzymes and growth factors needed for the wound healing. Issue 1/2012 Nobel Biocare NEWS 9 Recent Findings TiUnite® 10-year, Immediate Loading Early wound healing: The fibrin matrix will be broken down by the enzyme plasmin and their debris will be removed by neutrophils (green, left) and later macrophages. The healing site will be invaded by fibroblasts and the blood clot replaced by the provisional extracellular matrix. Eventually, osteogenic cells (red arrows) stream to the implant surface. Once they reach it, they migrate by active locomotion using their pseudopodia and the open pores as attachment points (yellow arrow) to the front of bone formation. Already available as an ePub ahead of publication, an article in “Clinical Implant Dentistry and Related Research” documents the 10-year outcome of immediately loaded implants with the TiUnite surface. “10-Year Follow-Up of Immediately Loaded Implants with TiUnite Porous Anodized Surface,“ by Drs. Marco Degidi, Diego Nardi and Adriano Piattelli reports on a prospective study the authors carried out to assess the 10-year performance of TiUnite implants supporting fixed prostheses placed with an immediate loading approach in both postextractive and healed sites. All the patients in this study received a fixed provisional restoration supported by parallel design, self-tapping implants with a TiUnite surface, and an external hexagonal connection. Success and survival rate for restorations and implants, changes in marginal peri-implant bone level, probing depth measurements, biological or technical complications, and any other adverse event were recorded at yearly follow-ups. The implants placed in healed and post-extractive sites, respectively, achieved a 98.05% and a 96.52% cumulative survival rate and the authors conclude that positive results—in terms of bone maintenance in the long-term perspective—are to be expected using immediately Osteoconductive bone formation: Human histology six months following insertion shows bone anchored in the TiUnite pores (left). In extraction sockets, newly formed bone crosses the gap between local bone (LB) and the implant surface by distance osteogenesis (middle, yellow arrow). As soon as the implant surface is reached, new bone spreads over the surface by contact osteogenesis (middle, red arrow) characterized by woven bone deposited directly on and along the surface (right). from the previous page provisional extracellular matrix (ECM) by secreting collagen and fibronectin. In angiogenesis, new blood vessels are formed by vascular endothelial cells. In contraction, the wound is made smaller by the action of myofibroblasts, which establish a grip on the wound edges and contract themselves. Now the benefit of the TiUnite topography comes into play as the moderately rough surface diminishes the ECM retraction from the surface—when compared to smooth surfaces—and inhibits its retraction from the surface. This is a prerequisite for osteoconductive bone formation as osteogenic cells, again attracted by the chemical signals of the platelets, may reach the surface only if the ECM remains attached. Day 5 to 7 – Osteoconductive bone formation Once the osteogenic cells have reached the TiUnite surface, they migrate to the front of bone formation, i.e. where wound edges of the local bone of the osteotomy are in contact with the implant surface or where bone newly formed by distance osteogenesis already has reached the surface. At the front of bone formation they will become differentiated to osteoblasts. The latter will form the bone collagenous bone matrix, which eventually becomes mineralized, and woven bone is formed. The strength of TiUnite in this phase of the wound healing is obvious: the porous surface is an ideal substrate for the migration of osteogenic cells along the surface (Schüpbach et al, ) and the surface properties (with Ra < μm and Rm Conclusions Taken together, the unique TiUnite properties allow teamplay between topography-related as well as chemistry-related factors to accelerate osseointegration. Therefore, it’s not surprising that a variety of animal and human studies have demonstrated enhanced osseointegration, both in terms of speed loaded implants with a TiUnite surface in both post-extractive and healed sites when adequate levels of oral hygiene are maintained. www.nobelbiocare.com/tiunite-10-year-abstract 7-year TiUnite® Overdenture Study Also available as an ePub, another study to be published in “Clinical Implant Dentistry and Related Research” follows up seven years of experience with the implant-supported mandibular overdentures that have become a popular treatment alternative for edentulous patients desiring increased retention of complete dentures. “Seven-year Follow-up Results of TiUnite Implants Supporting Mandib- “The TiUnite surface has improved our results, especially in grafted bone and in bone of low density. It has, without question, significantly reduced our early failure rate as well.” — Professor Bertil Friberg, Sweden ular Overdentures: Early versus Delayed Loading,” by Drs. Ilser Turkyilmaz, Tolga F. Tozum, Dana M. Fuhrmann and Celal Tumer, evaluates and presents treatment outcomes of mandibular overdentures retained by two unsplinted, early-loaded implants and compares these results with those for delayed-loaded implants. No implant was lost in this clinical trial, and the results show that there is no significant difference in the clinical and radiographic outcomes of patients treated with mandibular overdentures supported by TiUnite implants that are either early or delayed loaded. > μm) are optimal for the differentiation of stem cells into osteogenic cells (Schwartz et al, ). According to these characteristics, TiUnite is highly osteoconductive and new bone formation occurs rapidly and directly on and along the implant surface. Moreover, the osteoblasts, being polarized cells, secrete collagen matrix only perpendicularly to the surface—and thereby directly into the open TiUnite pores (Schüpbach et al, ). A kinetic study about early bone formation with TiUnite showed initial bone formation and its direct anchorage already around day , thereby maintaining the primary stability (Schüpbach et al, in prep.). and amount of bone-to-implant contact on par with that of hydroxyapatite surfaces, which many still consider the gold standard for osteoconductivity (Zechner et al, ). From a clinical perspective, TiUnite has enabled the predictable application of very short implants and implants placed in very demanding bone conditions. Moreover, TiUnite has both reduced the healing time necessary before functional implant loading can take place, and lifted immediate function solutions to a very high and very reliable level of success (Glauser ). < www.nobelbiocare.com/overdenture-abstract Over 11 million TiUnite® Implants Sold to Date! Scientific studies on TiUnite have demonstrated over and over again this surface’s ability to increase the predictability and speed of dental implant osseointegration. Help us celebrate a decade of success by reading all about it: More to explore: nobelbiocare.com/resources 10 Nobel Biocare NEWS Issue 1/2012 Statistics can be Deceiving Be forewarned: Everyone has an axe to grind, a point to prove, or a product to sell. Tables instead of graphs? Presentations of results and conclusions are often based on statistical analyses. Their reliability depends not only on the quality and the manner of presentation, but their interpretation by the reader as well. Interpretation varies depending on the background of the reader and how the material is presented. It is crucial for the reader to be critical. Many questions need to be asked. A few examples: Is it reasonable to draw the conclusions being presented from the figures available? Is it reasonable to talk about -year results when only of subjects in a study have attended the -year checkup? What is the objective of the report? Who may profit from the results? Diagrams can be used when presenting material. They can provide the reader, i.e. the interpreter, with both numerical and visual information, but it is important to understand that such visual information can easily be manipulated by simple modifications of the diagram. Data can also be presented in tables. Good tables must be easy to read and easy to interpret; otherwise the reader will easily lose interest. Some tables are so detailed that it is impossible to determine which are the important parts of the table. Identifying the columns in the table by letters or abbreviations can also make it more difficult to interpret. When comparing different groups within a population or when comparing different populations, the manner in which the groups/populations have been selected should be described as well as their respective size(s). For example, the number of failed fixtures is of interest only if you know the total number of fixtures in the specific groups/population. When comparing different groups, it is necessary to mention both the total number and the number of the compared sub-groups. Cut-offs exaggerate A diagram axis can be “cut off ” to produce more dramatic differences. Lifetable A lifetable includes both actual and relative numbers (results) and can be appropriately used to present the results of a long-term follow-up study (see figure ), and the long- 95% 40% 94% 20% 93% b 95 93 c a b c Figure 1: Two diagrams that describe the same result. The frequency axis has been “cut off” to exaggerate the percentage differences. Lasting impressions 10 10 8 8 6 6 4 4 2 2 a b c d a b c d Figure 2: Broader bars make differences in a bar chart appear less dramatic. 60 5 Quality and format S 60% a 97 96% 50 4 tatistics make it possible to organize material for systematic analysis and can be used to present findings as clear, objective figures instead of vague, subjective words (the most common of them being: “a few” and “usually”). There is quite a difference between saying: “He usually does well at competitions” and “Three times out of , he has done well at competitions.” “Usually” means different things to different people. Statistics serve well to define the relationship between any two variables. By using broader bars in a bar graph, the differences between different bars will appear less dramatic. Broader bars look shorter than thin ones as can be seen in figure . Another way of changing the visual impression of a bar chart is to change the axes so the frequency is represented along the horizontal axis (x-axis) instead of the vertical axis (y-axis) as can be seen in figure . The vertical axis should, whenever possible, be the frequency axis because a horizontal frequency axis makes the differences in the chart appear to be smaller. 80% 40 30 3 To give the reader an impression of dramatically decreasing numbers of failed fixtures, the author can choose to show only the numbers of failed fixtures during successive time periods (see figure A). This obscures for the reader the fact that the number of controlled implants during the periods in question has decreased successively at the same time (see figure B) and that the success rate figures hardly vary at all from one time period to the next (see figure C). In order to give the reader an overall picture when presenting the results of a comparison, it is important to carefully state what actually has been compared. The size of the comparative groups should be stated; not the results of the comparison alone. The objective of the investigation and the method of investigation ought to be declared. It is also important to spell out the plan of investigation for the reader. The loss of subjects due to dropout, infirmity or death is a difficulty faced in most clinical trials. The effects can be far-reaching. Suppose the objective of a study is to resolve the proportion of implanted fixtures that survive years after the operation. If data is only collected on of the fixtures and of the have failed, the failure rate may appear to be percent but, if the other have failed, it means that percent is a more reasonable figure. On the other hand, if the uncontrolled fixtures are all survivals it means that only percent have actually failed. In some cases, figures must be rounded off. If the result is presented with figures that show “great precision” (i.e. use many decimals) it looks as if the result is much more exact than the size of the sample may justify. An article can look trustworthy if numerous statistical analyses are 97% 97 95 93 20 2 Optical illusions 100% 10 Group 1 2 3 4 5 1 term final results can be forecast with a lifetable even if the study is not yet completed. Nonetheless, it is important to be aware that more than percent of the initial group must remain in the study (including any failed fixtures) to draw any reliable conclusions. The reader will find it difficult to interpret the results if only one part of the lifetable is presented, especially if only the cumulative success rates (CSR) are presented. Group By Christina Bergström If it is the intention of the author to exaggerate the differences between narrow range values (%, % and %, for example) a diagram axis can be “cut off ” as seen in figure . Proportions are lost with a “cutoff ”, that is, the correct proportions of the data cannot be seen. Instead of giving each single unit equal space, only a specific part of the table has been presented in figure . If a cut-off of the axis is necessary to make a point, the cut-off should be clearly marked to aid in interpretation. No. of failed implants No matter where we turn today, we find statistics all around us. In this classic, yet still up-to-date Nobelpharma News report, one of Ulf Lekholm’s co-authors, and a statistical expert in her own right, explains how figures are used to tell a story—or sometimes to exaggerate one. Depending on how they are presented, statistics can be reliable or misleading. 10 20 30 40 50 60 No. of failed implants Figure 3: A change in axis gives a different impression. Time period No. of inserted/ controlled implants No. of failed implants No. of withdrawn implants Success rate Cumulative success rate (CSR) 0–1 year 1000 16 85 98.4% 98.4% 1–2 years 700 8 49 98.9% 97.3% 2–3 years 550 5 45 99.1% 96.4% 3–4 years 250 3 55 98.8% 95.2% 4–5 years 100 1 31 99.0% 94.3% 5 years 12 Figure 4: A lifetable. used to demonstrate the results. This gives the reader the impression that the study encompasses well-controlled material and does not need to be brought into question. Nonetheless, statistical analyses can be deceptive. It is quite possible that the reader is not familiar with the methodology used and that the analyses therefore do not provide any comprehensible information. If that is the case, then the statistical analyses used are of little value. Once again, it is the duty of the author to make sure that the article can be understood by the vast majority of those for whom it has been written. Correlation Many statistical analyses are carried out to examine the relation between two variables (within a single group of subjects) in order to assess whether or not the two variables are associated. One may conclude a relation- more on following page 11 Nobel Biocare NEWS Issue 1/2012 Research Put into Practice Know your implant procedures: the use of torque drivers and implant screws Implant screws are deceptively simple and exquisitely intricate at the same time. By Dr. Chandur Wadhwani I 2 3 A. 4 5 6 Year 2 3 B. 4 100 250 5 6 Year Rule number 4 Int Journ Oral Maxillofac Implants. Re-use of screws: Limit the number of times the screw is tightened and loosened. Each time this is done, the subsequent force needed to undo the screw is reduced. This affects both the screw and the implant to such a degree that after six tightening/loosening events—even if a new screw is used—it does not improve the fastening properties of the joint. As a general rule, only tighten/ loosen the screw a maximum of five times. < 2008. Jaarda M. et al. “Comparison of ‘look-alike’ implant retaining screws.” J Prosthod. 1995. Pai and Hess. “Experimental study of loosening of threaded fasteners due to dynamic shear loads.” Journal Sound and Vibration. 2002. McCracken M. et al. “Variability of mechanical torque-limiting devices in clinical service at a US dental school.” Int J Prosthodont. 2009. Weiss et al. “Effect of repeated closures on opening torque values More to explore: Theoharidou et al. “Abutment in seven abutment-implant sys- screw loosening in single-implant tems.” Journal Prosthet Dent. restorations – a systemic review.” 2000. Precision-milled Abutments For Major Implant Systems 50% 550 1 Suvival rate 1 100% Use as directed. If the manufacturer states a given torque, the screw has been designed and tested to that value. Using a lower or higher torque than prescribed will result in unpredictable joint behavior. Check that your torque wrench is delivering the correct force required. A recent study showed after repeated use some devices produce forces far in excess of that needed, some far less. In general, it is recommended that you choose the beam type (see the illustration) as it delivers more consistent force. If you have the toggle type (not recommended) calibrate or replace your device yearly—ask Nobel Biocare for details. 12 Year Rule number 2 No. of controlled implants 10 No. of failed implants 20 Always use original Nobel Biocare manufacturers components and parts. “Compatible parts” may look Tips and Techniques Rule number 3 1000 Rule number 1 T&T Use of lubricants, ointments and medications affects the implant/ abutment joint, especially under vibration. It is not advised and may lead to premature screw loosening. 700 A systemic review of abutment screw loosening in single-implant restorations found that abutment screw loosening is a rare event regardless of the geometry of the implant abutment connection, provided that appropriate anti-rotation features exist and proper torque is employed. the same but cannot be guaranteed to work the same. Even “compatible” screws have different thread pitch and patterns. Studies show that even though they may look the same, they do not work in the same way. 1000 The Science A beam type torque wrench is the type recommended by the author because it delivers more consistent force than the toggle type. 500 mplant abutments are commonly fixed to the implant using a screw. Screw mechanics take advantage of the metal structure that can be stretched as the tightening process occurs. Elongating the screw by using the recommended torque setting turns the screw into a “spring” that clamps the components together, improving the joint fixation more than if the screw is simply tightened. This produces a robust joint, capable of withstanding the rigors of the oral environment during function. But certain rules must be followed in order to get the most out of this joint. 1 2 3 C. 4 5 6 Figure 5: Three different ways to present the results of the figure 4 lifetable can be seen in the three diagrams here. A: The number of failed implants during different years. B: The number of controlled implants during the same years. C: The survival rate during the same years for the same fixtures. from the previous page ship between two variables if one variable varies simultaneously with another. This is called a correlation; it implies no cause/effect relationship. Although there may be a cause/effect relationship, even a third vari- able could be the cause of both of the observed changes. When reading articles that include statistical analyses in medical magazines or journals, in newspapers or the popular press—just to name a few examples—the reader has to be critical and look for the figures that underlie the values under study. If those figures cannot be found, it is possible that the writer has consciously chosen to present his or her results in a vague manner. Be skeptical when you read and you’ll get more out of the materials you find interesting. < Clinical screw with unique TorqTite surface included NobelProcera™ nobelbiocare.com/nobelprocera 12 Nobel Biocare NEWS Issue 1/2012 Excellent Initial Stability and Perfect Esthetic Results NobelActive™ is the most versatile choice for your implant dentistry practice. Nobel Biocare. This patented, biocompatible surface has been scientifically proven both in the long and short term to enhance osseointegration and increase the predictability of implant treatment (Glauser, Zembic, et al, ; and Glauser, Portmann, et al, ). Many prosthetic solutions NobelActive now offers a new, true 3.0 mm small-diameter implant for successful restorations in the anterior region where space is limited and good esthetics essential. A third-generation dental implant, NobelActive has been designed to meet the high demands of dental implant surgery and implant prosthetics efficiently. Reliably high initial stability for immediate loading clearly sets NobelActive apart from conventional implant systems. By Drs. Kai Klimek and Roberto Sleiter W ith its innovative thread design, NobelActive condenses the bone during insertion at every turn, which differentiates it from other self-tapping implants available on the market. The expanding, tapered implant body of NobelActive features a double-lead thread design, which also contributes to the high initial stability characteristic of this implant. The innovative implant tip allows fine adjustments in implant orientation to be made during insertion to optimize the final position of the implant in the bone, without jeopardiz- ing initial stability. The implant thread allows gradual atraumatic narrow ridge expansion and was developed to attain high initial stability even in compromised bone situations. Furthermore, NobelActive has two reverse-cutting flutes. Rotating the implant by half-a-turn counterclockwise engages the cutting capability of these flutes. The coronal region of NobelActive is back-tapered and designed to maximize alveolar bone volume around the implant collar for improved soft tissue support. These new attributes provide significant advantages for the subsequent prosthetic management and facilitate co-operation between the surgical and prosthetic teams. Groovy™ Macroscopically visible surface grooves not only promote, but also accelerate new bone formation in conjunction with the TiUnite surface of this implant (Hall et al, ). TiUnite is a highly crystalline and phosphate-enriched titanium oxide surface, available exclusively from NobelActive has an internal conical connection. The connection offers the clinician the option of restoring the tooth with a wide range of prefabricated prosthetics as well as with NobelProcera. Using NobelProcera, the implant can be restored with a comprehensive combination of prosthetic options (e.g. with abutments made either of zirconia or titanium), to assure the best possible function and esthetics. NobelProcera Abutments can be designed with practically any angle, taper, finish line, height, width and cross-section to optimally adapt the form, arch and axis of the prosthesis to the peri-implant structures. Each NobelProcera restoration is individually designed using state-of-the-art D computer-aided design software (CAD) and then milled from highstrength zirconia or titanium in a computer-assisted manufacturing (CAM) process. properties of this implant. Nobel Biocare therefore strongly recommends participating in a practical training course before using NobelActive. Science first and foremost Nobel Biocare is currently conducting a number of multi-center clinical trials to assess the success, soft tissue maintenance and bone remodeling of NobelActive implants over time. One is a five-year, randomized, controlled, prospective study examining the NobelActive implant in the anterior and posterior regions of the maxilla and mandible, and shows that NobelActive can be used under the demanding treatment conditions of immediate loading, with stable bone and soft tissue levels after two years in function. < More to explore To peruse the scientific literature being accumulated on NobelActive, visit nobelbiocare.com/resources. For full references cited in this article, please visit our enhanced digital edition at: nobelbiocare.com/ newsletter Initial situation using NobelActive NP 3.5 x 11.5: 36-year-old female patient in good overall health, non-smoker, no parafunctional habits Fig. 1. Extraction of the left upper central incisor after fracture. Fig. 2. 10 weeks post-extraction, flapless insertion of a NobelActive NP 3.5 x 11.5 implant, delayed loading. Fig. 3. The situation 20 weeks after extraction. Fig. 4. Treatment 20 weeks after extraction, impression taking with impression coping. Fig. 5. Fitting of the NobelProcera Zirconia Abutment. Fig. 6. Fitting of the NobelProcera Zirconia Abutment. Fig. 7. Inserted NobelProcera single zirconia crown left upper central incisor, 1 week after insertion. Fig. 8. Inserted NobelProcera single zirconia crown left upper central incisor, 21 months after insertion. Getting it right from the start Product development at Nobel Biocare is based upon the principles established by Professor Per-Ingvar Brånemark, namely that all innovation should be based on sound scientific research and subjected to systematic clinical evaluation before entering full-scale commercial distribution. That is why NobelActive went through rigorous clinical trials, eight months of clinical testing and extensive technical study in the prelaunch phase. Dentists from every corner of the globe participated in the endeavor. At the beginning of this eightmonth period, when over , implants were used, the clinicians received extensive training with regard to the implant’s remarkable potential. Experience gained from clinical use and the subsequent feedback reports confirmed the effectiveness of this unique implant design. The clinician’s response also confirmed how important previous training was in order to make the most of the novel and innovative The photos in figures 1–8 courtesy of Roberto Sleiter (Switzerland). Issue 1/2012 13 Nobel Biocare NEWS NobelActive™ Expands its Range of Components A few words from the clinical perspective on Nobel Biocare responsiveness The clinicians who use Nobel Biocare products often provide the feedback the company needs to better adapt its range of products to clinical demands. By Dr. Nik Sisodia E ver since its launch four years ago, I have been using NobelActive. Because I have found that the surgical versatility and conical connection of this multi-purpose implant are so good, I have switched over to it completely. I am now exclusively using NobelActive for all cases and indications. Having a secure and strong conical connection offers built-in platform shifting and has meant that I see crestal bone heights remaining stable to the top of the implant in many more cases than previously. A pleasure to work with Many of us who were using the NobelActive implant early-on found that—thanks to the new conical connection—implants could now be placed deeper when required. Of course, this also meant that we needed a range of prosthetic components that were taller in order to make transmucosal healing possible. As always, the people at the R&D department of Nobel Biocare welcomed our queries, were openminded and explored the possibility. I think it is safe to say that as a direct result of clinical demand, Nobel Biocare very quickly added a taller mm healing abutment to the NobelActive range. Without doubt, this new healing abutment will make management of the soft tissues far easier in those cases where the implant is placed deeper. For me, it is a very welcome addition to the Nobel Biocare product portfolio. < More to explore: Check out all the NobelActive components at: nobelbiocare.com/healing Restorative Flexibility 7 mm tall healing abutment to accommodate sub-crestal placement and thick soft tissue. Modified bridge components – Healing abutment and impression coping with natural emergence profile. – Healing abutments in three heights for restorative flexibility (3, 5 and 7 mm). These new restorative components are for use with both NobelActive and NobelReplace Conical Connection. Immediate Loading of a Molar, Post-extraction NobelActive™ – a solution for the restoration of both single- and multi-rooted teeth Here is a case study of implant placement immediately after a molar extraction using NobelActive in conjunction with immediate temporary loading. By Dr. Ira Schecter T his patient is a healthy, middleaged male with no medical preconditions and satisfactory oral hygiene. Figure 1 illustrates a lower left first molar that had a previous root canal treatment and was obviously failing. Retreatment endodontically was deemed to be unpredictable at best, and the treatment option selected was to extract the tooth and place an immediate dental implant into the socket site. Figure 2 illustrates how the tooth was extracted atraumatically, preserving as much of the surrounding bone as possible. We chose a NobelActive dental implant because its surgical protocol dictates minimal osteotomy preparation and thus allowed me to utilize the available inter-septal bone between the two root socket sites. The implant was submerged below the adjacent crestal bone heights and was totally engaged in host bone. No bone grafting was carried out in the adjacent sockets as we expected the sockets to fill-in via the natural host healing process. The implant was torque challenged to greater than Ncm and was tested for initial stability in the host bone utilizing an Osstell Mentor frequency resonator. Figure 3. The implant passed all tests for initial biomechanical stability, and an impression was taken at the time of placement after suturing the tissue. Figure 4. An immediate acrylic temporary restoration was made, which was secured to the implant and inserted hours post-op. Figures 5–7. The surrounding bone was allowed to heal for a period of six months and a new impression was taken to index the healed tissue around the temporary acrylic crown restoration. A custom NobelProcera Titanium Abutment was inserted and torqued to Ncm and then an all ceramic NobelProcera Zirconia Crown restoration was cemented on top of the abutment, completely covering the metal underneath. Fulfilling high expectations Patients today want to be treated in an efficient and expedient manner. For years, we have been able to ex- Fig. 1. The molar to be extracted. Fig. 2. X-ray of Immediate temporary. Fig. 3. Immediate placement and impression. Fig. 4. Immediately loaded temporary. Fig. 5. Custom NobelProcera Titanium Abutment. Fig. 6. X-ray of NobelProcera Titanium Abutment. tract single-rooted teeth, place implants immediately into the socket sites and immediately load the implants thanks to well-developed protocols for such cases. With the NobelActive implant, we can now do the same in multi-rooted teeth situations—and with very pre- dictable long-term results, I believe—as long as we carefully follow the surgical and implant placement guidelines. < More to explore: nobelbiocare.com/nobelactive Fig. 7. Permanent NobelProcera Crown. 14 Nobel Biocare NEWS Issue 1/2012 Micromotion and Dental Implants A research update in two parts – with thought-provoking consequences for longevity A well-known and oftenquoted pioneer in the field of biomechanics—who not incidentally holds the position of Senior Research Engineer, Division of Plastic & Reconstructive Surgery at Stanford University in California— sends us this report on the state of the art. By Professor John B. Brunski M ost clinicians already appreciate that it is beneficial to insert dental implants “tightly” (e.g., with adequate primary stability) into a freshly-prepared bone site. But how “tight” is tight? What constitutes “adequate” primary stability? And if an implant is somewhat “loose”, how does this looseness relate to “micromotion”? Moreover, why is the “tightness” vs. “looseness” of an implant important from a mechanical and biological (i.e. biomechanical) standpoint? Finding some answers starts with two initial points. Point 1 First, an implant that is not firmly anchored in bone won’t be clinically useful in a functional, load-bearing sense when that implant is called upon to support a prosthesis. This is easy to see from a simple example with six implants installed in a lower jaw to support a typical full-arch prosthesis that’s screwed or cemented onto all six implants (Figure a). Suppose that two out of the six implants are not as “tightly” attached to the surrounding bone as the other four. (This situation around the two implants could be caused by one or both of the following problems: [] the bone around the implants was quite porous and therefore much more deformable, leading to a somewhat “soft” interface; [] the surgery to install the implants might have damaged more bone than normal, also thereby leading to a “softer”, less stiff interface.) Now, we know from both measurements and calculations that when relatively “stiff ” implants exist in the same distribution as “less stiff ” implants, then the stiffer implants end up taking most of the load—effectively converting a six-implant situation (in this example) into a four-implant case (Figure b). Overall, the general result is that when a prosthesis is supported by multiple dental implants, load-sharing among the implants depends on the relative stiffness of the implants, with “softer” (less stiff) implants taking less load than the “stiffer” implants. It follows that if one wants all six implants to perform to their full load-bearing capability, they should all be equally well “fixed” (or “tight”) in the bone. Point 2 The second reason why “loose” implants are a problem stems from the biological consequences of the associated “micromotion” at the bone-implant interface. The term “micromotion” refers to relative displacements of a loaded implant with respect to the surrounding interfacial bone. A simple example of rather extreme micromotion is to imagine a mm diameter implant that’s loaded after being placed into a . mm diameter hole; such an implant would not be engaged with the bony walls of the hole and would therefore not be well-supported when any load is exerted on it; and as a result the implant will tend to “wobble around”—i.e., experience micromotion—in the hole. But why is this micromotion a biological problem (besides the fact that the implant would not function well in load support)? The answer is that many studies demonstrate that micromotion—if it is “excessive”—will interfere with the biology of proper interfacial bone healing. For example, some authors have proposed that = All implants equally stiff = Implants no. 1 & 6 less stiff Vertical load 300 Estimated neutral axis of implants Axial load (N) 200 100 0 –100 –200 –300 | 6 | | | | 5 4 3 2 Implant number | 1 Fig. 1a & 1b. Changes in the force distribution when implants no. 1 and 6 have about 10 to 20 times lower stiffness than implants 2–5. THREAD THREAD Fig. 2a. Unstrained: Cells and fibrin are intact and not damaged in any way. Used and modified from Marx, 2008, with permission. “excessive” micromotion could be anywhere from to µm (depending on the author), i.e., this range of values represents the threshold beyond which there will be interference in bone healing. However, it is also clear that this threshold has not been established very precisely or whether it even pertains to all the differently-shaped im- R&D Research and Development plants that exist. Most significantly, the search is still on for the underlying mechanism(s) by which micromotion interacts with the interfacial biology to either negatively (as most authors believe) or perhaps positively (as at least some authors have suggested) influence interfacial reactions. Searching for clarity So, what is micromotion and how might it operate at an interface? We have been exploring the hypothesis that implant micromotion produces strain (deformation) in the interfacial tissue, and that it is this strain in the interfacial tissue—and not the implant micromotion per se—that is the key factor in regulating the interfacial biology of healing. So what’s involved with this hypothesis and how do we test it? First, it is instructive to consider some examples of the meaning of strain and how implant micromotion can create interfacial strain. Strain is an engineering term related to deformation. When it comes to strain in interfacial tissues, Figure depicts two highly magnified, idealized views of a bone-implant interface as it might look soon after implantation (e.g., seconds to a few Fig. 2b. Strained: In this example, implant threads move to the right, compressing the cells and fibrin against the bone. hours). Figures a and b show the “before” and “after” states of the interface following some amount of implant micromotion. In this example, the micromotion consists of a bodily displacement of the implant threads to the right, toward the cut edge of the bone that borders the interface. Figures a and b also show a small gap between the implant’s threads and the cut edge of the bone, which is meant to depict that at least in some regions of a typical interface, there is the possibility that the threads of a freshly-installed implant may not directly interdigitate with bone of the site. Figure a goes on to illustrate that, early after surgery, such a small gap between implant and cut bone will ordinarily fill with a blood clot comprised of fibrin, red blood cells, platelets, growth factors, etc. Strain of the interface comes about as we consider the difference between the state of affairs in Figure a (which depicts the implant threads before there has been any micromotion of the implant relative to the cut surface of the bone) and Figure b (after the threads of the implant have been displaced some distance to the right). In comparing these two images, we observe (Figure b) regions of deformation of the interface, e.g., regions of compression, tension (stretching), and shearing of the cells and fibrin in the gap region. So at least qualitatively, what this example shows is the idea that implant micromotion can end up deforming (straining) the interfacial tissue. So what? Before we answer that question in the next issue of Nobel Biocare News, a few more words on strain. For one thing, the nature and size (magnitude) of the interfacial strain will depend on location in the interfacial gap. That is, a comparison of Figures a and b reveals that in some regions there is compression (“squeezing”) of the red blood cells against the bone surface, while in other regions there is mainly stretching (tension, “pulling”) of the yellowish fibrin fibers. A detailed quantitative engineering strain analysis at discrete points in this image could be done, but the key take-home messages connected with strain are these: r "UBOZHJWFOiQPJOUuMPDBUJPO JO the interface, one can define a state of strain—which is also called the strain state at that point. r 5IJT TUSBJO TUBUF JO UIF JOUFSGBDF can depend on many factors—including the amount and direction of the implant’s micromotion as well as the implant’s shape and fit in the drill hole, etc. r 4USBJOBUBDFSUBJOQPJOUJOUIFJOterface can simultaneously involve more than one type of strain at the same spot, e.g., compression, stretching, and shearing can all exist simultaneously at the same location in a material. (A common example of this situation is during the stretching of a common rubber band: At any point in the middle of the rubber band there is simultaneously tension or stretching along the length dimension but also compression in the width and thickness directions.) r *O FOHJOFFSJOH UFSNT UIF TUSBJO state at a point is described by a mathematical quantity known as the strain tensor, a full explication of which goes far beyond the scope of this article, but one important feature of the strain tensor is that it allows us to compute the so-called principal strains, which are the largest and smallest magnitudes of strain at the point of interest. r -BTUMZBOZNBUFSJBMXJMMGBJMXIFO the strains (which are related to the stresses) become too large—a fact that applies for both biological materials (such as bone and soft tissue) and man-made materials (such as titanium). < There’s more to this story! Professor Brunski will return in the next issue to answer the question, “What are the biological consequences of micromotion and the associated interfacial strains?” If you can’t wait until then, both articles are available now in our enhanced digital edition at: nobelbiocare.com/newsletter Issue 1/2012 15 Nobel Biocare NEWS A Case in 12 Pictures NobelProcera bars on four NobelReplace implants in the mandible and six NobelReplace implants in the maxilla. By Dr. Stefan Holst Case history: A 73-year-old patient presented with a failing mandibular restoration necessitating removal of the remaining teeth and atrophied alveolar ridges in the edentulous maxilla. Due to extensive atrophy of the alveolar ridges and the amount of hard and soft tissue missing, fixed implant retained restorations were not an option. The Best Marketing Tool is a Satisfied Patient Dr. Ronald Goldstein says that meeting the patient on his or her own terms is essential in that crucial first conversation about implants. Is there any one best way to explain implant procedures to the patient? Goldstein: No, it all depends on the patient. The most successful offices have a good understanding of the psychological make-up of each patient. Initial insights from a treatment coordinator, dental hygienist, or even a dental assistant should be taken into consideration by the dentist. Q&A Questions and Answers Dr. Ronald E. Goldstein, is a dentist from Atlanta, Georgia, USA, an active speaker and a prolific writer of both consumer and academic literature on the topics of esthetic dentistry and implants. there. Practical benefits and the science that makes them possible should always be a part of the conversation. Comparison shoppers If a satisfied patient referred the new patient, he or she may just want to get started with the treatment. If, on the other hand, the new patient has approached you because of your website, then you need to realize that this patient has probably already done a considerable amount of homework. I like to ask patients like these what more they want to know and then build the presentation from Then there are the self-assured patients who already know—or think they know—everything they need to know about implants. They want to compare you to others. Tell them about your experience, any warranties you offer, and be specific about finances. Chances are, your treatment plan will differ from other offices’ so be prepared with back-up graphics and maybe even a video to let them know why your plan is the best choice. Remember, every patient is different. Before having that first conversation about implants, gather input from your staff about the patient’s interest, knowledge and motivation, and then listen carefully to what the patient has to say. < There’s more to this story! Dr. Goldstein answers more questions in our enhanced digital edition at: nobelbiocare.com/newsletter “The best decision I ever made!” Meet Pat, 69, who had her first implant 23 years ago. By Pat Farrell Treatment performed: Four implants were placed in the interforaminal area of the mandible and six implants in the maxilla for bar retained fixed-removable restorations. Case notes: The long-term success of an implant-retained restoration depends to a great extent on the accurate and precise fit of a superstructure, biocompatibility of materials selected and easy hygiene maintenance for the patient. If a patient’s manual skills are impaired or significant amounts of hard and soft tissue need to be replaced by prosthetic means, a fixed-removable overdenture is both a well-accepted and excellent treatment option, allowing for simple and easy handling. The CAD/CAM design of the NobelProcera Implant Bars Overdenture and the final restorations were made by DentalX, Munich, Germany. I feel very lucky, when I look at my friends who are around my age. They are mostly over seventy. Struggling with loose dentures, afraid to socialize because they cannot smile or chew properly—I knew early on in my life, that I never wanted to experience that. I always had problems with my teeth and oral health in general. I remember a time when I wasn’t comfortable to smile or open my mouth—which is difficult when you are a teacher. You are always in front of people, and obviously you serve as an example to others. I needed to be confident in my job. My dentist was a real life-saver. I suppose you could describe him as a pioneer, since he placed my first implant over twenty-three years ago! Since then, I have had a further fourteen placed, and I have never regretted it. My teeth feel like my own—so secure, that I know I never have to worry about them ever again. I socialize a lot, and love my foods. I play golf, and meet my friends—and when I spot someone with an old-fashioned denture, I feel so lucky. Getting implants is the best decision I have ever made! < Nobel Biocare NEWS Celebrating the Triumph of Osseointegration Revolutionary breakthroughs – 30 and 60 years on This year, scientific symposia will mark the dual anniversaries of the advent and acknowledgement of osseointegration. I Prof. George Zarb at this year’s first Nobel Biocare Symposium. Pioneers from the heady days of the Toronto Conference of , such as George Zarb and Ragnar Adell, were honored and other speakers reminded participants of how far PerIngvar Brånemark, Nobel Biocare and their band of supporters have brought osseointegration since those days of breakthrough and years ago. Eyes on the horizon The programs of all five of the remaining Nobel Biocare Symposia will celebrate the origins and evolution of osseointegration as a practical and trusted treatment modality over the last six decades. Each program will also include lectures on recent advances in treatment, presented from surgical, prosthetic and laboratory perspectives. Europe and Russia Austria Nobel Biocare Austria Phone: +43 1 892 89 90 Nobel Biocare NEWS Printed on non-chlorine bleached FSC-certified paper. Design and printing: www.linkgroup.ch Prefer e-mail delivery? Then visit: www.nobelbiocare.com/enews Headquarters Nobel Biocare Services AG P.O. Box 8058 Zürich-Flughafen, Switzerland Offices: Balsberg, Balz Zimmermann-Strasse 7 8302 Kloten, Switzerland Phone +41 43 211 42 00 Fax +41 43 211 42 42 Belgium Nobel Biocare Belgium Phone: +32 2 467 41 70 Denmark Nobel Biocare Denmark Phone: +45 39 40 48 46 Finland Nobel Biocare Finland Phone: +358 9 343 69 70 France Nobel Biocare France Phone: +33 1 49 20 00 30 Germany Nobel Biocare Germany Phone: +49 221 500 85 590 Hungary Nobel Biocare Hungary Phone: +36 1 279 33 79 Ireland Nobel Biocare Ireland Phone: toll free 1 800 677 306 Web contact: www.nobelbiocare.com/contact 300 Years of Experience Take 300 Years to Gain World-renowned experts are the voice of experience today Despite their small numbers, members of the Associated Brånemark Osseointegration Centers represent an enormous amount of cumulative experience in the field of osseointegration. by Frederic Love n , Per-Ingvar Brånemark discovered the principles of osseointegration in Sweden. Thirty years later, in , the discovery was acknowledged, and his subsequent findings confirmed, at an epoch-making meeting of dental authorities organized by George Zarb in Canada. Yet another thirty years have now passed, and Nobel Biocare is celebrating both these - and -year anniversaries in Sweden, Canada, and four other locations, too. Starting the year-long celebration in the hometown of osseointegration—Brånemark’s Gothenburg— Nobel Biocare brought together some of the best-known names in the field on March –. The event began with a surprise entrance from Brånemark himself who delivered advice and thoughts for the future. Ulf Lekholm then led experts not only from Scandinavia, but the far corners of the world, as they exchanged ideas and discussed promising areas for further exploration at this meeting. Issue 1/2012 Speakers will look towards the future as well, presenting current trends and possible future developments for bone-anchored restorative dentistry. Under the common theme, “Celebrating years of osseointegration and years of international acknowledgement,” meetings will be held in Avignon, France (June -), Odessa, Ukraine (June –), Hamburg, Germany (June –) and Rimini, Italy (October –), with the final symposium planned for Toronto, Canada (October –) where the international breakthrough for osseointegration first took place. < Mark your calendar now! For further information—or to register online—please go to: nobelbiocare.com/symposia2012 R ecently, a small group of osseointegration pioneers, all of them representatives of the Associated Brånemark Osseointegration Centers (ABOC), gathered in Gothenburg, Sweden, for the organization’s annual meeting. Among the well-known names in attendance were Drs. Per-Ingvar Brånemark, James Chow, Remesh Chowdhary, Edward Hui, Yataro Komiyama, Ulf Lekholm, Ulf Nannmark, Patrick Palacci, Laércio Vasconselos, Mats Wikström, William Becker and Lars Sennerby. Together, this small band of implant experts has accumulated more than years of experience of implant treatment ad modum Brånemark. In their discussions, one of the participants, Patrick Palacci, pointed out that “less is more” has always been the central philosophy behind the very successful original protocol itself—and its further development. “By respecting Mother Nature,” he said, “continuous development of simpler and safer techniques has been going on ever since the first patient was treated.” Yataro Komiyama added, “To provide predictable long-term prognoses for patients, we should reevaluate the past and respect living tissues. The living tissue is wiser than the human being.” According to Palacci, the members of the global ABOC network undertake to improve existing diagnostic, surgical and restorative techniques, and to spread awareness and knowledge of osseointegration. At the Gothenburg meeting, the group underlined the central importance of the team approach to successful outcomes, and in a formal statement prepared for publication in Clinical Implant Dentistry and Related Research, they also wrote that the “prerequisites for a successful longterm implant treatment outcome include good patient selection, adequate evaluation and correct diagnosis, careful planning, suitable techniques, and regular maintenance.” < More to explore: Read the entire reprint at nobelbiocare.com/300-years Italy Nobel Biocare Italy Phone: +39 039 683 61 Cust. support: toll free 800 53 93 28 Sweden Nobel Biocare Sweden Phone: +46 31 335 49 00 Cust. support: +46 31 335 49 10 Colombia Hospimedics S.A. 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Please contact the local Nobel Biocare sales office for current product assortment and availability. 16