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Three-dimensional finite-element analysis of functional stresses in different

bone locations produced by implants placed in the maxillary posterior region


of the sinus floor
Omer Lutfi Koca, DDS, PhD,a Gurcan Eskitascioglu, DDS, PhD,b and Aslihan Usumez, DDS, PhDc
Selcuk University, Faculty of Dentistry, Konya, Turkey
Statement of problem. Implants placed in the posterior maxilla have lower success rates compared to
implants placed in other oral regions. Inadequate bone levels have been suggested as a reason for this differential
success rate.
Purpose. The purpose of this study was to determine the amount and localization of functional stresses in
implants and adjacent bone locations when the implants were placed in the posterior maxilla in proximity to the
sinus using finite element analysis (FEA).
Material and methods. A 3-dimensional finite element model of a maxillary posterior section of bone (Type 3)
was used in this study. Different bony dimensions were generated to perform nonlinear calculations. A single-
piece 4.1 3 10–mm screw-shaped dental implant system (ITI solid implant) was modeled and inserted into
atrophic maxillary models with crestal bone heights of 4, 5, 7, 10, or 13 mm. In some models the implant
penetrated the sinus floor. Cobalt-Chromium (Wiron 99) was used as the crown framework material placed onto
the implant, and porcelain was used for occlusal surface of the crown. A total average occlusal force (vertical load)
of 300 N was applied at the palatal cusp (150 N) and mesial fossa (150 N) of the crown. The implant and
superstructure were simulated in finite element software (Pro/Engineer 2000i program).
Results. For the porcelain superstructure for bone levels, maximum von Mises stress values were observed on the
mesial fossae and palatal cusp. For the bone structure, the maximum von Mises stress values were observed in the
palatal cortical bone adjacent to the implant neck. There was no stress within the spongy bone. High stresses
occurred within the implants for all bone levels.
Conclusion. The maximum von Mises stresses in the implants were localized in the neck of implants for 4- and
5-mm bone levels, but for 7-, 10-, and 13-mm bone levels more even stresses occurred within the
implants. (J Prosthet Dent 2005;93:38-44.)

CLINICAL IMPLICATIONS
The results of this finite element study indicated that implants supported by 7-, 10-, or 13-mm
bone levels demonstrate more even von Mises stresses, localized in smaller areas of cortical bone,
than implants with 4- or 5-mm bone levels. However, long-term clinical trials are required to
determine the validity of the effects of bone levels in the maxillary posterior region on the long-
term success of implant treatment.

T he therapeutic regimen for treating patients with


missing teeth has been significantly expanded by mod-
of which is the maxillary sinus. Thus, implant placement
in the maxilla can be difficult for many reasons, includ-
ern implant methods. The prosthesis supported by os- ing inadequate posterior alveolus, increased pneumati-
seointegrated implants has become an integral part of zation of maxillary sinus, and close approximation of
restorative therapy for both completely and partially sinus to crestal bone.5 The thickness of bone beneath
edentulous patients.1-3 However, a prerequisite for suc- the maxillary sinus correlates with the degree of pneu-
cessful oral implants is sufficient bone volume.4 In using matization.5 Sinus pneumatization may minimize or
osseointegrated dental implants for partially edentulous completely eliminate the amount of vertical bone avail-
patients, clinicians frequently are confronted with ana- able.5,6 In addition to the problem of a compromised al-
tomic variations of the premolar and molar areas, one veolar ridge, the maxillary sinus can vary in size and
shape, making implant placement impossible without
surgical modification.7
a
Research Fellow, Department of Prosthodontics.
Several techniques and a variety of materials have
b
Professor and Chair, Department of Prosthodontics. been reported to increase posterior maxillary bone
c
Assistant Professor, Department of Prosthodontics. height to permit successful dental implant placement.8,9

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KOCA, ESKITASCIOGLU, AND USUMEZ THE JOURNAL OF PROSTHETIC DENTISTRY

Table I. Elastic properties of materials modeled Table II. Models consisted of elements and node
Modulus of Bone level Elements Node
elasticity, Poisson’s
Material E (MPa) ratio, v 4 mm 141,153 27,510
5 mm 156,916 29,843
Titanium46 110,000 0.35
7 mm 182,318 33,485
Cr-Co alloy45 218,000 0.33 10 mm 189,541 34,313
Porcelain43 68,900 0.28 13 mm 192,645 34,721
Cortical bone44 13,400 0.30
Spongy bone44 1370 0.30
tures occur, microdamage caused by stress greater
than normal levels may stimulate osteoclastic activity
Bruschi et al10 described a surgical technique for aug- to remove the damaged bone.34
menting an atrophic alveolus beneath the maxillary sinus The distribution of forces in peri-implant bone has
without utilizing bone grafts or membranes and termed been investigated by finite element analyses in several
it localized management of the sinus floor (LMSF). As de- studies.25,26,28,29,34,35,37 Recently, stress distribution
scribed, the LMSF technique offered the advantage of in bone correlated with implant-supported prosthesis
placing implants in a single stage in the posterior maxilla design has been investigated primarily by means of 2-di-
with as little as 5 mm of residual bone.10 Winter et al7 mensional (2-D) and 3-dimensional (3-D) finite ele-
evaluated the clinical success of placing titanium im- ment analyses (FEAs).38 Studies comparing the
plants in the maxillary posterior with less than 4 mm accuracy of these analyses found that, if detailed stress
of alveolar bone, utilizing the surgical principles of the information is required, then 3-D modeling is neces-
LMSF technique. Ellegaard et al11 placed implants sary.38,39 The 3-D FEA is considered an appropriate
into a minimum of 3 mm of alveolar bone with implants method for investigation of the stress throughout a
protruding more than 5 mm into the maxillary sinus, 3-D structure, and therefore this method was selected
without bone grafts. for bone and implants stress evaluation in this study.
Adequate bone volume available for maxillary im- The purpose of this study was to determine the amount
plant placement and loading is necessary to achieve and localization of functional stresses in implants placed
long-term function of implant-supported restorations. in different bone levels (4, 5, 7, 10, or 13 mm) in the
Increased problems of bone and implant loss have atrophic posterior maxilla using FEA. The hypothesis
been reported in the posterior maxilla.12 Animal experi- tested was that the amount and localization of func-
ments13,14 and clinical studies2,3,15-17 have shown that, tional stresses in implants placed in different bone levels
in the absence of plaque-related gingivitis, bone loss in the posterior maxilla is similar.
around implants is associated with unfavorable loading
MATERIAL AND METHODS
conditions. One of the reasons for short-term implant
failure is lack of primary stability. A 3-D finite element model of a maxillary section of
Impaired bone height and a paucity of dense cortical bone with a missing second premolar and its superstruc-
bone contribute significantly to such diminished im- ture was used in this study. According to the classifica-
plant survival.14 While late implant failures are primarily tion system by Lekholm and Zarb,40 a maxillary bone
related to biomechanical complications, the major factor model, simulating D3-type bone (thin porous cortical
leading to such failures may be lack of understanding of bone on the crest and trabeculer bone within) was se-
biomechanical factors.18,19 The contribution of several lected. Average and atrophic maxillary alveolar crests
factors, including biomechanical overload,20 direction were modeled according to measurements of Misch.41
and amplitude of forces,21-24 inadequate bone vol- Therefore, different bone dimensions were generated
ume,11,25-27 bone density,28-30 number of supporting to perform nonlinear calculations. The implant was
implants,23,31 angulation of implants in bone,32 and placed into an atrophic maxilla, with crestal bone heights
type of prosthesis33,34 make the in vivo examination of of 4, 5, 7, 10, or 13 mm. Spongy bone was modeled as
biomechanical factors related to implants too complex. a solid structure in cortical bone.28,42 Cortical bone
The load transferred to bone through the prosthesis thicknesses used in this study were an internal thickness
and implant, and careful planning and execution of the of 0.35 mm and external thickness of 0.7 mm beneath
prosthetic therapy, are important factors in achieving the maxillary sinus for all bone levels.
appropriate stress distribution in the bone.35,36 The A single-piece, 4.1 3 10–mm screw-shaped dental
manner in which bone is loaded may be essential to its implant system (solid implant, ITI; Institut Straumann
response. Bone is usually subjected to cyclic loads, AG, Waldenburg, Switzerland) was selected for this
with results that differ from static loads.34 If a sufficient study. Cobalt-Chromium (Wiron 99; Bego, Bremen,
number of repetitive load cycles are applied, stress mi- Germany) was simulated as a crown framework material,
crofractures in bone may occur. After bone microfrac- and feldspathic porcelain was used for the occlusal

JANUARY 2005 39
THE JOURNAL OF PROSTHETIC DENTISTRY KOCA, ESKITASCIOGLU, AND USUMEZ

Fig. 1. Values and distribution of loads applied to finite


element model.

Fig. 3. Localization areas of bone structure. CR-BCB, Crestal


ridge-buccal cortical bone; CR-PCB, crestal ridge-palatal
cortical bone; CR-MCB, crestal ridge-mesial cortical bone;
CR-DCB, crestal ridge-distal cortical bone; LW-MT, lateral
wall-middle third; LW-AT, lateral wall-apical third.

elastic, homogenous, and isotropic.26,28,29,34,43 The


corresponding elastic properties such as Young’s modu-
lus (E) and Poisson ratio (m) were determined from the
literature43-46 and are summarized in Table I. Models
consisting of elements and nodes are summarized in
Table II. A fixed bond between the bone and the im-
plant along the interface was presumed. An average oc-
clusal force of 300 N was used.20,38 A vertical load was
applied at the palatal cusp (150 N) and mesial fossa
(150 N) locations (Fig. 1).47
The final element on the x-axis for each design was as-
sumed to be fixed, which defined the boundary condi-
tion. The geometry of the tooth model has been
described by Wheeler.48 The applied forces were static.
Stress levels were calculated using von Mises stresses49
values. The von Mises stresses are the most commonly
reported in FEA studies to summarize the overall stress
state at a point.22-26,28,29,34,34 The analyses were per-
formed on a computer (Dual Pentium IV 2.0 GHz;
Toshiba Information Equipment, Manila, Philippines)
using software (COSMOSM, version 2.5; Structural
Fig. 2. Finite element model (4-mm bone level). Research and Analysis Corp, Los Angeles, Calif and
Pro/Engineer 2000i; Parametric Technology Corp).
surface. The implant and its superstructure were simulated Boundary conditions, loading, and mathematical mod-
using finite element software (Pro/Engineer 2000i; els were prepared with finite element software. The out-
Parametric Technology Corp, Needham, Mass). The puts were transferred to the COSMOSM program to
metal thickness used in this study was 1.0 mm with a por- display stress values and distributions. Data for stresses
celain thickness of 0.35 mm. Cement thickness layer was were produced numerically and color-coded. Figure 2
not modeled.42 All materials were presumed to be linear displays the FE-model.

40 VOLUME 93 NUMBER 1
KOCA, ESKITASCIOGLU, AND USUMEZ THE JOURNAL OF PROSTHETIC DENTISTRY

Fig. 4. Distribution of stresses within implant and cortical bone.

Fig. 5. Distribution of stresses within cortical bone for all bone levels.

Table III. Maximum stress values in all localizations (MPa)


Bone
Levels CR-BCB CR-PCB CR-MCB CR-DCB LW-MT LW-AT

4 mm 50 50 31 25 12 18
5 mm 50 50 25 18 12 18
7 mm 31 50 18 12 12 12
10 mm 25 50 12 12 12 12
13 mm 16 44 12 6 6 6
CR-BCB, Crestal ridge-buccal cortical bone; CR-PCB, crestal ridge-palatal
cortical bone; CR-MCB, crestal ridge-mesial cortical bone; CR-DCB, crestal
ridge-distal cortical bone; LW-MT, lateral wall-middle third; LW-AT, lateral
wall-apical third.

Bone structure was specified for 6 localized areas:


ridge crest, buccal cortical bone adjacent to implant Fig. 6. Maximum von Mises stress values in cortical bone, in
neck (CR-BCB); palatal cortical bone adjacent to im- all bone levels and in all localization areas.
plant neck (CR-PCB); mesial cortical bone adjacent to
implant neck (CR-MCB); distal cortical bone adjacent
RESULTS
to implant neck (CR-DCB); the middle third of the lat-
eral wall of the sinus (LW-MT); the apical third of lateral Figure 4, A, represents stress distribution within the
wall of the sinus, close to zygomatic process (LW-AT) porcelain superstructure. For all bone levels, maximum
(Fig. 3). von Mises stress values of 84 to 168 MPa were observed,

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THE JOURNAL OF PROSTHETIC DENTISTRY KOCA, ESKITASCIOGLU, AND USUMEZ

Fig. 7. Distribution of stresses within implants and abutments in all bone levels.

particularly on the mesial fossae and palatal cusp where levels in the posterior maxilla. The 7-, 10-, and 13-mm
the stresses were applied. Figures 4, B, and 5 represent bone levels predicted more even von Mises stresses
the stress distribution within the bone structure. There within the implant, and the stresses were localized in
was no stress within the spongy bone. The maximum smaller areas at cortical bone than 4-mm and 5-mm
von Mises stress values were observed in the cortical bone levels.
bone adjacent to the implant neck. In the past 2 decades, FEA has become an increas-
For the buccal cortical bone on the ridge crest, the ingly useful tool for the prediction of the effects of stress
maximum von Mises stress value was observed at the on the implant and surrounding bone. Vertical and
4-mm and 5-mm bone levels (50 MPa), and the low- transverse loads from mastication induce axial forces
est stress value was observed at the 13-mm bone level and bending moments and result in stress gradients in
(18 MPa). For the palatal cortical bone on the ridge the implants, as well as in the bone. A key factor for
crest, the maximum stress value was observed at 4-, the success or failure of a dental implant is the manner
5-, 7-, and 10-mm bone levels (50 MPa), and the in which stresses are transferred to surrounding bone.
lowest stress value was observed at the 13-mm bone FEA allows investigators to predict stress distribution
level (44 MPa). For the mesial cortical bone the max- in the contact area of implants with cortical bone and
imum stress value was observed at the 4-mm bone around the apex of implants in spongy bone.36
level (31 MPa), and the lowest stress value was ob- The model used in the present study made several as-
served at the 10- and 13-mm bone levels (12 MPa). sumptions regarding the simulated structures. The
For the distal cortical bone the maximum stress value structures in the model were all assumed to be homoge-
was observed at the 4-mm bone level (25 MPa), and neous, isotropic, and to possess linear elasticity. The
the lowest stress value was observed at the 13-mm properties of the materials modeled in this study, partic-
bone level (6 MPa). ularly the living tissues, however, are different.
For the middle third of the lateral wall of the sinus, Additionally, a 100% implant-bone interface was simu-
the maximum stress value was observed at the 4-, 5-, lated, which does not necessarily simulate clinical situa-
7-, and 10-mm bone levels (12 MPa), and lowest stress tions.20 Also, it is important to note that the stress
value was observed at the 13-mm bone level (6 MPa). In distribution patterns may have been different depending
the apical third of the lateral wall of the sinus, the max- on the materials and properties assigned to each layer of
imum stress value was observed at the 4-mm and 5-mm the model and the model used in the experiments.
bone levels (18 MPa), and the lowest stress value was ob- Furthermore, the cement layer was not modeled.
served at the 13-mm bone level (6 MPa). The maximum Thus, the inherent limitations in this study should be
stress values of localization areas shown in Table III and considered.
Figure 6. When applying FEA to dental implants, it is impor-
Figure 7 represents stress distributions within the im- tant to consider not only axial loads and horizontal
plant and abutment. At the 4- and 5-mm bone levels, the forces (moment-causing loads) but also a combined
maximum stresses were localized at the neck of the im- load (oblique occlusal force), because the latter repre-
plant, but at the 7-, 10-, and 13-mm bone levels, sents more realistic occlusal directions and, for a given
more even stresses were observed within the implants. force, will result in localized stress in cortical bone.22
In the current study, only vertical loads were considered.
The design of the occlusal surface of the model can
DISCUSSION
influence the stress distribution pattern. In the present
The results obtained do not support the research hy- study, the locations for the force applications were spe-
pothesis of an expected similar amount and localization cifically described as cusp tip and mesial fossa.
of functional stresses in implants placed in different bone However, the geometric form of the tooth surface can

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KOCA, ESKITASCIOGLU, AND USUMEZ THE JOURNAL OF PROSTHETIC DENTISTRY

produce a pattern of stress distribution that is specific for CONCLUSIONS


the modeled form. The pattern could be different with
Within the limitations of this study the following
even moderate changes to the occlusal surface of the
conclusions were drawn:
crown. Although this occlusal form exists for this model,
the same form would not represent all premolar teeth. In 1. For supporting bone levels of 4 and 5 mm, the
the present study, a 4.1 3 10-mm screw ITI dental im- maximum stresses were localized in wide areas, and for
plant was selected because no report on ITI standard levels of 7, 10, and 13 mm, the maximum stresses
4.1-mm diameter solid screw implant fractures could were localized in narrow areas.
be found in literature.21 2. At 4- and 5-mm bone levels, the maximum
Crestal bone loss is often seen clinically and is stresses were localized at the neck of implant, but at 7-,
a phenomenon which has been observed in different 10-, and 13-mm bone levels, more even stresses oc-
stages of implant loading as a decrease of radiological curred within the implants.
marginal bone level.26 In a number of radiological 3. The maximum stresses were localized on the pala-
long-term studies,17 FEA analyses,22-26,28,29,34,37-39 tal cortical bone for all bone levels. Only at the 4-mm
and photoelastic analyses,11,24 loaded implants and 5-mm bone levels did maximum von Mises stresses
showed typical bone loss around the implant neck. occur on both buccal and palatal surfaces.
The results of the current study indicated that maxi-
mum von Mises stresses occurred mainly at the palatal
surfaces of cortical bone adjacent to implant necks for
all models. Only at 4-mm and 5-mm bone levels did REFERENCES
maximum von Mises stresses occur on both the buccal 1. Adell R, Eriksson B, Lekholm U, Branemark PI, Jemt T. Long-term follow-
up study of osseointegrated implants in the treatment of totally edentulous
and palatal surfaces. jaws. Int J Oral Maxillofac Implants 1990;5:347-59.
The stresses were concentrated in the neck of implant 2. Jemt T, Lekholm U. Oral implant treatment in posterior partially edentu-
and were probably due to the rigid connection between lous jaws: a 5-year follow-up report. Int J Oral Maxillofac Implants
1993;8:635-40.
the implant and bone. The elastic modulus of cortical 3. Zarb GA, Schmitt A. The longitudinal clinical effectiveness of osseointe-
bone is higher than spongy bone and for this reason cor- grated dental implants in posterior partially edentulous patients. Int J Pros-
tical bone is stronger and more resistant to deforma- thodont 1993;6:189-96.
4. Knabe C, Hoffmeister B. The use of implant-supported ceramometal tita-
tion.12,30,35 A consistent observation from the current nium prostheses following sinus lift and augmentation procedures: a clin-
study was the concentration of maximum stress at the ical report. Int J Oral Maxillofac Implants 1998;13:102-8.
bone-implant interface and at the level of cortical 5. Garg AK. Augmentation grafting of the maxillary sinus for placement of
dental implants: anatomy, physiology, and procedures. Implant Dent
bone. According to the results of the present study, it 1999;8:36-46.
is suggested that loading an implant with low-volume 6. Misch CE. Maxillary sinus augmentation for endosteal implants: orga-
bone beneath the sinus floor might cause increased nized alternative treatment plans. Int J Oral Implantol 1987;4:49-58.
7. Winter AA, Pollack AS, Odrich RB. Placement of implants in the severely
stress concentration in the cortical bone, especially atrophic posterior maxilla using localized management of the sinus floor:
around the coronal portion of the implant. a preliminary study. Int J Oral Maxillofac Implants 2002;17:687-95.
Subsequently, marginal bone resorption might be initi- 8. Tatum H Jr. Maxillary and sinus implants reconstructions. Dent Clin North
Am 1986;30:207-29.
ated, if the load-bearing capacity of bone is surpassed. 9. Boyne PJ, James RA. Grafting of the maxillary sinus floor with autogenous
This may explain the decreased success rates that result marrow and bone. J Oral Surgery 1980;38:613-6.
when implants are placed in posterior sites with less 10. Bruschi GB, Scipioni A, Calesini G, Bruschi E. Localized management of
sinus floor with simultaneous implant placement: a clinical report. Int J
than 5 mm of bone. Oral Maxillofac Implants 1998;13:219-26.
For all bone levels tested, the highest stresses oc- 11. Ellegaard B, Kolsen-Petersen J, Baelum V. Implant therapy involving max-
curred within implants. This is likely due to the higher illary sinus lift in periodontally compromised patients. Clin Oral Implants
Res 1997;8:305-15.
modulus of elasticity of titanium that peaked at 155 12. Gross MD, Nissan J. Stress distribution around maxillary implants in ana-
MPa (Fig. 7). As titanium alloys are known to tolerate tomic photoelastic models of varying geometry: Part II. J Prosthet Dent
stresses of up to 900 MPa without irreversible deforma- 2001;85:450-4.
13. Isidor F. Loss of osseointegration caused by occlusal load of oral implants.
tion,37 the force of 300 N applied to the system was un- A clinical and radiographic study in monkeys. Clin Oral Implants Res
likely to cause implant failure. 1996;7:143-52.
Many finite element and photoelastic studies were 14. Sennerby L, Thomsen P, Ericson LE. A morphometric and biomechanic
comparison of titanium implants inserted in rabbit cortical and cancellous
based on block-shaped, nonanatomic models that bone. Int J Oral Maxillofac Implant 1992;7:62-71.
showed principal stress concentration at the apex of cyl- 15. Quirynen M, Naert I, van Steenberghe D. Fixture design and overload in-
inder-shaped implants on axial loading. These models fluence marginal bone loss and fixture success in the Branemark System.
Clin Oral Implants Res 1992;3:104-11.
did not simulate the hollow intricate anatomy of the 16. Block MS, Gardiner D, Kent JN, Misiek DJ, Finger IM, Guerra L. Hydroxy-
maxilla and facial skeleton.24 In the present study, differ- apatite-coated cylindrical implants in the posterior mandible: 10-year
ent patterns of stress distributions were demonstrated observations. Int J Oral Maxillofac Implants 1996;11:626-33.
17. Benn DK. Estimating the validity of radiographic measurements of mar-
around a maxillary implant with simulated maxillary si- ginal bone height changes around osseointegrated implants. Implant
nus geometry. Dent 1992;1:79-83.

JANUARY 2005 43
THE JOURNAL OF PROSTHETIC DENTISTRY KOCA, ESKITASCIOGLU, AND USUMEZ

18. Taylor TD, Agar JR, Vogiatzi T. Implant prosthodontics: Current perspec- 36. Geng JP, Tan KBC, Liu GR. Application of finite element analysis in
tive and future directions. Int J Oral Maxillofac Implants 2000;15:66-75. implant dentistry: A review of the literature. J Proshet Dent 2001;85:
19. Iplikcioglu H, Akca K, Cehreli MC, Sahin S. Comparison of non-liner fi- 585-98.
nite element stress analysis with in vitro strain gauge measurements on 37. Tepper G, Haas R, Zechner W, Krach W, Watzek G. Three-dimensional
a morse taper implants. Int J Oral Maxillofac Implants 2003;18:258-65. finite element analysis of implant stability in the atrophic posterior max-
20. Brunski JB, Nanci A. Biomaterials and biomechanics of oral and maxillo- illa: a mathematical study of the sinus flor augmentation. Clin Oral Impl
facial implants: Current status and future developments. Int J Oral Maxil- Res 2002;13:657-65.
lofac Implants 2000;15:650-61. 38. Ismail YH, Pahountis LN, Fleming JF. Comparison of two-dimensional and
21. Chapman RJ. Principles of occlusion for implant prostheses: guidelines for three-dimensional finite element analysis of a blade implant. J Oral Im-
position, timing, and force of occlusal contacts. Quintessence Int 1989; plantol 1987;4:25-31.
20:473-80. 39. DeTolla DH, Andreana S, Patra A, Buhite R, Comella B. The role of the
22. Holmgren EP, Seckinger RJ, Kilgren LM, Mante F. Evaluating parameters of finite element model in dental implants. J Oral Implantol 2000;27:77-81.
osseointegrated dental implants using finite element analysis. A two di- 40. Lekholm U, Zarb GA. Patient selection and preparation. In:
mensional comparative study examining the effects of implant diameter, Branemark P-I, Zarb GA, Albrektsson T, editors. Tissue-ıntegrated prosthe-
implant shape and load direction. J Oral Implantol 1998;24:80-8. ses: osseointegration in clinical dentistry. Chicag: Quintessence; 1985. p.
23. Hobkirk JA, Havthoulas TK. The influence of mandibular deformation, im- 199-209.
plant numbers and loading position on detected forces in abutments sup- 41. Misch CE. Contemporary implant dentistry. 2nd ed. St. Louis: Mosby;
porting implant supersuctures. J Proshet Dent 1998;80:169-74. 1999. p. 193-203.
24. Gross MD, Nissan J, Samuel R. Stres distribution around maxillary im- 42. Matsushita Y, Kitoh M, Mizuta K, Ikeda H, Suetsugu T. Two dimensional
plants in anatomic photoelastic models of varying geometry: Part I. J Pros- FEM analysis of hydroxyapatite implants: diameter, effects on stress distri-
thet Dent 2001;85:442-9. bution. J Oral Implantol 1990;16:6-11.
25. Clelland NL, Lee JK, Bimbent OC, Brantley WA. A three-dimensional fi- 43. Papavasiliou G, Kamposiora P, Bayne SC, Felton DA. 3D- FEA of osseoin-
nite element stres analysis of angled abutments for an implant placed in tegration percentages and patterns on implant bone interfacial stresses. J
anterior maxilla. Int J Prosthodont 1995;4:95-100. Dent 1997;25:485-91.
26. Meyer U, Vollmer D, Christoph B, Joos U. Bone loading pattern around 44. Farah JW, Craig RG, Meroueh KA. Finite element analysis of three- and
implants in average and atrophic edentulous maxillae: A finite-element four-unit bridges. J Oral Rehabil 1989;16:603-11.
analysis. J Cranio-Maxillofac Surg 2001;29:100-5. 45. Moroi HH, Okimoto K, Moroi R, Terada Y. Numeric approach to the bio-
27. Fugazzotto PA, Wheleer SL, Lindsay JA. Success and failure rates of im- mechanical analysis of thermal effects in coated implants. Int J Prostho-
plants in type IV bone. J Periodontol 1993;64:1085-7. dont 1993;6:564-72.
28. Holmes DC, Loftus JT. Influence of bone quality on stress distribution for 46. O’Brien JW. Dental materials and their selection. 2nd ed. Chicago: Quin-
endoosseos implants. J Oral Implantol 1997;3:104-11. tessence; 1997. p. 383-7.
29. Tada S, Stegaroiu R, Kitamura E, Miyakawa O, Kusakari H. Influence of 47. Eskitasxcxıoğlu G, Üsxümez A, Sevimay M, Soykan E, Ünsal E. The influence
implant design and bone quality on stres/strain distribution in bone of occlusal loading location on stresses transferred to implant-supported
around implants: A 3-dimensional finite element analysis. Int J Oral Max- prostheses and supporting bone: a three-dimensional finite element study.
illofac Implants 2003;18:357-68. J Prosthet Dent 2004;91:144-50.
30. Ichikawa T, Kanitani H, Kawamato N, Matsumato N, Wigianto R. Influ- 48. Wheeler RC, Ash MM. Atlas of tooth form. 5th ed. Philadelphia: W B
ence of bone quality on the stress distribution. An in vitro experiment. Saunders; 1984. p. 68.
Clin Oral Implants Res 1997;8:18-22. 49. Timoshenko S, Young DH. Elements of strength of materials. 5th ed. Flor-
31. Duyck J, Van Oosterwyck H, Vander Sloten J, De Cooman M, Puers R, ence: Wadsworth; 1968. p. 377.
Neart I. Magnitude and distribution of occlusal forces on oral implants
supporting fixed prostheses: An in vivo study. Clin Oral Implants Res Reprint requests to:
2000;11:465-75. DR ASLIHAN USUMEZ
32. Krekmanov L, Kahn M, Rangert B, Lindström H. Tilting of posterior man- SELCUK UNIVERSITY, FACULTY OF DENTISTRY, DEPARTMENT OF PROSTHODONTICS
dibular or maxillary implants for improved prosthesis support. Int J Oral CAMPUS / KONYA
Maxillofac Implants 2000;15:405-14. TURKEY 42079
33. Glantz P-O, Rangert B, Svensson A, Stafford GD, Arnvidarson B, Randow FAX: 190-332-2410062
K, et al. On clinical loading of osseointegrated implants. A methodolog- E-MAIL: asli_u@hotmail.com
ical and clinical study. Clin Oral Implants Res 1993;4:99-105.
34. Papavasiliou G, Kamposiora P, Bayne SC, Felton DA. Three dimensional 0022-3913/$30.00
finite element analysis of stress distribution around single tooth implants Copyright Ó 2005 by The Editorial Council of The Journal of Prosthetic
as a function of bony support, prosthesis type and loading during function. Dentistry
J Prosthet Dent 1996;76:633-40.
35. Stegaroiu R, Sato T, Kusakari H, Miyakawa O. Influence of restoration type
on stress distribution in bone around implants: a three-dimensional finite
element analysis. Int J Oral Maxillofac Implants 1998;13:82-90. doi:10.1016/j.prosdent.2004.10.001

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