Implant Complications
Implant Complications
Implant Complications
edical interventions involving surgical procedures for the insertion of devices such as stents, hip or knee prostheses, orthopedic devices, or dental implants are associated with risk. Before undergoing such interventions, the risks for failure or complications and chances of survival or success need to be carefully weighed by patients and professionals. A qualitative description of risk would relate a greater overall risk to a greater loss and greater likelihood that an event occurs.
In medicine, a risk factor is a variable associated with an increased risk of disease or infection. Risks are correlational and not necessarily causal. Risk factors are evaluated by comparing the risk of those exposed to the potential risk factor to those not exposed. For the purpose of the present review, mechanical and technical risks were defined as follows: Mechanical risk: Risk of a complication or failure of a prefabricated component caused by mechanical forces. Technical risk: Risk of a complication or failure of the laboratory-fabricated suprastructure or its materials. Mechanical and technical risks play a major role in implant dentistry. They may lead to increased rates of repairs and remakes, and to a waste of time and financial resources, and may even affect the patients quality of life. During treatment planning, constellations known to be associated with increased risk should be avoided. Risks associated with different treatment options must also be related to the financial consequences, especially when considerable price differences exist between the prosthetic options.
1Vice
Chairman and Graduate Program Director in Periodontology, Department of Periodontology, School of Dental Medicine, University of Bern, Bern, Switzerland. 2Chairman, Division for Fixed Prosthodontics, School of Dental Medicine, University of Bern, Bern, Switzerland. The authors reported no conflict of interest. Correspondence to: Prof Urs Brgger, Division for Fixed Prosthodontics, School of Dental Medicine, University of Bern, Freiburgstrasse 7, CH-3010 Bern, Switzerland. Fax: +41 31 632 4931. Email: urs.braegger@zmk.unibe.ch This review paper is part of the Proceedings of the Fourth ITI Consensus Conference, sponsored by the International Team for Implantology (ITI) and held August 2628, 2008, in Stuttgart, Germany.
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A series of systematic reviews were launched to estimate and compare the failure/complication rates to be expected with various types of fixed reconstructions on teeth and implants.18 With some of the reconstructions, considerably increased rates of failures were estimated to occur over 10 years of function6: fixed dental prostheses (FDPs) with cantilever extensions on teeth (19.6%), combined toothimplant-supported FDPs (22.3%), and resin-bonded FDPs (35.0%). The protocols of the systematic reviews mentioned above were designed to include publications reporting on the prosthetic failure and complication rates with a particular design of a reconstruction, ie, full-arch FDPs on implants/teeth, short-span FDPs on implants and teeth, and single crowns, over at least 5 years. Excluding multiple other factors that may mask a correlation with a particular risk factor seems to be difficult when combining data from cohort studies being performed at various centers. According to the definition of risk factor mentioned above, long-term studies that evaluated and compared the risk of those patients/reconstructions exposed to a certain risk factor to those not exposed to that risk factor in the same environment are of particular interest. Therefore, the aim of this review was to systematically screen the literature for information answering the following focused question: Which mechanical/ technical risk factors have an impact on implant-supported reconstructions?
Selection Criteria
Randomized controlled trials (RCTs), controlled trials, and prospective and retrospective cohort studies with a mean follow-up time of at least 4 years were included. The material evaluated in one study had to include cases with the risk factor and cases without exposure to the risk factor. The following inclusion criteria were used: Mean follow-up time 4 years At least five patients included Studies on fully and partially edentulous patients Studies on fixed and/or removable implant-supported dental prostheses Studies on fixed dental prostheses with cantilever extension(s) Studies on implant-supported single-unit crowns Studies on implant- and/or tooth-implant-supported reconstructions Studies on cylindrical and/or cylindrical-conical solid-screw implants Clinical examination at the follow-up visits Detailed information on the characteristics of the implants and their supported reconstructions The following exclusion criteria were used: Animal studies in vitro studies Studies based on patients records, surveys, questionnaires, or interviews Studies focusing exclusively on finite element analysis (FEA) Studies focusing exclusively on implant length and/or diameter Studies focusing exclusively on patient-centered outcomes Reviews Case reports Abstracts
Validity Assessment
Two reviewers (UB and GES) screened titles and abstracts identified through the search for possible inclusion. The discrepancies were resolved by discussion. Publications of potential interest were obtained in order to evaluate the full text. Both reviewers screened the included publications independently using the inclusion criteria. Again, any disagreement was resolved by discussion between the two reviewers.
Data Extraction
Collectively, the outcome variables included:
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Implant-related mechanical and technical risk factors Abutment-related mechanical and technical risk factors Suprastructure-related mechanical and technical risk factors Depending on the presence or absence of a specific mechanical or technical risk factor, survival and success rates of implants, abutments, and related suprastructures were extracted from the publications. Sur vival was defined as presence of the implant, abutment, and/or its suprastructure in situ in its original extension at follow-up examination with or without complications. Success was defined as presence of the implant, abutment, and/or suprastructure in situ without any mechanical or technical complications during the entire follow-up period. From the included papers, the following information was extracted: the number of patients examined, the mean age of the patients, the mean observation time, the number of implants restored, the implant system used, the designs of the reconstructions under examination, and the study design applied. Finally, the major findings related to harm to the suprastructure, prosthetic components of the implant systems, peri-implant tissues, implants, and results of statistical analyses were noted and grouped according to potential risk factors.
Potentially relevant publications identified from the online search (n = 3,568) Publications excluded on the bases of title and abstract evaluation (n = 3,457) Potentially relevant full-text articles retrieved for detailed evaluation (n = 111) Publications excluded on the basis of full-text evaluation (n = 78) Publications included based on the MEDLINE database search (n = 33) Publications included based on the manual search (n = 2) Publications included in the present systematic review (n = 35) Fig 1 tions. Selection process used to identify the included publica-
RESULTS
Of the 3,568 titles resulting from the online search, 111 were selected for full text review after reading the abstract. From the 111 full-text articles, 33 were included for data extraction. Two additional articles were included based on a manual search (Fig 1). The data from 35 publications were grouped according to 10 risk factors identified after screening the literature: Type of retentive elements supporting overdentures Cantilever extension(s) on fixed dental prostheses (FDPs) Cemented versus screw-retained FDPs Angled/angulated abutments Bruxism Crown-to-implant ratio Length of the suprastructure Prosthetic materials Number of implants supporting an FDP History of mechanical/technical complications
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Table 1 Randomized Controlled Trials with Edentulous Mandibles Restored with Various Overdenture Designs on Different Implant Systems: Results after 5 and 10 Years of Observation
Study
63.7 (3685) 60 mo 72 Nobel Biocare 12 Dolder bar 12 magnet 12 ball Prospective randomized RCT
Year
No. of patients
Mean Mean age, observation No. of y (range) time implants Implant system Overdenture design Type of study Summary of results
Naert et al10
1999
36
Gotfredsen et al11
2000
26
Meijer et al12
2004
90
Timmerman et al15
2004
110/103
Meijer et al13
2000
61
Visser et al16
2005
60
Meijer et al14
2004
61
Naert et al10
2004
36
Table 2
Study
66 62 mo 115 Nobel Biocare (12106 mo) 8-y life table Round bar/ball 18 maxillary/ 32 mandibular RCT 75 round bar or ball versus 44 rigid bar Consecutive patients Random assignment
Year
Mean No. of age, y patients (range) Implant system Findings Designs of reconstruction Study design
1998
49
2002
119
63 (4090)
9.3 y (515 y)
258
Straumann
Nedir et al19 NR 8-y life table 60 mo 180 Straumann Consecutive patients 145 Straumann 41 ball/14 bar Consecutive patients
2006
55
Oetterli et al20
2001
Risk of complication: old components, new components Bone anchoragelever arm was a risk factor More denture fractures with bar versus ball (no framework) More implant loss in maxilla (25%) versus mandible (0%) No risk factor for implant loss No significant difference in time to change of retention mechanism between resilient and rigid Rate of prosthetic maintenance service = event per patient per year at 5 years (no significant difference between the 2 retention systems) For resilient: more complications with retainers, more denture base resin fractures, hyperplasia, relining For rigid: fracture of bar extension, retightening of female part Rates at 5 years similar, advantage for rigid related to time needed for service. No risk factor for implant loss Event rate per year: 1.5 with ball, recurrent events 0.9 mm with bar Free of complications 57.1% with bar, 24% with ball (P < .04) Supportive surface and position of implant as well as retention mechanism No risk factor for implant loss
2002
233
Supportive surface, bent clipbars, U-shaped extension bars, mandible o: angle between axis connecting implants and mandibular hinge axis Maxilla: full-arch prosthesis 55; Milled bar 19; Dolder bar 16 Mandible: full-arch prosthesis 40; Milled bar 84 Dolder bar 44
Prospective multicenter
2001
48
Survival of prosthesis: Maxilla: full-arch prosthesis 96.4%; Milled bar 94.7%; Dolder bar 87.5% Mandible: full-arch prosthesis 100%; Ball anchor 99%; Dolder bar 98% Implant success: Maxilla: full-arch prosthesis 92.1%; Milled bar 92.2%; Dolder bar 86.9% Mandible: full-arch prosthesis 96.2%; Ball anchor 93.7%; Dolder bar 93.9% Catastrophic results: 50% of overdentures were remade, 30% required a reline Only 83% implant survival HA implants lost a lot of bone
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bar (11 cases, 1.0 events per year).11 Over 5 years, 48 complications/repairs were observed in the ball group and 53 in the bar group. Mainly during the first year of function, there were statistically significantly more complications/repairs in the bar group. However, some of the technical complications were related to the devices needed for radiographic standardization. Meijer et al12 followed overdentures with Dolder bars on three different implant systems (IMZ, Nobel Biocare, and Straumann). Over 5 years, there was no effect on the implants and no information was presented on prosthetic aspects. In an earlier report by the same group comparing overdentures on IMZ and Nobel Biocare implants, multiple prosthetic revisions were noted.13 When the same patients were followed over 10 years,14 the 56 surviving overdentures with round bars and Ackermann clips required 256 prosthetic actions, including replacement of broken abutments and loose clip screws, placement of new bars or gold cylinders and new or fastening clips, relining of maxillary or mandibular dentures, repair of denture bases or teeth, readjustment of occlusion, and provision of new maxillary and mandibular dentureswith no obvious difference between the IMZ and Nobel Biocare groups. A clinical implant performance scale was used to score the events. With a mean score of 1.3 for the IMZ group and 1.2 for the Nobel Biocare group, the clinical outcomes appeared to be similar. Three types of overdenture designs were compared comprehensively using a computerized random allocation procedure.15 Thirty-six overdentures were attached to two ball anchors, 37 to a bar on two implants, and 37 to a bar on four implants. General satisfaction with phonetics, esthetics, and social functioning remained high. The score reflecting satisfaction with retention and stability of the overdenture decreased significantly in the group with two ball attachments. Comparing 30 overdentures with bars on two implants to 30 overdentures with bars on four implants, Visser et al16 found a tendency for more biological complications with four implants but a higher need for prosthetic aftercare on two implants (not statistically significant). Six additional studies were found in which overdentures with different attachment systems were compared longitudinally. In these studies, allocation of the groups was not performed using randomization (Table 2). Forty-nine patients with maxillary and mandibular overdentures were followed over 62 months (range 12 to 106 months).17 When patients received overdentures either on ball anchors or on a round bar, the overdentures that were not reinforced with a metal
74 Volume 24, Supplement, 2009
framework were at high risk of fracturing. In the bar group, 30 of 36 patients required denture repairs. In the maxilla, 25% of the originally placed implants were lost compared to none in the mandible. The amount of bone anchorage in relation to the lever arm was higher in the lost implants (mean lever armbone anchorage ratio of 1.3) than in all implants placed (a mean lever armbone anchorage ratio of about 1). Over an observation period of 5 to 15 years (mean 9.3 years), 119 patients with implant-supported overdentures were monitored at regular intervals.18 The rate of prosthetic maintenance per patient over 5 years was similar for the resilient and rigid types of fixation applied. However, the characteristics of the complications differed. Whereas resilient attachments had more complications with retainers, more denture base resin fractures, mucosal hyperplasia, and denture relines, the rigid support attachments had more fractures of bar extensions and needed retightening of female parts. It was obvious that rigid fixation was an advantage, since less time was required for services. The time to the first change of a component was not significantly different for resilient versus rigid attachments. The amount of aftercare in patients with overdentures was assessed cumulatively up to 8 years by Nedir et al.19 The percentage of overdentures remaining free from complications was 57% for the bar devices but only 24% for overdentures with ball anchors (P < .04); 1.5 events per year were noted in the ball attachment group, whereas 0.9 events per year per patient occurred in the bar group. Anatomical, morphologic, and prosthetic variables are considered to be of importance when selecting a particular implant position. Oetterli et al20 evaluated the casts and clinical parameters of 90 edentulous patients, each one with two intraforaminal implants supporting an overdenture. The angle between the virtual axis connecting both implants and the mandibular hinge axis was measured on mounted casts. The supporting surface was identified between bent clip bars and U-shaped extension bars. Seventy patients could be evaluated clinically after 5 years. The positions and retention mechanism of mandibular implants supporting an overdenture had little influence on the clinical parameters assessed. No data related to technical/mechanical complications were reported. The long-term function (10-year life table) of overdentures was compared to the clinical outcome with full-arch fixed prostheses in a study including 233 patients receiving 163 overdentures and 95 fixed fullarch prostheses.21 The survival rates for overdentures on Dolder bars were 87.5% for the maxilla and 97.7%
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for the mandible. Survival of full-arch prosthses was 96.4% in the maxilla and 100% in the mandible. Overdentures on milled bars had a 94.7% survival rate in the maxilla, and overdentures on ball anchors in the mandible had a 98.8% survival rate. One study reported a dramatic incidence of implant loss (27% over 4 to 6 years), remakes of overdentures (50%), and relinings (30%).22 Handling such frequent catastrophic events would be highly impracticable in daily clinical practice.
edentulous patients. Fifteen of the FDPs had a distal cantilever extension and 34 a mesial cantilever extension. After a mean follow-up of 4 years, no negative effects related to the presence of the mesial or the distal cantilever extension were found.
Table 3
Extension
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Study
130 Astra Tech Consecutive patients 5-y survival
Year
Wennstrm et al24
2004
45
Shackleton et al23
1994
25
Romeo et al25
2004
NR
Nedir et al19
2006
NR
Table 4
Study
NR 4 y after loading 50.8 mo Straumann 40 I-I 58 T-T 18 I-T 24 Biomet 3i 12 cemented
Year
Mean No. of age, y patients (range) No. of implants Implant system Designs of reconstruction
Study design
12 screw-retained
Findings
Vigolo et
al27
2004
12
2001
85
Retrospective cohorts
Prospective randomly assigned No complications at all No influence on bone and soft tissue 13/79 cemented with complications 3/26 screw-retained with complications (ns) No influence on implant loss 8-year life table Consecutive
2006
NR
De Boever et al29
2006
105
No significant difference in complication rate No influence on implant loss 29 complications out of 127 (22.8%) 26 complications out of 45 (57%) P < .001 No influence on implant loss
NR = not recorded; ns = not significant; FDP = fixed dental prosthesis; I-I = implant-to-implant FDP; I-T = implant-to-tooth FDP; T-T = tooth-to-tooth FDP.
Table 5
Observation No. of time implants Factors No information on prosthetic complications No increased risk of technical complications Finding for reconstruction Finding for implants Survival probability for implants NS 10 y 3,101 Ankylos Implant system
Study
Year
No. of patients
Sethi et al30
2002
NR
2007
38
5y
69
Astra Tech
From 045 degrees; 264 implants > 15 degrees, 352 implants 15 degrees 36 axial (04 degrees inclination) versus 33 nonaxial (1230 degrees)
Table 6
Bruxism
Study
55.7 (2383) NR NR 301 Nobel Biocare 56.8 mo 103 (142 teeth) Straumann FDPs: 40 I-I; 58 T-T; 18 I-T
Year
No. of patients
Mean observation Mean age, time y (range) (range) No. of implants Implant system Design of reconstructions Type of study
Retrospective cohorts Clustered failures as test group versus matched control group
Findings
Brgger et
al28
2001
85
Ekfeldt et al32
2001
54
13/75 nonbruxers (17.3%) had technical complications and 6/10 bruxers (60%) had complications P < .01 No influence on implant loss In the test group with clustered losses, there were 7 patients with bruxism Heavy influence on implant loss
105
Consecutive
17/43 (39%) had complications in the bruxing group 29/126 (23%) had complications in the non-bruxing group; P < .001 No influence on implant loss
2006
109
Nobel Biocare
Consecutive patients
22.6% of the patients were defined as bruxers; they had 50% of the veneer fractures; however, ns No significant influence on implant loss Straumann Consecutive No statistically significant increase in complication rate for FDPs and overdentures NS
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Nedir et al19
2006
NR = not recorded; FDP = fixed dental prosthesis; NS = not significant; I-I = implant-to-implant FDP; I-T = implant-to-tooth FDP; T-T = tooth-to-tooth FDP.
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Bruxism (Table 6)
Based on clinical experience, probably every dentist would group bruxers into a high-risk category for technical and mechanical complications and failures. Even implant fractures seem to occur more frequently in bruxers according to case reports. The present literature search indicated five studies in which bruxers were compared to nonbruxers. In two of the clinical reports, statistically significantly higher rates of mechanical/technical complications (ie, 17.3% and 23%) and failures (ie, 60% and 39%) were found in bruxers compared with nonbruxers.28,29 In two additional publications, trends toward more frequent mechanical/technical complications and implant losses were observed in bruxers.32,33 Nedir et al,19 however, found no increased rate of complications in FDPs and overdentures in bruxers compared to nonbruxers.
Table 7
Crown-to-Implant Ratio
Study
59.6 (2280) 53 mo 262 Nobel Biocare Consecutive patients Consecutive patients Consecutive patients
Year
Mean observation time (range) No. of implants Implant system Crown-to implant ratio
No influence on bone loss No risk factor for implant loss No influence on bone loss No risk factor for implant loss No influence on bone loss No risk factor for implant loss
Tawil et
al33
2006
109
2005
74
2007
83
123 FDPs ranged from C:I < 1 to > 2 for 234 implants 30 were < 1, 8 > 2 22: 1.0 157: 1.12.0 20: > 2.0 8: 00.99 133: 11.99 51: 2
Table 8
Length of Reconstruction
Study
2586 62.5 25.3 mo 283 Straumann
Year
Type of study
Consecutive patients
Design of reconstruction
80 SC 39 two connected crowns 38 3- to 4-unit FDP
Findings
25% of SC had complications 35% of two connected crowns had complications 44% of 3- to 4-unit FDP had complications, P < .04
De Boever et
al29
2006
105
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DISCUSSION
Data Extraction
The main objective of this report was to extract published evidence related to mechanical/technical risk factors for any kind of damage to an implant-supported reconstruction. We searched for technical and/or biological complications or failure rates experienced with or without exposure to a certain mechanical/technical characteristic. Studies related to implant sur faces, loading protocols, toothimplantsupported reconstructions, implant length, and width of the platform were excluded.
Table 9
Material Aspects
Study
60 5y NR Astra Tech 13 FDP mandible Chicago IV gold alloy A 13 FDP Palliag M silver palladium B Not randomized
Year
Mean Mean age, observation No. of y (range) time (range) implants Implant system Design of reconstruction/ materials used
Murphy et
al36
2002
26
Jemt et al37 56 11 50 12 5y 170 Nobel Biocare Groups arranged at random, split mouth
2003
42
2004
36
Consecutive
2003
32/30
21 FDP ceramometal cast framework left 21 FDP ceramometal cast framework right with low-fusing porcelain 21 with titanium framework prosthesis with low-fusing porcelain 27 prostheses with abutment 19 at implant level, Cresco Ti Precision 53 ceramic abutments (Ceradapt alumina ceramic) 50 titanium abutments 19 FDP on ceramic abutments 17 FDP on titanium abutments/29 left Short FDP Consecutive
Similar number of events for technical complications No influence on bone loss; no risk factor for implant loss No difference in prosthesis survival, more porcelain chips with titanium 19% versus 10% (P > 0.3) No risk factor for implant loss No more bone loss No difference in complication rates No difference in bone loss around implants Patients satisfied with esthetics Only one ceramic abutment failed No influence on implant bone loss
Table 10
Number of Implants
Study
65 (3291) 9.5 (518) y 375 Nobel Biocare
Year
No. of patients
Mean Mean age, observation No. of y (range) time (range) implants Implant system
Type of study
Not randomized
Findings
Eliasson et
al41
2006
178
2004
34
Nobel Biocare
30 FDP on 2 implants 74 FDP on 3 implants Nobel Biocare Maxilla: 14 FDP on 4 implants 70 FDP on 6 implants Mandible: 13 FDP on 4 implants 59 FDP on 6 implants
Brnemark et al40 NR 10 y
1995
156
882
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Survival rate 96.8%/97.6% More screw loosening with 2 implants; P < .05 More porcelain fractures with 3 implants; P = .05 No influence on implant loss and bone loss Small difference in ISQ value No influence on reconstruction No influence on implant loss Function of prostheses over 10 y was same All mandibular prostheses stable 1/14 on 4 implants lost 6/70 on 6 implants lost in the maxilla Survival of implants 88.4%/ 93.4% Higher risk to lose an implant if only 4 were placed
NR = not recorded; ISQ = implant stability quotient; FDP = fixed dental prosthesis.
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0: Success, no complications 1: Minor complications, such as: gingival hyperplasia, relining of maxillary or mandibular dentures, readjustment of occlusion, clip loosening, coping/ screw loosening, broken abutment, a slight disturbance of the mental nerve, probing depth = 6 mm, or x-ray score 1 with PPD 5 mm 2: Complications with a chance of recovery or stabilization of the present situation, such as: correction of a non-fitting superstructure, fracture of the superstructure, a severe disturbance of the mental nerve, x-ray score 1 with PPD 6 mm, or x-ray score 2 with PPD 5 mm 3: Serious complications that may lead to failure of the implant system: X-ray score 2 with PPD 6 mm or x-ray score 3 4: Failure of the implant system: removal of one or two implants after placement of the suprastructure The x-ray score 0 related to no apparent bone loss; 1, to a reduction < 1/3 of the length of the implant; 2, to a reduction between > 1/3 and < 1/2 of the implant length; and 3, to a reduction > 1/ 2 of the implant length. Pooling wide ranges of biological and technical complications in the same category may mask clinically important differences between groups.43 In 2006, Nedir et al grouped prosthetic complications of overdentures into foreseeable and nonforeseeable events. 19 Change of female parts of the spherical attachment, change of the clip, and relining were categorized as foreseeable. Mechanical retention problems, repair and replacement of the overdenture, and complications of the opposing complete denture were unforeseeable complications in the overdenture group. For the fixed restoration group, complications were graded as minor or major. A fracture was considered major if it affected esthetics, caused the metal framework to be visible, resulted in a missing interproximal contact point, or caused the patient to complain of tongue- or masticatory-related discomfort. Major fractures resulted in a prosthesis remake; minor fractures did not lead to remakes. In a series of systematic reviews on complication and failure rates reported with various types of reconstructions on teeth and implants, the extracted data were listed as the estimated event rates per 100 reconstructions per year, considering the actual exposure time and assuming no change in the longterm risk intensity. 6 Statistically significantly increased failures rates were calculated for cantilever FDPs on teeth and tooth-implantsupported FDPs compared to FDPs on teeth without extension, implant-supported FDPs, and single crowns on implants over 10 years. In addition, statistically signifi-
Type of study
Consecutive
Prospective
Of 30 failures with reconstructions, 15 had major so-called retrievable complications before Odds ratio 3.55; P < .001 Loss of retention leading to technical failure; Odds ratio 17.6 (3.686.4); P < .001 Fracture of porcelain leading to technical failure; Odds ratio 11.0 (2.157.9); P < .004 Brgger et al44
SC = single crowns; FDP = fixed dental prosthesis; I-I = implant-to-implant FDP; I-T = implant-to-tooth FDP.
Findings
No. of implants
Brnemark
No. of patients
152
1997
Parein et al43
Table 11
Study
2005
Year
89
58.9 (2888)
55.7 (1490)
10 (812) y
4.2 y
392
Straumann
Implant system
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cantly increased complication rates were calculated for loss of vitality and loss of retention when comparing cantilever FDPs with conventional FDPs. The 5year complication rates were similar for the implant-supported FDPs and single crowns.
identified as a risk factor. Both of two extracted papers on angled abutments did not indicate that angulations > 15 degrees for the abutments and the prosthesis had any effect on the outcome. The patient risk factor bruxism resulted in significantly increased event rates in two studies, in trends for higher rates in two studies, and in no difference in one report. From a retrospectively assessed cohort of 368 patients with 838 endosseous implants, 19 cases were selected in which there were technical/ mechanical complications such as implant fractures, abutment fractures, screw loosening, occlusal wear, or damage to the prosthesis.46 The 19 patients were evaluated for sleep bruxism using polysomnographic analysis. Most of the bruxism episodes occurred during light sleep and did not cause arousal, and the patients were unaware of the nocturnal parafunctional habits. Bruxism was reported to have continued despite the fact that all these patients were provided with a nightguard. Crown-to-root ratio, material aspects, and the number of implants placed were not identified as risk factors for increased failure/complication rates. The complexity of a reconstruction, expressed as the number of units, was identified as a risk in only one study, and having had a previous complication was identified as a risk in two. The implant length in relation to the height of the suprastructure as well as the number of implants needed to physically support an FDP and assure its function are risk factors related to the quality and quantity of the osseointegration and the torque needed to disrupt the chemical and histologic bonding between the supporting bone and the implant surface. Efforts to improve osseointegration in implant dentistry by modifying the surface characteristics, such as the topography and chemistry, have led to much more reliable clinical results compared to the original machined implants when using shorter and fewer implants.47,48
Limitations/Critical Remark
The fact that some of the mechanical/technical characteristics evaluated were not identified as true risk factors in this review does not mean that they are not, in fact, risks. Limitations of the study designs, too many uncontrollable variables, small number of subjects, etc, may have hidden the actual facts in some of the studies.
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CONCLUSIONS
Mandibular overdentures: Independent of the retentive element system used, patients required multiple prosthetic services during the observation period (six RCTs). Technical/mechanical complications occurred more frequently with a ball attachment than with a bar retentive system (one RCT). With respect to retention, patients were most satisfied with a bar retentive system, followed by ball anchors, and least satisfied with magnets (one RCT). Metal frameworks protected overdentures from fractures (one consecutive case study). The presence of cantilever extensions was not associated with increased mechanical/technical risks for implants supporting short-span FDPs (three consecutive case studies). The presence of cantilever extensions > 15 mm was associated with an increased risk of full-arch FDP fracture compared with the presence of cantilever extensions 15 mm (one consecutive case study). No increased mechanical/technical risks for FDPs were observed in three of four studies (one prospective, one retrospective, and one consecutive case study) comparing screw-retained versus cemented reconstructions. The presence of angled/angulated abutments was not associated with increased mechanical/technical risks for implant-supported FDPs (one consecutive case study). Increased mechanical/technical risks for FDPs were observed in bruxers in four of five studies (two retrospective and two consecutive case studies) comparing bruxers and nonbruxers. The crown-to-implant ratio was not associated with implant loss and marginal bone loss of implants supporting FDPs (2 consecutive case studies). Increased mechanical/technical risks for FDPs were observed in 1 study (consecutive cases) comparing 3- to 4-unit FDPs with single crowns and double crowns. Increased mechanical/technical risks for FDPs were observed in two studies (consecutive case studies) comparing FDPs with and without a history of complications. Regarding the survival/success rate of the implant, none of the 10 listed mechanical/technical risks had an influence.
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