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Article
IPS e.max for All-Ceramic Restorations: Clinical
Survival and Success Rates of Full-Coverage Crowns
and Fixed Partial Dentures
Silvia Brandt 1, * , Anna Winter 2, Hans-Christoph Lauer 1, Fritz Kollmar 3,
Soo-Jeong Portscher-Kim 1and Georgios E. Romanos 4,5
1Department of Prosthodontics, Center for Dentistry and Oral Medicine (Carolinum), Johann Wolfgang
Goethe University, Theodor-Stern-Kai 7, 60596 Frankfurt, Germany; h.c.lauer@em.uni-frankfurt.de (H.-C.L.);
s.kim@med.uni-frankfurt.de (S.-J.P.-K.)
2Department of Prosthodontics, Center for Dentistry, Oral Medicine, Julius Maximilian University,
Pleicherwall 2, 97070 Würzburg, Germany; e-winter_a3@ukw.de
3Private Practice Dr. Fritz Kollmar, Friedrich-Ebert-Straße 55, 34117 Kassel, Germany; fitz@dreskollmar.de
4Department of Oral Surgery and Implant Dentistry, Center for Dentistry and Oral Medicine (Carolinum),
Johann Wolfgang Goethe University, Theodor-Stern-Kai 7, 60596 Frankfurt, Germany;
georgios.romanos@stonybrook.edu
5Germany and Department of Periodontology, School of Dental Medicine, Stony Brook University, Stony
Brook, NY 11794, USA
*Correspondence: hajjaj@med.uni-frankfurt.de; Tel.: +49-69-6301-83617; Fax: +49-69-6301-3711
Received: 17 December 2018; Accepted: 29 January 2019; Published: 2 February 2019
Abstract:
The IPS e.max system by Ivoclar Vivadent, offering a variety of products and indications,
is widely used for all-ceramic restorations. We analyzed the clinical track record of these products in
daily clinical practice, associating their restorative survival rate with various parameters to define
recommendations for long-term stability. A total of 1058 full-coverage crowns and fixed partial
dentures (FPDs) were evaluated retrospectively over up to 66.48 (37.05
±
18.4) months. All were
made of IPS e.max Press, IPS e.max CAD, IPS e.max Ceram or IPS e.max ZirPress and had been
delivered by a private dental practice within three years. Uses not recommended by the manufacturer
were also deliberately included. The five-year cumulative survival was 94.22% (i.e., 94.69% or
90.58% for glass-ceramic crowns or FDPs and 100% or 90.06% for zirconia-based crowns or FDPs).
Significantly superior outcomes emerged for conventional vs. adhesive cementation and for vital vs.
non-vital abutment teeth, but not for recommended vs. non-recommended uses. Caution is required
in restoring non-vital teeth, but the spectrum of recommended uses should generally be reconsidered
and expanded, given our finding of high survival and success rates for IPS e.max ceramics, even for
uses not currently recommended by the manufacturer.
Keywords:
IPS e.max system; full-contour crown restorations; fixed partial dentures; survival rate;
success rate
1. Introduction
Patients increasingly know about the availability of dental materials that are both esthetically
pleasing and biocompatible [
1
,
2
]. All-ceramic restorations combine high biocompatibility with good
optical and material properties [
3
], thus meeting both patient expectations and clinical requirements [
4
].
This is why this particular segment of the dental market has been growing for some decades [
2
].
All-ceramic restorations may be considered an evidence-based treatment modality, given a large
number of available studies [
5
–
7
]. All-ceramic crowns have been shown
in vitro
to be a good alternative
Materials 2019,12, 462; doi:10.3390/ma12030462 www.mdpi.com/journal/materials
Materials 2019,12, 462 2 of 10
to metal-ceramic crowns [
8
] and clinical results to the same effect were provided by Etman and
Woolford [9].
On closer examination, however, many studies have limitations such as narrow indications or
small case numbers [
10
–
13
]. Another problem is strict inclusion and exclusion criteria, resulting in
the overrepresentation of stable periodontal health and good oral hygiene [
12
–
17
] while turning a
blind eye to cases involving temporomandibular dysfunction [
11
–
13
]. Hence, the qualifications that
often get attached to the study of restorations have a way of removing the cases studied from daily
clinical practice, where clinicians need to consider a variety of patient-specific risk factors whenever
they plan and deliver dental restorations. Sometimes they conclude that pushing beyond the spectrum
of indications for a given material is the way to go and, with the patient’s consent, will proceed to
implement this plan.
There is a need for these clinicians to select from a multitude of ceramic materials that are intended
for different indications, require different procedures and come with different recommendations for
retention. IPS e.max (Ivoclar Vivadent, Ellwangen, Germany) is a lithium-disilicate system encompassing
a comprehensive range of products for diverse uses and processing techniques. Being a glass-ceramic
material, lithium silicate combines the advantages of permitting, although not requiring, adhesive
luting for retention [
18
] in addition to offering maximum esthetics [
10
] and high fracture resistance [
19
].
Thanks to these benefits, it is a material widely used in clinical practice.
Given the increasing use of all-ceramic restorations in clinical practice, it is only reasonable
to investigate them under real-life clinical conditions as well. To fill the aforementioned gaps left
by the limiting inclusion and exclusion criteria of previous studies, we designed a retrospective
investigation into the survival rates of all-ceramic IPS e.max restorations with no exclusion criteria
applied, specifically including uses of the material not currently recommended by its manufacturer.
Another goal was to analyze how the restorative failures involved were related to specific clinical
parameters, thus helping to avoid errors and improve survival in daily clinical practice.
2. Materials and Methods
All restorations here evaluated had been delivered in a private practice in Germany between June
2011 and June 2014. The baseline totality of eligible restorations was 1101 full-coverage crowns and
fixed partial dentures (FPDs) made from IPS e.max Press, IPS e.max CAD, IPS e.max Ceram or IPS
e.max ZirPress (Ivoclar Vivadent). All these restorations met our requirement of having been fabricated
in the same dental laboratory in accordance with the manufacturer’s instructions. For evaluation in
this study, we additionally required that the patients complied with follow-up visits.
Given that 43 of these 1101 restorations were not followed up in the years to come, a total
of 1058 restorations eventually met all inclusion criteria for evaluation. Since our intention was to
evaluate the IPS e.max system under real-life conditions, we applied no exclusion criteria, thus specifically
including uses of the material not currently recommended by its manufacturer. Table 1gives an overview
of how the various restorative products were distributed across the 1058 evaluable restorations.
Table 1. Distribution of restorative materials across the 1058 restorations.
Materials n Distribution
Total 1058 100.00%
IPS e.max Press 861 81.38%
Zirconia framework + IPS e.max
ZirPress 87 8.22%
IPS e.max CAD 50 4.73%
Zirconia framework + IPS e.max
Ceram 30 2.84%
IPS e.max Press + IPS e.max
Ceram 27 2.55%
IPS e.max Ceram 3 0.28%
Materials 2019,12, 462 3 of 10
For statistical analysis, general information (age, gender, anonymized patient ID) and additional
treatment-related details were entered in spreadsheet software (Microsoft Excel). The patients were
divided into different groups according to their age at the time of incorporation (
≤
30 years, 31–50 years,
51–70 years,
≥
70 years). The parameters thus recorded included: abutment topography; type
of support by implant and or natural abutment(s); vitality or non-vitality of natural abutments;
nature of the opposing dentition; restorative design; restorative material; use for a recommended
or non-recommended indication; luting technique; technician in charge of fabrication; interval from
delivery to latest follow-up; as well as occurrence and management of complications and failures.
Any complete loss of a restoration was defined as a restorative failure influencing the survival
curve of the time-to-event analysis. Kaplan–Meier probabilities of survival time could then be
estimated, based on the number of failures documented throughout the observation period, for any
of the crowns and FPDs considered. Aside from these survival rates, success rates were obtained
separately by performing the respective Kaplan–Meier calculations based on all complications rather
than on failures only. The aforementioned parameters were analyzed by log-rank testing for significant
associations with restorative survival.
All statistical calculations were performed with BiAS (Biometric Analysis of Samples) software
(rev. 11.05; Epsilon Verlag, Nordhastedt, Germany) and differences were considered significant at
p≤0.05
. Approval for the study was obtained from the institutional review board (reference number:
17/2015).
3. Results
3.1. Baseline Data
The 1058 restorations meeting all inclusion criteria were evaluable over an observation period
of up to 66.48 (37.05
±
18.4) months. They included 922 single or splinted crowns and 136 FPDs in
368 (206 female and 162 male) patients aged 57.84 years at the time of delivery. Maxillary restorations
accounted for 58.57% (540/922) of the crowns and 50.74% (69/136) of the FPDs. Adhesive cementation
were used in 53.31% and conventional cementation in 46.69% of cases. Table 2summarizes pertinent
patient data, the distribution of the 1058 evaluable restorations by type (crowns or FDPs) and jaw
(maxilla or mandible) and the cementation methods used.
Table 2. Patient demographics, restoration types and cementation methods.
Patients Evaluable Restorations
Total (n) 368 Total (n) 1058
Female/male (n) 206/162 Full-coverage crowns (n) 922
Mean age (years) 57.84 Maxilla (n) 540
Cementation Mandible (n) 382
Total (n) 1058
Fixed partial dentures (n)
136
Adhesive (n) 564 Maxilla (n) 69
Conventional (n) 494 Mandible (n) 67
3.2. Non-Recommended Uses and Restoration Subtypes
The manufacturer currently recommends IPS e.max Press and IPS e.max CAD for laminate/occlusal
veneers, inlays/onlays, partial/full-coverage crowns, hybrid abutments/hybrid abutment crowns and
for FPDs not extending beyond second premolars [
20
,
21
]. IPS e.max ZirPress and IPS e.max Ceram are
used for framework veneering. Non-recommended uses accounted for 158 of the 1058 restorations
here investigated, including FPDs supported by teeth (n = 32), implants (n = 9) or combinations of
both (n = 2); splinted crowns supported by teeth (n = 101), implants (n = 9) or both (n = 4); and one
tooth-supported single crown with a cantilever unit (n = 1). Table 3gives a detailed listing of the
restoration subtypes included in our evaluable overall sample of 1058 restorations.
Materials 2019,12, 462 4 of 10
Table 3. Detailed listing of the evaluable crowns and fixed partial dentures (FPDs).
Restorations n Distribution
All restorations 1058 100.00%
Tooth-supported single crowns 615 58.13%
Implant-supported single crowns 156 14.74%
Tooth-supported splinted crowns 126 11.91%
Tooth-supported FPDs 83 7.84%
Implant-supported FPDs 44 4.16%
Other 121 1.98%
Implant-supported splinted
crowns 13 1.23%
1For example, tooth/implant-supported or cantilever FPDs (9)/crowns (12).
3.3. Overall Success and Survival
A total of 35 restorations (3.3%) failed during the observation period, including 27 crowns and
eight FDPs. The cumulative success rates were 97.36% (12 months), 96.32% (24 months), 90.37%
(48 months) and 87.99% (60 months). Based on complete losses, the survival rates illustrated by the
cumulative Kaplan–Meier curve were 98.83% (12 months), 98.41% (24 months), 96.93% (36 months),
95.52% (48 months) and 94.22% (60 months). Based on only the restorations used for non-recommended
indications, five restorations (three crowns and two FPDs) had failed—all of these being failures
concerning IPS e.max Press as a restorative material. The survival rate of non-recommended uses
scarcely differed (and hence not significantly) from recommended uses (p= 0.85). Table 4gives an
overview of the five-year survival rates broken down by restoration types and the two major restorative
materials involved.
Table 4. Five-year Kaplan–Meier survival rates.
Restorations n Survival
Cumulative (all restorations) 1058 94.22%
All full-coverage crowns 922 94.90%
Recommended uses 807 94.51%
Lithium-disilicate crowns 1768 94.69%
Veneered zirconia-based crowns 39 100.00%
Non-recommended uses 115 94.95%
All fixed partial dentures 136 89.44%
Recommended uses 93 88.47%
Lithium-disilicate FDPs 143 90.58%
Veneered zirconia-based FDPs 50 90.06%
Non-recommended uses 43 95.35%
1Made from IPS e.max products (CAD, IPS, Press with e.Ceram veneers or Ceram).
3.4. Results for the Crown Restorations
Based on the 922 crown restorations, the survival rate was found to vary significantly with gender
and age, being higher in male than female patients (log-rank test: p= 0.005) and within the age group
of 31–50 years (log-rank test: p= 0.0043). Significant reductions in survival were seen for non-vitality
compared to the vitality of abutment teeth (log-rank test: p= 0.0063) and for adhesive compared to
conventional cementation (log-rank test: p= 0.0003). The 115 crowns used for non-recommended
indications exhibited a survival rate almost identical to the crowns used for recommended indications
(see Table 4). Figure 1illustrates the Kaplan–Meier survival curve for all 922 crown restorations
(five-year survival: 94.90%). Table 5lists the different causes of all 27 failures.
Materials 2019,12, 462 5 of 10
Table 5. Reasons for biological or technical failure of crown restorations.
Causes of Failure n Distribution
All full-coverage crowns
922
100.00%
Total number of failures 27 2.93%
Fracture of the restoration 5 0.54%
Apical osteitis 5 0.54%
Loss of retention 4 0.43%
Hypersensitivity 4 0.43%
Pre-prosthetic core fracture 3 0.33%
Chipping 2 0.22%
Root fracture 2 0.22%
Loss of implant 1 0.11%
Secondary caries 1 0.11%
Materials 2019, 12 FOR PEER REVIEW 5
Table 5. Reasons for biological or technical failure of crown restorations.
Causes of Failure n Distribution
All full-coverage crowns 922 100.00%
Total number of failures 27 2.93%
Fracture of the restoration 5 0.54%
Apical osteitis 5 0.54%
Loss of retention 4 0.43%
Hypersensitivity 4 0.43%
Pre-prosthetic core fracture 3 0.33%
Chipping 2 0.22%
Root fracture 2 0.22%
Loss of implant 1 0.11%
Secondary caries 1 0.11%
Figure 1. Kaplan–Meier survival curve for crown restorations.
Results for the FPD Restorations
Based on the 136 FPDs, adhesive cementation was again found to reduce the survival rate
compared to non-adhesive cementation (log-rank test: p
=
0.0318). Unlike with the crown restorations,
however, log-rank testing did not yield any significant differences for any of the other parameters
based on FPDs. Non-recommended uses concerned 43 FPDs. They included the failure of two tooth-
supported FPDs, but the resultant five-year Kaplan–Meier survival rate was actually (though not
significantly) higher for the non-recommended than for the recommended uses (95.35% versus
88.40%; see Table 4). Figure 2 illustrates the Kaplan–Meier survival curve for the 136 FPDs (five-year
survival: 89.44%). Table 6 lists the eight failures involved.
Table 6. Reasons for biological or technical failure of FPD restorations.
Causes of Failure n Distribution
All fixed partial dentures (FPDs) 136 100.00%
Total number of failures 8 5.88%
Endodontic complications 3 2.21%
Ceramic chipping/fracture 2 1.47%
Root fracture 2 1.47%
Preprosthetic core fracture 1 0.74%
Figure 1. Kaplan–Meier survival curve for crown restorations.
3.5. Results for the FPD Restorations
Based on the 136 FPDs, adhesive cementation was again found to reduce the survival rate
compared to non-adhesive cementation (log-rank test: p= 0.0318). Unlike with the crown restorations,
however, log-rank testing did not yield any significant differences for any of the other parameters
based on FPDs. Non-recommended uses concerned 43 FPDs. They included the failure of two
tooth-supported FPDs, but the resultant five-year Kaplan–Meier survival rate was actually (though
not significantly) higher for the non-recommended than for the recommended uses (95.35% versus
88.40%; see Table 4). Figure 2illustrates the Kaplan–Meier survival curve for the 136 FPDs (five-year
survival: 89.44%). Table 6lists the eight failures involved.
Table 6. Reasons for biological or technical failure of FPD restorations.
Causes of Failure n Distribution
All fixed partial dentures (FPDs)
136
100.00%
Total number of failures 8 5.88%
Endodontic complications 3 2.21%
Ceramic chipping/fracture 2 1.47%
Root fracture 2 1.47%
Preprosthetic core fracture 1 0.74%
Materials 2019,12, 462 6 of 10
Materials 2019, 12 FOR PEER REVIEW 6
Figure 2. Kaplan–Meier survival curve for FPD restorations.
4. Discussion
Our results demonstrate the high survival and success rates of IPS e.max materials over up to 60
months. They do diverge somewhat from previous reports. Yang et al. [17], in a similar study design,
reported a cumulative survival rate of 96.6% for 6855 restorations made of IPS e.max Press over five
years. Part of the explanation for our different five-year survival of 94.22% might be that we
investigated not only IPS e.max Press, but the whole IPS e.max range of products. Also, that previous
group conducted their study under defined conditions linked to a military university hospital. The
present study, by contrast, used patient files on record in a private practice. Given that no exclusion
criteria were applied, more of these restorations were bound to be affected by patient-specific risk
factors such as poor oral hygiene or periodontal problems. Also, we deliberately included uses of
materials not currently recommended by the manufacturer.
In 2017, Rauch et al. [12] reported an 87.6% survival rate of lithium-disilicate single crowns after
six years, which is lower than the rate presented here despite fewer risk factors due to defined
exclusion criteria. One should, however, bear in mind the longer observation period in that study
and its low case number of 25 crowns. These crowns were fabricated and inserted in both a private
practice and a prosthetic university department, which incidentally yielded a (though not
significantly) higher complication rate for the university-fabricated restorations. Our 100% survival
rate for zirconia-based single crowns is consistent with another very high survival rate of 98.5%
reported by Miura et al. [22]. Despite the provenance of our data (private practice) and our inclusion
of non-recommended uses, our 90.58% survival rate for glass-ceramic FPDs is virtually identical to
the 90.6% reported by Yang et al. [17], although both of these rates are lower than the 100% five-year
survival for three-unit FPDs reported by Kern et al. [7], which again might be due to the different
local scenarios involved.
Note, however, that all previous studies analyzed restorations conforming to the manufacturer’s
recommendations. For example, Clausen et al. [23] investigated single crowns made of IPS e.max
Press and Obermeier et al. [24] investigated implant-supported crowns made of IPS e.max CAD. The
present study, by contrast, also includes 158 non-recommended uses. While five of these restorations
failed (all of them made of IPS e.max Press), a significant difference between recommended and non-
recommended uses was not observed. Despite this non-significant difference and the limited number
of cases involved, it is nevertheless interesting to note that the non-recommended restorations
actually showed higher survival rates. As a departure from previous studies, it is therefore fair to
suggest that the range of indications listed by the manufacturer should be reconsidered and
expanded where appropriate.
However, one point to consider in comparing our results to those of previous studies is that
consistent definitions of ‘complication’ and ‘failure’ have often been lacking. Different causes of
failure emerged. Technical complications included ceramic defects in the form of full-blown fractures
Figure 2. Kaplan–Meier survival curve for FPD restorations.
4. Discussion
Our results demonstrate the high survival and success rates of IPS e.max materials over up to
60 months. They do diverge somewhat from previous reports. Yang et al. [
17
], in a similar study
design, reported a cumulative survival rate of 96.6% for 6855 restorations made of IPS e.max Press
over five years. Part of the explanation for our different five-year survival of 94.22% might be
that we investigated not only IPS e.max Press, but the whole IPS e.max range of products. Also,
that previous group conducted their study under defined conditions linked to a military university
hospital. The present study, by contrast, used patient files on record in a private practice. Given that no
exclusion criteria were applied, more of these restorations were bound to be affected by patient-specific
risk factors such as poor oral hygiene or periodontal problems. Also, we deliberately included uses of
materials not currently recommended by the manufacturer.
In 2017, Rauch et al. [
12
] reported an 87.6% survival rate of lithium-disilicate single crowns after
six years, which is lower than the rate presented here despite fewer risk factors due to defined exclusion
criteria. One should, however, bear in mind the longer observation period in that study and its low
case number of 25 crowns. These crowns were fabricated and inserted in both a private practice and
a prosthetic university department, which incidentally yielded a (though not significantly) higher
complication rate for the university-fabricated restorations. Our 100% survival rate for zirconia-based
single crowns is consistent with another very high survival rate of 98.5% reported by
Miura et al.
[
22
].
Despite the provenance of our data (private practice) and our inclusion of non-recommended uses,
our 90.58% survival rate for glass-ceramic FPDs is virtually identical to the 90.6% reported by
Yang et al.
[
17
], although both of these rates are lower than the 100% five-year survival for three-unit
FPDs reported by Kern et al. [7], which again might be due to the different local scenarios involved.
Note, however, that all previous studies analyzed restorations conforming to the manufacturer’s
recommendations. For example, Clausen et al. [
23
] investigated single crowns made of IPS e.max Press and
Obermeier et al. [
24
] investigated implant-supported crowns made of IPS e.max CAD. The present study,
by contrast, also includes 158 non-recommended uses. While five of these restorations failed (all of
them made of IPS e.max Press), a significant difference between recommended and non-recommended
uses was not observed. Despite this non-significant difference and the limited number of cases
involved, it is nevertheless interesting to note that the non-recommended restorations actually showed
higher survival rates. As a departure from previous studies, it is therefore fair to suggest that the range
of indications listed by the manufacturer should be reconsidered and expanded where appropriate.
However, one point to consider in comparing our results to those of previous studies is that
consistent definitions of ‘complication’ and ‘failure’ have often been lacking. Different causes of failure
emerged. Technical complications included ceramic defects in the form of full-blown fractures or
Materials 2019,12, 462 7 of 10
chipping. Events of this kind have been reported previously to constitute a frequent complication
of all-ceramic single crowns, as evidenced in a 2017 review article by Aldegheishem et al. [
25
] and
supported by Monaco et al. [
8
]. Consistent with statements by Reich et al. [
13
], we also noted failures
resulting from endodontic complications such as hypersensitivity or apical osteitis, as well as from
secondary caries of abutment teeth.
We also demonstrated a statistically significant association between survival rate and cementation
type. Both conventional and adhesive cementation can be used with the IPS e.max system.
Adhesive bonding is meant to increase the fracture resistance of restorations [
26
–
28
] but is highly
technique-sensitive. Perfect drying/isolation [
29
] and appropriate etchability of the residual tooth
structure are required. Also, the quality of the bond is amenable to surface conditioning, as has been
demonstrated by applying different methods of cleaning to restorations after etching [
30
]. Although
Kern et al. [
7
] and Esquivel-Upshaw et al. [
31
] observed no difference to this effect, conventional
cementation emerged as superior in the present study. Again, one might implicate our different
study design in this finding, considering that the restorations we analyzed were inserted in a private
practice, where changing clinicians and practice-related circumstances may have played a role. Yet,
on the flip side of this argument, Rauch et al. [
12
] reported in their study a higher complication rate
for restorations delivered at a German university hospital than for those delivered by dentists in
private practice.
Another statistically significant finding of the present study was the lower survival rate of crowns
retained on non-vital than on vital teeth. Huettig et al. [
32
] and Fedorowicz et al. [
33
] previously
reported a similarly increased rate of complications for non-vital abutment teeth, suspecting that these
were biologically inferior to vital abutments. On another confirmatory note, Toman et al. [
34
] reported
that the survival rate of crowns was significantly reduced on non-vital teeth and suggested that any
restoration of non-vital teeth with lithium-disilicate crowns must be subject to rigorous case selection.
It should be considered that all restorations in our study had been fabricated from products
of the same system (IPS e.max) and manufacturer (Ivoclar Vivadent). A comparable material by
another manufacturer could not be included for comparison because no such material was available
until very recently. This is over and above the fact that such a comparison would not have been
readily feasible, given a clinical background of retrospectively evaluating data from a private practice.
Similar study protocols in which specific materials were evaluated without comparison have been used
previously [
12
,
17
]. Most importantly, the opportunity to assess one system as used in daily clinical
practice across a wide spectrum of indications clearly outweighed the shortcoming that no different
products were available for comparison.
The present study was designed as a non-experimental, analytical, retrospective cohort study on
the basis of patient files archived in a private dental practice. Given this design, the correctness and
completeness of the existing documentation had to be taken for granted. While the possibility of any
issues in this regard should not be dismissed, this is a caveat inherent in most retrospective studies [
35
].
Given a large data base and a balanced distribution between maxillary and mandibular restorations,
our approach did turn out to be appropriately suited to evaluating the clinical track record of the IPS
e.max system and potential modifying factors.
As a case in point, the documentation available to us indicated for each restoration the dental
laboratory where it had been fabricated. This allowed us to include only restorations known to have
been fabricated by the same laboratory under the supervision of the same master dental technician,
thus ensuring consistent fabrication standards, which can contribute greatly to favorable complication
rates [
36
]. The detailed patient records also allowed us to consider the fabrication procedures in
evaluating the outcomes. Previous reports on the survival rates of lithium-disilicate restorations
were also based on standardized fabrication processes, but the samples they considered were heavily
qualified [
11
–
17
]. Given our different study objective, which was to verify a real-life track record in
daily clinical practice, we deliberately minimized criteria in compiling our sample. Also, our survival
Materials 2019,12, 462 8 of 10
rates should be considered keeping in mind that any non-recommended uses of the studied material
were specifically included.
Any complications that occurred were recorded during annual recall appointments, although
the retrospective study design did imply very dissimilar follow-up times and observation periods,
the latter ranging up to 66.48 months (mean 37.05
±
18.4 months). While this may appear short
compared with a follow-up time of up to 10 years in other studies, it has been shown repeatedly that
most complications with IPS e.max restorations occur in the initial phase after insertion [
16
,
17
,
32
].
Hence, the observation period does seem to be adequately long for a conclusive evaluation of the
material under study.
The present study produced a multitude of results. Thanks to a high case number and a wide
spectrum of products and uses, we were able to address different questions that normally would have
been addressed in separate studies. The fact that we deliberately refrained from exclusion criteria
and used data that had accumulated in daily clinical practice enabled us to review the outcomes
with IPS e.max products in real life. We could only achieve this by accepting risk factors such as
bruxism, poor oral hygiene, periodontal problems, or non-recommended uses with their implications
for long-term success. The high survival rates we obtained despite this background paints a favorable
picture of the clinical track record of IPS e.max in everyday practice. The fact that these rates are highly
consistent with the available literature on the subject underscores the conclusiveness of our findings.
Also, a research focus on implant-borne IPS e.max restorations would be useful, given the increasing
popularity of all-ceramic restorations for implants and that previous studies on the subject, while
showing favorable material properties and survival rates, have covered limited samples or observation
periods [37,38].
5. Conclusions
Within the limitations of this study, the use of IPS e.max may be recommended in clinical
practice. Caution should be exercised in restoring non-vital teeth and in selecting luting techniques.
High survival rates were obtained even for non-recommended uses of IPS e.max prompted by
patient-specific considerations. Hence, the spectrum of indications for these products should generally
be reconsidered and expanded where appropriate. Although we reviewed previous reports and filled
some of the gaps they left, there is a need for further investigations similar in case number and design.
Author Contributions:
Conceptualization, S.B.; methodology, S.B.; software, S.B.; validation, H.-C.L., A.W. and
S.B.; formal analysis, S.B., A.W. and S.-J.P.-K.; investigation, F.K., S.-J.P.-K., H.-C.L. and G.E.R.; resources, S.B. and
F.K.; data curation, F.K. and G.E.R.; writing—original draft preparation, A.W.; writing—review and editing, S.B.,
G.E.R. and H.-C.L.; visualization, S.B.; supervision, G.E.R. and H.-C.L.; project administration and final editing of
the manuscript, S.B.
Conflicts of Interest: The authors declare no conflict of interest.
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