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Systemic Conditions and Treatments as Risks for Implant Therapy
Michael M. Bornstein, Dr Med Dent1/Norbert Cionca, Dr Med Dent2/Andrea Mombelli, Prof Dr Med Dent3
Purpose: To evaluate whether systemic diseases with/without systemic medication increase the risk ofimplant failure and therefore diminish success and survival rates of dental implants. Materials andMethods: A MEDLINE search was undertaken to find human studies reporting implant survival in sub-jects treated with osseointegrated dental implants who were diagnosed with at least one of 12 systemicdiseases. Results: For most conditions, no studies comparing patients with and without the conditionin a controlled setting were found. For most systemic diseases there are only case reports or caseseries demonstrating that implant placement, integration, and function are possible in affectedpatients. For diabetes, heterogeneity of the material and the method of reporting data precluded a for-mal meta-analysis. No unequivocal tendency for subjects with diabetes to have higher failure ratesemerged. The data from papers reporting on osteoporotic patients were also heterogeneous. The evi-dence for an association between osteoporosis and implant failure was low. Nevertheless, somereports now tend to focus on the medication used in osteoporotic patients, with oral bisphosphonatesconsidered a potential risk factor for osteonecrosis of the jaws, rather than osteoporosis as a risk factorfor implant success and survival on its own. Conclusions: The level of evidence indicative of absoluteand relative contraindications for implant therapy due to systemic diseases is low. Studies comparingpatients with and without the condition in a controlled setting are sparse. Especially for patients withmanifest osteoporosis under an oral regime of bisphosphonates, prospective controlled studies areurgently needed. INT J ORAL MAXILLOFAC IMPLANTS 2009;24(SUPPL):12–27
Key words: bisphosphonates, diabetes, implant failure, osseointegration, osteoporosis, systemic disease
The replacement of missing teeth with endosseous first described by the two research groups of Bråne-
implants for the rehabilitation of edentulous or
mark and Schroeder. Fundamental experimental
partially edentulous patients has become a standard
studies demonstrated that titanium implants regu-
of care in the past two decades. This significant
larly heal with direct bone-to-implant contact, a
progress is based on the concept of osseointegration,
process termed osseointegration1 or functional anky-losis.2 To achieve and maintain osseointegration, indi-cations and contraindications must be carefully
1Assistant Professor, Department of Oral Surgery and Stomatology,
balanced, and proper patient selection is thus a key
School of Dental Medicine, University of Bern, Bern, Switzerland.
issue in treatment planning.3 Contraindications can
2Graduate Student, Department of Periodontology, School of Den-
be divided into local and systemic/medical. In a paper
tal Medicine, University of Geneva, Geneva, Switzerland.
prepared for the second ITI (International Team of
Professor and Chairman, Department of Periodontology, Schoolof Dental Medicine, University of Geneva, Geneva, Switzerland.
Oral Implantology) Consensus Conference, Buser andcoworkers4 (2000) proposed to subdivide the general
None of the authors reported a conflict of interest.
medical/systemic risk factors into two groups:
Correspondence to: Dr Michael Bornstein, Department of OralSurgery and Stomatology, School of Dental Medicine, University
Group 1 (very high risk): Patients with serious sys-
of Bern, Freiburgstrasse 7, CH-3010 Bern, Switzerland. Fax: +41
temic disease (rheumatoid arthritis, osteomalacia,
31 632 25 03. Email: Michael.bornstein@zmk.unibe.ch
osteogenesis imperfecta); immunocompromisedpatients (HIV, immunosuppressive medications);
This review paper is part of the Proceedings of the Fourth ITI Consen-
drug abusers (alcohol); noncompliant patients
sus Conference, sponsored by the International Team for Implan-tology (ITI) and held August 26–28, 2008, in Stuttgart, Germany.
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 13
Group 2 (significant risk): Patients with irradiated
reviews,3,6,7,11–14 a list of systemic diseases suspected
bone (radiotherapy), severe diabetes (especially
of having a negative impact on the success of
type 1), bleeding disorders (hemorrhagic diathe-
osseointegration therapy was generated. Severe and
sis, drug-induced anticoagulation), heavy smoking
acute medical conditions for which implant therapy
has always been considered a contraindication (eg,acute infections, severe bronchitis or emphysema,
Systemic diseases may affect oral tissues by
severe anemia, uncontrolled diabetes, uncontrolled
increasing their susceptibility to other diseases or by
hypertension, abnormal liver function, nephritis,
interfering with healing. In addition, systemic condi-
severe psychiatric disease, conditions with severe risk
tions may be treated with medications or other thera-
of hemorrhage, endocarditis or myocardial infarction)
pies that potentially affect implants and the tissues
carrying them. Several authors have identified dis-
As the present review paper is also an update of
eases for which dental implants are not recom-
the paper published in 2006 by Mombelli and
mended, or are at least questionable,3,5–7 but it often
Cionca,15 key word selection was additionally based
remains unclear on what type of evidence these
on the search terms used in the former publication.
The diseases and conditions retained for further
Patients receiving dental implants generally fall
analysis were: scleroderma, Sjögren syndrome, neu-
into the first two physical status categories of the
ropsychiatric disorders/Parkinson disease, lichen
Classification System of the American Society of
ruber planus/oral lichen planus, HIV infection, ecto-
Anesthesiology (ASA): P1, a normal healthy patient; or
dermal dysplasia, long-term immunosuppression
P2, a patient with mild systemic disease.8,9 For very
after organ transplantation, cardiovascular disease,
severe and acute medical problems, calculating the
Crohn disease, diabetes, osteoporosis, oral bisphos-
risk of failure in affected subjects seems impossible,
phonate medication, and use of radiotherapy for the
simply because patients with such conditions hardly
treatment of oral squamous cell carcinoma (OSCC).
ever receive implants. These patients fall into the ASAphysical status categories P3 to P6: patients with
severe systemic disease (P3); patients with severe sys-
In patients treated with dental implants, to what
temic disease that is a constant threat to life (P4);
extent does a history of scleroderma, Sjögren syn-
moribund patients who are not expected to survive
drome, neuropsychiatric disorders/Parkinson disease,
without an operation (P5); and subjects declared
oral lichen planus, HIV infection, ectodermal dyspla-
brain dead whose organs may be removed for donor
sia, long-term immunosuppression after organ trans-
purposes (P6). A recent publication stated that elec-
plantation, cardiovascular disease, Crohn disease,
tive dental treatment of patients classified as P4 or
diabetes, osteoporosis, medication with oral bisphos-
higher should ideally be postponed until the patient’s
phonates, or irradiated bone due to the treatment of
medical condition has stabilized and improved to at
OSCC increase the risk for implant failure?
Implant failure was selected as the primary study
The purpose of this review was to evaluate the
parameter, and it was further divided into early and
impact of systemic diseases, and/or medications used
to treat systemic diseases, on the success of dentalimplant therapy. The analysis was focused on condi-
tions that are not generally considered to be an
Using EndNote X1, 13 MEDLINE searches were con-
absolute contraindication. The role of systemic factors
ducted based on the process mentioned previously.
in early failures (ie, during the healing period up to
The search was conducted up to and including March
initiation of prosthetic treatment) and late failures (ie,
2008 using the following strategy: implant AND (oral
after implant loading) was analyzed.
2. Sjögren’s syndrome and/or Sjögren3. Neuropsychiatric disorders and/or Parkinson
To select the most important key words, a preliminary
assessment was made of the potentially relevant lit-
erature. This was achieved by “scoping” searches,
including searching for existing reviews. Incorporat-
ing opinions expressed in seven nonsystematic
The International Journal of Oral & Maxillofacial Implants 13
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 14
10. Diabetes or insulin therapy or glucose intolerance
11. Osteoporosis or osteoporotic12. Oral bisphosphonates
Scleroderma, Lichen Planus, and Ectodermal
13. Radiotherapy or irradiation or irradiated
DysplasiaNo controlled studies were found for scleroderma,
This search strategy was designed for high recall
oral lichen planus, or ectodermal dysplasia to demon-
rather than high precision in the first instance. There
strate any positive or negative effects on the out-
come of implant therapy. For all three conditions onlycase reports or case series could be identified.
Scleroderma is defined as a multisystem disorder
characterized by inflammatory, vascular, and sclerotic
The primary study inclusion criteria were:
changes of the skin and various internal organs, espe-cially the lungs, heart, and gastrointestinal tract. Typi-
Study includes human subjects with the respec-
cal clinical features in the facial region are a masklike
appearance (patients look younger), thinning of the
Subjects have osseointegrated dental implants.
lips, microstomia, radial perioral furrowing, sclerosis of
Study reports implant failure, survival, and/or suc-
the sublingual ligament, and indurations of the
tongue.16 These symptoms cause the skin of the face
Case series include at least five subjects with the
and lips as well as the intraoral mucosa to become
respective diagnosis. If case reports with fewer
taut, thereby hindering dental treatment and compli-
treated subjects were the only available source of
cating or even preventing the insertion of dental
prostheses. Only five case reports with up to twopatients treated with dental implants could be found
Two independent reviewers screened titles and
in the literature.17–21 Therefore, the level of evidence
abstracts of the search results (MB, NC). Any disagree-
for the efficacy of dental implants in these patients is
ment regarding inclusion was resolved by discussion
including the third independent reviewer (AM). The full
Oral lichen planus (OLP) is a common T-cell–medi-
text of all studies of possible relevance was then
ated autoimmune disease of unknown cause that
obtained by two reviewers (MB, NC) for independent
affects stratified squamous epithelium virtually exclu-
assessment of the stated inclusion criteria. Additional
sively.22 OLP has been considered a contraindication
studies were sought by scanning the references cited in
for the placement of dental implants possibly because
the retained papers and by personal communication.
of the altered capacity of the oral epithelium to
The methodological quality was assessed using the
adhere to the titanium surface.5 In the literature there
levels of evidence proposed by the Oxford Centre for
are only case reports with up to three patients treated,
Evidence-based Medicine (http://www.cebm.net/
including symptomatic23 and asymptomatic21,24 forms
levels_of_evidence.asp), ranging from lowest (level 5,
of lichen planus. Nevertheless, OLP is a potentially
expert opinion without explicit critical appraisal, or
malignant condition, which in rare cases may result in
based on physiology, bench research, or first princi-
malignant transformation.25 Only one case report
ples) to highest (level 1a, systematic reviews with
describing an OSCC originating from OLP in associa-
homogeneity of randomized clinical trials).
tion with dental implants was identified.26 With the lit-erature available at present (level 4), oral lichen planus
as a risk factor for implant surgery and long-term suc-
The following data were sought, separately for each
condition, for subjects with and without the specific
Ectodermal dysplasia (ED) is a hereditary disease
diagnosis (if available): implant type, number of sub-
characterized by congenital dysplasia of one or more
jects, number of implants, number of subjects with
ectodermal structures. Common extra- and intraoral
early failures, number of early failing implants, years
manifestations include defective hair follicles and
of follow-up, number of subjects followed up, number
eyebrows, frontal bossing, nasal bridge depression,
of implants followed up, number of subjects with late
protuberant lips, hypo- or anodontia, conical teeth,
failures, number of late failing implants. Failures were
and generalized spacing.27 Most search results for ED
defined as implants lost, and were subdivided into
were case reports demonstrating treatment success
losses occurring before and those occurring after the
with dental implants.21,28–37 A few larger case series
functional loading (early and late).
report survival and success rates of implants in suchpatients38–42 (Table 1). However, due to the lack ofcontrols, it cannot be determined how these results
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 15
Table 1 Implant Failures: Case Series of Patients with Ectodermal Dysplasia Treated with Implants
%Subj = subject-based rate; %Impl = implant-based rate; Y = years of follow-up after restoration; ND = no data available.
compare to those expected in subjects without the
dal diseases characterized by rigidity and tremor,51
condition. All studies reported significantly lower sur-
there are some case reports suggesting that successful
vival and success rates in the maxilla than in the
implant placement is possible.52,53 Therefore, the level
of evidence for the efficacy of dental implants in thesepatients is low (level 4). For many neuropsychiatric dis-
orders there is no literature available.
Sjögren syndrome (SS) is a chronic autoimmune dis-ease affecting the exocrine glands, primarily the sali-
vary and lacrimal glands. At present, the etiology of
The introduction of highly active antiretroviral ther-
SS is far from being understood.43 The most common
apy (HAART) for HIV infection has significantly post-
symptoms of SS are extreme tiredness, along with dry
poned the outbreak of AIDS-defining diseases,
eyes (keratoconjunctivitis sicca) and dry mouth
reduced the rates of clinically manifested opportunis-
(xerostomia). Xerostomia can eventually lead to diffi-
tic infections and oral HIV-associated mucosal lesions,
culty in swallowing, severe and progressive tooth
and extended life expectancy considerably.54 Several
decay, or oral infections. Currently, there is no cure for
case reports have demonstrated successful implant-
SS, and treatment is mainly palliative.44
prosthetic rehabilitation of these immunocompro-
Literature on implant performance in patients with
mised but immunologically stable patients.55–58 The
SS is scarce. There are no controlled studies available,
authors of a recent report conclude that no modifica-
and only one case series study with eight patients
tion of routine dental treatment is needed in HIV-pos-
included was found (level of evidence 4).45 The eight
itive patients, provided that their immune status is
patients in this study were all women receiving a total
stable.59 Optimized oral hygiene, regular recall inter-
of 54 implants (18 in the maxilla, 36 in the mandible)
vals, screening for HIV-related oral lesions, and detec-
with a machined surface. At abutment connection
tion of hyposalivation/xerostomia are preventive
seven of these implants (12.9%) were found not to be
therapies used to treat HAART side effects. Only one
osseointegrated at abutment connection. During the
study was found that investigated the short-term
first year of function, two additional implants in the
clinical outcome of implant placement in a group of
mandible were lost, resulting in an implant-based fail-
HIV-positive patients compared to results with an
ure rate of 16.7% (patient-based 50%; four patients
HIV-negative control group.60 In this study, 20 HIV-
out of eight lost at least one implant).
positive subjects and 9 HIV-negative control patientswere followed for 6 months after loading of the
implants. The success rates for both groups were
100%; no differences in clinical outcome were noted
There is virtually no literature available on implant per-
between the two groups (a level 3b study).
formance in patients with neuropsychiatric disorders. There are no controlled studies or even case series on
defined pathological entities to evaluate implant sur-
Crohn disease is an idiopathic chronic inflammatory
vival and success in these situations. Only case reports
disorder of the gastrointestinal tract that may also
on selected psychiatric diseases or neurologic disabili-
involve the oral cavity. The disease process is charac-
ties—such as Down syndrome, autism, Huntington dis-
terized by recurrent exacerbations and remissions.61
ease, and schizophrenia—have been published.46–50
The literature regarding the performance of dental
For Parkinson disease, one of a group of extrapyrami-
implants in patients with Crohn disease is scarce, with
The International Journal of Oral & Maxillofacial Implants 15
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 16
a level of evidence 4.62 In a retrospective study with
pathologies—ranging from recent myocardial infarc-
observation up to 1 week after second-stage surgery,
tion to congestive heart failure to atherosclerosis and
two of three patients with Crohn disease had implant
hypertension—are referred to as CVD. In a preliminary
failures (3 out of 10 inserted implants were lost).63
retrospective study with a total of 246 patients receiv-
The authors speculated that the presence of anti-
ing dental implants, three different groups were sepa-
body-antigen complexes might lead to autoimmune
rately analyzed for early implant failures72: group I, CVD
inflammatory processes in several parts of the body,
(39 patients); group II, healthy subjects (98 patients);
including the bone-implant interface. However, in
group III, other systemic disease (109 patients). The
both of these patients with early implant failures,
patient-based failure rates varied between 12.2% and
other medical and local risk factors were also present:
13.8% in the three groups, and differences were not
claustrophobia, smoking, and poor bone quantity.
statistically significant (evidence level 3b).
In a follow-up study, patients treated from 1982 to
One center has published three papers on this
2003 were evaluated to assess the influence of sys-
subject. The influence of systemic and local factors on
temic and local factors on the occurrence of early
implant failure, again only up to 1 week after second-
implant failures.64 Crohn disease was significantly
stage surgery, was evaluated in a retrospective analy-
related to early implant failure, exhibiting an odds
sis of patients receiving implants.63 CVD was not
ratio of 7.95 (95% CI of 3.47 to18.24)—the highest
associated with an increased incidence of early
odds ratio of all systemic factors evaluated in the
implant failures. In a second retrospective analysis of
study. Unfortunately, the authors did not provide the
a much larger patient population, hypertension and
exact number of patients with Crohn disease treated
cardiac problems also were not significantly related
or the number of implant failures in these patients.
to early implant failure.64 In a third study, the authors
In a recent prospective study from the same
prospectively evaluated the occurrence of early fail-
group, the influence of various systemic and local fac-
ures of implants with a modified, oxidized titanium
tors on the occurrence of early failures was once
surface, again only up to second-stage surgery.65
more evaluated. This time the implants had a modi-
Once more, hypertension and cardiac problems were
fied, oxidized titanium surface.65 Between November
not factors contributing to early implant failure.
2003 and June 2005, 11 of 12 implants placed in
A retrospective cohort study including patients
patients with Crohn disease integrated successfully.
consecutively treated with dental implants between
Unfortunately, the authors again did not provide the
1982 and 2003 revealed that hypertension and car-
exact number of patients with Crohn disease treated.
diac disease were not significant factors associatedwith implant failure.73
Transplantation (Heart/Liver/Renal Transplant)
Patients receiving transplanted organs generally
undergo long-term immunosuppressive therapy, usu-
There are two major types of diabetes: Type 1 (previ-
ally consisting of cyclosporine A combined with
ously termed “insulin-dependent”) is caused by an
steroids, which have anti-inflammatory proper-
autoimmune reaction destroying the beta cells of the
ties.66,67 Several animal studies have demonstrated
pancreas, leading to insufficient production of insulin.
that cyclosporine may negatively influence bone
Type 2 (previously termed “non–insulin-dependent”)
healing around dental implants and may even impair
is viewed as a resistance to insulin in combination
the mechanical retention of dental implants previ-
with an incapability to produce additional compen-
ously integrated in bone.68–70 With regard to studies
satory insulin.74 Type 2 diabetes, often linked to obe-
in humans, there is no information available in the lit-
sity,75 is the predominant form, notably in the adult
erature addressing heart or renal transplantations
population in need of implant therapy. Diabetes melli-
and the performance of subsequently placed or
tus is associated with various systemic complications,
already present dental implants (evidence level 5).
including retinopathy, nephropathy, neuropathy,
There is one case report describing the placement of
micro- and macrovascular disturbances, and impaired
two interforaminal implants 6 months after liver
wound healing. In the oral cavity, xerostomia, caries,
transplantation, providing anecdotal evidence of sta-
and periodontitis have been linked to diabetes melli-
bility 10 years after insertion71 (evidence level 4).
tus. The increased susceptibility to periodontitis isthought to be due to a negative influence of diabetes
on inflammatory mechanisms and apoptosis, resulting
The literature addressing dental implants and their
in a deregulated host defense, deficits in wound heal-
success and failure rates in patients with cardiovascu-
ing, and microvascular problems (for review, see Taylor
lar diseases (CVD) is scarce. In addition, very different
and coworkers [2004],76 Graves et al [2006]77).
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 17
Table 2 Implant Failures: Case Series of Diabetic Patients Treated with Implants
%Subj = subject-based rate.;%Impl = implant-based rate; Y = years of follow-up; ND = no data available.
The present authors have analyzed the literature
reports, the numbers of subjects and implants avail-
published up to October 2005 in a previous paper.15
able to calculate early and late failure rates do not
At that time, a search using the terms implant AND
always correspond (n indicating the number of
(oral OR dental) AND (diabetes OR insulin therapy OR
treated subjects). Thus, estimated overall failure rates
glucose intolerance) yielded 73 articles. The primary
are not identical to the sum of early and late failure
screening excluded 60 of these papers because they
either did not report results from humans, did not
Because the data compiled in Table 2 were hetero-
include diabetic subjects, did not deal with osseointe-
geneous with regard to the length of time the cases
grated implants, or did not quantitatively report fail-
were followed, the proportion of implants and sub-
ure/success/survival. Scanning the reference lists of
jects monitored throughout the entire period varied,
the retained studies yielded one additional paper.
and large parts of sought information were unavail-
Furthermore, one MSc thesis78 found through per-
able, a meta-analysis was not possible. Within the lim-
sonal communication was added. A repetition of the
itations of the collected material, the following trends
same search in April 2008 yielded a limited amount of
were recognized: (1) more failures in diabetic patients
additional original data published with regard to dia-
occurred early, and (2) the percentage of diabetic
betes: one case report of successful implants in a dia-
patients experiencing failures seemed to be relatively
betic patient,79 one prospective cohort study,80 and
high, but the percentage of failing implants appeared
two papers from the same center presenting retro-
spective data of a patient population that included
Nine studies reported data on failures in cohorts
including some diabetic subjects. Specific attribution
Data were extracted from 18 articles.63,64,65,73,78,80–92
of failures to the diabetic status was not reported in
Three types of reports were found: (1) case series of
one of them.82 The other eight studies are listed in
diabetic patients treated with implants; (2) cross-sec-
tional, longitudinal, or retrospective evaluations of
Again heterogeneity of the material and the
groups of subjects treated with implants, including
method of data reporting precluded any further
some diabetic patients; and (3) one matched control
analysis. The diabetic patients in general had well-
retrospective chart survey (evidence level 3a).
controlled blood glucose levels, at least before and
Table 2 lists eight papers, each reporting results
immediately after implant therapy. No unequivocal
from multiple diabetic patients treated with implants.
tendency for subjects with diabetes to have higher
One paper is a 1-year interim report83 of the same
failure rates emerged. However, the largest study
patient population presented with a 5-year follow-up
reporting early and late failures, the retrospective
in another publication.88 From the data in these
cohort analysis of Moy and coworkers (2005) already
papers, an attempt was made to calculate early, late,
mentioned in the context of CVD, included 48 dia-
and overall failure rates. However, it was noted that
betic and 1,092 nondiabetic patients treated consec-
due to incomplete follow-up of subjects in these
utively by one surgeon over a period of 21 years.73
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Table 3 Implant Failures: Studies Including Diabetic (D) and Nondiabetic (non-D) Subjects
%Subj = subject-based rate; %Impl = implant-based rate; Y = years of follow-up; ND = no data available. *Cumulative (variable time).
This study indicated a statistically significant increase
tion, opposing arch, and duration of edentulism.78 In
in the relative risk of implant failure with diabetes (RR
this study, diabetic patients had no increased risk of
2.75, 95% CI: 1.46 to 5.18, P < .05).
implant failure and a similar number of prosthodon-
The most recent publications were limited to
tic complications compared to matched nondiabetic
reporting the rate of early failures: 50 implants placed
in a cohort of 35 subjects, including 25 patients with
The present review focused on failure. In the
diabetes (10 well controlled, 12 moderately con-
recent literature, biological complications not neces-
trolled, 3 poorly controlled), showed 100% success at
sarily leading to failure, ie, peri-implant mucositis and
the 4-month follow-up.80 No apparent influence of
peri-implantitis, have become an issue of investiga-
diabetes on 252 implant failures in 178 patients was
tion as well. A cross-sectional survey of 212 subjects
noted in the retrospective assessment of Alsaadi and
with 578 implants included 29 diabetics.93 In diabetic
coworkers (2007)64 including 2,004 subjects treated
patients, peri-implant mucositis was diagnosed in
with 6,946 implants (only odds ratios reported; case
59% of the cases and peri-implantitis in 24%. In sub-
numbers not known). In the recent report of the same
jects with no diabetes, the prevalence of mucositis
group, 14 early failing implants in 14 patients out of
was similar (66%) but peri-implantitis was signifi-
283 subjects treated with 720 implants are
reported.65 This data set includes one subject withdiabetes type 1, who had an early failure, and reports
4% early failures in patients with diabetes type 2, in
Osteoporosis has been defined as a decrease in bone
comparison to 1.9% in nondiabetic subjects.
mass and bone density and an increased risk and/or
At the highest available level of evidence, a group
incidence of fracture. However, it has been noted that
of 15 diabetics, retrospectively identified in a pool of
subjects without fractures may have also lost a signif-
387 consecutively treated patients, were each
icant amount of bone, while many patients with frac-
matched to two control subjects by age, sex, location
tures display levels of bone mass similar to those of
of implants (jaw and zone), type of prosthetic restora-
control subjects.94,95 Thus, definitions of osteoporosis
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 19
based on reduced bone mass or nonviolent fracture
endocrinopathies can cause osteoporosis. These
are not perfectly synonymous. In addition, the rela-
drugs are used for a variety of conditions, including,
tionship between skeletal and mandibular or maxil-
but not limited to, Crohn disease, asthma, pemphigus,
lary bone mass is limited.96–98 The World Health
and polyarthritis. Cases have been reported in which
Organization has established diagnostic criteria for
dental implants were placed, and successfully main-
osteoporosis based on bone density measurements
tained, under such circumstances.62,106,107
determined by dual energy X-ray absorptiometry: A
In 2005 a number of papers were published evalu-
diagnosis of osteoporosis is made if the bone mineral
ating implant therapy, including subjects with and
density level is 2.5 standard deviations below that in
without a diagnosis of osteoporosis. A repetition of
the same search in April 2008 yielded two additional
In October 2005, a search using the terms implant
papers in this category. They have already been men-
AND (oral OR dental) AND (osteoporosis OR osteo-
tioned previously in the context of CVD and dia-
porotic) yielded 66 articles. The primary screening
betes64,65 and will be discussed below in the context
excluded 54 of these papers because they either did
not report results from humans, did not include sub-
Van Steenberghe and coworkers63 counted 27
jects with osteoporosis, did not deal with osseointe-
early failures among 1,263 consecutively inserted
grated implants, or did not quantitatively report
implants in 399 patients. Two implants were placed in
failure/success/survival rates. Three papers were case
patients diagnosed with osteoporosis and both were
reports of individual osteoporotic females, all success-
a success. In 2007, however, the same center reported
fully treated with osseointegrated implants.100–102 One
a significant association between osteoporosis and
paper reported a case of implant failure after therapy
early implant failure.64 In a third paper by the same
with an oral bisphosphonate for osteoporosis.103 In
group, none of their 29 implants placed in patients
this report, the patient lost all five implants, which had
with osteoporosis failed early, whereas 2% of the
been inserted to retain a fixed hybrid mandibular
implants in nonosteoporotic subjects failed.65
prosthesis, approximately 2.5 years after insertion. The
Von Wowern and Gotfredsen108 measured changes
patient’s initial medical history was significant for
in mineral content of the mandibular bone in 7 osteo-
osteoporosis, hyperparathyroidism, nephrolithiasis,
porotic and 11 nonosteoporotic women 5 years after
thyroidectomy, cholecystectomy, hysterectomy, an
functional loading of their implants. Although no
ankle fracture, and a hip fracture with total hip
implant failure was observed in any patient, a signifi-
replacement. Two years after implant placement, ther-
cant difference was noted in the marginal bone loss
apy for osteoporosis was commenced with etidronate,
between the two groups. One retrospective study
an oral bisphosphonate known as Didronel. In the fol-
found no difference in failure rates between women
lowing routine appointment, all five implants exhib-
receiving (n = 25) or not receiving (n = 91) hormone
ited massive radiolucency all around the implants. The
replacement therapy (HRT).109 In the study by Moy et
authors concluded that bisphosphonates should be
al,73 already discussed in the context of diabetes, post-
avoided in patients who have undergone implant
menopausal hormone replacement therapy (or lack
placement, and implants should not be placed in
thereof ) was also evaluated. Compared to the total of
patients who require bisphosphonates. This case
1,140 patients, the relative risk for implant failure was
report is the first article to mention bisphosphonates
increased by 2.55 (95% CI: 1.72 to 3.77, P < .05) in the
as a potential risk factor for oral implantology. In light
161 women on HRT. Implant failure rates of
of the current controversy (see next section on bis-
postmenopausal women, with or without estrogen
phosphonates), it is important to note that etidronate
replacement therapy, were compared to those of pre-
is one of the least potent bisphosphonates known
menopausal women by August and coworkers.110
today and is administered via an oral route only.
Postmenopausal women without HRT (n = 168) had
Another paper reported three cases of mandibular
the highest maxillary failure rate (13.6%), a rate signifi-
fractures following implant placement, two of them
cantly greater than that of premenopausal women
in elderly women with advanced mandibular
(n = 114) (6.3%). The difference in the maxillary failure
atrophy.104 Sixteen women, all with a diagnosis of
rates of HRT-supplemented postmenopausal women
osteoporosis (low bone density or the occurrence of
(n = 75) (8.1%) and unsupplemented women did not
low-trauma fractures), were assessed in one retro-
reach statistical significance. Implants placed in the
spective study with regard to the success of implants
mandible did not show statistically significant differ-
placed between 6 months and 11 years previously.
The reported overall success rate was 97.0% for max-
With regard to age, the opposite was found by Dao
illary implants and 97.3% for mandibular implants.105
et al111 in an informal review of the Toronto implant
The administration of corticosteroids or other
study patient series (93 women and 36 men, aged 20
The International Journal of Oral & Maxillofacial Implants 19
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 20
to 76 years): The highest failure rates were noted in
The second type are nonmalignant bone diseases,
the youngest age group. The heterogeneity and qual-
the most common of which are osteoporosis and
ity of the data presented in these studies precluded
Paget disease.116 Marx first showed a connection
between bisphosphonate cancer therapy and
Thirty-nine women aged 48 to 70 years, 19 with a
osteonecrosis of the jawbones in 2003.117 He
densitometric diagnosis of osteoporosis in the lum-
described 36 cases of osteonecrosis: 80.5% in the
bar spine and femoral neck and 20 controls with a
mandible, 14% in the maxilla, 5.5% in both jaws
normal densitometric diagnosis, were compared by
simultaneously. All affected subjects were being
Amorim and coworkers.112 Bone mineral density was
treated with intravenous bisphosphonates, either
measured in the patients and controls by dual-energy
pamidronate (brand name Aredia) or zoledronate
x-ray absorptiometry. Eighty-two osseointegrated
(Zometa). In 28 of these patients the clinical onset
dental implants were placed in the mandible, 39 of
was preceded by a tooth extraction. Since then,
them in the osteoporosis group and 43 in the control
numerous centers have reported similar observa-
group. The loss of one implant (1.2%) could not be
tions, with incidences of osteonecrosis as high as 12%
attributed to systemic osteoporosis.
for patients treated with intravenous bisphospho-
Two publications including a collection of cases
nates.118,119 Today, intravenous bisphosphonate ther-
with failures and a group of control patients with suc-
apy is considered a major risk for jaw necrosis
cessful implants analyzed factors associated with
(bisphosphonate-related osteonecrosis of the jaw
implant integration failure.113,114 The analysis by
[BRONJ]).120 Elective oral surgery, including the inser-
Blomqvist et al113 included 11 patients with severely
tion of dental implants, is generally contraindicated
atrophied maxillary alveolar processes who had lost
for subjects on this type of medication.121–123
43% of implants placed in a one-stage procedure
The risk for BRONJ appears to be much lower for
together with sinus-floor bone grafts. Mean relative
oral than for intravenous drug administration,119 but
bone mass density was significantly lower in these
appears to increase with the duration of bisphospho-
subjects than in 11 control subjects, matched for sex
nate therapy.120,123 Especially oral administration of the
and age, who had received the same reconstructive
potent aminobisphosphonates with N-containing side
treatment but no grafts. Becker and coworkers114
groups (alendronate/Fosamax; risedronate/Actonel;
compared a case population of 49 individuals who
ibandronate/Boniva or Bonvivia) over several years has
had experienced implant loss to a control population
consisting of 49 successful recall patients. The groups
The use of bisphosphonates in the treatment of
had the same gender distribution but were
osteopenia/osteoporosis requires oral administration
unmatched for age. Ten patients in the test group and
of much lower dosages than in the context of cancer
7 in the control group had a history of osteoporosis.
therapy. The risk for complications of implant therapy
Generalized estimating equations were used to eval-
in such patients—implant failure or BRONJ—is cur-
uate the likelihood of an individual having at least
rently unknown and the subject of controversy.120,125
one implant failure. There was no association
The present literature search yielded only three clini-
between bone density assessed at the radius and
cal studies addressing this issue. As these studies are
ulna and the risk of implant failure. The clinical esti-
very different in design, they will be discussed indi-
mation of local bone quality, however, was related to
vidually without a direct comparison.
implant failure, suggesting that a simple visual
In a report from 2006 presenting data from two
assessment of bone quality at a site considered for
controlled studies, oral bisphosphonate usage was
implantation may be more informative than bone
not associated with osteonecrosis of the jaws.126 In
density measures obtained at peripheral bones.
the first study, the effects of alendronate on alveolar
Based on the results reported above, the evidence
bone loss in patients with moderate or severe perio-
for the efficacy of dental implants in patients with
dontal disease were explored using a double-blind
osteoporosis is on the level of multiple case-control
placebo-controlled design. Patients were randomized
to either 70 mg alendronate or a placebo once weeklyfor 2 years. No BRONJ was observed in this study. The
second study was a parallel-arm controlled study of
Bisphosphonates reduce or even suppress osteoclast
patients with dental implants receiving oral bisphos-
function and can therefore be used in the treatment
phonates (alendronate or risedronate) versus control
of various disorders causing abnormal bone resorp-
dental implant patients over the course of at least 3
tion. The first type of disorders includes malignancies
years. After the observation period, 100% of the
affecting the bone, such as multiple myeloma and
implants in the test group and 99.2% of the implants
bone metastases of breast and prostate cancer.115
in the control group (no bisphosphonates) were con-
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 21
sidered successful, thus exhibiting no statistically sig-
Radiotherapy or Irradiation or Irradiated
nificant difference between the two groups. Also in
With regard to cancer, two aspects need to be consid-
this study, no evidence of BRONJ was observed (evi-
ered: the effect of the disease and the effect of its treat-
ment on the tissues containing the implants.The cancer
In a retrospective analysis of private practice case
may have been treated before the implants were
records, patients with a history of oral bisphospho-
placed, or treatment may become necessary in subjects
nates (alendronate or risedronate; mean time of drug
who already have implants. Furthermore, implants may
usage 3.3 years) and treatment with implant place-
be inserted in residual or grafted bone. Due to the het-
ment at the time of tooth removal or in an edentu-
erogeneity of disease conditions, combinations of treat-
lous area were analyzed for possible side effects.127
ments (radiotherapy and chemotherapy), sequence of
The implants were left to heal for 6 weeks before initi-
events, time of follow-up, and parameters used for
ation of prosthodontic restoration. Patients were fol-
assessment, it was decided to analyze the risk factor
lowed for 12 to 24 months after implant placement,
radiotherapy for dental implant placement in a descrip-
and hard and soft tissue complications were noted.
tive manner, with special emphasis on existing system-
One patient exhibited exposed bone 1 week after
atic reviews. As pointed out in two reviews, several
implant insertion. No other postoperative sequelae or
factors may potentially influence success rates in irradi-
complications were noted in any patients, and all
ated patients. They include, but are not limited to: the
implants were classified as successful 12 to 24
source, dose, and fractionation of irradiation; concomi-
months postinsertion. The authors concluded that
tant therapies (ie, chemotherapy, hyperbaric oxygen
the incidence of BRONJ after an average of 3.3 years
therapy); the anatomic region of implantation; and the
of bisphosphonate intake following implant insertion
timing of medical and dental therapies.130,131
with or without tooth extraction is minimal, and it is
In a recent systematic review, the literature from
comparable to complication rates in patients without
1990 to 2006 was searched for implant failure rates to
a history of oral bisphosphonate therapy (evidence
compare the outcomes of preimplantation radiother-
apy and postimplantation radiotherapy.132 The
The design of the study mentioned above was crit-
authors found similar failure rates for the time points
icized in a letter to the editor of the Journal of Peri-
(3.2% versus 5.4%, respectively; evidence level 2c), but
odontology for the following reasons128: the mean
cautioned that it was difficult to compare the studies
duration of oral bisphosphonates before implant
included because of differences in the exact site of
placement was relatively short; the dosage of alen-
implant placement in relation to the region of radio-
dronate taken by the included patients was low (only
therapy, in lengths of follow-up periods, in implant
four subjects used 70 mg; the remaining patients
systems used, and in the use of prostheses, and
used 35 mg); and the sample size, with 61 patients,
because there were other confounding variables, such
as systemic disease, smoking, and parafunction. When
A retrospective questionnaire was mailed to 1,319
implants were inserted after radiotherapy, the implant
patients in the United States who received implants in
failure rate was lower for the mandible (4.4%) than for
the years 1998 to 2006129; 458 of these patients
the maxilla (17.5%). The authors could not find evi-
returned the questionnaire (34.7%). Anamnestically,
dence in the literature to support delaying implant
115 patients receiving 468 implants reported that they
placement after radiotherapy for 6 to 12 months to
had been taking oral bisphosphonates at the time. Of
maximize implant success. No implant failures were
these 468 inserted implants, all but 2 integrated. The
found to occur below a radiation dose of 45 Gy.
115 patients were asked to come for a clinical visit, and
In a study analyzing the long-term survival rates of
72 patients presented. In these 72 patients, no BRONJ
316 dental implants placed in the mandible in 71
could be diagnosed. The implant failure rate for
patients after radiotherapy and radical surgery, three
patients taking oral bisphosphonates was similar to
different groups were evaluated: (1) implants in non-
that observed for a healthy control population. The
irradiated residual bone, (2) implants in irradiated
authors therefore concluded that oral bisphospho-
residual bone, and (3) implants in grafted bone.133 In
nates represent no risk factor for osteonecrosis in
this study, the patients were treated with implants
implant surgery. Nevertheless, they limited this conclu-
after cancer surgery and after receiving a total
sion to a duration of bisphosphonate intake not
radiochemotherapy dose of 50 Gy. The survival rates
longer than 3 years and also warned against simulta-
2, 3, 5, and 8 years after implant insertion were 95%,
neous medication with corticosteroids (evidence level
94%, 91%, and 75%, respectively. Implants placed in
irradiated bone showed significantly lower survivalrates than implants in nonirradiated mandibularbone. The survival rates for the three groups com-
The International Journal of Oral & Maxillofacial Implants 21
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 22
pared in this study were 95% (group 1), 72% (group
implants (71 IMZ and 178 Brånemark implants) in the
2), and 54% (group 3). The authors could not show
irradiated maxilla and mandible, osteoradionecrosis
that the amount of time between irradiation and
occurred in 2 patients in the mandible, and necrosis
implantation significantly influenced the results.
of soft tissues in the floor of the mouth occurred in 3
A retrospective study reported the survival rates of
patients following implant placement. Osteora-
631 implants inserted in cancer patients over a
dionecrosis resulted in continuity defects of the
period of 25 years.134 This group of irradiated patients
mandible and loss of the implants in the region.
was compared to a control group of nonirradiated
Some authors even state that this severe complica-
patients receiving 614 implants at the same clinic
tion may be underreported in the literature.131
during the same period. The mean time of follow-up
To minimize the risk of osteoradionecrosis due to
in this study was 6.3 years, with a range of 0.5 to 23
implant placement in irradiated bone and to improve
years. During this period, 147 implants in patients
survival and success rates of implants inserted in irra-
undergoing radiotherapy were lost (23.3%), and 76
diated jawbones, hyperbaric oxygen (HBO) therapy
implants (12.4%) failed in the control group. High
has been advocated.139–142 The rationale for the use of
implant failure rates were especially seen after high-
HBO therapy is based on its effect on osteogenesis
dose radiotherapy and a long time after irradiation.
through stimulation of capillary ingrowth, fibroblastic
Failures occurred in all craniofacial regions, but the
proliferation, collagen synthesis, and capillary angio-
greatest risk of implant failures was found for the
genesis.140,143–145 Therefore, HBO has been recom-
frontal bone, zygoma, mandible, and nasal maxilla.
mended for all elective surgery in irradiated tissues, for
In another retrospective study, the survival of den-
the prevention and treatment of osteoradionecro-
tal implants placed in the interforaminal region dur-
sis,146,147 and to improve osseointegration of implants
ing oral cancer surgery was evaluated in relation to
inserted in patients undergoing radiotherapy.131,140–142
postoperative radiotherapy.135 In 48 patients with a
Nevertheless, the use of HBO in irradiated patients
squamous cell carcinoma of the oral cavity, a total of
remains controversial in the literature, with some
139 implants were placed. Of these patients, 21 (with
authors considering it ineffective.148,149 In a recent sys-
61 implants) received postoperative radiotherapy
tematic review from the Cochrane collaboration,
with 10 to 68 Gy on the symphyseal area, while 27
Esposito and coworkers compared the success, mor-
patients (78 implants) were treated with surgery
bidity, patient satisfaction, and cost effectiveness of
alone. The average time interval between surgery and
dental implant treatment performed with and with-
the commencement of radiotherapy was 6 weeks.
out HBO in irradiated patients150 (evidence level 1b).
The success rate of the dental implants was 97% in
After screening of the eligible studies, only one ran-
the postoperative irradiated group and 100% in the
domized controlled clinical trial was identified.151 In
nonirradiated group. The prosthetic success was
this study, endosseous implants were placed in the
lower, irrespective of radiation administration,
anterior part of the mandible either under antibiotic
because in 12 patients a denture could not be fabri-
prophylaxis alone (13 patients) or under antibiotic
cated due to death of the patient (7 patients), psycho-
prophylaxis combined with pre- and postsurgery HBO
logical reasons (4), and loss of an implant (1). The
treatment (13 patients). In the HBO group 85.2% of
authors concluded that postoperative radiotherapy
implants survived, and in the non-HBO group 93.3%
did not negatively affect the osseointegration of
survived. Interestingly, osteoradionecrosis developed
implants placed during oral cancer surgery.
in one patient in the HBO group only. In their system-
Regarding the papers evaluating multiple local
atic review, Esposito and coworkers concluded that
and systemic risk factors for dental implant failure
HBO therapy in irradiated patients requiring dental
(already mentioned above in the context of Crohn
implants may not offer any evident clinical benefits.150
disease, diabetes, osteoporosis, and cardiovasculardiseases), radiotherapy was identified by two studies
as being a statistically significant variable. 63,73 The
When discussing the impact of various medical con-
calculated relative risk of failure for implants due to
ditions on implant failure, it is necessary to keep in
radiation therapy was 2.73 (95% CI 1.10 to 3.77). Two
mind that recorded data may be interrelated. Poten-
papers did not find a significant association between
tial risk factors, particularly those found more fre-
implant failure and irradiation of the patient due to
quently in older adults in general—systemic chronic
diseases, medications taken on a long-term basis,
Besides the problem of implant failure, the risk of
reduced salivary flow—may not be independent of
induction of osteoradionecrosis is always pre-
each other. On the other hand, one single factor alone
sent.136–138 Esser and Wagner137 reported that in their
may not influence the risk measurably, whereas a
group of 64 patients rehabilitated with a total of 249
combination of multiple independent factors may
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 23
have a significant impact. This is supported by retro-
spective investigations showing, for example, that thecombination of specific interleukin-1 gene polymor-
On the basis of the data found in the literature, the
phisms and smoking could be associated with peri-
implant bone loss, whereas only one of these factorsalone is not.152–154 Established risk factors for osteo-
porosis include advanced age, smoking, and alcohol
The level of evidence indicating absolute and relative
consumption, steroid therapy, inadequate calcium
contraindications for oral implant therapy due to sys-
intake, genetic predisposition, and menopause.
temic conditions and treatments is low. Many condi-
There have been attempts in recent years to ana-
tions have been listed as potential risk factors, but
lyze several factors jointly. Ekfeldt and coworkers155
studies comparing patients with and without the
recorded age, gender, smoking habits, alcohol and
condition in a controlled setting are sparse. In gen-
other drug abuse, as well as medical conditions such
eral, the available literature is restricted to case
as diabetes, osteoporosis, cytostatic treatment or
radiotherapy, impaired immune defense, psychologi-
The problem of positive publication bias exists in
cal disorders, and bruxism in 27 subjects with multi-
case reports and smaller case series.
ple implant failures and 27 matched controls. Patients
No data exist for the more severe medical condi-
in the failure group had less favorable bone condi-
tions, simply because implant therapy has not been
tions (bone volume) in general, and bruxism was
noted only in this group. But this group also includedmore subjects with signs of addiction to alcohol, nar-
cotics, and tobacco. In addition, this group also
Based on the published literature it is not possible to
included one subject under cortisone treatment, one
distinguish between subtypes of systemic diseases
with uncontrolled diabetes mellitus, and two psycho-
such as diabetes type 1 and 2 or primary and sec-
logically stressed individuals. In the retrospective
study of Moy and coworkers,73 the database of 1,140
The supposition that subjects with diabetes tend
implant patients, including 170 with implant failures,
to have higher failure rates is equivocal. The only
was subjected to multiple regression analysis to
available matched-control retrospective survey indi-
explore predictors of the number of failed implants
cated no increased risk of failure. The largest study, a
per patient. Using this approach, the variables sex,
retrospective cohort analysis of patients with type 2
age, implant location, smoking, hypertension, coro-
diabetes treated by one clinician, indicated a statisti-
nary artery disease, asthma, diabetes, steroids,
cally significant increase in the relative risk of implant
chemotherapy, head and neck radiation therapy, and
postmenopausal HRT were evaluated. The only vari-
The density of peripheral bone, as currently used
ables identified as having significant predictive value
for the diagnosis of osteoporosis, showed only a weak
for implant failure were location in the maxillary arch,
association with the risk of implant failure in two
diabetes, smoking, and head and neck irradiation.
Observations made in case series can reflect
For bisphosphonate therapy and implant surgery,
cohort effects; for example, results specific to the gen-
the duration, route, and the dosage of the medica-
eration studied that may not be seen in subsequent
tion, as well as the type of bisphosphonate are
generations. There may be differences in dental sta-
reported to play an important role in potential bis-
tus and dental awareness (today’s young generation
phosphonate-related osteonecrosis of the jaws. There
may reach old age with more and better maintained
are not enough data to estimate the risk for oral bis-
teeth), changes in dietary patterns and in the use and
phosphonates in the context of implant therapy, with
abuse of substances (based on availability, prefer-
only one prospective and two retrospective clinical
ences, and the awareness of side effects), and
changes in general health conditions (as environ-
A systematic review of implants placed before and
mental hazards shift and new therapies and pharma-
after radiotherapy reported failure rates of between
ceutical products become available). These may
0% and 12.6% for a follow-up period up to 12 years.
account for many differences that we ascribe to
Osteoradionecrosis following implant placement has
aging.156 It remains to be investigated which changes
been reported in the literature. A recent systematic
observed in older subjects today are truly a conse-
review found no beneficial effect of hyperbaric oxy-
quence of the physiological aging process (and not
due to other extraneous factors), and thus can beexpected to occur in future generations as well.
The International Journal of Oral & Maxillofacial Implants 23
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 24
22. Scully C, Carrozzo M. Oral mucosal disease: Lichen planus. Br J
Oral Maxillofac Surg 2008;46:15–21.
1. Brånemark PI, Adell R, Breine U, Hansson BO, Lindström J,
23. Esposito SJ, Camisa C, Morgan M. Implant retained overden-
Ohlsson A. Intra-osseous anchorage of dental prostheses. I.
tures for two patients with severe lichen planus: A clinical
Experimental studies. Scand J Plast Reconstr Surg
report. J Prosthet Dent 2003;89:6–10.
24. Reichart PA. Oral lichen planus and dental implants. Report of
2. Schroeder A, Pohler O, Sutter F. Gewebsreaktion auf ein Titan-
3 cases. Int J Oral Maxillofac Surg 2006;35:237–240.
Hohlzylinderimplantat mit Titan-Spritzschichtoberfläche.
25. Bornstein MM, Kalas L, Lemp S, Altermatt HJ, Rees TD, Buser D.
Schweiz Monatsschr Zahnheilkd 1976;86:713–727.
Oral lichen planus and malignant transformation. A retro-
3. Blanchaert RH. Implants in the medically challenged patient.
spective follow-up study regarding clinical and histopatho-
logic data. Quintessence Int 2006;37:261–271.
4. Buser D, von Arx T, ten Bruggenkate CM, Weingart D. Basic sur-
26. Czerninski R, Kaplan I, Almoznino G, Maly A, Regev E. Oral
gical principles with ITI implants. Clin Oral Implants Res
squamous cell carcinoma around dental implants. Quintes-
5. Sugerman PB, Barber MT. Patient selection for endosseous
27. Itthagarun A, King NM. Ectodermal dysplasia: A review and
dental implants: Oral and systemic considerations. Int J Oral
case report. Quintessence Int 1997;28:595–602.
Maxillofac Implants 2002;17:191–201.
28. Bergendal T, Eckerdal O, Hallonsten AL, Koch G, Kurol J, Kvint S.
6. Hwang D, Wang HL. Medical contraindications to implant
Osseointegrated implants in the oral habilitation of a boy
therapy: Part I: Absolute contraindications. Implant Dent
with ectodermal dysplasia: A case report. Int Dent J
7. Hwang D, Wang HL. Medical contraindications to implant
29. Smith RA, Vargervik K, Kearns G, Bosch C, Koumjian J. Place-
therapy: Part II: Relative contraindications. Implant Dent
ment of an endosseous implant in a growing child with ecto-
dermal dysplasia. Oral Surg Oral Med Oral Pathol
8. Chanavaz M. Patient screening and medical evaluation for
implant and preprosthetic surgery. J Oral Implantol
30. Davarpanah M, Moon JW, Yang LR, Celletti R, Martinez H. Den-
tal implants in the oral rehabilitation of a teenager with hypo-
9. American Society of Anesthesiologists. Physical Status Classi-
hidrotic ectodermal dysplasia: Report of a case. Int J Oral
fication. http://www.asahq.org/clinical/physicalstatus.htm.
Maxillofac Implants 1997;12:252–258.
31. Guckes AD, McCarthy GR, Brahim J. Use of endosseous
10. Maloney WJ, Weinberg MA. Implementation of the American
implants in a 3-year-old child with ectodermal dysplasia: Case
Society of Anesthesiologists physical status classification sys-
report and 5-year follow-up. Pediatr Dent 1997;19:282–285.
tem in periodontal practice. J Periodontol 2008;79:1124–1126.
32. Escobar V, Epker BN. Alveolar bone growth in response to
11. Beikler T, Flemmig TF. Implants in the medically compromised
endosteal implants in two patients with ectodermal dyspla-
patient. Crit Rev Oral Biol Med 2003;14:305–316.
sia. Int J Oral Maxillofac Surg 1998;27: 445–447.
12. van Steenberghe D, Quirynen M, Molly L, Jacobs R. Impact of
33. Bergendal B. Prosthetic habilitation of a young patient with
systemic diseases and medication on osseointegration. Peri-
hypohidrotic ectodermal dysplasia and oligodontia: A case
report of 20 years of treatment. Int J Prosthodont
13. Wood MR, Vermilyea SG. A review of selected dental literature
on evidence-based treatment planning for dental implants:
34. Kargül B, Alcan T, Kabalay U, Atasu M. Hypohidrotic ectoder-
Report of the Committee on Research in Fixed Prosthodon-
mal dysplasia: Dental, clinical, genetic and dermatoglyphic
tics of the Academy of Fixed Prosthodontics. J Prosthet Dent
findings of three cases. J Clin Pediatr Dent 2001;26:5–12.
35. Giray B, Akça K, Iplikçioglu H, Akça E. Two-year follow-up of a
14. Paquette DW, Brodala N, Williams RC. Risk factors for
patient with oligodontia treated with implant- and tooth-
endosseous dental implant failure. Dent Clin North Am
supported fixed partial dentures: A case report. Int J Oral Max-
15. Mombelli A, Cionca N. Systemic diseases affecting osseointe-
36. Peñarrocha-Diago M, Uribe-Origone R, Rambla-Ferrer J, Guari-
gration therapy. Clin Oral Implants Res 2006;17(suppl
nos-Carbó J. Fixed rehabilitation of a patient with hypo-
hidrotic ectodermal dysplasia using zygomatic implants. Oral
16. Wolff K, Johnson RA, Suurmond D. Fitzpatrick’s Color Atlas &
Surg Oral Med Oral Pathol Oral Radiol Endod
Synopsis of Clinical Dermatology, ed 5. New York: McGraw-
37. Kramer FJ, Baethge C, Tschernitschek H. Implants in children
17. Jensen J, Sindet-Pedersen S. Osseointegrated implants for
with ectodermal dysplasia: A case report and literature
prosthetic reconstruction in a patient with scleroderma:
review. Clin Oral Implants Res 2007;18:140–146.
Report of a case. J Oral Maxillofac Surg 1990:48:739–741.
38. Guckes AD, Brahim, JS, McCarthy GR, Rudy SF, Cooper LF. Using
18. Langer Y, Cardash HS, Tal H. Use of dental implants in the
endosseous dental implants for patients with ectodermal
treatment of patients with scleroderma: A clinical report. J
dysplasia. J Am Dent Assoc 1991;122:59–62.
39. Kearns G, Sharma A, Perrott D, Schmidt B, Kaban L, Vargervik K.
19. Patel K, Welfare R, Coonar HS. The provision of dental implants
Placement of endosseous implants in children and adoles-
and a fixed prosthesis in the treatment of a patient with scle-
cents with hereditary ectodermal dysplasia. Oral Surg Oral
roderma: A clinical report. J Prosthet Dent 1998;79:611–612.
Med Oral Pathol Oral Radiol Endod 1999;88:5–10.
20. Haas SE. Implant-supported, long-span fixed partial denture
40. Guckes AD, Scurria MS, King TS, McCarthy GR, Brahim J.
for a scleroderma patient: A clinical report. J Prosthet Dent
Prospective clinical trial of dental implants in persons with
ectodermal dysplasia. J Prosthet Dent 2002;88:21–25.
21. Öczakir CS, Balmer S, Mericske-Stern R. Implant-prosthodontic
41. Sweeney IP, Ferguson, JW, Heggie AA, Lucas JO. Treatment out-
treatment for special care patients: A case series study. Int J
comes for adolescent ectodermal dysplasia patients treated
with dental implants. Int J Pediatr Dent 2005;15:241–248.
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 25
42. Umberto G, Maiorana C, Ghiglione V, Marzo G, Santoro F,
63. van Steenberghe D, Jacobs R, Desnyder M, Maffei G, Quirynen
Szabó G. Osseointegration and guided bone regeneration in
M. The relative impact of local and endogenous patient-
ectodermal dysplasia. J Craniofac Surg 2007;18:1296–1304.
related factors on implant failure up to the abutment stage.
43. Delaleu N, Jonsson R, Koller MM. Sjögren’s syndrome. Eur J
Clin Oral Implants Res 2002;13:617–622.
64. Alsaadi G, Quirynen M, Komárek A, van Steenberghe D. Impact
44. Mathews SA, Kuien BT, Scofield RH. Oral manifestations of Sjö-
of local and systemic factors on the incidence of oral implant
gren’s syndrome. J Dent Res 2008;87:308–318.
failures, up to abutment connection. J Clin Periodontol
45. Isidor F, Brondum K, Hansen HJ, Jensen J, Sindet-Pedersen S.
Outcome of treatment with implant-retained dental prosthe-
65. Alsaadi G, Quirynen M, Michiles K, Teughels W, Komárek A, van
ses in patients with Sjögren syndrome. Int J Oral Maxillofac
Steenberghe D. Impact of local and systemic factors on the
incidence of failures up to abutment connection with modi-
46. Jackowski J, Andrich J, Käppeler H, Zöllner A, Jöhren P, Müller
fied surface oral implants. J Clin Periodontol 2008;35:51–57.
M. Implant-supported denture in a patient with Huntington’s
66. Tarantino A, Montagnino G, Ponticelli C. Corticosteroids in kid-
disease: Interdisciplinary aspects. Spec Care Dentist
ney transplant recipients. Safety issues and timing of discon-
tinuation. Drug Saf 1995;13:145–156.
47. Ambard A, Mueninghoff L. Rehabilitation of a bulimic patient
67. Dumont RJ, Ensom MH. Methods for clinical monitoring of
using endosteal implants. J Prosthodont 2002;11:176–180.
cyclosporin in transplant patients. Clin Pharmacokinet
48. Lustig JP, Yanko R, Zilberman U. Use of dental implants in
patients with Down syndrome: A case report. Spec Care Den-
68. Sakakura CE, Margonar R, Holzhausen M, Nociti FH Jr, Alba RC
Jr, Marcantonio E Jr. Influence of cyclosporin A therapy on
49. Ekfeldt A. Early experience of implant-supported prostheses
bone healing around titanium implants: A histometric and
in patients with neurologic disabilities. Int J Prosthodont
biomechanic study in rabbits. J Periodontol 2003;74:976–981.
69. Sakakura CE, Marcantonio E Jr, Wenzel A, Scaf G. Influence of
50. Addy L, Korszun A, Jagger RG. Dental implant treatment for
cyclosporin A on quality of bone around integrated dental
patients with psychiatric disorders. Eur J Prosthodont Restor
implants: A radiographic study in rabbits. Clin Oral Implants
51. Jolly DE, Paulson RB, Paulson GW, Pike JA. Parkinson’s disease:
70. Sakakura CE, Margonar R, Holzhausen M, Nociti FH Jr, Alba RC
A review and recommendations for dental management.
Jr, Marcantonio E Jr. Influence of cyclosporin A therapy on
bone healing around titanium implants: A histometric and
52. Heckmann SM, Heckmann JG, Weber HP. Clinical outcomes of
biomechanic study in rabbits. J Periodontol 2007;74:976–981.
three Parkinson’s disease patients treated with mandibular
71. Heckmann SM, Heckmann JG, Linke JJ, Hohenberger W,
implant overdentures. Clin Oral Implants Res
Mombelli A. Implant therapy following liver transplantation:
Clinical and microbiological results after 10 years. J Periodon-
53. Kubo K, Kimura K. Implant surgery for a patient with Parkin-
son’s disease controlled by intravenous midazolam: A case
72. Khadivi V, Anderson J, Zarb GA. Cardiovascular disease and
report. Int J Oral Maxillofac Implants 2004;19:288–290.
treatment outcomes with osseointegration surgery. J Pros-
54. Burgoyne RW, Tan DHS. Prolongation and quality of life for
HIV-infected adults treated with highly active antiretroviral
73. Moy PK, Medina D, Shetty V, Aghaloo TL. Dental implant failure
therapy (HAART): A balancing act. J Antimicrob Chemother
rates and associated risk factors. Int J Oral Maxillofac Implants
55. Rajnay ZW, Hochstetter RL. Immediate placement of an
74. Skamagas M, Breen TL, LeRoith D. Update on diabetes melli-
endosseous root-form implant in an HIV-positive patient:
tus: Prevention, treatment, and association with oral disease.
Report of a case. J Periodontol 1998;69:1167–1171.
56. Baron M, Gritsch F, Hansy AM, Haas R. Implants in an HIV-posi-
75. Kahn BB, Flier JS. Obesity and insulin resistance. J Clin Invest
tive patient: A case report. Int J Oral Maxillofac Implants
76. Taylor GW, Manz MC, Borgnakke WS. Diabetes, periodontal
57. Shetty K, Achong R. Dental implants in the HIV-positive
diseases, dental caries, and tooth loss: A review of the litera-
patient—Case report and review of the literature. Gen Dent
ture. Compend Contin Educ Dent 2004;25:179–190.
77. Graves DT, Liu R, Alikhani M, Al-Mashat H, Trackman PC. Dia-
58. Achong RM, Shetty K, Arribas A, Block MS. Implants in HIV-pos-
betes-enhanced inflammation and apoptosis—Impact on
itive patients: 3 case reports. J Oral Maxillofac Surg
periodontal pathology. J Dent Res 2006;85:15–21.
78. Accursi GE. Treatment outcomes with osseointegrated Bråne-
59. Strietzel FP, Rothe S, Reichart PA, Schmidt-Westhausen AM.
mark implants in diabetic patients: A retrospective study [MSc
Implant-prosthetic treatment in HIV-infected patients receiv-
thesis]. Toronto: University of Toronto, 2000.
ing highly active antiretroviral therapy: Report of cases. Int J
79. Balshi SF, Wolfinger GJ, Balshi TJ. An examination of immedi-
Oral Maxillofac Implants 2006;21:951–956.
ately loaded dental implant stability in the diabetic patient
60. Stevenson GC, Riano PC, Moretti AJ, Nichols CM, Engelmeier
using resonance frequency analysis (RFA). Quintessence Int
RL, Flaitz CM. Short-term success of osseointegrated dental
implants in HIV-positive individuals: A prospective study. J
80. Dowell S, Oates TW, Robinson M. Implant success in people
with type 2 diabetes mellitus with varying glycemic control: A
61. Scheper HJ, Brand HS. Oral aspects of Crohn’s disease. Int Dent
pilot study. J Am Dent Assoc 2007;138:355–361.
81. Smith RA, Berger R, Dodson TB. Risk factors associated with
62. Steiner M, Ramp WK. Endosseous dental implants and the glu-
dental implants in healthy and medically compromised
cocorticoid-dependent patient. J Oral Implantol
patients. Int J Oral Maxillofac Implants 1992;7:367–372.
The International Journal of Oral & Maxillofacial Implants 25
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 26
82. Mericske-Stern R, Zarb GA. Overdentures: An alternative
103. Starck WJ, Epker BN. Failure of osseointegrated dental
implant methodology for edentulous patients. Int J Prostho-
implants after diphosphonate therapy for osteoporosis: A
case report. Int J Oral Maxillofac Implants 1995;10:74–78.
83. Shernoff AF, Colwell JA, Bingham SF. Implants for type II dia-
104. Mason ME, Triplett RG, Van Sickels JE, Parel SM. Mandibular
betic patients: Interim report. VA Implants in Diabetes Study
fractures through endosseous cylinder implants: Report of
Group. Implant Dent 1994;3:183–185.
cases and review. J Oral Maxillofac Surg 1990;48:311–317.
84. Kapur KK, Garrett NR, Hamada MO, et al. A randomized clinical
105. Friberg B, Ekestubbe A, Mellstrom D, Sennerby L. Branemark
trial comparing the efficacy of mandibular implant-sup-
implants and osteoporosis: A clinical exploratory study. Clin
ported overdentures and conventional dentures in diabetic
Implant Dent Relat Res 2001;3:50–56.
patients. Part I: Methodology and clinical outcomes. J Prosthet
106. Cranin AN. Endosteal implants in a patient with corticosteroid
dependence. J Oral Implantol 1991;17:414–417.
85. Balshi TJ, Wolfinger GJ. Dental implants in the diabetic
107. Friberg B. Treatment with dental implants in patients with
patient: A retrospective study. Implant Dent 1999;8:355–359.
severe osteoporosis: A case report. Int J Periodontics Restora-
86. Fiorellini JP, Chen PK, Nevins M, Nevins ML. A retrospective
study of dental implants in diabetic patients. Int J Periodon-
108. von Wowern N, Gotfredsen K. Implant-supported overden-
tics Restorative Dent 2000;20:366–373.
tures, a prevention of bone loss in edentulous mandibles? A
87. Morris HF, Ochi S, Winkler S. Implant survival in patients with
5-year follow-up study. Clin Oral Implants Res 2001;12:19–25.
type 2 diabetes: Placement to 36 months. Ann Periodontol
109. Minsk L, Polson AM. Dental implant outcomes in post-
menopausal women undergoing hormone replacement.
88. Olson JW, Shernoff AF, Tarlow JL, Colwell JA, Scheetz JP, Bing-
Compend Contin Educ Dent 1998;19:859–864.
ham SF. Dental endosseous implant assessments in a type 2
110. August M, Chung K, Chang Y, Glowacki J. Influence of estrogen
diabetic population: A prospective study. Int J Oral Maxillofac
status on endosseous implant osseointegration. J Oral Max-
illofac Surg 2001;59:1285–1289; discussion 1290–1291.
89. Rutar A, Lang NP, Buser D, Bürgin W, Mombelli A. Retrospective
111. Dao TT, Anderson JD, Zarb GA. Is osteoporosis a risk factor for
assessment of clinical and microbiological factors affecting
osseointegration of dental implants? Int J Oral Maxillofac
periimplant tissue conditions. Clin Oral Implants Res
112. Amorim MA, Takayama L, Jorgetti V, Pereira RM. Comparative
90. Abdulwassie H, Dhanrajani PJ. Diabetes mellitus and dental
study of axial and femoral bone mineral density and parame-
implants: A clinical study. Implant Dent 2002;11:83–86.
ters of mandibular bone quality in patients receiving dental
91. Farzad P, Andersson L, Nyberg J. Dental implant treatment in
implants. Osteoporosis Int 2007;18:703–709.
diabetic patients. Implant Dent 2002;11:262–267.
113. Blomqvist JE, Alberius P, Isaksson S, Linde A, Hansson BG. Fac-
92. Peled M, Ardekian L, Tagger-Green N, Gutmacher Z, Machtei
tors in implant integration failure after bone grafting: An
EE. Dental implants in patients with type 2 diabetes mellitus:
osteometric and endocrinologic matched analysis. Int J Oral
A clinical study. Implant Dent 2003;12:116–122.
93. Ferreira SD, Silva GL, Cortelli JR, Costa JE, Costa FO. Prevalence
114. Becker W, Hujoel PP, Becker BE, Willingham H. Osteoporosis
and risk variables for peri-implant disease in Brazilian sub-
and implant failure: An exploratory case-control study. J Peri-
jects. J Clin Periodontol 2006;33:929–935.
94. Cummings SR. Are patients with hip fractures more osteo-
115. Hubner RA, Houston SJ. Bisphosphonates’ use in metastatic
porotic? Review of the evidence. Am J Med 1985;78:487–494.
bone disease. Hosp Med 2005;66:414–419.
95. Melton LJ 3rd, Wahner HW. Defining osteoporosis. Calcif Tis-
116. Miller PD. Optimizing the management of postmenopausal
osteoporosis with bisphosphonates: The emerging role of
96. von Wowern N, Melsen F. Comparative bone morphometric
intermittent therapy. Clin Ther 2005;27:361–376.
analysis of mandibles and iliac crests. Scand J Dent Res
117. Marx RE. Pamidronate (Aredia) and zoledronate (Zometa)
induced avascular necrosis of the jaws: A growing epidemic. J
97. von Wowern N, Storm TL, Olgaard K. Bone mineral content by
Oral Maxillofacial Surg 2003;61:1115–1118.
photon absorptiometry of the mandible compared with that
118. Durie BGM, Katz M, Crowley J. Osteonecrosis of the jaws and
of the forearm and the lumbar spine. Calcif Tissue Int
bisphosphonates. N Engl J Med 2005;353:99–102.
119. American Association of Oral and Maxillofacial Surgeons,
98. Jacobs R, Ghyselen J, Koninckx P, van Steenberghe D. Long-
Advisory Task Force on Bisphosphonate-Related Osteonecro-
term bone mass evaluation of mandible and lumbar spine in
sis of the Jaws. American Association of Oral and Maxillofacial
a group of women receiving hormone replacement therapy.
Surgeons position paper on bisphosphonate-related
osteonecrosis of the jaws. J Oral Maxillofac Surg
99. Glaser DL, Kaplan FS. Osteoporosis. Definition and clinical pre-
sentation. Spine 1997;22 (24, suppl):12S–16S.
120. Dello Russo NM, Jeffcoat MK, Marx RE, Fugazzotto P.
100. Fujimoto T, Niimi A, Nakai H, Ueda M. Osseointegrated
Osteonecrosis in the jaws of patients who are using oral bis-
implants in a patient with osteoporosis: A case report. Int J
phosphonates to treat osteoporosis [JOMI current issues
Oral Maxillofac Implants 1996;11:539–542.
forum]. Int J Oral Maxillofacial Implants 2007;22:146–153.
101. Eder A, Watzek G. Treatment of a patient with severe osteo-
121. Scully C, Madrid C, Bagan J. Dental endosseous implants in
porosis and chronic polyarthritis with fixed implant-sup-
patients on bisphosphonate therapy. Implant Dent
ported prosthesis: A case report. Int J Oral Maxillofac Implants
122. Wang HL, Weber D, McCauley LK. Effect of long-term oral bis-
102. Degidi M, Piattelli A. Immediately loaded bar-connected
phosphonates on implant wound healing: Literature review
implants with an anodized surface inserted in the anterior
and a case report. J Periodontol 2007;78:84–594.
mandible in a patient treated with diphosphonates for osteo-
123. Marx RE. Bisphosphonate-induced osteonecrosis of the jaws:
porosis: A case report with a 12-month follow-up. Clin Implant
A challenge, a responsibility, and an opportunity [editorial].
Int J Periodontics Restorative Dent 2008;28:5–6.
12_1a_bornstein.qxp 9/8/09 3:04 PM Page 27
124. Otomo-Corgel J. Implants and oral bisphosphonates: Risky
141. Granström G, Tjellström A, Brånemark PI. Osseointegrated
business? [commentary]. J Periodontol 2007;78:373–376.
implants in irradiated bone: A case-controlled study using
125. Mulligan R, Sobel S. Osteoporosis: Diagnostic testing, interpre-
adjunctive hyperbaric oxygen therapy. J Oral Maxillofac Surg
tations, and correlations with oral health—Implications for
dentistry. Dent Clin North Am 2005;49:463–484.
142. Granström G. Placement of dental implants in irradiated
126. Jeffcoat MK. Safety of oral bisphosphonates: controlled stud-
bone: The case for using hyperbaric oxygen. J Oral Maxillofac
ies on alveolar bone. Int J Oral Maxillofac Implants 2006;21:
143. Greenwood TW, Gilchrist AG. Hyperbaric oxygen and wound
127. Fugazzotto PA, Lightfoot WS, Jaffin R, Kumar A. Implant place-
healing in post-irradiation head and neck surgery. Br J Surg
ment with or without simultaneous tooth extraction in
patients taking oral bisphosphonates: Postoperative healing,
144. Mainous EG, Hart GB. Osteoradionecrosis of the mandible.
early follow-up, and incidence of complications in two private
Treatment with hyperbaric oxygen. Arch Otolaryngol
practices. J Periodontol 2007;78:1664–1669.
128. Elad S, Yarom M, Khamaisi M. Comment on: Fugazzoto PA,
145. Hart GB, Mainous EG. The treatment of radiation necrosis with
Lightfoot WS, Jaffin R, Kumar A. Implant placement with or
hyperbaric oxygen (OHP). Cancer 1976;37:2580–2585.
without simultaneous tooth extraction in patients taking oral
146. Marx RE, Johnson RP, Kline SN. Prevention of osteoradionecro-
bisphosphonates: Postoperative healing, early follow-up, and
sis: A randomized prospective clinical trial of hyperbaric oxy-
incidence of complications in two private practices. J Perio-
gen versus penicillin. J Am Dent Assoc 1985;111:49–54.
147. Marx RE, Ehler WJ, Tayapongsak P, Pierce LW. Relationship of
129. Grant BT, Amenedo C, Freeman K, Kraut RA. Outcomes of plac-
oxygen dose to angiogenesis induction in irradiated tissue.
ing dental implants in patients taking oral bisphosphonates:
A review of 115 cases. J Oral Maxillofac Surg 2008;66:223–230.
148. Keller EE. Placement of dental implants in the irradiated
130. Chiapasco M. Implants for patients with maxillofacial defects
mandible: A protocol without adjunctive hyperbaric oxygen. J
and following irradiation. In: Lang NP, Karring T, Lindhe J (eds).
Oral Maxillofac Surg 1997;55:972–980.
Proceedings of the 3rd European Workshop on Periodontol-
149. Donoff RB. Treatment of the irradiated patient with dental
ogy. Berlin: Quintessence, 1999:557–607.
implants: The case against hyperbaric oxygen treatment. J
131. Granström G. Radiotherapy, osseointegration and hyperbaric
Oral Maxillofac Surg 2006;64:819–822.
oxygen therapy. Periodontol 2000 2003;33:145–162.
150. Esposito M, Grusovin MG, Patel S, Worthington HV, Coulthard
132. Colella G, Cannavale R, Pentenero M, Gandolfo S. Oral implants
P. Interventions for replacing missing teeth: Hyperbaric oxy-
in radiated patients: A systematic review. Int J Oral Maxillofac
gen therapy for irradiated patients who require dental
implants. Cochrane Database Syst Rev 2008;CD003603.
133. Yerit KC, Posch M, Seemann M, et al. Implant survival in
151. Schoen PJ, Raghoebar GM, Bouma J, et al. Rehabilitation of
mandibles of irradiated oral cancer patients. Clin Oral
oral function in head and neck cancer patients after radio-
therapy with implant-retained dentures: Effects of hyperbaric
134. Granström G. Osseointegration in irradiated cancer patients:
oxygen therapy. Oral Oncol 2007;43:379–388.
An analysis with respect to implant failures. J Oral Maxillofac
152. Feloutzis A, Lang NP, Tonetti MS, et al. IL-1 gene polymorphism
and smoking as risk factors for peri-implant bone loss in a well-
135. Schepers RH, Slagter AP, Kaanders JHAM, van den Hoogen
maintained population. Clin Oral Implants Res 2003;14:10–17.
FJA, Merkx MAW. Effect of postoperative radiotherapy on the
153. Gruica B, Wang HY, Lang NP, Buser D. Impact of IL-1 genotype
functional result of implants placed during ablative surgery
and smoking status on the prognosis of osseointegrated
for oral cancer. Int J Oral Maxillofac Surg 2006;35:803–808.
implants. Clin Oral Implants Res 2004:15:393–400.
136. Watzinger F, Ewers R, Henninger A, Sudasch G, Babka A, Woelfl
154. Lachmann S, Kimmerle-Müller E, Axmann D, Scheideler L,
G. Endosteal implants in the irradiated lower jaw. J Cran-
Weber H, Haas R. Associations between peri-implant crevicu-
iomaxillofac Surg 1996;24:237–244.
lar fluid volume, concentrations of crevicular inflammatory
137. Esser E, Wagner W. Dental implants following radical oral can-
mediators, and composite IL-1A -889 and IL-1b + 3954 geno-
cer surgery and adjuvant radiotherapy. Int J Oral Maxillofac
type. A cross-sectional study on implant recall patients with
and without clinical signs of peri-implantitis. Clin Oral
138. Wagner W, Esser E, Ostkamp K. Osseointegration of dental
implants in patients with and without radiotherapy. Acta
155. Ekfeldt A, Christiansson U, Eriksson T, et al. A retrospective
analysis of factors associated with multiple implant failures in
139. Jisander S, Grenthe B, Alberius P. Dental implant survival in the
maxillae. Clin Oral Implants Res 2001;12:462–467.
irradiated jaw: A preliminary report. Int J Oral Maxillofac
156. Mombelli A. Aging and the periodontal and peri-implant
microbiota. Periodontol 2000 1998;16:44–52.
140. Larsen PE. Placement of dental implants in the irradiated
mandible: A protocol involving adjunctive hyperbaric oxygen. J Oral Maxillofac Surg 1997;55:967–971.
The International Journal of Oral & Maxillofacial Implants 27
Preparing for an HG pregnancy Personal Worksheet Disclaimer: None of the information provided on this website is meant to suggest any medical course of action. Instead the information is intended to inform and to raise awareness so that these issues can be discussed by / with qualified Healthcare Professionals with their patients. The responsibility for any medical treatment rests with t
MIT Department of Biology: H. Robert Horvitzhttp://web.mit.edu/biology/www/facultyareas/facresearch/horvitz. Home Faculty and Areas of Research H. Robert Horvitz OVERVIEW Medical InstitutePh.D. 1974, Harvard Universitytransduction, cell lineage, cell fate, and morphogenesis, with some emphasis on nervous system development. Study ofthe cellular and molecular