osteo integrated implant in maxillofacial rehabilitaiton hed23993

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Osseointegrated Implant Based Dental Rehabilitation in Head and Neck Reconstruction Patients Sydney Ch’ng, MD, PhD 1,2,3, Roman J. Skoracki, MD 1 , Jesse C. Selber, MD 1 , Peirong Yu, MD 1 , Jack W. Martin, DDS, MS 4 , Theresa M. Hofstede, DDS 4 , Mark S. Chambers, DMD, MS 4 , Jun Liu, MD, PhD 1 , Matthew M. Hanasono, MD 1 1 Department of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA 2 Department of Plastic Surgery, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia 3 The Institute of Academic Surgery, University of Sydney, New South Wales, Australia 4 Dental Oncology Section, Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA Running Title: Osseointegrated Implants Funding: No funding was received for this study. Presented at: American Association of Plastic Surgeons 2013 Annual Meeting, New Orleans, LA Key Words: Head and Neck Cancer; Osseointegrated Implants; Microvascular Free Flaps; Fibula Free Flap; Prosthodontics CORRESPONDING AUTHOR Matthew M. Hanasono, M.D. Department of Plastic Surgery University of Texas M. D. Anderson Cancer Center 1515 Holcombe Boulevard, Unit 443 Houston, Texas 77030 Telephone: 713-794-1247 Fax: 713-794-5492 Email: [email protected] This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process which may lead to differences between this version and the Version of Record. Please cite this article as an ‘Accepted Article’, doi: 10.1002/hed.23993 This article is protected by copyright. All rights reserved.

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  • Osseointegrated Implant Based Dental Rehabilitation in Head and Neck

    Reconstruction Patients

    Sydney Chng, MD, PhD1,2,3, Roman J. Skoracki, MD1, Jesse C. Selber,

    MD1, Peirong Yu, MD1, Jack W. Martin, DDS, MS4, Theresa M. Hofstede,

    DDS4, Mark S. Chambers, DMD, MS4, Jun Liu, MD, PhD1, Matthew M.

    Hanasono, MD1

    1Department of Plastic Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA 2Department of Plastic Surgery, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia 3The Institute of Academic Surgery, University of Sydney, New South Wales, Australia 4Dental Oncology Section, Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA

    Running Title: Osseointegrated Implants Funding: No funding was received for this study. Presented at: American Association of Plastic Surgeons 2013 Annual Meeting, New Orleans, LA Key Words: Head and Neck Cancer; Osseointegrated Implants; Microvascular Free Flaps; Fibula Free Flap; Prosthodontics

    CORRESPONDING AUTHOR

    Matthew M. Hanasono, M.D. Department of Plastic Surgery University of Texas M. D. Anderson Cancer Center 1515 Holcombe Boulevard, Unit 443 Houston, Texas 77030 Telephone: 713-794-1247 Fax: 713-794-5492 Email: [email protected]

    This article has been accepted for publication and undergone full peer review but has not beenthrough the copyediting, typesetting, pagination and proofreading process which may lead todifferences between this version and the Version of Record. Please cite this article as anAccepted Article, doi: 10.1002/hed.23993

    This article is protected by copyright. All rights reserved.

  • 2

    Abstract

    Background: Dental restoration is an integral part of head and neck cancer

    reconstruction.

    Methods: We evaluated the success rate of osseointegrated implants in head

    and neck cancer patients, comparing outcomes between implants placed in

    fibula free flaps to those placed in native mandibular and maxillary bone.

    Results: A total of 1132 implants were placed in 246 patients. The overall

    implant loss rate was 3.7% and was higher in fibula flaps (8.2%) compared to

    the native mandible (2.6%) and maxilla (2.2%), although these differences did

    not reach statistical significance (p=0.059 and p=0.053, respectively). The

    failure rate was 8.0% for implants placed after radiation and 3.6% in patients

    who did not undergo radiation (p=0.097). Osteoradionecrosis occurred in 19

    patients (7.7%) following implant placement, and tobacco use was found to be

    a risk factor (p=0.027).

    Conclusions: Osseointegrated implants are reliable in head and neck cancer

    patients including those undergoing bony free flap reconstruction.

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  • 3

    Introduction

    Advances in reconstructive surgery, particularly in the area of

    microvascular reconstruction, have resulted in improved aesthetic and

    functional outcomes for patients with head and neck cancer. However, in spite

    of increasingly sophisticated reconstructive techniques, head and neck cancer

    patients frequently lack functional dentition, which not only affects mastication,

    but speech, swallowing, and appearance as well. Dental rehabilitation with

    conventional prostheses following radiation therapy, tumor resection, and/or

    flap reconstruction is often unsuccessful due to altered tissue contours and

    lack of adequate dentition for fixation. In many cases, stable prosthetic

    retention can only be achieved with the use of osseointegrated implants.1,2

    The reliability and efficacy of osseointegrated implants have been well

    documented in the non-cancer, edentulous population.3 In contrast, the

    reliability, safety, and utility of osseointegrated implant placement in the head

    and neck cancer population remains incompletely defined, mainly due to the

    limited availability of large, single-center reports in the literature. Successful

    dental restoration with implants is more challenging in this population given

    the surgical resection of bone and mucosa and irradiation of oral cavity

    tissues, as well as a high prevalence of tobacco use and other risk factors for

    impaired healing. Additionally, implants in this population are often placed

    into osseous free flaps.4-6 While successful osseointegration into osseous free

    flaps has been reported in several case series, it is unclear whether they are

    as reliable as implants placed into native mandibular and maxillary bone.

    Our primary objective was to determine implant success rates in head

    and neck cancer patients, comparing the outcomes of osseointegrated

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  • 4

    implants in vascularized osseous free flaps to implants placed in native

    mandibular and maxillary bone. A secondary objective was to assess the

    effect of risk factors associated with poor healing, such as radiation therapy,

    chemotherapy, tobacco use, and diabetes mellitus. Finally, we evaluated how

    many patients completed dental restoration, including implant placement,

    uncovering, abutment placement, and prosthesis delivery.

    Methods

    This is a retrospective review of head and neck cancer patients who

    underwent osseointegrated implant placement at our institution between 2005

    and 2011, during which data was prospectively collected on patients who

    received osseointegrated implants for dental restoration. Institutional review

    board approval was obtained prior to undertaking this study. Dental

    oncologists trained in prosthodontics placed all implants.

    In our practice, patients with satisfactory remaining dentition and

    dentoalveolar architecture are rehabilitated with conventional non-implant-

    retained prostheses. In patients who were judged to require osseointegrated

    implants for adequate prosthetic stability or had failed a trial of conventional

    prosthesis use, implants were recommended provided the patient was

    motivated to undergo the multi-stage procedure and would agree to regular

    follow-up and practice adequate hygiene care. Insurance preauthorization

    was sought in all potential osseointegrated implant candidates, and, as other

    centers have experienced, only obtained in a subset of patients. Those

    whose insurance would not reimburse for implant rehabilitation were given the

    option of bearing the costs on their own.

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  • 5

    Implant success was defined as a painless and stable fixture without

    evidence of peri-implant infection or radiographic lack of osseointegration.

    The implant survival time was defined as the time interval from date of implant

    placement to the date of implant failure or last follow-up date, whichever

    occurred first. The Kaplan-Meier product-limit method was used to estimate

    the cumulative survival rates. A log-rank test was used to compare the

    cumulative time to first-implant-loss rate among the various groups.

    A generalized estimating equation (GEE) model was applied in testing

    for risk factors associated with implant loss, accounting for within-patient

    correlation in the estimation. The chi-square and Fishers exact tests were

    used as appropriate to investigate the association between various

    parameters and successful completion of oral rehabilitation. Using step-wise

    model selection, a multivariate logistic regression model was used to estimate

    the odds ratios (OR) associated with significant risk factors for the

    development of osteoradionecrosis. All tests were two-sided. A p-value of

  • 6

    extraction if indicated) prior to commencement of radiation therapy. All

    osseous free flaps receiving osseointegrated implants in this study were fibula

    free flaps.

    Astra Tech implants (Dentsply Implants, Mannheim, Germany) were

    used in all patients. When present, titanium reconstruction plates and screws

    were partially or entirely removed if they interfered with proper placement of

    osseointegrated implants in the delayed setting. Free flap skin paddle

    debulking was performed as needed to optimize the soft tissue contour over

    the alveolar ridge or fibula for prosthetic fitting.

    Stage 2. The implants were uncovered, tested for stability (manually,

    rather than by resonance frequency analysis, which is an objective measure

    of magnet-induced vibration, not available at out center), and fitted with

    abutments. Any unstable implants were removed or not used. Final soft tissue

    modifications, including further free flap skin paddle debulking and

    vestibuloplasty, which involved deepening the gingivolabial or gingivobuccal

    sulcus and full-thickness skin grafting held in place with a bolster for 5 days,

    were performed when necessary to create an optimal soft tissue platform for

    the dental prosthesis. After healing, a removable dental prosthesis was

    fashioned to complete the restoration, and revised subsequently as

    necessary. Completion of Stage 2, with prosthesis fabrication and functional

    loading of the implants, was considered a surrogate marker for successful

    completion of dental implant oral rehabilitation in this study.

    Results

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    A total of 1132 implants were placed in 246 head and neck cancer

    patients, including 166 males and 80 females, with a median age of 59 years.

    Other demographic information, including potential risk factors for implant loss

    is shown in Table 1. The dose of radiation ranged from 60 to 72 Gray and

    intensity modulated radiation therapy (IMRT) was the modality used. Due to

    the retrospective nature of the study, the precise radiation fields could not be

    obtained and, therefore, it was not possible to estimate dosimetry to each of

    the implant sites. Active tobacco use was defined as cigarette smoking within

    30 days of implant placement. The diagnosis of diabetes mellitus included

    patients with non-insulin dependent diabetes mellitus requiring treatment with

    oral hypoglycemics (rather than diet-controlled) or insulin-dependent diabetes

    mellitus. Primary tumor types, sites, and T and N classifications are shown in

    Table 2.

    Osseointegrated implants were placed immediately (at the time of

    surgical ablation) in 115 patients (46.7%), and delayed in 90 patients (36.6%).

    An additional 41 study patients (16.7%) did not undergo resection or flap

    reconstruction. This group was treated with definitive radiation therapy or

    combined radiation and chemotherapy, and underwent implant placement

    following dental extraction 4 to 6 weeks prior to starting radiation therapy.

    Osseointegrated implants were placed prior to beginning radiation therapy in

    147 patients (59.8%) and after the conclusion of radiation therapy in 18

    (7.3%). Eighty-one patients (32.9%) did not receive any radiation.

    Sixty-six patients (26.8%) received soft tissue free flap reconstruction,

    including radial forearm free flap (n=32), anterolateral thigh free flap (n=27),

    ulnar artery perforator flap (n=4), rectus abdominis myocutaneous free flap

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    (n=2), and lateral arm free flap (n=1). Sixty-seven patients (27.2%) had

    osseous reconstruction using a fibula free flap. Fifty-four patients (22%) had a

    total of 243 osseointegrated implants placed in their fibula free flaps (mean

    number of implants, 4.5; range, 2-9). One hundred eighty-five patients had a

    total of 618 implants placed in the native mandible, and 90 patients had a total

    of 271 implants placed in the native maxilla (Table 3). The rate of successful

    implant osseointegration and retention in the mandible, maxilla and fibula free

    flap were 97.4%, 97.8% and 91.8%, respectively. There was a trend for

    reduced implant survival in fibula free flaps as compared with the native

    mandible and maxilla that did not reach statistical significance (p=0.059 and

    p=0.057, respectively).

    Overall, 42 of the 1132 implants (3.7%) were lost in 22 of 246 patients

    (8.9%) at a median time of 33.7 months (range, 0.9 to 92.7 months). Further

    analysis revealed that the implant failure rate was progressive over time,

    increasing from 1.4% at 12 months to 3.9% with follow-up greater than 36

    months, and to 5.1% for those followed over 60 months (Table 4). Most of the

    implants lost in the native mandible and maxilla occurred in the first 3 years,

    but implants placed in fibula free flaps experienced increasing attrition beyond

    60 months (Figure 1). In the group that received surgery with or without

    chemoradiation, 37 implants out of 964 were lost (3.8% loss rate). In the

    group that received only radiation or radiation plus chemotherapy, 5 out of

    168 implants were lost (3.0% loss rate). This difference was not statistically

    significant (p=0.82).

    Implant failure was more common in the subgroup that had implants

    placed after radiation therapy (8.0%), compared to those who did not undergo

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  • 9

    radiation therapy (3.6%). This difference, however, was not statistically

    significant (p=0.097) (Table 5 and Figure 2). Further analysis based on the

    site of implant placement showed that implants placed in a fibula that never

    received radiation were less likely to fail than those placed in bone that had

    received radiation prior to or following radiation (5.1% vs.13.0% and 18.6%,

    p

  • 10

    A univariate analysis examining age>65, diabetes mellitus, active

    smoking (vs. prior smoking and nonsmoking status), chemotherapy, and free

    flap type (none vs. soft tissue free flap vs. fibula free flap), demonstrated

    active smoking to be a significant risk factor for the development of ORN

    (p=0.027; other data not shown). Similarly, a multivariate logistic regression

    model for the development of ORN also found active smoking to be a

    significant risk factor (OR=2.84; 95% confidence interval (CI)=1.01-7.98;

    p=0.048).

    Long-term follow-up information was incomplete for 16 patients (6.5%),

    including 10 who pursued dental rehabilitation at another institution. Of the

    remaining 230 patients (93.5%), 184 (80.0%) completed Stage 2 (i.e.,

    fabrication of and functional loading with permanent prosthesis). The median

    time from implant placement until completion of Stage 2 was 7.0 months

    (range, 1.1 to 23.2 months).

    Disease recurrence was associated with failure to complete Stage 2

    (p

  • 11

    Osseointegrated implants provide prosthetic retention that is generally

    superior to traditional dentures secured by clasps to the remaining teeth or

    dental adhesives in the edentulous. Osseointegrated implants also result in

    retention of bone height, while traditional dentures are associated with gradual

    bone loss. In edentulous patients, bone loss is frequently progressive over

    time to the point that stable fixation is impossible. This is an outcome study of

    osseointegrated implant dental rehabilitation in a large oncologic patient

    cohort from a single institution. The results demonstrate that osseointegrated

    implants are very reliable, even in a cohort of highly challenging patients.

    Our overall implant survival rate of 96.3% at a median follow-up period

    of 33.7 months (92.8% and 92.2% for those followed up to 3 and 5 years,

    respectively) is within the range of figures previously reported in the literature,

    which includes implant survival rates of 81 to 99%, averaging 87% in studies

    ranging from 0 to 10 years in head and neck cancer patients.2,5-12 In keeping

    with Shaw et al.2 and Watzinger et al.,13 but in contrast to Schliephake et al.,14

    we found the vascularized free flaps to be less reliable in retaining

    osseointegrated implants, though still with a relatively high survival rate of

    91.8%.2,13,14

    In this study, the administration of radiation therapy, and the sequence

    of radiation therapy in relation to implant placement did not significantly affect

    the implant survival rate, except in fibula free flaps. In our series, 59.8% of

    patients who underwent surgical resection of a primary tumor either

    underwent implant placement at the time of ablative surgery into the native

    mandible or maxilla, or in cases of microvascular osseous free flap

    reconstruction, as a secondary staged procedure into the neomandible that

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  • 12

    took place prior to commencement of radiation therapy while 7.3% of patients

    had implant placement following the completion of radiation therapy. Primary

    or early implant placement has been thought to be more reliable because the

    detrimental effects of radiation therapy on bone do not seem to begin until

    about 6 weeks after radiation therapy has started.15 Since radiation therapy

    does not usually begin until 4 to 6 weeks following the ablative surgery, it is

    believed that there is sufficient time for osseointegration to take place prior to

    exposure to the damaging effects of radiation therapy.4

    The proponents of secondary implant placement have argued that a

    delayed approach allows for more comprehensive assessment of disease

    status, oral function, and patient motivation, as well as more precise

    prosthetic planning.4 Several clinical studies, supplemented by histology

    studies in animals, have demonstrated that dental osseointegrated implants

    placed in irradiated recipient bed are reliable.2,3,16-18 Most, however, advocate

    for a delay of at least nine months following radiation therapy to allow for

    recovery of the bony tissue from the deleterious effects of irradiation on

    cellularity and vascularity.19,20 While our failure rates for implants placed into

    irradiated native mandibular and maxillary bone was 0%, the 18.6% failure

    rate for implants placed into fibular bone suggests that irradiation might be

    considered a relative contraindication to implant placement in osseous free

    flaps.

    The incidence of ORN occurring after implant placement in our patient

    cohort was 7.7%. A recent paper by Tsai et al.21 from our institution quoted a

    7.5% ORN rate among 402 oropharyngeal cancer patients receiving definitive

    radiation therapy between 2000 and 2008. Epstein et al.22 found the incidence

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  • 13

    of mandibular ORN in head and neck cancer patients to range from 5.8 to

    44.2% based on approximately 4000 subjects in 13 studies combined. These

    disparate figures may result from the subjectivity in diagnosis, with the

    spectrum of presentation ranging from a clinically inconsequential small area

    of bone exposure to a complex orocutaneous fistula or a pathologic fracture,

    and the varying clinicodemographic parameters within different patient

    population. In our series, several pathologic fractures were noted in implanted

    patients and required segmental mandibulectomy and bony free flap

    reconstruction. Our experience with implant loss secondary to ORN in fibula

    free flaps is limited, but, in all 4 cases recorded, resulted in complete loss of

    all implants placed into the free flap, and fibular fracture in 1 case.

    Active smoking was a predictor for ORN in our patients. Other factors

    reported in the literature to be associated with ORN include radiation therapy

    to more than 50% volume of the mandibular body, alcohol consumption,

    larger tumors, advanced age, increased radiation dose, hyperfractionation,

    dentate (versus edentulous) state, post-radiation dental extractions, tumor

    location (retromolar trigone at increased risks), poor oral hygiene and poor

    nutritional status. Given the morbidity of ORN observed in our series, we

    would recommend that active smoking in irradiated patients be considered a

    contraindication to secondary implant placement in all patients, and that it

    probably even be considered a contraindication to implant loading in patients

    who have had implant placement prior to irradiation.

    Some evidence suggests that hyperbaric oxygen (HBO) therapy is

    associated with improved outcomes in preventing and healing late radiation

    tissue injury in the head and neck.23 However, it has not been found, based

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  • 14

    on the limited amount of clinical research available, to offer any appreciable

    clinical benefits specifically in irradiated patients requiring dental implants.24

    Because HBO is employed as treatment rather than prophylaxis for ORN in

    our practice, we are unable to answer the question of whether it is effective in

    preventing implant loss with our data.

    In this series the oral rehabilitation completion rate was 80%. Other

    studies have quoted completion rates of 35 to 75%.7 While patient selection in

    this series may be considered liberal, our practice is governed to a large

    extent by practicality; many of our patients are referred from distant locations,

    and desire to consolidate surgical procedures, favoring primary implant

    placement. Patients are asked to opt for implant placement many times at the

    start of their cancer treatment, in order to minimize the number of surgical

    procedures as well as to avoid implant placement following radiation therapy.

    However, at that time, the final oral function (i.e., speech and swallowing) is

    unknown, as is the potential other functional problems, such as oral

    incompetence or trismus that might result in patients not completing dental

    rehabilitation. In this initial experience, we did try to select for patients who

    had good oncologic and functional prognosis to undergo implant placement,

    but acknowledge that functional outcomes in head and neck cancer are often

    hard to predict and may change over time, resulting in failure to complete

    dental restoration or a prosthesis that is primarily cosmetic in nature, which

    may still be of considerable value to many patients. Because cancer

    recurrence is the predominant obstacle to completion of oral rehabilitation, an

    argument can be made for delaying implant placement, for example, until after

    the median time to diagnosis of recurrence (11.2 months following definitive

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  • 15

    treatment), particularly in patients with more advanced disease. Of note, in

    our practice, osseointegrated implant dental rehabilitation has been generally

    funded by health insurance or, less commonly, self-funded.

    Some have advocated the replacement of free flap skin paddle around

    osseointegrated implant with mucosal grafts because the latter protect against

    marginal bone loss and peri-implant inflammation.25 We routinely debulk the

    fibula free flap soft tissue and skin paddle for implant placement, but have not

    found peri-implant skin to be problematic enough to prompt a change in

    practice. In non-irradiated patients in whom the soft tissue component is

    bulky, the skin paddle can be excised in a delayed setting and the periosteum

    left to mucosalize.

    One challenge in studying implant loss is the most appropriate way to

    count and analyze endpoints.13 Comparison of outcomes from previously

    published papers on osseointegrated dental rehabilitation has to be

    undertaken with caution. There is reasonable overall agreement on the criteria

    for implant survival/success, but there continues to be a lack of consensus on

    the most appropriate form of statistical analysis. Varied treatment protocols

    and reconstructive techniques further compound making effective

    comparisons. We decided to study our patients undergoing osseointegrated

    implant placement utilizing a simple input/output analysis when presenting

    implant survival/loss, Kaplan-Meier curves to depict time to first implant loss in

    a patient, and a GEE model in testing for risk factors associated with implant

    survival in order to account for within-patient correlation.

    Conclusions

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    Osseointegrated dental rehabilitation is safe and reliable in head and

    neck cancer patients. Implant failure rates are higher in fibula free flaps

    compared to the native mandible or maxilla, but success rates still exceed

    91%. Radiation therapy adversely affects implant survival in fibula free flaps

    but not the native mandible or maxilla. Disease recurrence is the biggest

    impediment to successful completion of rehabilitation.

    Based on our findings, we consider patients who have received or will

    receive cancer treatment for curative intent, demonstrate motivation for dental

    rehabilitation and compliance with proper oral hygiene, and have the financial

    and social resources to complete the dental rehabilitation process candidates

    for osseointegrated implant placement. If patients have received prior

    irradiation, we require that they not be active smokers. We consider prior

    irradiation a relative contraindication to implant placement in fibula free flap

    bone. We are now actively exploring the effect of hyperbaric oxygen on

    improving success rates in this subgroup.

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  • 19

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    Interventions for replacing missing teeth: hyperbaric oxygen therapy for

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    irradiated patients who require dental implants. Cochrane Database Syst

    Rev 2008, Issue 1. Art. No.: CD003603.

    25. Chang YM, Wallace CG, Tsai CY, Shen YF, Wei FC. Dental implant

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    Figure Legend

    Figure 1. Time to first osseointegrated implant loss by osseointegrated

    implant site.

    Figure 2. Time to first implant osseointegrated loss by timing of radiotherapy.

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    Tables Table 1. Patient characteristics

    Variable No. of Patients (%) (n=246)

    No. of Implants (%) (n=1132)

    Age >65 Years 88 (35.8) 383 (33.8)

    Preoperative Radiation 18 (7.3) 100 (8.8)

    Postoperative Radiation 147 (59.8) 695 (61.4)

    Chemotherapy 99 (40.2) 480 (42.4)

    Tobacco Use 102 (41.5) 471 (41.6)

    Diabetes mellitus 38 (15.5) 153 (13.5)

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    Table 2. Primary tumor type, site, and classification. Subsite

    Type Buccal FOM Lip Mandible Nasal/

    Maxillary

    Pharynx Skin Tongue

    ACC 0 2 0 1 4 1 0 2

    Adenocarcinoma 0 0 0 1 2 0 0 0

    Ameloblastic

    Carcinoma

    0 0 0 4 2 0 0 0

    Desmoid Tumor 0 0 0 4 0 0 0 0

    Fibrosarcoma 0 0 0 2 1 0 0 0

    Hemangio-

    endothelioma

    0 0 0 0 1 0 0 0

    Melanoma 0 0 0 1 2 0 0 0

    MEC 0 0 0 2 1 0 0 0

    ORN 0 0 0 22 3 0 0 0

    Osteosarcoma 0 0 0 6 1 0 0 0

    SCC 9 23 3 46 16 41 5 39

    T1 0 4 1 0 0 2 0 0

    T2 4 5 1 5 2 7 0 13

    T3 2 2 1 3 3 13 3 10

    T4 3 9 0 32 11 10 4 8

    N0 2 13 3 23 4 9 0 10

    N1 0 3 0 4 2 6 1 0

    N2a 2 0 0 11 0 2 0 0

    N2b 3 4 0 2 3 7 0 13

    N2c 1 1 0 0 5 5 0 8

    N3 1 0 0 0 0 3 0 0

    Recurrent 0 2 0 6 2 9 0 8

    Abbreviations: ACC, adenoid cystic carcinoma; FOM, floor of mouth; MEC,

    mucoepidermoid carcinoma; ORN, osteoradionecrosis; SCC, squamous cell

    carcinoma.

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    Table 3. Osseointegrated implant loss by sites

    Site

    Median Follow- up Time (Yrs.)

    Total No. of Patients

    No. of Patients With Implant Loss (%)

    Total No. of Implants

    No. of Implant Loss (%)

    All patients

    2.8 246 22 (8.9) 1132 42 (3.7)

    Mandible 2.8 185 9 (4.9) 618 16 (2.6)

    Maxilla 2.6 90 3 (3.3) 271 6 (2.2)

    Fibula 3.1 54 10 (18.5) 243 20 (8.2)*

    *The implant loss rate in fibula flaps was not significantly lower than in the

    native mandible (p=0.059) or native maxilla (p=0.057).

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    Table 4. Cumulative osseointegrated implant loss rate

    Cumulative implant loss rate

    Site 1 year 3 years 5 years

    All patients 1.4% 3.9% 5.1%

    Free flap 2.6% 7.4% 7.4%

    Mandible 0.9% 3.3% 4.5%

    Maxilla 1.3% 2.0% 4.7%

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    Table 5. Univariate analysis of risk factors for osseointegrated implant loss

    Variable No. of Successful Implants (%)

    No. of Implants Lost (%)

    p-Value

    Age >65 years 363 (94.8) 20 (5.2) 0.322

    Preoperative Radiation 92 (92) 8 (8) 0.097

    Postoperative Radiation 673 (96.8) 22 (3.2) 0.734

    Pre- or Postoperative Radiation

    765 (96.2) 30 (3.8) 0.704

    Active Smoking 457 (97) 14 (3) 0.441

    Diabetes Mellitus 147 (96.1) 6 (3.9) 0.832

    Chemotherapy 471 (98.1) 9 (1.9) 0.162

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    Table 6. Osseointegrated implant loss by site and timing of radiotherapy

    Site Timing of Radiation

    Total no. of implants placed

    Total no. of implants lost (%)

    p-Value

    No Radiation 177 9 (5.1)

    Fibula Preoperative Radiation

    43 8 (18.6) 0.041

    Postoperative Radiation

    23 3 (13.0)

    No Radiation 123 2 (1.6)

    Mandible Preoperative Radiation

    38 0 0.769

    Postoperative Radiation

    457 14 (3.1)

    No Radiation 37 1 (2.7)

    Maxilla Preoperative Radiation

    19 0 0.303

    Postoperative Radiation

    215 5 (2.3)

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    Table 7. Univariate analysis of parameters in completion of dental rehabilitation*

    Variable No. of Patients Completing Oral Rehabilitation

    p-Value

    Age >65 Years 69 (82.1%) 0.609

    Preoperative Radiation 12 (66.7%) 0.357

    Postoperative Radiation 110 (82.7%) 0.471

    Pre- or Postoperative Radiation 122 (80.8%) 0.729

    Chemotherapy 69 (75.8%) 0.239

    Tobacco Use 73 (77.7%) 0.505

    Diabetes Mellitus 27 (75%) 0.496

    Recurrence 31 (60.8%)

  • 253x253mm (300 x 300 DPI)

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  • 253x253mm (300 x 300 DPI)

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