Strategic use of obturator prostheses for the rehabilitation of oral cancer patients during the COVID-19 pandemic.

During the current pandemic scenario, maxillofacial rehabilitation specialists involved with supportive care in cancer must transform its practice to cope with COVID-19 and improve protocols that could quickly return the oral function of complex cancer patients who cannot wait for surgical complex rehabilitation. This includes the role of the maxillofacial prosthodontist for the rehabilitation of surgically treated patients with maxillary cancers by the means of filling obturator prostheses that are considered an optimal scientific-based strategy to reduce hospital stay with excellent pain control, oral function (speech, swallowing, mastication, and facial esthetics), psychologic and quality of life outcomes for the patients following intraoral cancer resection. Therefore, the aim of this commentary was to bring new lights to the strategic use of obturator prostheses for the rehabilitation of oral cancer patients during the COVID-19 pandemic as well as to present a protocol for managing such cases.

The Role of Maxillofacial Prosthetics for the Surgically Treated Patient at National Cancer Institute-Designated Comprehensive Cancer Centers.

OBJECTIVES/HYPOTHESIS: The current role of maxillofacial prosthetic care for head and neck cancer patients is not well understood. Additionally, perceived barriers for service provision are unknown. The purpose of this study was to evaluate the current role of maxillofacial prosthetic care at National Cancer Institute (NCI)-designated comprehensive cancer centers and to identify perceived barriers to care. STUDY DESIGN: Multicenter, cross-sectional survey of head and neck division leaders at NCI-designated comprehensive cancer centers. METHODS: Each head and neck division leader from the 47 NCI-designated comprehensive cancer centers was invited to participate. The main outcomes of this study were: 1) to evaluate the current role of maxillofacial prosthetics for the surgically treated head and neck cancer patient within NCI-designated comprehensive cancer centers and 2) to identify perceived barriers to care. Measured outcomes were obtained from an anonymous online survey and reported. RESULTS: Twenty-eight of the 47 head and neck service chiefs responded (60% response rate). Respondents expressed preference for prosthetic rehabilitation for hard palate/upper gum, auricular, and nasal defects. Local flap or free tissue transfer was preferred for lower gum and soft palate defects. Cost-related factors were among the most reported perceived barriers to maxillofacial prosthetic care. CONCLUSIONS: Maxillofacial prosthetics have an important role in the rehabilitation of the head and neck cancer patient. Perceived barriers for services exist, particularly as it relates to cost. Providers should be aware that these issues are likely to be more severe in regional or community centers. LEVEL OF EVIDENCE: NA Laryngoscope, 129:409-414, 2019.

Clinical survey over the past 35 years at the clinic for maxillofacial prosthetics Tokyo Medical and Dental University.

PURPOSE: The purpose of this survey was to examine the overview of maxillofacial prosthetic treatment at our department, in order to ascertain the actual status of patients and discuss future needs. METHODS: Subjects were all patients who visited Clinic for Maxillofacial Prosthetics, Dental Hospital, Tokyo Medical and Dental University (TMDU) in the period from January 1, 1980 to December 31, 2014. Using medical records of the Clinic for Maxillofacial Prosthetics, Dental Hospital, TMDU, patients' data including sex, address, referring institution, and primary condition were analyzed throughout the period. RESULTS: The number of patients over 35 years was 6219, with a man-to-woman ratio of 6:4. The number of patients in their 60s, 70s, and 80s showed an increasing trend. Patients with tumors accounted for about 50 % of cases in 1980-1984 and increased to 80 % in 2010-2014. CONCLUSIONS: The survey showed an increasing number of elderly patients and patients with tumors. This suggests that more awareness and education about maxillofacial prosthetics are needed.

[Maxillomandibular advancement surgery as an optional therapy for patiens with severe obstructive sleep apnoea]. / Bimaxillaire osteotomie als mogelijke behandeling voor ernstig obstructieve slaapapneu.

Obstructive sleep apnoea (OSA) is a common chronic disorder which often requires lifelong treatment. Its prevalence in the Netherlands is estimated to be around 300.000 people. In this study 12 patients with severe OSA were treated with maxillomandibular advancement surgery between 2011 and 2012. The mean advancement during surgery was 8.7 mm and the mean postoperative admission was 4 days. All patients underwent polysomnography at 3 months. Three months after surgical treatment, the apnoea-hypopnea index had decreased with 74.9% (57.3 to 14.4). The subjective sleepiness of the patients had also decreased with a mean of 57.5%. The literature indicates comparable results in patients with severe OSAS, specifically a reduction of the apnoea-hypopnea index of 80-90%. Considering the successful results following maxillomandibular advancement surgery, this therapy is an appropriate alternative for patients who cannot cope with 'continuous positive airway pressure' or patients who want a permanent therapeutic solution. Further research is recommended to achieve higher levels ofevidence for maxillomandibular advancement surgery in patients with OSA.

[Oral appliances or maxillomandibular advancement osteotomy for severe obstructive sleep apnoea in patients refusing CPAP]. / Orthèse d'avancée mandibulaire ou ostéotomie maxillo-mandibulaire pour le traitement des syndromes d'apnées obstructives du sommeil sévères refusant la PPC.

OBJECTIVES: The management of patients with severe obstructive sleep apnea syndrome (OSAS) refusing or not tolerating continuous positive pressure ventilation (CPAP) remains problematic. We evaluated the effectiveness of oral appliances and of maxillomandibular advancement osteotomy. METHODS: One hundred and two patients with severe OSAS were included between 2001 and 2006. Maxillo-mandibular advancement osteotomy was proposed to patients less than 60 years of age, non obese and without comorbidities. The other patients were treated with oral appliances. All patients underwent polysomnography at 3 months. RESULTS: Group A: 25 patients with mean apnea-hypopnea index (AHI) at 45/h were treated by maxillo-mandibular advancement. Three months after the surgery, AHI had decreased from 45 to 7. The success rate was 89% when AHI was less than 15/h and 74% when AHI was less than 10/h. Sixteen patients performed a polysomnography one year after surgery with similar results. There were no major postoperative complications. Group B: 77 patients with a mean AHI at 41/h were treated with oral appliances. Only 23 patients underwent polysomnography at 3 months. The mean AHI had decreased from 41/h to 22/h. The success rate was 56% when AHI was less than 15/h and 30% when AHI was less than 10/h. DISCUSSION: We are confronted with an increasing number of severe OSAS patients with CPAP failure or intolerance. Surgery for maxillo-mandibular advancement is an effective alternative. However, it is not always indicated or accepted by the patient. So an oral appliance remains a useful therapeutic option despite its moderate success rate.

Necesidad de prótesis buco-maxilofacial en el municipio Matanzas en el año 1999 / Need for oral-maxillofacial protheses in Matanzas municipality in the year 1999

Se realizó este trabajo con el objetivo de conocer la necesidad de prótesis buco-máxilo-facial en el municipio Matanzas, así como el comportamiento de estas y su relación con el sexo, la edad y la etiología. Se realizó un estudio descriptivo de corte transversal donde se tomó como referencia la población perteneciente a las distintas áreas de salud de este municipio. Para la obtención de la muestra se aplicó un diseño muestral estratificado por conglomerado, la cual quedó constituida por 1 937 personas, y a aquellas que reunieron los criterios de inclusión, se les aplicó la encuesta de necesidad de rehabilitación buco-maxilofacial. Se obtuvo como resultado que existía necesidad de prótesis buco-maxilofacial con preferencia por la del tipo ocular, sexo masculino y pacientes jóvenes. La etiología traumática fue la predominante como causa de lesión para ambos sexos, seguida por la oncológica. Las regiones auriculares y maxilares estuvieron afectadas en el sexo masculino en mayor cuantía que en el femenino. En las regiones orbital, nasal, mandibular y compleja no hubo afectaciones(AU)

An 8-year assessment of maxillofacial prosthetic patients treated in a Department of Prosthetic Dentistry.

The Department of Prosthetic Dentistry at the University of the Witwatersrand, Johannesburg, serves as a referral centre for maxillofacial prosthetic patients from the surrounding general hospitals and local private clinics. This places a time and financial constraint on the department. The aim of this study was to establish the number of new patients seen annually, the causative factors associated with the various types of defects, the treatment provided and the cost per patient in terms of clinical hours and prosthesis fees. The data were taken from the records of patients treated in the maxillofacial prosthetics clinic during an 8-year period, from January 1991 to December 1998. The total number of new patients was calculated and the data were collated according to the year in which treatment commenced. Results were tabulated according to the number of new cases in each group, the aetiology of the defects, prosthetic treatment provided and the costs in terms of clinical hours and prostheses. The results of this study indicate that there is a need for a specialised Maxillofacial Prosthetic Unit. Although the present fee schedule needs to be revised, there is still a need for a substantial amount of state subsidy.

Color stability and colorant effect on maxillofacial elastomers. Part I: colorant effect on physical properties.

STATEMENT OF PROBLEM: The average clinical life span of a maxillofacial prosthesis is approximately 6 months, at which point it needs to be refabricated, mainly because of degradation of the color and physical properties of the prosthesis. PURPOSE: This first part of a 3-part study evaluated the effect of coloring agents on the physical properties of maxillofacial elastomers. METHODS AND MATERIAL: Five dumbbell-shaped and 5 trouser-shaped specimens were fabricated for each of the combinations of the 3 elastomers (Silastic medical adhesive type A, Silastic 4-4210, and Silicone A-2186) and 6 colorants (dry earth pigments, rayon fiber flocking, artist's oil paints, kaolin, liquid cosmetics, and no-colorants), for a total of 180 specimens. Evaluations of hardness and tear strength were made with the trouser-shaped specimens. Evaluations of the ultimate tensile strength and the percentage elongation were made with the dumbbell-shaped specimens. A within elastomer analysis compared the 6 colorants using a 1-way analysis of variance for each of the 4 physical properties. When significant differences were observed, the Student-Newman-Keuls multiple range test was used to identify differences between groups at a significance level of.05. RESULTS: Physical properties of maxillofacial elastomers were changed by the incorporation of coloring agents. Dry earth pigments, kaolin, and rayon flocking acted as a solid filler without bonding to the Silicone, and artists' oils and liquid cosmetics acted as a liquid phase without bonding to the silicone matrix. CONCLUSION: No clearly superior colorant-elastomer combination was demonstrated in all the tests in this study.

Color stability and colorant effect on maxillofacial elastomers. Part II: weathering effect on physical properties.

STATEMENT OF PROBLEM: The clinical life of a maxillofacial prosthesis averages about 6 months, before it needs to be refabricated. Degradation of the color and physical properties of the prosthesis are the principle reasons for replacement. PURPOSE: This second part of a 3-part in vitro investigation evaluated the change in physical properties of popular colorant-elastomer combinations as a result of weather exposure. MATERIAL AND METHODS: Fifteen dumbbell-shaped and 15 trouser-shaped specimens were fabricated for each of the 3 elastomers (Silastic medical adhesive type A, Silastic 4-4210, and Silicone A-2186) and 6 colorant combinations (dry earth pigments, rayon fiber flocking, artist's oil paints, kaolin, liquid cosmetics, and no-colorants) for a total of 540 specimens. The 15 dumbbell-shaped and trouser-shaped specimens of each elastomer colorant combination were separated into 5 of each shape among 3 test condition groups (control, time passage, and natural weathering). Control specimens were evaluated within 1 month of fabrication. The time passage group was sealed in glass containers and kept in the dark for 6 months before testing. The natural-weathering groups were placed on the roof of the dental school for 6 months and exposed to sunlight and weathering. Evaluations of hardness and tear strength were made on trouser-shaped specimens, and evaluations of the ultimate tensile strength and percentage elongation on dumbbell-shaped specimens. Physical property data for each elastomer-colorant combination were subjected to a 1-way analysis of variance to examine effects among the test conditions. When significant differences were observed, the Student-Newman-Keuls multiple range test was performed to identify differences in elastomer-colorant combinations among each test condition at a significance level of .05. RESULTS: Exposure to weathering and time changes of the physical properties of many colorant-elastomer combinations indicated that properties of a clinical prosthesis can change with time. CONCLUSION: The addition of colorants to the silicones altered the effects of weathering. In addition, the silicones were not as stable as previously assumed.

Color stability and colorant effect on maxillofacial elastomers. Part III: weathering effect on color.

STATEMENT OF PROBLEM: Maxillofacial prostheses are serviceable for approximately 6 months, after which they need to be refabricated because of the deterioration of color and physical properties. PURPOSE: This third article in a 3-part series evaluated the color stability of commonly used colorant-elastomer combinations as a result of exposure to weathering. METHODS AND MATERIAL: Fifteen specimens were fabricated for each of the 3 elastomers (Silastic medical adhesive type A, Silastic 4-4210, and Silicone A-2186) and 6 colorants (dry earth pigments, rayon fiber flocking, artist's oil paints, kaolin, liquid cosmetics, and no colorant) for a total of 270 specimens (18 groups of 15 specimens). The 15 specimens of each elastomer-colorant combination were separated into 3 test condition groups (control, time passage, and natural weathering) of 5 specimens per test condition group. Control specimens were evaluated within 1 month of fabrication. The time passage group was sealed in glass containers and kept in the dark for 6 months before testing. The natural weathering groups were placed on the roof of the dental school for 6 months and exposed to sunlight and weathering. Color and optical density data for each elastomer-colorant combination were subjected to a 1-way analysis of variance to examine effects among test conditions (control, time passage, and weathering). When significant differences were observed, the Student-Newman-Keuls multiple range test was performed to identify differences in elastomer-colorant combinations among each test condition at a significance level of .05. RESULTS: Changes in color, as a result of weathering, were noted in many of the colorant-elastomer combinations. Also, color change occurred not only to the colored, but also to uncolored materials over time without exposure to weathering. CONCLUSION: Clinically, the addition of colorants could have a stabilizing effect on the elastomer color when it is exposed to weathering.

Wettability of silicone rubber maxillofacial prosthetic materials.

STATEMENT OF PROBLEM: Maxillofacial prosthetic materials that contact skin or mucosa should have good wettability. A material that is easily wetted will form a superior lubricating layer between the supporting tissues and, thus, reduce friction and patient discomfort. The surface energy of a maxillofacial prosthetic material will give an indication of the amount of energy available for adhesion and of the susceptibility of the material to bacterial adhesion. PURPOSE: This study evaluated the wettability and surface energies of a range of commercially available silicone rubber maxillofacial prosthetic materials. MATERIAL AND METHODS: Contact angles and surface energies were measured by using a dynamic contact angle measuring technique. Four commonly used silicone maxillofacial materials were tested and their properties compared with those of an acrylic resin denture base material and a widely used denture soft lining material. RESULTS: There were no significant differences in the wettability of the silicone rubber materials. All materials were significantly less wetted than the denture acrylic resin material. There were no significant differences in the surface energies of the silicone rubber materials, but all were significantly lower than denture acrylic resin material. CONCLUSIONS: The Cahn dynamic contact angle analyzer was a quick and reproducible method for determining the contact angles and surface energies of maxillofacial materials. Further work is needed to improve the wettability of silicone rubber materials used for maxillofacial prostheses, thus, reducing their potential to produce friction with tissues.

Properties of maxillofacial silicone elastomers reinforced with silica powder.

Compounds of a silicone elastomer suitable for preparing maxillofacial prostheses, reinforced with various amounts of silica powder, have been studied for their mechanical response and wetting properties in terms of contact angle. Tensile strength and elongation at break showed an increase with increasing silica volume fraction up to 35%, whereas the Young modulus displayed small dependence on the silica content and the resistance to tear increased continuously with filler volume fraction (Vf). The wetting properties assessed via the contact angle, seemed to degrade with increasing silica Vf, but a dependence on the elastomer network density has also been recorded.

The relative value of provider work for maxillofacial prosthetic services.

The results of a national survey of members of the American Academy of Maxillofacial Prosthetics who estimated the relative value of provider work for nine existing and two proposed coded maxillofacial prosthetic services is reported. The work estimates are a necessary component of a larger effort by the Health Care Financing Administration to establish a resource-based relative value scale for reimbursement for all Medicare services. Analysis of the survey data reveals agreement regarding the relative value of work for maxillofacial services compared with other established medical procedures and that the median values for each service are acceptable initial estimates.

Maxillectomy--to reconstruct or obturate? Results of a UK survey of oral and maxillofacial surgeons.

Post-maxillectomy defects may be restored either by surgical reconstruction or by prostheses and there is continuing controversy about the most appropriate method of rehabilitation in any particular case. A questionnaire was designed to assess the current practices of oral and maxillofacial surgeons in the UK after resection of the maxilla for malignant disease. Maxillectomies were carried out by 83% of surgeons; most surgeons do 1-5 cases a year; 38% of surgeons do reconstruct surgically, but only in 10% of cases. Only 65% of surgeons have access to the services of a restorative dentist; this did influence 19% of surgeons' decision about whether to reconstruct surgically or restore by prosthetic means.

The provision of hospital maxillo-facial prosthetic services in Scotland.

Maxillo-facial prosthetics can contribute much to the quality of life of patients with congenital problems or those treated surgically for a head and neck neoplasm. The availability of an adequate service varies internationally. The present study examines the current provision and requirements for such a service in Scotland. A questionnaire survey of 90 oral, plastic and ENT surgeons was carried out. Information was sought on numbers and types of cases seen, prosthetic treatment provided and involvement of Consultants in Restorative Dentistry in their management. The results show that most surgeons only treat a small number of such patients with a consequent dilution of experience, and with a possible need for supra-regional specialist centres. In addition there is a need for improvement of multi-disciplinary planning clinics for such cases.

Maxillofacial prosthetics: vital signs.

A maxillofacial prosthetics survey was designed to record the response rate of prosthodontists regarding the frequency of maxillofacial procedures and insurance coverage in 1991. The survey explored variability with respect to membership in professional organizations, region, education, primary activity, and age of the prosthodontist. A total of 342 survey instruments were received from a total of 690 mailed. A total of 18,410 maxillofacial procedures were performed by the survey population. Members of the American Academy of Maxillofacial Prosthetics performed procedures at a significantly higher rate than did the members of the American College of Prosthodontists. A greater procedure rate was observed for prosthodontists in the South Midwest and Southwestern regions; the hospital setting; with 2 plus 1 year additional postgraduate maxillofacial training; and the 45- to 54-year age group. Insurance covered most maxillofacial procedures, but was not uniformly distributed within predictor variables nor between procedures.

Craniofacial osseointegration: the Canadian experience.

A survey was undertaken to determine the number of centers in Canada with an active involvement in extraoral osseointegration. It was found that six centers had placed 222 implants in 91 patients in Canada. The individual implant success rates for the Canadian experience were compared with the published Swedish and United States' experience. The Canadian experience is combined with the Swedish and United States' experience to provide retrospective multinational multicenter data. The data given should be viewed as providing trends only and not as definitive expectations of predictable success rates. The success rates are considered likely to change with time as the number of patients treated increases and the duration of follow-up is extended. The mastoid region in nonradiated patients is considered to provide a high degree of predictable individual implant success. The success rates in radiated patients yield far lower success rates, which vary with anatomic location. The criteria for success in using craniofacial implants need to be defined and should reflect the differences between extraoral and intraoral implants.

Effects of environmental factors on maxillofacial elastomers: Part II--Report of survey.

Part II of a four-part report presents an international survey that was conducted to determine the most frequently used materials in the fabrication of facial and somatoprostheses. The survey also solicited information about advantages and disadvantages, methods of coloring, and the perceived properties of an "ideal" material. The results of the survey indicated that the majority of prosthodontists and prosthetists are using room temperature-vulcanized silicone products, intrinsically colored with dry earth pigments or artist's pigments. The need for further research in materials for external prostheses was clearly indicated.