Outcomes after definitive surgery for mandibular osteoradionecrosis.

OBJECTIVES: To analyze charges, complications, survival, and functional outcomes for definitive surgery of mandibular osteoradionecrosis (ORN). MATERIALS AND METHODS: Retrospective analysis of 76 patients who underwent segmental mandibulectomy with reconstruction from 2000 to 2009. RESULTS: Complications occurred in 49 (65%) patients and were associated with preoperative drainage (odds ratio [OR] 4.40, 95% confidence interval [CI] 1.01-19.27). The adjusted median charge was $343 000, and higher charges were associated with double flap reconstruction (OR 8.15, 95% CI 2.19-30.29) and smoking (OR 5.91, 95% CI 1.69-20.72). Improved swallow was associated with age <67 years (OR 3.76, 95% CI 1.16-12.17) and preoperative swallow (OR 3.42, 95% CI 1.23-9.51). Five-year ORN-recurrence-free survival was 93% while overall survival was 63% and associated with pulmonary disease (HR [hazard ratio] 3.57, 95% CI 1.43-8.94). CONCLUSIONS: Although recurrence of ORN is rare, surgical complications are common and charges are high. Poorer outcomes and higher charges are associated with preoperative factors.

Antimicrobial efficacy of oral topical agents on microorganisms associated with radiated head and neck cancer patients: an in vitro study.

OBJECTIVE: A variety of oral topical agents have been used for prevention and management of radiotherapy-induced adverse effects. The antimicrobial nature of some of the commonly used agents is unknown. The purpose of this study was to evaluate antimicrobial efficacies of various oral topical agents on common microorganisms associated with radiated head and neck cancer patients. METHOD AND MATERIALS: Seven commonly used topical oral agents-0.12% chlorhexidine with alcohol, 0.12% chlorhexidine without alcohol, baking soda-salt rinse, 0.4% stannous fluoride gel, 0.63% stannous fluoride rinse, calcium phosphate mouthrinse, and acemannan hydrogel (aloe vera) rinse-were evaluated in vitro for their antimicrobial efficacies against four common microorganisms. A combination of baking soda-salt rinse and 0.4% stannous fluoride gel was evaluated as the eighth agent. The microorganisms used were Staphylococcus aureus, group B Streptococcus, Escherichia coli, and Candida albicans. An ELISA reader was used to measure the turbidity of microbial culture wells and optical density (OD) values for each of the 960 wells recorded. Mean OD values were rank ordered based on their turbidity. One-way ANOVA with Tukey HSD post hoc analysis was used to study differences in OD values (P < .05). RESULTS: Mean OD values classified for topical agents from lowest to highest were chlorhexidine with alcohol, chlorhexidine without alcohol, baking soda- salt, calcium phosphate rinse, and the combination of baking soda-salt and stannous fluoride gel. Mean OD values classified for microorganisms from lowest to highest were Escherichia coli, Staphylococcus aureus, group B Streptococcus, and Candida albicans. CONCLUSION: A significant difference among the antimicrobial efficacies of topical agents was evident for each of four microorganisms (P < .05). There was also a significant difference among the antimicrobial efficacies of the same topical agent on the four microorganisms tested (P < .05).

Adhesive retention of silicone and chlorinated polyethylene for maxillofacial prostheses.

STATEMENT OF PROBLEM: A key factor of a successful facial prosthesis is the retention of the prosthesis to the patient's skin, especially when there is no mechanical means and the retention depends primarily on medical skin adhesives. Studies determining which medical adhesives provide the best bond strength for maxillofacial prostheses are needed. PURPOSE: The purpose of this study was to quantify the force required to detach strips of Silastic Adhesive A/MDX4-4,210 silicone elastomer with a urethane liner (A/M-U) and experimental chlorinated polyethylene elastomer (CPE) from the skin of human subjects coated with a protective dressing using 1 of 2 medical adhesives. MATERIAL AND METHODS: With IRB approval, 8 A/M-U and CPE rubber strips (total of 208) were applied in a predetermined random order to the left and right ventral forearms of 26 human subjects. Skin-Prep Protective Dressing (SP) was applied to half of the sites just before Epithane-3 (E3) and Secure(2) Medical Adhesive (SMA) were used to adhere the strips. Strips were peeled 6 hours later in a universal testing machine at 10 cm/min. Data are reported in newton/meter (N/m). The data was compared using a 3-way, within-groups, multivariate analysis of variance (MANOVA) and the Fisher exact test (alpha=.05). Values for N/m under various conditions relating to the subjects were compared by the Tukey HSD Test for unequal N (alpha=.05). Data are reported as mean (SD). RESULTS: Statistical analysis revealed no differences (mean (SD)) and no significant interactions between the independent variables (A/M-U = 94.6 (62.1) and CPE = 98.4 (69.6) N/m, SP = 93.0 (58.8) and no SP = 99.8 (72.1) N/m, E3 = 97.6 (69.8) and SMA = 95.3 (61.8) N/m; P=.984). Debonding occurred at the skin interface for both adhesives, as evidenced by residue on prosthetic materials (Fisher exact test; P<.005). CONCLUSIONS: The adhesive bond strengths of both SMA and E3, with and without the presence of SP, were not significantly different between A/M-U and CPE maxillofacial prosthetic materials. Adhesive failure occurred at the skin interface.