OEHS Academy: New and Aspiring Principals Responsibilities
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Professionally applied fluoride Dr. Rihab Abdul Hussein Ali B.D.S , M.Sc. , PhD.
Studies of the use of professional topical fluoride applications (by dental personnel) for the control of dental caries began in the early 1940s. Since that time, it has been generally accepted that the fluoride content of enamel is inversely related to the prevalence of dental caries. Materials used available in form of solutions, gel, foam, varnishes, pumices, fluoride release devices and fluoridated restorative materials. It was assumed that it was necessary to administer a thorough dental prophylaxis prior to the topical application of fluoride.
Indications of use in: Patients at high risk of caries on smooth surfaces and root surfaces. Patients with rampant caries. Sensitive teeth. Non-fluoridated area. Special groups like patients with reduced salivary flow rate, patients undergoing head and neck irradiation as well as patients with orthodontic treatment.
Professional fluoride-delivery methods The two most common methods are: 1- Paint-on technique: The patient instructed to rinse the mouth. Teeth are isolated using cotton roll and saliva ejector, the patient position in upright and the head tilted forward, fluoride material applied to teeth by cotton or brush. The fluoridated agent applied following dryness of teeth for 1-4 minutes following the manufacturer s instructions. The amount of agent used must not exceed 4ml to prevent acute toxicity. Used un waxed dental floss to push the material between teeth.
After the treatment, the patient should be asked to expectorate several times and instructed not eat or drink for at least 30 minutes. It was found that significantly greater fluoride deposition occurred when the patients were not permitted to rinse, eat, or drink following the fluoride treatment. This method is better to be used for patient suffers of gaging reflex. It is the appropriate method for gels and solutions.
2- Tray technique A small amount of fluoride is adding to a tray without overloading, this allow the flow of gels or foams to cover the teeth surfaces. The patient should be seated in upright position. The materials should be left in place following the manufacture instructions. Trays come in different shapes and types as custom vinyl.
Reports have shown that 10 to 30 mg of fluoride may be inadvertently swallowed during the application procedure, and the ingestion of these quantities of fluoride by young children may contribute to the development of dental fluorosis in those teeth that are unerupted and in the developmental stage. The precautions to reduce the amount of inadvertently swallowed fluoride to less than 2 mg, which may be expected to be of little consequence.
Application Frequency The frequency of topical applications should be dictated by the conditions and needs presented by each patient. Thus, it is recommended that new patients, regardless of age, with active caries be given an initial series of four topical fluoride applications within a period of 2 to 4 weeks. If desired, the initial application may be preceded by a thorough prophylaxis, the remaining three applications constituting the initial treatment series should be preceded by tooth brushing to remove plaque and oral debris.
This series of treatments may be combined with the plaque control, dietary counseling, and initial restorative programs. Then patient should be given single, topical applications at intervals of 3, 6, or 12 months, depending on his or her caries status. Patients with little evidence of existing or anticipated caries should be given single applications every 12 months as a preventive measure.
Three different fluoride systems have been adequately evaluated and approved for use professionally by dentist. These three systems are: 2% sodium fluoride system. 8% stannous fluoride system. Acidulated phosphate fluoride system containing 1.23% fluoride.
Sodium Fluoride (NaF) This material is available in powder, gel, and liquid form. The compound is recommended for use in a 2% concentration (= 9200 ppm), which may be prepared by dissolving 0.2 g of powder in 10 mL of distilled water. The prepared solution or gel has a basic pH and is stable if stored in plastic containers. It should not be store in a glass container, it will react with the silica of the glass forming silicon dioxide fluoride reducing fluoride anticaries effect.
Ready-to-use 2% solutions and gels of NaF are commercially available; because of the relative absence of taste considerations with this compound, these solutions generally contain little flavoring or sweetening agents. This material is not irritant to the gingiva, and does not cause discoloration of teeth. The only disadvantage is requiring four visits weekly (Knutson s technique). It is recommended to be applied at ages 3, 7, 11 and 13 years. Coinciding the eruption time of permanent and primary teeth.
Mechanism of action: NaF reacts with hydroxyl apatite crystals in enamel forming calcium fluoride. A thick layer formed and interfered with the further dissolution of fluoride from the topical agent. The CaF2 formed reacts with the hydroxyl apatite crystals to form fluoridated hydroxyl apatite which in turn makes the tooth surface resistant against caries attack. Ca10 (PO4)6(OH)2 +20F- 10CaF2+ 6PO43-+ 2OH- CaF2+ 2Ca5 (PO4)3OH 2Ca5 (PO4)3 F+ Ca(OH)2
Stannous Fluoride (SnF2) This compound is available in powder form either in bulk containers or pre-weighed capsules. The recommended and approved concentration is 8%, (19,500 ppm) which is obtained by dissolving 0.8 g of the powder in 10 mL of distilled water. Stannous fluoride solutions are quite acidic, with a pH of about 2.4 to 2.8. Aqueous solutions of SnF2 are not stable because of the formation of stannous hydroxide and, subsequently, stannic oxide, which is visible as a white precipitate. As a result, solutions of this compound must be prepared immediately prior to use (Muhlar technique).
SnF2 solutions have a bitter, metallic taste. To eliminate the need to prepare this solution from the powder and to improve patient acceptance, a stable, flavored solution can be prepared with glycerine and sorbitol to retard hydrolysis of the SnF2 and with any of a variety of compatible flavoring agents. SnF2 may cause irritation to gingiva, pigmentation around the margins of restoration and discoloration of hypocalcified regions of the teeth. SnF2 used for sensitive teeth and effective in prevention and reduction of caries greater than sodium fluoride.
Mechanism of action: SnF2 reacts with hydroxyl apatite crystals in enamel, the tin of stannous fluoride also reacts with enamel and new crystalline gets formed called stannous-tri-fluorophosphate is more resistant to caries. Tin hydroxyphosphate (gets dissolved in oral fluids and is responsible for the metallic taste) is formed when SnF2 is applied in low concentration. While at high concentration of SnF2, calcium tri-fluoro stannate gets formed along with tin-tri-fluorophosphate which is render the tooth structure more stable and less susceptible to caries. CaF2 is the end product in low and high concentration.
The reaction at low concentration is: Ca5 (PO4)3OH + 2SnF2 2CaF2 + Sn2(OH) PO4 + Ca3(PO4)2 The reaction at high concentration is: Ca5 (PO4)3OH + 16SnF2 CaF2 + 2SnF3F3PO4 (Tin-tri-fluorophosphate)+ Sn2(OH)PO4 (Tin hydroxyphosphate)+ 4CaF2(SnF3)2 (Calcium tri-fluoro stannate) 2Ca5 (PO4)3OH + CaF2 2 Ca5(PO4)3F + Ca(OH)2
There are two ways of speeding the reactions and lead to formation of fluoroapetite. 1. Increase the concentration of fluoride ions in the agents. 2. Lowering the pH that is making the solution more acidic. The success of any topical fluoridated agent depend on it is capability of depositing fluoride ions in the enamel as fluoroapetite and not on only calcium fluoride.
Acidulated Phosphate Fluoride (APF) This treatment system is available as either a solution or gel, both of which are stable and ready to use. Both forms contain 1.23% fluoride (12,300 ppm), generally obtained by the use of 2.0% sodium fluoride and 0.34% hydrofluoric acid. Phosphate is usually provided as orthophosphoric acid in a concentration of 0.98%. The pH of true APF systems should be about 3.5.
Gel preparations feature a greater variation in composition, particularly with regard to the source and concentration of phosphate. In addition, the gel preparations generally contain thickening (binders), flavoring, and coloring agents. The gelling agent is in form of methylcellulose or hydroxyethyl cellulose is added to solution and the pH is 4-5. The Brudevold s solution prepared by dissolving 20 gm of sodium fluoride in 1 liter of 0.1M phosphoric acid.
Another form of acidulated phosphate fluoride for topical applications called thixotropic gels. The term thixotropic denotes a solution that sets in a gel-like state but is not a true gel. On the application of pressure, thixotropic gels behave like solutions; it has been suggested that these preparations are more easily forced into the interproximal spaces than conventional gels. The active fluoride system in thixotropic gels is identical to conventional APF solutions. To help prevent ingestion it is recommended that the patient sits upright and does not swallow.
No more than 2.5 ml of gel per tray should be applied, and custom or properly fitted stock trays with absorptive liners should be used. Suction devices should be used during and after treatment and excess gel removed with gauze. Patients should spit out thoroughly after treatment. The gels are usually recommended to be used twice yearly, but when more severe caries is present they may be used more frequently. A significant reductions in caries incidence have been achieved using these products.
Within the past few years, a foam form of APF has become available. The primary advantage of foam preparations is that appreciably less material is used for a treatment and therefore lesser amounts are likely to be inadvertently swallowed by young children during the professional application. AFP is stable in plastic container and not staining the teeth. Repeated exposure of porcelain or composite restoration to AFP can lead to loss of material and roughening because of its high acidity.
Mechanism of action: AFP applied on teeth leads to dehydration and shrinkage in the volume of hydroxyapatite crystals which forms dicalcium phosphate dihydrate (DCPD)(Ca HPO4 2H2O). Fluoride penetrates deeply and leads to formation of fluorapatite (FA)( Ca5(PO4)3F). When acidic fluoride at high concentrations is applied to the tooth surface calcium is etched from the surface of the tooth. The free calcium that is released, and calcium that is present in saliva, react with the fluoride ions present in the topical fluoride to form calcium fluoride.
When the saliva returns the plaque pH to neutral, the calcium fluoride precipitates and deposits as tiny granules of insoluble fluoride that occupy the etched areas. Later, when a cariogenic food is consumed and lactic acid is produced by plaque, the pH drops and the calcium fluoride spheres dissolve, releasing fluoride ions locally.
Varnishes Fluoride varnishes have been used in dental office and community programs since 1960s. They are generally used to provide fluoride at risk sites or surfaces within the mouth and are usually applied at intervals of 3 or 6 months. They contain high levels of fluoride and are designed to harden on the tooth to aid retention. Varnishes have been shown to work as well as gels, and the varnishes are preferred because less fluoride is ingested.
Teeth should be relatively dry before applying fluoride varnish. The paint brush that comes with the product is used to paint the varnish on all selected tooth surfaces. Patients should be instructed that some varnishes leave a temporary, yellow stain that can last for 24 hours. Varnishes are highly indicated for sensitive teeth and for children under 6 years old that can be applied on the affected surface only. While it is contraindicated in patients with gingivitis.
The most widely used is Duraphat varnish, containing 5% sodium fluoride (22,600 ppm F) that sets on contact with saliva. Patients are instructed not to eat within two hours. Duraphat usually remains on the tooth surfaces for about 24 hours. It is believed that delivery of high doses of fluoride of this type results in the local formation of calcium fluoride, which can act as a reservoir for the slow release of fluoride. Fluor protector varnish is polyurethane-based varnish 0.9 wt % silane fluoride. The varnish is acidic and hardened in air into colorless within 2-3 minutes. It is retained on the teeth for 1-2 weeks. Another type is Bifluoride 12 varnishcontains 6% NaF and 6% CaF. It is retained on the tooth surfaces for days and it used also for treatment of hypersensitive exposed root dentin.
Slow-release fluoride devices An optimum fluoride-delivery system would be one that supplies small amounts of fluoride throughout the day so that consistent, elevated plaque fluoride levels are maintained with little or no individual effort required. To be effective the fluoride release has to be constant and sustainedand the device must be retained in the mouth without causing damage to soft tissues or becoming loose.
Materials used are (plastic or glass beads containing fluoride), the copolymer membrane type and recently used a mixture of NaF and hydroxyapatite. Slow-release glass materials retained on the buccal surface of molar teeth have shown effectiveness, and bioadhesive tablets and other systems have also been evaluated.
Fluoridated prophylactic paste Before application of fluoride agents, it is recommended to clean teeth and polishing with rubber cup using pumice. Different types of Fluoridated prophylactic paste are available as: 1. Zirconium silicate contadins stannous fluoride. 2. Silicon dioxide contains acidulated phosphate fluoride. These pastes are not a substitute for the topical agents, they are used in order to increase the accessibility of fluoride ions in tooth surface. Polishing will remove a thin layer of enamel (1-4 m), thus it is always recommended using F pumice to replenish the minerals that abraded during polishing.
Restorative materials containing fluoride An alternative approach is to use dental materials to provide fluoride delivery. It is important that addition of fluoride does not compromise the required properties of the restorative material. Materials such as the old silicate restorative materials and glass-ionomer cements contain between 15 and 20% fluoride, and resin modified glass ionomers, polyacid-modified composite resin (compomers), fissure sealants, fluoride has also been added to other dental materials such as composite and amalgam.
While Fluoride releasing materials include the addition of ytterbium fluoride (YbF3) to commercial glass-ionomer cement, organic fluorides in the form of amine fluorides (AmF). These materials could potentially provide a fluoride reservoir to help prevent secondary caries and to prevent or help remineralize caries in adjacent teeth or surfaces. These materials may feature greater longevity, a reduced incidence of marginal failure, an elevated concentration of fluoride in plaque, together with an antibacterial action when compared with non-fluoride releasing materials.
In addition, fluoride-releasing materials may perform better in caries inhibition in artificial caries model studies than non-fluoridated materials. Initially, fluoride release from most methods tends to be high, but it reduces as the available reservoir depletes. Nevertheless, even 1 year after application of a glass-ionomer cement fluoride levels were six times higher than normal in unstimulated saliva. It is believed that glass ionomer cements may act as a reservoir by absorbing fluoride from other sources such as toothpaste and slowly releasing this as fluoride levels diminish in the oral cavity.
Recommendations for fluoride-delivery methods 1- Fluoride is topically available in the oral cavity at concentrations that can significantly affect the ongoing de- mineralization and remineralization process 2- Ingestion of fluoride is minimized. 3- The method of delivery is cost-effective.