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Biomedical subjects

G Dolci

Publications and source records attributed to G Dolci.

At least 19 recordsLinked to original sources

A between-patient disinfection method to control water line contamination and biofilm inside dental units.

The aim of the present study was to evaluate the efficacy of a between-patient disinfection procedures to maintain low bacterial counts in dental unit water line (DUWL) effluents, and control dental water line biofilms. Six dental units already in use, that had never been cleaned, were monitored for three weeks. During the first week only baseline contamination levels were assessed with no treatment of the system. In the second week lines were flushed with water for 30 s before treating each patient. During the third week, a disinfection procedure with 0.26% peracetic acid, followed by a water flush, was implemented before treating each patient. DUWL samples were collected both at the beginning and at the end of 216 dental procedures (72 during each period), plated on R2A agar and incubated at room temperature for seven days to obtain total bacterial counts in colony forming units per millilitre. To assess biofilm control, nine dental units (five never used and four old dental units with established biofilm) were used for 30 days in routine dental practice undergoing five between-patient DUWL disinfecting cycles every day. Water line samples were removed at baseline and at the end of the study and examined by scanning electron microscopy to determine the presence or absence of biofilms. A significant difference (P < 0.01) in mean DUWL bacterial counts was found between the three sets of observations. Biofilms were not present in any of the new dental units and a demonstrable reduction in the biofilms from the four dental units with previous presence of established biofilms was observed at the end of the study. In this study, a between-patient disinfection procedure consisting of flushing DUWL with peracetic acid with use of water was efficacious in the control of both microbial contamination of dental treatment water and dental water line biofilms.

Biofilms↗

Infection through sprays in medical devices for dentistry. A controllable epidemiological impact.

The risk of infections via dental sprays has been confirmed once again by the detection, inside dental unit waterlines, of bacterial and viral contaminations, both from water supplies and from the oral cavity of patients. Conventional means of prevention, flushing of the ducts before any dental treatment and anti-retraction devices intended to avoid contamination originating from the patient, evaluated in laboratory and clinical conditions, have been shown to be ineffective in controlling the risk. Tests carried out in vitro, with circuit models, and with the dental unit in service, have confirmed the efficacy of a method to disinfect the waterlines with a disinfecting solution based on TAED and Peroxidant, which in aqueous solution develop peracetic ions (Autosteril method). Zero bacterial count, zero viral charge and a complete biofilm demolition were achieved both in lab conditions and in service units. After hygienic treatment, the same disinfection method, once installed on old units that had been in service for years and without any hygienic device, allowed us to restore and to maintain the microbiological quality of the irrigant also in dental units of old design, and significantly reduced biofilm formation inside the waterlines. Therefore, on the basis of scientific findings, a microbiologic monitoring protocol is proposed in order to verify the hygienic conditions of units which are in service.

Clinical Protocols↗

Detection of DNA from periodontal pathogenic bacteria in biofilm obtained from waterlines in dental units.

Direct person-to-person transmission of periodontal bacteria through saliva has recently been widely reported and dental units have been demonstrated to retract saliva from patients under treatment and to release it into the mouths of subjects undergoing the next operation. In this study the presence of a group of periodontal pathogenic bacteria inside waterlines in dental units was investigated using polymerase chain reaction (PCR) based methods. Briefly, 18 dental units of three different manufacturers were studied. Dental units were divided into two groups according to their prevalent use in routine practice. The first group consisted of nine dental units characterized by the frequent use of high-speed dental hand-pieces directly inside the mouth and in contact with patients' saliva. The second group, as a control, consisted of nine dental units where high-speed dental hand-pieces were not in use. A one cm section of the waterline tubing connected to the high-speed hand-piece was removed from each dental unit to evaluate the presence of DNA of Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Bacteroides forsythus, Treponema denticola. Two specimens were positive for Prevotella intermedia DNA. All the positive results were from samples obtained from dental units categorised in the first group. These findings clearly suggest that dental units have the potential to transmit periodontal pathogens. Manufacturers should be invited to design dental units that incorporate automated devices to disinfect DUWLs between patients with minimal effort by dental staff.

Aggregatibacter actinomycetemcomitans↗

Effectiveness of two devices designed to prevent fluid retraction in a high-speed handpiece.

STATEMENT OF PROBLEM: Contaminated fluid can be retracted into the turbine air chamber of a high-speed handpiece when it stops rotating. PURPOSE: This study attempted to evaluate 2 operating systems recently equipped with antiretraction devices installed inside the handpiece (Kavo) or inside the unit (Castellini) and to compare the results with those obtained from an operating system without any antisuction device (Bien Air). MATERIAL AND METHODS: Two test conditions (bur immersed approximately 5 mm into a dye solution or completely immersed in dye solution) were conducted using potassium bichromate dye to simulate a fluid contaminant. RESULTS: During the first procedure dye influx for the Kavo unit was 0.08 +/- 0.1 microL, 0.06 +/- 0.1 microL for the Castellini unit, and 12.4 +/- 5.2 microL for the Bien Air unit (F=28.3; P <.01). During the second procedure, the results of the dye influx were Kavo unit 2.52 +/- 1.3 microL, Castellini unit 0.1 +/- 0.1 microL, and Bien Air unit 22.22 +/- 4.0 microL (F=123; P <.01). Mean values were significantly different between Castellini and Kavo units during the second procedure. CONCLUSION: Antisuction devices can reduce dye penetration into the air chamber of a high-speed handpiece. Better results may be obtained with devices installed inside the unit and designed to increase the air pressure in the air chamber when the turbine stops running.

Air Pollution, Indoor↗

Calcium phosphates produced by physical methods in the treatment of dentin hypersensitivity.

BACKGROUND: The aim of this paper is to study the properties of innovative materials based on defective calcium phosphates produced by physical methods in the therapy of dentin hypersensitivity. METHODS: In particular, the effects of gels, aqueous solutions and toothpastes containing the above mentioned materials on dentinal permeability measured as dentin hydraulic conductance have been studied. The calcium phosphates have been characterized by X-ray powder diffraction (Rietveld analysis) and Fourier transform infra-red analysis. In addition, scanning electron microscopy has been performed to study the surface of dentin and enamel after treatment with the phosphates. In particular sound occlusal dentin, sound cervical dentin, carious occlusal dentin, sound buccal enamel and carious buccal enamel have been observed. RESULTS: The results have shown that these biocompatible materials can be produced with chemical and physical characteristics very similar to dentin and/or enamel. By forming a protective layer inside and outside the dentin tubuli, the calcium phosphates significantly reduce the dentinal hypersensitivity. CONCLUSIONS: These phosphates seem to be a promising material for clinical application.

Calcium Phosphates↗

Bioactivity of chitosan in dentistry. Preliminary data on chitosan-based cements.

BACKGROUND: The chemical association of chitosan with inorganic salts, such as calcium phosphate, finds a promising application in dentistry as room-temperature self-hardening cement. We present the physical, chemical and crystallographic characterization of newly-developed cements made of 1) calcium-phosphate and a chitosan gel obtained by acetic acid treatment, and 2) calcium phosphate and a chitosan gel obtained by ascorbic acid treatment. Both cements are self-hardening at room temperature. METHODS: The cements were characterized by X-ray diffractography, scanning electron microscopy and fluorine-selective electrode analysis. RESULTS: The chitosan-hydroxyapatite cements had hardness comparable to spongy bone and above that of PMMA. CONCLUSIONS: The cements are promising for application in endodontics and restorative dentistry.

Biocompatible Materials↗

Dentin dysplasia type I. Report of case and ultrastructural study.

Radicular dentin dysplasia (DD-I) is a rare hereditary dental alteration. It is characterized clinically by almost normal looking crowns and severe hypermobility of the teeth. The radiographic analysis, on the other hand, discloses the obliteration of all pulp chambers, the short, malformed roots and plenty of periapical bone radiolucencies on noncarious teeth. A case of radicular dentin dysplasia is presented. In this 43-year-old woman the diagnosis was supported, besides the clinical and radiographic analysis, by the pedigree of the proband, which showed the autosomal dominant pattern of feature transmission. Further-more, the electron microscopic analysis of one extracted molar revealed the atubular structure of the secondary dentin, and its globular organization.

Adult↗

Evaluation of piroxicam-beta-cyclodextrin, piroxicam, paracetamol and placebo in post-operative oral surgery pain.

Two hundred ninety-eight patients with post-operative pain after the surgical removal of an impacted third molar were randomly assigned, on a double-blind basis, to receive a single oral dose of piroxicam 20 mg, or piroxicam-beta-cyclodextrin equivalent to 20 mg piroxicam, or paracetamol 500 mg, or placebo. Using a semi-quantitative self-rating scale, patients rated their pain and its relief at 30-min intervals for the first 2 h, and then hourly for 4 h after treatment administration. All active medications were reported to be significantly superior to placebo. The three active drugs were comparable for the degree of analgesia up to the third hour, after which the effect of paracetamol decreased significantly as compared to piroxicam-beta-cyclodextrin and piroxicam. Piroxicam-beta-cyclodextrin and paracetamol were more rapid than piroxicam in inducing analgesia. The tolerability for the active drugs was comparable to that for placebo.

Acetaminophen↗

[Analgesic efficacy and the tolerance for piroxicam-beta-cyclodextrin compared to piroxicam, paracetamol and placebo in the treatment of postextraction dental pain].

INTRODUCTION: Acute postoperative pain is a common experience in oral surgery practice. Non-steroidal anti-inflammatory drugs (NSAIDs) are quite effective against mild to moderate pain and they are generally better suited in ambulatory outpatients than narcotic analgesics. The analgesic activity of piroxicam, a well known NSAID has been documented in many pain states. Piroxicam can be administered once daily because of its long half-life, but its absorption in the gastrointestinal tract is slow as it is its onset of action. Piroxicam-beta-cyclodextrin (PBCD) is a new formulation of piroxicam which is the product of supermolecular encapsulation of piroxicam with the cyclic oligosaccharide beta-cyclodextrin. PBCD is absorbed much faster than standard piroxicam, and its action as an analgesic is consequently more rapid. The purpose of this study was to assess the efficacy and the rapidity of action of piroxicam-beta-cyclodextrin in comparison with standard piroxicam, paracetamol and placebo following surgical extraction of impacted third molars. MATERIALS AND METHODS: The study population was composed of 32 patients of both sexes and in good health. To be included into the study, patients must have had third molar removal resulting in acute post-surgical pain of at least moderate intensity. The patients were then randomly assigned to one of four treatment groups. PBCD 20 mg tablets; piroxicam 20 mg capsules; paracetamol 500 mg tablets, or placebo. The study was conducted according to a double-blind, double-dummy design. Pain intensity and pain relief were recorded at 0.5, 1, 1.5, 2, 3, 4 hours after a single dose of the study drugs, by means of a Keele-type rating scale. Rescue analgesics were not allowed before one and a half hour after taking the study drugs. A global evaluation of study drugs was expressed by patients at the end of the observation period. RESULTS: Treatment groups were homogeneous for demographic characteristics of the patients and for pain intensity at the time of medication with study drugs. All patients who received placebo requested supplemental analgesics, while none of the patients treated with the active drugs needed rescue analgesics. PBCD and paracetamol were comparable for their analgesic effect, while the time lag before a significant reduction of pain intensity with piroxicam was longer. Piroxicam and PBCD were superior to paracetamol because they showed a substantial analgesic effect through the 4-hour study duration, while paracetamol did not induce a complete relief from pain. DISCUSSION: One of the most commonly utilized model for the evaluation of analgesics is the third molar extraction pain. Our study clearly differentiated between active drugs and placebo. Furthermore, while PBCD and paracetamol showed a rapid effect, piroxicam was slow in inducing pain relief. The analgesic and anti-inflammatory activity of PBCD and piroxicam brought about the resolution of pain and inflammation consequent to the dental extraction. Paracetamol, a pure analgesic, was not equally active and pain persisted, even if at a low grade, throughout the observation period; probably this was due to local inflammation and edema. The results of our study appear to confirm the pharmacokinetic data on PBCD, which showed that therapeutic blood levels are reached faster with PBCD than with the standard piroxicam formulation. This results should be confirmed in studies with an adequate number of patients.

Acetaminophen↗

[The morphology of the base of the cranium in prognathism. A cephalometric study of adult patients].

The cranial base of 60 adults affected by mandibular prognathism was studied with the aid of a computerized cephalometric analysis. The means and standard deviations of the values measured on the sample where compared with the cephalometric standards of the University of Michigan. The studied sample showed a significant reduction in length of the floor of the anterior cranial fossa, the cranial base angle showed no deviation from the control but the whole cranial base was backward and upward rotated in relation to the Frankfurt plane. The cranial base morphology was similar in patients with or without maxillary retrusion. The data in our possession may indicate that mid-facial sagittal growth in patients affected by mandibular prognathism is somehow impaired by altered cranial base growth. In any case the sagittal projection of the frontal and nasal bones appears to be reduced in our patients and this data must be kept in mind when studying these patients with the aid of cephalometry.

Adult↗