Apical extrusion of intracanal bacteria following use of various instrumentation techniques

Aim To evaluate the number of bacteria extruded apically from extracted teeth ex vivo after canal instrumentation using a manual technique and three engine‐driven techniques utilizing nickel–titanium instruments (K3, RaCe, and FlexMaster). Methodology Seventy extracted human mandibular premolar teeth with similar dimensions were used. Access cavities were prepared and root canals were then contaminated with a suspension of Enterococcus faecalis and then dried. The contaminated roots were divided into four experimental groups of 15 teeth each and one control group of 10 teeth. G1. RaCe group: the root canals were instrumented using RaCe instruments. G2. K3 group: the root canals were instrumented using K3 instruments. G3. FlexMaster group: the root canals were instrumented using FlexMaster instruments. G4. Manual technique group: the root canals were instrumented using K‐type stainless steel instruments. G5. Control group: no instrumentation was attempted. Bacteria extruded from the apical foramen during instrumentation were collected into vials. The resultant microbiological samples were removed from the vials and then incubated in culture media for 24 h. The number of colony‐forming units (CFU) was determined for each sample. The data obtained were analysed using the Kruskal–Wallis one‐way analysis of variance and Mann–Whitney U‐tests, with α = 0.05 as the level for statistical significance. Results There was a significant difference between experimental‐control and engine‐driven‐manual technique groups (P < 0.05). The manual technique was associated with the greatest extrusion of microorganism. Conclusions All instrumentation techniques extruded intracanal bacteria apically. No significant difference was found in the number of CFU among the engine‐driven techniques; manual techniques extruded significantly more microorganisms.     

An in vitro investigation of peak insertion torque values of six commercially available mini-implants

This study compared peak insertion torque values of six commercially available self-drilling mini-implants [Mini Spider? screw (1.5 × 8 mm), Infinitas? (1.5 × 9 mm), Vector TAS? (1.4 × 8 mm), Dual Top? (1.6 × 8 mm), Tomas Pin? (1.6 × 8 mm), and Ortho-Easy? (1.7 × 6, 8, and 10 mm)]. Twenty implants each were drilled into acrylic rods at a speed of 8 rpm using a motorized torque measurement stand, and the values were recorded in Newton centimetres (Ncm). A further 20 Ortho-Easy? implants with a length of 6 and 10 mm were tested at 8 rpm; 20 implants of 6 mm length were also tested at 4 rpm. Kaplan-Meier estimates of the peak torque values were compared using the log-rank test with multiple comparisons evaluated by Sidak's test. There were significant differences in the maximum torque values for different mini-implants with the same length. The Mini Spider? screw and Infinitas? showed the lowest average torque values (6.5 and 12.4 Ncm) compared with Vector TAS?, Dual ToP?, Tomas Pin?, and Ortho-Easy? (30.9, 29.4, 25.4, and 24.8 Ncm, respectively). There was no correlation between the diameter of the implants and torque values. The Tomas Pin? showed the largest standard deviation (7.7 Ncm) and the Dual Top? implant the smallest (0.6 Ncm). Different insertion speeds did not result in significant differences in peak torque values but the 6 mm mini-implants showed significantly higher torque values than the 8 and 10 mm implants. Using a 'torque limiting' screwdriver or pre-drilling cortical bone to reduce insertion, torque appears justified for some of the tested implants.     

Predoctoral implant dentistry curriculum survey: European dental schools

PURPOSE: In 2002 a survey of European dental schools was conducted. The purpose of the survey was to determine the curricular structure, teaching philosophies and materials used in predoctoral implant dentistry courses. MATERIALS AND METHODS: Fifty-six European dental schools were randomly selected from the Association for Dental Education in Europe representing 33 countries. A questionnaire was mailed to the predoctoral implant dentistry director/chairperson of the selected European dental schools. Of these, 40 schools returned the completed survey, resulting in a response rate of 71%. The mean, median and range of responses were computed where applicable. RESULTS: The results from this survey show that 80% of the responding schools required a course in implant dentistry. Between 1997 and 1999 over a third of responding schools (36%) incorporated a predoctoral implant dentistry course into their curriculum. Eighty-seven per cent of the schools have some prosthodontists teaching the course. Thirty-seven per cent of schools are offering a laboratory course in conjunction with the implant course. Sixty-three per cent of the schools are not restoring implant cases at the predoctoral level. However, 68% of schools reported students are required to be present during implant surgery. Ten per cent of schools require that the implant-related laboratory work be completed by the students. CONCLUSIONS: Predoctoral implant dentistry educational programmes vary from school to school. Yet a large percentage of schools agree on certain topics, including the importance of including implant education in predoctoral dental programmes.     

A comparison of two methods for the evaluation of the daily urinary fluoride excretion in Romanian pre-school children

OBJECTIVE: To compare two different methods of estimating daily fluoride urinary excretion in pre-school children under stable fluoride intake conditions. DESIGN: Thirty-five healthy kindergarten children, permanent residents of Targu-Mures, Romania, where the average drinking water fluoride concentration is 0.12 mg F/L, participated on two separate occasions, when they were aged 4-6 and 5-7 years, respectively in the collection of a) a mid-morning spot urine sample and b) a 16-h time-controlled urine sampling. In case a), the ratio of concentrations of fluoride and creatinine were measured, while in case b) the rates of fluoride excretion in two separate 8-hour periods were used to estimate the 24-hour fluoride urinary excretion. RESULTS: The estimated average daily fluoride urinary excretion values (S.D.) were 0.318 (0.182) mg F/day for method a) and 0.341 (0.193) mg F/day for method b). These values were not significantly different (Mann-Whitney U test; p = 0.49). The estimated daily fluoride doses were 0.040 (0.021) and 0.043 (0.022) mg F/kg body weight/day, respectively. The latter values were not significantly different (Mann Whitney U test; p = 0.38). CONCLUSIONS: Results obtained suggest that under stable F-intake conditions the estimation of the daily fluoride urinary excretion by means of a mid-morning spot urine sample yields comparable results to those obtained with the more involved method of separate, two 8 h (16 h) time-controlled urine sampling recommended by the WHO. Use of spot urine sampling appears to be particularly useful for epidemiological studies.     

Platelet-derived growth factor-B gene delivery sustains gingival fibroblast signal transduction

Background and Objective: Platelet‐derived growth factor‐BB is a potent mediator of tooth‐supporting periodontal tissue repair and regeneration. A limitation of the effects of topical platelet‐derived growth factor‐BB application is its short half‐life in vivo. Gene therapy has shown strong promise for the long‐term delivery of platelet‐derived growth factor in both skin ulcer healing and periodontal tissue engineering. However, little is known regarding the extended effects of platelet‐derived growth factor‐B on cell signaling via gene delivery, especially at the level of phosphorylation of intracellular kinases. This study sought to evaluate the effect of gene transfer by Ad‐PDGF‐B on human gingival fibroblasts (HGFs) and the subsequent regulation of genes and cell‐surface proteins associated with cellular signaling. Material and Methods: HGFs from human subjects were treated by adenoviral PDGF‐B, PDGF‐1308 (a dominant negative mutant of PDGF) and recombinant human platelet‐derived growth factor‐BB, and then incubated in serum‐free conditions for various time points and harvested at 1, 6, 12, 24, 48, 72 and 96 h. Exogenous PDGF‐B was measured by RT‐PCR and Western blot. Cell proliferation was evaluated by [methyl‐³H]thymidine incorporation assay. We used proteomic arrays to explore phosphorylation patterns of 23 different intracellular kinases after PDGF‐B gene transfer. The expression of α and β PDGFR and Akt were measured by Western blot analysis. Results: Sustained in vitro expression of PDGF‐B in HGFs by Ad‐PDGF‐B transduction was seen at both the mRNA and protein levels. Compared to rhPDGF‐BB and Ad‐PDGF‐1308, Ad‐PDGF‐B maintained cell growth in serum‐free conditions, with robust increases in DNA synthesis. Gene delivery of PDGF‐B also prolonged downregulation of the growth arrest specific gene (gas) PDGFαR. Of the 23 intracellular kinases that we tested in proteomic arrays, Akt revealed the most notable long‐term cell signaling effect as a result of the over‐expression of Ad‐PDGF‐B, compared with pulse recombinant human platelet‐derived growth factor BB. Prolonged Akt phosphorylation was induced by treatment with Ad‐PDGF‐B, for at least up to 96 h. Conclusion: These findings further demonstrate that gene delivery of PDGF‐B displays sustained signal transduction effects in human gingival fibroblasts that are higher than those conveyed by treatment with recombinant human platelet‐derived growth factor‐BB protein. These data on platelet‐derived growth factor gene delivery contribute to an improved understanding of these pathways that are likely to play a role in the control of clinical outcomes of periodontal regenerative therapy.     

Macrophages in periapical lesions

Macrophages are major constituents of periapical granulomas. They have a central protective role in both innate immunity and adoptive, antigen-specific immune response. Macrophage activation may occur in periapical granulomas by cytokines produced by antigen-activated T-lymphocytes; by bacterial endotoxin, as part of the innate immunity; or by both these processes. Recent studies in athymic animals have shown that periapical granulomas may develop independently of T-lymphocytes. This observation reveals the major role that the activated macrophage may have in the formation of periapical lesions. Only a few of the macrophages in the periapical granuloma are activated. Current studies indicate that these activated cells are the source of the bone-resorbing cytokines in the periapical granuloma. Understanding the central role of the activated macrophage in the formation as well as the perpetuation of periapical lesions may lead to the development of new diagnostic and therapeutic tools in endodontics.     

Macrophages in periapical lesions

Abstract – Macrophages are major constituents of periapical granulomas. They have a central protective role in both innate immunity and adoptive, antigen‐specific immune response. Macrophage activation may occur in periapical granulomas by cytokines produced by antigen‐activated T‐lymphocytes; by bacterial endotoxin, as part of the innate immunity; or by both these processes. Recent studies in athymic animals have shown that periapical granulomas may develop independently of T‐lymphocytes. This observation reveals the major role that the activated macrophage may have in the formation of periapical lesions. Only a few of the macrophages in the periapical granuloma are activated. Current studies indicate that these activated cells are the source of the bone‐resorbing cytokines in the periapical granuloma. Understanding the central role of the activated macrophage in the formation as well as the perpetuation of periapical lesions may lead to the development of new diagnostic and therapeutic tools in endodontics.