Dag Ørstavik

An Evaluation of Microbial Leakage in Roots Filled with a Thermoplastic Synthetic Polymer-Based Root Canal Filling Material (Resilon)

The purpose of this study was to compare bacterial leakage using Streptococcus mutans and Enterococcus faecalis through gutta-percha and a thermoplastic synthetic polymer-based root filling (Resilon) using two filling techniques during a 30-day period. Teeth were decoronated, roots prepared to a length of 16 mm, and instrumented to ISO sizes 40 to 50. A total of 156 roots were randomly divided into 8 groups of 15 roots (groups 1-8) and 3 control groups (12 roots each). Roots were filled using lateral and vertical condensation techniques with gutta-percha and AH 26 sealer (groups 1 and 2) or with gutta-percha and Epiphany sealer (groups 3 and 4). Groups 5 and 6 were filled with Resilon and Epiphany sealer using the lateral or vertical condensation techniques. A split chamber microbial leakage model was used in which S. mutans placed in the upper chamber could reach the lower chamber only through the filled canal. Groups 7 and 8 were identical to groups 5 and 6 respectively; however, E. faecalis was used to test the leakage. Positive controls were filled with Resilon (12 roots) and gutta-percha (12 roots) without sealer and tested with bacteria, whereas negative controls (12 roots) were sealed with wax to test the seal between chambers. All but one positive control leaked within 24 h, whereas none of the negative controls leaked. Resilon showed minimal leakage (group 8: one leakage; groups 5-7: each with two leakages), which was significantly less than gutta-percha, in which approximately 80% of specimens with either technique or sealer leaked. Kruskal-Wallis test showed statistical significance when all groups were compared (p < 0.05). Mann-Whitney U test compared the respective groups and found Resilon groups superior to gutta-percha groups (p < 0.05).

Reduction of Intracanal Bacteria Using Nickel-Titanium Rotary Instrumentation and Various Medications

The purpose of this study was to evaluate the extent of bacterial reduction with nickel-titanium rotary instrumentation and 1.25% NaOCl irrigation. Also, the additional antibacterial effect of calcium hydroxide for >1 wk was tested. Forty-two subjects with radiographic and clinical signs of chronic apical periodontitis were recruited. The canals were sampled before treatment, during and after instrumentation, and after treatment with calcium hydroxide and the samples incubated anaerobically for 7 days at 37 degrees C. The bacteria from each sample were quantified and the log10 values were used for calculations and comparisons. The initial sample confirmed infection of the canals. There was a significantly greater pattern of reduction of bacteria when NaOCl was used as an irrigant, compared with sterile saline (p < 0.05). After instrumentation with NaOCl irrigation, 61.9% of canals were rendered bacteria-free. The placement of calcium hydroxide for at least 1 wk rendered 92.5% of the canals bacteria free. This was a significant reduction, compared with NaOCl irrigation alone (p = 0.0001). The results of this study indicate that NaOCl irrigation with rotary instrumentation is an important step in the reduction of canal bacteria during endodontic treatment. However this method could not consistently render canals bacteria-free. The addition of calcium hydroxide intracanal medication should be used to more predictably attain this goal.

The effectiveness of increased apical enlargement in reducing intracanal bacteria.

It has been suggested that the apical portion of a root canal is not adequately disinfected by typical instrumentation regimens. The purpose of this study was to determine whether instrumentation to sizes larger than typically used would more effectively remove culturable bacteria from the canal. Forty patients with clinical and radiographic evidence of apical periodontitis were recruited from the endodontic clinic. Mandibular cuspids (n = 2), bicuspids (n = 11), and molars (mesial roots) (n = 27) were selected for the study. Bacterial sampling was performed upon access and after each of two consecutive instrumentations. The first instrumentation utilized 1% NaOCI and 0.04 taper ProFile rotary files. The cuspid and bicuspid canals were instrumented to a #8 size and the molar canals to a #7 size. The second instrumentation utilized LightSpeed files and 1% NaOCl irrigation for further enlargement of the apical third. Typically, molars were instrumented to size 60 and cuspid/bicuspid canals to size 80. Our findings show that 100% of the cuspid/bicuspid canals and 81.5% of the molar canals were rendered bacteria-free after the first instrumentation sizes. The molar results improved to 89% after the second instrumentation. Of the (59.3%) molar mesial canals without a clinically detectable communication, 93% were rendered bacteria-free with the first instrumentation. Using a Wilcoxon rank sum test, statistically significant differences (p < 0.0001) were found between the initial sample and the samples after the first and second instrumentations. The differences between the samples that followed the two instrumentation regimens were not significant (p = 0.0617). It is concluded that simple root canal systems (without multiple canal communications) may be rendered bacteria-free when preparation of this type is utilized.

Virulence Factors of Enterococcus faecalis: Relationship to Endodontic Disease

Enterococcus faecalis is a micro-organism that can survive extreme challenges. Its pathogenicity ranges from life-threatening diseases in compromised individuals to less severe conditions, such as infection of obturated root canals with chronic apical periodontitis. In the latter situation, the infecting organisms are partly shielded from the defense mechanisms of the body. In this article, we review the virulence factors of E. faecalis that may be related to endodontic infection and the periradicular inflammatory response. The most-cited virulence factors are aggregation substance, surface adhesins, sex pheromones, lipoteichoic acid, extracellular superoxide production, the lytic enzymes gelatinase and hyaluronidase, and the toxin cytolysin. Each of them may be associated with various stages of an endodontic infection as well as with periapical inflammation. While some products of the bacterium may be directly linked to damage of the periradicular tissues, a large part of the tissue damage is probably mediated by the host response to the bacterium and its products.

Bacterial reduction with nickel-titanium rotary instrumentation.

The purpose of this study was to compare intracanal bacterial reduction on teeth instrumented with 0.04 tapered nickel-titanium (NiTi) rotary instrumentation to bacterial reduction when using a stainless-steel K-file step-back technique using sterile saline irrigation. Forty-eight patients with apical periodontitis were randomly assigned treatment type. The canals were sampled before, during, and after instrumentation. The samples were incubated anaerobically for 7 days at 37 degrees C, colony-forming unit numbers calculated, and a log transformation performed to normalize the counts. Teeth exhibiting apical periodontitis were uniformly infected, whereas vital control teeth were not. A similar and uniform reduction occurred with progressive filing, regardless of technique (p < 0.0001). There was no detectable difference in colony-forming unit count after NiTi rotary or stainless-steel hand instrumentation (p = 0.42). Neither technique could predictably render canals free of bacteria. The results of this study indicate NiTi rotary and stainless-steel hand K-file step-back instrumentation techniques were not significantly different in their ability to reduce intracanal bacteria.

Dimensional change following setting of root canal sealer materials.

OBJECTIVE The study was designed to evaluate a method proposed for measuring dimensional changes of endodontic sealers, and to assess the dimensional changes of 11 commercial sealers after prolonged storage in water. METHODS The method for linear dimensional change described in the draft standard for endodontic sealers was applied to 11 different types of endodontic sealers. One material (Sealapex) could not be tested by the method. The other 10 materials were followed for dimensional change over 48 weeks. RESULTS The sealers showed markedly different dimensional properties. For most materials, the greatest dimensional changes took place within the first 4 weeks. Zinc-oxide-eugenol based sealers generally showed shrinkage ranging from 0.3 to 1%, while one product (Proco-Sol) exhibited expansion exceeding 6% after prolonged storage. The epoxy-based materials, AH 26 and AH 26 silverfree, exhibited a large, initial expansion of 4-5%. AH Plus expanded from 0.4% after 4 weeks up to 0.9%. Apexit, a Ca(OH)2-based material, showed only minor variation round baseline value, -0.14 to +0.19%. Roeko-Seal expanded to 0.2% within 4 weeks, but was stable thereafter. SIGNIFICANCE The test methodology adequately assessed dimensional changes exceeding +/-0.2%, but some brands of material either could not be made into adequate test specimens or showed surface changes which interfered with dimensional change measurements. Theoretical approaches to the consequences of expansion by materials of low bulk strength question the necessity of a strict requirement against expansion, whereas bacterial penetration may be a real threat from sealers shrinking as little as 1%.

Inactivation of the Antibacterial Activity of Iodine Potassium Iodide and Chlorhexidine Digluconate Against Enterococcus faecalis by Dentin, Dentin Matrix, Type-I Collagen, and Heat-Killed Microbial Whole Cells

The antibacterial activity of chlorhexidine digluconate and iodine potassium iodide on Enterococcus faecalis A197A was tested in the presence of dentin, dentin matrix, dentin pretreated by EDTA and citric acid, collagen, and heat-killed cells of Enterococcus faecalis and Candida albicans. Medications were preincubated for 1 h with each of the potential inhibitors and tested for their antibacterial activity against E. faecalis, strain A197A. Surviving bacteria were sampled after 1 and 24 h of incubation. Dentin matrix and heat-killed microbial cells were the most effective inhibitors of chlorhexidine, whereas dentin pretreated by citric acid or EDTA showed only slight inhibition. Dentin and skin collagen showed some inhibition at 1 h but not after 24 h. Iodine potassium iodide was effectively inhibited by dentin, dentin matrix, and heat-killed microbial cells. Skin collagen and dentin pretreated by EDTA or by citric acid showed little or no inhibitory effect on iodine potassium iodide. Different components of dentin are responsible for the divergent patterns of inhibition of the antibacterial activity of chlorhexidine digluconate and iodine potassium iodide. Chemical treatment of dentin before applying the medication into the root canal may alter the antibacterial effect of the medication.

Adhesion of endodontic sealers: scanning electron microscopy and energy dispersive spectroscopy.

The microscopic details of the debonded interfaces between endodontic sealers and dentin or gutta-percha were assessed in this study. Dentin, conditioned with 37% H3PO4 for 30 s, 25% citric acid for 30 s, 17% EDTA for 5 min, or a rinse with 10 ml of distilled H2O (control), and gutta-percha surfaces were coated with freshly mixed sealer: Grossmans sealer, Apexit, Ketac-Endo, AH Plus, RoekoSeal Automix, or RoekoSeal Automix with an experimental primer. The surfaces were pressed together and the sealers were allowed to set. After tensile bond strength testing, the morphological aspects of the fractured surfaces were assessed by scanning electron microscopy and energy dispersive spectroscopy. The energy dispersive spectroscopy successfully traced sealer components to the debonded surfaces. Some of the sealers penetrated into the dentinal tubules when the dentin surface had been pretreated with acids. However, these sealer tags remained occluding the tubules after bond failure in some instances only (Grossmans sealer, RoekoSeal Automix with an experimental primer, AH Plus/EDTA). Penetration of the endodontic sealers into the dentinal tubules when the smear layer was removed was not associated with higher bond strength.

Radiopacity of root canal sealers

A standardized and reproducible method of radiopacity measurements of dental materials is presented. The method entails densitometric comparison of standard-sized specimens with an aluminum step wedge under controlled conditions for exposure and film processing. Methodologic aspects have been evaluated and discussed. Measurements of forty root canal sealers demonstrated wide variations among the different types. Visual examination could not provide reproducible measurements of the radiopacity of the materials.

Histopathology and X-ray microanalysis of the subcutaneous tissue response to endodontic sealers

One-hundred and twenty-three polyethylene tube implants of 12 endodontic sealers were placed subcutaneously into rats. The implants were left in situ for periods of 14 and 90 days. The tissue response was analyzed histologically and by scanning X-ray microanalysis. The tissue responses differed markedly in the intensity, extent, and cellular characteristics. A slight long-term tissue response was noted for polymeric resin-based materials; zinc oxide-eugenol-based sealers gave a stronger reaction; and a chloroform-based and two paste-type materials caused the least favorable reactions. X-ray microanalysis of tissue sections revealed material components in the reactive capsule and in the peripheral connective tissue of most specimens investigated. Implants of the resin-based sealers, AH26 and Hydron, were surrounded by macrophages, phagocytosing heavy metal components (Bi, Ba) of the materials. Zinc oxide-eugenol- and chloroform-based materials appeared more frequently to fragment into particles of sizes too large for monocellular phagocytosis.