[Treatment of a fractured endodontical instrument in the root canal]. / Behandeling van een gefractureerd endodontisch instrument in het wortelkanaal.

A 53-year-old woman with continuing pain coming from a lower first molar was diagnosed with apical periodontitis, with a retained fractured instrument in the root canal. There are a variety of treatment options for dealing with a corpus alienum in a root canal. In this case it was decided to treat the tooth endodontically, and leave the fractured instrument fragment in situ. The selection of this treatment option was made on the basis of knowledge of the original diagnosis and the success rates of the various treatment options as described in the relevant literature, weighed against the possible risks and their effects on the prognosis. This suggested that the use of a dental operating microscope has a positive impact on the success rates of endodontic treatment The prognosis for endodontic treatment when a fractured instrument fragment is left within the root canal, as in this case, is not significantly reduced. The presence of preoperative periapical pathology, however, is a more clinically significant prognostic indicator.

[Root canal preparation: shaping and cleaning of the root canal]. / De wortelkanaalpreparatie: vormgeven om te reinigen.

Primary shaping is of paramount importance for a succesfull root canal treatment. In this article the basis principles of apical terminus location, shape, size and diameter are discussed. The use of NiTi instruments and crown-down preparation techniques are explained.

[Disinfection of the root canal system during endodontic treatment]. / Desinfectie van het wortelkanaalstelsel bij de endodontische behandeling.

In this article an overview is given of the disinfectants used in root canal therapy. The different properties of anti-microbials and their effect on the endodontic microflora are discussed. A clinical guideline for effective disinfection is included.

Periapical healing of endodontically treated teeth in one and two visits obturated in the presence or absence of detectable microorganisms.

AIM: The purpose of the present study is to evaluate the healing of periapical lesions of teeth with positive and negative canal cultures at the time of obturation, and to evaluate the periapical healing of teeth treated in one visit (without) or in two visits with an interappointment dressing of calcium hydroxide. METHODOLOGY: Thirty-nine patients received root-canal treatment. In the first visit, teeth were instrumented, and 18 of these teeth were filled (after microbiological sampling) with calcium hydroxide in sterile saline. The other 21 teeth were obturated with gutta-percha and AH-26 sealer after microbiological sampling. Four weeks later, the teeth with calcium hydroxide were accessed again and after microbiological sampling they were obturated with gutta-percha and AH-26 sealer. Healing of periapical radiolucency was recorded over a period up to 4.5 years. RESULTS: In both the treatment groups, the size of the periapical lesions reduced significantly during the follow-up period. Complete radiographic healing was observed in 81% of the cases in the one-visit group, and in 71% of the cases in the two-visit group. The probability of success increased continuously over time for both treatment groups. Seven out of eight cases (87.5%) that showed a positive root-canal culture at the time of obturation healed. The number of colony forming units (CFU) in six out of eight positive canals was <10(2) CFU mL(-1). CONCLUSIONS: Within the limitations of this study, no significant differences in healing of periapical radiolucency was observed between teeth that were treated in one visit (without) and two visits with inclusion of calcium hydroxide for 4 weeks. The presence of a positive bacterial culture (CFU<10(2)) at the time of filling did not influence the outcome of treatment.

Combinations of bacterial species in endodontic infections.

AIM: This study was undertaken to investigate combinations of bacteria found in root-canal infections of teeth with periapical bone destruction without clinical signs and symptoms. METHODOLOGY: Endodontic samples from 58 root canals were cultured anaerobically and microorganisms were counted and identified. Eighty-one combinations of microorganisms were found and tested for a symbiotic relationship using the Fisher's exact test and Odds ratio calculation. RESULTS: All samples contained microorganisms with a median CFU mL(-1) of 8x10(4) per sample. Strict anaerobic species accounted for 87% of the microflora. The most prevalent bacteria were Prevotella intermedia, Peptostreptococcus micros and Actinomyces odontolyticus, present in 33, 29 and 19%, respectively, of the cultured canals. A significant relationship (P<0.05) and an Odds ratio >2 were found between P. intermedia and P. micros, P. intermedia and P. oralis, A. odontolyticus and P. micros, Bifidobacterium spp. and Veillonella spp. CONCLUSIONS: These results indicate that endodontic pathogens do not occur at random but are found in specific combinations.

Effects of instrumentation, irrigation and dressing with calcium hydroxide on infection in pulpless teeth with periapical bone lesions.

AIM: The aim of this study was to evaluate the fate of microorganisms in root canals of teeth with infected pulps and periapical bone lesions with and without the use of calcium hydroxide medication. METHODOLOGY: Endodontic samples were cultured and microorganisms were counted and identified in 43 teeth before (sample 1) and after (sample 2) treatment during the first visit and before (sample 3) and after (sample 4) treatment during the second visit. In the first visit teeth were instrumented and half of the teeth were filled with a thick slurry of calcium hydroxide in sterile saline. The other teeth were obturated with gutta-percha and AH-2 6 sealer. After 4 weeks the teeth with calcium-hydroxide were accessed again and after microbiological sampling they were obturated with gutta-percha and AH-26 sealer. RESULTS: The mean total colony forming unit (CFU) counts of positive samples dropped significantly as a result of canal preparation during the first visit from 1.0 x 10(6) to 1.8 x 10(3) (between samples 1 and 2) but increased to 9.3 x 10(3) in the period between the two visits (sample 2 and 3). There was no difference in mean total CFU counts of positive samples between the end of the first (sample 2) and the end of the second visit (sample 4). The most frequently isolated species were Prevotella intermedia, Capnocytophaga spp.. Actinomyces odontolyticus. Propionibacterium acnes and Peptostreptococcus micros. CONCLUSIONS: Although a calcium hydroxide paste was placed in the prepared canals, the number of positive canals had increased in the period between visits. However, the number of microorganisms had only increased to 0.93% of the original number of CFU (sample 1). It is concluded that a calcium hydroxide and sterile saline slurry limits but does not totally prevent regrowth of endodontic bacteria.

Viable bacteria in root dentinal tubules of teeth with apical periodontitis.

Two sets of teeth with apical periodontitis were collected at different geographic locations to study the identity of bacteria left in the root dentinal tubules. Root dentin of 20 of these teeth was cultured from three locations between pulp and cementum (A, B, and C). In addition dentin from eight teeth was examined histologically. Using the culturing technique bacteria were found in 77% of the dentin samples from set 1 (Amsterdam) and in 87.5% of the dentin samples from set 2 (Glasgow). At greater distance, in layer C, from the pulp bacteria were found in 62% (13 of 21) of the dentin samples. Twenty-three percent (3 of 13) of set 1 and 25% (2 of 8) of set 2 contained >50,000 colony-forming units/mg of dentin in layer C. In layers closer to the pulp higher numbers of anaerobic bacteria and gram-positive rods were found, as well as a larger number of bacterial species. Histological sections showed bacterial penetration in dentinal tubules in 5 of 8 teeth. In the other three teeth where the colony-forming units/mg recovered was <10,000, no histological signs of tubule penetration was seen. It seems clear that, in more than half of the infected roots, bacteria are present in the deep dentin close to the cementum and that anaerobic culturing of dentin is more sensitive than histology to detect these bacteria.

Penetration of bacteria in bovine root dentine in vitro.

AIM: The aim of this study was to develop a test model to quantify the penetration of bacteria into dentinal tubules. METHODOLOGY: The model consisted of two compartments separated by a bovine dentine specimen with a thickness of 1.5-3.1 mm. The root cementum was removed from the root surface and the specimens were oriented in the model with the pulpal side facing the inoculated chamber of the test model. One compartment contained the test organism and the other was filled with sterile broth that was evaluated for growth of the test organism. The depth of bacterial penetration was measured in the dentine with or without a smear layer using both a histological and a quantitative recovering grinding technique, after 6 weeks of exposure to the microorganisms. RESULTS: E. faecalis penetrated dentine significantly deeper than A. israelii (P < 0.001). After removal of the smear layer with EDTA, E. faecalis penetrated significantly deeper than in dentine pretreated with saline only (P < 0.01) or with a combination of saline and sodium hypochlorite (P < 0.01). Microorganisms were found in 89% of the cultured specimens and in 80% of the specimens that were evaluated with light microscopy. Total penetration through the dentine specimen and infection of the broth in the test compartment of the model occurred in only two out of 72 specimens. CONCLUSION: Collection and immediate culturing of infected dentine dust and counting colony forming units (CFU) allowed an overview of the number of bacteria per sample and was more sensitive than microscopy. Removal of the smear layer enhanced bacterial penetration.

Soft tissue management in endodontic surgery.

This article provides an overview of the factors influencing the wound healing of oral soft tissues before, during, and after surgical endodontics. In more detail, the effects of flap design, handling of tissues, and wound closure are discussed.

The fate and the role of bacteria left in root dentinal tubules.

In this article the question of the relevance and consequences of bacteria remaining in the tubules of root dentine after cleaning and shaping of the root canal space is addressed. A second aim is to discuss the necessity of clinical measures taken to eradicate those bacteria that are presumed to survive there. The available clinical and experimental evidence supports the use of antibacterial dressings in cases where the root canal space remains temporarily unobturated after removal of necrotic and infected pulp tissue. There is no evidence, however, that special measures should be taken to kill the bacteria in the dentinal tubules. Should time permit, a sound obturation technique immediately following the cleaning, shaping and disinfection phases allows the remaining bacteria in the tubules to be either inactivated or prevented from repopulating the (former) canal space. In the vast majority of cases, those bacteria appear not to jeopardize the successful outcome of root canal treatment.

A comparison of leakage of filling materials in demineralized and non-demineralized resected root ends under vacuum and non-vacuum conditions.

A study was conducted to compare the marginal apical leakage of root-end filling materials under vacuum and non-vacuum conditions, and to assess the effect of demineralization by application of citric acid to the root ends on the apical marginal leakage of root end filling materials. The root canals of 148 extracted human canines and premolars were handfiled and sealed with gutta-percha and Roth's 801 sealer using cold lateral condensation. The teeth were divided into 8 groups that received retrofilling materials. The materials tested were amalgam, IRM and gutta-percha/sealer with and without successive application of citric acid. Half of the specimens were placed under vacuum conditions in methylene blue dye, and the other half were placed in the dye for the same time period without exhausting air from the flask. The teeth were split longitudinally and the extent of dye penetration was determined with a stereomicroscope and eyepiece micrometer. The most evident difference in dye penetration was found between the positive control groups. Under vacuum conditions, the positive controls showed complete penetration of the unobturated canal system with dye. With passive immersion only partial penetration of the unobturated canal system occurred. Application of citric acid to the root end did not adversely affect the seal of amalgam, IRM or gutta-percha/sealer.

[Efficiency and endodontic access cavity preparation]. / Een goede opening, een efficiënt begin.

A description of the principles and techniques of the endodontic access cavity is given.

[Principles for the preparation of the access cavity in teeth]. / Het endodontisch openen van elementen. Principes en technieken.

In this article the general principles and techniques for the preparation of the endodontic access cavity are presented. Problems encountered during preparation are discussed more thoroughly, as are problems encountered while trying to locate the canal orifice(s). Instructions are given to prevent failure during this stage of endodontic treatment.