Effect of passive ultrasonic activation on microorganisms in primary root canal infection: a randomized clinical trial.

OBJECTIVE: This clinical study sought to evaluate the effectiveness of passive ultrasonic activation (PUA) in eliminating microorganisms in primary endodontic infection (PEI) after instrumentation of root canals using microbiological culture and checkerboard DNA-DNA hybridization. METHODOLOGY: Twenty root canals with PEI and apical periodontitis were selected. The root canals were instrumented and then randomly divided into 2 groups, according to the irrigation method: PUA and conventional needle irrigation (CNI). Microbiological samples were collected before instrumentation (S1), after instrumentation (S2) and after irrigation with 17% EDTA (S3). The samples were subjected to anaerobic culture technique and checkerboard DNA-DNA hybridization analysis. RESULTS: A statistically significant difference was found between CNI (23.56%) and PUA (98.37%) regarding the median percentage values for culturable bacteria reduction (p<0.05). In the initial samples, the most frequently detected species was S. constellatus (50%), and after root canal treatment was E. faecalis (50%). CONCLUSION: Both treatments significantly decreased the number of bacterial species compared with the initial sample. However, no statistical difference in the total microbial load between PUA and CNI groups was detected. The number of cultivable anaerobic bacteria reduced significantly using PUA, and the bacterial composition and number of bacterial species after using either CNI or PUA was similar.

Effect of passive ultrasonic activation on microorganisms in primary root canal infection: a randomized clinical trial

Abstract Objective: This clinical study sought to evaluate the effectiveness of passive ultrasonic activation (PUA) in eliminating microorganisms in primary endodontic infection (PEI) after instrumentation of root canals using microbiological culture and checkerboard DNA-DNA hybridization. Methodology: Twenty root canals with PEI and apical periodontitis were selected. The root canals were instrumented and then randomly divided into 2 groups, according to the irrigation method: PUA and conventional needle irrigation (CNI). Microbiological samples were collected before instrumentation (S1), after instrumentation (S2) and after irrigation with 17% EDTA (S3). The samples were subjected to anaerobic culture technique and checkerboard DNA-DNA hybridization analysis. Results: A statistically significant difference was found between CNI (23.56%) and PUA (98.37%) regarding the median percentage values for culturable bacteria reduction (p<0.05). In the initial samples, the most frequently detected species was S. constellatus (50%), and after root canal treatment was E. faecalis (50%). Conclusion: Both treatments significantly decreased the number of bacterial species compared with the initial sample. However, no statistical difference in the total microbial load between PUA and CNI groups was detected. The number of cultivable anaerobic bacteria reduced significantly using PUA, and the bacterial composition and number of bacterial species after using either CNI or PUA was similar.

Effectiveness in the Removal of Endotoxins and Microbiological Profile in Primary Endodontic Infections Using 3 Different Instrumentation Systems: A Randomized Clinical Study.

INTRODUCTION: This clinical study was conducted to correlate the microbiological profile and levels of endotoxins found in primary endodontic infection with the presence of clinical features and to evaluate the removal of microorganisms and endotoxins using rotary, reciprocating, and hybrid systems for biomechanical preparation. METHODS: Thirty single root canals with primary endodontic infection were evaluated with signs and symptoms and were randomly divided into 3 groups according to the instrumentation system used (n = 10) as follows: rotary Mtwo instruments (VDW, Munich, Germany) with 8 files, the reciprocating Reciproc system (VDW) with a single file, and Genius hybrid instruments with 3 files (1 rotary and 2 reciprocating files) with irrigation using 24 mL 2.5% sodium hypochlorite. Samples were collected before (S1) and after instrumentation (S2) before being submitted to microbiological culture (colony-forming units/mL) and the checkerboard DNA-DNA hybridization test. Endotoxins were quantified using the limulus amebocyte lysate assay. RESULTS: Microbiological culture showed statistical differences in the reduction of colony-forming units/mL with all systems tested (P < .05), but no statistical difference was found among the groups. The most frequently detected species were Capnocytophaga ochracea (53%) and Fusobacterium nucleatum (53%) at S1 and F. nucleatum (50%) and Leptotrichia buccalis (50%) at S2. As for the reduction of endotoxins at S2, Mtwo presented the best results (95.05%) followed by the Genius (91.85%) and Reciproc (64.68%) groups, but no statistical difference was found among the groups. Previous pain, tenderness to percussion, and presence of a sinus tract were associated with specific microorganisms (P < .05). CONCLUSIONS: Signs and symptoms were correlated with microorganisms. Endodontic treatment was effective in reducing bacteria and endotoxins but was not capable of completely removing them from the root canal.

Estudo comparativo de sistemas rotatório, reciprocante e híbrido no preparo de canais radiculares em dentes com infecção endodôntica primária: perfil microbiano e quantificação de endotoxinas / Comparative estudy of rotatory, reciprocating and hybrid systems on the instrumentation of root canals in teeth with primary endodontic infection: microbiological profile and endotoxin quantification

Os objetivos deste trabalho são: 1) Quantificar por checkerboard a carga microbiana e pelo método de LAL endotoxinas (EU/mL) nas infecções endodônticas primárias; 2) Realizar o monitoramento dos níveis de endotoxinas (EU/mL) e de carga microbiana antes do tratamento, após o preparo biomecânico com sistemas de instrumentação rotatória, reciprocante e híbrida e após o uso da medicação intracanal; 3) Relacionar sinais e sintomas clínicos com níveis de endotoxinas, micro-orgnismos e com complexos bacterianos; 4) Relacionar volumetria dos canais radiculares por meio de TCFC com níveis de endotoxina, micro-organismos e complexos bacterianos. Trinta dentes com infecção endodôntica primária e presença de lesão periapical foram submetidos a TCFC antes do tratamento e avaliados quanto a presença de sinais e sintomas clínicos. Após abertura coronária, foi realizada a coleta inicial nos canais radiculares, e em seguida, procedeu-se com o tratamento endodôntico, sendo os dentes divididos em diferentes grupos experimentais de acordo com o sistema de instrumentação utilizado (n=10): rotatório Mtwo (MTWO), reciprocante Reciproc (REC), e híbrido Genius (GEN). Durante o preparo biomecânico, os canais foram irrigados com 24 mL de NaOCl 2,5%. Foram realizadas coletas do conteúdo dos canais radiculares: logo após a abertura coronária (1 col), após a instrumentação (2 col), e após a MIC por 14 dias, realizada com pasta de hidróxido de cálcio associada a solução salina fisiológica (3 col). A detecção de micro-organimos foi realizada pelo teste checkerboard DNA-DNA hybridization. A quantificação de endotoxinas foi realizada pelo teste cinético cromogênio do lisado de amebócito de Limulus. As volumetrias dos canais radiculares foram realizadas com auxílio do software Nemotec®. Todos os dados foram analisados estatisticamente. Os resultados mostraram a detecção de micro-organismos e endotoxinas em 100% das amostras iniciais, sendo as bactérias C. ochracea e F. nucleatum as mais prevalentes (53%). Após o PBM, os micro-organismos mais encontrados foram F. nucleatum e L. buccalis (50%); e após a MIC C. gracilis (53,3%). Não houve diferença estatística entre os grupos quanto à redução da carga microbiana. Quanto as endotoxinas, logo após o PBM, o grupo que mais reduziu foi o MTWO, seguido por GEN e REC; após a MIC, o grupo que mais reduziu foi o GEN, seguido pelo MTWO e REC, porém todos os grupos se comportaram de maneira semelhante. Dor espontânea foi relacionada com P. nigrescens; dor a percussão com P. gingivalis, V. parvula, S. sputigena, P. nigrescens e E. saburreum; presença de fístula foi relacionada com o complexo laranja, Grampositivas e anaeróbios facultativos, e micro-organismos E. corrodens, P. micra, C. showae e E. saburreum. O maior volume do canal radicular foi correlacionado fortemente com anaeróbios estritos, com o complexo laranja e o micro-organismo P. micra. O PBM foi efetivo na redução de bactérias e endotoxinas do canal radicular, mas sem diferença estatística entre os três sistemas utilizados. Conclui-se que o PBM com NaOCl 2,5% é eficaz na redução de endotoxinas e na remoção de micro-organimos do canal radicular; sinais e sintomas são relacionados com micro-organismos, assim como a volumetria do canal radicular (AU)

The aims of this study are: 1) Quantify by checkerboard test the microbial load and endotoxins through LAL method (EU/ml) in primary endodontic infections; 2) To monitore levels of endotoxin (EU/ml) and microbial load before treatment, after biomechanical preparation with rotatory, reciprocating and hybrid instrumentation systems, and after use of intracanal medication; 3) To associate clinical signs and symptoms with endotoxin levels, microorganism and bacterial complexes; 4) To relate volumes of root canals through cone beam computed tomography (CBCT), with endotoxin levels, microorganisms and bacterial complexes. Thirty teeth with primary endodontic infection and periapical lesion were submitted to endodontic treatment after CBCT and evaluated the presence of clinical signs and symptoms. After coronary opening, the initial samples were collected to verify the presence of infection in root canals. Then, teeth were divided into different experimental groups according to the instrumentation system used (n=10): rotatory Mtwo (MTWO), reciprocating Reciproc (REC), and hybrid Genius (GEN). During biomechanical preparation, the canals were irrigated with 24 mL of 2.5% NaOCl. Samples were collected: after coronary opening (S1), after the instrumentation (S2) and after intracanal medication for 14 days with calcium hydroxide paste and physiological saline solution (S3). The detection of microorganisms was performed by checkerboard DNA-DNA hybridization technique. The endotoxin quantification was performed by chromogenic kinetic test of the Limulus amoebocyte lysate. The root canal volumetries were performed by Nemotec® software. All data were analyzed statistically. The results showed the detection of microorganisms and endotoxins in 100% of the S1, with the most prevalent bacteria being C. ochracea and F. nucleatum (53%). After biomechanical preparation, the most found microorganisms were F. nucleatum and L. buccalis (50%); And after intracanal medication C. gracilis (53.3%). There was no statistical difference between the groups regarding the reduction of the microbial load. In relation to endotoxins, after biomechanical preparation, the group with greatest reduction was MTWO, followed by GEN and REC; after intracanal medication, the group with greatest reduction was GEN, followed by MTWO and REC, but there was no statistical difference between them. Spontaneous pain was associated to P. nigrescens; tenderness to percussion with P. gingivalis, V. parvula, S. sputigena, P. nigrescens and E. saburreum; sinus tract was related to the orange complex, Gram-positive and facultative anaerobes, and microorganisms E. corrodens, P. micra, C. showae and E. saburreum. The root canal volume was strongly correlated with strict anaerobes, with the orange complex and the P. micra microorganism. Biomechanical preparation was effective in decreasing bacteria and endotoxin, but with no statistical difference were found between the three systems. Microorganisms are related to signs and symptoms and to root canal volume. In conclusion, biomechanical preparation with 2.5% NaOCl was effective on reducing endotoxins and decreasing microorganisms from root canals; signs and symptoms are related to microorganisms as well as root canal volumetry (AU)

Avaliação do metabolismo epitelial em cistos radiculares pela técnica de AgNORS / Epithelial metabolism evaluation in radicular cysts by the AGNOR technique

Introdução: A formação do Cisto Radicular (CR) está associada à proliferação dos restos epiteliais de Malassez por estímulos inflamatórios, provenientes da proliferação bacteriana do canal radicular de um dente não vital. Quando o dente é removido, esse cisto passa a ser denominado Cisto Residual (CRe). O tratamento de escolha para o CR é endodôntico, com o objetivo de eliminar a inflamação presente no periápice. No entanto, em alguns casos, o cisto pode continuar a crescer, necessitando de tratamento cirúrgico, o que ocorre na maioria dos casos de CRe. Objetivo: Avaliar o metabolismo do epitélio de revestimento de CR e CRe, utilizando a quantificação das AgNORs, e verificar a influência da presença de inflamação sobre o crescimento desses cistos. Material e método: Vinte casos de CR e dez de CRe foram submetidos à técnica de AgNOR. A análise quantitativa das NORs foi realizada utilizando-se o software 'Contando células'. O teste estatístico pós-hock de Newman-keuls foi realizado para a comparação do número médio de AgNORs entre CR e CRe, e entre áreas inflamadas e não inflamadas. Resultado: Diferença estatisticamente significante (p=0,0094) foi observada entre áreas inflamadas (1,86±0,26) e não inflamadas (1,65±0,20). Na comparação entre CR (1,81±0,28) e CRe (1,73±0,16), não houve diferença estatisticamente significante (p=0,37). Conclusão: A inflamação interfere no metabolismo epitelial de CR e CRe, o que reflete a ação de fatores de crescimento na proliferação do epitélio, contribuindo para o crescimento do cisto, independentemente da presença do fator etiológico associado com a origem da lesão. .

Introduction: Radicular Cyst (RC) development is associated with the activation and proliferation of epithelial rests of Malassez. This occurs due to inflammatory stimuli resulting from bacteria proliferation in the root canal of a non-vital tooth. When the tooth is removed, the cyst becomes known as Residual Cyst (ReC). The RC common treatment is the endodontic therapy, with the aim of eliminating the inflammation in the periapical region. Nonetheless, this treatment is not always effective and the cyst may continue to grow, what happens in most cases of ReC. Objective: To evaluate the metabolism of the RC and ReC epithelial lining through the technique of AgNOR quantification and of the influence of the presence of inflammation in the growth of these cysts. Material and method: 20 cases of RC and 10 of ReC, were processed by the AgNOR technique. The AgNOR quantitative analysis was performed using the "Counting cells" software. The statistical post-hock Newman-Keuls test was applied to compare the RC and ReC mean number of AgNORs in inflamed and non-inflamed areas. Result: Statistically significant difference (p=0.0094) was observed between inflamed (1.86±0.26) and non-inflamed (1.65±0.20) areas. No statistically significant difference (p=0.37) was observed in the comparison between RC (1.81±0.28) and ReC (1.73±0.16). Conclusion: Inflammation interferes in the epithelial metabolism of RC and ReC, reflectings the action of growth factors in epithelial proliferation and contributing to the growth of the cyst, regardless the presence of the etiologic factor associated with the injury origin. .