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Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems

AIMS AND OBJECTIVES: Instrumentation techniques may cause extrusion of microorganisms and their products into the periapical region resulting inflammation and treatment failure. The aim of this ex vivo study was comparing the apical bacterial extrusion in canals prepared with single file versus mult...

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Autores principales: Saberi, Eshaghali, Zahedani, Shahram Shahraki, Ebrahimipour, Sediqe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629858/
https://www.ncbi.nlm.nih.gov/pubmed/29026702
http://dx.doi.org/10.4103/jispcd.JISPCD_199_17
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author Saberi, Eshaghali
Zahedani, Shahram Shahraki
Ebrahimipour, Sediqe
author_facet Saberi, Eshaghali
Zahedani, Shahram Shahraki
Ebrahimipour, Sediqe
author_sort Saberi, Eshaghali
collection PubMed
description AIMS AND OBJECTIVES: Instrumentation techniques may cause extrusion of microorganisms and their products into the periapical region resulting inflammation and treatment failure. The aim of this ex vivo study was comparing the apical bacterial extrusion in canals prepared with single file versus multiple file rotary systems. MATERIALS AND METHODS: Ninety-two human single-rooted mandibular first premolars were used. Endodontic access cavities were prepared, and root canals were contaminated with an Enterococcus faecalis (E. faecalis) suspension. The samples were incubated at 37°C for 30 days; the contaminated teeth were divided into four groups of 20 specimens each (1: Reciproc, 2: Mtwo, 3: Neoniti A1, 4: Safesider). Six teeth were not infected and each were prepared with one of the above instruments were considered as negative and six teeth which had been previously infected, were used as positive control groups. Extruded bacteria from the apical foramen during instrumentation were collected into vials containing 0.9% NaCl. The microbial samples were taken from the vials and incubated in brain heart agar medium for 24 h. The resulting bacterial titer, in colony-forming units per mL, was determined. The data entered into SPSS 18 software and were analyzed by Kruskal–Wallis and Mann–Whitney U-tests at 0.05 significance level. RESULTS: Mtwo multifile system showed significantly less bacterial extrusion than Safesider (P = 0.015) and Neoniti A1 (P = 0.042) but did not show significant difference with Reciproc system (P = 0.25). CONCLUSIONS: All instrumentation systems extruded bacteria beyond the apical foramen. However, this study showed that Mtwo multifile rotary system extruded fewer bacteria.
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spelling pubmed-56298582017-10-12 Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems Saberi, Eshaghali Zahedani, Shahram Shahraki Ebrahimipour, Sediqe J Int Soc Prev Community Dent Original Article AIMS AND OBJECTIVES: Instrumentation techniques may cause extrusion of microorganisms and their products into the periapical region resulting inflammation and treatment failure. The aim of this ex vivo study was comparing the apical bacterial extrusion in canals prepared with single file versus multiple file rotary systems. MATERIALS AND METHODS: Ninety-two human single-rooted mandibular first premolars were used. Endodontic access cavities were prepared, and root canals were contaminated with an Enterococcus faecalis (E. faecalis) suspension. The samples were incubated at 37°C for 30 days; the contaminated teeth were divided into four groups of 20 specimens each (1: Reciproc, 2: Mtwo, 3: Neoniti A1, 4: Safesider). Six teeth were not infected and each were prepared with one of the above instruments were considered as negative and six teeth which had been previously infected, were used as positive control groups. Extruded bacteria from the apical foramen during instrumentation were collected into vials containing 0.9% NaCl. The microbial samples were taken from the vials and incubated in brain heart agar medium for 24 h. The resulting bacterial titer, in colony-forming units per mL, was determined. The data entered into SPSS 18 software and were analyzed by Kruskal–Wallis and Mann–Whitney U-tests at 0.05 significance level. RESULTS: Mtwo multifile system showed significantly less bacterial extrusion than Safesider (P = 0.015) and Neoniti A1 (P = 0.042) but did not show significant difference with Reciproc system (P = 0.25). CONCLUSIONS: All instrumentation systems extruded bacteria beyond the apical foramen. However, this study showed that Mtwo multifile rotary system extruded fewer bacteria. Medknow Publications & Media Pvt Ltd 2017 2017-09-18 /pmc/articles/PMC5629858/ /pubmed/29026702 http://dx.doi.org/10.4103/jispcd.JISPCD_199_17 Text en Copyright: © 2017 Journal of International Society of Preventive and Community Dentistry http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Saberi, Eshaghali
Zahedani, Shahram Shahraki
Ebrahimipour, Sediqe
Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems
title Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems
title_full Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems
title_fullStr Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems
title_full_unstemmed Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems
title_short Apical Extrusion of Intracanal Bacteria with Single File and Multifile Rotary Instrumentation Systems
title_sort apical extrusion of intracanal bacteria with single file and multifile rotary instrumentation systems
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629858/
https://www.ncbi.nlm.nih.gov/pubmed/29026702
http://dx.doi.org/10.4103/jispcd.JISPCD_199_17
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