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Effect of different intracanal medicaments on the fracture resistance of the human root

BACKGROUND: The effect of different intracanal medicaments on root fracture resistance has not been thoroughly investigated in the short and long term. To assess the effect of calcium hydroxide (CH), CH combined with Chlorhexidine (CHX), double antibiotic paste (DAP), and simvastatin as intracanal m...

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Autores principales: Rahimi, Saeed, Ghasemi, Negin, Jabbari, Golchin, Zaheri, Zahra, Torabi, Zahra Sadat, Darehchi, Naghmeh Rahimi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927953/
https://www.ncbi.nlm.nih.gov/pubmed/35308444
http://dx.doi.org/10.4103/1735-3327.336694
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author Rahimi, Saeed
Ghasemi, Negin
Jabbari, Golchin
Zaheri, Zahra
Torabi, Zahra Sadat
Darehchi, Naghmeh Rahimi
author_facet Rahimi, Saeed
Ghasemi, Negin
Jabbari, Golchin
Zaheri, Zahra
Torabi, Zahra Sadat
Darehchi, Naghmeh Rahimi
author_sort Rahimi, Saeed
collection PubMed
description BACKGROUND: The effect of different intracanal medicaments on root fracture resistance has not been thoroughly investigated in the short and long term. To assess the effect of calcium hydroxide (CH), CH combined with Chlorhexidine (CHX), double antibiotic paste (DAP), and simvastatin as intracanal medicaments on the fracture resistance of the human root. One hundred and twenty single-rooted mandibular premolars which were extracted for periodontal reasons were collected for this in vitro study. MATERIALS AND METHODS: This was an in vitro study. All teeth were decoronated. Root canals were prepared by the Pro taper system, and %2.5 NaOCl was used for irrigation. The smear layer was removed using %5.25 NaOCl and 17% ethylenediaminetetraacetic acid each for 3 min. The samples were randomly divided into five groups based on the medicament: (1) CH (2) CH + CHX (3) Simvastatin (4) DAP (5) Control group. All specimens in each group were incubated for 1 week (Subgroup A) and 1 month (Subgroup B). Then, medicaments were removed and filled with gutta-percha and AH26 sealer. All samples were tested for fracture resistance. The data were statistically evaluated with the SPSS software 17. ANOVA and Mann–Whitney U and Wilcoxon tests were used for the analysis of the data. P = 0.05 was considered statistically significant. RESULTS: Although CH and CH + CHX increased the fracture resistance in a 1-week period, there was no significant difference between the groups after 1 month. CONCLUSION: Under the limitations of this study, CH and CH + CHX, DAP and simvastatin do not have a negative effect on root fracture resistance when used as intracanal medicaments for <1 month.
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spelling pubmed-89279532022-03-18 Effect of different intracanal medicaments on the fracture resistance of the human root Rahimi, Saeed Ghasemi, Negin Jabbari, Golchin Zaheri, Zahra Torabi, Zahra Sadat Darehchi, Naghmeh Rahimi Dent Res J (Isfahan) Original Article BACKGROUND: The effect of different intracanal medicaments on root fracture resistance has not been thoroughly investigated in the short and long term. To assess the effect of calcium hydroxide (CH), CH combined with Chlorhexidine (CHX), double antibiotic paste (DAP), and simvastatin as intracanal medicaments on the fracture resistance of the human root. One hundred and twenty single-rooted mandibular premolars which were extracted for periodontal reasons were collected for this in vitro study. MATERIALS AND METHODS: This was an in vitro study. All teeth were decoronated. Root canals were prepared by the Pro taper system, and %2.5 NaOCl was used for irrigation. The smear layer was removed using %5.25 NaOCl and 17% ethylenediaminetetraacetic acid each for 3 min. The samples were randomly divided into five groups based on the medicament: (1) CH (2) CH + CHX (3) Simvastatin (4) DAP (5) Control group. All specimens in each group were incubated for 1 week (Subgroup A) and 1 month (Subgroup B). Then, medicaments were removed and filled with gutta-percha and AH26 sealer. All samples were tested for fracture resistance. The data were statistically evaluated with the SPSS software 17. ANOVA and Mann–Whitney U and Wilcoxon tests were used for the analysis of the data. P = 0.05 was considered statistically significant. RESULTS: Although CH and CH + CHX increased the fracture resistance in a 1-week period, there was no significant difference between the groups after 1 month. CONCLUSION: Under the limitations of this study, CH and CH + CHX, DAP and simvastatin do not have a negative effect on root fracture resistance when used as intracanal medicaments for <1 month. Wolters Kluwer - Medknow 2022-01-28 /pmc/articles/PMC8927953/ /pubmed/35308444 http://dx.doi.org/10.4103/1735-3327.336694 Text en Copyright: © 2022 Dental Research Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Rahimi, Saeed
Ghasemi, Negin
Jabbari, Golchin
Zaheri, Zahra
Torabi, Zahra Sadat
Darehchi, Naghmeh Rahimi
Effect of different intracanal medicaments on the fracture resistance of the human root
title Effect of different intracanal medicaments on the fracture resistance of the human root
title_full Effect of different intracanal medicaments on the fracture resistance of the human root
title_fullStr Effect of different intracanal medicaments on the fracture resistance of the human root
title_full_unstemmed Effect of different intracanal medicaments on the fracture resistance of the human root
title_short Effect of different intracanal medicaments on the fracture resistance of the human root
title_sort effect of different intracanal medicaments on the fracture resistance of the human root
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8927953/
https://www.ncbi.nlm.nih.gov/pubmed/35308444
http://dx.doi.org/10.4103/1735-3327.336694
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