AI Article Synopsis

  • - The study investigated how different pulpotomy base materials (PBMs)—IRM, MTA, and GI—affect Enterococcus Faecalis colonization in the pulp chambers of extracted primary teeth using confocal laser scanning microscopy (CLSM).
  • - Results showed that the Glass Ionomer (GI) group had a greater extent of bacterial staining compared to both IRM and MTA, indicating more bacterial presence, while MTA showed the lowest levels of bacteria.
  • - Bacterial penetration into dentinal tubules reached depths of up to 695μm, with no significant differences between the materials used, but the ratio of live to dead bacteria was higher in the GI group than in IRM and MTA groups

Article Abstract

the study aimed to evaluate Enterococcus Faecalis colonization in the pulp chamber in pulpotomized extracted human teeth filled by different pulpotomy base materials (PBMs), using confocal laser scanning microscopy (CLSM). : Cavity preparations were made in 70 extracted primary molars. The pulp chambers were filled using either Intermediate restorative material (IRM), Mineral Trioxide Aggregate (MTA) or Glass ionomer (GI). Twenty-five teeth served controls. The specimens were sterilized, and coronally filled with bacterial suspension for 21 days. The specimens were cut through the furcation area, stained using LIVE/DEAD BacLight Bacterial Viability Kit and evaluated using CLSM. The extent of fluorescent staining was larger in the GI group, compared to the IRM and MTA groups, and larger in the IRM group compared to the MTA group (P<0.05). The minimal and maximal bacterial penetration depths into the dentinal tubules were 55 and 695μm, respectively (mean 310μm), without differences between the materials (GI, IRM, MTA, p>0.05). The ratio of live bacteria to dead bacteria within the evaluated areas was higher in the GI group compared to the IRM and the MTA groups, and higher in the IRM group compared to the MTA group (P<0.05). There were no differences between the mesial, distal and apical parts in any of the evaluations (p>0.05). bacteria colonize the interface between the PBM and dentin and penetrate deeply into the dentinal tubules. The extent and the vitality of the colonized bacteria may be affected by the type of PBM.

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http://dx.doi.org/10.17796/1053-4625-44.2.3DOI Listing

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