Cementation of Glass-Ceramic Posterior Restorations: A Systematic Review
Aim. The aim of this comprehensive review is to systematically organize the current knowledge regarding the cementation of glass-ceramic materials and restorations, with an additional focus on the benefits of Immediate Dentin Sealing (IDS). Materials and Methods. An extensive li...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2015-01-01
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Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2015/148954 |
Summary: | Aim. The aim of this comprehensive review is to systematically
organize the current knowledge regarding the cementation of glass-ceramic
materials and restorations, with an additional focus on the benefits of Immediate
Dentin Sealing (IDS). Materials and Methods. An extensive literature
search concerning the cementation of single-unit glass-ceramic posterior restorations
was conducted in the databases of MEDLINE (Pubmed), CENTRAL (Cochrane Central
Register of Controlled Trials), and EMBASE. To be considered for inclusion,
in vitro and in vivo studies should compare different
cementation regimes involving a “glass-ceramic/cement/human tooth” complex.
Results and Conclusions. 88 studies were included in total.
The in vitro data were organized according to the following topics:
(micro)shear and (micro)tensile bond strength, fracture strength, and marginal gap
and integrity. For in vivo studies survival and quality of survival
were considered. In vitro studies showed that adhesive systems
(3-step, etch-and-rinse) result in the best (micro)shear bond strength values compared
to self-adhesive and self-etch systems when luting glass-ceramic substrates
to human dentin. The highest fracture strength is obtained with adhesive cements
in particular. No marked clinical preference for one specific procedure could be
demonstrated on the basis of the reviewed literature. The possible merits of IDS
are most convincingly illustrated by the favorable microtensile bond strengths.
No clinical studies regarding IDS were found. |
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ISSN: | 2314-6133 2314-6141 |