Professional Documents
Culture Documents
_Introduction
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luting techniques have been documented1519, but little has been reported on the laboratory procedures involved in fabricating FRCFPDs. This report describes
the clinical and laboratory procedures entailed in fabricating fibre-reinforced composite inlay-fixed partial dentures (FRCIFPDs); the method can be used to
restore missing teeth in an aesthetic, functional, and
time-saving manner, without any surgical steps. In
particular, a laboratory technique is described that
uses a plexiglass flask; light-curing, pre-impregnated
glass fibres; and light-curing composites.
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_FRCFPD fabrication
While fabricating the FRCIFPD, the technician
must carefully plan each step, to optimise framework design. Several studies1,2,13,14 have shown that
survival of FRCIFPDs depends on the mechanical
performance of the framework and on the quality
of adhesion between veneering material and fibres. Fracture of the principal structure in the connector areas and delamination of the composite
are the main causes of FRCIFPD failure.11,2326 The
framework design must be optimised: the framework should be the same shape as the final restoration but reduced in size.23,24 If it is designed thus,
loads applied to the structure will be transferred
from the veneering composite to the framework,
averting the delamination due to tensile forces
acting on the composite-framework interface.26
The framework wax-up is the first and most critical step in the entire procedure for FRCIFPD fabrication (Fig. 8). A specific silicone for stents (Temp
putty, 95 shore, Micerium S.p.a., Italy) is placed in a
plexiglass flask for composites (Tender flask,
Micerium). Before the silicone hardens, the framework wax-up is immersed in the putty. In order to
ensure light polymerisation of the composite,
transparent silicone (Temp Clear Silicone, 55 shore,
Micerium) is used to fill the flask, which is immediately closed. After about 15 minutes, the flask is
opened and the two components are separated, in
order to remove the wax-up (Fig. 9). When the silicone stamps have dried completely, fabrication of
the fibre framework may begin. An initial layer of
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A silane coupling agent is applied to the framework surface prior to composite resin veneering.
The first layer consists of opaque dentine (Enamel
Plus HFO Tender, Micerium), which reduces the
transparency of the glass fibre (Fig. 13). Various
dentine shades and brown stains are then applied
so that the restoration and the surrounding intact
teeth are aesthetically similar. Veneering is completed with enamel composites and characterisation (Enamel Plus HFO dentine stain and enamel,
Micerium). Finishing and polishing procedures,
using diamond burs, dedicated brushes, gums,
and diamond pastes, must be performed very
carefully (Fig. 14).
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_Discussion
Currently, interest in using FRCs for many dental applications is growing11, and acceptable success rates in long-term FRC prosthetic solutions,
such as crowns and FPDs, have been reported.1013
The main causes of failure of FRC devices in high
stress-bearing applications are fracture5,12, delamination of veneering composite, and de-cementation of the prosthesis.28 In order to increase
the survival rate of the FRCs structure, clinical and
laboratory procedures need to be optimised to reduce the risk of mechanical failure. In vivo studies
and FE analyses have shown that FRCFPD connectors are the most critical areas with regard to
stress concentration.20,21 Repeated, strong masticatory forces can contribute to formation of micro-cracks, eventually leading to fracture of the
composite, especially in the connector areas. In
order to reduce this risk, the clinician should in-
crease the space available to the technician, enabling him or her to apply the correct amount of
fibre and composite on the abutment teeth.5
Fracture of veneering composite at the connectors is thus correlated to box preparation design
(Figs. 18, 19). When space is inadequate, composite wear may result in early failure of the restoration or in fibre exposure, which may lead to plaque
accumulation and hydrolysis of the fibre.29 Another important strategy to reduce fracture at the
connector areas is to optimise the concentration
of fibres. The manufacturing processes and specific equipment described in this report, if applied
with care, enable fibre compaction to be maximised, decreasing voids in the framework, and
making the technique more predictable.30 In addition, use of the flask allows an anatomic framework design to be created, ensuring better stress
distribution within the tooth-restoration complex. This is very important, not only to reduce the
risk of composite fracture at the connectors, but
also to prevent delamination of the veneering material in the pontic element.
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_author info
_Conclusion
Dr Daniele Rondoni has a private practice in Savona, Italy.
The clinical and laboratory procedures required
to fabricate FRCFPDs are described, paying particular attention to strategies that can reduce the risk
of failure. Prospective clinical trials will be required,
to investigate long-term survival of this prosthetic
solution._
Editorial Note: A complete list of references is
available from the publisher.
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