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Rudd
Fig. 2. Waxed dentures and aluminum plates placed in flask to check height of artificial teeth
and aluminum plates. A, Maxillary denture; B, mandibular denture.
Fig. 3. Aluminum plates placed in stone mixture. A, Maxillary denture; B, mandibular den-
ture.
Fig. 4. Top portion of stone molds removed and metal plates exposed. A, Maxillary denture.
B, Mandibular denture.
Fig. 5. Lingual stone portions loosened towards groove by plaster knife. A, Maxillary denture;
B, mandibular denture.
Fig. 6. Upper (A) and lower (B) halves of stone portions removed.
Flasking edges of the anterior teeth and the tips of the cusps
of the posterior teeth.
1. Check the height of the denture teeth in the flask 6. Lubricate the metal plates with petroleum jelly to
so that approximately 4 to 6 mm of space is avail- facilitate their removal and place them into a verti-
able between the teeth and the top of the flask. cal position at midline, while the artificial stone is
2. Fix the trial denture in the bottom half of the flask still soft (Fig. 3). Ensure that the posterior edge of
with artificial stone. the metal plates is in contact with the inner surface
3. Paint all of the stone surface in the lower half of of the flask. This will facilitate removal of the metal
the flask with a separating medium. plates and prying of the lingual and palatal artificial
4. With the upper half in the flask in position, check stone.
the height of the metal plates. Position the plate 7. Paint the stone surface with a separating medium
vertically in the palatal or lingual space of the trial and then pour the stone onto the surface filling the
dentures at midline (Fig. 2). The upper edge of the flask. Place the lid of the flask in position.
metal plate should be approximately 2 mm above 8. Allow the stone to set, eliminate the wax, and iso-
the occlusal surfaces of the posterior teeth and late the stone.
incisal edges of the anterior teeth, and 2 mm below 9. Fill the mold space with the resin denture base
the top of the flask. material and process the denture in the conven-
5. Pour a thin mix of artificial stone up to the incisal tional manner.
Fig. 7. Upper (A) and lower (B) stone portions removed completely from lingual surfaces of
dentures.
Fig. 8. Processed maxillary (A) and mandibular (B) dentures after complete deflasking.
Deflasking SUMMARY
1. Remove all parts of the flask from the stone mold This procedure is easy and helps to facilitate the
that contains the processed denture. Do not sepa- removal of the palatal and lingual portions of flasking
rate the top part from the bottom of the mold. stone. Thus, it reduces the hazards of denture base
2. Pry away the top portion, the last pour of stone fracture or deformation during deflasking of the
from the mold, with a plaster knife (Fig. 4), and processed denture. An additional advantage of this pro-
remove the metal plates from the stone. (This will cedure is that it reduces both the flasking and deflask-
leave a groove in the stone.) ing time.
3. With the plaster knife, cut the stone adjacent to the
lingual surface of the maxillary tuberosity and REFERENCES
retromolar pad, then pry the stone sections toward
1. Hickey JC, Zarb GA, Bolender CL. Prosthodontic treatment for edentulous
the groove and remove them (Figs. 5 through 7).
patients. 9th ed. St Louis: CV Mosby; 1985. p. 458-73.
4. Separate the other parts of the stone from the buc- 2. Craig RG, Restorative dental materials. 8th ed. St Louis: CV Mosby; 1989.
cal and labial surfaces of the denture (Fig. 8). p. 509-59.
3. Phillips RW. Science of dental materials. 9th ed. Philadelphia: WB Saun- Copyright © 1998 by The Editorial Council of The Journal of Prosthetic
ders; 1991. p. 177-213. Dentistry.
4. Javid NS, Boucher CO. Flasking for easy deflasking. J Prosthet Dent 0022-3913/98/$5.00 + 0. 10/1/91643
1973;29:581-5.
5. Morrow RM, Rudd KD, Eissman HF. Dental laboratory procedures: com-
plete dentures. Vol. 1. St Louis: CV Mosby; 1980. p. 284-304.
6. Rahn AO, Heartwell CM Jr. Textbook of complete dentures. 5th ed.
Philadelphia: Lea and Febiger; 1993. p. 373-86.
Purpose. Endosseous implants to support prostheses in the treatment of partially edentulous jaws
was developed from the successful application of implant support for prostheses in completely
edentulous jaws. However, it is recognized that the partial edentulous condition is distinctly dif-
ferent from the complete edentulous condition. Microbiologic environment, occlusion, ridge
contour, and mechanical factors differ in these 2 edentulous states. This article documented treat-
ment outcomes when implants were used to support prostheses in partially edentulous jaws.
Material and methods. The first 88 patients with a total of 97 partially edentulous spans treat-
ed at the University of Toronto Implant Prosthodontic Unit were documented. Inclusion and
exclusion criteria were described. Changes in proposed treatment, due to the use of implants for
orthodontic treatment, the loss of implants, or the decision to treat with implant-supported
removable prostheses, resulted in the removal of 11 patients (13 edentulous areas) from the study.
The demographic data of the remaining 77 patients is described. All the 230 Brånemark implants
(Nobel Biocare AB) were placed and surgically uncovered as a 2-stage procedure. Implants were
categorized as anterior (zone 1) or posterior (zone 2) relative to the position of the premolar
teeth. All prostheses were fabricated by staff (n = 39) or supervised residents (n = 58). Success
criteria follow literature standards.
Results. A total of 15 patients experienced complications between stage 1 and stage 2 surgery
with 11 implant dehiscences, 1 persistent mucosal inflammation, 1 altered nerve sensation, and 2
implant losses. After prosthesis placement, 15 documented cases of mucosal inflammation were
noted for 9 prostheses, 9 prostheses had abutment screw complications (10 abutment screw frac-
tures in 4 prostheses and 10 abutment screws loosened in 7 prostheses), and 15 prostheses expe-
rienced prosthesis screw loosening. Prosthetic complications occurred in 25 prostheses with 23
incidents of acrylic resin fracture and 2 prostheses that were remade as a result of inadequate fit.
Prosthesis replacement occurred 21 times, in 6 of these situations the replacement was due to
implant failure and the remaining prostheses were replaced to improve esthetics after the intro-
duction of new prosthetic components. Of the 230 implants that were placed, 14 were lost. Of
the 14 lost, 11 of these were replaced, 3 were put to sleep, and 3 were used to support remov-
able prostheses. The Kaplan-Meier cumulative implant survival rate was 92.5% with a mean sur-
vival time of 11.34 years.
Discussion. Complications in implant-supported fixed prostheses seem to cluster in a small num-
ber of prostheses rather than being evenly distributed throughout all prostheses. Implant loss
occurred before prosthesis insertion 50% of the time. Implant failure rate was not correlated with
anatomic location. Implant survival in this study was comparable to survival rates described in
other studies. 24 References. —SE ECKERT