The Endocrown: A Different Type of All-Ceramic Reconstruction for Molars

Authors
Michel Fages
Suffix
DDS, PhD
Authors
Bertrand Bennasar
Suffix
DDS
Cite this as: J Can Dent Assoc ;79:d140
Topics
endodontics
restorations
treatment
 

Abstract

The endocrown is indicated for the endodontic restoration of severely damaged molars. This monolithic, ceramic adhesive restoration requires specific preparation techniques to satisfy criteria that are primarily biomechanical in nature: a cervical margin in the form of a butt joint and a preparation of the pulp chamber that does not extend into the root canals. The remaining tooth substance is thus more robust, resulting in increased longevity. This simple and efficient concept is compatible with the philosophy of biointegrated prostheses. This type of reconstruction, which is still uncommon, should be more widely known and used.

For many practitioners, the use of complete glass ceramic crown restorations for severely damaged and endodontically treated molars remains problematic.1 Proposed in 1999 by Bindl and Mörmann2 as an alternative to the full post-and-core supported crown, the “endocrown” is a one-piece ceramic construction, based on concepts developed by Pissis.3In 2008, Lander and Dietschi4 presented a clinical report on endocrowns, and, in 2009, Magne and Knezevic,5 who were concerned about the choice of reconstruction materials, considered ceramics versus composites for endocrown molar restorations. Various studies suggested extending the concept to maxillary premolars6 and maxillary incisors,7 but these proposals remain controversial.

The main objective is to dispense with metal and achieve an all-ceramic bonded reconstruction that is minimally invasive of root canals, as the use of root canals for anchoring has been cited as an important factor in weakening the tooth.8-11 Thus, the preparation for endocrowns is different from that for conventional complete crowns.12,13

The endocrown is described as a monolithic (one-piece) ceramic bonded construction14-18 characterized by a supra-cervical19 butt joint, retaining maximum enamel to improve adhesion. The endocrown invades the pulpal chamber, but not the root canals. It is milled using computer-aided techniques16,18 or by molding ceramic materials under pressure20,21 (Fig. 1a and b). New generations of ceramics and adhesives may lead to a view of this therapeutic device as an alternative to conventional crown-root anchored restorations.22,23 The specific preparation and bonding result in a particularly favourable reconstruction in terms of biomechanics.5,24,25

NOTE: Click to enlarge images.

Figure 1: An endocrown machined using computer-aided design and computer-aided manufacture (a). A pressed endocrown, with sprue attached, positioned on a master mold (b).

 

The purpose of this paper is to describe the preparation and insertion of endocrowns as well as the materials used to achieve a reliable and durable result.

Methods

Occlusal Preparation

The goal in preparation is to achieve an overall reduction in the height of the occlusal surface of at least 2 mm in the axial direction. This reduction can be achieved by drilling 2-mm-deep grooves as guides (Fig. 2), then using a green diamond wheel bur to reduce the occlusal surface.

The bur is oriented along the major axis of the tooth and held parallel to the occlusal plane (Fig. 3). Its shape allows control of the orientation of the reduction and ensures a flat surface, which determines the position of the cervical margin or “cervical sidewalk.” The cervical margin should be supragingival; however, if clinical factors or esthetics require, the margin can follow the gingival margin. Differences in level between the various parts of the cervical margin must be linked by a slope of no more than 60° to avoid a staircase effect. Enamel walls less than 2 mm thick should be removed.

Figure 2: Making the guide grooves in an isolated tooth and in situ.

 

Figure 3: Preparation of the cervical margin or “cervical sidewalk” using a wheel bur held parallel to the occlusal plane.

 

Axial Preparation

This step primarily involves eliminating undercuts in the access cavity. A cylindrical-conical green diamond bur with a total occlusal convergence of 7° is used to make the coronal pulp chamber and endodontic access cavity continuous (Fig. 4). With the bur orientated along the long axis of the tooth, the preparation is carried out without excessive pressure and without touching the pulpal floor. Removing too much tissue from the pulp chamber walls will reduce their thickness and the width strip of enamel. The depth of the cavity should be at least 3 mm.

Figure 4: Axial preparation using a cylindro-conical drill to make the coronal pulp chamber continuous with the access cavity.

 

Polishing the Cervical Band

The bur used in this step has the same taper as the one used in axial preparation, but a larger diameter and a finer particle size. It should be guided around the entire surface of the cervical band to remove micro-irregularities and produce a flat, polished surface (Fig. 5). The margin line should appear as a regular line with a sharp edge (Fig. 6a and b).

Figure 5: Polishing the cervical band.

 

Figure 6: Cervical margin before (a) and after (b) polishing.

 

Preparation of the Cavity Floor

The entrance to the pulpal canal is opened. Gutta percha is removed to a depth not exceeding 2 mm to take advantage of the saddle-like anatomy of the cavity floor. This should be done with a nonabrasive instrument to maintain the integrity of the canals entrance. No drilling of dentin is carried out.

Cleaning the Pulp Chamber

Ultrasound is recommended to clean the pulp chamber and its floor thoroughly. Abrasion is not indicated.

Bonding

Adhesives such as self-adhesive RelyX Unicem (3M, St. Paul, Minn.) or composites such as Multilink (Ivoclar, Schaan, Liechtenstein) are used for bonding the endocrown to the prepared tooth (Fig. 7).

Figure 7: Prepared tooth (a), endocrown (b) and final result after bonding (c).

 

Discussion

Longevity and Effectiveness

In an evaluation of adhesively placed endocrowns after 2 years, Bindl and Mörmann2 concluded that “the overall clinical quality of the endocrowns was very good.” In another 2-year evaluation, Bernhart et al.14 concluded that endocrowns “represent a very promising treatment alternative for endodontically treated molars.” In 2012, Biacchi and Basting26compared the fracture strength of 2 types of full ceramic crowns: indirect conventional crowns retained by glass fibre posts and endocrowns. They concluded that endocrowns were more resistant to compressive forces than conventional crowns. More recently, finite element analysis highlighted the role of endocrowns in stress distribution.27

Indications and Contraindications

The endocrown is suitable for all molars, particularly those with clinically low crowns, calcified root canals or very slender roots. The endocrown is contraindicated if adhesion cannot be assured, if the pulpal chamber is less than 3 mm deep or if the cervical margin is less than 2 mm wide for most of its circumference.

Choice of Materials

Glass-ceramic: Glass-ceramic has the advantages of biocompatibility and biomimicry,15 and its wear coefficient is close to that of the natural tooth.16 In addition, the single interface of a 1-piece restoration enhances cohesion.

Bonding Agent: The bonding material constitutes the critical interface between the restoration and the prepared tooth.21 In addition to its adhesive properties, its modulus of elasticity is important as it must be able to absorb pressure, just as the dentin enamel junction (DEJ) does.22 The interface includes all prepared surfaces. Products that must be photopolymerized require the use of a high-power lamp that must be able to reach light-triggered initiators on the pulpal floor, under layers of ceramic that sometimes exceed 7 mm.

Preparation

The butt joint, or cervical sidewalk, is the base of the restoration — with a band of peripheral enamel that optimizes bonding.19 Unlike chamfer or shoulder preparation techniques, crimping is prohibited. The goal is to achieve a wide, even, stable surface that resists the compressive stresses that are most common on molars.8 The prepared surface is parallel to the occlusal plane to ensure stress resistance along the major axis of the tooth.

The pulpal chamber cavity ensures retention and stability. Its shape — trapezoidal in mandibular molars and triangular in maxillary molars — enhances the restoration’s stability.

There is no need for additional preparation. The saddle form of the pulpal floor enhances stability. This anatomy, along with the adhesive qualities of the bonding material, makes it unnecessary to attempt further use of post involving root canals. Actually the root canals do not require any specific shape; therefore they are not weakened by the drilling11 and they will not be subject to the stresses associated with the use of post.8,9 The compressive stresses are reduced, being distributed over the cervical butt joint and the walls of the pulp chamber.

Conclusion

The preparation for endocrowns is rational and simple and can be performed quickly. Root canals are not involved in the process, and the procedure is less traumatic than alternatives. The supragingival position of the cervical margin preserves the marginal periodontium, facilitates impression taking and maintains the solid substance of the remaining tooth. The all-ceramic monolithic-type construction, made by pressure molding or machining, endows the endocrown with mechanical strength. From a biomechanical standpoint, the restoration allows adaptation to strains at the bonded joint. These forces are distributed over the cervical butt joint (compression) and axial walls (shear force), thus moderating the load on the pulpal floor. The endocrown fits perfectly with the concept of biointegration and belongs among the restorative options for posterior endodontically treated and badly damaged molars.

THE AUTHORS

 
 

Dr. Fages is assistant lecturer, department of prosthodontics, dental faculty, University of Montpellier 1, France.
 

Dr. Bennasar is assistant lecturer, department of prosthodontics, dental faculty, University of Montpellier 1, France.

Correspondence to: Dr. Michel Fages, 11 av. Célestin Arnaud, 34110 la Peyrade, France. Email: mifages@wanadoo.fr

The authors have no declared financial interests in any company manufacturing the types of products mentioned in this article.

This article has been peer reviewed.

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Gallery of all Figures in article.