Elsevier

Dental Materials

Volume 26, Issue 10, October 2010, Pages 993-1000
Dental Materials

Review
Clinical performance of cervical restorations—A meta-analysis

https://doi.org/10.1016/j.dental.2010.06.003Get rights and content

Abstract

Objectives

To carry out a meta-analysis in order to assess the influencing factors on retention loss and marginal discoloration of cervical restorations made of composites and glass ionomer (derivates).

Methods

The literature was searched for prospective clinical studies on cervical restorations with an observation period of at least 18 months.

Results

Fifty clinical studies involving 40 adhesive systems matched the inclusion criteria. On average, 10% of the cervical fillings were lost and 24% exhibited marginal discoloration after 3 years. The variability ranged from 0% to 50% for retention loss and from 0% to 74% for marginal discoloration. Hardly any secondary caries was detected. When linear mixed models with a study and experiment effect were used, the analysis revealed that the adhesive/restorative class had the most significant influence, with 2-step self-etching adhesive systems performing best and 1-step self-etching adhesive systems performing worst; 3-step etch-and-rinse systems, glass ionomers/resin-modified glass ionomers, 2-step etch-and-rinse systems and polyacid-modified resin composites were ranked in between. Restorations placed in teeth whose dentin/enamel had been prepared/roughened showed a statistically significant higher retention rate than those placed in teeth with unprepared dentin (p < 0.05). Beveling of the enamel and the type of isolation used (rubberdam/cotton rolls) had no significant influence.

Significance

The clinical performance of cervical restorations is significantly influenced by the type of adhesive system used and/or the adhesive class to which the system belonged and whether the dentin/enamel is prepared or not. 2-Step self-etching- and 3-step etch&rinse systems shall be chosen over 1-step self-etching systems and glass ionomer derivates. The dentin (and enamel) surface shall be roughened before placement of the restoration.

Introduction

About a quarter of the population do have non-carious cervical lesions, and the lesions are significantly more prevalent at older ages (<50%), with premolars being the most affected teeth [1]. There is consensus that the etiology is multifactorial with mechanical-abrasive (toothbrush/toothpaste) and erosive (acids from food and beverages) processes. Occlusal overloading and/or eccentric movements may be found as co-factors because of some confounding effects, but are unlikely causal factors [2]. There is no biological reason to restore non-carious lesions other than esthetics. Under some circumstances, when the lesion has significantly compromised tooth structure or is progressing at a fast rate, can restoring the lesion prevent further tooth damage. A questionnaire conducted among US general practitioners in the 90s revealed that more than half of the dentists interviewed did not restore non-carious cervical lesions [3].

Loss of retention and marginal discoloration are still the main shortcomings of cervical restorations (Class V) placed with adhesive technology [1], [4]. Both clinical incidents compromise the esthetic appearance, especially if they occur in anterior teeth. The prevalence of retention loss rises sharply with increasing observation periods [5]. On the other hand, Class V non-carious non-retentive lesions are frequently used to clinically evaluate the effectiveness of adhesive systems.

In non-carious cervical lesions, restoratives are placed with either preparation of dentin and/or enamel. In contrast to intact or caries-affected dentin, non-carious cervical lesions exhibit a high degree of sclerosis and have a high amount of minerals, which renders the establishment of a hybrid layer more difficult [6]. Some clinicians roughen the dentin and enamel with a diamond bur and/or bevel the enamel margin to improve the bond to the hard tissues. The results of some clinical studies on the topic of preparation are inconclusive [7]. The influence of absolute versus relative isolation of the treatment field is another topic that is subject to controversy. A meta-analysis revealed no influence of the type of isolation on the survival rate in posterior composite restorations [8]. A systematic analysis of clinical studies on cervical restorations has, to date, not been carried to investigate these operative aspects.

The type of adhesive system and/or the belonging to a specific class of adhesives as proposed by Van Meerbeek [6] may play an important role on the longevity of the restoration. A review of clinical trials on the effectiveness of adhesive systems in non-carious cervical lesions measured as retention loss arrived at the conclusion that glass ionomer cements had the lowest rate of retention loss and 1-step self-etching adhesives the highest [4].

The American Dental Association (ADA) previously defined an adhesive system to be adequate and acceptable for clinical use (“full acceptance”) if the retention rate of restorations placed in non-carious lesions is higher than 90% after an observation period of 1.5 years [9]. Many of the newer adhesive systems, especially the 1-step self-etching systems, would not have received ADA acceptance. The ADA acceptance program was abandoned by the end of 2008 [10].

The goal of the present study was to assess the influence of the following factors on the clinical outcome:

  • -

    operative technique: beveling of enamel, preparation/roughening of dentin/enamel, absolute versus relative isolation;

  • -

    the type of adhesive system and/or restorative material;

  • -

    observation period.

The following hypotheses were examined:

  • 1.

    Beveling of enamel and/or preparation/roughening of dentin/enamel results in less retention loss and marginal discoloration.

  • 2.

    The type of isolation does not influence the clinical outcome.

  • 3.

    The type of adhesive system or restorative material has an influence on the performance of cervical restorations.

Section snippets

Selection of clinical trials on Class V restorations

Prospective clinical studies on Class V restorations were searched in MEDLINE (search period 12/2008) and IADR abstracts (1994–2008). The search words were “Class V” or “cervical” or “abfraction lesion” and “clinical”. The inclusion criteria were as follows:

  • 1.

    Prospective clinical trial involving at least one adhesive system in Class V cavities.

  • 2.

    Minimal duration of 18 months.

  • 3.

    The study had to report about the following outcome variables: retention, marginal discoloration, marginal integrity,

Results

Clinical data from 50 studies have been included in the systematic review (see Appendix A) containing 105 in vivo experiments with 40 different adhesives, 39 different composites, and 63 different combinations adhesives/composites. The type of adhesive and composite/restorative material is listed in the table of the Appendix A. The clinical index could be calculated for 67 experiments at 12 months, 25 at 18 months, 76 at 24 months and 35 at 36 months. Overall, only 14/203 = 7% of the values were

Discussion

The rationale for creating a clinical index is that a better statistical analysis can be carried out. The same index has been used in another study when in vitro and in vivo data on adhesive systems had been compared [11]. The weighing of the three outcome variables was based on the following considerations: (1) Retention loss is the most obvious sign of failure of a cervical restoration and is the most reliable diagnostic evaluation criterion with little variability between different

References (20)

There are more references available in the full text version of this article.

Cited by (129)

View all citing articles on Scopus
View full text