Introduction

There seems to be emerging evidence in recent years that pathological tooth wear is an increasing problem, particularly in young adults. The Children's Dental Health Survey UK (2003)1 noted increased prevalence of localised anterior tooth wear affecting 33% of 15-year-olds. This showed a six percentage point increase in the proportion of affected young adults compared to the previous decade. This increase in prevalence is true for individuals of all socioeconomic backgrounds.

The aetiology and clinical appearance of tooth wear is frequently documented with the terms 'erosion', 'abrasion', 'attrition' and more recently 'abfraction'. However, in reality, the multifactorial nature of tooth wear means that these conditions usually occur in combination.2,3 In a large number of patients, the rate of tooth wear is slow. As tooth wear progresses with the reduction in the clinical crown height, the occlusal vertical dimension is frequently maintained by compensatory effects that attempt to maintain functional occlusal contacts. Dento-alveolar compensation occurs through continued tooth eruption, alveolar bone growth and apical cementum deposition, thus reducing the interocclusal space available for restoration.4 This phenomenon is common in patients with localised anterior tooth wear and restoration of these teeth becomes a challenge.

One of the options for creating interocclusal space is through relative axial tooth movement. In 1975, Dahl et al.5 described the use of a removable cobalt-chromium partial bite-raising appliance to create interocclusal space in a patient with localised maxillary anterior tooth wear. It proved to be effective by a combination of orthodontic intrusion of teeth contacting the appliance and continued eruption of those held out of contact.6 The authors reported a 100% success rate in achieving the desired interocclusal space in the subsequent 20 cases treated. The technique offered the obvious advantage in reducing the need to remove tooth tissue in order to accommodate any planned restorations. Several studies in the literature since have reported success in achieving the desired relative axial tooth movement using the Dahl principle, ranging from 93% to 100% of all cases.7,8,9,10,11

The science and technology of composite dental restorative materials have advanced considerably over the years. Although composites have not evolved to the point of being an ideal restorative material, they have become a viable option to manage localised anterior tooth wear. The successful use of composite resin restorations placed at an increased occlusal vertical dimension as 'Dahl' type appliances has been demonstrated over the short-term.7,8,9,10,11,12 This simple technique offers better patient compliance compared to the traditional removable Dahl appliance, ease of maintenance, conservation of tooth tissue and immediate improvement in aesthetics. The minimally invasive and conservative nature of the treatment regime offers an obvious advantage when restoring the already compromised worn anterior teeth. The aim of this study was therefore to evaluate the long term (ten years) survival and clinical performance of resin-based composite 'Dahl' type restorations provided at an increased occlusal vertical dimension (OVD) used to manage localised anterior tooth wear.

Method

Sample

The study was granted with a favourable ethical opinion by the NHS National Research Ethics Service, Charing Cross Research Ethics Committee. The sample involved a group of 26 patients, 18 males and 8 females, treated for localised anterior tooth wear with composite resin 'Dahl' restorations placed at an increased occlusal vertical dimension. The oldest patient was 80 years old and the youngest was 28 years old. These patients were treated between April 1994 and April 1999 at the Eastman Dental Hospital. All patients included in the study had the initial treatment provided at least ten years before the point of recall for this study. In the past, these patients were reviewed every six months for the first two years following the initial treatment, followed by a five-year review. Informed consent was obtained from all the patients enrolled in the study.

A total of 283 restorations were reviewed in the 26 patients after a ten year follow-up period. This included restorations that were initially placed and any subsequent replacement over the ten-year period. All the restorations that were replaced were considered as new restorations. The restorations that were subsequently replaced with crowns were classified as failed restorations. The composite resin restorations provided at the initial treatment were placed as either direct restorations, indirect restorations, or a combination of these. For teeth that were restored with a combination of direct and indirect restorations, the restorations were considered as single restorations.

A total of 186 teeth were restored, 78.5% being in the maxilla and 21.5% in the mandible. Out of all the 283 restorations reviewed, 77 were on the canines, 87 on lateral incisors and 119 on central incisors.

Around 75% of the restorations were placed by consultants and the remaining 25% were placed by senior clinical staff and postgraduate students.

Collection of data

The collection of data involved a full history and clinical examination; reference to clinical records; assessment of restorations using modified United States Public Health Services (USPHS) criteria; radiographic analysis; and statistical analysis following database creation of the clinical findings.

Clinical records

Access to past dental records enabled confirmation of all details pertinent to the aetiology and the initial placement of the restorations. Similarly, the clinical records of all restorations that were repaired or replaced could be noted on the data collection pro-forma. The clinical records, including some previous intra-oral photographs and study casts, served to rectify any discrepancies that became evident during data collection.

Recall examination

At recall, a history and clinical examination was carried out where data were collected. This involved recording of the following information:

  • Patient details (name, hospital number, date of birth, gender)

  • Treatment details (treatment date, operator, and aetiology of tooth wear)

  • Restoration details (material used, opposing dentition, and occlusal relationship)

  • Restoration assessment (USPHS criteria scores)

  • Restoration failure details (history and date of repair or replacement, tooth involved, and cause of failure)

  • Patient satisfaction (based on existing restorations and willingness to have the same treatment again).

Intra-oral digital clinical photographs and study casts were obtained and compared to the patient's previous clinical photographs and study casts.

Radiographic examination was undertaken where clinically indicated and in the best interest of the patient. All patients had a radiographic assessment as part of their initial treatment management. These radiographs were part of their clinical records and allowed comparison and analysis with any radiographs taken at recall.

Restoration assessment

Restorations were clinically assessed by direct evaluation using the modified United States Public Health Service (USPHS) criteria13,14,15 and allocated a score of 1, 2 or 3 as shown in Table 1. Calibration of a single assessor revealed an unweighted inter-examiner kappa score of 0.779, indicating substantial agreement, and an intra-examiner score of 0.886, indicative of almost perfect agreement.16

Table 1 Clinical assessment criteria used to assess the restorations

Patient satisfaction

Patient satisfaction was assessed at two levels: the aesthetic satisfaction of the surviving restorations, and the overall experience of the initial treatment.

Patients were asked to comment on the aesthetics of the surviving restorations as a whole. The response was graded according to the following:

  1. 1

    Patient has no complaints and is pleased with the aesthetics

  2. 2

    Patient has some reservations but accepts the aesthetics

  3. 3

    Patient is unhappy about the aesthetics and requests intervention.

Finally, the response to the willingness of having the initial treatment again, if appropriate, was graded as follows:

  1. 1

    Yes; very happy with the initial treatment

  2. 2

    Maybe; not sure if would like the treatment again

  3. 3

    No; unhappy with the initial treatment.

Survival analysis

The data collated was entered on a spreadsheet run by the software Statistical Programme for Social Sciences (SPSS.14) and STATA Version 10. The objective of the analysis was to assess the survival function of the restorations and to ascertain what clinical factors may exert a significant effect on the survival of restorations placed using this treatment regime. The variables included in the analysis were:

  1. 1

    Patient gender

  2. 2

    Operator

  3. 3

    Aetiology of tooth wear (Table 2)

  4. 4

    Material (Table 3)

  5. 5

    Nature of opposing dentition (Table 4)

  6. 6

    Incisal relationship (Table 5).

The baseline date was taken as the date of restoration placement. Survival of a restoration was defined as the interval between the date of placement and the date of failure. A restoration that was replaced was re-entered as a new restoration. Those restorations that did not fail at the end of the period of study were considered to be surviving and included in the statistical analysis.

Survival analysis was carried out at two different levels of failure:

  1. 1

    Major failure: defined as any restorations that required complete replacement and included any recall restoration that had a USPHS score of 3

  2. 2

    Combined major and minor failure: included all restorations in the major failure group, all those that had required repair or refinishing for any reason, and those that were placed in the USPHS score of 2 for any of the assessment criteria. Exception to this was when restorations were surviving and the only USPHS score of 2 was related to wear, the rest of the assessment criteria scoring a USPHS score of 1. As wear of the restorations was an almost universal finding, there remained a risk of giving an inaccurate impression of overall performance. This methodology was consistent with the previous study by Redman et al.11

Survival analysis was performed on each variable initially using the Kaplan-Meier approach to assess the effect of that variable on survival. Log rank tests were performed addressing the null hypothesis that there are no differences in the overall survival times in the categories of the variable of interest. If the log rank test gave p <0.05, it was concluded that the categories of that variable differed significantly in their effect on the survival of the restorations. Where p <0.05 and the variable had more than two categories, each pair of categories was compared by the log rank test to establish where the differences lay and to assist in calculating baseline hazards for the subsequent Cox proportional hazards model. This Cox proportional hazards regression analysis was used to evaluate the independent effects of the different variables included in the model on the survival of the restorations.

Results

Re-establishment of posterior occlusion

All the patients were reviewed earlier by Redman et al.11 who noted re-establishment of posterior tooth contact in all the patients, ranging from just under 2 months to 18 months, with a mean of 7 months.

Of the 26 patients reviewed for this study, 21 patients (81%) carried on to exhibit complete re-establishment of posterior occlusion with Shimstock foil holding firmly between all pairs of posterior teeth. The remaining five patients (19%) exhibited occlusal contacts between most but not all the pairs of posterior teeth. Invariably, this lack of occlusal contact occurred in the first molar and premolar region.

Failure of restorations

More than 50% of the restorations had major failures. These included the ones that had been subsequently replaced by new restorations and any restorations that were surviving but had failed and required replacements. Around 7% of the restorations surviving were successful and exhibited no failure modes.

The majority of the minor failures that had an intervention involving repair in the past were due to minor fracture of the restorations, most notably along the incisal edges. Other reasons included staining and marginal discolouration, and recementation of indirect restorations.

When considering all the failures, combining major and minor failures, the majority of the restorations failed as a result of wear (45.5%), marginal discolouration (28.9%) and fracture (21.6%) (Table 6).

Table 2 Distribution of tooth wear aetiology
Table 3 Restorative material distribution among sample
Table 4 Nature of opposing dentition
Table 5 Number of restorations placed in different incisal relations
Table 6 Restoration failure modes – major and minor failures

Survival analysis

The median survival time (MST) for all the restorations was 7.0 years when considering major failure modes only (Fig. 1). This means that considering the group as a whole, there was a 50% probability that a composite restoration placed using this treatment regime would survive 7.0 years. However, when considering the survival of restorations placed as replacements, the MST for these restorations was 4 years and 9 months (Fig. 2). At combined major and minor failure levels the MST was 5 years and 9 months (Fig. 3).

Figure 1
figure 1

Kaplan-Meier survival plot for major failures in all restorations (95% confidence interval)

Figure 2
figure 2

Kaplan-Meier survival plot for major failures in restorations that were replaced

Figure 3
figure 3

Kaplan-Meier survival plot for combined major and minor failures in all restorations (95% confidence interval)

Further statistical analysis involving log rank tests and Cox proportional hazards model revealed incisal relation, aetiology, and nature of opposing dentition as significant variables affecting survival rates when considering major failures (Table 7). The incisal relation Class I, the aetiological factor of abrasion, and the opposing porcelain surface significantly reduced the survival rates of the composite restorations. However, at combined major and minor failure level, only the aetiological factor of abrasion and indirect placement of composite material were significantly associated with reduced survival.

Table 7 Significant clinical variables affecting survival outcome (p <0.05)

Biological complications

Of the 26 patients, one patient had received root fillings on two of the teeth three years after the initial restorations were placed as a result of irreversible pulpitis. Another patient had three restorations replaced due to secondary caries. Although these complications may be related to the composite treatment provided, the precise causes remain uncertain as this was not objectively analysed during the period of the study, and the findings were purely incidental at the point of recall.

Biological complications that were unlikely to be due to the composite treatment included a patient who had a single root filling that was completed before the initiation of the treatment due to previous trauma. Another case presented with generalised adult chronic periodontal disease, with the anterior teeth exhibiting radiographic signs of moderate bone loss and clinical mobility of grade II. A third patient had two restorations replaced by post crowns, both presenting with apical radiolucency and clinical signs of chronic apical periodontitis. Apart from these findings, no other pathology was observed.

Patient satisfaction

In four of the patients reviewed, a total of 23 restored teeth were subsequently replaced by cast restorations. Of the remaining 22 patients, eight had no complaints and were still pleased with the results (Figs 4,5,6,7). Around ten patients had some reservations (Figs 8 and 9), and only four were unhappy and requested intervention (Figs 10 and 11). All these patients were very satisfied with the initial treatment they had received and expressed willingness to have the same treatment again when necessary.

Figure 4: PATIENT A.
figure 4

Anterior view of teeth at initial presentation in May 1994

Figure 5: PATIENT A.
figure 5

Occlusal view of anterior teeth at initial presentation in May 1994

Figure 6: PATIENT A.
figure 6

Restorations in October 2008, patient expressed high satisfaction

Figure 7: PATIENT A.
figure 7

Occlusal view of the restorations in October 2008, then in service and successful

Figure 8: PATIENT B.
figure 8

Postoperative view of restorations in November 1994

Figure 9: PATIENT B.
figure 9

Restorations in September 2008. Patient expressed some reservations with regards to marginal staining

Figure 10: PATIENT C.
figure 10

Restorations after placement in August 1997

Figure 11: PATIENT C.
figure 11

Major failure of restorations as noted in March 2008. Patient expressed dissatisfaction and requested intervention

Discussion

This study shows that the use of composite resin restorations has proved to be a viable medium-term option to treat localised anterior tooth wear at an increased OVD. The desired tooth movements occur in a manner and timescale similar to that of other Dahl appliances. However, more than 90% of the restorations exhibited minor or major failure over the preceding ten years and required intervention and maintenance. The restorations commonly failed due to wear, marginal discolouration and fracture, frequently occurring in combination. The failure modes expose the limited mechanical and physical properties of composite resin used in this way.

The MST of 5 years and 9 months is comparable to the previous study by Redman et al.11 who noted a MST of 4 years and 9 months over a six-year period when all types of failure were considered. Interestingly, the restorations placed as replacements exhibited a reduced survival rate when considering major failures. The replacement of restorations in these compromised teeth will often involve bonding to dentine. The limitations of bonding composite resin to dentine despite the use of dentine bonding agents are well documented.17,18

At both levels of failure, major and combined major and minor, patients with abrasion as the primary aetiological factor had restorations with significantly poorer survival outcome when compared to erosion, attrition, or combined aetiology. However, only two patients had abrasion diagnosed as a primary aetiological factor and had a habit of chewing pencils. These two patients constituted a small proportion of the sample and the results need to be interpreted with caution. Both the patients were continuing their habits when reviewed.

The statistical analysis suggest that for major failures requiring replacement of the restorations, there was no significant difference between direct, indirect, or for the technique utilising the combination of the materials. These findings are similar to those found by Wassell et al.19,20 and Van Dijken21 where no significant differences in longevity were noted between directly and indirectly fabricated composite Class II restorations. There seems to be a significantly greater degree of minor failures with indirect restorations compared to direct or combined restorations. However, frequency analysis of the common failure modes of wear, fracture and marginal discolouration did not reveal significant predilection for indirect composites. The results may be explained by the fact that fewer indirect composites were placed compared to direct composites. As severity of wear and the number of teeth affected increased, the decision to treat with indirect restorations was more likely. The disproportionate sample in this category again may explain why failure events for indirect composites appear to be significant.

The different structure and physical properties of tooth substance and dental restorative material in dynamic occlusion eventually results in their differential wear. There is no current restorative material that is able to satisfy the requirements of an ideal restorative material from this respect. The results suggest that at a major failure level, composite restorations performed significantly worse when opposed by porcelain. There was no significant difference in the longevity of the restorations when opposed by similar composite resin materials or natural teeth. However, only five restorations were opposed by porcelain which may bias this finding. Nevertheless, several studies have shown the marked abrasive nature of porcelain compared to other restorative materials such as gold alloy and composite resin.22,23 In contrast to porcelain, Willems et al.24 have demonstrated modern composite resin restorations to have similar wear rates to human enamel, supporting its use in the management of tooth wear.

The nature of the incisal relationships has been suggested to affect the survival outcome of composite resin restorations placed using this treatment regime. Redman et al.11 noted the Class II Division 2 group to have significantly reduced survival outcome at both major and combined failures levels. The possibly unfavourable and higher shear and tensile forces placed on the restorative material associated with Class II Division 2 and Class III occlusions may result in higher failure rates. However, the analysis of results from this study suggest otherwise. At the major failures level, there was a statistically significant difference between Class III and both Class I and Class II Division 2. The restorations in Class III groups had significantly better survival outcome than Class I or Class II Division 2 groups. The samples within these groups were uniformly proportionate. It was therefore surprising to see that patients with a Class I occlusion appeared to have a relatively poor performance with composite restorations used in this study. The amount of parafunction may be more important than the incisal relationship but this was not measured. Some patients may have initially presented with a pseudo-Class III occlusion and restored to a Class I. The progressive wear of the restorations may then resume a pseudo-Class III occlusion again. The incisal relationship was not a significant factor when considering all failures, both major and minor.

The biological complications associated with this treatment regime were very low. Only 2% of all the restorations that had major failures were replaced as a result of secondary caries. Only one patient had two teeth develop symptoms of irreversible pulpitis three years after the initial placement of the restorations. In reality, it is impossible to assess accurately the pulpal condition of the tooth which has been compromised by tooth wear. The condition will depend on the cumulative effects of pathological and iatrogenic insults imposed on the tooth with time.25 It may therefore be possible that the pulp, or some part of the pulp, already showed signs of irreversible pulpitis but these were not manifested clinically at the time of initial placements. This compares favourably to conventional crowns where endodontic complications develop in 19% of the restored teeth.26

The patient satisfaction remained high despite long-term failures and maintenance involved. Only four patients were unhappy about the aesthetic results at this stage of recall. These patients presented with restorations that had major failures, and invariably required intervention. All the patients when questioned stated that they were happy with the initial treatment. Comments were made about the simplicity of the procedure, tolerance of the procedure, immediate improvement in symptoms and aesthetics, and ease of maintenance. The technique takes time but is conservative of tooth structure and avoids or delays the need for conventional preparation.

It was interesting to find that five of out of the 26 patients reviewed presented with only partial stability of posterior occlusion after a ten year follow-up period. None of these patients were aware of their partial stability or reported any concerns. Further studies may consider the factors that can be used to predict the eruptive potential of the dentition and the long-term consequences of a partially established posterior occlusion.

Conclusion

Repeated use of composite resin restorations placed at an increased occlusal vertical dimension as a 'Dahl' type appliance to manage localised anterior tooth wear is a viable treatment option in the short- to medium-term. The restorations are susceptible to failures and require a degree of maintenance. However, the biological complications associated with this treatment regime are rare and patient satisfaction remains high.