Abstract
The progression of non-carious cervical lesions (NCCLs) leads to gingival recession (GR), which is restored with restorative materials, using different periodontal plastic surgery procedures. There is no consensus on which technique is superior to others. Therefore, the present systematic review aimed to assess the effectiveness of root coverage (RC) procedures in the restored and unrestored NCCLs in terms of clinical and patient-centered outcomes.
We used the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) while searching 5 databases in addition to the gray literature. The Medical Subject Headings (MeSH) terms and keywords in the title and abstract fields, as well as in headings, were used to search the existing literature for the relevant publications on the effectiveness of RC procedures with the restoration of NCCLs over the past 3 decades (January 1990–July 2021). After applying the inclusion and exclusion criteria, 13 articles were read in full and critically analyzed. The quality analysis was performed using the Cochrane RevMan software.
A total of 222 potentially relevant titles and abstracts were found after the initial electronic and manual search, and after removing duplicates. Applying the inclusion and exclusion criteria yielded 23 publications that were further analyzed for relevance and applicability. Following critical analysis, 13 publications were used for validity assessment and data extraction.
In the teeth with NCCLs and GR, the restoration of NCCLs does not affect the percentage RC. However, it significantly decreases dentin hypersensitivity, and the patients’ perception of esthetics and satisfaction.
Keywords: gingival recession, root coverage, non-carious cervical lesions, periodontal plastic surgery, mucogingival surgery
Introduction
Due to the reduction of caries prevalence in worldwide populations, the teeth are functional for more extended periods.1 This may expose the teeth to conditions other than caries, such as non-carious cervical lesions (NCCLs). Non-carious cervical lesions are saucer- or wedge-shaped defects present at the cementoenamel junction (CEJ), characterized by a gradual, slow loss of mineralized dental tissue in the absence of dental caries. The progression of NCCLs causes the loss of CEJ, leading to crown and root involvement.2 Most of the NCCL coronal zone may be formed by the exposed dentin of the anatomical crown, and the apical zone involves the dentin of the anatomical root. Furthermore, the apical shift of the gingival margin with the exposure of the root surface leads to gingival recession (GR).3 Non-carious cervical lesions are restored with various materials, like glass ionomer cement (GIC), resin-modified glass ionomer cement (RMGIC) or composites. These restorations reduce dentinal hypersensitivity, but do not provide root coverage (RC) and improve esthetics.4
The successful treatment of NCCLs associated with GR is based on clinically predictable periodontal plastic surgery procedures with the restoration of NCCLs. Periodontal plastic surgery procedures may comprise the coronally advanced/positioned flap or the connective tissue graft (CTG) over the restored root surfaces. Various studies have shown that GR associated with NCCLs can be successfully treated with a restorative procedure combined with a periodontal plastic surgery procedure to obtain optimal functional and esthetic results. The restoration of NCCLs followed by mucogingival surgery is indicated when cervical abrasion is associated with GR of more than 3 mm.5, 6, 7
The RC of the restored surfaces depends on the extent of NCCL and GR, the amount of interdental bone and soft tissue loss, the type of restoration used, and the periodontal procedure performed.8
Several RC procedures have been demonstrated to correct GR, but there is no consensus on which is superior. Regarding the restorations, various materials have been shown to effectively restore NCCLs, claiming superiority over one another. However, there is no consensus on which treatment is better at correcting this complex lesion of RC associated with GR. Therefore, the present systematic review was undertaken to assess the effectiveness of RC procedures in the restored and unrestored NCCLs in terms of clinical and patient-centered outcomes.
The focused question was: What is the success rate of root coverage procedures in patients with GR associated with NCCLs?
Material and methods
Report and protocol
This review was prepared in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement,9 the Cochrane Collaboration guidelines, and used a review checklist based on the proposed focused question. It was registered with PROSPERO (https://www.crd.york.ac.uk/PROSPERO) under the registration number CRD42021258035.
Inclusion and exclusion criteria
The inclusion criteria for this systematic review were based on the PICOS acronym:
– (P) types of participants: patients suffering from GR defects associated with NCCLs;
– (I) types of interventions: any type of NCCL restoration followed by any RC procedure;
– (C) comparisons between interventions: all possible comparisons among the groups, including the restored and unrestored NCCL with RC procedures;
– (O) type of outcome measures:
- • primary outcome: recession height (RH); keratinized tissue thickness (KTT); and keratinized tissue height (KTH);
- • secondary outcome: probing depth (PD); clinical attachment loss (CAL); plaque index (PI); and gingival index (GI);
– (S) types of studies: only randomized controlled trials (RCTs) with at least 6 months of follow-up and including at least 15 patients in each arm.
The exclusion criteria were as follows: non-randomized controlled trials; defects other than NCCLs; and less than 6 months of follow-up.
Search strategy
An initial search strategy with no restrictions regarding the status or publication language was performed to identify relevant studies published up to and including July 31, 2021, that met the inclusion criteria. The studies selected for the review were RCTs with at least a 6-month follow-up that utilized tooth-colored restorative materials for NCCLs and RC procedures.
The keywords used: ‘non-carious cervical lesions’; ‘cervical abrasion’; ‘cervical restoration’; ‘tooth-colored restorative materials’; ‘root coverage’; ‘gingival recession’; ‘periodontal plastic surgery’; ‘coronally advanced flap’; ‘laterally displaced flap’; ‘denuded root surface’; ‘abfraction’; ‘subepithelial connective tissue graft’; and ‘mucogingival surgery’.
Electronic search
The MEDLINE (via PubMed) search strategy relied on the Cochrane Highly Sensitive Search Strategy for identifying randomized trials in MEDLINE: Sensitivity-maximizing version (2008 revision); PubMed format.10 The following electronic databases were searched: MEDLINE via PubMed; Scopus; the Cochrane Central Register of Controlled Trials (CENTRAL); Embase; and the Web of Science.
Hand-searching and the gray literature
The following leading journals were hand-searched twice by the 2 review authors (KC and LG): “Journal of Periodontology”; “Journal of Clinical Periodontology”; “Journal of Periodontal Research”; “International Journal of Periodontics and Restorative Dentistry’; and “Journal of Indian Society of Periodontology”.
The gray literature was explored using the Conference Proceedings Citation Index (CPCI) within the Web of Science, the System for Information on Grey Literature in Europe (SIGLE) database, and the Scopus Web and Patent results sets. Dissertations and theses were searched using the ProQuest Dissertations & Theses Global (PQDT)™ full-text database. To locate unpublished and ongoing trials related to the review question, the Current Controlled Trials (www.controlled-trials.com) and ClinicalTrials.gov (www.clinicaltrials.gov) trial registries were consulted.
The review authors checked twice the bibliographies of all the RCTs and relevant review articles included.
Each study identified by at least one review author through the various search strategies was involved in the next stage (study selection).
Study selection
The titles and abstracts (when available) of all reports (222 articles) identified through the electronic and manual search were screened independently by the 2 review authors. The full texts were obtained if the studies appeared to meet the inclusion criteria or if there was insufficient data in the title and abstract to make a clear decision. The complete reports obtained from all electronic sources and with other searching methods were assessed independently by the 2 review authors to establish whether or not the studies met the inclusion criteria. The 2 review authors discussed any disagreement to resolve conflicts. Initially, 23 articles were selected after screening, and 10 not meeting the criteria were excluded, with the reasons for exclusion after the full-text analysis recorded.11, 12, 13, 14, 15, 16, 17, 18, 19, 20 Thirteen studies meeting the inclusion criteria were then included, and underwent validity assessment and data extraction. The screening and selection of articles are depicted in Figure 1.
Data extraction
The 2 review authors extracted data from the included studies independently, using the preferred data extraction forms. If necessary, trial authors were contacted for clarification or the missing information. For each trial included in the study, the following data was recorded:
– general information: year of publication; correspondence details; country of origin; and setting (university or clinical);
– methods: study design; and number of centers;
– participants: number of participants and their characteristics (age, gender and systemic health); and criteria for inclusion and exclusion;
– interventions and comparisons: number of intervention groups; types of intervention (restored or unrestored NCCLs); and surgical technique (type of RC procedure used – coronally advanced flap (CAF), CTG, or a combination);
– outcomes: details of the outcomes collected (types – RH, KTT, KTH, PD, CAL, PI, GI, time points, and patient-centered outcomes);
– results: number of participants allocated to each intervention group; dropouts; characteristics of patients in each group (age, gender and systemic health); and results for each outcome considered;
– study funding: information about the possible study funding.
Risk of bias assessment
The assessment of the risk of bias was carried out independently and in duplicate by the 2 review authors as part of the data extraction process, with any disagreement discussed between the same 2 review authors. It was conducted using the recommended approach for assessing the risk of bias in studies (Figure 2) by the Cochrane Collaboration21 and reported using the RevMan software, v. 5 (Copenhagen, Denmark: The Nordic Cochrane Centre, the Cochrane Collaboration).
Randomization
All trials were reported as RCTs, but not all of them reported randomization and allocation in detail.
Allocation
All trials presented an adequate method of allocation concealment except 2 studies.6, 22
Masking
Examiner masking was not practical in most of the studies,6, 7, 23, 24, 25, 26, 28, 29, 30, 31 as it was easy to note whether the restoration was present. The investigators who recruited patients and the examiner were masked to the procedure in the study by Mathias-Santamaria et al.27
Data synthesis and reporting
This systematic review included 13 research articles that were analyzed for quantitative data. The literature analysis revealed that most studies were conducted from 2007 until now. Table 1 demonstrates the baseline characteristics of the RCTs included.
Table 2 reports the outcomes of the studies on which the meta-analysis was performed.
Statistical analysis
Data was extracted and coded using Microsoft Excel (Microsoft Corporation, Redmond, USA). The outcomes of interest were the mean RC, PD, KTH, keratinized tissue width (KTW), and CAL. The effect sizes and weights were calculated for each outcome from each study. The χ2-based test of homogeneity was performed using Cochran’s Q statistic. The I2 statistic (<50%) indicated that there was homogeneity between the studies, hence a fixed effects model was considered. Forest plots were constructed for each outcome.
Table 3 and Figure 3 show the forest plot of the studies included in the meta-analysis. The point estimate is the effect size of PD between the interventions administered to the treatment and control arms. As can be observed from the figure, Isler et al.,6 Santamaria et al.,7, 23, 24 Dursun et al.,26 Lucchesi et al.,28 and Ramireddy et al.29 reported a significant difference in the PD value between the 2 arms in their experiments.
Table 4 and Figure 4 show the forest plot of the studies included in the meta-analysis. The point estimate is the effect size of KTH/KTT between the interventions administered to the treatment and control arms. As can be observed from the figure, Isler et al.,6 Lucchesi et al.,28 Ramireddy et al.,29 and Lemos Reis et al.30 reported a significant difference in the KTH/KTW value between the 2 arms in their experiments.
Table 5 and Figure 5 show the forest plot of the studies included in the meta-analysis. The point estimate is the effect size of relative CAL(rCAL)/CAL between the interventions administered to the treatment and control arms. As shown in the figure, Isler et al.,6 Santamaria et al.7 and Ramireddy et al.29 reported a significant difference in the rCAL/CAL value between the 2 arms in their experiments.
Table 6 and Figure 6 show the forest plot of the studies included in the meta-analysis. The point estimate is the effect size of relative RH (rRH)/relative GR (RGR) between the interventions administered to the treatment and control arms. As seen in the figure, Isler et al.,6 Santamaria et al.7, 23, 24 and Ramireddy et al.29 reported a significant difference in the rRH/RGR value between the 2 arms in their experiments.
Table 7 and Figure 7 show the forest plot of the studies included in the meta-analysis. The point estimate is the effect size of the percentage RC between the interventions administered to the treatment and control arms.
Table 8 tabulates dentin sensitivity (DS) for the evaluation of patient-centered outcomes.
Table 9 and Figure 8 show the effect size for the esthetic scores (ESs) obtained from the studies outlined in the meta-analysis. Changes in the visual analog scale (VAS) score for the esthetic outcome were observed for both treatment groups, and the differences between the effect sizes were used to compare the outcomes between the studies analyzed in the meta-analysis. As shown in Table 9, the summary score calculated showed a statistically significant difference in ES between the 2 groups assessed in each study.
Table 10 and Figure 9 show the effect size for DS from the studies outlined in the meta-analysis. Changes in the VAS score for DS were observed for both treatment groups, and the differences between the effect sizes were used to compare the outcomes between the studies. Table 10 summarizes the score calculated from the studies and shows a statistically significant difference in DS between the 2 groups assessed in each study.
A summary of ESs is recorded in Table 11.
Table 12 and Figure 10 show the risk ratio for DS obtained from the studies outlined in the meta-analysis. Change in the proportion of cases with DS were observed for both treatment groups, and the differences between the risk ratios were used to compare the outcomes between the studies. As seen in Table 12, the summary score calculated for the studies showed a statistically significant difference in DS between the 2 groups assessed in each study.
Results
A total of 222 potentially relevant papers were identified through the search strategy, of which 199 were excluded after screening the titles and abstracts. The full texts of 23 papers were assessed based on the inclusion and exclusion criteria, with 13 articles fulfilling the eligibility criteria and included in the review. The reasons for the exclusion of 10 articles are shown in Figure 1.
Included studies
A total of 428 patients were enrolled in the 13 included articles, 12 studies6, 7, 8, 22, 23, 25, 26, 27, 28, 29, 30, 31 completed the follow-up periods and 1 RCT24 reported dropouts. The characteristics of the studies are shown in Table 1.
Age groups
The age of patients ranged from 19 to 71 years. Four RCTs7, 22, 23, 24 included participants with Miller’s class 1 GR, 3 RCTs8, 25, 29 included Miller’s class 1 and 2 GR, and 5 studies6, 26, 28, 30, 31 did not mention the GR classification. One study by Mathias-Santamaria et al.27 included GR based on a different classification system32 (a single recession type (RT)-132 associated with class B+ or B– NCCL,33 forming a combined defect on a vital canine or premolar).
Follow-up
The maximum follow-up period for 5 RCTs7, 22, 28, 29, 30 was 6 months, 6 RCTs6, 8, 25, 26, 27, 31 followed up for 1 year, and Santamaria et al.23 and Santamaria et al.24 for 2 years.
Study design
Three studies22, 23, 30 had a split-mouth design, while the others used a parallel group design. Eleven RCTs6, 7, 22, 23, 24, 25, 26, 28, 29, 30, 31 performed complete NCCL restoration, whereas 2 – by Santamaria et al.8 and Mathias-Santamaria et al.27 employed partial restoration.
Type of material used
Various materials were used for NCCL restoration, with 4 studies6, 26, 28, 29 using RMGIC, and others employing giomer,6 nano-ionomer cement (NIC),26 micro-filled resin composite (MRC),28 or nano-filled resin composite (NRC) alone25, 27 or in combination.6, 26 However, no evidence suggested that the material type affected the surgical outcome.
Type of surgical root coverage procedure
Seven studies7, 22, 27, 28, 29, 30, 31 performed the coronally advanced/positioned flap and 6 studies6, 8, 23, 24, 25, 26 used CTG for RC.
Esthetic scores
Five studies6, 8, 26, 27, 31 recorded ES and reported that the restoration of NCCLs in combination with any RC procedure provided better esthetic results. Dursun et al.26 also reported that ES was similar in the RMGIC and NIC groups (9.06 ±1.43). Two studies involved professional esthetic assessment by recording the root coverage esthetic score (RES)26, 31 and the modified root coverage esthetic score (mRES).27
Dentin hypersensitivity
Three of the RCTs6, 27, 31 recorded the VAS scores for DS and reported decreased dentin hypersensitivity as perceived by the patient. Cairo et al.31 recorded the VAS scores for patient satisfaction at 1 year and reported no significant difference between the 2 groups.
Six studies7, 22, 25, 26, 29, 31 reported the percentage of sites with DS. All of these studies reported a statistically significant difference in the percentage of dentin hypersensitivity, and there was a more significant decrease in the percentage of dentin hypersensitivity in the restored NCCL group.
Discussion
From among the 13 included studies, only 3 RCTs6, 7, 29 compared the restored NCCLs with the unrestored NCCLs. All 13 studies demonstrated that the restoration of NCCLs had a significant impact on PD, rCAL/CAL and rRH/RGR.
Complete root coverage (CRC) was the most used and indicated primary outcome, as it is the main objective of RC procedures. Nonetheless, there was no significant difference in RC when comparing GR without NCCL with the GR of the root surface with NCCL, suggesting that root surface restoration did not markedly affect the outcome of the surgical procedure.
In RC procedures using soft tissue augmentation, such as platelet-rich fibrin (PRF),29 CTG6, 8, 23, 24, 25, 26 or the acellular dermal matrix,30 there was an increase in KTT. However, there was no significant difference in the outcome of the surgical procedure in terms of RC.
No data indicated the sequence of restoration, or whether restoration should be complete or partial, with only one study analyzing partial restoration.27 Most of the studies employed restoration before surgical procedures, maybe due to better isolation conditions.
The risk of bias is an indicator of the methodological quality of the studies included. As shown in Figure 2, the studies had a low risk of bias. In these studies, it was not possible to attain blinding or masking, as it was easy to notice if the NCCL was restored.
Conclusions
In the teeth with NCCLs and GR, the restoration of NCCL does not affect the percentage RC. However, it significantly decreases dentin hypersensitivity, and the patient’s perception of esthetics and satisfaction.
Ethics approval and consent to participate
Not applicable.
Data availability
All data generated and/or analyzed during this study is included in this published article.
Consent for publication
Not applicable.