Protocol and registration
The study protocol was registered and is available in PROSPERO (International Prospective Register of Systematic Reviews) under the registration number CRD42021240984 and reported in accordance with the PRISMA 2020 Statement26.
Deviation from protocol
As per our research protocol, we had initially planned to research both topics together: Extensive caries lesion and DDE; however, due to the complexity of the search, it was adapted only to teeth with DDE and the economic analysis was not conducted. Therefore, the eligibility criteria and PICO question used were revised.
As the included studies did not always present comparative groups for the treatment of DDE, deviating from what was initially planned in the registry, it was not possible to conduct a network meta-analysis.
Search sources and strategy
The systematic search of the available studies was conducted up to May 31, 2023, in the electronic databases MEDLINE/PubMed, Scopus, Web of Science, Embase, and the Cochrane Central Register of Controlled Trials (CENTRAL). Additionally, the reference lists of potentially eligible studies were checked to ensure that all relevant studies were analyzed. Grey literature search was carried out in the ProQuest database. For the development of the search strategy, the following PICO question was formulated:
What is the best management strategy (I) when compared among the available options (C) concerning longevity and perception/acceptability (O) for posterior deciduous or young permanent teeth with enamel developmental defects presenting post-eruptive fractures or dentin cavities in children up to 14 years old (P)?
The search strategy was developed for the MEDLINE/Pubmed database and then adapted for each consulted database, as described in SI Table 1.
Table 1
– Characteristics of Studies on Molar-Incisor Hypomineralization (MIH).
Authors (Year/Country) | Patient Count | Patient Age | Treatment Count per Group | Involved Tooth Type | Type of Cavity / Severity | Number of Involved Surfaces | Study Design | Evaluated Intervention | Evaluated Outcome | Success Assessment Tools | Follow-up Time | Longevity Rate | Treatment Acceptability Rate | Economic Analysis Conducted | Perception |
Biondi et al.,20221/Argentina | 153 | - | 236 with HM/359 without HM = 595 | Firts permanent molars | Moderate/Severe | - | Retrospective | glass ionomers, steel crown, onlay,inlay, composite resins | Longevity | Clinical examination - modified Ryge criteria /USPHS | 61.7 ± 20.1 without MH/ 57.5 ± 23.9 with MH | 77% with MH/ 100%without MH. | - | - | - |
Dhareula et al.,201934/India | 30 | 8–13 years | 21 per group = 42 | First permanent morlar | Severe | > 2 | RCT | Metal onlay/ indirect resin onlay | Clinical Success | Clinical and radiographic examination - (USPHS) | 36 months | 87.6% for both the groups combined and 90% for metal and 85.7% for the composite group | - | | |
Farias et al.,202235 /Colombia | 115 | 7–10 years | 61 Composite resin/ 54 Stainless steel crown | First permanent molars | Mild, Moderate, Severe | At least 1 | Retrospective | RC/SSC | Longevity | Clinical evaluated with the criteria proposed by Innes et al., to assess restorations of SSC and CR | 24 months | SSC 94,4%/ RC 49.2% | - | - | For CR, 1 patient (1.6%) classified it as very low, 3 (4.9%) as low, 27 (44.3%) as moderate, 23 (37.7%) as intense and 7 (11.5%) as very intense. For SSC, 18 patients (33.3%) rated the discomfort as very low, 19 (35.2%) as low, 14 (25.9%) as moderate, 3 (5.6%) as intense and none as very intense. |
Fragelli et al.,201536 /Brazil | 21 | 6–9 years | 48 | First permanent molars | Morderate/Severe | - | Prospective | 5% fluoride varnish + Glass ionomer cement | Clinical success | Clinical examination - USPHS-Modified | 12 months | 78% | - | - | - |
Gatón-Hernandéz et al.,202037/Spain | 326 | 6-8years | 281 | First permanent molar with open apex | Severe | Occlusal with or without proximal involvement | Longitudinal | Glass ionomer cement and after 6 months Resin Composit | Clinical Success | clinically and radiographically ex- amination | 24 months | In 272 teeth (96.8%), clinical and radiographic success | - | - | - |
Grossi et al.,201833 /Brazil | 44 | 7–13 years | 60 | First permanent molar and Incisors | Severe | > 1 | Prospective | ART - glass hybrid restorative | Longevity | Clinical examination - using the modi- fied ART criterion | 12 months | Success rate was 98.3%, | - | - | - |
Kotsanos et al.,200538 /Greece | 36 | mean age 7.5 | 136 HMI/130 control | First permanent molars | - | At least 1 | Retrospective | RC fillings, Stainless steel, Amalgam, sealants, RC restorarion | Longevity | Clinical examination | 2–5 years | HMI 75% CG 87,7% | - | - | - |
Lygidakis et al.,200339 /Greece | 46 | 8–10 years | 52 Composite restorations | Permanent Molars | Atypical | > 2 | Prospective | Composite restorations | Longevity | Clinical examination - The criteria of Ryge | 48 months | 49 49 teeth reassessed, none requiring retreatment; 4 (8%)with changes in positioning. | - | - | - |
Linner et al.,202040 /Germany | 52 | Mean age 11.2 | 28 GIC restorations/ 126 non-invasive composite restorations/ 27 conventional composite restorations/ 23 CAD/CAM-fabricated ceramic restorations = 204 | Permanent incisors and molars teeth | Moderate/Severe | - | Retrospective | GIC restorations/ non-invasive composite restorations/ conventional composite restorations/ CAD/CAM-fabricated ceramic restorations | Longevity | Clinical FDI criteria for fracture of material and retention examination | 42.9 months | CAD/ CAM group 100.0%/ Conventional composite 76,2%/non-invasive composite restorations29.9%/ GIC restorations 7.0% | - | - | - |
Rolim et al.,202041 /Brazil | 35 | 7–16 years | 33 total etch/31 self etch | First permanent molars | Moderate/Severe | At least 1 | RCT | SE/TE both with universal adhesive and bulk-fill resin composite | Longevity/dental pain/dental anxiety | Clinical examination - USPHS modified | 12 months | 80.8% (TE) and 62.3% (SE) | - | - | Reduction in self-reported pain after 12 months in both groups |
Singh et al., 202131 /India | 46 | 8–15 years | 20 per group = 60 | First permanent molars | Severe | > 2 | RCT | zirconia, lithium disilicate, and cast metal crowns | Clinical Success | Clinical examination - USPHS criteria | 24 months | 6–12 months 100% / 24 months: Metal crown 100%; lithium disilicate and and zirconia crowns 98,3% | Parents: 80% of parents were highly satisfed and 20% were satisfed with the treatment. As for the child, 78.3% were highly satis- fed and 18.3% and satisfed. | | - |
Souza et al.,201732 /Brazil | 18 | 6–8 years | SEA 19/ TEA 22 = 41 | First permanent molars | Severe | - | RCT | self-etching adhesive (SEA) and total-etch adhesive (TEA) + RC | Longevity | Clinical examination - the USPHS-modified criteria | 18 months | were 68% for SEA and 54% for TEA | - | - | - |
Eligibility criteria
The articles were considered eligible when they met the following inclusion criteria:
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Being related to the scope of the review in question: Evaluating the treatment of DDE with dentin cavities or post-eruptive fractures in posterior deciduous and/or young permanent teeth, up to 14 years of age.
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Evaluating the child's or caregiver's perception/acceptability or treatment longevity.
After the initial assessment, articles that met the inclusion criteria were read in their entirety. Articles showing at least one of the following exclusion criteria were considered ineligible:
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Being conducted in specific groups (patients with special needs or undergoing medical treatment).
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Not providing separate data for posterior deciduous or young permanent teeth.
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Not evaluating management strategies for teeth with DDE with dentin cavities or post-eruptive fractures.
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Not being a clinical study.
There were no restrictions on the language or publication date of the included studies. The authors have proficiency in comprehending articles in both Portuguese and English. In cases where articles in other languages were available, an online website (www.deepl.com) was used.
Study selection
The article selection process was conducted using the Rayyan program (Ouzzani et al. 2016) by two independent reviewers (AMPC, BTAS) in duplicate and blinded. Initially, both reviewers assessed the titles and abstracts in accordance with the inclusion criteria. In cases where there was insufficient data to make a decision, in the absence of an abstract, or when the abstract did not provide clear information, the article was then selected for the next phase. Subsequently, the two reviewers (AMPC, RMR), independently, in duplicate and blinded, evaluated the eligible articles in their entirety based on the exclusion criteria. A third researcher (TKT), with experience in systematic reviews related to restorative treatment, was consulted in cases of conflict or uncertainty.
Data extraction
The same reviewers (AMPC, BT, RM), independently and in duplicate, conducted data extraction from eligible articles, including: publication details (authors and year), sample characteristics (number and age of participants, number of treatments performed per group, type of tooth involved, cavity type/severity, number of surfaces involved, and type of enamel development defect), study methodology (design, evaluated interventions, evaluated outcomes, assessment tools for success), and outcome information (follow-up time, longevity rate, and treatment acceptability). Additionally, it was collected the perception/acceptability of the child and/or their caregivers.
Risk of bias assessment
The risk of bias in the included studies was assessed by 2 reviewers (AMPC and TKT), independently and in duplicate, using the Cochrane risk-of-bias tool for randomized trials 2 (RoB 2.0) for randomized clinical trials and the Risk Of Bias In Non-randomized Studies - of Interventions (ROBINS-I) for non-randomized intervention studies.
The RoB 2 tool comprises five domains: bias in the randomization process, bias due to deviations from intended interventions, bias due to missing outcome data, bias in outcome measurement, and bias in the selection of reported results. Reviewers categorized the domains as "low risk of bias," "high risk of bias," or "some concern regarding bias." When all domains received a low risk of bias rating, the study was considered low risk. If at least one domain received a "some concern regarding bias" or "high risk of bias" rating, the studies were then given these respective classifications27.
On the other hand, the ROBINS-I tool consists of seven domains: bias due to confounding, bias in the selection of participants, bias in the classification of interventions, bias due to deviations from intended interventions, bias due to missing data, bias in outcome measurement, and bias in the selection of reported results. In this tool, the domains were categorized as low, moderate, serious, or critical risk of bias, or "no information" (unable to identify information or uncertainties about possible bias)28. The overall risk of bias rating received, similar to the RoB 2.0 tool, the least favorable categorization among the risks assessed for each domain.
Data synthesis and statistical methods for meta-analyses
Since only similar studies on restorative treatments for MIH were found, meta-analyses were conducted considering this substrate type. Qualitative data synthesis was performed for the other DDE.
The I2 test was conducted to assess heterogeneity among the studies, and the tau2 test was used to estimate the variance within the studies. Subsequently, single-arm meta-analyses were conducted to assess the cumulative success rate of restorative treatments according to the follow-up time – 6, 12, and 24 months. Success was evaluated in alignment with the criteria delineated by the included articles. Subgroup analyses were conducted to explore the influence of different types of restorative treatment on the success rate. Sensitivity analyses were performed to investigate the potential influence of individual studies on outcome estimates when there was moderate or high heterogeneity. Publication bias was investigated through visual funnel plot asymmetry analysis and the Begg test when ten or more studies were included.
The meta-analyses were conducted using the "meta," "metafor," "metaprop," and "metabias" packages in the RStudio Team software (RStudio Team, 2022, Boston, MA). The cumulative proportion rate and corresponding 95% confidence intervals (95% CI) were then calculated.
Certainty of evidence
The GRADE (Grading of Recommendations Assessment, Development, and Evaluation) tool was used to assess the certainty of evidence for the results through GRADEpro in the meta-analyses according to the outcome, classified as high, moderate, low, or very low29. The following parameters were considered for the analysis of the certainty of evidence: methodological limitations (risk of bias), inconsistency, indirect evidence, imprecision, and publication bias.