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Multifactorial Contributors to the Longevity of Dental Restorations: An Integrated Review of Related Factors

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28 June 2024

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01 July 2024

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Abstract
Purpose: This integrated review aims to identify and analyze the multifactorial contributors to the longevity of direct restorations, focusing on tooth-, patient-, and dentist-related factors. Materials and Methods: A literature search was performed using an electronic database, PubMed/Medline, Web of Science, and Scopus, between 1980 and 2024. Titles and abstracts of papers that evaluated aspects categorized into tooth-related, patient-related, and dentist-related factors influencing restoration failure were selected and screened. Full-text assessments were conducted, and the extracted data were compiled, summarized, and synthesized. The reference lists of the collected papers were also screened, and relevant citations were included in this review. Data were gathered from clinical and laboratorial studies, systematic reviews, and meta-analyses to provide a comprehensive understanding of restoration longevity. Results: Among the tooth-related factors, multiple-surface restorations, deep margins, tooth location, and tooth vitality significantly impact restoration survival. Patient-related factors such as medical conditions, risk predictors of caries, age, sex, parafunctional habits, smoking, periodontal health, number of restorations, and socioeconomic status all play crucial roles. Regarding dentist-related factors, the decision-making process, age, experience, and dentist manual dexterity are vital aspects. Furthermore, the technique used, including isolation methods for moisture control, as well as the type of dental practice (large group vs. small practice), notably influenced the restoration survival. Conclusions: The longevity of dental restorations is influenced by a complex interplay of tooth-related, patient-related, and dentist-related factors. Strategies to improve restoration outcomes should consider all these multifactorial contributors. Continuing professional education, diligent patient guidance on the factors that influence restoration survival, careful material selection and restorative technique, and tailored individual treatment are crucial factors to reduce failure rates and improve the lifespan of restorations.
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Subject: Public Health and Healthcare  -   Other

1. Introduction

Direct restorations are widely used to treat dental caries lesions due to several factors, including their reduced treatment complexity, cost-effectiveness, decreased chair time, and fewer clinical sessions. The primary materials employed for direct restorations are composite resin, amalgam, resin-modified glass ionomer (RMGI) and glass ionomer cement (GIC) [1]. Despite their widespread use, the longevity of direct restorations varies, with approximately half of all restorations placed in general dental practice being replacements for defective or failed restorations [2,3,4,5]. This leads to significant costs, with global expenses estimated at US$ 298 billion yearly, corresponding to an average of 4.6% of global health expenditure [6]. The annual failure rate for amalgam restorations ranges from 0.16% to 2.83% [7], while for composite restorations, it varies between 1% and 4% [8,9,10]. Research indicates that dental students can attain satisfactory clinical outcomes using posterior composites, with an average yearly failure rate of 2.8% [11]. Indeed, strict adherence to adhesive protocols and proper placement of direct composite restorations can result in them lasting for up to three decades, demonstrating clinically satisfactory performance [12]. GIC restorations, on the other hand, exhibit an annual failure rate of 7%, mainly due to deficiencies in the material [13,14,15,16,17].
The failure of restorations imposes a burden on both the healthcare system and patients due to additional financial commitments and time resources. Furthermore, the frequent replacement of restorations can lead to additional trauma to the tooth, including further reduction of dental tissue, loss of tooth vitality, and reduced patient trust [18,19,20,21,22]. Studies have identified moderately strong evidence indicating a genetic contribution to caries susceptibility, particularly involving genes related to enamel formation, salivary properties, and immune regulation [23,24]. However, genetic risk is further modified by lifestyle and environmental factors. Patients' lifestyle, behavior, dietary habits, and systemic diseases have been proven to influence the development of dental caries and periodontal diseases [23]. Fermentable carbohydrates are the most significant dietary risk factor for caries disease. Their breakdown results in acid production and biofilm formation, which lowers pH and favors acid-producing microorganisms. The concentration, availability, and adhesiveness of these carbohydrates in food also contribute significantly [23,25].
The most frequent causes of failure for direct restorations may vary slightly according to the restorative material. For amalgam restorations, these include secondary caries, tooth/restoration fracture, marginal deficiencies, restoration dislodgement, and overhang [26]. The main reasons for composite resin restoration failure include secondary caries, tooth/restoration fracture, use of a thick layer of glass ionomer liner, absence of peripheral enamel bonding, and enamel beveling deficiency [27]. For GIC/RMGI restorations, the primary factors for failure are secondary caries and loss of glass-ionomer material [28].
Understanding the factors that influence the success and failure of dental restorations is essential for improving clinical outcomes, decreasing the need for repairs or replacements, and reducing the financial burden on healthcare systems. To enhance the success rates of direct, it is vital to identify the causes of early restoration failure and develop strategies to mitigate these failures. This study aims to analyze the multifactorial contributors to the longevity of dental restorations through an integrated review of tooth-related, patient-related, and dentist-related factors.

2. Materials and Methods

A literature search was performed using an electronic database, PubMed/Medline, Web of Science, and Scopus, between 1980 and 2024. Titles and abstracts of papers that evaluated aspects categorized into tooth-related, patient-related, and dentist-related factors influencing restoration failure were selected and screened. Full-text assessments were conducted, and the extracted data were collected, summarized, and combined. The reference lists of the collected papers were also screened, and relevant citations were included in this review. Data were gathered from clinical and laboratorial studies, systematic reviews, and meta-analyses to provide a comprehensive understanding of restoration longevity. Inclusion criteria: English language; prospective and retrospective clinical trials; laboratorial studies; meta-analyses; systematic review; literature review. Exclusion criteria: papers published before 1980; studies conducted in primary teeth; in vitro studies conducted on bovine teeth; duplicated studies.

3. Discussion

Factors Affecting the Longevity of Direct Restorations

Patient-Related Factors

Behavioral factors of an individual, such as snacking frequency and toothbrushing habits, can directly affect oral environmental conditions, which in turn influence the survival of restorations [29]. Biochemical challenges, such as biofilm accumulation and temperature fluctuations, create harsh environmental conditions for tooth structure and adhesive interfaces. These challenges can lead to processes like hydrolysis, leaching, fatigue, and cracking [30]. Dietary habits play a crucial role in maintaining or disturbing the homeostasis of the oral environment. Frequent exposure to sugars and fermentable carbohydrates leads to prolonged plaque acidification [31], resulting in microbiota metabolic activity and tooth demineralization. This acidification can severely damage composite restoration surfaces [32].
Salivary fluid is essential for the formation of the oral microbiome and biofilm [33]. It has been demonstrated that proteins secreted into saliva within the oral cavity are valuable for testing and diagnosing dental caries, underlining the significance of saliva in both the progression and detection of this condition [34]. Salivary proteins, such as proline-rich proteins, mucins, histatins, cystatins, and statherins, protect the tooth surface by attracting calcium ions and promoting remineralization. The pellicle they form slows demineralization and reduces microbial adherence, shielding the tooth surface from pH fluctuations. This also enhances the buffering action, leading to acid neutralization from bacterial or non-bacterial sources [35]. Furthermore, they positively influence the reorganization of infected or affected carious dentin. A significant reduction in bacterial counts observed after cavity sealing highlights the antimicrobial activity of salivary proteins [36,37,38]. Salivary proteins include powerful enzymes that naturally inhibit bacterial growth by penetrating bacterial cell walls and neutralizing their pathogenicity. These enzymes also exhibit antifungal and antiviral properties [39]. Various studies have found that the texture of saliva is a crucial factor as well. Saliva that is thick, sticky, and frothy, particularly when it exhibits increased viscosity, has been associated with a higher susceptibility to dental caries [40].
Xerostomia, characterized by reduced quality and quantity of saliva, can elevate the prevalence of caries, and it is more common in female individuals over 50 years old [41,42]. Patients with xerostomia often experience decreased survival rates of dental restorations, particularly those with large composite restorations [43]. Under normal conditions, saliva is oversaturated with calcium hydroxyapatite, which helps prevent dental demineralization. Diseases that affect the quality and quantity of saliva, such as Sjogren's syndrome, viral infections (HIV and HCV), uncontrolled diabetes, Alzheimer's disease, hypertension, depression, and cancer, can impact the health of intraoral soft and hard tissues, leading to dental caries and gingivitis [44]. Burning Mouth Syndrome (BMS), associated with bruxism and considered an oral psychosomatic condition, which often aligns with salivary gland dysfunction [45]. Bulimia nervosa, characterized by self-induced vomiting and binge eating, has also been linked to altered salivary function. Studies indicate that both resting and stimulated salivary flow rates are reduced in patients with sialadenosis, while total protein and amylase levels are increased [44]. Additionally, xerostomia is associated with over 500 medications, with polypharmacy being the most prevalent cause [46]. Many patients on xerogenic medications are unaware of their risk for oral complications such as dental caries. Medications that contribute to xerostomia include antipsychotics, antihistamines, antiemetics, antiretroviral therapy, decongestants, appetite suppressants, and diuretics [44]. Chemotherapy and radiotherapy of head and neck can also lead to changes in saliva quality and quantity [44]. It has been verified that while direct damage to teeth or restorations from radiation itself may not be the primary cause of early restoration failure in radiation-related caries, changes in saliva quantity and quality, challenges in maintaining oral hygiene, and an increased cariogenic diet may play more significant roles [41,42]. Furthermore, several studies have associated smoke exposure with an increased risk of caries, linked to alterations in saliva [47,48].
The use of caries risk assessment (CRA) can help identify risk factors and is crucial for tailoring patient treatment, as it is directly related to the rate of dental restoration failure [49,50]. Patients with a high or medium caries risk have a 2 to 3 times higher risk of restoration failure [14]. A study found that patients with a high DMFT index (Decayed, Missing, and Filled Teeth) have a 2.45 to 4.40 times greater risk of restoration failure compared to those with a low index [51,52]. Additionally, the absence of teeth and inadequate proximal contacts have also been related to lower survival rates for restorations [53].
Missing teeth may lead to the use of partial removable dentures, which can compromise the survival of restorations, as patients with removable dentures frequently struggle to clean them effectively [54,55]. Ulcerations of the gums and/or oral mucosa have been reported in these patients due to poor denture fit and improper use, further complicating their oral hygiene compliance [56]. Additionally, the presence of non-oral pathogenic bacteria and significant biofilm formation in the oral cavities of patients using dentures have been shown to increase the risk of systemic infections and complicate oral hygiene management [57]. Furthermore, compromised periodontal status has also been linked to a higher likelihood of restoration failure, as optimal restoration success is achieved when the surrounding tissues are healthy and stable [58]. Eliminating periodontal disease before, during, and after restorative procedures is crucial for the longevity of restorations [59].
Psychological factors also play a significant role in enhancing restoration survival [55,60]. Caries risk may increase in any age group due to physiological changes, which are associated with increased medication use and reduced interest in self-care. Additionally, stress factors can manifest in behaviors such as parafunctional habits, including bruxism, which can induce occlusal stress and pose mechanical challenges to both restorations and adhesive interfaces, potentially resulting in wear and/or cracking of teeth and restorations [60]. Patients with bulimia have shown an elevated rate of restoration failure due to erosion [61]. In patients experiencing erosion, the cause of the wear is a risk factor for restorative treatment if it remains uncontrolled. The longevity of the restoration is reduced due to compromised marginal integrity, leading to a higher incidence of microleakage and secondary caries [62].
Several studies have shown the correlation between age and restoration failure. Increased failure rates for direct resin composite restorations were observed during adolescence and after age 65 [29,30,63]. While adolescents are more prone to frequent sugary snacks and soft drinks [13], older patients are more likely to have older restorations, and caries incidence is higher due to changes in their stomatognathic system, impaired motor function, reduced salivary flow, changes to softer diets, general health issues, increased use of medications, and their inability to maintain oral hygiene [64].
Regarding gender, some studies have reported lower restoration survival in male patients [29,65]. while others did not find any correlation [66]. This discrepancy may be due to men typically having stronger bite forces than women, leading to higher rates of material fatigue, fractures, and restoration failures [67]. Additionally, women, being more health-conscious, tend to attend dental hygiene consultations more regularly, which contributes to better oral health outcomes [68,69].
Socioeconomic deprivation has been reported as an important factor in the survival rate of composite restorations [49,50]. Cultural, educational, sociological, and psychological factors also play crucial roles in influencing oral care and, consequently, the longevity of dental restorations [70,71,72,73]. People from poorer socioeconomic strata experience more restoration failures than those from wealthier backgrounds. Restorations in clinics in deprived areas have higher annual failure rates (5.6%) compared to areas with medium (4.2%) and high (5.1%) socioeconomic status [74]. The educational level of patients and their access to oral health services can affect clinical outcomes [65]. Poor adherence to oral health advice [55], irregular dental visits [75], and lower maternal education at childbirth [76] are other socioeconomic-related factors strongly associated with restoration failure. Conversely, studies have identified a direct correlation between the frequency of dental checkups per year and the failure rates of direct restorations [63]. Records from the General Dental Services of England and Wales indicate that patients who frequently visit dental practices experience significantly reduced survival rates of direct restorations [77,78]. This suggests that a proactive or aggressive approach by dentists may potentially lead to over-treatment [79,80]. This suggests that a proactive or aggressive approach by dentists may potentially lead to over-treatment [79,80]. This phenomenon can also be explained by the method of determining recall intervals, which takes into account patient-related factors such as oral hygiene, dental history, and age. As a result, patients with poorer indicators are scheduled for shorter intervals between checkups.
Furthermore, research has shown that patients who frequently change dentists are more likely to have their restorations replaced. Dentists who did not place the original restoration are more inclined to replace it than those who did [81,82,83,84,85]. This tendency may stem from dentists having greater trust in their own work than in the work of their peers. Additionally, when addressing a defective restoration in a new patient, dentists lacking baseline information for an accurate prognosis are more likely to replace the entire restoration rather than repair it [86].

3.1. Operator-Related Factors

The operator's technique plays a pivotal role in enhancing the longevity of dental restorations [13,87,88,89]. Proper moisture control and meticulous adherence to restorative protocols are crucial during the execution of technique-sensitive steps in adhesive dentistry [20]. Additional considerations include employing the correct light-curing technique, which depends on factors such as the type of light-curing unit (LCU), the duration of light exposure, the thickness of the resin composite, and positioning the light-curing tip as close to the work area as possible. For surfaces that are difficult to reach, extending the light-curing time is recommended [74,90,91,92,93,94,95,96,97,98,99]. It is crucial for clinicians to understand and optimize the photopolymerization process of resin-based composites to enhance material properties. A previous study by Kopperud et al. (2017) revealed that the majority of Norwegian dental practitioners lacked adequate knowledge in this area. Additionally, a significant portion of the participants (78.3%) were not aware of the irradiance values of their light-curing units (LCUs). The study also found that the same percentage of dentists neglected regular maintenance of their LCUs [100]. Composite restorations require adequate radiant exposure to properly polymerize, ensuring optimal mechanical and physical properties [101]. Insufficient photopolymerization may lead to color changes over time [102,103,104], which could mistakenly be interpreted as recurrent caries. Additionally, inadequate polymerization is linked to lower microhardness values [105], degradation of the restoration, weakening of its mechanical properties, and an increased risk of microleakage [106].
An interesting observation is the higher annual failure rates of dental restorations placed in large group practices compared to those performed by a single dentist or in smaller practices [29]. This finding may be related to the fact that patients in larger practices are often seen by different dentists. It has been previously observed that changing dentists leads to a higher rate of restoration replacements [77,78]. Additionally, long-term studies on posterior composites placed by general practitioners indicate that their survival rates are comparable to those placed by specialists [107].
The dentist's decision-making process is another critical factor that can significantly impact the longevity of restorations [14,108]. This process is often underestimated and involves various complex co-variables [74]. The presence of additional risk factors, such as tooth vitality [109], the number of remaining walls [110,111], and the use of removable partial dentures [112], further complicates decision-making. Moreover, securing the patient's consent for proposed treatment options adds another layer of complexity in selecting the most suitable treatment when planning the restoration of a defective tooth [11,13,113,114,115,116,117,118,119,120,121,122]. A potential explanation for the wide variation in annual failure rates (AFRs) observed for composite restorations relates to whether dentists adopt a proactive or reactive approach to aged restorations. Proactive dentists, who prefer to intervene early rather than monitor a questionable restoration, may contribute to shorter restoration longevity compared to reactive, more conservative dentists who wait to observe disease progression before intervening. Additionally, a proactive approach does not necessarily guarantee that the new restoration will outlast the original [74]. Success and survival rates tend to decrease when dentists choose to repair or replace restorations due to minor issues such as marginal staining, gaps, chipping, or wear [63]. In a retrospective study spanning up to 18.5 years, restorations that underwent more frequent annual check-ups exhibited higher failure rates than those with fewer check-ups. The variability in dentists evaluating the restorations significantly affected the time until failure [63]. While some studies have verified the influence of the operator on survival rates, the dentist's impact on the outcomes is not always clear [77,78,108].
Regarding the operator's age, studies present conflicting findings about the impact of a dentist's experience and age on the survival of dental restorations. Some studies indicate that restorations performed by less experienced dentists or those who graduated more recently have higher annual failure rates [30]. Conversely, other studies suggest that restorations placed by younger dentists tend to last longer [123]. Additionally, one study found that restorations performed by dentists who graduated within the past 19 years are less likely to fail compared to those done by dentists who graduated over 19 years ago [107]. This study showed that the time from initial restoration placement to the need for reintervention is shorter for restorations placed by older dentists [77]. evolution of materials and techniques may explain this fact, as older dentists may not always be up to date with the most recent materials and restorative protocols.
Regarding the dentist’s gender, a study found that restorations placed by male clinicians were less likely to fail compared to those placed by female clinicians [123]. This may be related to another finding that part-time practitioners have higher failure rates than full-time practitioners, with a higher proportion of women working in part-time positions compared to men [124,125,126,127]. The differences identified in multivariable analysis could also stem from varying diagnosis patterns; for instance, women might be more likely to report a restoration as a failure, whereas men might not.
It has also been shown that dentists' motivation and workload potentially influence their treatment outcomes [77]. Practice workload emerged as a significant predictor, though the reasons behind this observation remain unclear. Interestingly, dentists reporting a need for more patients tend to have a success rate approximately twice that of balanced or slightly busy clinicians. One might speculate that a dentist with sufficient time could dedicate more attention to detail and take longer with a procedure. However, clinicians describing their practice as excessively busy may also exhibit a high success rate, possibly indicating greater efficiency. Practices categorized as very busy or not busy demonstrated restorations with higher survival rates, suggesting a complex interplay of practice style, work environment, and clinical approach [64,128].

3.2. Tooth-Related Factors

Teeth with larger cavities or fewer cavity walls, especially when marginal ridges are removed, present increased cuspal deflection during function [129]. This leads to a higher likelihood of fractures and increased Annual Failure Rate (AFR) [130,131]. Teeth with Class I restorations rarely fracture due to excessive loads, as the remaining walls and the presence of marginal ridges—considered reinforcing structures by connecting facial and lingual walls—provide stability. In Class II restorations, the wedge effect combined with the load remains within the cavity, causing additional stresses that may lead to fracture the cavity walls [132]. The width of the isthmus has a significant impact on Class II preparations. An isthmus measuring one-fourth of the intercuspal distance can provide increased strength to the prepared tooth [130]. Marginal ridges reinforce the tooth by connecting the facial and lingual walls. MOD cavities, which involve significant loss of dentin, are considered the most prone to fractures and have a higher annual failure rate (AFR) [133].
Regardless of the treatment used, studies suggest a strong relationship between the amount of remaining tooth tissue and restorations survival [16,134,135]. Opdam (2014) reported that the risk of AFR increased by 30% to 40% for each additional missing wall. Furthermore, resin composite restorations failed 3.3 times more often in posterior teeth with fewer than 2 remaining walls compared to those with 4 walls [136]. Additionally, endodontically treated molars with restorations covering more than 4 surfaces exhibited higher failure rates [10]. Studies shown that the reasons for the failure of composite restorations vary depending on the time of evaluation. Failures during the follow-up period of one to four years are mostly related to restoration fractures. In contrast, secondary caries and the need for endodontic treatment become the predominant causes of failure over a ten-year evaluation period [135,137].
The quality of the remaining tooth structure is another crucial factor for enhancing restoration longevity. Factors such as the presence of cracks, sclerotic and deep dentin compared to sound and superficial dentin, and the position of cervical margins are important aspects influencing the survival rate of restorations [27,138,139]. Furthermore, restorations placed due to fractures were more prone to fail than those placed due to caries [30]. Additionally, the presence of deep caries lesions showed a four times higher risk of failure, while cavities with pulp exposure had a 14 times higher failure risk compared to restorations localized in the dentin [140].
Relating to tooth vitality, the need for endodontic treatment is a critical factor influencing the prognosis, long-term survival, and success of teeth and restorations. A practice-based study with over 430,000 restorations reported that fewer than 20% of restorations placed in endodontically treated teeth survived after 10 years. The main reasons for failures included secondary caries, root and cusp fractures, loss of retention, and restoration fractures. In vital teeth, composite restorations mainly fail due to secondary caries and restoration fractures [60,65,123]. Endodontic treatment has been shown to reduce the stiffness of teeth by 5%, while an occlusal restoration can reduce stiffness by 20%, and a MOD restoration can reduce tooth stiffness by 63% [141]. A previous study reported that the annual failure rate (AFR) for endodontically treated teeth was 10.9%, compared to 4.5% for vital teeth [29]. Root-filled teeth undergo a reduction in free water content within the dentine matrix and tubules, affecting their viscoelastic properties. Dehydration is suggested as a contributing factor to vertical root fractures. The most critical factor is the loss of tooth structure, and there is general consensus that cuspal coverage of endodontically treated posterior teeth enhances their survival [142].
Tooth position and antagonistic contacts can also play a significant role in the longevity of restorations [53]. The superior visibility of occlusal tooth surfaces facilitates easier and earlier detection of secondary caries and other restoration deficiencies [143]. Molars generally have lower restoration survival rates than other teeth due to larger restorations and greater occlusal forces [64]. The first molar, the most frequently restored tooth, showed the highest AFR [30]. Additionally, studies indicated that restorations might last longer in premolars than in molars [14]. Restorations in the upper arch had a higher risk of failure compared to those in the lower arch. A study found that after 5 years, direct composite restorations exhibited more wear in the upper arch than in the lower arch, though the reason for this remained unclear [144]. Contrary to these findings, Lucarotti (2018) reported that the restoration survival rate over 15 years varies by tooth type, with upper molars having the highest survival rate. Another study revealed that the AFR of restorations was similar across the four quadrants [30].
In conclusion, this review underscores the need for a holistic approach in dental practice, where understanding and addressing multifactorial contributors can lead to improved restoration success rates and reduced failure rates. Continuous education and training for dental professionals, coupled with comprehensive patient management, are recommended to optimize the longevity of dental restorations. By addressing patient-related, tooth-related, and dentist-related factors contributing to restoration failure, dental professionals can ensure better patient outcomes, reduce the need for frequent replacements, and ultimately enhance the overall quality of dental care. Several studies have emphasized the need for tailored treatment based on individual patient conditions. Furthermore, a more conservative approach with an emphasis on prevention has been the ultimate goal. The findings in this review indicate that the survival of direct restorations is not solely dependent on tooth-related factors but is also significantly influenced by the complex interplay of several factors. By addressing these multifactorial contributors through a comprehensive and informed approach, dental professionals can significantly improve dental restoration outcomes, benefiting both patients and healthcare systems.

References

  1. Parolia, A.; Kundabala, M.; Gupta, V.; Verma, M.; Batra, C.; Shenoy, R.; et al. Microleakage of bonded amalgam restorations using different adhesive agents with dye under vacuum: An in vitro study. Indian J. Dent. Res. 2011, 22, 252–255. [Google Scholar] [CrossRef]
  2. Jokstad, A.; Mjor, I.A.; Qvist, V. The age of restorations in situ. Acta Odontol. Scand. 1994, 52, 234–242. [Google Scholar] [CrossRef] [PubMed]
  3. Pink, F.E.; Minden, N.J.; Simmonds, S. Decisions of practitioners regarding placement of amalgam and composite restorations in general practice settings. Oper. Dent. 1994, 19, 127–132. [Google Scholar] [PubMed]
  4. Mjör, I.A.; Moorhead, J.E.; Dahl, J.E. Reasons for replacement of restorations in permanent teeth in general dental practice. Int. Dent. J. 2000, 50, 360–366. [Google Scholar] [CrossRef] [PubMed]
  5. McDaniel, R.J.; Davis, R.D.; Murchison, D.F.; Cohen, R.B. Causes of failure among cuspal-coverage amalgam restorations: A clinical survey. J. Am. Dent. Assoc. 2000, 131, 173–177. [Google Scholar] [CrossRef] [PubMed]
  6. Listl, S.; Galloway, J.; Mossey, P.A.; Marcenes, W. Global economic impact of dental diseases. J. Dent. Res. 2015, 94, 1355–1361. [Google Scholar] [CrossRef] [PubMed]
  7. Kapoor, B.; Ahmed, L. The war between amalgam and composite: A critical review. J. Oral Res. Rev. 2021, 13, 133–138. [Google Scholar] [CrossRef]
  8. Manhart, J.; Chen, H.; Hamm, G.; Hickel, R. Buonocore Memorial Lecture. Review of the clinical survival of direct and indirect restorations in posterior teeth of the permanent dentition. Oper. Dent. 2004, 29, 481–508. [Google Scholar] [PubMed]
  9. Heintze, S.D.; Rousson, V. Clinical effectiveness of direct class II restorations: A meta-analysis. J. Adhes. Dent. 2012, 14, 407–431. [Google Scholar] [CrossRef] [PubMed]
  10. Demarco, F.F.; Cenci, M.S.; Montagner, A.F.; de Lima, V.P.; Correa, M.B.; Moraes, R.R.; Opdam, N.J.M. Longevity of composite restorations is definitely not only about materials. Dent. Mater. 2023, 39, 1–12. [Google Scholar] [CrossRef] [PubMed]
  11. Opdam, N.J.M.; Loomans, B.A.C.; Roeters, F.J.M.; Bronkhorst, E.M. Five-year clinical performance of posterior resin composite restorations placed by dental students. J. Dent. 2004, 32, 379–383. [Google Scholar] [CrossRef] [PubMed]
  12. Da Rosa Rodolpho, P.A.; Rodolfo, B.; Collares, K.; Correa, M.B.; Demarco, F.F.; Opdam, N.J.M.; et al. Clinical performance of posterior resin composite restorations after up to 33 years. Dent. Mater. 2022, 38, 680–688. [Google Scholar] [CrossRef] [PubMed]
  13. Bernardo, M.; Luis, H.; Martin, M.D.; Leroux, B.G.; Rue, T.; Leitão, J.; DeRouen, T.A. Survival and reasons for failure of amalgam versus composite posterior restorations placed in a randomized clinical trial. J. Am. Dent. Assoc. 2007, 138, 775–783. [Google Scholar] [CrossRef] [PubMed]
  14. Demarco, F.F.; Correa, M.B.; Cenci, M.S.; Moraes, R.R.; Opdam, N.J. Longevity of posterior composite restorations: Not only a matter of materials. Dent. Mater. 2012, 28, 87–101. [Google Scholar] [CrossRef] [PubMed]
  15. Demarco, F.F.; Collares, K.; Coelho-de-Souza, F.H.; Correa, M.B.; Cenci, M.S.; Moraes, R.R.; et al. Anterior composite restorations: A systematic review on long-term survival and reasons for failure. Dent. Mater. 2015, 31, 1214–1224. [Google Scholar] [CrossRef] [PubMed]
  16. Opdam, N.J.M.; Van De Sande, F.H.; Bronkhorst, E.; Cenci, M.S.; Bottenberg, P.; Pallesen, U.; et al. Longevity of posterior composite restorations: A systematic review and meta-analysis. J. Dent. Res. 2014, 93, 943–949. [Google Scholar] [CrossRef] [PubMed]
  17. Goldstein, G.R. The longevity of direct and indirect posterior restorations is uncertain and may be affected by a number of dentist-, patient-, and material-related factors. J. Evid. Based Dent. Pract. 2010, 10, 30–31. [Google Scholar] [CrossRef] [PubMed]
  18. Silvani, S.; Trivelato, R.F.; Nogueira, R.D.; Gonçalves, Lde S.; Geraldo-Martins, V.R. Factors affecting the placement or replacement of direct restorations in a dental school. Contemp. Clin. Dent. 2014, 5, 54-58. [CrossRef]
  19. Nassar, H.; El-Shamy, H. Bonding system choice and practices among senior dental students. J. Int. Soc. Prev. Community Dent. 2017, 7, S143–S148. [Google Scholar] [CrossRef] [PubMed]
  20. Wong, C.; Blum, I.R.; Louca, C.; Sparrius, M.; Wanyonyi, K. A retrospective clinical study on the survival of posterior composite restorations in a primary care dental outreach setting over 11 years. J. Dent. 2021, 106, 103586. [Google Scholar] [CrossRef] [PubMed]
  21. Jingarwar, M.M.; Bajwa, N.K.; Pathak, A. Minimal intervention dentistry — a new frontier in clinical dentistry. J. Clin. Diagn. Res. 2014, 8, ZE04–ZE08. [Google Scholar] [CrossRef]
  22. Lucarotti, P.S.K.; Burke, F.J.T. The ultimate guide to restoration longevity in England and Wales. Part 1: Methodology. Br. Dent. J. 2018, 224, 709–716. [Google Scholar] [CrossRef] [PubMed]
  23. Chapple, I.L.; Bouchard, P.; Cagetti, M.G.; Campus, G.; Carra, M.C.; Cocco, F.; Nibali, L.; Hujoel, P.; Laine, M.L.; Lingstrom, P.; Manton, D.J.; Montero, E.; Pitts, N.; Rangé, H.; Schlueter, N.; Teughels, W.; Twetman, S.; Van Loveren, C.; Van der Weijden, F.; Vieira, A.R.; Schulte, A.G. Interaction of lifestyle, behaviour or systemic diseases with dental caries and periodontal diseases: Consensus report of group 2 of the joint EFP/ORCA workshop on the boundaries between caries and periodontal diseases. J. Clin. Periodontol. 2017, 44, S39–S51. [Google Scholar] [CrossRef] [PubMed]
  24. Opal, S.; Garg, S.; Jain, J.; Walia, I. Genetic factors affecting dental caries risk. Aust. Dent. J. 2015, 60, 2–11. [Google Scholar] [CrossRef] [PubMed]
  25. Pitts, N.B.; Twetman, S.; Fisher, J.; Marsh, P.D. Understanding dental caries as a non-communicable disease. Br. Dent. J. 2021, 231, 749–753. [Google Scholar] [CrossRef] [PubMed]
  26. Wilson, N.; Lynch, C.D.; Brunton, P.A.; Hickel, R.; Meyer-Lueckel, H.; Gurgan, S.; et al. Criteria for the replacement of restorations: Academy of Operative Dentistry European Section. Oper. Dent. 2016, 41, S48–S57. [Google Scholar] [CrossRef] [PubMed]
  27. Kuper, N.K.; Opdam, N.J.; Ruben, J.L.; de Soet, J.J.; Cenci, M.S.; Bronkhorst, E.M.; et al. Gap size and wall lesion development next to composite. J. Dent. Res. 2014, 93, 108–113. [Google Scholar] [CrossRef] [PubMed]
  28. Scholtanus, J.D.; Huysmans, M.C.D. Clinical failure of class-II restorations of a highly viscous glass-ionomer material over a 6-year period: A retrospective study. J. Dent. 2007, 35, 156–162. [Google Scholar] [CrossRef]
  29. Laske, M.; Opdam, N.J.M.; Bronkhorst, E.M.; Braspenning, J.C.C.; Huysmans, M.C.D.N.J.M. Ten-year survival of class II restorations placed by general practitioners. JDR Clin. Transl. Res. 2016, 1, 292–299. [Google Scholar] [CrossRef] [PubMed]
  30. Laske, M.; Opdam, N.J.; Bronkhorst, E.M.; Braspenning, J.C.; Huysmans, M.C. Risk factors for dental restoration survival: A practice-based study. J. Dent. Res. 2019, 98, 414–422. [Google Scholar] [CrossRef] [PubMed]
  31. Marsh, P.D. Are dental diseases examples of ecological catastrophes? Microbiology 2003, 149, 279–294. [Google Scholar] [CrossRef]
  32. Beyth, N.; Bahir, R.; Matalon, S.; Domb, A.J.; Weiss, E.I. Streptococcus mutans biofilm changes surface-topography of resin composites. Dent. Mater. 2008, 24, 732–736. [Google Scholar] [CrossRef] [PubMed]
  33. Proctor, G. B. The physiology of salivary secretion. Periodontology 2000, 2016, 70, 11-25. [CrossRef]
  34. Hong, S. W.; Seo, D. G.; Baik, J. E.; Cho, K.; Yun, C. H.; Han, S. H. Differential profiles of salivary proteins with affinity to Streptococcus mutans lipoteichoic acid in caries-free and caries-positive human subjects. Mol. Oral Microbiol. 2014, 29, 208–218. [Google Scholar] [CrossRef] [PubMed]
  35. Van Nieuw Amerongen, A.; Bolscher, J. G.; Veerman, E. C. Salivary proteins: protective and diagnostic value in cariology? Caries Res. 2004, 38, 247–253. [Google Scholar] [CrossRef]
  36. Pinheiro, S. L.; da Rocha, N. N.; Peres, M. D. L. H. M. Capacity of a hydroxyapatite–lysozyme combination against Streptococcus mutans for the treatment of dentinal caries. J. Conserv. Dent. Endod. 2016, 19, 465–468. [Google Scholar] [CrossRef] [PubMed]
  37. Shimada, J.; Moon, S. K.; Lee, H. Y.; Takeshita, T.; Pan, H.; Woo, J. I.; Lim, D. J. Lysozyme M deficiency leads to an increased susceptibility to Streptococcus pneumoniae-induced otitis media. BMC Infect. Dis. 2008, 8, 1–11. [Google Scholar] [CrossRef] [PubMed]
  38. Kagan, B. L.; Selsted, M. E.; Ganz, T.; Lehrer, R. I. Antimicrobial defensin peptides form voltage-dependent ion-permeable channels in planar lipid bilayer membranes. Proc. Natl. Acad. Sci. U.S.A. 1990, 87, 210–214. [Google Scholar] [CrossRef]
  39. Żelechowska, P.; Agier, J.; Brzezińska-Błaszczyk, E. Endogenous antimicrobial factors in the treatment of infectious diseases. Cent. Eur. J. Immunol. 2016, 41, 419–425. [Google Scholar] [CrossRef] [PubMed]
  40. Kaur, A.; Kwatra, K. S.; Kamboj, P. Evaluation of non-microbial salivary caries activity parameters and salivary biochemical indicators in predicting dental caries. J. Indian Soc. Pedod. Prev. Dent. 2012, 30, 212–217. [Google Scholar] [CrossRef]
  41. Nederfors, T.; Isaksson, R.; Mörnstad, H.; Dahlöf, C. Prevalence of perceived symptoms of dry mouth in an adult Swedish population-relation to age, sex and pharmacotherapy. Community Dent. Oral Epidemiol. 1997, 25, 211–216. [Google Scholar] [CrossRef] [PubMed]
  42. Villa, A.; Polimeni, A.; Strohmenger, L.; Cicciù, D.; Gherlone, E.; Abati, S. Dental patients’ self-reports of xerostomia and associated risk factors. J. Am. Dent. Assoc. 2011, 142, 811–816. [Google Scholar] [CrossRef] [PubMed]
  43. Jukka, L.; Hannu, V.; Ellinoora, R.; Laura, J.; Ritva, N.; Vuokko, A. The survival time of restorations is shortened in patients with dry mouth. J. Dent. 2021, 113, 103794. [Google Scholar] [CrossRef]
  44. Iorgulescu, G. Saliva between normal and pathological. Important factors in determining systemic and oral health. J. Med. Life 2009, 2, 303. [Google Scholar] [PubMed]
  45. Mott, A. E.; Grushka, M.; Sessle, B. J. Diagnosis and management of taste disorders and burning mouth syndrome. Dent. Clin. North Am. 1993, 37, 33–71. [Google Scholar] [CrossRef] [PubMed]
  46. Scully, C. Drug effects on salivary glands: dry mouth. Oral Dis. 2003, 9, 165–176. [Google Scholar] [CrossRef] [PubMed]
  47. Benedetti, G.; Campus, G.; Strohmenger, L.; Lingström, P. Tobacco and dental caries: a systematic review. Acta Odontol. Scand. 2013, 71, 363–371. [Google Scholar] [CrossRef] [PubMed]
  48. Jiang, X.; Jiang, X.; Wang, Y.; Huang, R. Correlation between tobacco smoking and dental caries: A systematic review and meta-analysis. Tob. Induc. Dis. 2019, 17. [CrossRef]
  49. Peres, M. A.; Peres, K. G.; De Barros, A. J. D.; Victora, C. G. The relation between family socioeconomic trajectories from childhood to adolescence and dental caries and associated oral behaviours. J. Epidemiol. Community Health 2007, 61, 141–145. [Google Scholar] [CrossRef]
  50. Thomson, W. M.; Poulton, R.; Milne, B. J.; Caspi, A.; Broughton, J. R.; Ayers, K. M. S. Socioeconomic inequalities in oral health in childhood and adulthood in a birth cohort. Community Dent. Oral Epidemiol. 2004, 32, 345–353. [Google Scholar] [CrossRef] [PubMed]
  51. Opdam, N. J.; Bronkhorst, E. M.; Roeters, J. M.; Loomans, B. A. A retrospective clinical study on longevity of posterior composite and amalgam restorations. Dent. Mater. 2007, 23, 2–8. [Google Scholar] [CrossRef] [PubMed]
  52. Trachtenberg, F.; Maserejian, N. N.; Tavares, M.; Soncini, J. A.; Hayes, C. Extent of tooth decay in the mouth and increased need for replacement of dental restorations: the New England Children's Amalgam Trial. Pediatr. Dent. 2008, 30, 388–392. [Google Scholar] [PubMed]
  53. Linnemann, T.; Kramer, E. J.; Schwendicke, F.; Wolf, T. G.; Meyer-Lueckel, H.; Wierichs, R. J. Longevity and risk factors of post restorations after up to 15 years: a practice-based study. J. Endod. 2021, 47, 577–584. [Google Scholar] [CrossRef] [PubMed]
  54. Laske, M.; Opdam, N. J. M.; Bronkhorst, E. M.; Braspenning, J. C. C.; Huysmans, M. C. D. N. J. M. Longevity of direct restorations in Dutch dental practices. Descriptive study out of a practice-based research network. J. Dent. 2016, 46, 12–17. [Google Scholar] [CrossRef] [PubMed]
  55. Wong, F. M.; Ng, Y. T.; Leung, W. K. Oral health and its associated factors among older institutionalized residents—a systematic review. Int. J. Environ. Res. Public Health 2019, 16, 4132. [Google Scholar] [CrossRef] [PubMed]
  56. Ganesh, V.; Drever, S.; Agilinko, J.; Vallamkondu, V.; Majumdar, S.; Shakeel, M. Management of a swallowed denture: our experience with 34 patients. GMS Ger. Med. Sci. 2021, 19. [CrossRef]
  57. Derafshi, R.; Bazargani, A.; Ghapanchi, J.; Izadi, Y.; Khorshidi, H. Isolation and identification of nonoral pathogenic bacteria in the oral cavity of patients with removable dentures. J. Int. Soc. Prev. Community Dent. 2017, 7, 197–201. [Google Scholar] [CrossRef] [PubMed]
  58. Skupien, J. A.; Opdam, N. J.; Winnen, R.; Bronkhorst, E. M.; Kreulen, C. M.; Pereira-Cenci, T. Survival of restored endodontically treated teeth in relation to periodontal status. Braz. Dent. J. 2016, 27, 37–40. [Google Scholar] [CrossRef]
  59. Goldberg, P. V.; Higginbottom, F. L.; Wilson, T. G., Jr. Periodontal considerations in restorative and implant therapy. Periodontology 2000, 25, 100–109. [Google Scholar] [CrossRef] [PubMed]
  60. Lempel, E.; Lovász, B. V.; Bihari, E.; Krajczár, K.; Jeges, S.; Tóth, Á. Long-term clinical evaluation of direct resin composite restorations in vital vs endodontically treated posterior teeth — retrospective study up to 13 years. Dent. Mater. 2019, 35, 1308–1318. [Google Scholar] [CrossRef] [PubMed]
  61. Bartlett, D.; Sundaram, G. An up to 3-year randomized clinical study comparing indirect and direct resin composites used to restore worn posterior teeth. Int. J. Prosthodont. 2006, 19, 6. [Google Scholar]
  62. Loomans, B.; Opdam, N.; Attin, T.; Bartlett, D.; Edelhoff, D.; Frankenberger, R.; ... & Wilson, N. Severe tooth wear: European consensus statement on management guidelines. J. Adhes. Dent. 2017, 19, 111-119. [CrossRef]
  63. Wierichs, R.J.; Kramer, E.J.; Meyer-Lueckel, H. Risk factors for failure of direct restorations in general dental practices. J. Dent. Res. 2020, 99, 1039–1046. [Google Scholar] [CrossRef] [PubMed]
  64. McCracken, M.S.; Gordan, V.V.; Litaker, M.S.; Funkhouser, E.; Fellows, J.; Shamp, D.; Qvist, V.; Meral, J.S.; Gilbert, G.H. A 24-month evaluation of amalgam and resin-based composite restorations. J. Am. Dent. Assoc. 2013, 144, 583–593. [Google Scholar] [CrossRef] [PubMed]
  65. Burke, F.J.; Lucarotti, P.S. The ultimate guide to restoration longevity in England and Wales. Part 4: resin composite restorations: time to next intervention and to extraction of the restored tooth. Br. Dent. J. 2018, 224, 945–946. [Google Scholar] [CrossRef] [PubMed]
  66. Van de Sande, F.H.; Opdam, N.J.; Rodolpho, P.A.; Correa, M.B.; Demarco, F.F.; Cenci, M.S. Patient risk factors' influence on survival of posterior composites. J. Dent. Res. 2013, 92, 78S–83S. [Google Scholar] [CrossRef] [PubMed]
  67. Koc, D.; Dogan, A.; Bek, B. Bite force and influential factors on bite force measurements: a literature review. Eur. J. Dent. 2010, 4, 223–232. [Google Scholar] [CrossRef] [PubMed]
  68. Silva, A.E.; Demarco, F.F.; Feldens, C.A. Oral health–related quality of life and associated factors in Southern Brazilian elderly. Gerodontology 2015, 32, 35–45. [Google Scholar] [CrossRef] [PubMed]
  69. Crocombe, L.A.; Broadbent, J.M.; Thomson, W.M.; Brennan, D.S.; Poulton, R. Impact of dental visiting trajectory patterns on clinical oral health and oral health-related quality of life. J. Public Health Dent. 2012, 72, 36–44. [Google Scholar] [CrossRef] [PubMed]
  70. Bauer, J.; Vasilache, I.; Schlegel, A.K.; et al. Esthetics and Psyque-Part 1: Assessment of the influence of patient perceptions of body image and body experience on selection of existing natural tooth color. Int. J. Prosthodont. 2012, 25, 36–43. [Google Scholar] [PubMed]
  71. Witt, M.; Flores-Mir, C. Laypeople’s preferences regarding frontal dentofacial esthetics: periodontal factors. J. Am. Dent. Assoc. 2011, 142, 925–937. [Google Scholar] [CrossRef] [PubMed]
  72. Gul-e-Erum; Fida, M. Changes in smile parameters as perceived by orthodontists, dentists, artists, and laypeople. World J. Orthod. 2008, 9, 132-140.
  73. Patzer, G. Understanding the causal relationship between physical attractiveness and self-esteem. J. Esthet. Dent. 1996, 3, 144–147. [Google Scholar] [CrossRef] [PubMed]
  74. Demarco, F.F.; Collares, K.; Correa, M.B.; Cenci, M.S.; Moraes, R.R.; Opdam, N.J. Should my composite restorations last forever? Why are they failing? Braz. Oral Res. 2017, 31, e56. [Google Scholar] [CrossRef] [PubMed]
  75. Camargo, M.B.J.; Dumith, S.C.; Barros, A.J. Regular use of dental care services by adults: patterns of utilization and types of services. Cad. Saude Publica 2009, 25, 1894–1906. [Google Scholar] [CrossRef] [PubMed]
  76. Correa, M.B.; Peres, M.A.; Peres, K.G.; Horta, B.L.; Barros, A.J.; Demarco, F.F. Do socioeconomic determinants affect the quality of posterior dental restorations? A multilevel approach. J. Dent. 2013, 41, 960–967. [Google Scholar] [CrossRef] [PubMed]
  77. Lucarotti, P.S.K.; Holder, R.L.; Burke, F.J.T. Outcome of direct restorations placed within the general dental services in England and Wales (Part 3): variation by dentist factors. J. Dent. 2005, 33, 827–835. [Google Scholar] [CrossRef] [PubMed]
  78. Burke, F.J.T.; Lucarotti, P.S.K. How long do direct restorations placed within the general dental services in England and Wales survive? Br. Dent. J. 2009, 206, E2. [Google Scholar] [CrossRef] [PubMed]
  79. Bader, J.D.; Shugars, D.A.; Rozier, G.; Lohr, K.N.; Bonito, A.J.; Nelson, J.P.; Jackman, A.M. Diagnosis and management of dental caries. Evid. Rep. Technol. Assess. 2001, 36, 1–4. [Google Scholar]
  80. Brouwer, F.; Askar, H.; Paris, S.; Schwendicke, F. Detecting secondary caries lesions: a systematic review and meta-analysis. J. Dent. Res. 2016, 95, 143–151. [Google Scholar] [CrossRef] [PubMed]
  81. Elderton, R.J. The quality of amalgam restorations. Assess. Qual. Dent. Care 1977, 45–81. [Google Scholar] [CrossRef]
  82. Elderton, R.J.; Nuttall, N.M. Variation among dentists in planning treatment. Br. Dent. J. 1983, 154, 201–206. [Google Scholar] [CrossRef] [PubMed]
  83. Davies, J.A. The relationship between change of dentist and treatment received in the General Dental Service. Br. Dent. J. 1984, 157, 322–324. [Google Scholar] [CrossRef] [PubMed]
  84. Boyd, M.A. Amalgam replacement: are decisions based on fact or tradition. Qual. Eval. Dent. Restor. Criteria Placement Replace. 1989, 73–82. [Google Scholar]
  85. Bader, J.D.; Shugars, D.A. Understanding dentists' restorative treatment decisions. J. Public Health Dent. 1992, 52, 102–110. [Google Scholar] [CrossRef] [PubMed]
  86. Gordan, V.V.; Riley, J.L., III; Geraldeli, S.; Rindal, D.B.; Qvist, V.; Fellows, J.L.; ... & Dental Practice-Based Research Network lareslaborative Group. Repair or replacement of defective restorations by dentists in The Dental Practice-Based Research Network. J. Am. Dent. Assoc. 2012, 143, 593-601. [CrossRef]
  87. Soncini, J.A.; Maserejian, N.N.; Trachtenberg, F.; Tavares, M.; Hayes, C. The longevity of amalgam versus compomer/composite restorations in posterior primary and permanent teeth: findings From the New England Children's Amalgam Trial. J. Am. Dent. Assoc. 2007, 138, 763–772. [Google Scholar] [CrossRef] [PubMed]
  88. Simecek, J.W.; Diefenderfer, K.E.; Cohen, M.E. An evaluation of replacement rates for posterior resin-based composite and amalgam restorations in US Navy and marine corps recruits. J. Am. Dent. Assoc. 2009, 140, 200–209. [Google Scholar] [CrossRef] [PubMed]
  89. Van Nieuwenhuysen, J.P.; D'Hoore, W.; Carvalho, J.; Qvist, V. Long-term evaluation of extensive restorations in permanent teeth. J. Dent. 2003, 31, 395–405. [Google Scholar] [CrossRef] [PubMed]
  90. Samaha, S.; Bhatt, S.; Finkelman, M.; Papathanasiou, A.; Perry, R.; Strassler, H.; Kugel, G.; Garcia-Godoy, F.; Price, R. Effect of instruction, light curing unit, and location in the mouth on the energy delivered to simulated restorations. Am. J. Dent. 2017, 30, 343–349. [Google Scholar] [PubMed]
  91. Ferracane, J.L.; Lawson, N.C. Probing the hierarchy of evidence to identify the best strategy for placing class II dental composite restorations using current materials. J. Esthet. Restor. Dent. 2021, 33, 39–50. [Google Scholar] [CrossRef] [PubMed]
  92. Karacolak, G.; Turkun, L.S.; Boyacioglu, H.; Ferracane, J.L. Influence of increment thickness on radiant energy and microhardness of bulk-fill resin composites. Dent. Mater. J. 2018, 37, 206–213. [Google Scholar] [CrossRef] [PubMed]
  93. Jandt, K.D.; Mills, R.W. A brief history of LED photopolymerization. Dent. Mater. 2013, 29, 605–617. [Google Scholar] [CrossRef] [PubMed]
  94. Brambilla, E.; Gagliani, M.; Ionescu, A.; Fadini, L.; García-Godoy, F. The influence of light-curing time on the bacterial colonization of resin composite surfaces. Dent. Mater. 2009, 25, 1067–1072. [Google Scholar] [CrossRef] [PubMed]
  95. Fan, P.L.; Schumacher, R.M.; Azzolin, K.; Geary, R.; Eichmiller, F.C. Curing-light intensity and depth of cure of resin-based composites tested according to international standards. J. Am. Dent. Assoc. 2002, 133, 429–434. [Google Scholar] [CrossRef] [PubMed]
  96. Al-Zain, A.O.; Platt, J.A. Effect of light-curing distance and curing time on composite microflexural strength. Dent. Mater. J. 2021, 40, 202–208. [Google Scholar] [CrossRef]
  97. Par, M.; Repusic, I.; Skenderovic, H.; Milat, O.; Spajic, J.; Tarle, Z. The effects of extended curing time and radiant energy on microhardness and temperature rise of conventional and bulk-fill resin composites. Clin. Oral Investig. 2019, 23, 3777–3788. [Google Scholar] [CrossRef] [PubMed]
  98. Leprince, J.G.; Palin, W.M.; Hadis, M.A.; Devaux, J.; Leloup, G. Progress in dimethacrylate-based dental composite technology and curing efficiency. Dent. Mater. 2013, 29, 139–156. [Google Scholar] [CrossRef] [PubMed]
  99. Hussain, M.; Wang, Y. Influence of prolonged light-curing time on the shear bonding strength of resin to bleached enamel. Oper. Dent. 2010, 35, 672–681. [Google Scholar] [CrossRef]
  100. Kopperud, S.E.; Rukke, H.V.; Kopperud, H.M.; Bruzell, E.M. Light curing procedures-performance, knowledge level and safety awareness among dentists. J. Dent. 2017, 58, 67–73. [Google Scholar] [CrossRef] [PubMed]
  101. Maktabi, H.; Balhaddad, A.A.; Alkhubaizi, Q.; Strassler, H.; Melo, M.A.S. Factors influencing success of radiant exposure in light-curing posterior dental composite in the clinical setting. Am. J. Dent. 2018, 31, 320–328. [Google Scholar] [PubMed]
  102. Eshmawi, Y.T.; Al-Zain, A.O.; Eckert, G.J.; Platt, J.A. Variation in composite degree of conversion and microflexural strength for different curing lights and surface locations. J. Am. Dent. Assoc. 2018, 149, 893–902. [Google Scholar] [CrossRef] [PubMed]
  103. Janda, R.; Roulet, J.F.; Latta, M.; Steffin, G.; Rüttermann, S. Color stability of resin-based filling materials after aging when cured with plasma or halogen light. Eur. J. Oral Sci. 2005, 113, 251–257. [Google Scholar] [CrossRef] [PubMed]
  104. Maktabi, H.; Ibrahim, M.; Alkhubaizi, Q.; Weir, M.; Xu, H.; Strassler, H.; Melo, M.A.S. Underperforming light curing procedures trigger detrimental irradiance-dependent biofilm response on incrementally placed dental composites. J. Dent. 2019, 88, 103110. [Google Scholar] [CrossRef] [PubMed]
  105. Ciccone-Nogueira, J.C.; Borsatto, M.C.; Souza-Zaron, W.C.D.; Ramos, R.P.; Palma-Dibb, R.G. Microhardness of composite resins at different depths varying the post-irradiation time. J. Appl. Oral Sci. 2007, 15, 305–309. [Google Scholar] [CrossRef] [PubMed]
  106. Aggarwal, N.; Jain, A.; Gupta, H.; Abrol, A.; Singh, C.; Rapgay, T. The comparative evaluation of depth of cure of bulk-fill composites–An in vitro study. J. Conserv. Dent. Endod. 2019, 22, 371–375. [Google Scholar] [CrossRef]
  107. Da Silva Pereira, R.A.; da Silva, G.R.; Barcelos, L.M.; Cavalcanti, K.G.B.A.; Herval, Á.M.; Ardenghi, T.M.; Soares, C.J. Practice-based analysis of direct posterior dental restorations performed in a public health service: Retrospective long-term survival in Brazil. PLoS ONE 2020, 15, e0243288. [Google Scholar] [CrossRef] [PubMed]
  108. Frankenberger, R.; Reinelt, C.; Petschelt, A.; Krämer, N. Operator vs. material influence on clinical outcome of bonded ceramic inlays. Dent. Mater. 2009, 25, 960–968. [Google Scholar] [CrossRef]
  109. Morgano, S.M.; Rodrigues, A.H.; Sabrosa, C.E. Restoration of endodontically treated teeth. Dent. Clin. N. Am. 2004, 48, 397–416. [Google Scholar] [CrossRef] [PubMed]
  110. Opdam, N.J.; Bronkhorst, E.M.; Loomans, B.A.; Huysmans, M.C. 12-year survival of composite vs. amalgam restorations. J. Dent. Res. 2010, 89, 1063–1067. [Google Scholar] [CrossRef]
  111. Trushkowsky, R.D. Restoration of endodontically treated teeth: criteria and technique considerations. Quintessence Int. 2014, 45, 557–567. [Google Scholar] [CrossRef] [PubMed]
  112. Kawata, T.; Kawaguchi, T.; Yoda, N.; Ogawa, T.; Kuriyagawa, T.; Sasaki, K. Effects of a removable partial denture and its rest location on the forces exerted on an abutment tooth in vivo. Int. J. Prosthodont. 2008, 21, 50–52. [Google Scholar] [PubMed]
  113. Kramer, N.; Garcia-Godoy, F.; Reinelt, C.; Feilzer, A.J.; Frankenberger, R. Nanohybrid vs. fine hybrid composite in extended class II cavities after six years. Dent. Mater. 2011, 27, 455–464. [Google Scholar] [CrossRef] [PubMed]
  114. Manhart, J.; Chen, H.Y.; Hickel, R. Clinical evaluation of the posterior composite Quixfil in class I and II cavities: 4-year follow-up of a randomized controlled trial. J. Adhes. Dent. 2010, 12, 237–243. [Google Scholar] [CrossRef] [PubMed]
  115. Plasmans, P.J.; van ’t Hof, M.A. A 4-year clinical evaluation of extensive amalgam restorations description of the failures. J. Oral Rehabil. 1993, 20, 561–570. [Google Scholar] [CrossRef]
  116. Shi, L.; Wang, X.; Zhao, Q.; Zhang, Y.; Zhang, L.; Ren, Y. Evaluation of packable and conventional hybrid resin composites in class I restorations: three-year results of a randomized, double-blind and controlled clinical trial. Oper. Dent. 2010, 35, 11–19. [Google Scholar] [CrossRef] [PubMed]
  117. Akerboom, H.B.; Advokaat, J.G.; van Amerongen, W.E.; Borgmeijer, P.J. Long-term evaluation and restoration of amalgam restorations. Community Dent. Oral Epidemiol. 1993, 21, 45–48. [Google Scholar] [CrossRef]
  118. Kiremitci, A.; Alpaslan, T.; Gurgan, S. Six-year clinical evaluation of packable composite restorations. Oper. Dent. 2009, 34, 11–17. [Google Scholar] [CrossRef] [PubMed]
  119. Kohler, B.; Rasmusson, C.G.; Odman, P. A five-year clinical evaluation of class II composite resin restorations. J. Dent. 2000, 28, 111–116. [Google Scholar] [CrossRef] [PubMed]
  120. Kopperud, S.E.; Tveit, A.B.; Gaarden, T.; Sandvik, L.; Espelid, I. Longevity of posterior dental restorations and reasons for failure. Eur. J. Oral Sci. 2012, 120, 539–548. [Google Scholar] [CrossRef] [PubMed]
  121. Lin, H.; Wang, J.; Yan, W. [A three-year clinical evaluation of five light-cured composite resins in fillings of posterior teeth]. Zhonghua Kou Qiang Yi Xue Za Zhi 1997, 32, 242–245. [Google Scholar] [PubMed]
  122. Mjor, I.A.; Jokstad, A. Five-year study of Class II restorations in permanent teeth using amalgam, glass polyalkenoate (ionomer) cement and resin-based composite materials. J. Dent. 1993, 21, 338–343. [Google Scholar] [CrossRef] [PubMed]
  123. Burke, F.J.; Lucarotti, P.S. The ultimate guide to restoration longevity in England and Wales. Part 10: key findings from a ten million restoration dataset. Br. Dent. J. 2018, 225, 1011–1016. [Google Scholar] [CrossRef] [PubMed]
  124. del Aguila, M.A.; Leggott, P.J.; Robertson, P.B.; Porterfield, D.L.; Felber, G.D. Practice patterns among male and female general dentists in a Washington State population. J. Am. Dent. Assoc. 2005, 136, 790–796. [Google Scholar] [CrossRef] [PubMed]
  125. Walton, S.M.; Byck, G.R.; Cooksey, J.A.; Kaste, L.M. Assessing differences in hours worked between male and female dentists: an analysis of cross-sectional national survey data from 1979 through 1999. J. Am. Dent. Assoc. 2004, 135, 637–645. [Google Scholar] [CrossRef] [PubMed]
  126. Ayers, K.M.; Thomson, W.M.; Rich, A.M.; Newton, J.T. Gender differences in dentists’ working practices and job satisfaction. J. Dent. 2008, 36, 343–350. [Google Scholar] [CrossRef] [PubMed]
  127. Newton, J.T.; Buck, D.; Gibbons, D.E. Workforce planning in dentistry: the impact of shorter and more varied career patterns. Community Dent. Health 2001, 18, 236–241. [Google Scholar] [PubMed]
  128. Coppola, M.N.; Ozcan, Y.A.; Bogacki, R. Evaluation of performance of dental providers on posterior restorations: does experience matter? A data envelopment analysis (DEA) approach. J. Med. Syst. 2003, 27, 445–456. [Google Scholar] [CrossRef] [PubMed]
  129. Collares, K.; Opdam, N.J.; Laske, M.; Bronkhorst, E.M.; Demarco, F.F.; Correa, M.B.; et al. Longevity of anterior composite restorations in a general dental practice-based network. J. Dent. Res. 2017, 96, 1092–1099. [Google Scholar] [CrossRef] [PubMed]
  130. Mondelli, J.; Steagall, L.; Ishikiriama, A.; de Lima Navarro, M.F.; Soares, F.B. Fracture strength of human teeth with cavity preparations. J. Prosthet. Dent. 1980, 43, 419–422. [Google Scholar] [CrossRef] [PubMed]
  131. González-López, S.; De Haro-Gasquet, F.; Vílchez-Díaz, M.A.; Ceballos, L.; Bravo, M. Effect of restorative procedures and occlusal loading on cuspal deflection. Oper. Dent. 2006, 31, 33–38. [Google Scholar] [CrossRef] [PubMed]
  132. Gabel, A.B. The American textbook of operative dentistry. 1954.
  133. Rocca, G.T.; Krejci, I. Crown and post-free adhesive restorations for endodontically treated posterior teeth: from direct composite to endocrowns. Eur. J. Esthet. Dent. 2013, 8, 156–179. [Google Scholar] [PubMed]
  134. Moura, F.R.; Romano, A.R.; Lund, R.G.; Piva, E.; Rodrigues Junior, S.A.; Demarco, F.F. Three-year clinical performance of composite restorations placed by undergraduate dental students. Braz. Dent. J. 2011, 22, 111–116. [Google Scholar] [CrossRef] [PubMed]
  135. Afrashtehfar, K.I.; Emami, E.; Ahmadi, M.; Eilayyan, O.; Abi-Nader, S.; Tamimi, F. Failure rate of single-unit restorations on posterior vital teeth: A systematic review. J. Prosthet. Dent. 2017, 117, 345–353. [Google Scholar] [CrossRef] [PubMed]
  136. Da Rosa Rodolpho, P.A.; Cenci, M.S.; Donassollo, T.A.; Loguercio, A.D.; Demarco, F.F. A clinical evaluation of posterior composite restorations: 17-year findings. J. Dent. 2006, 34, 427–435. [Google Scholar] [CrossRef] [PubMed]
  137. Beck, F.; Lettner, S.; Graf, A.; Bitriol, B.; Dumitrescu, N.; Bauer, P.; Moritz, A.; Schedle, A. Survival of direct resin restorations in posterior teeth within a 19-year period (1996-2015): A meta-analysis of prospective studies. Dent. Mater. 2015, 31, 958–985. [Google Scholar] [CrossRef] [PubMed]
  138. Kang, S.H.; Kim, B.S.; Kim, Y. Cracked teeth: Distribution, characteristics, and survival after root canal treatment. J. Endod. 2016, 42, 557–562. [Google Scholar] [CrossRef] [PubMed]
  139. Nuamwisudhi, P.; Jearanaiphaisarn, T. Oral functional behaviors and tooth factors associated with cracked teeth in asymptomatic patients. J. Endod. 2021, 47, 1383–1390. [Google Scholar] [CrossRef] [PubMed]
  140. Auschill, T.M.; Koch, C.A.; Wolkewitz, M.; Hellwig, E.; Arweiler, N.B. Occurrence and causing stimuli of postoperative sensitivity in composite restorations. Oper. Dent. 2009, 34, 3–10. [Google Scholar] [CrossRef] [PubMed]
  141. Reeh, E.S.; Messer, H.H.; Douglas, W.H. Reduction in tooth stiffness as a result of endodontic and restorative procedures. J. Endod. 1989, 15, 512–516. [Google Scholar] [CrossRef] [PubMed]
  142. Bhuva, B.; Giovarruscio, M.; Rahim, N.; Bitter, K.; Mannocci, F. The restoration of root filled teeth: a review of the clinical literature. Int. Endod. J. 2021, 54, 509–535. [Google Scholar] [CrossRef] [PubMed]
  143. Raedel, M.; Hartmann, A.; Bohm, S.; Priess, H.W.; Samietz, S.; Konstantinidis, I.; Walter, M.H. Four-year outcomes of restored posterior tooth surfaces—a massive data analysis. Clin. Oral Investig. 2017, 21, 2819–2825. [Google Scholar] [CrossRef] [PubMed]
  144. Rodolpho, P.A.D.R.; Rodolfo, B.; Collares, K.; Correa, M.B.; Demarco, F.F.; Opdam, N.J.; et al. Clinical performance of posterior resin composite restorations after up to 33 years. Dent. Mater. 2022, 38, 680–688. [Google Scholar] [CrossRef] [PubMed]
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