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The influence of the gingival phenotype on implant survival rate and clinical parameters: a systematic review.
Q3 Dentistry Pub Date : 2025-02-05 DOI: 10.1038/s41432-025-01114-x
Diego Marques da Silva, Filipe Castro, Bruno Martins, Javier Flores Fraile, Juliana Campos Hasse Fernandes, Gustavo Vicentis Oliveira Fernandes

Objective: The goal of this systematic review was to verify whether the gingival phenotype (thick or thin) could impact the dental implant survival rate by affecting the marginal bone.

Methods: The search was carried out on PubMed/MedLine, PubMed Central, and B-On databases. The research question was: "Does gingival phenotype positively or negatively influence marginal bone loss around dental implants?" The inclusion criteria were: any clinical trial/study, comparative study, prospective or retrospective articles, systematic review that addressed at least a 1-year follow-up with an assessment of the marginal bone loss (MBL) around dental implants, articles that reported the gingival phenotype (thin or thick) and were published in the last 13 years. The exclusion criteria were narrative or other reviews, letters to the editor, and commentaries. Data extraction included the author's name, year of publication, type of study, sample size, number of implants, method used, and outcomes presented. The extracted data was summarized and presented in the results section. Critical Appraisal tool in JBI Systematic Reviews was used to determine the possibility of bias.

Results: A total of 62 articles were found, but eight articles were relevant to compose this study. After deep evaluation, it was possible to observe the implant success rate for both gingival phenotypes, thin and thick, was greater than 91% within a follow-up of up to 5 years. Therefore, it is unclear whether the thickness of the gingival tissue surrounding the implant can directly influence the marginal bone level. The gingival phenotype may be indirectly involved in the survival rate of dental implants, as it can be a risk factor for peri-implantitis, leading to marginal bone loss beyond what is expected.

Discussion: The thin gingival phenotype is one of the main risk factors for additional bone loss. It is crucial to know how to preserve the healthy condition.

Conclusion: Within the results found, the gingival phenotype is indirectly related to implant survival rate and clinical parameters, which were respectively high and non-conclusive. Therefore, a higher risk of peri-implantitis is suggested when a thin phenotype is present.

{"title":"The influence of the gingival phenotype on implant survival rate and clinical parameters: a systematic review.","authors":"Diego Marques da Silva, Filipe Castro, Bruno Martins, Javier Flores Fraile, Juliana Campos Hasse Fernandes, Gustavo Vicentis Oliveira Fernandes","doi":"10.1038/s41432-025-01114-x","DOIUrl":"https://doi.org/10.1038/s41432-025-01114-x","url":null,"abstract":"<p><strong>Objective: </strong>The goal of this systematic review was to verify whether the gingival phenotype (thick or thin) could impact the dental implant survival rate by affecting the marginal bone.</p><p><strong>Methods: </strong>The search was carried out on PubMed/MedLine, PubMed Central, and B-On databases. The research question was: \"Does gingival phenotype positively or negatively influence marginal bone loss around dental implants?\" The inclusion criteria were: any clinical trial/study, comparative study, prospective or retrospective articles, systematic review that addressed at least a 1-year follow-up with an assessment of the marginal bone loss (MBL) around dental implants, articles that reported the gingival phenotype (thin or thick) and were published in the last 13 years. The exclusion criteria were narrative or other reviews, letters to the editor, and commentaries. Data extraction included the author's name, year of publication, type of study, sample size, number of implants, method used, and outcomes presented. The extracted data was summarized and presented in the results section. Critical Appraisal tool in JBI Systematic Reviews was used to determine the possibility of bias.</p><p><strong>Results: </strong>A total of 62 articles were found, but eight articles were relevant to compose this study. After deep evaluation, it was possible to observe the implant success rate for both gingival phenotypes, thin and thick, was greater than 91% within a follow-up of up to 5 years. Therefore, it is unclear whether the thickness of the gingival tissue surrounding the implant can directly influence the marginal bone level. The gingival phenotype may be indirectly involved in the survival rate of dental implants, as it can be a risk factor for peri-implantitis, leading to marginal bone loss beyond what is expected.</p><p><strong>Discussion: </strong>The thin gingival phenotype is one of the main risk factors for additional bone loss. It is crucial to know how to preserve the healthy condition.</p><p><strong>Conclusion: </strong>Within the results found, the gingival phenotype is indirectly related to implant survival rate and clinical parameters, which were respectively high and non-conclusive. Therefore, a higher risk of peri-implantitis is suggested when a thin phenotype is present.</p>","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143255105","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Second chances for smiles: a systematic review of implants in failed sites.
Q3 Dentistry Pub Date : 2025-02-05 DOI: 10.1038/s41432-025-01113-y
Sundas Jamil

Aim: It has been proven that implants are predictable substitutes for replacing teeth. However, the effectiveness and survival of implants placed in sites previously affected by failure, as well as the optimal treatment strategies, remain poorly defined. This systematic review aimed to evaluate implant survival and peri-implant health in such cases, focusing on comparing immediate versus delayed implant placement and the role of augmentation. Four electronic databases were systematically searched, and meta-analyses were conducted with subgroup analyses (PROSPERO CRD42024548610). Of 1,798 records identified, 24 studies met the inclusion criteria.

Results: The 1-year survival rate for implants placed as replacements was 96.7% (95% CI: 92.8-99.3%). No significant differences were found between immediate and delayed placement (P = 0.31), or between immediate and delayed augmentation (P = 0.85). Although implants with immediate augmentation showed a higher survival rate (97.6%, 95% CI: 93.4-99.9%) compared to those with delayed augmentation (91.7%, 95% CI: 83.4-97.5%), this difference was not statistically significant (P = 0.26). Peri-implant health outcomes, including marginal bone loss, were consistent across subgroups.

Conclusion: Replacing failed implants is often an attractive treatment option. While implants placed as replacements generally have lower survival rates compared to primary implants, immediate implant placement remains a viable option when adequate bone volume is present. The review supports the effectiveness of implant re-placement, with generally favourable.

Clinical relevance: Dental implants are widely used for replacing missing teeth, but implant failure is a known complication. Understanding the outcomes of implants placed in sites where implants have failed is important as this situation can present challenges, such as insufficient bone or altered soft tissue conditions. This article provides data on the survival and health outcomes of implants placed in these failed sites, which may provide benefit to clinicians in these scenarios.

{"title":"Second chances for smiles: a systematic review of implants in failed sites.","authors":"Sundas Jamil","doi":"10.1038/s41432-025-01113-y","DOIUrl":"https://doi.org/10.1038/s41432-025-01113-y","url":null,"abstract":"<p><strong>Aim: </strong>It has been proven that implants are predictable substitutes for replacing teeth. However, the effectiveness and survival of implants placed in sites previously affected by failure, as well as the optimal treatment strategies, remain poorly defined. This systematic review aimed to evaluate implant survival and peri-implant health in such cases, focusing on comparing immediate versus delayed implant placement and the role of augmentation. Four electronic databases were systematically searched, and meta-analyses were conducted with subgroup analyses (PROSPERO CRD42024548610). Of 1,798 records identified, 24 studies met the inclusion criteria.</p><p><strong>Results: </strong>The 1-year survival rate for implants placed as replacements was 96.7% (95% CI: 92.8-99.3%). No significant differences were found between immediate and delayed placement (P = 0.31), or between immediate and delayed augmentation (P = 0.85). Although implants with immediate augmentation showed a higher survival rate (97.6%, 95% CI: 93.4-99.9%) compared to those with delayed augmentation (91.7%, 95% CI: 83.4-97.5%), this difference was not statistically significant (P = 0.26). Peri-implant health outcomes, including marginal bone loss, were consistent across subgroups.</p><p><strong>Conclusion: </strong>Replacing failed implants is often an attractive treatment option. While implants placed as replacements generally have lower survival rates compared to primary implants, immediate implant placement remains a viable option when adequate bone volume is present. The review supports the effectiveness of implant re-placement, with generally favourable.</p><p><strong>Clinical relevance: </strong>Dental implants are widely used for replacing missing teeth, but implant failure is a known complication. Understanding the outcomes of implants placed in sites where implants have failed is important as this situation can present challenges, such as insufficient bone or altered soft tissue conditions. This article provides data on the survival and health outcomes of implants placed in these failed sites, which may provide benefit to clinicians in these scenarios.</p>","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143255101","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effectiveness of school-based approaches for reduction of sugar and sugar-sweetened beverages in children: a systematic review and meta-analysis.
Q3 Dentistry Pub Date : 2025-02-05 DOI: 10.1038/s41432-024-01103-6
Sneha Malhotra, Deepali Aggarwal, Bharathi M Purohit, Rahul Morankar, Amrita Chawla, Ritu Duggal, Nilima Nilima, Upendra Singh Bhadauria, Manali Deb Barma, Harsh Priya

Objective: To verify the effectiveness of school-based interventions (SBI) aimed at reducing sugar-sweetened beverage (SSB) consumption among children to create or enhance public health initiatives.

Background: An important source of sugar consumption is SSBs, which are defined as any consumable non-alcoholic water-based beverage containing considerable amounts of free sugars. A growing number of people are using SSBs as their main source of sugar. Obesity and overweight in children and adolescents is a serious public health concern. The frequent consumption of excess amounts of SSBs is a risk factor for obesity, type 2 diabetes, cardiovascular disease and dental caries. The majority of earlier studies have concentrated on the association between SSB intake and obesity, regulatory and policy initiatives on SSB purchase and consumption. Numerous behavioural interventions have been reported to target the reduction of sugary drink consumption among children; however, there is a lack of conclusive evidence regarding their effectiveness. We aimed to evaluate the effectiveness of SBI on the factors that influence the reduction of sugary beverage consumption in a school setting.

Material and methods: Systematic review of school-based interventions involving children.

Setting: The following databases were investigated: MEDLINE/PubMed, PsycINFO, CINAHL and EMBASE.

Results: A total of forty-seven studies were included in the review. Most of the studies were found to be of moderate quality. All of the interventions, irrespective of whether they targeted individuals, their environment or both, were effective in decreasing SSB consumption.

Conclusions: School-based interventions have demonstrated encouraging outcomes in decreasing sugary soft drink intake among teenagers. Several recommendations are made to improve future studies. The included trials demonstrated a moderate quality of evidence, suggesting that educational and behavioural interventions yielded only a modest effect in reducing sugar-sweetened beverage (SSB) consumption.

{"title":"Effectiveness of school-based approaches for reduction of sugar and sugar-sweetened beverages in children: a systematic review and meta-analysis.","authors":"Sneha Malhotra, Deepali Aggarwal, Bharathi M Purohit, Rahul Morankar, Amrita Chawla, Ritu Duggal, Nilima Nilima, Upendra Singh Bhadauria, Manali Deb Barma, Harsh Priya","doi":"10.1038/s41432-024-01103-6","DOIUrl":"https://doi.org/10.1038/s41432-024-01103-6","url":null,"abstract":"<p><strong>Objective: </strong>To verify the effectiveness of school-based interventions (SBI) aimed at reducing sugar-sweetened beverage (SSB) consumption among children to create or enhance public health initiatives.</p><p><strong>Background: </strong>An important source of sugar consumption is SSBs, which are defined as any consumable non-alcoholic water-based beverage containing considerable amounts of free sugars. A growing number of people are using SSBs as their main source of sugar. Obesity and overweight in children and adolescents is a serious public health concern. The frequent consumption of excess amounts of SSBs is a risk factor for obesity, type 2 diabetes, cardiovascular disease and dental caries. The majority of earlier studies have concentrated on the association between SSB intake and obesity, regulatory and policy initiatives on SSB purchase and consumption. Numerous behavioural interventions have been reported to target the reduction of sugary drink consumption among children; however, there is a lack of conclusive evidence regarding their effectiveness. We aimed to evaluate the effectiveness of SBI on the factors that influence the reduction of sugary beverage consumption in a school setting.</p><p><strong>Material and methods: </strong>Systematic review of school-based interventions involving children.</p><p><strong>Setting: </strong>The following databases were investigated: MEDLINE/PubMed, PsycINFO, CINAHL and EMBASE.</p><p><strong>Results: </strong>A total of forty-seven studies were included in the review. Most of the studies were found to be of moderate quality. All of the interventions, irrespective of whether they targeted individuals, their environment or both, were effective in decreasing SSB consumption.</p><p><strong>Conclusions: </strong>School-based interventions have demonstrated encouraging outcomes in decreasing sugary soft drink intake among teenagers. Several recommendations are made to improve future studies. The included trials demonstrated a moderate quality of evidence, suggesting that educational and behavioural interventions yielded only a modest effect in reducing sugar-sweetened beverage (SSB) consumption.</p>","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143255084","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Do implant overdentures improve chewing ability and quality of life despite no effect on nutritional status?
Q3 Dentistry Pub Date : 2025-02-01 DOI: 10.1038/s41432-025-01107-w
Nithya Nandhini, Praveen Chandrashekaraiah, Reshma Benzigar, Ramya Shivananjan, A Selva Arockiam

Data sources: This prospective study involved 35 edentulous adults aged 50 years and older, treated at a dental clinic. Data were collected across four time points: baseline (T0), 3 months post-application of conventional complete dentures (CD; T1), and 3 and 6 months after the transition to implant-supported overdentures (IOD; T2 and T3). Patient outcomes were assessed using: Mini Nutritional Assessment (MNA): To evaluate nutritional status, Oral Health Impact Profile (OHIP-14): To measure oral health-related quality of life (OHRQoL) and Chewing Ability Questionnaire: To document functional improvements.

Results: Mini Nutritional Assessment (MNA) scores declined initially after transitioning to CDs (T0-T1) but stabilized following implant overdenture placement. Significant improvements were reported, with chewing difficulty decreasing from 91.4% at baseline to 51.4% at T3. Marked enhancements in OHIP-14 scores at T2 and T3, indicating better oral health perception.

Conclusion: While implant overdentures significantly improved chewing ability and quality of life, they did not lead to measurable improvements in nutritional status. The findings highlight the functional and psychosocial benefits of implant overdentures for older adults, suggesting that oral rehabilitation enhances overall well-being even without direct nutritional effects. This study provides a moderate level of evidence based on its prospective design, validated outcome measures, and clear findings related to chewing ability and oral health-related quality of life. However, the small sample size, lack of long-term follow-up, and absence of significant improvements in nutritional status suggest the need for further research to validate and strengthen these findings. Future studies with larger populations and extended observation perimplant overdentures are essential to enhance the robustness and generalizability of the evidence.

{"title":"Do implant overdentures improve chewing ability and quality of life despite no effect on nutritional status?","authors":"Nithya Nandhini, Praveen Chandrashekaraiah, Reshma Benzigar, Ramya Shivananjan, A Selva Arockiam","doi":"10.1038/s41432-025-01107-w","DOIUrl":"https://doi.org/10.1038/s41432-025-01107-w","url":null,"abstract":"<p><strong>Data sources: </strong>This prospective study involved 35 edentulous adults aged 50 years and older, treated at a dental clinic. Data were collected across four time points: baseline (T0), 3 months post-application of conventional complete dentures (CD; T1), and 3 and 6 months after the transition to implant-supported overdentures (IOD; T2 and T3). Patient outcomes were assessed using: Mini Nutritional Assessment (MNA): To evaluate nutritional status, Oral Health Impact Profile (OHIP-14): To measure oral health-related quality of life (OHRQoL) and Chewing Ability Questionnaire: To document functional improvements.</p><p><strong>Results: </strong>Mini Nutritional Assessment (MNA) scores declined initially after transitioning to CDs (T0-T1) but stabilized following implant overdenture placement. Significant improvements were reported, with chewing difficulty decreasing from 91.4% at baseline to 51.4% at T3. Marked enhancements in OHIP-14 scores at T2 and T3, indicating better oral health perception.</p><p><strong>Conclusion: </strong>While implant overdentures significantly improved chewing ability and quality of life, they did not lead to measurable improvements in nutritional status. The findings highlight the functional and psychosocial benefits of implant overdentures for older adults, suggesting that oral rehabilitation enhances overall well-being even without direct nutritional effects. This study provides a moderate level of evidence based on its prospective design, validated outcome measures, and clear findings related to chewing ability and oral health-related quality of life. However, the small sample size, lack of long-term follow-up, and absence of significant improvements in nutritional status suggest the need for further research to validate and strengthen these findings. Future studies with larger populations and extended observation perimplant overdentures are essential to enhance the robustness and generalizability of the evidence.</p>","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074399","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
What are the success rates of anterior restorations used in localised wear cases?
Q3 Dentistry Pub Date : 2025-02-01 DOI: 10.1038/s41432-025-01112-z
Bryan Murchie, Nikita Jiwan, David Edwards
<p><strong>Objective: </strong>A systematic review and meta-analysis of the literature was carried out assessing the success and survival rate of anterior restorations used in localised wear cases. This also included assessment of posterior teeth re-establishing occlusal contact following use of the Dahl approach.</p><p><strong>Data sources: </strong>Two large databases; Medline via OVID, and Scopus were used to identify existing literature. The review followed Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) and Meta-analyses guidelines and used the PIO framework [1]. Grey literature was also searched.</p><p><strong>Study selection: </strong>Publications written in English were included between Jan 1970 and Nov 2020.</p><p><strong>Population: </strong>participants with localised anterior tooth loss.</p><p><strong>Intervention: </strong>anterior composite restorations.</p><p><strong>Outcome: </strong>success and survival rates of the composite restorations. Six cohort studies were included in the final analysis, with three prospective and three retrospective. These studies evaluated the success and survival rates of direct and indirect composite restorations, with a follow-up period ranging from 5 months to 10 years, which took place between 2000 to 2016.</p><p><strong>Data extraction and synthesis: </strong>Extracted data included: author(s) and year, study type, number and age of participants, number of restorations, location for intervention, type of intervention (direct vs indirect), type of composite, increase in OVD (amount of increase and period to re-establish posterior occlusion), follow up period, definition of failure, number of failed restorations, assessment of intervention and longevity/survival rate. Risk of bias in individual studies was assessed using The Newcastle Ottawa quality assessment scale (NOS) for cohort studies. Outcome measures were standardised as success or survival: Success - restoration assigned category A on the modified US Public Health Service (USPHS) criteria. Survival - restoration assigned category A or B on the modified USPHS criteria. The restoration was considered a failure if any other grades were allocated on the modified USPHS criteria. Results were visualised using forest plots. Heterogeneity between studies was measured by I-squared statistic. Sensitivity analysis was performed for each outcome.</p><p><strong>Results: </strong>The survival rates for composite restorations (direct and indirect) at 2-10 years follow-up was 88% (95% CI, 70-90%; I<sup>2</sup> = 97%). When significant outliers from one study were removed, and re-analysed, the survival rates increased to 93% at 2-7 years follow-up (95% CI, 85-98%; I<sup>2</sup> = 83%). Success rates for composite restorations over the same 2-10 year period was 68% (95% CI, 44-87%; I<sup>2</sup> = 98%). Heterogeneity was generally considered high due to large variations in study design, sample size, type of intervention, and follow
{"title":"What are the success rates of anterior restorations used in localised wear cases?","authors":"Bryan Murchie, Nikita Jiwan, David Edwards","doi":"10.1038/s41432-025-01112-z","DOIUrl":"https://doi.org/10.1038/s41432-025-01112-z","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;A systematic review and meta-analysis of the literature was carried out assessing the success and survival rate of anterior restorations used in localised wear cases. This also included assessment of posterior teeth re-establishing occlusal contact following use of the Dahl approach.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Data sources: &lt;/strong&gt;Two large databases; Medline via OVID, and Scopus were used to identify existing literature. The review followed Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) and Meta-analyses guidelines and used the PIO framework [1]. Grey literature was also searched.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study selection: &lt;/strong&gt;Publications written in English were included between Jan 1970 and Nov 2020.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Population: &lt;/strong&gt;participants with localised anterior tooth loss.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Intervention: &lt;/strong&gt;anterior composite restorations.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Outcome: &lt;/strong&gt;success and survival rates of the composite restorations. Six cohort studies were included in the final analysis, with three prospective and three retrospective. These studies evaluated the success and survival rates of direct and indirect composite restorations, with a follow-up period ranging from 5 months to 10 years, which took place between 2000 to 2016.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Data extraction and synthesis: &lt;/strong&gt;Extracted data included: author(s) and year, study type, number and age of participants, number of restorations, location for intervention, type of intervention (direct vs indirect), type of composite, increase in OVD (amount of increase and period to re-establish posterior occlusion), follow up period, definition of failure, number of failed restorations, assessment of intervention and longevity/survival rate. Risk of bias in individual studies was assessed using The Newcastle Ottawa quality assessment scale (NOS) for cohort studies. Outcome measures were standardised as success or survival: Success - restoration assigned category A on the modified US Public Health Service (USPHS) criteria. Survival - restoration assigned category A or B on the modified USPHS criteria. The restoration was considered a failure if any other grades were allocated on the modified USPHS criteria. Results were visualised using forest plots. Heterogeneity between studies was measured by I-squared statistic. Sensitivity analysis was performed for each outcome.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;The survival rates for composite restorations (direct and indirect) at 2-10 years follow-up was 88% (95% CI, 70-90%; I&lt;sup&gt;2&lt;/sup&gt; = 97%). When significant outliers from one study were removed, and re-analysed, the survival rates increased to 93% at 2-7 years follow-up (95% CI, 85-98%; I&lt;sup&gt;2&lt;/sup&gt; = 83%). Success rates for composite restorations over the same 2-10 year period was 68% (95% CI, 44-87%; I&lt;sup&gt;2&lt;/sup&gt; = 98%). Heterogeneity was generally considered high due to large variations in study design, sample size, type of intervention, and follow","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
How effective is CBCT-guided endodontic access over 'brain-guided' accesses, and is this a likely addition to the general dental practitioner's armamentarium?
Q3 Dentistry Pub Date : 2025-01-31 DOI: 10.1038/s41432-025-01116-9
Sandeep Pai, David Edwards, Greig Taylor

Design: Non-randomised prospective single-arm controlled clinical trial. The main inclusion criteria for both guided and freehand access groups was pulp canal obliteration (PCO). All teeth underwent cone-beam CT (CBCT) scan prior to access. Null hypothesis was that there is no difference in technical failure between guided and unguided access. The primary outcome was canal location success as a discrete measure (found, not found, perforated). The secondary outcome was conservativeness of drill pathway using discrete measures (optimal precision, acceptable precision, technical failure (included canal not found and perforation)). Patients underwent one subsequent annual follow-up.

Case selection: Patients attended for consultation at one centre (University Hospital Leuven, Belgium). PCO extent was assigned using periapical radiograph followed by CBCT. Cases graded as 'high difficulty' (via qualitative assessment) by briefed endodontists within the centre were selected for the study. Control group was taken from historical records as assigning an active patient to the freehand over the guided group was considered unethical.

Data analysis: Sample size calculation to achieve conventional 80% power and statistical significance of 0.05% was undertaken, mandating 60 teeth per group. An analysis including all data, without matching, was performed by a generalized linear model for binary data using a logit link function with the primary outcome (canal found or not found/perforation) as response variable and the technique (guided or freehanded) as explanatory variable. p  ≤  0.05 was considered statistically significant. Blinding of operators was not possible. Teeth were matched (paired) per group to achieve group homogeneity.

Results: Guided access yielded a 98.3% (n = 59/60) success rate with only one case unsuccessful (canal not found). In comparison, freehand access yielded 81% (n = 59/73) success rate, with 9.5% (n = 7/73) of teeth with canals unfound, and 9.5% (n = 7/73) of teeth perforated. Null hypothesis rejected given statistical significance of results (p = 0.011).

Conclusions: Cases presenting with PCO that undergo guided access show optimal outcomes both from an endodontic and from a conservational perspective, with significant increased chances of canal location in a conservative manner. Freehand correction in guided access cases can be used to inform changes to initial guided access if the canal is not found.

{"title":"How effective is CBCT-guided endodontic access over 'brain-guided' accesses, and is this a likely addition to the general dental practitioner's armamentarium?","authors":"Sandeep Pai, David Edwards, Greig Taylor","doi":"10.1038/s41432-025-01116-9","DOIUrl":"https://doi.org/10.1038/s41432-025-01116-9","url":null,"abstract":"<p><strong>Design: </strong>Non-randomised prospective single-arm controlled clinical trial. The main inclusion criteria for both guided and freehand access groups was pulp canal obliteration (PCO). All teeth underwent cone-beam CT (CBCT) scan prior to access. Null hypothesis was that there is no difference in technical failure between guided and unguided access. The primary outcome was canal location success as a discrete measure (found, not found, perforated). The secondary outcome was conservativeness of drill pathway using discrete measures (optimal precision, acceptable precision, technical failure (included canal not found and perforation)). Patients underwent one subsequent annual follow-up.</p><p><strong>Case selection: </strong>Patients attended for consultation at one centre (University Hospital Leuven, Belgium). PCO extent was assigned using periapical radiograph followed by CBCT. Cases graded as 'high difficulty' (via qualitative assessment) by briefed endodontists within the centre were selected for the study. Control group was taken from historical records as assigning an active patient to the freehand over the guided group was considered unethical.</p><p><strong>Data analysis: </strong>Sample size calculation to achieve conventional 80% power and statistical significance of 0.05% was undertaken, mandating 60 teeth per group. An analysis including all data, without matching, was performed by a generalized linear model for binary data using a logit link function with the primary outcome (canal found or not found/perforation) as response variable and the technique (guided or freehanded) as explanatory variable. p  ≤  0.05 was considered statistically significant. Blinding of operators was not possible. Teeth were matched (paired) per group to achieve group homogeneity.</p><p><strong>Results: </strong>Guided access yielded a 98.3% (n = 59/60) success rate with only one case unsuccessful (canal not found). In comparison, freehand access yielded 81% (n = 59/73) success rate, with 9.5% (n = 7/73) of teeth with canals unfound, and 9.5% (n = 7/73) of teeth perforated. Null hypothesis rejected given statistical significance of results (p = 0.011).</p><p><strong>Conclusions: </strong>Cases presenting with PCO that undergo guided access show optimal outcomes both from an endodontic and from a conservational perspective, with significant increased chances of canal location in a conservative manner. Freehand correction in guided access cases can be used to inform changes to initial guided access if the canal is not found.</p>","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074401","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Is periodontal disease associated with gestational diabetes? Exploring the evidence.
Q3 Dentistry Pub Date : 2025-01-31 DOI: 10.1038/s41432-025-01110-1
Lata Goyal, Mehak Gupta, Shipra Gupta

Data sources: A comprehensive literature search was carried out via PubMed, Cochrane, Embase and Virtual health libraries till April 2024. Articles with full text were selected in English, Spanish, French, and Portuguese language. Only observational studies were included.

Study selection: All selected studies were observational in nature and published in full text in English, Spanish, French, or Portuguese language. Gestational diabetes mellitus was diagnosed based on the American Diabetes Association's guidelines, and periodontal disease was diagnosed using international criteria by expert personnel.

Data extraction and synthesis: Two examiners did data extraction and synthesis. To identify the relationship between periodontal disease and gestational diabetes mellitus, an Odds ratio with 95% confidence interval was used. The inverse of the variance fixed effects model was applied. The Der Simonian and Laird random effects model was used if the homogeneity test using the Q statistic and the I2 revealed heterogeneity (p < 0.1). Eggers's test was used for bias assessment, and a funnel plot was also used to determine publication bias. Newcastle -Ottawa criteria were used to evaluate the quality of the included studies. Stata 17 was used in the entire data extraction process. Later on, a meta-analysis was done with seven articles with an adjusted Odds ratio.

Results: A total of 187 studies were found after a literature search, later on, duplicates were removed, leaving behind 176 studies. After screening the articles based on inclusion and exclusion criteria, 11 articles were finally included in the systematic review. Out of 11 included studies, 3 studies were cohort studies, and 8 were case-control. A total of 2032 patients were evaluated, out of which 572 developed gestational diabetes mellitus. 10 studies were considered to be of high quality, and one study was of intermediate quality. Six of the eleven studies reported a link between periodontal disease and gestational diabetes mellitus, whereas five did not yield any meaningful findings. The results showed a statistically significant p-value of less than 0.0017 and an odds ratio (OR) of 1.83 with a 95% confidence interval (CI) of 1.25 to 2.69.

Conclusion: This systematic review and meta-analysis suggest that periodontal disease is related to gestational diabetes mellitus. Several studies support the hypothesis that the presence of periodontal disease increases the risk of the development of gestational diabetes mellitus, more strong evidence is required before the same is established inconclusively.

{"title":"Is periodontal disease associated with gestational diabetes? Exploring the evidence.","authors":"Lata Goyal, Mehak Gupta, Shipra Gupta","doi":"10.1038/s41432-025-01110-1","DOIUrl":"https://doi.org/10.1038/s41432-025-01110-1","url":null,"abstract":"<p><strong>Data sources: </strong>A comprehensive literature search was carried out via PubMed, Cochrane, Embase and Virtual health libraries till April 2024. Articles with full text were selected in English, Spanish, French, and Portuguese language. Only observational studies were included.</p><p><strong>Study selection: </strong>All selected studies were observational in nature and published in full text in English, Spanish, French, or Portuguese language. Gestational diabetes mellitus was diagnosed based on the American Diabetes Association's guidelines, and periodontal disease was diagnosed using international criteria by expert personnel.</p><p><strong>Data extraction and synthesis: </strong>Two examiners did data extraction and synthesis. To identify the relationship between periodontal disease and gestational diabetes mellitus, an Odds ratio with 95% confidence interval was used. The inverse of the variance fixed effects model was applied. The Der Simonian and Laird random effects model was used if the homogeneity test using the Q statistic and the I2 revealed heterogeneity (p < 0.1). Eggers's test was used for bias assessment, and a funnel plot was also used to determine publication bias. Newcastle -Ottawa criteria were used to evaluate the quality of the included studies. Stata 17 was used in the entire data extraction process. Later on, a meta-analysis was done with seven articles with an adjusted Odds ratio.</p><p><strong>Results: </strong>A total of 187 studies were found after a literature search, later on, duplicates were removed, leaving behind 176 studies. After screening the articles based on inclusion and exclusion criteria, 11 articles were finally included in the systematic review. Out of 11 included studies, 3 studies were cohort studies, and 8 were case-control. A total of 2032 patients were evaluated, out of which 572 developed gestational diabetes mellitus. 10 studies were considered to be of high quality, and one study was of intermediate quality. Six of the eleven studies reported a link between periodontal disease and gestational diabetes mellitus, whereas five did not yield any meaningful findings. The results showed a statistically significant p-value of less than 0.0017 and an odds ratio (OR) of 1.83 with a 95% confidence interval (CI) of 1.25 to 2.69.</p><p><strong>Conclusion: </strong>This systematic review and meta-analysis suggest that periodontal disease is related to gestational diabetes mellitus. Several studies support the hypothesis that the presence of periodontal disease increases the risk of the development of gestational diabetes mellitus, more strong evidence is required before the same is established inconclusively.</p>","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074403","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Tooth vitality and periapical healing: is Biodentine at par with MTA in regenerative endodontics?
Q3 Dentistry Pub Date : 2025-01-31 DOI: 10.1038/s41432-025-01109-8
Shubham Sareen, Prabhleen Kaur Brar, Shipra Gupta, Lata Goyal
<p><strong>Design: </strong>The study is a prospective, double-blinded randomised control trial that compares the mineral trioxide aggregate (MTA) and Biodentine as the pulp space barrier material after induction of a periapical blood clot by over-instrumentation for endodontic regeneration in single-rooted mature permanent anterior tooth (closed apex) with apical periodontitis (periapical pathology of more than 3 mm) and having necrosed pulp. A total of 36 patients were included in the study and after randomisation were allocated equally to both the groups out of which 31 patients returned for follow-up over an 18-month period. The treatment protocol consisted of two separate appointments. At the first appointment, a standardised and custom-made radiographic guide was prepared for each patient to ensure uniformity and repeatability of the radiographs at subsequent follow-up visits. This was followed by access to the pulp chamber and biomechanical preparation of the single canal up to master apical file size. The irrigant used in each case was 1.5% sodium hypochlorite and also calcium hydroxide intracanal medicament was placed during this visit. The interval between the two appointments was not fixed and depended on the patient's symptoms following the first visit; however, the maximum allowable time frame was set at 3 weeks. During the second visit after irrigation with 17% ethylenediaminetetraacetic acid (EDTA) over instrumentation was done to induce bleeding that was allowed to fill the canal. The clot was stabilised by collagen plug and the pulp space sealer (either MTA or Biodentine) was placed below the cementoenamel junction following which composite restoration was done. The radiographs were taken before the treatment, after both the appointments and at 6, 9, 12 and 18 months subsequently by a single experienced examiner. Pre-operatively, a periapical index score (PAI) was given to each case and the sensibility test was performed at 6, 12, 18 months postoperatively using an electric pulp tester (EPT).</p><p><strong>Case selection: </strong>Participants were recruited from the Department of Endodontics outpatient clinic. The patients were aged between 10-35 years and had no systemic conditions. For inclusion in the study, participants were required to have mature anterior tooth (single root canal) with closed apex associated with apical periodontitis and necrotic pulp having periapical radiolucency of more than 3 mm on the radiograph. Patients suffering from periodontitis (ensured by periodontal probing) and those having developmental anomalies of the teeth were excluded from the study.</p><p><strong>Data analysis: </strong>The normalcy of the data was assessed by Shapiro-Wilk test. Continuous data was analysed by Mann Whitney U test and the categorical data was analysed by Chi-square test and Fisher's exact test. With the level of significance set at 0.05.</p><p><strong>Results: </strong>Firstly, the author presented the overall healing o
{"title":"Tooth vitality and periapical healing: is Biodentine at par with MTA in regenerative endodontics?","authors":"Shubham Sareen, Prabhleen Kaur Brar, Shipra Gupta, Lata Goyal","doi":"10.1038/s41432-025-01109-8","DOIUrl":"https://doi.org/10.1038/s41432-025-01109-8","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Design: &lt;/strong&gt;The study is a prospective, double-blinded randomised control trial that compares the mineral trioxide aggregate (MTA) and Biodentine as the pulp space barrier material after induction of a periapical blood clot by over-instrumentation for endodontic regeneration in single-rooted mature permanent anterior tooth (closed apex) with apical periodontitis (periapical pathology of more than 3 mm) and having necrosed pulp. A total of 36 patients were included in the study and after randomisation were allocated equally to both the groups out of which 31 patients returned for follow-up over an 18-month period. The treatment protocol consisted of two separate appointments. At the first appointment, a standardised and custom-made radiographic guide was prepared for each patient to ensure uniformity and repeatability of the radiographs at subsequent follow-up visits. This was followed by access to the pulp chamber and biomechanical preparation of the single canal up to master apical file size. The irrigant used in each case was 1.5% sodium hypochlorite and also calcium hydroxide intracanal medicament was placed during this visit. The interval between the two appointments was not fixed and depended on the patient's symptoms following the first visit; however, the maximum allowable time frame was set at 3 weeks. During the second visit after irrigation with 17% ethylenediaminetetraacetic acid (EDTA) over instrumentation was done to induce bleeding that was allowed to fill the canal. The clot was stabilised by collagen plug and the pulp space sealer (either MTA or Biodentine) was placed below the cementoenamel junction following which composite restoration was done. The radiographs were taken before the treatment, after both the appointments and at 6, 9, 12 and 18 months subsequently by a single experienced examiner. Pre-operatively, a periapical index score (PAI) was given to each case and the sensibility test was performed at 6, 12, 18 months postoperatively using an electric pulp tester (EPT).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Case selection: &lt;/strong&gt;Participants were recruited from the Department of Endodontics outpatient clinic. The patients were aged between 10-35 years and had no systemic conditions. For inclusion in the study, participants were required to have mature anterior tooth (single root canal) with closed apex associated with apical periodontitis and necrotic pulp having periapical radiolucency of more than 3 mm on the radiograph. Patients suffering from periodontitis (ensured by periodontal probing) and those having developmental anomalies of the teeth were excluded from the study.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Data analysis: &lt;/strong&gt;The normalcy of the data was assessed by Shapiro-Wilk test. Continuous data was analysed by Mann Whitney U test and the categorical data was analysed by Chi-square test and Fisher's exact test. With the level of significance set at 0.05.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Firstly, the author presented the overall healing o","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143064563","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Similar patient-reported satisfaction and professional appraisal of implant-supported fixed dental prosthesis fabricated by different workflows.
Q3 Dentistry Pub Date : 2025-01-29 DOI: 10.1038/s41432-025-01111-0
Aditi Nanda, Vikender Singh Yadav, Kanika Makker, Anika Dawar
<p><strong>Design: </strong>A triple-armed, double-blind randomized controlled trial with cross-over design investigated patient-reported satisfaction and objective dental evaluation of a 3-unit, monolithic zirconium dioxide (ZrO2), implant-supported fixed dental prosthesis (iFDP) fabricated with 2 completely digital workflows and 1 mixed analog-digital workflow.</p><p><strong>Case selection: </strong>Participants enrolled required rehabilitation of 2 dental implants in posterior region of either of the arches with a 3-unit, ZrO2 iFDP. A total of 20 participants received the 3 types of ZrO2, iFDP fabricated by 3 different methods. Thus, a total of 60 iFDPs were fabricated in the study. 20 iFDP were fabricated by complete digital workflow by using 3Shape Trios 3 Intraoral scanner (IOS) and 3 Shape designing software (Test-1). In second group (Test-2) 20 iFDPs were fabricated by using Dental Wings Virtuo Vivo IOS and Dental Wings original software (DWOS) for CAD designing. 20 iFDPs (control) were fabricated by mixed analogue-digital workflow by using Polyether impression and Exocad Lab software. The primary clinical outcome was blinded, subjective evaluation on visual analogue scale (VAS) by the participant, and an objective evaluation on VAS by a dentist at the time of prosthetic try-in of each of the 3 types of prosthesis. Secondary outcome was patients' perception about the impression procedures in the 3 different workflows on VAS.</p><p><strong>Study timeline: </strong>The study was conducted at 2 instances during the prosthetic rehabilitation. The primary outcomes were assessed at the time of prosthetic try-in. The secondary outcome was observed after the impression session.</p><p><strong>Data analysis: </strong>Clinical parameters were measured on VAS from 0 to 100 score. For the primary outcome, VAS score was recorded for each iFDP as observed for patient perception (satisfaction) and dentist evaluation (objective). The perception about impression was also recorded on VAS. Descriptive analysis of all scores was done by mean and standard deviation. ANOVA test was used for comparisons among the 3 different types of iFDP. Tukey's HSD was used for pairwise comparisons within ANOVA. Linear regression analyses was done to compare overall satisfaction of the patients and the dentist within each group. The level of significance was set at α = 0.05.</p><p><strong>Results: </strong>After the start of recruitment in January 2020, there were no losses and exclusions. VAS for patient satisfaction was higher than VAS for dentist evaluation. Patient satisfaction among Test-1, Test-2, and Control showed no significant difference (P = 0.876). Dentist satisfaction among workflows were also not significantly different (P = 0.22). The relationship between VAS scores of patients and dentists was weak for Test-1 (R-value = -0.424, P = 0.062), Test-2 (R-value = 0.116, P = 0.068), and Control (R-value = -0.183, P = 0.441). Significant differences for patients' perc
{"title":"Similar patient-reported satisfaction and professional appraisal of implant-supported fixed dental prosthesis fabricated by different workflows.","authors":"Aditi Nanda, Vikender Singh Yadav, Kanika Makker, Anika Dawar","doi":"10.1038/s41432-025-01111-0","DOIUrl":"https://doi.org/10.1038/s41432-025-01111-0","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Design: &lt;/strong&gt;A triple-armed, double-blind randomized controlled trial with cross-over design investigated patient-reported satisfaction and objective dental evaluation of a 3-unit, monolithic zirconium dioxide (ZrO2), implant-supported fixed dental prosthesis (iFDP) fabricated with 2 completely digital workflows and 1 mixed analog-digital workflow.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Case selection: &lt;/strong&gt;Participants enrolled required rehabilitation of 2 dental implants in posterior region of either of the arches with a 3-unit, ZrO2 iFDP. A total of 20 participants received the 3 types of ZrO2, iFDP fabricated by 3 different methods. Thus, a total of 60 iFDPs were fabricated in the study. 20 iFDP were fabricated by complete digital workflow by using 3Shape Trios 3 Intraoral scanner (IOS) and 3 Shape designing software (Test-1). In second group (Test-2) 20 iFDPs were fabricated by using Dental Wings Virtuo Vivo IOS and Dental Wings original software (DWOS) for CAD designing. 20 iFDPs (control) were fabricated by mixed analogue-digital workflow by using Polyether impression and Exocad Lab software. The primary clinical outcome was blinded, subjective evaluation on visual analogue scale (VAS) by the participant, and an objective evaluation on VAS by a dentist at the time of prosthetic try-in of each of the 3 types of prosthesis. Secondary outcome was patients' perception about the impression procedures in the 3 different workflows on VAS.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Study timeline: &lt;/strong&gt;The study was conducted at 2 instances during the prosthetic rehabilitation. The primary outcomes were assessed at the time of prosthetic try-in. The secondary outcome was observed after the impression session.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Data analysis: &lt;/strong&gt;Clinical parameters were measured on VAS from 0 to 100 score. For the primary outcome, VAS score was recorded for each iFDP as observed for patient perception (satisfaction) and dentist evaluation (objective). The perception about impression was also recorded on VAS. Descriptive analysis of all scores was done by mean and standard deviation. ANOVA test was used for comparisons among the 3 different types of iFDP. Tukey's HSD was used for pairwise comparisons within ANOVA. Linear regression analyses was done to compare overall satisfaction of the patients and the dentist within each group. The level of significance was set at α = 0.05.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;After the start of recruitment in January 2020, there were no losses and exclusions. VAS for patient satisfaction was higher than VAS for dentist evaluation. Patient satisfaction among Test-1, Test-2, and Control showed no significant difference (P = 0.876). Dentist satisfaction among workflows were also not significantly different (P = 0.22). The relationship between VAS scores of patients and dentists was weak for Test-1 (R-value = -0.424, P = 0.062), Test-2 (R-value = 0.116, P = 0.068), and Control (R-value = -0.183, P = 0.441). Significant differences for patients' perc","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143064487","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Can monolithic zirconia frameworks in implant-supported cross-arch prostheses deliver reliable long-term outcomes?
Q3 Dentistry Pub Date : 2025-01-29 DOI: 10.1038/s41432-025-01108-9
Nidhi Parmar

Design: A retrospective cohort study assessing the mid-to-long-term outcomes and risk factors affecting the prosthetic success and survival of implant-supported cross-arch fixed dental prostheses (IFCDPs) with monolithic zirconia frameworks.

Cohort selection: Forty-seven patients received a total of 51 cross-arch prostheses (27 maxillary and 24 mandibular prostheses), supported by 302 implants. Comprehensive clinical and radiographic records were available over a follow-up period ranging from 5 to 13 years. A strict inclusion criteria ensured the use of screw-retained implants and monolithic zirconia frameworks fabricated using standardised CAD/CAM protocols, without cemented titanium bases. Exclusion criteria included systemic conditions affecting healing, bruxism, uncontrolled periodontitis, smoking, and significant health changes during the follow-up period.

Data analysis: Descriptive statistics summarised implant and prosthesis outcomes, while complications were evaluated for peri-implantitis at an implant level and framework fractures at a prosthesis level. Peri-implantitis was identified through clinical signs, including bleeding on probing, suppuration, and radiographic evidence of bone loss. Prosthetic outcomes were classified using the modified USPHS criteria. Mixed-effects Cox regression models were applied to analyse risk factors. Hazard ratios were calculated for peri-implantitis and framework fractures, with statistical significance set at p < 0.05.

Results: The implant survival rate was 97.64%, with peri-implantitis observed in 27 implants, predominantly in the mandible, resulting in an overall implant success rate of 91.06%. Prosthesis survival was 82.35%, with nine framework fractures reported, eight of which occurred in mandibular prostheses. The mandible was identified as a significant risk factor for both framework fractures (HR = 11.64, p = 0.024) and peri-implantitis (HR = 10.88, p = 0.003).

Conclusion: IFCDPs with monolithic zirconia-based frameworks exhibited favourable clinical outcomes over a 5-13-year period. However, mandibular prostheses were more prone to framework fractures and peri-implantitis, highlighting the need to consider mandibular flexure in prosthetic design to enhance long-term success and durability.

{"title":"Can monolithic zirconia frameworks in implant-supported cross-arch prostheses deliver reliable long-term outcomes?","authors":"Nidhi Parmar","doi":"10.1038/s41432-025-01108-9","DOIUrl":"https://doi.org/10.1038/s41432-025-01108-9","url":null,"abstract":"<p><strong>Design: </strong>A retrospective cohort study assessing the mid-to-long-term outcomes and risk factors affecting the prosthetic success and survival of implant-supported cross-arch fixed dental prostheses (IFCDPs) with monolithic zirconia frameworks.</p><p><strong>Cohort selection: </strong>Forty-seven patients received a total of 51 cross-arch prostheses (27 maxillary and 24 mandibular prostheses), supported by 302 implants. Comprehensive clinical and radiographic records were available over a follow-up period ranging from 5 to 13 years. A strict inclusion criteria ensured the use of screw-retained implants and monolithic zirconia frameworks fabricated using standardised CAD/CAM protocols, without cemented titanium bases. Exclusion criteria included systemic conditions affecting healing, bruxism, uncontrolled periodontitis, smoking, and significant health changes during the follow-up period.</p><p><strong>Data analysis: </strong>Descriptive statistics summarised implant and prosthesis outcomes, while complications were evaluated for peri-implantitis at an implant level and framework fractures at a prosthesis level. Peri-implantitis was identified through clinical signs, including bleeding on probing, suppuration, and radiographic evidence of bone loss. Prosthetic outcomes were classified using the modified USPHS criteria. Mixed-effects Cox regression models were applied to analyse risk factors. Hazard ratios were calculated for peri-implantitis and framework fractures, with statistical significance set at p < 0.05.</p><p><strong>Results: </strong>The implant survival rate was 97.64%, with peri-implantitis observed in 27 implants, predominantly in the mandible, resulting in an overall implant success rate of 91.06%. Prosthesis survival was 82.35%, with nine framework fractures reported, eight of which occurred in mandibular prostheses. The mandible was identified as a significant risk factor for both framework fractures (HR = 11.64, p = 0.024) and peri-implantitis (HR = 10.88, p = 0.003).</p><p><strong>Conclusion: </strong>IFCDPs with monolithic zirconia-based frameworks exhibited favourable clinical outcomes over a 5-13-year period. However, mandibular prostheses were more prone to framework fractures and peri-implantitis, highlighting the need to consider mandibular flexure in prosthetic design to enhance long-term success and durability.</p>","PeriodicalId":12234,"journal":{"name":"Evidence-based dentistry","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2025-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143064486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Evidence-based dentistry
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