Pub Date : 2024-11-16DOI: 10.1007/s00784-024-06025-2
Wafaa Saleh, Fatma Ata, Nessma A Nosser, Bassant Mowafey
Objectives: The current literature lacks the correlation between serum levels of vitamin D and interleukin-8 (IL-8) to the stages of periodontitis. The present research objectives are to evaluate the serum levels of vitamin D and IL-8 in periodontitis participants and healthy controls and to measure their correlation with the stages of periodontitis.
Methods: The current case-control study was conducted on patients with periodontitis and healthy controls. After obtaining a questionnaire from the participants, the following clinical parameters were measured; periodontal probing depth (PPD), clinical attachment loss (CAL), plaque index (PI), gingival index (GI), bleeding on probing (BOP), and tooth count. The serum levels of vitamin D and IL-8 were measured using ELISA kits. Then, we measured the correlation of the stages of periodontitis with the serum levels of vitamin D and IL-8.
Results: Ninety-eight participants; 52 with periodontitis and 46 healthy controls were included. The patients with periodontitis showed a significantly lower level of vitamin D, higher PPD, CAL, BOP, and lower number of teeth than the controls. In addition, serum vitamin D significantly correlated with the stages of periodontitis. Serum IL-8 showed no significant difference between the study and control groups while it does not significantly correlate with the stages of periodontitis.
Conclusion: The current study's findings suggest a potential association between serum level of vitamin D with severity of periodontitis which necessitates screening vitamin D status in patients with periodontitis and investigating the possibility of vitamin D supplementation in decreasing the progression of periodontitis.
研究目的目前的文献缺乏血清中维生素D和白细胞介素-8(IL-8)水平与牙周炎阶段的相关性。本研究的目的是评估牙周炎患者和健康对照者血清中维生素 D 和 IL-8 的水平,并测量它们与牙周炎分期的相关性:本病例对照研究的对象是牙周炎患者和健康对照组。在获得参与者的调查问卷后,测量了以下临床参数:牙周探诊深度(PPD)、临床附着丧失(CAL)、牙菌斑指数(PI)、牙龈指数(GI)、探诊出血量(BOP)和牙齿数量。使用 ELISA 试剂盒测定了血清中维生素 D 和 IL-8 的水平。然后,我们测定了牙周炎分期与血清中维生素 D 和 IL-8 水平的相关性:结果:98 名参与者中包括 52 名牙周炎患者和 46 名健康对照者。与对照组相比,牙周炎患者的维生素 D 水平明显较低,PPD、CAL、BOP 较高,牙齿数量较少。此外,血清维生素 D 与牙周炎的分期有明显的相关性。血清 IL-8 在研究组和对照组之间无明显差异,与牙周炎的分期也无明显相关性:目前的研究结果表明,血清维生素 D 水平与牙周炎的严重程度可能存在关联,因此有必要对牙周炎患者的维生素 D 状态进行筛查,并研究补充维生素 D 以减少牙周炎恶化的可能性。
{"title":"Correlation of serum vitamin D and IL-8 to stages of periodontitis: a case-control analysis.","authors":"Wafaa Saleh, Fatma Ata, Nessma A Nosser, Bassant Mowafey","doi":"10.1007/s00784-024-06025-2","DOIUrl":"10.1007/s00784-024-06025-2","url":null,"abstract":"<p><strong>Objectives: </strong>The current literature lacks the correlation between serum levels of vitamin D and interleukin-8 (IL-8) to the stages of periodontitis. The present research objectives are to evaluate the serum levels of vitamin D and IL-8 in periodontitis participants and healthy controls and to measure their correlation with the stages of periodontitis.</p><p><strong>Methods: </strong>The current case-control study was conducted on patients with periodontitis and healthy controls. After obtaining a questionnaire from the participants, the following clinical parameters were measured; periodontal probing depth (PPD), clinical attachment loss (CAL), plaque index (PI), gingival index (GI), bleeding on probing (BOP), and tooth count. The serum levels of vitamin D and IL-8 were measured using ELISA kits. Then, we measured the correlation of the stages of periodontitis with the serum levels of vitamin D and IL-8.</p><p><strong>Results: </strong>Ninety-eight participants; 52 with periodontitis and 46 healthy controls were included. The patients with periodontitis showed a significantly lower level of vitamin D, higher PPD, CAL, BOP, and lower number of teeth than the controls. In addition, serum vitamin D significantly correlated with the stages of periodontitis. Serum IL-8 showed no significant difference between the study and control groups while it does not significantly correlate with the stages of periodontitis.</p><p><strong>Conclusion: </strong>The current study's findings suggest a potential association between serum level of vitamin D with severity of periodontitis which necessitates screening vitamin D status in patients with periodontitis and investigating the possibility of vitamin D supplementation in decreasing the progression of periodontitis.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"645"},"PeriodicalIF":3.1,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11568973/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142643895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-15DOI: 10.1007/s00784-024-06034-1
Camilla Lennholm, Hanna Andreasen, Anna Westerlund, Henrik Lund
Objectives: To evaluate at which thickness marginal bone becomes visible to the observer on cone-beam computed tomography (CBCT) images and how reconstruction technique and viewing mode affect assessment.
Materials and methods: Fourteen anterior teeth from six human mandibles were examined with two CBCT resolution protocols: standard- and high-resolution. Distance from the cementoenamel junction to the visible marginal bone level (MBL) was measured in three groups of reconstructed CBCT images: multiplanar reformation (MPR) with grey scale, MPR with inverted grey scale, and 3D rendering. These measurements were used to identify the bone level where marginal bone width should be measured on histological photographs of sliced teeth. Gold standards comprised measurements of bone thickness at the superior MBL on histological photographs.
Results: MPR grey scale images exposed at high-resolution settings yielded highest validity: bone widths of 0.173 mm (buccal) and 0.356 mm (lingual) were necessary for visibility on a CBCT image. 3D-rendered lingual surfaces exposed with high-resolution settings had lowest validity. Intra-observer agreement for all CBCT and histological measurements was high.
Conclusion: The best CBCT resolution protocol, reconstruction technique, and viewing mode for analyzing buccal and lingual surfaces of the alveolar bone margin are images exposed with a high-resolution protocol, reconstructed using MPR, and viewed in grey scale. Bone thickness required to be visualized was twice lingually compared to buccally.
Clinical relevance: The visualization of bone thickness in CBCT requires a greater thickness on the lingual side compared to the buccal side. 3D-rendered reconstructions should be avoided when evaluating thin bony structures.
{"title":"Visibility of alveolar bone thicknesses on CBCT images-a study on minimum bone requirements using various reconstruction techniques, viewing modes, and resolutions.","authors":"Camilla Lennholm, Hanna Andreasen, Anna Westerlund, Henrik Lund","doi":"10.1007/s00784-024-06034-1","DOIUrl":"10.1007/s00784-024-06034-1","url":null,"abstract":"<p><strong>Objectives: </strong>To evaluate at which thickness marginal bone becomes visible to the observer on cone-beam computed tomography (CBCT) images and how reconstruction technique and viewing mode affect assessment.</p><p><strong>Materials and methods: </strong>Fourteen anterior teeth from six human mandibles were examined with two CBCT resolution protocols: standard- and high-resolution. Distance from the cementoenamel junction to the visible marginal bone level (MBL) was measured in three groups of reconstructed CBCT images: multiplanar reformation (MPR) with grey scale, MPR with inverted grey scale, and 3D rendering. These measurements were used to identify the bone level where marginal bone width should be measured on histological photographs of sliced teeth. Gold standards comprised measurements of bone thickness at the superior MBL on histological photographs.</p><p><strong>Results: </strong>MPR grey scale images exposed at high-resolution settings yielded highest validity: bone widths of 0.173 mm (buccal) and 0.356 mm (lingual) were necessary for visibility on a CBCT image. 3D-rendered lingual surfaces exposed with high-resolution settings had lowest validity. Intra-observer agreement for all CBCT and histological measurements was high.</p><p><strong>Conclusion: </strong>The best CBCT resolution protocol, reconstruction technique, and viewing mode for analyzing buccal and lingual surfaces of the alveolar bone margin are images exposed with a high-resolution protocol, reconstructed using MPR, and viewed in grey scale. Bone thickness required to be visualized was twice lingually compared to buccally.</p><p><strong>Clinical relevance: </strong>The visualization of bone thickness in CBCT requires a greater thickness on the lingual side compared to the buccal side. 3D-rendered reconstructions should be avoided when evaluating thin bony structures.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"641"},"PeriodicalIF":3.1,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11564398/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616161","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-13DOI: 10.1007/s00784-024-06040-3
Vinícius Taioqui Pelá, Mariana Miranda de Brito, Gustavo Cassalate da Silva, Even Akemi Taira, Carolina Ruis Ferrari, Talita Mendes Oliveira Ventura, Larissa Tercilia Grizzo Thomassian, Flávio Henrique-Silva, Eduardo Pereira de Souza, Thais Fernanda Carlos, Thiago Saads Carvalho, Andrea Soares da Costa Fuentes, Karina Fan, Reinaldo Marchetto, Adrian Lussi, Marília Afonso Rabelo Buzalaf
Objective: This study aimed to examine and compare the efficacy of mouthwashes containing different proteins and peptide on the prevention of enamel erosion in vivo, as well as to evaluate the participants' satisfaction with the formulations.
Methods: Twelve participants were selected and underwent five cross-over mouthwash phases: Water (control); 0.1 mg/mL CaneCPI-5; 0.5 mg/mL MaquiCPI-3; 0.1 mg/mL CsinCPI-2; and 0.037 mg/mL Stn15pSpS. After prophylaxis, the participants rinsed (1 min), followed by the acquired enamel pellicle (AEP) formation (2 h). An erosive challenge was made (biopsy, citric acid 1%, 15s) on the buccal surface of the central maxillary incisors. The Relative Surface Reflection Intensity (%SRI) was assessed and analyzed by ANOVA/Tukey's tests. The calcium release in acid was measured by the Arsenazo method and verified by Kruskal-Wallis/Dunn's tests. The Spearman's correlation was used between analyses. A questionnaire evaluated the satisfaction of participants.
Results: For both analyses, the results showed that mouthwashes containing the proteins or peptide were significantly more effective in preventing enamel erosion compared to deionized water, with no significant differences among the active ingredients (p < 0.05). Also, there was a significant negative correlation between %SRI and calcium released (r=-0.5754). The questionnaire revealed that the volunteers were satisfied with the taste of the products. In addition, the experimental procedures were well tolerable, and no side effects were reported.
Conclusion: All mouthwashes containing proteins or peptide were acceptable and effective in protecting enamel against initial dental erosion in vivo.
Clinical significance: This study highlights the potential of these pioneer organic components for the development of mouthwashes designed for people with risk of erosive tooth wear.
{"title":"Designing mouthwash formulations with innovative molecular components to control initial dental erosion in vivo.","authors":"Vinícius Taioqui Pelá, Mariana Miranda de Brito, Gustavo Cassalate da Silva, Even Akemi Taira, Carolina Ruis Ferrari, Talita Mendes Oliveira Ventura, Larissa Tercilia Grizzo Thomassian, Flávio Henrique-Silva, Eduardo Pereira de Souza, Thais Fernanda Carlos, Thiago Saads Carvalho, Andrea Soares da Costa Fuentes, Karina Fan, Reinaldo Marchetto, Adrian Lussi, Marília Afonso Rabelo Buzalaf","doi":"10.1007/s00784-024-06040-3","DOIUrl":"https://doi.org/10.1007/s00784-024-06040-3","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to examine and compare the efficacy of mouthwashes containing different proteins and peptide on the prevention of enamel erosion in vivo, as well as to evaluate the participants' satisfaction with the formulations.</p><p><strong>Methods: </strong>Twelve participants were selected and underwent five cross-over mouthwash phases: Water (control); 0.1 mg/mL CaneCPI-5; 0.5 mg/mL MaquiCPI-3; 0.1 mg/mL CsinCPI-2; and 0.037 mg/mL Stn15pSpS. After prophylaxis, the participants rinsed (1 min), followed by the acquired enamel pellicle (AEP) formation (2 h). An erosive challenge was made (biopsy, citric acid 1%, 15s) on the buccal surface of the central maxillary incisors. The Relative Surface Reflection Intensity (%SRI) was assessed and analyzed by ANOVA/Tukey's tests. The calcium release in acid was measured by the Arsenazo method and verified by Kruskal-Wallis/Dunn's tests. The Spearman's correlation was used between analyses. A questionnaire evaluated the satisfaction of participants.</p><p><strong>Results: </strong>For both analyses, the results showed that mouthwashes containing the proteins or peptide were significantly more effective in preventing enamel erosion compared to deionized water, with no significant differences among the active ingredients (p < 0.05). Also, there was a significant negative correlation between %SRI and calcium released (r=-0.5754). The questionnaire revealed that the volunteers were satisfied with the taste of the products. In addition, the experimental procedures were well tolerable, and no side effects were reported.</p><p><strong>Conclusion: </strong>All mouthwashes containing proteins or peptide were acceptable and effective in protecting enamel against initial dental erosion in vivo.</p><p><strong>Clinical significance: </strong>This study highlights the potential of these pioneer organic components for the development of mouthwashes designed for people with risk of erosive tooth wear.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"640"},"PeriodicalIF":3.1,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616146","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-12DOI: 10.1007/s00784-024-06024-3
Fumika Tsuda, Keiichi Yoshida, Takashi Sawase
Objectives: To assess the influence of different primer compositions-silane (S), 10-methacryloyloxydecyl dihydrogen phosphate (MDP), and the combination of silane and MDP (S + MDP)-on the bonding performance of MDP-free and MDP-containing resin cements to highly translucent zirconia.
Materials and methods: Tribochemical silica-coated zirconia plates were pretreated with one of three experimental primers, S, MDP, or S + MDP, with untreated specimens serving as controls. Subsequently, these plates were bonded to stainless-steel rods using either two MDP-free or two MDP-containing resin cements. Tensile bond strength was measured after 24 h (TC0) and following thermal cycling (4-60 °C for 10,000 cycles; TC10,000). Data were analyzed using a three-way analysis of variance (ANOVA), followed by one-way ANOVA and Tukey-Kramer post hoc tests (α = 0.05). X-ray photoelectron spectroscopy (XPS) assessed the elemental mass concentrations on the zirconia surfaces.
Results: For MDP-free resin cements, MDP-treated specimens exhibited significantly greater bond strengths than controls, regardless of the aging conditions. However, a significant reduction in bond strength was observed between TC0 and TC10,000 in most of the MDP-free resin cement groups, except for one S + MDP group. Conversely, for MDP-containing resin cements, the S + MDP group exhibited no statistically significant differences between aging conditions. Notably, XPS analysis detected silicon, zirconium, and aluminum on the zirconia surfaces.
Conclusions: No significant difference in tensile bond strength was observed between aging conditions for MDP-containing resin cements bonded to tribochemical silica-coated zirconia primed with S + MDP.
Clinical relevance: The combination of MDP-containing primers and resin cements demonstrated superior bonding performance to tribochemical silica-coated zirconia.
{"title":"Effects of primer components of silane and 10-methacryloyloxydecyl dihydrogen phosphate on resin bonding to tribochemical silica-coated highly translucent zirconia.","authors":"Fumika Tsuda, Keiichi Yoshida, Takashi Sawase","doi":"10.1007/s00784-024-06024-3","DOIUrl":"https://doi.org/10.1007/s00784-024-06024-3","url":null,"abstract":"<p><strong>Objectives: </strong>To assess the influence of different primer compositions-silane (S), 10-methacryloyloxydecyl dihydrogen phosphate (MDP), and the combination of silane and MDP (S + MDP)-on the bonding performance of MDP-free and MDP-containing resin cements to highly translucent zirconia.</p><p><strong>Materials and methods: </strong>Tribochemical silica-coated zirconia plates were pretreated with one of three experimental primers, S, MDP, or S + MDP, with untreated specimens serving as controls. Subsequently, these plates were bonded to stainless-steel rods using either two MDP-free or two MDP-containing resin cements. Tensile bond strength was measured after 24 h (TC0) and following thermal cycling (4-60 °C for 10,000 cycles; TC10,000). Data were analyzed using a three-way analysis of variance (ANOVA), followed by one-way ANOVA and Tukey-Kramer post hoc tests (α = 0.05). X-ray photoelectron spectroscopy (XPS) assessed the elemental mass concentrations on the zirconia surfaces.</p><p><strong>Results: </strong>For MDP-free resin cements, MDP-treated specimens exhibited significantly greater bond strengths than controls, regardless of the aging conditions. However, a significant reduction in bond strength was observed between TC0 and TC10,000 in most of the MDP-free resin cement groups, except for one S + MDP group. Conversely, for MDP-containing resin cements, the S + MDP group exhibited no statistically significant differences between aging conditions. Notably, XPS analysis detected silicon, zirconium, and aluminum on the zirconia surfaces.</p><p><strong>Conclusions: </strong>No significant difference in tensile bond strength was observed between aging conditions for MDP-containing resin cements bonded to tribochemical silica-coated zirconia primed with S + MDP.</p><p><strong>Clinical relevance: </strong>The combination of MDP-containing primers and resin cements demonstrated superior bonding performance to tribochemical silica-coated zirconia.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"638"},"PeriodicalIF":3.1,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616149","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-12DOI: 10.1007/s00784-024-06032-3
Ana Paula Perroni, Fabíola Jardim Barbon, Eduardo Trota Chaves, Simone Alberton da Silva, Rafael Ratto de Moraes, Noéli Boscato
Objective: This study evaluated the influence of tooth shade, resin-based luting agent shade values, and ceramic thickness on the optical properties of CLVs.
Materials and methods: The study involved 16 participants who received 95 CLVs. CIE L*, a*, b* color coordinates were assessed with a clinical spectrophotometer. Variables considered were: luting agent value in three levels (high, medium, low); tooth shade before and after preparation in two levels (lighter and darker shades); and CLV thickness in two levels (< 1 mm, ≥ 1 mm). The color difference (ΔE00) was analyzed under four scenarios, utilizing statistical methods suitable for non-normal distributions.
Results: Ninety-five CLVs (n = 95) were analyzed, ceramic thicknesses mean (SD) values were 0.70 (± 0.15) for < 1 mm group and 1.19 (0.20) for ≥ 1 mm group. ΔE00 values ranging from 2.93 to 9.72, all exceeding the thresholds of perceptibility and acceptability. Significant variations were observed in optical outcomes based on the clinical variables studied, particularly showing that high-value luting agents are more effective over darker substrates (p = 0.043). Thicker ceramics significantly improved masking capabilities, demonstrating their critical role in esthetic treatments (p = 0.024). No significant differences were found regarding the tooth shade after preparation (p = 0.215).
Conclusion: The study confirmed that luting agent shade values and ceramic thickness, critically influence the final optical properties of CLVs. High-value luting agents and thicker ceramics effectively achieved acceptable color differences, especially over darker tooth substrates. These findings underscore the importance of carefully selecting materials and techniques to optimize optical outcomes in CLV restorations.
Clinical significance: Luting agent's value and ceramic thickness plays a critical role in achieving natural-looking ceramic laminate veneers, especially on darker tooth substrates. These factors significantly impact the final color matching and esthetic outcome.
{"title":"Exploring the influence of tooth, ceramic, and resin luting agent variations on laminate veneer optical characteristics: a prospective clinical investigation.","authors":"Ana Paula Perroni, Fabíola Jardim Barbon, Eduardo Trota Chaves, Simone Alberton da Silva, Rafael Ratto de Moraes, Noéli Boscato","doi":"10.1007/s00784-024-06032-3","DOIUrl":"https://doi.org/10.1007/s00784-024-06032-3","url":null,"abstract":"<p><strong>Objective: </strong>This study evaluated the influence of tooth shade, resin-based luting agent shade values, and ceramic thickness on the optical properties of CLVs.</p><p><strong>Materials and methods: </strong>The study involved 16 participants who received 95 CLVs. CIE L*, a*, b* color coordinates were assessed with a clinical spectrophotometer. Variables considered were: luting agent value in three levels (high, medium, low); tooth shade before and after preparation in two levels (lighter and darker shades); and CLV thickness in two levels (< 1 mm, ≥ 1 mm). The color difference (ΔE<sub>00</sub>) was analyzed under four scenarios, utilizing statistical methods suitable for non-normal distributions.</p><p><strong>Results: </strong>Ninety-five CLVs (n = 95) were analyzed, ceramic thicknesses mean (SD) values were 0.70 (± 0.15) for < 1 mm group and 1.19 (0.20) for ≥ 1 mm group. ΔE<sub>00</sub> values ranging from 2.93 to 9.72, all exceeding the thresholds of perceptibility and acceptability. Significant variations were observed in optical outcomes based on the clinical variables studied, particularly showing that high-value luting agents are more effective over darker substrates (p = 0.043). Thicker ceramics significantly improved masking capabilities, demonstrating their critical role in esthetic treatments (p = 0.024). No significant differences were found regarding the tooth shade after preparation (p = 0.215).</p><p><strong>Conclusion: </strong>The study confirmed that luting agent shade values and ceramic thickness, critically influence the final optical properties of CLVs. High-value luting agents and thicker ceramics effectively achieved acceptable color differences, especially over darker tooth substrates. These findings underscore the importance of carefully selecting materials and techniques to optimize optical outcomes in CLV restorations.</p><p><strong>Clinical significance: </strong>Luting agent's value and ceramic thickness plays a critical role in achieving natural-looking ceramic laminate veneers, especially on darker tooth substrates. These factors significantly impact the final color matching and esthetic outcome.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"639"},"PeriodicalIF":3.1,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616150","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-11DOI: 10.1007/s00784-024-06013-6
Menna Moataz Aboelnor, Khaled Aly Nour, Heba Mohamed Ahmed Al-Sanafawy
Objective: The objective of this study is to evaluate the effectiveness of two different viscosities of short fiber-reinforced composite resin (SFRC) cores and two different viscosities of veneering composite resins on the fracture strength of direct occlusal veneers.
Materials and methods: One maxillary premolar was virtually prepared for an occlusal veneer and printed into resin dies. In total, (n = 48) resin dies were printed and assigned into three groups according to the type of core material of the occlusal veneer; mono-structured without a SFRC core, a high viscosity SFRC core, and a low viscosity SFRC core. Each group was re-divided into two subgroups (n = 8) according to the veneering composite resin; packable composite resin and injectable composite resin. Mono-structured and bi-structured direct occlusal veneers were fabricated on the resin dies using the mentioned core and veneering materials with the occlusal replica technique. Fracture strength was evaluated using a universal testing machine and the mode of failure was inspected. Statistical analysis to compare the core and veneering materials was performed using independent t test (P ≤ 0.05) and one-way ANOVA followed by tukey's post hoc test (Pa ≤ 0.0166) when appropriate. Interactions between subgroups were tested using two-way ANOVA, and one-way ANOVA was used to compare all subgroups followed by tukey's post hoc test (Pa ≤ 0.0033). Intergroup comparison between failure modes were performed using chi square test (Pa ≤ 0.0033).
Results: The presence of a SFRC core significantly improved the fracture strength of the specimens. There was no significant difference between the fracture strength of high viscosity SFRC and low viscosity SFRC cores. Specimens veneered with injectable composite resin had significantly superior fracture strength compared to packable composite resin. Additionally, there was a weak correlation between fracture strength and mode of failure.
Conclusion: Short fiber reinforced composite resin significantly increases the fracture strength of direct occlusal veneers. Injectable composite resin has significantly higher fracture strength than packable composite resin as veneering materials of direct occlusal veneers.
Clinical relevance: Bi-structured direct occlusal veneers fabricated of injectable composite resin with low viscosity SFRC cores can withstand high masticatory forces in stress-bearing areas.
{"title":"Fracture strength of direct occlusal veneers with different short fiber-reinforced composite cores and veneering materials: an in-vitro study.","authors":"Menna Moataz Aboelnor, Khaled Aly Nour, Heba Mohamed Ahmed Al-Sanafawy","doi":"10.1007/s00784-024-06013-6","DOIUrl":"10.1007/s00784-024-06013-6","url":null,"abstract":"<p><strong>Objective: </strong>The objective of this study is to evaluate the effectiveness of two different viscosities of short fiber-reinforced composite resin (SFRC) cores and two different viscosities of veneering composite resins on the fracture strength of direct occlusal veneers.</p><p><strong>Materials and methods: </strong>One maxillary premolar was virtually prepared for an occlusal veneer and printed into resin dies. In total, (n = 48) resin dies were printed and assigned into three groups according to the type of core material of the occlusal veneer; mono-structured without a SFRC core, a high viscosity SFRC core, and a low viscosity SFRC core. Each group was re-divided into two subgroups (n = 8) according to the veneering composite resin; packable composite resin and injectable composite resin. Mono-structured and bi-structured direct occlusal veneers were fabricated on the resin dies using the mentioned core and veneering materials with the occlusal replica technique. Fracture strength was evaluated using a universal testing machine and the mode of failure was inspected. Statistical analysis to compare the core and veneering materials was performed using independent t test (P ≤ 0.05) and one-way ANOVA followed by tukey's post hoc test (Pa ≤ 0.0166) when appropriate. Interactions between subgroups were tested using two-way ANOVA, and one-way ANOVA was used to compare all subgroups followed by tukey's post hoc test (Pa ≤ 0.0033). Intergroup comparison between failure modes were performed using chi square test (Pa ≤ 0.0033).</p><p><strong>Results: </strong>The presence of a SFRC core significantly improved the fracture strength of the specimens. There was no significant difference between the fracture strength of high viscosity SFRC and low viscosity SFRC cores. Specimens veneered with injectable composite resin had significantly superior fracture strength compared to packable composite resin. Additionally, there was a weak correlation between fracture strength and mode of failure.</p><p><strong>Conclusion: </strong>Short fiber reinforced composite resin significantly increases the fracture strength of direct occlusal veneers. Injectable composite resin has significantly higher fracture strength than packable composite resin as veneering materials of direct occlusal veneers.</p><p><strong>Clinical relevance: </strong>Bi-structured direct occlusal veneers fabricated of injectable composite resin with low viscosity SFRC cores can withstand high masticatory forces in stress-bearing areas.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"635"},"PeriodicalIF":3.1,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11551077/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616160","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-11DOI: 10.1007/s00784-024-05973-z
Hongpeng Zhang, Shuo Liu, Rui Hao, Jing Yao
<p><strong>Objective: </strong>To compare the effectiveness of autologous dental bone powder grafts with deproteinized bovine bone mineral (DBBM) allografts in oral implant bone deficiency.</p><p><strong>Methods: </strong>Between January 2021 and January 2023, we enrolled 120 patients with inadequate bone for oral implantation, dividing them into an experimental group and a control group (60 each). The experimental group received autologous dental bone powder grafts, while the control group received DBBM allografts. Wound healing was assessed using the early healing index (EHI) with 5 days of closure as the baseline timeline, as Grade I: full closure without a fibrin line, Grade II: closure with a fibrin line, and Grade III: closure with fibrin covering the incision. Additional outcomes included buccal and palatal alveolar bone height, alveolar bone width at 3 (W1), 7 (W2), and 11 mm (W3) below the top of the alveolar ridge, and bone density measured before and 3 months after tooth extraction. The altered shape of the alveolar bone at the extraction site was assessed at 3- and 6-months post-extraction. Implant success rate was also evaluated at 15 days and 1 month after implantation. Comparisons were made using independent t-tests, paired t-tests, χ² tests, and Z tests, as appropriate.</p><p><strong>Results: </strong>The experimental group had a lower wound healing time and a greater prevalence of EHI categorization class I compared to the control group (P < 0.05). Three months after tooth extraction, there was no statistically significant difference in buccal and palatal alveolar bone heights between the experimental group and the pre-treatment measurements (P > 0.05). However, the control group showed a decrease in buccal and palatal alveolar bone heights compared to the pre-treatment period, while the experimental group had greater bone heights than the control group (P < 0.05). Three months after extraction, the widths of W1, W2, and W3 decreased in both groups. However, the experimental group maintained greater widths compared to the control group (P < 0.05). At 3 months post-extraction, both groups showed an increase in alveolar bone density at the extraction site. Notably, the experimental group had a higher bone density compared to the control group as well as new bone contour score of the alveolar bone at the extraction site (P < 0.05). However, at 6 months after extraction, there was no statistically significant difference in the new bone contour score of the alveolar bone at the extraction site between the two groups (P > 0.05). There was no significant difference in the implant success rate between the two groups. (P > 0.05).</p><p><strong>Conclusions: </strong>Autologous dental bone powder grafting promotes initial alveolar bone regeneration, enhances wound healing, and increases new bone density, providing favorable surgical conditions for dental implants. However, by 6 months, there was no significant difference in bone contour com
{"title":"Comparative evaluation of autologous dental bone powder and deproteinized bovine bone mineral allografts for oral implant bone deficits.","authors":"Hongpeng Zhang, Shuo Liu, Rui Hao, Jing Yao","doi":"10.1007/s00784-024-05973-z","DOIUrl":"https://doi.org/10.1007/s00784-024-05973-z","url":null,"abstract":"<p><strong>Objective: </strong>To compare the effectiveness of autologous dental bone powder grafts with deproteinized bovine bone mineral (DBBM) allografts in oral implant bone deficiency.</p><p><strong>Methods: </strong>Between January 2021 and January 2023, we enrolled 120 patients with inadequate bone for oral implantation, dividing them into an experimental group and a control group (60 each). The experimental group received autologous dental bone powder grafts, while the control group received DBBM allografts. Wound healing was assessed using the early healing index (EHI) with 5 days of closure as the baseline timeline, as Grade I: full closure without a fibrin line, Grade II: closure with a fibrin line, and Grade III: closure with fibrin covering the incision. Additional outcomes included buccal and palatal alveolar bone height, alveolar bone width at 3 (W1), 7 (W2), and 11 mm (W3) below the top of the alveolar ridge, and bone density measured before and 3 months after tooth extraction. The altered shape of the alveolar bone at the extraction site was assessed at 3- and 6-months post-extraction. Implant success rate was also evaluated at 15 days and 1 month after implantation. Comparisons were made using independent t-tests, paired t-tests, χ² tests, and Z tests, as appropriate.</p><p><strong>Results: </strong>The experimental group had a lower wound healing time and a greater prevalence of EHI categorization class I compared to the control group (P < 0.05). Three months after tooth extraction, there was no statistically significant difference in buccal and palatal alveolar bone heights between the experimental group and the pre-treatment measurements (P > 0.05). However, the control group showed a decrease in buccal and palatal alveolar bone heights compared to the pre-treatment period, while the experimental group had greater bone heights than the control group (P < 0.05). Three months after extraction, the widths of W1, W2, and W3 decreased in both groups. However, the experimental group maintained greater widths compared to the control group (P < 0.05). At 3 months post-extraction, both groups showed an increase in alveolar bone density at the extraction site. Notably, the experimental group had a higher bone density compared to the control group as well as new bone contour score of the alveolar bone at the extraction site (P < 0.05). However, at 6 months after extraction, there was no statistically significant difference in the new bone contour score of the alveolar bone at the extraction site between the two groups (P > 0.05). There was no significant difference in the implant success rate between the two groups. (P > 0.05).</p><p><strong>Conclusions: </strong>Autologous dental bone powder grafting promotes initial alveolar bone regeneration, enhances wound healing, and increases new bone density, providing favorable surgical conditions for dental implants. However, by 6 months, there was no significant difference in bone contour com","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"637"},"PeriodicalIF":3.1,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616143","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-11DOI: 10.1007/s00784-024-06020-7
Aylin Pasaoglu Bozkurt, Ece Buyukbasaran
Objectives: Wounds may occur in the mouth during orthodontic treatment. Orthodontists use a variety of substances to eliminate the irritation. This randomized clinical trial aimed to examine the effect of orthodontic wax and ora-aid material on wound healing, the duration of staying in the mouth, and the effect on pain and to evaluate the effect on the patient's quality of life.
Materials and methods: The study included two hundred forty patients aged 11-14 years. At the end of 1 week, patients with no wound were determined as the control group G1(n:65), patients using Ormco orthodontic wax as G2(n:86), and patients using Ora-aid as G3(n:89). The patients were asked to fill out the questionnaire given to them five times in total, as T0 when the wound occurred, T1 after 24 h, T2 after 48 h, T3 after 96 h, and T4 after 168 h.
Results: The study's results demonstrated no significant differences in the level of pain between males and females. For all post-baseline time points, the Ora aid group had a lower VAS for pain when compared with the Ormco orthodontic wax group (P < 0.01).
Conclusions: This study demonstrated that ora-aid effectively reduces the mucosal discomfort associated with orthodontic appliances, and this product may be a suitable alternative to traditional orthodontic wax material for dealing with oral mucosal injuries during orthodontic treatment.
Clinical relevance: This product may be a suitable alternative to traditional orthodontic wax material for dealing with oral mucosal injuries during orthodontic treatment.
目标:在正畸治疗期间,口腔内可能会出现伤口。正畸医生会使用各种物质来消除刺激。这项随机临床试验旨在研究正畸蜡和 ora-aid 材料对伤口愈合、在口腔内停留时间和疼痛的影响,并评估对患者生活质量的影响:研究对象包括 240 名 11-14 岁的患者。一周后,无伤口的患者被确定为对照组 G1(n:65),使用 Ormco 正畸蜡的患者为对照组 G2(n:86),使用 Ora-aid 的患者为对照组 G3(n:89)。患者共需填写五次问卷,分别为伤口发生时的 T0、24 小时后的 T1、48 小时后的 T2、96 小时后的 T3 和 168 小时后的 T4:研究结果表明,男性和女性的疼痛程度没有明显差异。在基线后的所有时间点上,Ora aid 组与 Ormco 正畸蜡组相比,疼痛 VAS 值均较低(P 结论:Ora aid 组与 Ormco 正畸蜡组相比,疼痛 VAS 值均较低(P):本研究表明,ora-aid 能有效减轻正畸装置引起的粘膜不适感,该产品可能是正畸治疗期间处理口腔粘膜损伤的传统正畸蜡材料的合适替代品:本产品可替代传统正畸蜡材料,用于处理正畸治疗过程中的口腔黏膜损伤。
{"title":"Effects of orthodontic wax and ora-aid on pain and discomfort at the beginning of orthodontic treatment.","authors":"Aylin Pasaoglu Bozkurt, Ece Buyukbasaran","doi":"10.1007/s00784-024-06020-7","DOIUrl":"https://doi.org/10.1007/s00784-024-06020-7","url":null,"abstract":"<p><strong>Objectives: </strong>Wounds may occur in the mouth during orthodontic treatment. Orthodontists use a variety of substances to eliminate the irritation. This randomized clinical trial aimed to examine the effect of orthodontic wax and ora-aid material on wound healing, the duration of staying in the mouth, and the effect on pain and to evaluate the effect on the patient's quality of life.</p><p><strong>Materials and methods: </strong>The study included two hundred forty patients aged 11-14 years. At the end of 1 week, patients with no wound were determined as the control group G1(n:65), patients using Ormco orthodontic wax as G2(n:86), and patients using Ora-aid as G3(n:89). The patients were asked to fill out the questionnaire given to them five times in total, as T0 when the wound occurred, T1 after 24 h, T2 after 48 h, T3 after 96 h, and T4 after 168 h.</p><p><strong>Results: </strong>The study's results demonstrated no significant differences in the level of pain between males and females. For all post-baseline time points, the Ora aid group had a lower VAS for pain when compared with the Ormco orthodontic wax group (P < 0.01).</p><p><strong>Conclusions: </strong>This study demonstrated that ora-aid effectively reduces the mucosal discomfort associated with orthodontic appliances, and this product may be a suitable alternative to traditional orthodontic wax material for dealing with oral mucosal injuries during orthodontic treatment.</p><p><strong>Clinical relevance: </strong>This product may be a suitable alternative to traditional orthodontic wax material for dealing with oral mucosal injuries during orthodontic treatment.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"636"},"PeriodicalIF":3.1,"publicationDate":"2024-11-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142616148","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-11-08DOI: 10.1007/s00784-024-06037-y
Lana Cardoso-Silva, Bianca Caroline Gomes, Roberta Paula de Faria Melo, Isabella Silva Catananti, Beatriz Kelly Barros Lopes, Izadora Ramos de Almeida, Alexandra Mussolino de Queiroz, Francisco Wanderley Garcia de Paula-Silva, David John Manton, Fabricio Kitazono de Carvalho
Objective: The aim of this observational study was to compare the chewing patterns of children with unilateral Molar Incisor Hypomineralization (MIH) to those of children without MIH and to assess how the MIH severity influences the risk of chewing deviation. The hypothesis was that children with unilateral MIH would prefer to chew on the side opposite the defect.
Methods: A total of 121 children were included in this investigation and evaluated for their preferred chewing side (PCS). This study population comprised 45 children with unilateral mild MIH (G1), 42 with unilateral severe MIH (G2), and 34 children in the control group (CG) who had no MIH but presented with unilateral chewing complaints.
Results: The PCS pattern differed among the groups, with 31% of the children with MIH and 55.9% of the CG showing bilateral chewing. The chewing deviation prevalence was 24% in the CG and 52% in G2 (χ2 test; p = 0.03). Binomial logistic regression analysis revealed that both severities of MIH influenced the likelihood of chewing deviation (χ2 = 7.33, p = 0.026). Children with unilateral severe MIH were 3.57 times more likely to exhibit chewing deviation than were those without MIH.
Conclusions: The null hypothesis was rejected, indicating that unilateral MIH affects children's masticatory patterns, increasing the risk of chewing deviation.
Clinical relevance: Unilateral chewing may be associated with various health issues, such as temporomandibular disorders (TMDs), decreased hearing, and vision problems. Unilateral MIH is a potential risk factor for unilateral chewing.
{"title":"Unilateral molar Incisor hypomineralization influences the chewing side? an observational study in children.","authors":"Lana Cardoso-Silva, Bianca Caroline Gomes, Roberta Paula de Faria Melo, Isabella Silva Catananti, Beatriz Kelly Barros Lopes, Izadora Ramos de Almeida, Alexandra Mussolino de Queiroz, Francisco Wanderley Garcia de Paula-Silva, David John Manton, Fabricio Kitazono de Carvalho","doi":"10.1007/s00784-024-06037-y","DOIUrl":"https://doi.org/10.1007/s00784-024-06037-y","url":null,"abstract":"<p><strong>Objective: </strong>The aim of this observational study was to compare the chewing patterns of children with unilateral Molar Incisor Hypomineralization (MIH) to those of children without MIH and to assess how the MIH severity influences the risk of chewing deviation. The hypothesis was that children with unilateral MIH would prefer to chew on the side opposite the defect.</p><p><strong>Methods: </strong>A total of 121 children were included in this investigation and evaluated for their preferred chewing side (PCS). This study population comprised 45 children with unilateral mild MIH (G1), 42 with unilateral severe MIH (G2), and 34 children in the control group (CG) who had no MIH but presented with unilateral chewing complaints.</p><p><strong>Results: </strong>The PCS pattern differed among the groups, with 31% of the children with MIH and 55.9% of the CG showing bilateral chewing. The chewing deviation prevalence was 24% in the CG and 52% in G2 (χ2 test; p = 0.03). Binomial logistic regression analysis revealed that both severities of MIH influenced the likelihood of chewing deviation (χ2 = 7.33, p = 0.026). Children with unilateral severe MIH were 3.57 times more likely to exhibit chewing deviation than were those without MIH.</p><p><strong>Conclusions: </strong>The null hypothesis was rejected, indicating that unilateral MIH affects children's masticatory patterns, increasing the risk of chewing deviation.</p><p><strong>Clinical relevance: </strong>Unilateral chewing may be associated with various health issues, such as temporomandibular disorders (TMDs), decreased hearing, and vision problems. Unilateral MIH is a potential risk factor for unilateral chewing.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"634"},"PeriodicalIF":3.1,"publicationDate":"2024-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142603612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: Platelet concentrates are biomaterials with significant potential in tissue regeneration, functioning as scaffolds with greater leukocyte inclusion and a flexible fibrin mesh. However these concentrates have different preparation methods and biological properties. The objective of this clinical investigation was to evaluate the effects of utilizing platelet-rich fibrin (PRF) materials (L-PRF and A-PRF) as a palatal bandage following free gingival graft (FGG) on patients' morbidity and oral health-related quality of life.
Materials and methods: Thirty-nine participants received FGG to promote keratinized tissue and treat gingival recession. Participants were randomly assigned to L-PRF, A-PRF, and control groups, with 13 participants in each. They used a visual analog scale (VAS) to rate their pain, analgesic medication use, dietary changes, discomfort, and bleeding at 1-7 days, 14 days and 1 month during the healing process. Patients' quality of life was assessed using the Oral Health Impact Profile (OHIP-14) at baseline, 1-7 days, 14 days, 1 month, and 6 months.
Results: There was no difference in anxiety levels between the all groups. (p > 0.05). The control group had higher OHIP-14 total scores than the other groups, but the differences were not statistically significant, especially in the first seven days (p > 0.05). In addition, the PRF groups showed an improvement in quality of life after 14 days, 1 month, and 6 months (p < 0.05). Patients' pain and suffering decreased with healing. The control group took more postoperative analgesics than PRF groups. In addition, there was a significant decrease in patient complaints about medicine intake, bleeding, pain, perceived sensitivity, and dietary modifications in all groups during follow-up.
Conclusions: PRF palatal bandages may improve patient's quality of life, donor site healing, postoperative pain and morbidity.
Clinical relevance: This study found that preserving the palate in FGG and employing PRF materials that speed palate healing reduce discomfort and morbidity.
{"title":"Impact of platelet-rich fibrin derivatives on patient morbidity and quality of life in palatal donor sites following free gingival graft surgery: a randomized clinical trial.","authors":"Dilek Özkan Şen, Betül Irız Şengül, Fatma Uçan Yarkaç, Elif Öncü","doi":"10.1007/s00784-024-06023-4","DOIUrl":"https://doi.org/10.1007/s00784-024-06023-4","url":null,"abstract":"<p><strong>Objectives: </strong>Platelet concentrates are biomaterials with significant potential in tissue regeneration, functioning as scaffolds with greater leukocyte inclusion and a flexible fibrin mesh. However these concentrates have different preparation methods and biological properties. The objective of this clinical investigation was to evaluate the effects of utilizing platelet-rich fibrin (PRF) materials (L-PRF and A-PRF) as a palatal bandage following free gingival graft (FGG) on patients' morbidity and oral health-related quality of life.</p><p><strong>Materials and methods: </strong>Thirty-nine participants received FGG to promote keratinized tissue and treat gingival recession. Participants were randomly assigned to L-PRF, A-PRF, and control groups, with 13 participants in each. They used a visual analog scale (VAS) to rate their pain, analgesic medication use, dietary changes, discomfort, and bleeding at 1-7 days, 14 days and 1 month during the healing process. Patients' quality of life was assessed using the Oral Health Impact Profile (OHIP-14) at baseline, 1-7 days, 14 days, 1 month, and 6 months.</p><p><strong>Results: </strong>There was no difference in anxiety levels between the all groups. (p > 0.05). The control group had higher OHIP-14 total scores than the other groups, but the differences were not statistically significant, especially in the first seven days (p > 0.05). In addition, the PRF groups showed an improvement in quality of life after 14 days, 1 month, and 6 months (p < 0.05). Patients' pain and suffering decreased with healing. The control group took more postoperative analgesics than PRF groups. In addition, there was a significant decrease in patient complaints about medicine intake, bleeding, pain, perceived sensitivity, and dietary modifications in all groups during follow-up.</p><p><strong>Conclusions: </strong>PRF palatal bandages may improve patient's quality of life, donor site healing, postoperative pain and morbidity.</p><p><strong>Clinical relevance: </strong>This study found that preserving the palate in FGG and employing PRF materials that speed palate healing reduce discomfort and morbidity.</p>","PeriodicalId":10461,"journal":{"name":"Clinical Oral Investigations","volume":"28 12","pages":"631"},"PeriodicalIF":3.1,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142590170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}