Pub Date : 2025-07-22eCollection Date: 2025-09-01DOI: 10.34172/japid.025.3658
Parichehr Behfarnia, Reza Birang, Amineh Ghaznavi, Seyed Amir Mirghaderi
Background: The present study evaluated the synergistic effect of 808 nm and 660 nm diode lasers on the processes of healing and pain management following crown lengthening surgery.
Methods: This randomized clinical trial involved 20 patients who underwent surgical crown lengthening on both sides of their jaw. Following the surgery, one tooth from each patient was randomly assigned to either the case group (irradiated with 808 nm and 660 nm diode lasers as photobiomodulation [PBM] therapy) or the control group (laser device remained switched off). The early healing index (EHI), comprising clinical signs of inflammation (CSI), clinical signs of homeostasis (CSH), and clinical signs of re-epithelialization (CSR), was assessed on days 3 and 7. Pain severity was quantified on the day of surgery and 1, 3, and 7 days after surgery using a visual analog scale. The data were analyzed using the Wilcoxon test.
Results: No significant differences were observed in CSR on days 3 (P=0.18) and 7 (P=1.0), nor in CSI on day 3 (P=0.477) after surgery. However, a significant difference was identified in CSI on day 7 and in CSH on both days 3 and 7 (P<0.05) after surgery. Furthermore, the level of postoperative pain demonstrated a significant difference (P≤0.005).
Conclusion: PBM demonstrably enhanced CSI by day 7 and improved CSH by days 3 and 7, in addition to decreasing postoperative pain.
{"title":"Effect of photobiomodulation on wound healing and pain after crown lengthening surgery: A randomized clinical trial.","authors":"Parichehr Behfarnia, Reza Birang, Amineh Ghaznavi, Seyed Amir Mirghaderi","doi":"10.34172/japid.025.3658","DOIUrl":"10.34172/japid.025.3658","url":null,"abstract":"<p><strong>Background: </strong>The present study evaluated the synergistic effect of 808 nm and 660 nm diode lasers on the processes of healing and pain management following crown lengthening surgery.</p><p><strong>Methods: </strong>This randomized clinical trial involved 20 patients who underwent surgical crown lengthening on both sides of their jaw. Following the surgery, one tooth from each patient was randomly assigned to either the case group (irradiated with 808 nm and 660 nm diode lasers as photobiomodulation [PBM] therapy) or the control group (laser device remained switched off). The early healing index (EHI), comprising clinical signs of inflammation (CSI), clinical signs of homeostasis (CSH), and clinical signs of re-epithelialization (CSR), was assessed on days 3 and 7. Pain severity was quantified on the day of surgery and 1, 3, and 7 days after surgery using a visual analog scale. The data were analyzed using the Wilcoxon test.</p><p><strong>Results: </strong>No significant differences were observed in CSR on days 3 (<i>P</i>=0.18) and 7 (<i>P</i>=1.0), nor in CSI on day 3 (<i>P</i>=0.477) after surgery. However, a significant difference was identified in CSI on day 7 and in CSH on both days 3 and 7 (<i>P</i><0.05) after surgery. Furthermore, the level of postoperative pain demonstrated a significant difference (<i>P</i>≤0.005).</p><p><strong>Conclusion: </strong>PBM demonstrably enhanced CSI by day 7 and improved CSH by days 3 and 7, in addition to decreasing postoperative pain.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 3","pages":"172-178"},"PeriodicalIF":0.0,"publicationDate":"2025-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501482/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145254048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-28eCollection Date: 2025-09-01DOI: 10.34172/japid.025.3543
Saurabh Kamat, Senthil Murugan M, Edlyn Rodrigues, Jochima Eudora Cota, Vikas Dhupar, Francis Akkara
Background: This study evaluated the impact of different regenerative biomaterial combinations on bone quality and implant stability in guided bone regeneration (GBR).
Methods: A pilot study was conducted from September 2020 to October 2023 to compare the quality of bone regeneration and implant stability following GBR using three composite graft combinations. Forty-seven patients participated in the study in three experimental groups: group A (deproteinized cancellous bovine bone [xenograft] with injectable platelet-rich fibrin [i-PRF]), group B (xenograft with autogenous bone graft in a 2:1 ratio with i-PRF), and group C (xenograft with autogenous bone graft in a 1:1 ratio with i-PRF). The implant stability quotient (ISQ) was measured at the time of implant placement. Crestal bone biopsy procedures were performed.
Results: The study found that group C, using a 1:1 ratio of xenograft and autogenous graft with i-PRF, achieved the highest new bone formation (65.83%) and demonstrated moderately high vascularization and osteoclastic activity, indicative of good remodeling potential. ISQ measurements for all groups indicated good primary stability of implants, ranging from 55 to 65 at the time of placement.
Conclusion: Combining xenograft with autogenous graft in a 1:1 ratio, along with i-PRF, yielded optimal outcomes for new bone formation in GBR procedures. However, further research is needed to address the limitations associated with i-PRF, such as lack of rigidity and faster degradation, to enhance its application in GBR procedures.
{"title":"A pilot study and histological examination of xenograft and autogenous bone combinations with i-PRF in guided bone regeneration.","authors":"Saurabh Kamat, Senthil Murugan M, Edlyn Rodrigues, Jochima Eudora Cota, Vikas Dhupar, Francis Akkara","doi":"10.34172/japid.025.3543","DOIUrl":"10.34172/japid.025.3543","url":null,"abstract":"<p><strong>Background: </strong>This study evaluated the impact of different regenerative biomaterial combinations on bone quality and implant stability in guided bone regeneration (GBR).</p><p><strong>Methods: </strong>A pilot study was conducted from September 2020 to October 2023 to compare the quality of bone regeneration and implant stability following GBR using three composite graft combinations. Forty-seven patients participated in the study in three experimental groups: group A (deproteinized cancellous bovine bone [xenograft] with injectable platelet-rich fibrin [i-PRF]), group B (xenograft with autogenous bone graft in a 2:1 ratio with i-PRF), and group C (xenograft with autogenous bone graft in a 1:1 ratio with i-PRF). The implant stability quotient (ISQ) was measured at the time of implant placement. Crestal bone biopsy procedures were performed.</p><p><strong>Results: </strong>The study found that group C, using a 1:1 ratio of xenograft and autogenous graft with i-PRF, achieved the highest new bone formation (65.83%) and demonstrated moderately high vascularization and osteoclastic activity, indicative of good remodeling potential. ISQ measurements for all groups indicated good primary stability of implants, ranging from 55 to 65 at the time of placement.</p><p><strong>Conclusion: </strong>Combining xenograft with autogenous graft in a 1:1 ratio, along with i-PRF, yielded optimal outcomes for new bone formation in GBR procedures. However, further research is needed to address the limitations associated with i-PRF, such as lack of rigidity and faster degradation, to enhance its application in GBR procedures.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 3","pages":"132-139"},"PeriodicalIF":0.0,"publicationDate":"2025-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12504848/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145260170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-11eCollection Date: 2025-09-01DOI: 10.34172/japid.025.3478
Nasrin Faal Rastegar, Farzane Vaziri, Seyed Mostafa Mahmoudi
Background: The reduction of alveolar ridge volume after tooth extraction can be decreased through ridge preservation. According to previous studies, statin drugs induce osteogenesis. Therefore, this study aimed to evaluate the effect of simvastatin on the preservation and ossification of the alveolar ridge after tooth extraction.
Methods: In this single-center randomized clinical trial, 40 dental sockets in 40 patients were randomly divided into the treatment group (collagen with simvastatin) and the control group (collagen only). Histologic bone examination was performed under a light microscope two months after socket preservation at the time of dental implants. The predictable variable was using simvastatin in dental sockets. In the treatment group, collagen was used with simvastatin; in the control group, only collagen was used. The percentage of bone formation was the primary outcome, which was measured as the area of newly formed bone. In this study, inflammatory reaction, the amount of remaining bone substitute, and foreign body reaction were compared between the two groups. Covariates included age, sex, and tooth location. T-test was used for normally distributed data, while the Mann-Whitney test was used for non-normal data. P<0.05 was considered significant.
Results: The results showed that following eight weeks of simvastatin use in the treatment group, the percentage of new bone formation was significantly higher compared to the control group (treatment group vs. control group: 69.28±3.93 vs. 52.76±2.01; P=0.0001). No foreign body reaction and residual graft materials were observed in the treatment and control groups. Furthermore, the study showed an inflammatory reaction in only 23.5% of the samples in the control group (P=0.045).
Conclusion: Simvastatin significantly increased the formation of new bone in the dental socket in the treatment group.
背景:牙槽嵴保存可以减少拔牙后牙槽嵴体积的减少。根据以往的研究,他汀类药物可诱导成骨。因此,本研究旨在评价辛伐他汀对拔牙后牙槽嵴保存和骨化的影响。方法:采用单中心随机临床试验,将40例患者的40个牙套随机分为治疗组(含辛伐他汀胶原蛋白)和对照组(仅含胶原蛋白)。植牙时保存牙槽两个月后在光镜下进行骨组织学检查。可预测的变量是在牙槽内使用辛伐他汀。治疗组采用胶原蛋白联合辛伐他汀治疗;对照组只使用胶原蛋白。骨形成的百分比是主要结果,以新形成骨的面积来衡量。本研究比较两组的炎症反应、骨替代物剩余量、异物反应。协变量包括年龄、性别和牙齿位置。正态分布数据采用t检验,非正态分布数据采用Mann-Whitney检验。结果:治疗组在辛伐他汀治疗8周后,新生骨形成率明显高于对照组(治疗组vs对照组:69.28±3.93 vs 52.76±2.01;P=0.0001)。治疗组和对照组均未见异物反应和移植物残留。此外,研究显示对照组中只有23.5%的样本出现炎症反应(P=0.045)。结论:辛伐他汀治疗组可明显促进牙槽内新生骨的形成。
{"title":"Histologic evaluation of topical simvastatin effects on extraction sockets: A randomized controlled clinical trial.","authors":"Nasrin Faal Rastegar, Farzane Vaziri, Seyed Mostafa Mahmoudi","doi":"10.34172/japid.025.3478","DOIUrl":"10.34172/japid.025.3478","url":null,"abstract":"<p><strong>Background: </strong>The reduction of alveolar ridge volume after tooth extraction can be decreased through ridge preservation. According to previous studies, statin drugs induce osteogenesis. Therefore, this study aimed to evaluate the effect of simvastatin on the preservation and ossification of the alveolar ridge after tooth extraction.</p><p><strong>Methods: </strong>In this single-center randomized clinical trial, 40 dental sockets in 40 patients were randomly divided into the treatment group (collagen with simvastatin) and the control group (collagen only). Histologic bone examination was performed under a light microscope two months after socket preservation at the time of dental implants. The predictable variable was using simvastatin in dental sockets. In the treatment group, collagen was used with simvastatin; in the control group, only collagen was used. The percentage of bone formation was the primary outcome, which was measured as the area of newly formed bone. In this study, inflammatory reaction, the amount of remaining bone substitute, and foreign body reaction were compared between the two groups. Covariates included age, sex, and tooth location. T-test was used for normally distributed data, while the Mann-Whitney test was used for non-normal data. <i>P</i><0.05 was considered significant.</p><p><strong>Results: </strong>The results showed that following eight weeks of simvastatin use in the treatment group, the percentage of new bone formation was significantly higher compared to the control group (treatment group vs. control group: 69.28±3.93 vs. 52.76±2.01; <i>P</i>=0.0001). No foreign body reaction and residual graft materials were observed in the treatment and control groups. Furthermore, the study showed an inflammatory reaction in only 23.5% of the samples in the control group (<i>P</i>=0.045).</p><p><strong>Conclusion: </strong>Simvastatin significantly increased the formation of new bone in the dental socket in the treatment group.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 3","pages":"140-144"},"PeriodicalIF":0.0,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501483/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145254027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: The study aimed to compare the results of cytotoxicity and in vivo irritation and sensitization tests of a new antler-derived bone substitute with those of a bovine-derived xenograft.
Methods: This study included an in vitro cytotoxicity test based on ISO 10993-5 standard. Additionally, in vivo irritation and sensitization tests were carried out according to ISO 10993-10 standard protocol.
Results: The cytotoxicity test showed a viability of 99.46±1.09% for the antler-derived bone substitute and 98.42±1.84% for the bovine xenograft (P=0.445). Furthermore, after 24 hours, no differences in morphological grade were found in both samples. The irritation test indicated a primary irritation index (PII) score of 0 for both the antler and bovine xenografts. Likewise, the sensitization test demonstrated a sensitization score of 0 for both the antler and bovine xenografts. All animals appeared clinically normal throughout the study in both in vivo tests, and all sites of the test extract and the reagent control seemed normal.
Conclusion: Both the antler-derived and bovine xenografts were found to be non-toxic, non-irritating, and non-sensitizing. Further studies should be conducted on other essential laboratory tests and animal and clinical studies.
{"title":"Impact of animal source on biocompatibility of bone xenografts: A comparative animal study.","authors":"Ardeshir Lafzi, Reza Amid, Mahdi Kadkhodazadeh, Anahita Moscowchi, Javad Mehrani, Nima Ahmadi, Amirali Karimi Vasigh","doi":"10.34172/japid.025.3443","DOIUrl":"10.34172/japid.025.3443","url":null,"abstract":"<p><strong>Background: </strong>The study aimed to compare the results of cytotoxicity and in vivo irritation and sensitization tests of a new antler-derived bone substitute with those of a bovine-derived xenograft.</p><p><strong>Methods: </strong>This study included an in vitro cytotoxicity test based on ISO 10993-5 standard. Additionally, in vivo irritation and sensitization tests were carried out according to ISO 10993-10 standard protocol.</p><p><strong>Results: </strong>The cytotoxicity test showed a viability of 99.46±1.09% for the antler-derived bone substitute and 98.42±1.84% for the bovine xenograft (<i>P</i>=0.445). Furthermore, after 24 hours, no differences in morphological grade were found in both samples. The irritation test indicated a primary irritation index (PII) score of 0 for both the antler and bovine xenografts. Likewise, the sensitization test demonstrated a sensitization score of 0 for both the antler and bovine xenografts. All animals appeared clinically normal throughout the study in both in vivo tests, and all sites of the test extract and the reagent control seemed normal.</p><p><strong>Conclusion: </strong>Both the antler-derived and bovine xenografts were found to be non-toxic, non-irritating, and non-sensitizing. Further studies should be conducted on other essential laboratory tests and animal and clinical studies.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 3","pages":"157-162"},"PeriodicalIF":0.0,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501480/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145254060","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-05-20eCollection Date: 2025-09-01DOI: 10.34172/japid.025.2316
Amirhossein Farahmand, Ali Ghanbarzadeh, Zahra Salmani, Maryam Zohary, Marzieh Ghanbarzadeh
Background: Ketorolac is classified as a non-steroidal anti-inflammatory drug. It functions by inhibiting the production of prostaglandins, thereby diminishing the local inflammatory response. This medication has the potential to alleviate postoperative complications, including pain and swelling that may occur following surgical procedures.
Methods: Fifty patients with mild chronic periodontitis were randomly divided into two blinded groups of 25 patients. One group underwent scaling and root planing (SRP) with 2% ketorolac trometamol (KT) irrigation, and the other group received 0.2% chlorhexidine (CHX). Treatment was performed on the first and second molars in both mandibular quadrants. Various clinical periodontal parameters, such as plaque index (PI), bleeding on probing (BOP), pocket probing depth (PPD), clinical attachment loss (CAL ), and gingival index (GI) were carefully recorded. Patients were scheduled for follow-up visits at 3-month intervals.
Results: The CHX mouthwash and KT groups did not differ significantly in clinical periodontal parameters at baseline. Clinical outcomes demonstrated, as anticipated, statistically significant improvements in the percentages of PI, BOP, GI, PD, and CAL at 60 and 90 days compared to baseline in both groups (P<0.05). In contrast to the CHX group, the KT group's clinical periodontal parameters (PI, BOP, and GI) significantly decreased after the follow-up period.
Conclusion: KT can be recommended as a complementary treatment for individuals suffering from chronic periodontitis, as it is more effective in reducing PI, GI, and BOP compared with CHX.
{"title":"The impact of subgingival irrigation using ketorolac and chlorhexidine in patients with chronic periodontitis: A randomized, double-blind, controlled, clinical trial.","authors":"Amirhossein Farahmand, Ali Ghanbarzadeh, Zahra Salmani, Maryam Zohary, Marzieh Ghanbarzadeh","doi":"10.34172/japid.025.2316","DOIUrl":"10.34172/japid.025.2316","url":null,"abstract":"<p><strong>Background: </strong>Ketorolac is classified as a non-steroidal anti-inflammatory drug. It functions by inhibiting the production of prostaglandins, thereby diminishing the local inflammatory response. This medication has the potential to alleviate postoperative complications, including pain and swelling that may occur following surgical procedures.</p><p><strong>Methods: </strong>Fifty patients with mild chronic periodontitis were randomly divided into two blinded groups of 25 patients. One group underwent scaling and root planing (SRP) with 2% ketorolac trometamol (KT) irrigation, and the other group received 0.2% chlorhexidine (CHX). Treatment was performed on the first and second molars in both mandibular quadrants. Various clinical periodontal parameters, such as plaque index (PI), bleeding on probing (BOP), pocket probing depth (PPD), clinical attachment loss (CAL ), and gingival index (GI) were carefully recorded. Patients were scheduled for follow-up visits at 3-month intervals.</p><p><strong>Results: </strong>The CHX mouthwash and KT groups did not differ significantly in clinical periodontal parameters at baseline. Clinical outcomes demonstrated, as anticipated, statistically significant improvements in the percentages of PI, BOP, GI, PD, and CAL at 60 and 90 days compared to baseline in both groups (<i>P</i><0.05). In contrast to the CHX group, the KT group's clinical periodontal parameters (PI, BOP, and GI) significantly decreased after the follow-up period.</p><p><strong>Conclusion: </strong>KT can be recommended as a complementary treatment for individuals suffering from chronic periodontitis, as it is more effective in reducing PI, GI, and BOP compared with CHX.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 3","pages":"163-171"},"PeriodicalIF":0.0,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501475/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145254078","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-23eCollection Date: 2025-06-01DOI: 10.34172/japid.025.3475
Omid Moghaddas, Vanda Banazadeh
Background: This study aimed to compare insertion torque (IT) and implant stability quotient (ISQ) values immediately and three months after surgery with standard drilling (SD) and osseodensification (OD) drilling methods.
Methods: In this prospective study, 39 implants with the same diameter and length were placed in 21 patients using SD (23 implants) and OD (16 implants) methods in the posterior maxilla. The amounts of IT after surgery and ISQ after surgery and three months later were evaluated. The data were extracted and statistically analyzed with PASS2 software. The difference between IT and ISQ was determined by the two-way repeated-measures ANOVA at a significance level of 0.001.
Results: Immediately after surgery, the amount of IT using the OD drilling method was 37% higher than the SD drilling (P<0.001). ISQ values after surgery did not show a significant difference between SD and OD (P1<0.176). Three months after surgery, the ISQ values in both groups were not significantly different. ISQ values for all OD and SD group experimental parameters remained above the threshold value of 68. IT values showed a positive correlation with ISQ values at baseline.
Conclusion: In the present study, the OD technique provided a higher IT rate after surgery compared to the SD method; however, no difference was seen between the two groups regarding ISQ value either after surgery or three months later.
{"title":"Comparison of osseodensification and standard drilling methods on implant stability quotient and insertion torque values of implants.","authors":"Omid Moghaddas, Vanda Banazadeh","doi":"10.34172/japid.025.3475","DOIUrl":"10.34172/japid.025.3475","url":null,"abstract":"<p><strong>Background: </strong>This study aimed to compare insertion torque (IT) and implant stability quotient (ISQ) values immediately and three months after surgery with standard drilling (SD) and osseodensification (OD) drilling methods.</p><p><strong>Methods: </strong>In this prospective study, 39 implants with the same diameter and length were placed in 21 patients using SD (23 implants) and OD (16 implants) methods in the posterior maxilla. The amounts of IT after surgery and ISQ after surgery and three months later were evaluated. The data were extracted and statistically analyzed with PASS2 software. The difference between IT and ISQ was determined by the two-way repeated-measures ANOVA at a significance level of 0.001.</p><p><strong>Results: </strong>Immediately after surgery, the amount of IT using the OD drilling method was 37% higher than the SD drilling (<i>P</i><0.001). ISQ values after surgery did not show a significant difference between SD and OD (<i>P</i>1<0.176). Three months after surgery, the ISQ values in both groups were not significantly different. ISQ values for all OD and SD group experimental parameters remained above the threshold value of 68. IT values showed a positive correlation with ISQ values at baseline.</p><p><strong>Conclusion: </strong>In the present study, the OD technique provided a higher IT rate after surgery compared to the SD method; however, no difference was seen between the two groups regarding ISQ value either after surgery or three months later.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 2","pages":"59-64"},"PeriodicalIF":0.0,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261070/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144651346","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-22eCollection Date: 2025-06-01DOI: 10.34172/japid.025.3524
Abdusalam E Alrmali, Paolo Nava, Jacob Martin Zimmer, Syed Hanan Rufai, Andreas Onisiforou, Hom-Lay Wang
This article introduces a minimally invasive slim V-shaped surgical technique for labial frenectomy, specifically targeting high labial frenulum attachment. Proper frenulum management is critical in dental specialties, influencing aesthetics, phonetics, and prosthetic rehabilitation outcomes. The described technique is adaptable to various types of labial frenulum, including mucosal, gingival, papillary, and papilla penetrating. It involves a slim V-shaped incision, consecutive frenulum detachment, and repositioning within the vestibule, effectively addressing potential recurrence growth. Its minimally invasive nature reduces wound expansion into neighboring structures, ensuring optimal healing and minimizing postoperative discomfort. In conclusion, the slim V-shaped surgical technique offers a promising solution, minimizing complications and maximizing treatment success for high labial frenulum attachment.
{"title":"Slim V-shaped frenectomy: Description of a minimally invasive surgical technique.","authors":"Abdusalam E Alrmali, Paolo Nava, Jacob Martin Zimmer, Syed Hanan Rufai, Andreas Onisiforou, Hom-Lay Wang","doi":"10.34172/japid.025.3524","DOIUrl":"10.34172/japid.025.3524","url":null,"abstract":"<p><p>This article introduces a minimally invasive slim V-shaped surgical technique for labial frenectomy, specifically targeting high labial frenulum attachment. Proper frenulum management is critical in dental specialties, influencing aesthetics, phonetics, and prosthetic rehabilitation outcomes. The described technique is adaptable to various types of labial frenulum, including mucosal, gingival, papillary, and papilla penetrating. It involves a slim V-shaped incision, consecutive frenulum detachment, and repositioning within the vestibule, effectively addressing potential recurrence growth. Its minimally invasive nature reduces wound expansion into neighboring structures, ensuring optimal healing and minimizing postoperative discomfort. In conclusion, the slim V-shaped surgical technique offers a promising solution, minimizing complications and maximizing treatment success for high labial frenulum attachment.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 2","pages":"119-122"},"PeriodicalIF":0.0,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261069/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144651350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Excess cement is one of the most prevalent problems with cement-retained implant-supported prostheses. The excess cement may be considered an important source of inflammation during implant application. Optimizing the design procedure for reducing excess cement is necessary for successful and safe implant applications.
Methods: This study assessed the effect of two confounding factors, i.e., emergence profile and space gap size, on the level of excess cement. Three types of emergence profiles (concave, convex, and straight) and three different gap sizes (30, 60, and 90 µm) were considered for implant design, and the level of excess cement was measured for each design.
Results: Statistical analyses using one-way ANOVA followed by post hoc P value correction revealed that the best emergence profile with the lowest excess cement was the straight profile, with statistically lower excess cement compared with concave and convex profiles (P<0.05) and no significant difference between concave and convex profiles. Furthermore, analyses showed that lower gap size was associated with lower excess cement, even though increasing the gap size from a threshold (>60 µm) made the difference significant. Interaction analysis using two-way ANOVA also indicated the interaction between the emergence profile and space gap size.
Conclusion: The results emphasized that a straight profile with a smaller gap size should be considered to reduce the excess cement. However, due to the small sample size of the study, further analyses with different types of materials, angles of deformation, and gap sizes are required to reveal the exact relationship between excess cement and the design specifications.
{"title":"Effect of emergence profile and space gap size on excess cement in cement-retained implant reconstructions.","authors":"Fariborz Vafaee, Saeed Nikanjam, Arash Farahnaki, Meysam Mahabadi, Sajjad Farashi, Sara Khazaei, Shiva Shahabi","doi":"10.34172/japid.025.2292","DOIUrl":"10.34172/japid.025.2292","url":null,"abstract":"<p><strong>Background: </strong>Excess cement is one of the most prevalent problems with cement-retained implant-supported prostheses. The excess cement may be considered an important source of inflammation during implant application. Optimizing the design procedure for reducing excess cement is necessary for successful and safe implant applications.</p><p><strong>Methods: </strong>This study assessed the effect of two confounding factors, i.e., emergence profile and space gap size, on the level of excess cement. Three types of emergence profiles (concave, convex, and straight) and three different gap sizes (30, 60, and 90 µm) were considered for implant design, and the level of excess cement was measured for each design.</p><p><strong>Results: </strong>Statistical analyses using one-way ANOVA followed by post hoc <i>P</i> value correction revealed that the best emergence profile with the lowest excess cement was the straight profile, with statistically lower excess cement compared with concave and convex profiles (<i>P</i><0.05) and no significant difference between concave and convex profiles. Furthermore, analyses showed that lower gap size was associated with lower excess cement, even though increasing the gap size from a threshold (>60 µm) made the difference significant. Interaction analysis using two-way ANOVA also indicated the interaction between the emergence profile and space gap size.</p><p><strong>Conclusion: </strong>The results emphasized that a straight profile with a smaller gap size should be considered to reduce the excess cement. However, due to the small sample size of the study, further analyses with different types of materials, angles of deformation, and gap sizes are required to reveal the exact relationship between excess cement and the design specifications.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 2","pages":"65-70"},"PeriodicalIF":0.0,"publicationDate":"2025-04-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261064/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144651347","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-14eCollection Date: 2025-06-01DOI: 10.34172/japid.025.3722
Maziar Ebrahimi Dastgurdi, Douglas Deporter, Max Xia, Mohammad Ketabi
Background: Immediate molar implants (IMIs) have been shown to provide an effective treatment, but their placement comes with potential anatomically related risks.
Methods: CBCTs of>400 dental sites were analyzed for key anatomical features at mandibular molar sites that can impact the placement of IMIs. Features measured included distances from each molar furcation to points risking lingual plate perforation or inferior alveolar nerve (IAC) damage, distances from molar root apices to IAC, mesiodistal and buccolingual widths of molar inter-septal bone (ISB), and thicknesses of buccal and lingual cortical plates at first and second mandibular molar sites.
Results: Distances from molar furcations to contact with lingual cortical plates and to IAC decreased significantly from mesial to distal, as did distances from root apices to the mandibular canal. Both buccolingual and mesiodistal ISB widths and thicknesses of buccal and lingual cortical plates increased mesiodistally. Buccolingual ISB widths were largest coronally for both molar sites and decreased apically. The reverse was found with mesiodistal septal ISB widths, which increased coronoapically.
Conclusion: Risks of lingual perforations or IAC damage were significantly greater at second molars vs. first molars. The ability to place IMIs in ISB at first molars was estimated to be>twice as often as at second molars. Maximal implant lengths for IMIs placed in the furcal bone should not exceed 10 mm.
{"title":"CBCT data relevant in treatment planning for immediate mandibular molar implant placement.","authors":"Maziar Ebrahimi Dastgurdi, Douglas Deporter, Max Xia, Mohammad Ketabi","doi":"10.34172/japid.025.3722","DOIUrl":"10.34172/japid.025.3722","url":null,"abstract":"<p><strong>Background: </strong>Immediate molar implants (IMIs) have been shown to provide an effective treatment, but their placement comes with potential anatomically related risks.</p><p><strong>Methods: </strong>CBCTs of>400 dental sites were analyzed for key anatomical features at mandibular molar sites that can impact the placement of IMIs. Features measured included distances from each molar furcation to points risking lingual plate perforation or inferior alveolar nerve (IAC) damage, distances from molar root apices to IAC, mesiodistal and buccolingual widths of molar inter-septal bone (ISB), and thicknesses of buccal and lingual cortical plates at first and second mandibular molar sites.</p><p><strong>Results: </strong>Distances from molar furcations to contact with lingual cortical plates and to IAC decreased significantly from mesial to distal, as did distances from root apices to the mandibular canal. Both buccolingual and mesiodistal ISB widths and thicknesses of buccal and lingual cortical plates increased mesiodistally. Buccolingual ISB widths were largest coronally for both molar sites and decreased apically. The reverse was found with mesiodistal septal ISB widths, which increased coronoapically.</p><p><strong>Conclusion: </strong>Risks of lingual perforations or IAC damage were significantly greater at second molars vs. first molars. The ability to place IMIs in ISB at first molars was estimated to be>twice as often as at second molars. Maximal implant lengths for IMIs placed in the furcal bone should not exceed 10 mm.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 2","pages":"71-76"},"PeriodicalIF":0.0,"publicationDate":"2025-04-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261068/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144651345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-04-13eCollection Date: 2025-06-01DOI: 10.34172/japid.025.3467
Mouhamadou Lamine Guirassy, Folly Emmanuel Baglo, Ahmad Moustapha Diallo, Ndeye Lira Mbow, Diabel Thiam, Adam Seck-Diallo, Henri Michel Benoist
Background: Sickle cell disease is a genetic disorder that manifests itself in several organs. There is little consensus in the literature on oral manifestations, particularly dental and periodontal. This study aimed to identify the oral manifestations of sickle cell disease, focusing on dental and periodontal manifestations.
Methods: An electronic search was performed in PubMed, Embase, and African Index Medicus. Quality and risk of bias were assessed using the Newcastle-Ottawa Scale, the modified Newcastle-Ottawa Scale, and the 2013 Guideline CARE. This systematic review covered research published between 2000 and 2022.
Results: A total of 962 articles were identified, 26 of which were selected, including 13 case-control studies, 4 cohort studies, 7 cross-sectional studies, and 2 case reports. The risk of bias was high for 3.84% of the studies, medium for 38.46%, and low for 57.60%. Oral manifestations were reported in 24 studies, with a predominance of periodontal ones in 10 studies. An association between sickle cell disease and dental caries, pulpal necrosis, and delayed tooth eruption has been reported.
Conclusion: Several oral manifestations, particularly periodontal, of sickle cell disease have been reported. However, current data do not provide evidence of a possible association between sickle cell disease and oral symptoms, particularly periodontal manifestations.
背景:镰状细胞病是一种遗传性疾病,表现在几个器官。关于口腔的表现,尤其是牙齿和牙周方面的文献很少有共识。本研究旨在确定镰状细胞病的口腔表现,重点是牙齿和牙周表现。方法:在PubMed、Embase和African Index Medicus中进行电子检索。使用纽卡斯尔-渥太华量表、修改后的纽卡斯尔-渥太华量表和2013年指南CARE评估偏倚的质量和风险。该系统综述涵盖了2000年至2022年间发表的研究。结果:共纳入962篇文献,入选26篇,其中病例对照研究13篇,队列研究4篇,横断面研究7篇,病例报告2篇。高偏倚风险为3.84%,中等偏倚风险为38.46%,低偏倚风险为57.60%。24项研究报告了口腔表现,其中10项研究以牙周表现为主。镰状细胞病与龋齿、牙髓坏死和延迟出牙之间的关系已被报道。结论:镰状细胞病的几种口腔表现,特别是牙周表现已被报道。然而,目前的数据并没有提供证据表明镰状细胞病与口腔症状,特别是牙周表现之间可能存在关联。
{"title":"Oral manifestations of sickle cell disease and its effects on dental and periodontal health: A systematic review.","authors":"Mouhamadou Lamine Guirassy, Folly Emmanuel Baglo, Ahmad Moustapha Diallo, Ndeye Lira Mbow, Diabel Thiam, Adam Seck-Diallo, Henri Michel Benoist","doi":"10.34172/japid.025.3467","DOIUrl":"10.34172/japid.025.3467","url":null,"abstract":"<p><strong>Background: </strong>Sickle cell disease is a genetic disorder that manifests itself in several organs. There is little consensus in the literature on oral manifestations, particularly dental and periodontal. This study aimed to identify the oral manifestations of sickle cell disease, focusing on dental and periodontal manifestations.</p><p><strong>Methods: </strong>An electronic search was performed in PubMed, Embase, and African Index Medicus. Quality and risk of bias were assessed using the Newcastle-Ottawa Scale, the modified Newcastle-Ottawa Scale, and the 2013 Guideline CARE. This systematic review covered research published between 2000 and 2022.</p><p><strong>Results: </strong>A total of 962 articles were identified, 26 of which were selected, including 13 case-control studies, 4 cohort studies, 7 cross-sectional studies, and 2 case reports. The risk of bias was high for 3.84% of the studies, medium for 38.46%, and low for 57.60%. Oral manifestations were reported in 24 studies, with a predominance of periodontal ones in 10 studies. An association between sickle cell disease and dental caries, pulpal necrosis, and delayed tooth eruption has been reported.</p><p><strong>Conclusion: </strong>Several oral manifestations, particularly periodontal, of sickle cell disease have been reported. However, current data do not provide evidence of a possible association between sickle cell disease and oral symptoms, particularly periodontal manifestations.</p>","PeriodicalId":73584,"journal":{"name":"Journal of advanced periodontology & implant dentistry","volume":"17 2","pages":"103-110"},"PeriodicalIF":0.0,"publicationDate":"2025-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12261066/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144651349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}