Pub Date : 2025-02-20DOI: 10.1186/s40729-025-00601-1
Diana Heimes, Nadine Wiesmann-Imilowski, Timpe Heidebrecht, Sebastian Blatt, Andreas Pabst, Philipp Becker, Sandra Fuest, Jürgen Brieger, Ralf Smeets, Peer W Kämmerer
Purpose: Silk fibroin (SF) is a biomaterial derived from the cocoon of the mulberry silkworm. This study aimed to assess the capacity of SF matrices biologized with injectable platelet-rich fibrin (iPRF) or enamel matrix protein (EMP) to modulate angiogenesis and immune response in the chorioallantoic membrane (CAM) assay.
Methods: 300 eggs were divided into the following groups: CM + NaCl, CM + iPRF, CM + EMP, SF + NaCl, SF + iPRF, and SF + EMP. Matrices were applied to the CAM on embryonic development day (EDD) 7 after rehydration. Angiogenesis, represented by vascularized area, vessel density, and vessel junctions, was evaluated on EDD 10, 12, and 14. Additionally, gene expression of HIF-1ɑ, VEGF, MMP-13, and NOS2 was assessed via quantitative polymerase chain reaction (qPCR) on EDD 11 and 14.
Results: The number of vascularized specimens was notably higher in SF matrices regardless of the treatment applied, while in the CM group, only matrices biofunctionalized with iPRF demonstrated vascularization. On EDD 14, the CM + iPRF group exhibited the highest values for total vascularized area (CM + iPRF: 57.52%, SF + iPRF: 21.87%, p < 0.001), vessel density (CM + iPRF: 0.0067 μm/µm2, SF + iPRF: 0.0032 μm/µm2, p = 0.002), number of vessel junctions (CM + iPRF: 14.45, SF + iPRF: 4.82, p = 0.001). Gene expressions displayed high data variability and no significant differences between the groups.
Conclusions: Biofunctionalization with iPRF in CM leads to a high vascularization rate probably through their capability of retaining higher liquid volumes, suggesting improved intraoral wound healing after guided tissue regeneration (GTR). Despite biofunctionalization, SF matrices exhibit a high vascularization, indicating SF as a promising material for GTR.
目的:丝素蛋白(SF)是从桑蚕蚕茧中提取的生物材料。本研究旨在评估可注射富血小板纤维蛋白(iPRF)或搪瓷基质蛋白(EMP)生物化的SF基质在绒毛膜尿囊膜(CAM)实验中调节血管生成和免疫反应的能力。方法:300只鸡蛋分为CM + NaCl、CM + iPRF、CM + EMP、SF + NaCl、SF + iPRF和SF + EMP组。在胚胎发育第7天(EDD)补液后,将基质应用于CAM。在EDD 10、12和14上评估血管生成,以血管化面积、血管密度和血管连接为代表。此外,通过定量聚合酶链反应(qPCR)检测EDD 11和14上HIF-1、VEGF、MMP-13和NOS2的基因表达。结果:无论采用何种处理方法,SF基质中血管化标本的数量都显著增加,而在CM组中,只有经iPRF生物功能化的基质显示出血管化。在EDD 14, CM + iPRF组总血管化面积最高(CM + iPRF: 57.52%, SF + iPRF: 21.87%, p = 2, SF + iPRF: 0.0032 μm/µm2, p = 0.002),血管连接数最高(CM + iPRF: 14.45, SF + iPRF: 4.82, p = 0.001)。基因表达表现出较高的数据变异性,组间无显著差异。结论:iPRF在CM中的生物功能化可能通过其保留更高液体容量的能力导致高血管成形率,这表明引导组织再生(GTR)后改善了口内伤口愈合。尽管具有生物功能,但SF基质表现出高度的血管化,表明SF是一种很有前途的GTR材料。
{"title":"Biofunctionalization of silk fibroin scaffolds with enamel matrix protein and injectable platelet rich fibrin for soft tissue augmentation: an in-ovo study.","authors":"Diana Heimes, Nadine Wiesmann-Imilowski, Timpe Heidebrecht, Sebastian Blatt, Andreas Pabst, Philipp Becker, Sandra Fuest, Jürgen Brieger, Ralf Smeets, Peer W Kämmerer","doi":"10.1186/s40729-025-00601-1","DOIUrl":"10.1186/s40729-025-00601-1","url":null,"abstract":"<p><strong>Purpose: </strong>Silk fibroin (SF) is a biomaterial derived from the cocoon of the mulberry silkworm. This study aimed to assess the capacity of SF matrices biologized with injectable platelet-rich fibrin (iPRF) or enamel matrix protein (EMP) to modulate angiogenesis and immune response in the chorioallantoic membrane (CAM) assay.</p><p><strong>Methods: </strong>300 eggs were divided into the following groups: CM + NaCl, CM + iPRF, CM + EMP, SF + NaCl, SF + iPRF, and SF + EMP. Matrices were applied to the CAM on embryonic development day (EDD) 7 after rehydration. Angiogenesis, represented by vascularized area, vessel density, and vessel junctions, was evaluated on EDD 10, 12, and 14. Additionally, gene expression of HIF-1ɑ, VEGF, MMP-13, and NOS2 was assessed via quantitative polymerase chain reaction (qPCR) on EDD 11 and 14.</p><p><strong>Results: </strong>The number of vascularized specimens was notably higher in SF matrices regardless of the treatment applied, while in the CM group, only matrices biofunctionalized with iPRF demonstrated vascularization. On EDD 14, the CM + iPRF group exhibited the highest values for total vascularized area (CM + iPRF: 57.52%, SF + iPRF: 21.87%, p < 0.001), vessel density (CM + iPRF: 0.0067 μm/µm<sup>2</sup>, SF + iPRF: 0.0032 μm/µm<sup>2</sup>, p = 0.002), number of vessel junctions (CM + iPRF: 14.45, SF + iPRF: 4.82, p = 0.001). Gene expressions displayed high data variability and no significant differences between the groups.</p><p><strong>Conclusions: </strong>Biofunctionalization with iPRF in CM leads to a high vascularization rate probably through their capability of retaining higher liquid volumes, suggesting improved intraoral wound healing after guided tissue regeneration (GTR). Despite biofunctionalization, SF matrices exhibit a high vascularization, indicating SF as a promising material for GTR.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"13"},"PeriodicalIF":3.1,"publicationDate":"2025-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11842663/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143457754","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-17DOI: 10.1186/s40729-025-00595-w
Sabawun Paiwand, Sogand Schäfer, Alexander Kopp, Thomas Beikler, Imke Fiedler, Martin Gosau, Sandra Fuest, Ralf Smeets
Peri-implantitis is known as an inflammatory condition affecting the soft and hard tissue around dental implants. A promising strategy to prevent these conditions is the use of antibacterial implants. This study aimed to evaluate the antibacterial potential of titanium (Ti) dental implants modified using plasma-electrolytic oxidation (PEO). The modified surfaces were subsequently loaded with silver (Ag) (n = 6) and zinc (Zn) (n = 6) ions and compared to unloaded Ti specimens (n = 6), with untreated specimens serving as controls. The specimens (each n = 5) were incubated in a culture medium containing a mixture of specific anaerobic bacterial strains. Scanning electron microscopy (SEM) was used to visualize the bacterial biofilm on each specimen. In addition, total bacterial deoxxyribonucleic acid (DNA) and the number of viable bacteria were determined using quantitative real-time polymerase chain reaction (qrt-PCR) and colony forming unit analysis (CFU), respectively. The results of the CFU analysis showed a 2 log (99%) reduction in viable bacteria in the samples loaded with Ag and Zn compared to the unloaded control group (p < 0.05). Moreover, significantly lower bacterial DNA counts were detected with a 5 log reduction (99.999%) in the Ag and Zn samples compared to the positive control group (bacterial mixed culture solution, p < 0.05). Therefore, it was considered that Ag and Zn loaded Ti implants may be a promising addition to current approaches to enable advanced antibacterial dental implants. However, further studies should be conducted to evaluate the in vivo cytocompatibility of the developed specimens.
{"title":"Antibacterial potential of silver and zinc loaded plasma-electrolytic oxidation coatings for dental titanium implants.","authors":"Sabawun Paiwand, Sogand Schäfer, Alexander Kopp, Thomas Beikler, Imke Fiedler, Martin Gosau, Sandra Fuest, Ralf Smeets","doi":"10.1186/s40729-025-00595-w","DOIUrl":"10.1186/s40729-025-00595-w","url":null,"abstract":"<p><p>Peri-implantitis is known as an inflammatory condition affecting the soft and hard tissue around dental implants. A promising strategy to prevent these conditions is the use of antibacterial implants. This study aimed to evaluate the antibacterial potential of titanium (Ti) dental implants modified using plasma-electrolytic oxidation (PEO). The modified surfaces were subsequently loaded with silver (Ag) (n = 6) and zinc (Zn) (n = 6) ions and compared to unloaded Ti specimens (n = 6), with untreated specimens serving as controls. The specimens (each n = 5) were incubated in a culture medium containing a mixture of specific anaerobic bacterial strains. Scanning electron microscopy (SEM) was used to visualize the bacterial biofilm on each specimen. In addition, total bacterial deoxxyribonucleic acid (DNA) and the number of viable bacteria were determined using quantitative real-time polymerase chain reaction (qrt-PCR) and colony forming unit analysis (CFU), respectively. The results of the CFU analysis showed a 2 log (99%) reduction in viable bacteria in the samples loaded with Ag and Zn compared to the unloaded control group (p < 0.05). Moreover, significantly lower bacterial DNA counts were detected with a 5 log reduction (99.999%) in the Ag and Zn samples compared to the positive control group (bacterial mixed culture solution, p < 0.05). Therefore, it was considered that Ag and Zn loaded Ti implants may be a promising addition to current approaches to enable advanced antibacterial dental implants. However, further studies should be conducted to evaluate the in vivo cytocompatibility of the developed specimens.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"12"},"PeriodicalIF":3.1,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11833008/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143440886","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-11DOI: 10.1186/s40729-025-00588-9
Ömer Faruk Şarkbay, Ahmet Mihmanli, Hakan Cora
The aim of this study was to investigate in-vitro the temperature changes occurring in the bone during drilling with implant drills manufactured by different companies. Bone blocks obtained from fresh bovine ribs were used in the study. Bone blocks were drilled with drills manufactured by Ankylos, Astra Tech, Nobel Biocare, Bredent and Straumann implant brands at an ambient temperature of 30 ± 2° C under a constant pressure of 2 kg. Two K-type thermocouple sensors were placed on the bone blocks at 5th and 10th mm depths and the temperature changes were measured at a distance of 1 mm from the implant drill. In the study, working models were created under different conditions for implant socket preparation. In group 1, the first time drills were used at 150 rpm without irrigation, in group 2, the first time drills were used at 1200 rpm with 40 ml/min irrigation, in group 3, the 30th time drills were used at 150 rpm without irrigation, and in group 4, the 30th time drills were used at 1200 rpm with 40 ml/min irrigation. All osteotomy procedures were performed with 3.5 ± 0.3 mm diameter burs for a period of 8 s and the temperature values obtained at equal time intervals were recorded. Repeated Measures and Kruskall Wallis-H tests were used for statistical analysis of the data. No significant difference was observed between the implant drills and the temperature changes in the bone during drilling (p < 0.05). None of the groups reached critical temperature values (47° C+) throughout the study. At the 5th and 10th mm depths, the temperature changes in the sensors used were close to each other. It was also calculated that although the average temperatures were close to each other in the non-irrigated and irrigated systems, the difference values obtained by subtracting the initial temperature were significantly higher in the non-irrigated systems. The results showed that implant drills did not cause significant temperature increases in bone blocks depending on the difference in manufacturers (Ankylos, Astra Tech, Nobel Biocare, Bredent, Straumann) and the number of uses. It was also concluded that irrigated and non-irrigated systems are safe as long as they are used under the recommended conditions.
{"title":"In-vitro investigation of bone temperature changes in osteotomies performed with different brands of implant burs.","authors":"Ömer Faruk Şarkbay, Ahmet Mihmanli, Hakan Cora","doi":"10.1186/s40729-025-00588-9","DOIUrl":"10.1186/s40729-025-00588-9","url":null,"abstract":"<p><p>The aim of this study was to investigate in-vitro the temperature changes occurring in the bone during drilling with implant drills manufactured by different companies. Bone blocks obtained from fresh bovine ribs were used in the study. Bone blocks were drilled with drills manufactured by Ankylos, Astra Tech, Nobel Biocare, Bredent and Straumann implant brands at an ambient temperature of 30 ± 2° C under a constant pressure of 2 kg. Two K-type thermocouple sensors were placed on the bone blocks at 5th and 10th mm depths and the temperature changes were measured at a distance of 1 mm from the implant drill. In the study, working models were created under different conditions for implant socket preparation. In group 1, the first time drills were used at 150 rpm without irrigation, in group 2, the first time drills were used at 1200 rpm with 40 ml/min irrigation, in group 3, the 30th time drills were used at 150 rpm without irrigation, and in group 4, the 30th time drills were used at 1200 rpm with 40 ml/min irrigation. All osteotomy procedures were performed with 3.5 ± 0.3 mm diameter burs for a period of 8 s and the temperature values obtained at equal time intervals were recorded. Repeated Measures and Kruskall Wallis-H tests were used for statistical analysis of the data. No significant difference was observed between the implant drills and the temperature changes in the bone during drilling (p < 0.05). None of the groups reached critical temperature values (47° C+) throughout the study. At the 5th and 10th mm depths, the temperature changes in the sensors used were close to each other. It was also calculated that although the average temperatures were close to each other in the non-irrigated and irrigated systems, the difference values obtained by subtracting the initial temperature were significantly higher in the non-irrigated systems. The results showed that implant drills did not cause significant temperature increases in bone blocks depending on the difference in manufacturers (Ankylos, Astra Tech, Nobel Biocare, Bredent, Straumann) and the number of uses. It was also concluded that irrigated and non-irrigated systems are safe as long as they are used under the recommended conditions.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"11"},"PeriodicalIF":3.1,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11813834/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143399002","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-10DOI: 10.1186/s40729-025-00598-7
Serge Szmukler-Moncler, David Morales Schwarz, Jorge Manuel Perez, Florian Beuer
Background: Dental implant systems provide standard cylindrical healing abutments of various diameters; however, they do not match the larger shape of the complex emergence profile of the prosthetic crowns. Adaptation of the soft tissues from a circular emergence profile to the one that suits the prosthetic crown involves a simultaneous squeezing and stretching of the gingiva. Often, this translates into local blanching of the gingiva and the prosthodontist must assess that blanching is transient. There is no literature about how much strain exerted by the prosthetic crown is leading or not to gingiva blanching. Aim of this paper is to present a digital workflow that allows measuring, upon prosthesis delivery, how much the strained gingiva is displaced under the crown and leads or not to blanching of the peri-implant soft tissues.
Method and results: The digital workflow involves 3 intra-oral scans (IOS), IOS#1 at completion of the soft tissue healing, IOS#2 at prosthesis delivery, IOS#3 after soft tissue conditioning, and the STL files of the healing cap, the abutment, the implant and the prosthetic crown. The above are superposed and merged following a dedicated protocol that provides access to the distance the delivered crown deforms the strained gingiva. The present case study displayed distinct blanching intensities. Severe blanching was present when the strains applied to the gingiva caused a displacement of 1.3 mm and above; a displacement of 0.9 mm led to moderate blanching. No blanching was observed up to a displacement of 0.6 mm.
Conclusion: A digital protocol, involving the superposition and merging of IOSs taken along a defined timeline and STLs of the implant hardware, allowed measuring the displacement distances a prosthetic crown wields upon delivery on the gingiva beneath the prosthesis. Various intensities of gingiva blanching could be related to distinct displacement distances of the healed gingiva that were triggered by attaching a prosthetic crown to the implant neck.
{"title":"A digital way to assess the stain parameters that lead to soft tissue blanching when delivering an implant-supported crown.","authors":"Serge Szmukler-Moncler, David Morales Schwarz, Jorge Manuel Perez, Florian Beuer","doi":"10.1186/s40729-025-00598-7","DOIUrl":"10.1186/s40729-025-00598-7","url":null,"abstract":"<p><strong>Background: </strong>Dental implant systems provide standard cylindrical healing abutments of various diameters; however, they do not match the larger shape of the complex emergence profile of the prosthetic crowns. Adaptation of the soft tissues from a circular emergence profile to the one that suits the prosthetic crown involves a simultaneous squeezing and stretching of the gingiva. Often, this translates into local blanching of the gingiva and the prosthodontist must assess that blanching is transient. There is no literature about how much strain exerted by the prosthetic crown is leading or not to gingiva blanching. Aim of this paper is to present a digital workflow that allows measuring, upon prosthesis delivery, how much the strained gingiva is displaced under the crown and leads or not to blanching of the peri-implant soft tissues.</p><p><strong>Method and results: </strong>The digital workflow involves 3 intra-oral scans (IOS), IOS#1 at completion of the soft tissue healing, IOS#2 at prosthesis delivery, IOS#3 after soft tissue conditioning, and the STL files of the healing cap, the abutment, the implant and the prosthetic crown. The above are superposed and merged following a dedicated protocol that provides access to the distance the delivered crown deforms the strained gingiva. The present case study displayed distinct blanching intensities. Severe blanching was present when the strains applied to the gingiva caused a displacement of 1.3 mm and above; a displacement of 0.9 mm led to moderate blanching. No blanching was observed up to a displacement of 0.6 mm.</p><p><strong>Conclusion: </strong>A digital protocol, involving the superposition and merging of IOSs taken along a defined timeline and STLs of the implant hardware, allowed measuring the displacement distances a prosthetic crown wields upon delivery on the gingiva beneath the prosthesis. Various intensities of gingiva blanching could be related to distinct displacement distances of the healed gingiva that were triggered by attaching a prosthetic crown to the implant neck.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"10"},"PeriodicalIF":3.1,"publicationDate":"2025-02-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11811304/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143382348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-03DOI: 10.1186/s40729-025-00594-x
Christoph Mautsch, Jan Klenke, Thomas Kern, Stefan Wolfart, Jaana-Sophia Kern
Purpose: To retrospectively evaluate the outcome of implant-supported or combined tooth-implant-supported prostheses retained by electroplated double-crowns after 1-12 years.
Methods: Twenty-five patients were retrospectively examined in a private dental practice in Hamburg, Germany. All had been rehabilitated with a removable prosthesis retained by electroplated double-crowns, for at least one year. Fifteen patients had implant-supported prostheses and 10 had combined tooth-implant-supported prostheses in the maxilla or the mandible. Biological and technical complications were recorded at the clinical examination and extracted from the patient records. Kaplan-Meier implant and tooth survival rates were calculated. Potential risk factors for severe complications were identified. Oral health-related quality of life (OHRQoL) was measured by a short version of the Oral Health Impact Profile (OHIP) questionnaire. Patients reported subjective chewing function using a visual analogue scale.
Results: Kaplan-Meier survival rates were 100% for natural abutments and 90.9% for implants after 11.8 years (p = 0.54). Two implants in two patients were lost at 8 and 9 years due to peri-implantitis in the "solely implant" group. The most common complications were decementation of primary crowns and wear of the prosthetic teeth. The mean OHIP score for the group "tooth-implant-supported" was 5.2 ± 5.0, whereas the mean score for the "solely implant" group was 1.7 ± 2.9 (p = 0.039). Patients rated their subjective masticatory function very high with an average score of 9.4 ± 0.8 out of a possible 10.
Conclusions: Implant-supported or combined tooth-implant-supported prostheses retained by electroplated double-crowns are a viable method of treatment with a satisfactory outcome. Maintenance has been manageable and patients have reported very good subjective chewing function after several years of function.
{"title":"Electroplated double-crowns on implants and teeth after up to 12 years- a retrospective clinical study.","authors":"Christoph Mautsch, Jan Klenke, Thomas Kern, Stefan Wolfart, Jaana-Sophia Kern","doi":"10.1186/s40729-025-00594-x","DOIUrl":"10.1186/s40729-025-00594-x","url":null,"abstract":"<p><strong>Purpose: </strong>To retrospectively evaluate the outcome of implant-supported or combined tooth-implant-supported prostheses retained by electroplated double-crowns after 1-12 years.</p><p><strong>Methods: </strong>Twenty-five patients were retrospectively examined in a private dental practice in Hamburg, Germany. All had been rehabilitated with a removable prosthesis retained by electroplated double-crowns, for at least one year. Fifteen patients had implant-supported prostheses and 10 had combined tooth-implant-supported prostheses in the maxilla or the mandible. Biological and technical complications were recorded at the clinical examination and extracted from the patient records. Kaplan-Meier implant and tooth survival rates were calculated. Potential risk factors for severe complications were identified. Oral health-related quality of life (OHRQoL) was measured by a short version of the Oral Health Impact Profile (OHIP) questionnaire. Patients reported subjective chewing function using a visual analogue scale.</p><p><strong>Results: </strong>Kaplan-Meier survival rates were 100% for natural abutments and 90.9% for implants after 11.8 years (p = 0.54). Two implants in two patients were lost at 8 and 9 years due to peri-implantitis in the \"solely implant\" group. The most common complications were decementation of primary crowns and wear of the prosthetic teeth. The mean OHIP score for the group \"tooth-implant-supported\" was 5.2 ± 5.0, whereas the mean score for the \"solely implant\" group was 1.7 ± 2.9 (p = 0.039). Patients rated their subjective masticatory function very high with an average score of 9.4 ± 0.8 out of a possible 10.</p><p><strong>Conclusions: </strong>Implant-supported or combined tooth-implant-supported prostheses retained by electroplated double-crowns are a viable method of treatment with a satisfactory outcome. Maintenance has been manageable and patients have reported very good subjective chewing function after several years of function.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"9"},"PeriodicalIF":3.1,"publicationDate":"2025-02-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11790550/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143079839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-02-01DOI: 10.1186/s40729-025-00589-8
David Morales Schwarz, Serge Szmukler-Moncler, Hilde Morales Melendez, Florian Beuer
Background: Between adjacent dental implants, an interimplant distance (IID) of at least 3 mm has been recommended to avoid resorbing the interproximal crestal bone. The effect of a 2 mm IID on crestal bone loss has been investigated but the literature is scarce when it comes to an IID of 1 mm. There is a need to document such clinical situations when they occur and elucidate if such a narrow IID is deleterious or not to the interproximal crest. The present case deals with an IID of 1 mm in the premolar area where, for the first time, the fate of an interimplant crest is reported after a 10-year follow-up.
Case presentation: A 57-year-old patient attended with 2 hopeless maxillary premolars. The mesio-distal space available for implant rehabilitation was too narrow to receive standard diameter implants and keep an inter-implant distance (IID) of 3 mm as recommended by accepted guidelines. A protocol of immediate implant placement and provisionalization involving 2 implants of Ø 3.5 mm was implemented; placement in the extraction sockets resulted in an IID of 1 mm. After 3 months of healing the final prosthesis was delivered; the patient has been followed for 10 years now. Surprisingly, the findings showed that the interimplant crest was maintained 1.40 mm coronal to the shoulder of the neck of the implants. Bone completely filled the space between the prosthetic concave abutments and the interproximal papilla was closing the embrasure. The literature reports only 2 experimental studies involving a 1 mm IID; both showed that this did not lead to the resorption of the interproximal bone.
Conclusions: Unexpectedly, the present case with an IID of 1 mm did not lead to the resorption of the interproximal bone after 10 years. It is speculated that the reason for that is due to the implants displaying an internal conical connection, the platform-switching feature, concave abutments and subcrestal placement. The fate of the interproximal crest of implants placed with an IID of 1 mm lacks scientific evidence. More studies are warranted to elucidate this question in order to propose the best implant treatment in cases displaying a limited mesio-distal space.
{"title":"The impact of a 1 mm interimplant distance on the interproximal crestal bone height: a case report with a 10-year follow-up and literature review.","authors":"David Morales Schwarz, Serge Szmukler-Moncler, Hilde Morales Melendez, Florian Beuer","doi":"10.1186/s40729-025-00589-8","DOIUrl":"10.1186/s40729-025-00589-8","url":null,"abstract":"<p><strong>Background: </strong>Between adjacent dental implants, an interimplant distance (IID) of at least 3 mm has been recommended to avoid resorbing the interproximal crestal bone. The effect of a 2 mm IID on crestal bone loss has been investigated but the literature is scarce when it comes to an IID of 1 mm. There is a need to document such clinical situations when they occur and elucidate if such a narrow IID is deleterious or not to the interproximal crest. The present case deals with an IID of 1 mm in the premolar area where, for the first time, the fate of an interimplant crest is reported after a 10-year follow-up.</p><p><strong>Case presentation: </strong>A 57-year-old patient attended with 2 hopeless maxillary premolars. The mesio-distal space available for implant rehabilitation was too narrow to receive standard diameter implants and keep an inter-implant distance (IID) of 3 mm as recommended by accepted guidelines. A protocol of immediate implant placement and provisionalization involving 2 implants of Ø 3.5 mm was implemented; placement in the extraction sockets resulted in an IID of 1 mm. After 3 months of healing the final prosthesis was delivered; the patient has been followed for 10 years now. Surprisingly, the findings showed that the interimplant crest was maintained 1.40 mm coronal to the shoulder of the neck of the implants. Bone completely filled the space between the prosthetic concave abutments and the interproximal papilla was closing the embrasure. The literature reports only 2 experimental studies involving a 1 mm IID; both showed that this did not lead to the resorption of the interproximal bone.</p><p><strong>Conclusions: </strong>Unexpectedly, the present case with an IID of 1 mm did not lead to the resorption of the interproximal bone after 10 years. It is speculated that the reason for that is due to the implants displaying an internal conical connection, the platform-switching feature, concave abutments and subcrestal placement. The fate of the interproximal crest of implants placed with an IID of 1 mm lacks scientific evidence. More studies are warranted to elucidate this question in order to propose the best implant treatment in cases displaying a limited mesio-distal space.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"8"},"PeriodicalIF":3.1,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11785880/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143074461","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: The study aimed to examine the usefulness of a novel density measurement drill for evaluating cancellous bone density by examining the correlation between computed tomography (CT)-based Misch bone density classification and drilling torque value.
Methods: Bovine ribs were used as the drilling sites for implant placement. Multidetector CT (MDCT) was performed after contrast materials were attached to the drilling sites. CT value within the region of interest (ROI) on MDCT scan was measured and classified according to the Misch classification (D1 to D5). Drilling torque value was measured using a novel measurement drill. Next, histomorphometric analysis of the drilling site was performed to assess bone density, expressed as percentage of bone area within ROI.
Results: MDCT showed the presence of D2 (n = 87), D3 (n = 92), D4 (n = 133), and D5 (n = 52) at the measurement sites, however, no sites were classified as D1. The drilling torque values were 11.2 ± 3.2 Ncm for D2, 7.8 ± 3.3 Ncm for D3, and 3.0 ± 1.2 Ncm for D4, and 1.4 ± 0.6 Ncm for D5, with significant differences. A positive correlation was observed between CT value and drilling torque value (r = 0.99). Histomorphometric analysis revealed a positive correlation between drilling torque value and bone area ratio (r = 0.97).
Conclusions: The results of this limited study demonstrated the usefulness of the direct and objective cancellous bone density evaluation method using a novel measurement drill. This evaluation method will be informative for subsequent treatment decisions.
{"title":"Usefulness of a novel density measurement drill for evaluating cancellous bone density: correlation between CT value and drilling torque value in bovine ribs.","authors":"Kazuya Doi, Kaien Wakamatsu, Reiko Kobatake, Yoshifumi Oki, Yusuke Makihara, Masaru Konishi, Kazuhiro Tsuga","doi":"10.1186/s40729-025-00596-9","DOIUrl":"10.1186/s40729-025-00596-9","url":null,"abstract":"<p><strong>Purpose: </strong>The study aimed to examine the usefulness of a novel density measurement drill for evaluating cancellous bone density by examining the correlation between computed tomography (CT)-based Misch bone density classification and drilling torque value.</p><p><strong>Methods: </strong>Bovine ribs were used as the drilling sites for implant placement. Multidetector CT (MDCT) was performed after contrast materials were attached to the drilling sites. CT value within the region of interest (ROI) on MDCT scan was measured and classified according to the Misch classification (D1 to D5). Drilling torque value was measured using a novel measurement drill. Next, histomorphometric analysis of the drilling site was performed to assess bone density, expressed as percentage of bone area within ROI.</p><p><strong>Results: </strong>MDCT showed the presence of D2 (n = 87), D3 (n = 92), D4 (n = 133), and D5 (n = 52) at the measurement sites, however, no sites were classified as D1. The drilling torque values were 11.2 ± 3.2 Ncm for D2, 7.8 ± 3.3 Ncm for D3, and 3.0 ± 1.2 Ncm for D4, and 1.4 ± 0.6 Ncm for D5, with significant differences. A positive correlation was observed between CT value and drilling torque value (r = 0.99). Histomorphometric analysis revealed a positive correlation between drilling torque value and bone area ratio (r = 0.97).</p><p><strong>Conclusions: </strong>The results of this limited study demonstrated the usefulness of the direct and objective cancellous bone density evaluation method using a novel measurement drill. This evaluation method will be informative for subsequent treatment decisions.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"7"},"PeriodicalIF":3.1,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11785876/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143065385","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-24DOI: 10.1186/s40729-025-00591-0
Viveca Wallin Bengtsson, Akira Aoki, Koji Mizutani, Christel Lindahl, Stefan Renvert
Purpose: The study assessed the clinical outcomes following treatment of peri-implant mucositis using Er:YAG laser or an ultrasonic device over six months. Patients' experience of pain, aesthetics, and Quality of life were further assessed.
Methods: One dental implant, per included patient, diagnosed with peri-implant mucositis underwent treatment with an Er:YAG laser (test) or an ultrasonic scaler (control) randomly. Treatments were performed at baseline and months three and six. At each session, oral hygiene was instructed after plaque registration, and the patient was guided in proper cleaning technique using a toothbrush and interproximal aids as needed. Full mouth bleeding on probing (FMBoP), full mouth plaque score (FMPS), implant bleeding on probing (BoP), implant mean graded bleeding (mBI), implant probing pocket depts (PPD), implant suppuration and bone levels were assessed. Oral health-related Quality of life (OHQoL) and visual analog scales (VAS), which reflect aesthetic satisfaction and pain of the treatment, were also evaluated.
Results: Forty-six patients were included. FMBoP was significantly reduced from 30.1 to 21.5% (test) (p < 0.001) respectively from 35.0% to 30% (control) (p < 0.01). FMPS showed significant reduction from 61.5 to 32.7% (test) (p < 0.001) and from 58.7 to 39.1% (control) (p < 0.001). At the implant BoP reduced from 89.0 to 55.7% (test) (p < 0.001) respectively from 94.9 to 63.7% (control) (p < 0.001). mBI was reduced from 1.3 to 0.6 (test) (p < 0.01) and from 1.9 to 0.8 (control) (p < 0.001). Distribution of "no bleeding" increased from 13 to 61% (test) (p < 0.05) and from 0 to 35% (control) (p < 0.05). At month three, statistically significant intergroup differences were shown for PPD ≥ 4 mm with 43.5% (test) respectively 73.9% (control) (p < 0.05). At month six, statistically significant intergroup differences, were shown for FMBoP 21.5% (test) respectively 30% (control) (p < 0.05) and for plaque score at the implant 4.0% (test) respectively 26% (control) (p < 0.05). Less pain was reported in the laser group at three days 0.08 (test) respectively 0.2 (control) (p < 0.05).
Conclusions: Treatment of peri-implant mucositis was effective regardless of whether the treatment was performed with an Er:YAG laser or an ultrasonic scaler. Fewer diseased sites were diagnosed at six months following laser treatment.
{"title":"Treatment of peri-implant mucositis using an Er:YAG laser or an ultrasonic device: a randomized, controlled clinical trial.","authors":"Viveca Wallin Bengtsson, Akira Aoki, Koji Mizutani, Christel Lindahl, Stefan Renvert","doi":"10.1186/s40729-025-00591-0","DOIUrl":"10.1186/s40729-025-00591-0","url":null,"abstract":"<p><strong>Purpose: </strong>The study assessed the clinical outcomes following treatment of peri-implant mucositis using Er:YAG laser or an ultrasonic device over six months. Patients' experience of pain, aesthetics, and Quality of life were further assessed.</p><p><strong>Methods: </strong>One dental implant, per included patient, diagnosed with peri-implant mucositis underwent treatment with an Er:YAG laser (test) or an ultrasonic scaler (control) randomly. Treatments were performed at baseline and months three and six. At each session, oral hygiene was instructed after plaque registration, and the patient was guided in proper cleaning technique using a toothbrush and interproximal aids as needed. Full mouth bleeding on probing (FMBoP), full mouth plaque score (FMPS), implant bleeding on probing (BoP), implant mean graded bleeding (mBI), implant probing pocket depts (PPD), implant suppuration and bone levels were assessed. Oral health-related Quality of life (OHQoL) and visual analog scales (VAS), which reflect aesthetic satisfaction and pain of the treatment, were also evaluated.</p><p><strong>Results: </strong>Forty-six patients were included. FMBoP was significantly reduced from 30.1 to 21.5% (test) (p < 0.001) respectively from 35.0% to 30% (control) (p < 0.01). FMPS showed significant reduction from 61.5 to 32.7% (test) (p < 0.001) and from 58.7 to 39.1% (control) (p < 0.001). At the implant BoP reduced from 89.0 to 55.7% (test) (p < 0.001) respectively from 94.9 to 63.7% (control) (p < 0.001). mBI was reduced from 1.3 to 0.6 (test) (p < 0.01) and from 1.9 to 0.8 (control) (p < 0.001). Distribution of \"no bleeding\" increased from 13 to 61% (test) (p < 0.05) and from 0 to 35% (control) (p < 0.05). At month three, statistically significant intergroup differences were shown for PPD ≥ 4 mm with 43.5% (test) respectively 73.9% (control) (p < 0.05). At month six, statistically significant intergroup differences, were shown for FMBoP 21.5% (test) respectively 30% (control) (p < 0.05) and for plaque score at the implant 4.0% (test) respectively 26% (control) (p < 0.05). Less pain was reported in the laser group at three days 0.08 (test) respectively 0.2 (control) (p < 0.05).</p><p><strong>Conclusions: </strong>Treatment of peri-implant mucositis was effective regardless of whether the treatment was performed with an Er:YAG laser or an ultrasonic scaler. Fewer diseased sites were diagnosed at six months following laser treatment.</p><p><strong>Trial registration: </strong>Registered at www.</p><p><strong>Clinicaltrials: </strong>gov : study no, NCT05772299.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"6"},"PeriodicalIF":3.1,"publicationDate":"2025-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11759739/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143033119","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-01-23DOI: 10.1186/s40729-025-00590-1
Yuanxi Zhu, Mi Du, Ping Li, Hongye Lu, An Li, Shulan Xu
Purpose: This systematic review aims to assess the performance, methodological quality and reporting transparency in prediction models for the dental implant's complications and survival rates.
Methods: A literature search was conducted in PubMed, Web of Science, and Embase databases. Peer-reviewed studies that developed prediction models for dental implant's complications and survival rate were included. Two reviewers independently evaluated the risk of bias and reporting quality using the PROBAST and TRIPOD guidelines. The performance of the models were also compared in this study. The review followed the PRISMA guidelines and was registered with PROSPERO (CRD42019122274).
Results: The initial screening yielded 1769 publications, from which 14 studies featuring 43 models were selected. Four of the 14 studies predicted peri-implantitis as the most common outcome. Three studies predicted the marginal bone loss, two predicted suppuration of peri-implant tissue. The remaining five models predicted the implant loss, osseointergration or other complication. Common predictors included implant position, length, patient age, and a history of periodontitis. Sixteen models showed good to excellent discrimination (AUROC >0.8), but only three had undergone external validation. A significant number of models lacked model presentation. Most studies had a high or unclear risk of bias, primarily due to methodological limitation. The included studies conformed to 18-27 TRIPOD checklist items.
Conclusions: The current prediction models for dental implant complications and survival rate have limited methodological quality and external validity. There is a need for enhanced reliability, generalizability, and clinical applicability in future models.
目的:本系统综述旨在评估种植体并发症和存活率预测模型的性能、方法学质量和报告透明度。方法:在PubMed、Web of Science和Embase数据库中进行文献检索。同行评议的研究开发了牙种植体并发症和存活率的预测模型。两名审稿人使用PROBAST和TRIPOD指南独立评估偏倚风险和报告质量。本研究还比较了模型的性能。该审查遵循PRISMA指南,并在PROSPERO注册(CRD42019122274)。结果:最初的筛选产生了1769篇出版物,从中选择了14项研究,共43个模型。14项研究中有4项预测种植体周围炎是最常见的结果。3项研究预测边缘骨质流失,2项研究预测种植体周围组织化脓。其余5个模型预测种植体丢失、骨整合或其他并发症。常见的预测因素包括种植体位置、长度、患者年龄和牙周炎史。有16个模型具有良好到优异的识别能力(AUROC >0.8),但只有3个模型进行了外部验证。大量的模型缺乏模型表示。大多数研究的偏倚风险较高或不明确,主要是由于方法学的限制。纳入的研究符合TRIPOD检查表18-27项。结论:目前的种植牙并发症和存活率预测模型的方法学质量和外部有效性有限。在未来的模型中,需要提高可靠性、通用性和临床适用性。
{"title":"Prediction models for the complication incidence and survival rate of dental implants-a systematic review and critical appraisal.","authors":"Yuanxi Zhu, Mi Du, Ping Li, Hongye Lu, An Li, Shulan Xu","doi":"10.1186/s40729-025-00590-1","DOIUrl":"10.1186/s40729-025-00590-1","url":null,"abstract":"<p><strong>Purpose: </strong>This systematic review aims to assess the performance, methodological quality and reporting transparency in prediction models for the dental implant's complications and survival rates.</p><p><strong>Methods: </strong>A literature search was conducted in PubMed, Web of Science, and Embase databases. Peer-reviewed studies that developed prediction models for dental implant's complications and survival rate were included. Two reviewers independently evaluated the risk of bias and reporting quality using the PROBAST and TRIPOD guidelines. The performance of the models were also compared in this study. The review followed the PRISMA guidelines and was registered with PROSPERO (CRD42019122274).</p><p><strong>Results: </strong>The initial screening yielded 1769 publications, from which 14 studies featuring 43 models were selected. Four of the 14 studies predicted peri-implantitis as the most common outcome. Three studies predicted the marginal bone loss, two predicted suppuration of peri-implant tissue. The remaining five models predicted the implant loss, osseointergration or other complication. Common predictors included implant position, length, patient age, and a history of periodontitis. Sixteen models showed good to excellent discrimination (AUROC >0.8), but only three had undergone external validation. A significant number of models lacked model presentation. Most studies had a high or unclear risk of bias, primarily due to methodological limitation. The included studies conformed to 18-27 TRIPOD checklist items.</p><p><strong>Conclusions: </strong>The current prediction models for dental implant complications and survival rate have limited methodological quality and external validity. There is a need for enhanced reliability, generalizability, and clinical applicability in future models.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"5"},"PeriodicalIF":3.1,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11757661/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143023424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: This study aimed at investigating implant survival rate and marginal bone loss (MBL) around extra-short implants. The impact of the loading protocol and of the use of an intermediate abutment was also evaluated, to explore possible differences in terms of the outcome measures.
Materials and methods: Patients with single or multiple mandibular or maxillary posterior edentulism rehabilitated using extra-short 5-6 mm long implants were included. Different prosthetic protocols were used. Clinical and radiological follow-up was 5 years. The outcomes measures were implant survival and MBL.
Results: The analysis included 56 implants placed in 34 adults (12 males and 22 females; mean age 60 years, SD 11). Six implants failed during a median follow-up of 5 years and 4 of them were recorded in one patient at 2-year follow-up. The 5-year implant survival was 89% overall (87% in conventional and 94% in immediate loading). At univariate analysis, during follow-up immediate loading was associated with higher MBL (mean variation 0.21 mm, 95%CI 0.01 to 0.40; p = 0.02), while intermediate abutment was associated with lower MBL (mean variation -0.23 mm, 95%CI -0.39 to -0.09; p = 0.003). Multivariable analysis confirmed that immediate loading was associated with higher MBL.
Conclusion: Within its limitations, this study showed that extra-short implants under immediate loading conditions can be a reliable solution. The application of horizontal and vertical platform switching with the use of intermediate abutments seems to be able to contribute to the reduction of MBL.
目的:研究超短种植体种植体的成活率和边缘骨损失(MBL)。还评估了加载方案和使用中间基台的影响,以探讨结果测量方面可能存在的差异。材料和方法:采用超短5-6 mm长种植体修复单侧或多侧下颌或上颌后牙患者。使用了不同的假肢方案。临床及放射学随访5年。结果测量种植体存活和MBL。结果:分析包括34名成人(12名男性,22名女性;平均年龄60岁,SD 11)。在中位随访5年期间,有6例植入物失败,其中1例患者在随访2年时记录了4例植入物失败。5年种植体总体存活率为89%(常规种植体87%,即刻种植体94%)。在单因素分析中,在随访期间,立即加载与较高的MBL相关(平均变化0.21 mm, 95%CI 0.01至0.40;p = 0.02),而中间基台与MBL较低相关(平均变异-0.23 mm, 95%CI -0.39 ~ -0.09;p = 0.003)。多变量分析证实,立即加载与较高的MBL相关。结论:在其局限性内,本研究表明,在即时加载条件下,超短种植体是可靠的解决方案。水平和垂直平台切换的应用与使用中间基台似乎能够有助于减少MBL。
{"title":"Clinical and radiographic outcomes of extra-short implants (≤ 6 mm) in the posterior atrophic jaws: a retrospective cohort study.","authors":"Stefano Sivolella, Stefano Giovannini, Joana Berberi, Michele Stocchero, Giulia Brunello","doi":"10.1186/s40729-025-00592-z","DOIUrl":"10.1186/s40729-025-00592-z","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed at investigating implant survival rate and marginal bone loss (MBL) around extra-short implants. The impact of the loading protocol and of the use of an intermediate abutment was also evaluated, to explore possible differences in terms of the outcome measures.</p><p><strong>Materials and methods: </strong>Patients with single or multiple mandibular or maxillary posterior edentulism rehabilitated using extra-short 5-6 mm long implants were included. Different prosthetic protocols were used. Clinical and radiological follow-up was 5 years. The outcomes measures were implant survival and MBL.</p><p><strong>Results: </strong>The analysis included 56 implants placed in 34 adults (12 males and 22 females; mean age 60 years, SD 11). Six implants failed during a median follow-up of 5 years and 4 of them were recorded in one patient at 2-year follow-up. The 5-year implant survival was 89% overall (87% in conventional and 94% in immediate loading). At univariate analysis, during follow-up immediate loading was associated with higher MBL (mean variation 0.21 mm, 95%CI 0.01 to 0.40; p = 0.02), while intermediate abutment was associated with lower MBL (mean variation -0.23 mm, 95%CI -0.39 to -0.09; p = 0.003). Multivariable analysis confirmed that immediate loading was associated with higher MBL.</p><p><strong>Conclusion: </strong>Within its limitations, this study showed that extra-short implants under immediate loading conditions can be a reliable solution. The application of horizontal and vertical platform switching with the use of intermediate abutments seems to be able to contribute to the reduction of MBL.</p>","PeriodicalId":14076,"journal":{"name":"International Journal of Implant Dentistry","volume":"11 1","pages":"4"},"PeriodicalIF":3.1,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11747052/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143004911","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}