Influence of occlusal loading on peri-implant clinical parameters. A pilot study
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Influence of occlusal loading on peri-implant clinical parameters. A pilot study

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Influence of occlusal loading on peri-implant clinical parameters. A pilot study

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dc.contributor.author Pellicer Chover, Hilario es
dc.contributor.author Viña Almunia, José es
dc.contributor.author Romero Millán, Javier es
dc.contributor.author Peñarrocha Oltra, David es
dc.contributor.author García Mira, Berta es
dc.contributor.author Peñarrocha Diago, María es
dc.date.accessioned 2014-07-04T07:55:29Z
dc.date.available 2014-07-04T07:55:29Z
dc.date.issued 2014 es
dc.identifier.uri http://hdl.handle.net/10550/36883
dc.relation http://www.medicinaoral.com/pubmed/medoralv19_i3_p302.pdf es
dc.source Pellicer Chover, Hilario ; Viña Almunia, José ; Romero Millán, Javier ; Peñarrocha Oltra, David ; García Mira, Berta ; Peñarrocha Diago, María. Influence of occlusal loading on peri-implant clinical parameters. A pilot study. En: Medicina oral, patología oral y cirugía bucal. Ed inglesa, 2014, Vol. 19, No. 3: 302-307 es
dc.subject Odontología es
dc.subject Ciencias de la salud es
dc.title Influence of occlusal loading on peri-implant clinical parameters. A pilot study es
dc.type info:eu-repo/semantics/article en
dc.type info:eu-repo/semantics/publishedVersion en
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.description.abstractenglish Objectives: To investigate the relation between occlusal loading and peri-implant clinical parameters (probing depth, bleeding on probing, gingival retraction, width of keratinized mucosa, and crevicular fluid volume) in pa - tients with implant-supported complete fixed prostheses in both arches. Material and Methods: This clinical study took place at the University of Valencia (Spain) dental clinic. It included patients attending the clinic for regular check-ups during at least 12 months after rehabilitation of both arches with implant-supported complete fixed ceramo-metallic prostheses. One study implant and one control implant were established for each patient using the T-Scan®III computerized system (Tesco, South Boston, USA). The maxil - lary implant closest to the point of maximum occlusal loading was taken as the study implant and the farthest (with least loading) as the control. Occlusal forces were registered with the T-Scan® III and then occlusal adjust - ment was performed to distribute occlusal forces correctly. Peri-implant clinical parameters were analyzed in both implants before and two and twelve months after occlusal adjustment. Results: Before occlusal adjustment, study group implants presented a higher mean volume of crevicular fluid (51.3±7.4 UP) than the control group (25.8±5.5 UP), with statistically significant difference. Two months after occlusal adjustment, there were no significant differences between groups (24.6±3.8 UP and 26±4.5 UP respec - tively) ( p =0.977). After twelve months, no significant differences were found between groups (24.4±11.1 UP and 22.5±8.9 UP respectively) ( p =0.323). For the other clinical parameters, no significant differences were identified between study and control implants at any of the study times ( p >0.05). Conclusions: Study group implants receiving higher occlusal loading presented significantly higher volumes of crevicular fluid than control implants. Crevicular fluid volumes were similar in both groups two and twelve months after occlusal adjustment. es

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