首页> 外文期刊>The Journal of Prosthetic Dentistry >Clinical evaluation of all-ceramic crowns.
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Clinical evaluation of all-ceramic crowns.

机译:全瓷冠的临床评估。

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Statement of Problem. There are few in vivo studies on the clinical performance of all-ceramic crowns. Purpose. The aim of this study was to evaluate the clinical performance of IPS Empress crowns. Material and Methods. Thirty-seven all-ceramic IPS Empress crowns were placed in 20 patients. Twenty crowns were luted with Variolink II low-viscosity resin cement in combination with Syntac Classic dentin adhesive; the remaining 17 were luted with Variolink II in combination with Syntac Single Component. All procedural steps were performed by the same prosthodontist. Using the California Dental Association's (CDA) quality evaluation system, 2 calibrated evaluators examined the crowns for margin integrity, anatomic form, surface, and color for a period of 12 to 41 months, with a mean of 24.56 months after insertion. Kaplan-Meier statistical analysis was used to calculate the survival rate of the crowns. Values obtained for plaque and gingival conditions were compared to control teeth with use of the Wilcoxon signed ranks test (P<.05). Results. Based on the CDA criteria, 94.6% of the crowns were rated satisfactory. Fracture was registered in only 1 crown. One endodontically treated tooth failed due to the dislodgement of the prefabricated dowel. No significant difference was observed in the gingival health status of crowns that had margins placed above or at the level of the gingival margin. However, in crowns that had subgingival margin finish lines, the percentage of bleeding on probing was significantly higher than that of the contralateral control teeth. Conclusion. In this in vivo study, IPS Empress crowns luted with both dentin bonding agents functioned satisfactorily with a relatively low fracture rate over a mean evaluation period of 24.56 months.
机译:问题陈述。关于全瓷冠临床表现的体内研究很少。目的。这项研究的目的是评估IPS Empress牙冠的临床性能。材料与方法。在20位患者中放置了37个全陶瓷IPS Empress牙冠。用Variolink II低粘度树脂水泥与Syntac Classic牙本质胶结合使用,诱使20个牙冠脱落。其余17个与Variolink II和Syntac Single Component结合使用。所有程序步骤均由同一位修复医生执行。使用加州牙科协会(CDA)的质量评估系统,由两名经过校准的评估人员对牙冠的边缘完整性,解剖形态,表面和颜色进行了12到41个月的检查,平均在插入后24.56个月。 Kaplan-Meier统计分析用于计算牙冠的成活率。使用Wilcoxon符号秩和检验(P <.05),将获得的牙菌斑和牙龈状况的值与对照牙齿进行比较。结果。根据CDA标准,有94.6%的牙冠被评为满意。骨折仅记录在1个冠上。一根经牙髓治疗的牙齿由于预制销钉的脱落而失效。在边缘位于牙龈边缘以上或水平的冠部的牙龈健康状态没有观察到显着差异。但是,在具有龈下边缘终点线的牙冠中,探查时出血的百分比显着高于对侧对照牙齿。结论。在这项体内研究中,在两种牙本质粘合剂的情况下,IPS Empress牙冠在平均评估期24.56个月内均具有令人满意的功能,且骨折率相对较低。

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