...
【24h】

Clinical performance of indirect composite onlays and overlays: 2-year follow up

机译:间接复合覆盖物和覆盖物的临床表现:2年随访

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

This prospective clinical trial evaluated the clinical performance of indirect onlay and overlay restorations made of resin composite. From January 2012 to March 2013, a total of 60 patients (36 males, 24 females; mean age; 34.4 +/- 10 years) received 67 posterior onlay/overlay restorations in the maxilla or mandible made of laboratory-processed indirect composite (Gradia, GC, Japan). Patients were followed until March 2015. Two operators luted all restorations adhesively (Variolink II). Two independent calibrated examiners evaluated the restorations at baseline (2weeks), 6 months, and then annually, during regularly scheduled maintenance appointments, using the modified USPHS criteria for anatomic form, marginal adaptation, color match, surface roughness, marginal discoloration, secondary caries, and postoperative sensitivity. The observation periods involved 4 recalls during 24 months. Changes in the USPHS parameters were analyzed with the Friedman and Bonferroni-adjusted Wilcoxon signed-ranks tests (=.05). The mean observation period was 24.1 months. All restorations assessed were clinically acceptable with alfa scores predominating. Two restorations failed due to severe pain and subsequent extraction during the observation period. Not the color match (p>.05) but marginal adaptation (p<.05), marginal discoloration (p<.05), and surface roughness (p<.05) showed a significant difference between the baseline and the 2-year recall. No secondary caries or fractures were observed until the final follow-up. The indirect composite tested demonstrated to be successful for posterior onlay and overlays but deteriorations in qualitative parameters were observed during the 2-year clinical service.
机译:这项前瞻性临床试验评估了由树脂复合材料制成的间接镶嵌和覆盖修复体的临床性能。从2012年1月至2013年3月,共有60例患者(男36例,女24例;平均年龄; 34.4 +/- 10岁)在上颌或下颌骨中由实验室加工的间接复合材料制成的67个后牙覆盖/覆盖修复物(Gradia ,GC,日本)。对患者进行随访直至2015年3月。两名操作员用胶粘剂黏着所有修复体(Variolink II)。两名独立的经过校准的检查员在基线(2周),6个月之后,然后每年在定期安排的维护预约中,使用经过修改的USPHS解剖学形式,边缘适应性,颜色匹配,表面粗糙度,边缘变色,继发龋,和术后敏感性。观察期涉及24个月内的4次召回。 USPHS参数的变化通过Friedman和Bonferroni调整的Wilcoxon符号秩检验(= .05)进行分析。平均观察期为24.1个月。所有评估的修复体在临床上均可接受,阿尔法评分占优势。在观察期间,由于严重的疼痛和随后的拔除,两次修复均失败。不是颜色匹配(p> .05),而是边缘适应(p <.05),边缘变色(p <.05)和表面粗糙度(p <.05)在基线和2年之间显示出显着差异召回。直到最后一次随访才观察到继发性龋齿或骨折。间接复合材料测试证明后置覆盖物和覆盖物是成功的,但在2年临床服务期间观察到定性参数下降。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号