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两种可填充型后牙复合树脂的临床评估:两年随访

Clinical evaluation of two packable posterior composites: 2-year follow-up.

作者信息

Fagundes T C, Barata T J E, Bresciani E, Cefaly D F G, Jorge M F F, Navarro M F L

机构信息

Department of Operative Dentistry, Bauru School of Dentistry, University of São Paulo, São Paulo, 17012-901, Brazil.

出版信息

Clin Oral Investig. 2006 Sep;10(3):197-203. doi: 10.1007/s00784-006-0059-y. Epub 2006 Jul 6.

Abstract

The clinical performance of two packable posterior composites, Alert (A)-Jeneric/Pentron and SureFil (S)-Dentsply, was evaluated in 33 patients. Each patient received one A and one S restoration, resulting in a total of 66 restorations. The restorations were placed by one operator according to the manufacturer's specifications and were finished and polished after 1 week. Photographs were taken at baseline and after 2 years. Two independent evaluators conducted the clinical evaluation by using modified United States Public Health Service criteria. After 2 years, 60 restorations (30 A and 30 S), 27 class I (16 A and 11 S) and 33 class II (14 A and 19 S) were evaluated in 30 patients. Criterion A for recurrent caries, vitality, and retention was applicable to all 60 restorations. Criterion B was distributed among 40 restorations as follows: surface texture (15 A; 2 S), color (5 A; 6 S), postoperative sensitivity (1 S), marginal discoloration (8 A), marginal adaptation (3 A), and wear resistance (2 A). Data were analyzed using the Exact Fisher and McNemar tests. After 2 years, S showed a significantly better performance than A with respect to surface texture and marginal discoloration. The clinical performance of both materials was considered acceptable over the 2-year period. Further evaluations are necessary for a more in-depth analysis.

摘要

对33例患者使用的两种可填充型后牙复合树脂Alert(A,Jeneric/Pentron公司生产)和SureFil(S,登士柏公司生产)的临床性能进行了评估。每位患者分别接受一个A树脂修复体和一个S树脂修复体,共66个修复体。修复体由一名操作人员按照制造商的规格放置,1周后完成修整和抛光。在基线期和2年后拍摄照片。两名独立评估人员采用修改后的美国公共卫生服务标准进行临床评估。2年后,对30例患者的60个修复体(30个A修复体和30个S修复体)进行了评估,其中27个为I类修复体(16个A修复体和11个S修复体),33个为II类修复体(14个A修复体和19个S修复体)。复发性龋齿、活力和固位的A标准适用于所有60个修复体。B标准分布在40个修复体中,具体如下:表面质地(15个A修复体;2个S修复体)、颜色(5个A修复体;6个S修复体)、术后敏感(1个S修复体)、边缘变色(8个A修复体)、边缘适合性(3个A修复体)和耐磨性(2个A修复体)。使用精确费舍尔检验和麦克尼马尔检验对数据进行分析。2年后,S在表面质地和边缘变色方面的表现明显优于A。在2年期间,两种材料的临床性能均被认为是可接受的。需要进一步评估以进行更深入的分析。

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