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采用瓷聚体制作的嵌体和高嵌体修复体的短期临床评估

Short-term clinical evaluation of inlay and onlay restorations made with a ceromer.

作者信息

Monaco C, Baldissara P, dall'Orologio G D, Scotti R

机构信息

Department of Prosthetic Dentistry, School of Dentistry, University of Bologna, Italy.

出版信息

Int J Prosthodont. 2001 Jan-Feb;14(1):81-6.

Abstract

PURPOSE

This prospective clinical trial evaluated the clinical acceptability of a new material, ceromer, used for inlay and onlay restorations in single- or multisurface cavities of posterior teeth.

MATERIALS AND METHODS

Forty-three Targis inlay and onlay restorations were placed in 25 patients and evaluated using the United States Public Health Service criteria. The laboratory work was conducted by three dental technicians according to the manufacturer's recommendations. Twenty-five restorations were luted with Syntac bonding system and Variolink II, and 18 were luted with Scotchbond Multi Purpose and Opal Luting Composite. The recalls were done at 6, 12, and 18 months. Restorations were evaluated for six parameters and scored as ideal (A), clinically acceptable (B), or clinically unacceptable (C).

RESULTS

Indirect restorations received, after 18 months, scores of A at the following rates: color match 77%; marginal discoloration 93%; secondary caries 100%; anatomic form 93%; and marginal integrity 95%. For these parameters, statistical analysis indicated no significant differences at baseline and after 18 months. Postoperative hypersensitivity was reported by seven patients at baseline, but it decreased and there was no hypersensitivity at 12- and 18-month follow-ups.

CONCLUSION

Over an 18-month period the Targis restorative system yielded good clinical service.

摘要

目的

这项前瞻性临床试验评估了一种用于后牙单表面或多表面窝洞嵌体和高嵌体修复的新型材料——瓷聚体的临床可接受性。

材料与方法

在25例患者中放置了43个Targis嵌体和高嵌体修复体,并根据美国公共卫生服务标准进行评估。实验室工作由三名牙科技师按照制造商的建议进行。25个修复体用Syntac粘结系统和Variolink II粘结,18个用Scotchbond多功能粘结剂和Opal粘结复合树脂粘结。在6个月、12个月和18个月时进行复诊。对修复体的六个参数进行评估,并评为理想(A)、临床可接受(B)或临床不可接受(C)。

结果

18个月后,间接修复体在以下参数上获得A等级的比例为:颜色匹配77%;边缘变色93%;继发龋100%;解剖形态93%;边缘完整性95%。对于这些参数,统计分析表明基线时和18个月后无显著差异。7例患者在基线时报告有术后过敏,但过敏情况有所减轻,在12个月和18个月随访时无过敏情况。

结论

在18个月的时间里,Targis修复系统提供了良好的临床服务。

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