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乳牙活髓切断术中三氧化矿物凝聚体与生物活性玻璃陶瓷的评估与比较:临床与影像学研究

Evaluation and comparison of mineral trioxide aggregate and biodentine in primary tooth pulpotomy: Clinical and radiographic study.

作者信息

Carti O, Oznurhan F

机构信息

Faculty of Dentistry, Department of Pediatric Dentistry, Cumhuriyet University, Sivas, Turkey.

出版信息

Niger J Clin Pract. 2017 Dec;20(12):1604-1609. doi: 10.4103/1119-3077.196074.

Abstract

OBJECTIVES

Pulpotomy is the common therapy for cariously exposed pulps in symptom-free primary molar teeth. For many years, researchers have searched for an ideal material that allows regeneration of the residual pulp. The purpose of this study was to evaluate the efficacy of mineral trioxide aggregate (MTA), Biodentine as a pulpotomy medicament in primary teeth, both clinically and radiographically.

MATERIALS AND METHODS

A total of 25 children (50 human primary molar teeth) aged between 5 and 9 years were selected in this randomized clinical study. The patients were randomly assigned to receive the pulpotomy medicaments in either [Group 1]: MTA or [Group 2]: Biodentine. All pulpotomized teeth were restored with stainless steel crowns and evaluated clinically and radiologically at 1, 3, 6 and 12 months. Statistical analysis using Mann-Whitney U test and Fisher's exact test, and chi-square test was performed to determine the significant differences between the groups.

RESULTS

Clinical and radiological success rates were 96 and 80% in Group 1 and 96 and 60% in Group 2, respectively. There were no significant differences between the groups (P > 0.05). The radiographic success rates decreased in the controls, but there were no significant differences.

CONCLUSION

Biodentine showed similar clinical and radiographic results as MTA in the 12-month evaluation and can be safely used as a pulpotomy medicament.

摘要

目的

牙髓切断术是无症状的乳磨牙龋源性露髓的常用治疗方法。多年来,研究人员一直在寻找一种能使残留牙髓再生的理想材料。本研究的目的是从临床和影像学方面评估三氧化矿物凝聚体(MTA)、生物活性玻璃陶瓷作为乳牙牙髓切断术药物的疗效。

材料与方法

本随机临床研究共选取了25名年龄在5至9岁之间的儿童(50颗人类乳磨牙)。患者被随机分配接受牙髓切断术药物治疗,[第1组]:MTA或[第2组]:生物活性玻璃陶瓷。所有接受牙髓切断术的牙齿均用不锈钢冠修复,并在1、3、6和12个月时进行临床和影像学评估。采用曼-惠特尼U检验、费舍尔精确检验和卡方检验进行统计分析,以确定两组之间的显著差异。

结果

第1组的临床和影像学成功率分别为96%和80%,第2组分别为96%和60%。两组之间无显著差异(P>0.05)。对照组的影像学成功率有所下降,但无显著差异。

结论

在12个月的评估中,生物活性玻璃陶瓷与MTA的临床和影像学结果相似,可安全地用作牙髓切断术药物。

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