Clinical Radiographic and Histological Evaluation of Zinc Bioactive Glass as a Pulpotomy Medicament in Primary Molar Teeth: An In Vivo Study.

Q3 Dentistry
Venugopal N Reddy, Daneswari Reddy, Kasukurthi Snehitha, Sumanya Narahari, P Syam Prasad, Tarannum Rehaman
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引用次数: 0

Abstract

Background: In the past 20 years, research into pulpotomy materials has transitioned into the "biological era," marked by the emergence of innovative dental materials such as bioactive glass, which are bio-inductive and supportive of regeneration. This evolution represents significant advancements in dentistry.

Aim: To evaluate the clinical, radiographic, and histological success rate of zinc (Zn) bioactive glass as a pulpotomy medicament for primary molars.

Patients and methods: A total sample size of 40 primary molars was selected from 36 children aged 6-9 years. A regular conventional pulpotomy procedure was followed by the placement of Zn bioactive glass over the radicular orifice. The pulp chamber was filled with reinforced zinc oxide eugenol (ZOE). Patient recall was scheduled at 3, 6, 9, and 12 months, respectively. Further evaluation was done by scanning electron microscopy (SEM). Data were tabulated and subjected to statistical analysis.

Results: The present study shows 100, 97.44, 94.74, and 94.74% clinical success at the end of 3, 6, 9, and 12 months, respectively. The radiographic success was 100, 94.87, 92.11, and 92.11% at 3, 6, 9, and 12 months, respectively. SEM analysis showed a well-defined dentinal bridge formation between Zn bioactive glass and the pulp chamber.

Conclusion: Quite promising clinical, radiographic, and histological results of Zn bioactive glass in the present study show its potential as an additional pulpotomy medicament to the presently existing pulpotomy agents.

How to cite this article: Reddy VN, Reddy D, Snehitha K, et al. Clinical Radiographic and Histological Evaluation of Zinc Bioactive Glass as a Pulpotomy Medicament in Primary Molar Teeth: An In Vivo Study. Int J Clin Pediatr Dent 2025;18(1):34-39.

锌生物活性玻璃作为第一磨牙切髓药物的临床放射学和组织学评价:一项体内研究。
背景:近20年来,牙髓切开术材料的研究已经进入了“生物时代”,生物活性玻璃等创新性牙科材料的出现,具有生物诱导和支持再生的功能。这一演变代表了牙科的重大进步。目的:评价锌生物活性玻璃作为一种牙髓切开术的临床、影像学和组织学成功率。患者与方法:选取6 ~ 9岁儿童36例,总样本量40颗初生磨牙。常规牙髓切开术后,将锌生物活性玻璃放置在根孔上。髓腔内填充增强氧化锌丁香酚(ZOE)。患者召回分别安排在3、6、9和12个月。通过扫描电子显微镜(SEM)进一步评价。数据被制成表格并进行统计分析。结果:3个月、6个月、9个月和12个月的临床成功率分别为100%、97.44%、94.74%和94.74%。3个月、6个月、9个月和12个月的x线摄影成功率分别为100、94.87、92.11和92.11%。扫描电镜分析表明,锌生物活性玻璃与牙髓腔之间形成了明确的牙本质桥。结论:在本研究中,锌生物活性玻璃的临床、影像学和组织学结果非常有希望,表明它有潜力成为目前现有的牙髓切开剂之外的一种新的牙髓切开剂。本文引用方式:Reddy VN, Reddy D, Snehitha K等。锌生物活性玻璃作为第一磨牙切髓药物的临床放射学和组织学评价:一项体内研究。中华临床儿科杂志,2015;18(1):34-39。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.20
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发文量
135
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