用于牙槽窝保存技术的 3D 可打印生物聚合物:软组织反应:试验性随机临床研究。

IF 2.5 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Nicola De Angelis, Paolo Pesce, Wiwiek Poedjiastoeti, Trijani Suwandi, Rosalina Tjandrawinata, Francesco Bagnasco, Maria Menini
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引用次数: 0

摘要

背景:本平行临床研究的目的是评估3D打印生物聚合物与骨传导材料(β-磷酸三钙和羟基磷灰石)复合用于拔牙后软组织封闭的疗效。材料与方法:本研究遵循CONSORT报告指南;39例患者使用3D打印生物聚合物进行牙槽窝保存治疗,并随机分为3组(试验1组、试验2组和对照组)。所有病例在治疗过程中均不抬高皮瓣,仔细清洁和清创治疗部位,然后按以下方法随机密封:在 T1 组中,使用含有 10%羟基磷灰石的聚-D-乳酸 3D 打印盘;在 T2 组中,使用含有 20% β-磷酸三钙的聚-ε-己内酯 3D 打印盘;在 T3 组中,待窝洞愈合。在基线(拔牙时间)和拔牙后 6 周,对暴露率进行评估,并根据部位(前牙、后牙)进行分层:结果:在 6 周的随访中未发现脱落现象。所有部位均顺利愈合,无并发症。对于后牙,试验 1 和试验 2 显示软组织完全愈合,暴露面积分别从 46.5 ± 8.25 平方毫米减少到 0.6 ± 0.84 平方毫米和从 47.1 ± 8.67 平方毫米减少到 0.6 ± 0.7 平方毫米。对照组则从 45.6 ± 7.25 平方毫米减少到 1.2 ± 0.9 平方毫米。与对照组相比,试验 1 和试验 2 在统计学上都显示出更好的愈合效果(p < 0.05)。前牙在拔牙 4 周后牙槽窝完全闭合,试验组和对照组之间没有明显差异:本研究中使用的两种材料都证明达到了目的。伦理指南:根据 Trisakti 大学牙科学院健康研究伦理委员会的要求,本研究获得了参与者的书面知情同意,编号为:641/S3/KEPK/FKG/5/2023。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
3D-Printable Biopolymers for Socket Preservation Technique: Soft Tissues Response: A Pilot Randomised Clinical Study.

Background: The aim of the present parallel clinical study is to evaluate the efficacy of 3D-printed biopolymers compounded with osteoconductive material (beta-tricalcium phosphate and hydroxyapatite) for soft tissue closure after tooth extraction.

Materials and methods: this study followed the CONSORT reporting guidelines; 39 patients were treated with socket preservation using 3D-printed biopolymers and randomly divided into 3 groups (Test 1, Test 2, and Control). All cases were treated without flap elevation, careful cleaning and debridement of the sites, and then randomly sealed as follows: In T1, with a 3D-printed disk of poli-D-lactic acid with 10% of hydroxyapatite; in T2, using a 3D-printed disk of poli-ε caprolactone with 20% of β-tricalcium phosphate; and in T3, the socket was left open to heal. At baseline (extraction time) and 6 weeks after extraction, the rate of exposure was evaluated and stratified according to the site (anterior, posterior).

Results: No dropouts were observed during the 6 weeks follow-up. All sites underwent uneventful healing with no complications. For posterior teeth, Test 1 and Test 2 showed full healing of the soft tissues with a reduction of the exposed area from 46.5 ± 8.25 mm2 to 0.6 ± 0.84 mm2 and from 47.1 ± 8.67 mm2 to 0.6 ± 0.7 mm2, respectively. The Control group exhibited a reduction from 45.6 ± 7.25 mm2 to 1.2 ± 0.9 mm2. Both Tests 1 and 2, when compared to the Control group, showed statistically significant better healing (p < 0.05). Anterior teeth showed a complete closure of the socket 4 weeks after the extraction with no noticeable differences between Test and Control.

Conclusions: Both materials used in this study showed evidence to achieve the purpose. Ethical Guidelines: written informed consent was obtained from the participants of the study, as requested by the Ethics Committee for Health Research Faculty of Dentistry, Universitas Trisakti, with the following number: 641/S3/KEPK/FKG/5/2023.

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来源期刊
Dentistry Journal
Dentistry Journal Dentistry-Dentistry (all)
CiteScore
3.70
自引率
7.70%
发文量
213
审稿时长
11 weeks
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