Suppr超能文献

一项比较引导式与非引导式种植体植入的随机对照临床试验:以种植体为中心的 3 年随访结果。

A randomized controlled clinical trial comparing guided with nonguided implant placement: A 3-year follow-up of implant-centered outcomes.

机构信息

Assistant, Department of Oral Health Sciences, KU Leuven & Dentistry (Periodontology), University Hospitals Leuven, Leuven, Belgium.

Postdoctoral Researcher, Department of Oral Health Sciences, KU Leuven & Dentistry (Periodontology), University Hospitals Leuven, Leuven, Belgium.

出版信息

J Prosthet Dent. 2019 Jun;121(6):904-910. doi: 10.1016/j.prosdent.2018.09.004. Epub 2019 Feb 4.

Abstract

STATEMENT OF PROBLEM

Implant-based prosthetic solutions can be time consuming. If implants can be placed successfully with a guide, surgery time can be reduced.

PURPOSE

The purpose of this randomized controlled clinical trial was to assess implant outcomes, both clinical and radiological, comparing guided with nonguided implant placement after 3 years of follow-up.

MATERIAL AND METHODS

A total of 314 implants were placed in 72 jaws (60 participants). The jaws were randomly assigned to 1 of the 6 treatment groups: Materialise Universal/mucosa (Mat Mu), Materialise Universal/bone (Mat Bo), Facilitate/mucosa (Fac Mu), Facilitate/bone (Fac Bo), freehand navigation (Freehand), and a pilot-drill template (Templ). Radiographic and clinical parameters (bone loss, pocket probing depth, bleeding on probing, and plaque scores) were recorded at the time of implant placement, prosthesis installment (baseline), and 1-year, 2-year, and 3-year follow-up. Analysis was performed using a linear mixed model, and correction for simultaneous hypothesis was made according to Sidak (α=.05).

RESULTS

Three participants left the study before the 3-year follow-up; hence, 302 implants in 69 jaws were included in this study. None of the implants failed. The mean marginal bone loss after the third year of loading was 0.7 ±1.3 mm for the guided surgery group and 0.5 ±0.6 mm for the control group. No significant intergroup or follow-up period differences were observed (P>.05). In the guided surgery groups, the mean number of surfaces with bleeding on probing and plaque at 3-year follow-up was 1.7 ±1.5 and 1.7 ±1.7, respectively; for the control groups, this was 1.6 ±1.4 and 1.6 ±1.6, respectively. The mean pocket probing depth was 3.0 ±1.3 mm for the guided group and 2.6 ±1.0 mm for the control group. No significant differences were found (P>.1).

CONCLUSIONS

Within the limitation of this study, no statistically significant differences could be found between the guided group and the control group at the 3-year follow-up.

摘要

问题陈述

植入物修复体解决方案可能需要很长时间。如果可以使用引导器成功植入植入物,那么手术时间可以缩短。

目的

本随机对照临床试验的目的是评估 3 年随访后比较引导式和非引导式植入物放置的临床和影像学植入物结果。

材料和方法

总共在 72 个颌骨中植入了 314 个种植体(60 名参与者)。颌骨随机分配到 6 个治疗组中的 1 个:Materialise Universal/mucosa(Mat Mu)、Materialise Universal/bone(Mat Bo)、Facilitate/mucosa(Fac Mu)、Facilitate/bone(Fac Bo)、徒手导航(Freehand)和 Pilot-drill 模板(Templ)。在植入时、安装义齿时(基线)以及 1 年、2 年和 3 年随访时记录了影像学和临床参数(骨吸收、探诊深度、探诊出血和菌斑评分)。使用线性混合模型进行分析,并根据 Sidak(α=.05)进行同时假设校正。

结果

3 名参与者在 3 年随访前退出研究,因此本研究纳入了 302 个种植体和 69 个颌骨。没有种植体失败。负荷后第 3 年的平均边缘骨吸收量为引导手术组 0.7±1.3mm,对照组 0.5±0.6mm。未观察到组间或随访期差异(P>.05)。在引导手术组中,第 3 年随访时探诊出血和菌斑的平均表面数分别为 1.7±1.5 和 1.7±1.7;对照组分别为 1.6±1.4 和 1.6±1.6。引导组的探诊深度平均为 3.0±1.3mm,对照组为 2.6±1.0mm。未发现显著差异(P>.1)。

结论

在本研究的限制内,在 3 年随访时,引导组和对照组之间未发现统计学显著差异。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验