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美学导向的前牙即刻临时修复:一项前瞻性研究评估 3.0 毫米直径锥形种植体 5 年的结果。

Esthetically driven immediate provisionalization in the anterior zone: 5-year results from a prospective study evaluating 3.0-mm-diameter tapered implants.

机构信息

J. W. Goethe University, Frankfurt am Main, Germany.

Midwest Dental Implantology, St Charles, IL, USA.

出版信息

Clin Oral Investig. 2024 Jul 31;28(8):460. doi: 10.1007/s00784-024-05832-x.

Abstract

OBJECTIVES

Evaluate the 5-year safety and efficacy of a narrow-diameter (3.0 mm) implant that was immediately provisionalized with a single crown in the maxillary lateral incisor or mandibular central or lateral incisor area.

MATERIALS AND METHODS

An open, prospective, single-cohort, multicenter study was conducted, in which narrow-diameter implants were placed in fresh, healed extraction, or congenitally missing sites. All patients were required to meet strict criteria for immediate loading. The primary endpoints were marginal bone levels (MBL) and MBL changes (MBLC) from implant placement to 5-year follow-up. Secondary endpoints included cumulative 5-year survival and success rates, soft tissue health, and esthetic parameters.

RESULTS

A total of 91 implants were placed in 77 patients. The mean MBL remained stable from the 1-year (- 0.79 ± 0.73 mm, n = 75) to 5-year (- 0.74 ± 0.87 mm, n = 65) follow-up. A marginal bone gain of 0.11 ± 0.83 mm was observed from the 1-year to 5-year follow-up. The cumulative 5-year survival rate was 96.5%, and the cumulative 5-year success rate was 93%. The clinical parameters, including the modified plaque index, modified sulcus bleeding index, Jemt's papilla index, and pink esthetic score improved throughout the 5-year study.

CONCLUSIONS

The study demonstrated that narrow-diameter implants represent a safe and predictable treatment option for subjects suitable for immediate loading and with limited bone volume or limited inter-dental space.

CLINICAL RELEVANCE

Narrow-diameter implants with immediate provisionalization can be considered for use to restore missing or damaged teeth with predictable functional and esthetic outcomes. This trial was registered with ClinicalTrials.gov (NCT02184845).

摘要

目的

评估即刻单冠修复的 3.0mm 窄径种植体在上颌侧切牙、下颌中切牙或侧切牙区 5 年的安全性和疗效。

材料与方法

进行了一项开放性、前瞻性、单队列、多中心研究,其中将窄径种植体放置在新鲜愈合的拔牙窝或先天缺牙区。所有患者均需满足即刻负荷的严格标准。主要终点为从种植体植入到 5 年随访时的边缘骨水平(MBL)和 MBL 变化(MBLC)。次要终点包括 5 年累积生存率和成功率、软组织健康和美学参数。

结果

共有 77 名患者的 91 枚种植体被植入。从第 1 年(-0.79±0.73mm,n=75)到第 5 年(-0.74±0.87mm,n=65)的随访,平均 MBL 保持稳定。从第 1 年到第 5 年随访,观察到边缘骨增加了 0.11±0.83mm。5 年累积生存率为 96.5%,5 年累积成功率为 93%。临床参数,包括改良菌斑指数、改良龈沟出血指数、Jemt 牙龈乳头指数和粉红色美学评分,在整个 5 年研究中均得到改善。

结论

该研究表明,对于适合即刻负荷且骨量有限或牙间间隙有限的患者,窄径种植体是一种安全且可预测的治疗选择。

临床相关性

即刻临时修复的窄径种植体可用于修复缺失或受损的牙齿,获得可预测的功能和美学效果。本试验在 ClinicalTrials.gov(NCT02184845)注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74c2/11291535/9a140dca3c80/784_2024_5832_Fig1_HTML.jpg

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