Beier Ulrike Stephanie, Grunert Ingrid, Kulmer Siegfried, Dumfahrt Herbert
Clinical Department of Prosthetic Dentistry, Innsbruck Medical University, Innsbruck, Austria.
Int J Prosthodont. 2007 May-Jun;20(3):270-4.
This study aimed to evaluate the clinical success of a hydrophilic polyvinyl siloxane impression material for fixed dental restorations under various clinical conditions.
A total of 1,466 preparations for fixed restorations in maxillary and mandibular anterior and posterior teeth were evaluated. The study contained inlay, onlay, crown, veneer, post, and adhesive-wing preparations and implants for gold, porcelain-fused-to-metal, and ceramic restorations. The preparation finish line relative to the crest of the marginal gingiva, type of restoration, and position of the teeth were recorded. Three categories were established to rate impression quality: perfect impressions, with an absence of any voids or bubbles and perfect reproduction of the preparation finish line, were rated Criteria I; acceptable impressions, with minimal defects (< or = 2 mm) not involving the preparation finish line, were rated Criteria II; and unacceptable impressions, with larger voids or bubbles (> 2 mm) or defects involving the preparation finish line, were rated Criteria III.
Overall, 96.86% of the final impressions were clinically acceptable, 89.43% of which were rated Criteria I and 7.43% of which were rated Criteria II. Only 3.14% of the impressions were unacceptable and rated Criteria III. A significant influence on impression quality was found when the preparation finish line was more than 2 mm subgingival (P < .004), as well as when a beveled preparation was used (P < .004). The position of the teeth (P > .404) had no significant effect.
Surface-activated polyvinyl siloxane impression material offers high predictability to avoid bubbles and voids in the final impression.
本研究旨在评估一种亲水性聚乙烯基硅氧烷印模材料在各种临床条件下用于固定义齿修复的临床成功率。
共评估了1466例上颌和下颌前牙及后牙的固定修复体预备情况。该研究包括嵌体、高嵌体、全冠、贴面、桩、粘结翼板预备以及用于金、烤瓷熔附金属和陶瓷修复体的种植体。记录预备体边缘与龈缘嵴的相对位置、修复体类型和牙齿位置。建立了三类标准来评定印模质量:完美印模,无任何空隙或气泡且能完美再现预备体边缘线,评定为标准I;可接受印模,有最小缺陷(≤2mm)且不涉及预备体边缘线,评定为标准II;不可接受印模,有较大空隙或气泡(>2mm)或缺陷涉及预备体边缘线,评定为标准III。
总体而言,96.86%的最终印模在临床上是可接受的,其中89.43%评定为标准I,7.43%评定为标准II。只有3.14%的印模不可接受,评定为标准III。当预备体边缘线位于龈下超过2mm时(P<.004)以及使用有斜面的预备体时(P<.004),发现对印模质量有显著影响。牙齿位置(P>.404)没有显著影响。
表面活化的聚乙烯基硅氧烷印模材料具有很高的可预测性,可避免最终印模中出现气泡和空隙。