Kohal Ralf-J, Klaus Gerold, Strub Jörg R
Department of Prosthodontics, Albert-Ludwigs-University, University Hospital Freiburg, Hugstetter Strasse 55, 79106 Freiburg, Germany.
Clin Oral Implants Res. 2006 Oct;17(5):565-71. doi: 10.1111/j.1600-0501.2006.01252.x.
The purpose of this pilot investigation was to test whether zirconia implants restored with different all-ceramic crowns would fulfill the biomechanical requirements for clinical use. Therefore, all-ceramic Empress-1 and Procera crowns were cemented on zirconia implants and exposed to the artificial mouth. Afterwards, the fracture strength of the all-ceramic implant-crown systems was evaluated. Conventional titanium implants restored with porcelain-fused-to-metal (PFM) crowns served as controls.
Sixteen titanium implants with 16 PFM crowns and 32 zirconia implants with 16 Empress-1 crowns and 16 Procera crowns each--i.e., three implant-crown groups--were used in this investigation. The titanium implants were fabricated using the ReImplant system and the zirconia implants using the Celay system. The upper left central incisor served as a model for the fabrication of the implants and the crowns. Eight samples of each group were submitted to a long-term load test in the artificial mouth (1.2 million chewing cycles). Subsequently, a fracture strength test was performed with seven of the eight crowns. The remaining eight samples of each group were not submitted to the long-term load in the artificial mouth but were fracture-tested immediately. One loaded and one unloaded sample of each group were evaluated regarding the marginal fit of the crowns.
All test samples survived the exposure to the artificial mouth. Three Empress-1 crowns showed cracks in the area of the loading steatite ball. The values for the fracture load in the titanium implant-PFM crown group without artificial loading ranged between 420 and 610 N (mean: 531.4 N), between 460 and 570 N (mean: 512.9 N) in the Empress-1 crown group, and in the Procera crown group the values were between 475 and 700 N (mean: 575.7 N) when not loaded artificially. The results when the specimens were loaded artificially with 1.2 million cycles were as follows: the titanium implant-PFM crowns fractured between 440 and 950 N (mean: 668.6 N), the Empress-1 crowns between 290 and 550 N (mean: 410.7 N), and the Procera crowns between 450 and 725 N (mean: 555.5 N). No statistically significant differences could be found among the groups without artificial load. The fracture values for the PFM and the Procera crowns after artificial loading were statistically significantly higher than that for the loaded Empress-1 crowns. There was no significant difference between the PFM crown group and the Procera group.
Within the limits of this pilot investigation, it seems that zirconia implants restored with the Procera crowns possibly fulfill the biomechanical requirements for anterior teeth. However, further investigations with larger sample sizes have to confirm these preliminary results. As three Empress-1 crowns showed crack development in the loading area of the steatite balls in the artificial mouth, their clinical use on zirconia implants has to be questioned.
本初步研究的目的是测试用不同全瓷冠修复的氧化锆种植体是否能满足临床使用的生物力学要求。因此,将全瓷Empress-1冠和Procera冠粘结在氧化锆种植体上,并置于人工口腔中。之后,评估全瓷种植体-冠系统的断裂强度。用烤瓷熔附金属(PFM)冠修复的传统钛种植体作为对照。
本研究使用了16颗带有16个PFM冠的钛种植体以及32颗氧化锆种植体,后者分别配有16个Empress-1冠和16个Procera冠,即三个种植体-冠组。钛种植体采用ReImplant系统制作,氧化锆种植体采用Celay系统制作。左上中切牙作为制作种植体和牙冠的模型。每组八个样本在人工口腔中进行长期负荷测试(120万次咀嚼循环)。随后,对八个牙冠中的七个进行断裂强度测试。每组其余八个样本未在人工口腔中进行长期负荷测试,而是立即进行断裂测试。每组取一个负荷样本和一个未负荷样本评估牙冠的边缘适合性。
所有测试样本在人工口腔暴露后均存活。三个Empress-1冠在加载滑石球的区域出现裂缝。未进行人工加载时,钛种植体-PFM冠组的断裂负荷值在420至610 N之间(平均:531.4 N),Empress-冠组在460至570 N之间(平均:512.9 N),Procera冠组在475至700 N之间(平均:575.7 N)。当样本进行120万次人工加载时,结果如下:钛种植体-PFM冠在440至950 N之间断裂(平均:668.6 N),Empress-1冠在290至550 N之间断裂(平均:410.7 N),Procera冠在450至725 N之间断裂(平均:555.5 N)。未进行人工负荷的各组之间未发现统计学上的显著差异。人工加载后,PFM冠和Procera冠的断裂值在统计学上显著高于加载后的Empress-1冠。PFM冠组和Procera组之间无显著差异。
在本初步研究的范围内,似乎用Procera冠修复的氧化锆种植体可能满足前牙的生物力学要求。然而,需要更大样本量的进一步研究来证实这些初步结果。由于三个Empress-1冠在人工口腔中加载滑石球的区域出现裂缝发展,其在氧化锆种植体上的临床应用值得质疑。