Jung Britta A, Harzer Winfried, Gedrange Tomasz, Kunkel Martin, Moergel Maximilian, Diedrich Peter, Lüdicke Gabriele, Wehrbein Heiner
Department of Orthodontics, University Medical Center of Johannes Gutenberg University, Mainz, Germany.
J Orofac Orthop. 2010 Jul;71(4):273-80. doi: 10.1007/s00056-010-1007-7. Epub 2010 Jul 30.
To analyze the spectrum of indications for second-generation palatal implants in relation to two different loading concepts in a prospective, multicenter, randomized controlled trial (RCT).
Forty-one patients were recruited to the study from 2006 to 2009. All implants (Orthosystem, Straumann, Basel, Switzerland; dimensions: 4.1 mm x 4.2 mm) were inserted in the median or paramedian region of the anterior palate, and each patient was randomized to one of two loading groups (immediate loading within the first week after insertion versus conventional loading after a 12-week healing phase). In this interim evaluation, we report preliminary results obtained six months after functional loading.
All palatal implants were primarily stable at the time of insertion. One implant loss (12 weeks after surgical insertion) was documented in the cohort subjected to conventional loading, and one patient dropped out of the immediate-loading group. At the time of this investigation, 39 palatal implants are experiencing functional loads. Using both loading concepts, we had various orthodontic objectives, such as intrusion of anterior and/or posterior teeth, and the mesialization and distalization of posterior teeth. Both loading groups presented nearly identical indications, and the distribution of direct vs. indirect anchorage forms was also very similar during the active treatment.
Comparison of the two treatment concepts revealed no clinical differences in implant stability. Patients undergoing immediate-loading therapy were subject to no limitations regarding indications at 6 months after functional loading compared with the patients who experienced conventional loading.
在一项前瞻性、多中心、随机对照试验(RCT)中,分析与两种不同加载概念相关的第二代腭部种植体的适应证范围。
2006年至2009年招募了41名患者参与本研究。所有种植体(Orthosystem,士卓曼,瑞士巴塞尔;尺寸:4.1毫米×4.2毫米)均植入前腭部的正中或旁正中区域,每位患者被随机分配至两个加载组之一(植入后第一周内即刻加载与12周愈合期后传统加载)。在本次中期评估中,我们报告功能加载六个月后获得的初步结果。
所有腭部种植体在植入时基本稳定。在接受传统加载的队列中记录到一枚种植体脱落(手术植入后12周),一名患者退出即刻加载组。在本次调查时,39枚腭部种植体正在承受功能负荷。采用两种加载概念,我们有各种正畸目标,如前牙和/或后牙的压低,以及后牙的近中移动和远中移动。两个加载组的适应证几乎相同,在积极治疗期间直接与间接锚固形式的分布也非常相似。
两种治疗概念的比较显示种植体稳定性无临床差异。与接受传统加载的患者相比,接受即刻加载治疗的患者在功能加载六个月后适应证方面没有限制。