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首页> 外文期刊>European journal of oral implantology >Immediately loaded zygomatic implants vs conventional dental implants in augmented atrophic maxillae: 1-year post-loading results from a multicentre randomised controlled trial.
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Immediately loaded zygomatic implants vs conventional dental implants in augmented atrophic maxillae: 1-year post-loading results from a multicentre randomised controlled trial.

机译:立即装载颧植入物与增强萎缩颌骨上的常规牙科植入物:1年的多期式随机对照试验的加载后果。

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摘要

To compare the clinical outcome of immediately loaded cross-arch maxillary prostheses supported by zygomatic implants vs conventional implants placed in augmented bone. In total, 71 edentulous patients with severely atrophic maxillas without sufficient bone volumes for placing dental implants, or when it was possible to place only two implants in the anterior area (minimal diameter 3.5 mm and length of 8 mm) and less than 4 mm of bone height subantrally, were randomised according to a parallel group design to receive zygomatic implants (35 patients) to be loaded immediately vs grafting with a xenograft, followed after 6 months of graft consolidation by placement of six to eight conventional dental implants submerged for 4 months (36 patients). For immediate loading, zygomatic implants had to be inserted with an insertion torque superior to 40 Ncm. Screw-retained metal reinforced acrylic provisional prostheses were provided, to be replaced by definitive Procera Implant Bridge Titanium prostheses (Nobel Biocare, G?teborg, Sweden), with ceramic or acrylic veneer materials 4 months after initial loading. Outcome measures were: prosthesis, implant and augmentation failures, any complications, quality of life (OHIP-14), patients' number of days with total or partial impaired activity, time to function and number of dental visits, assessed by independent assessors. Patients were followed up to 1 year after loading. No augmentation procedure failed. Five patients dropped out from the augmentation group. Six prostheses could not be delivered or failed in the augmentation group vs one prosthesis in the zygomatic group, the difference being statistically significant (difference in proportions = -16.5%; P = 0.045; 95% CI: -0.34 to -0.01). Eight patients lost 35 implants in the augmentation group vs two patients who lost four zygomatic implants, the difference being statistically significant (difference in proportions = -20.1%; P = 0.037; 95% CI: -0.38 to -0.02). A total of 14 augmented patients were affected by 22 complications, vs 28 zygomatic patients (40 complications), the difference being statistically significant (difference in proportions = 34.8%; P = 0.005; 95% CI: 0.12 to 0.54). The 1-year OHIP-14 score was 3.93 ± 5.86 for augmented patients and 3.97 ± 4.32 for zygomatic patients with no statistically significant differences between groups (mean difference = 0.04; 95% CI: -2.56 to 2.65; P = 0.747). Both groups had significantly improved OHIP-14 scores from before rehabilitation (P < 0.001 for both augmented and zygomatic patients). On average, the number of days of total infirmity was 7.42 ± 3.17 for the augmented group and 7.17 ± 1.96 for the zygomatic group, the difference not being statistically significant (mean difference = -0.25; 95% CI: -1.52 to 1.02; P = 0.692). The number of days of partial infirmity were on average 14.24 ± 4.64 for the augmented group and 12.17 ± 3.82 for the zygomatic group, the difference being statistically significant (mean difference = -2.07; 95% CI: -4.12 to -0.02; P = 0.048). The mean number of days that needed to have a functional prosthesis was 444.32 ± 207.86 for augmented patients and 1.34 ± 2.27 for zygomatic patients, the difference being statistically significant (mean difference = -442.98; 95% CI: -513.10 to -372.86; P < 0.001). The average number of dental visits was 19.72 ± 12.22 for augmented patients and 15.12 ± 5.76 for zygomatic patients, the difference not being statistically significant (mean difference = -4.61; 95% CI: -9.31 to 0.92; P = 0.055). Preliminary 1-year post-loading data suggest that immediately loaded zygomatic implants were associated with statistically significantly fewer prosthetic failures (one vs six patients), implant failures (two vs eight patients) and time needed to functional loading (1.3 days vs 444.3 days) when compared to augmentation procedures and conventionally loaded dental implants. Even if more complications were reported for zygomatic implants
机译:为了比较颧骨植入物支持的立即加载的横拱上颌假体的临床结果与常规植入物放置在增强骨中。总共有71例患有严重萎缩的颌骨,没有足够的骨骼体积,用于放置牙科植入物,或者当可以在前面积(最小直径3.5mm和8mm)中只放置两个植入物并且小于4mm时伯高副高度根据平行组设计随机化,以接受颧植入物(35名患者)立即加载与异种移植物接枝,然后通过将六到八个常规牙科植入物浸没4个月后6个月后接枝覆盖。 (36名患者)。对于立即加载,必须将颧植入物插入到40ncm上的插入扭矩。提供螺旋保留的金属增强丙烯酸临时假体,由明确的Procera植入桥钛假体(诺贝尔Biocare,G?Tebric,瑞典)取代,初始装载后4个月内用陶瓷或丙烯酸贴面材料。结果措施是:假体,植入和增强失败,任何并发症,生活质量(OHIP-14),患者的数量或部分受损的活动,工作时间和牙科访问的数量,由独立评估师评估。装载后患者最多1年。没有增强程序失败。五名患者从增强组中掉出来。在颧骨组中的增强组Vs一个假体中不能递送或失败,差异存在统计学意义(比例差异= -16.5%; P = 0.045; 95%CI:-0.34至-0.01)。八名患者在增强组中丢失35例植入物与两名患有四个颧植入物的患者,差异有统计学意义(比例差异= -20.1%; P = 0.037; 95%CI:-0.38至-0.02)。共有14名增强患者受到22名并发症的影响,与28例颧骨患者(40个并发症),差异有统计学意义(比例差异= 34.8%; P = 0.005; 95%CI:0.12至0.54)。增强患者的1年OHIP-14得分为3.93±5.86,颧骨患者3.97±4.32患者在组之间没有统计学上显着差异(平均差异= 0.04; 95%CI:-2.56至2.65; P = 0.747)。两组两组在康复之前显着改善了OHIP-14分数(两个增强和颧骨患者的P <0.001)。平均而言,增强组的总产病数为7.42±3.17,为颧组组7.17±1.96,差异没有统计学意义(平均差异= -0.25; 95%CI:-1.52至1.02; P = 0.692)。部分虚弱的天数平均为增强组,12.24±4.64,颧骨组12.17±3.82,差异有统计学意义(平均差异= -2.07; 95%CI:-4.12至-0.02; P = 0.048)。用于增强患者的功能假体所需的平均天数为444.32±207.86,颧骨患者1.34±2.27,差异有统计学意义(平均差异= -442.98; 95%CI:-513.10至-372.86; p <0.001)。增强患者的平均牙科次数为19.72±12.22,颧骨患者15.12±5.76次,差异没有统计学意义(平均差异= -4.61; 95%CI:-9.31至0.92; P = 0.055)。初步1年后加载数据表明,立即加载的颧植入物与统计学上的假期失败(一个与六名患者),植入失败(两个与八名患者)和功能载荷所需的时间(1.3天与444.3天)相关联。与增强程序和常规装载的牙科植入物相比。即使报告了颧骨植入物的更多并发症

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