Immediately loaded zygomatic implants vs conventional dental implants in augmented atrophic maxillae: 1-year post-loading results from a multicentre randomised controlled trial.

Q1 Dentistry European Journal of Oral Implantology Pub Date : 2018-01-01
Rubén Davó, Pietro Felice, Roberto Pistilli, Carlo Barausse, Carlos Marti-Pages, Ada Ferrer-Fuertes, Daniela Rita Ippolito, Marco Esposito
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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, Göteborg, 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.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusions: </strong>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, they proved to be a better rehabilitation modality for severely atrophic maxillae. 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引用次数: 0

Abstract

Purpose: To compare the clinical outcome of immediately loaded cross-arch maxillary prostheses supported by zygomatic implants vs conventional implants placed in augmented bone.

Materials and methods: 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, Göteborg, 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.

Results: 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).

Conclusions: 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, they proved to be a better rehabilitation modality for severely atrophic maxillae. Long-term data are absolutely needed to confirm or dispute these preliminary results.

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即刻加载颧骨种植体与常规牙种植体在增强萎缩上颌:一项多中心随机对照试验加载后1年的结果
目的:比较颧骨种植体与常规种植体支撑的即刻负荷交叉弓上颌假体的临床效果。材料和方法:共有71例上颌严重萎缩无牙患者,没有足够的骨容量来放置牙种植体,或者当可能只在前侧区域放置两个种植体(最小直径3.5 mm,长度8 mm)且底部骨高度小于4 mm时,根据平行组设计随机分组,接受颧种植体(35例)立即加载与移植异种移植物。6个月后,36例患者将6 - 8个常规种植体浸入水中4个月。为了立即加载,颧骨植入物必须以大于40 Ncm的插入扭矩插入。提供螺钉保留的金属增强丙烯酸临时假体,在首次加载后4个月,用陶瓷或丙烯酸贴面材料替换最终Procera Implant Bridge Titanium假体(Nobel Biocare, Göteborg,瑞典)。结果测量是:由独立评估者评估的假体、种植体和增强体失败、任何并发症、生活质量(OHIP-14)、患者活动全部或部分受损的天数、功能恢复时间和牙科就诊次数。患者术后随访1年。结果:无隆胸手术失败。5名患者退出了强化组。隆胸组6个假体不能交付或失败,颧骨组1个假体,差异有统计学意义(比例差异= -16.5%;P = 0.045;95% CI: -0.34 ~ -0.01)。隆胸组8例患者丢失35个假体,2例患者丢失4个颧骨假体,差异有统计学意义(比例差异= -20.1%;P = 0.037;95% CI: -0.38 ~ -0.02)。14例增强患者共发生22例并发症,28例颧骨患者共发生40例并发症,差异有统计学意义(比例差异= 34.8%;P = 0.005;95% CI: 0.12 ~ 0.54)。增强型患者1年OHIP-14评分为3.93±5.86分,颧型患者1年OHIP-14评分为3.97±4.32分,组间差异无统计学意义(平均差异= 0.04;95% CI: -2.56 ~ 2.65;P = 0.747)。两组患者的OHIP-14评分均较康复前显著改善(增强型和颧骨型患者均P < 0.001)。平均而言,增强组的总衰弱天数为7.42±3.17天,颧骨组的总衰弱天数为7.17±1.96天,差异无统计学意义(平均差异= -0.25;95% CI: -1.52 ~ 1.02;P = 0.692)。增强组部分虚弱天数平均为14.24±4.64天,颧骨组平均为12.17±3.82天,差异有统计学意义(平均差异= -2.07;95% CI: -4.12 ~ -0.02;P = 0.048)。增强型患者需要植入功能性假体的平均天数为444.32±207.86天,颧骨型患者需要植入功能性假体的平均天数为1.34±2.27天,差异有统计学意义(平均差异= -442.98;95% CI: -513.10 ~ -372.86;P < 0.001)。颧突患者平均就诊次数为19.72±12.22次,颧突患者平均就诊次数为15.12±5.76次,差异无统计学意义(平均差异= -4.61;95% CI: -9.31 ~ 0.92;P = 0.055)。结论:加载后1年的初步数据表明,与隆胸和常规加载牙种植体相比,立即加载颧种植体的假体失败(1例对6例)、种植体失败(2例对8例)和功能加载所需时间(1.3天对444.3天)显著减少。尽管颧骨种植体有更多的并发症报道,但它们被证明是严重萎缩上颌较好的康复方式。要证实或质疑这些初步结果,绝对需要长期的数据。
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来源期刊
European Journal of Oral Implantology
European Journal of Oral Implantology DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
2.35
自引率
0.00%
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0
审稿时长
>12 weeks
期刊最新文献
Immediate loading of fixed prostheses in fully edentulous jaws - 1-year follow-up from a single-cohort retrospective study. Research in focus. Dental implants with internal versus external connections: 1-year post-loading results from a pragmatic multicenter randomised controlled trial. Research in focus. Immediate, early (6 weeks) and delayed loading (3 months) of single, partial and full fixed implant supported prostheses: 1-year post-loading data from a multicentre randomised controlled trial.
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