Bolle Caroline, Felice Pietro, Barausse Carlo, Pistilli Valeria, Trullenque-Eriksson Anna, Esposito Marco
Eur J Oral Implantol. 2018;11(1):31-47.
To evaluate whether 4.0 mm short dental implants could be an alternative to augmentation with xenographs in the maxilla and placement of at least 10.0 mm long implants in posterior atrophic jaws.
A group of 40 patients with atrophic posterior (premolar and molar areas) mandibles with 5.0 mm to 6.0 mm bone height above the mandibular canal and 40 patients with atrophic maxillas having 4.0 mm to 5.0 mm below the maxillary sinus, were randomised according to a parallel group design to receive between one and three 4.0 mm long implants or one to three implants of at least 10.0 mm long in augmented bone, at two centres. All implants had a diameter of 4.0 mm or 4.5 mm. Mandibles were vertically augmented with inter-positional equine bone blocks and resorbable barriers. Implants were placed 4 months after the inter-positional grafting. Maxillary sinuses were augmented with particulated porcine bone via a lateral window covered with resorbable barriers, and implants were placed simultaneously. Implants were not submerged and were loaded after 4 months with provisional screw-retained reinforced acrylic restorations replaced after another 4 months by definitive screw-retained metal-composite prostheses. Patients were followed up to 1 year post-loading. Outcome measures were: prosthesis and implant failures, any complication, and peri-implant marginal bone level changes.
Three patients dropped out; one from the maxillary augmented group, one from the mandibular augmented group, and one from the maxillary short implant group. In six augmented mandibles (30%) it was not possible to place implants of at least 10.0 mm, so shorter implants were placed instead. In mandibles, one implant from the augmented group failed vs two 4.0 mm implants in two patients from the short implant group. In maxillae, three short implants failed in two patients vs seven long implants in four patients (two long implants and one short implant dropped into the maxillary sinus). Two prostheses on short implants (one mandibular and one maxillary) were placed at a later stage because of implant failures, vs six prostheses (one mandibular and five maxillary) at augmented sites (one mandibular prosthesis not delivered, three maxillary prostheses delivered with delays, one not delivered, and one failed) at augmented sites. In particular, three patients in the augmented group (one mandible and two maxillae) were not wearing a prosthesis. There were no statistically significant differences in implant failures (P (chi-square test) = 0.693; difference in proportion = 0.03; CI 95% -0.11 to 0.17) or prostheses failures (P (chi-square test) = 0.126; difference in proportion = 0.10; CI 95% -0.03 to 0.24). At mandibular sites, nine augmented patients were affected by complications vs two patients treated with short implants (P (chi-square test) = 0.01; difference in proportion = 0.37; CI 95% 0.11 to 0.63), the difference being statistically significant. No significant differences were found for maxillae: nine sinus-lifted patients vs four short implant patients were affected by complications (P (chi-square test) = 0.091; difference in proportion = 0.25; CI 95% -0.03 to 0.53). At 1-year post-loading, average peri-implant bone loss was 0.51 mm at 4 mm long mandibular implants, 0.77 mm at 10 mm or longer mandibular implants, 0.63 mm at short maxillary implants and 0.72 mm at long maxillary implants. The difference was statistically significant in mandibles (mean difference -0.26 mm, 95% CI -0.39 to -0.13, P (ANCOVA) < 0.001), but not in maxillae (mean difference -0.09 mm, 95% CI -0.24 to 0.05, P (ANCOVA) = 0.196).
One year after loading 4.0 mm long implants achieved similar results, if not better, than longer implants in augmented jaws, but were affected by fewer complications. Short implants might be a preferable choice over bone augmentation, especially in mandibles, since the treatment is less invasive, faster, cheaper, and associated with less morbidity. However, 5 to 10 years post-loading data are necessary before making reliable recommendations.
评估4.0毫米短种植体是否可替代在上颌骨使用异种骨移植以及在下颌后牙区萎缩性牙槽嵴植入至少10.0毫米长的种植体。
将一组40例下颌后牙区(前磨牙和磨牙区)萎缩性牙槽嵴患者(下颌管上方骨高度为5.0至6.0毫米)和40例上颌骨萎缩患者(上颌窦下方骨高度为4.0至5.0毫米)按照平行组设计随机分组,在两个中心分别接受1至3枚4.0毫米长的种植体或在增量骨中植入1至3枚至少10.0毫米长的种植体。所有种植体直径为4.0毫米或4.5毫米。下颌骨采用间隙性马骨块和可吸收屏障进行垂直增量。在间隙性植骨后4个月植入种植体。上颌窦通过外侧开窗并用可吸收屏障覆盖,采用颗粒状猪骨进行增量,并同时植入种植体。种植体不进行埋入式处理,4个月后用临时螺丝固位的增强丙烯酸修复体加载,再过4个月更换为最终的螺丝固位金属复合假体。对患者进行加载后1年的随访。观察指标包括:修复体和种植体失败情况、任何并发症以及种植体周围边缘骨水平变化。
3例患者退出研究;1例来自上颌增量组,1例来自下颌增量组,1例来自上颌短种植体组。在6例增量下颌骨(30%)中,无法植入至少10.0毫米的种植体,因此改为植入较短的种植体。在下颌骨中,增量组有1枚种植体失败,而短种植体组的2例患者中有2枚4.0毫米种植体失败。在上颌骨中,2例患者中有3枚短种植体失败,4例患者中有7枚长种植体失败(2枚长种植体和1枚短种植体掉入上颌窦)。由于种植体失败,短种植体上的2个修复体(1个下颌和1个上颌)在后期放置,而增量部位有6个修复体(1个下颌和5个上颌)(1个下颌修复体未交付,3个上颌修复体延迟交付,1个未交付,1个失败)。特别是,增量组有3例患者(1例下颌和2例上颌)未佩戴修复体。种植体失败(P(卡方检验)=0.693;比例差异=0.03;95%CI -0.11至0.17)或修复体失败(P(卡方检验)=0.126;比例差异=0.10;95%CI -0.03至0.24)方面无统计学显著差异。在下颌部位,9例增量患者出现并发症,而短种植体治疗的患者中有2例出现并发症(P(卡方检验)=0.01;比例差异=0.37;95%CI 0.11至0.63),差异具有统计学意义。在上颌骨中未发现显著差异:9例上颌窦提升患者和4例短种植体患者出现并发症(P(卡方检验)=0.091;比例差异=0.25;95%CI -0.03至0.53)。在加载后1年,4毫米长的下颌种植体周围平均骨吸收为0.51毫米,10毫米或更长的下颌种植体为0.77毫米,上颌短种植体为0.63毫米,上颌长种植体为0.72毫米。在下颌骨中差异具有统计学意义(平均差异-0.26毫米,95%CI -0.39至-0.13,P(协方差分析)<0.001),但在上颌骨中无差异(平均差异-0.09毫米,95%CI -0.24至0.05,P(协方差分析)=0.196)。
加载后1年,4.0毫米长的种植体在增量牙槽嵴中取得了与较长种植体相似甚至更好的效果,但并发症较少。短种植体可能比骨增量更可取,尤其是在下颌骨,因为该治疗侵入性更小、速度更快、成本更低且发病率更低。然而,在做出可靠推荐之前,还需要加载后5至10年的数据。