Freitas Rubens Moreno de, Spin-Neto Rubens, Marcantonio Junior Elcio, Pereira Luís Antônio Violin Dias, Wikesjö Ulf M E, Susin Cristiano
Department of Oral Diagnosis and Surgery - Periodontics, UNESP - Universidade Estadual Paulista, Araraquara Dental School, Araraquara, SP, Brazil; Laboratory for Applied Periodontal & Craniofacial Regeneration, Department of Periodontics and Oral Biology, College of Dental Medicine, Department of Orthopedic Surgery, Medical College of Georgia, Georgia Regents University, Augusta, GA, USA.
Clin Implant Dent Relat Res. 2015 Jan;17 Suppl 1:e192-201. doi: 10.1111/cid.12156. Epub 2013 Sep 17.
The aim of this systematic review was to evaluate clinical and safety data for recombinant human bone morphogenetic protein-2 (rhBMP-2) in an absorbable collagen sponge (ACS) carrier when used for alveolar ridge/maxillary sinus augmentation in humans.
Clinical studies/case series published 1980 through June 2012 using rhBMP-2/ACS were searched. Studies meeting the following criteria were considered eligible for inclusion: >10 subjects at baseline and maxillary sinus or alveolar ridge augmentation not concomitant with implant placement.
Seven of 69 publications were eligible for review. rhBMP-2/ACS yielded clinically meaningful bone formation for maxillary sinus augmentation that would allow placement of regular dental implants without consistent differences between rhBMP-2 concentrations. Nevertheless, the statistical analysis showed that sinus augmentation following autogenous bone graft was significantly greater (mean bone height: 1.6 mm, 95% CI: 0.5-2.7 mm) than for rhBMP-2/ACS (rhBMP-2 at 1.5 mg/mL). In extraction sockets, rhBMP-2/ACS maintained alveolar ridge height while enhancing alveolar ridge width. Safety reports did not represent concerns for the proposed indications.
rhBMP-2/ACS appears a promising alternative to autogenous bone grafts for alveolar ridge/maxillary sinus augmentation; dose and carrier optimization may expand its efficacy, use, and clinical application.
本系统评价旨在评估重组人骨形态发生蛋白-2(rhBMP-2)在可吸收胶原海绵(ACS)载体中用于人类牙槽嵴/上颌窦增高时的临床和安全性数据。
检索1980年至2012年6月发表的使用rhBMP-2/ACS的临床研究/病例系列。符合以下标准的研究被认为 eligible for inclusion:基线时受试者>10例,且上颌窦或牙槽嵴增高不与种植体植入同时进行。
69篇出版物中有7篇 eligible for review。rhBMP-2/ACS对上颌窦增高产生了具有临床意义的骨形成,这将允许植入常规牙种植体,且rhBMP-2浓度之间无一致差异。然而,统计分析表明,自体骨移植后的窦腔增高显著大于rhBMP-2/ACS(rhBMP-2浓度为1.5mg/mL时)(平均骨高度:1.6mm,95%CI:0.5-2.7mm)。在拔牙窝中,rhBMP-2/ACS维持牙槽嵴高度,同时增加牙槽嵴宽度。安全性报告未显示对拟用适应症的担忧。
rhBMP-2/ACS似乎是牙槽嵴/上颌窦增高自体骨移植的一种有前景的替代方法;剂量和载体优化可能会扩大其疗效、用途和临床应用。
“eligible for inclusion”和“eligible for review”直译为“符合纳入条件的”和“符合审查条件的”,在中文语境中表述稍显生硬,可根据上下文灵活调整为“ eligible for inclusion”为“纳入标准”,“eligible for review”为“纳入综述” ,这里为了忠实原文未做调整。