Professor/Consultant in Oral Surgery, University of Plymouth Peninsula Dental School, Plymouth, UK.
Professor of Dental Public Health, Peninsula Dental School, University of Plymouth, Plymouth, UK.
Evid Based Dent. 2020 Dec;21(4):140-141. doi: 10.1038/s41432-020-0138-y.
Data sources PubMed, the Cochrane Oral Health Group Trials Register and Embase. Additionally, issues of the following journals between 2000 and April 2019 were hand-searched: Journal of Clinical Periodontology, Journal of Periodontology, International Journal of Periodontology and Restorative Dentistry, European Journal of Oral Implantology, Journal of Oral and Maxillofacial Surgery, Clinical Implant Dentistry and Related Research, and Clinical Oral Implants Research.Study selection Only randomised controlled trials (RCTs) involving soft tissue augmentation at dental implant sites were considered for inclusion. The selection was restricted to RCTs published in English language with at least ten patients per group and a minimum follow-up period of three months. A PICO method was used to organise the inclusion criteria and soft tissue augmentations were clustered into three groups; that is, before prosthetic treatment, after prosthetic treatment and at immediate implant placement.Data extraction and synthesis The screening of titles and abstracts was carried out by two reviewers and disagreements were moderated by a third reviewer. Eligibility was determined using full texts and data were extracted using purposefully designed forms. The Cochrane handbook for systematic reviews of interventions toolkit was used to assess the risk of bias. The studies were grouped according to the type of intervention and subjected to quantitative data synthesis. Continuous outcome measures were assessed using random-effects meta-analyses and pooled estimates were expressed as weighted mean differences (MDs) along with 95% confidence intervals (CIs).Results Following initial electronic and hand-searches, 2,119 studies were screened for title and abstract, and 32 studies were considered for full-text screening. Only 14 RCTs met the inclusion criteria and the remaining 18 studies were excluded from the systematic review. The included studies described soft tissue augmentation for 538 implants placed in 475 patients. Three studies (68 patients; 78 implants) reported improved soft tissue thickness with xenogenic collagen matrix (XCM) augmentation compared to no augmentation at the implant sites before prosthetic treatment (high/unclear risk of bias). One study (28 patients; 41 implants) reported improved height of keratinised tissue (KT) and marginal bone levels (MBLs) with free gingival graft (FGG) compared to no augmentation at the implant sites after prosthetic treatment (unclear risk of bias). Three RCTs (126 patients; 126 implants) focused on connective tissue grafting (CTG) and bone grafting versus no grafting in conjunction with immediate implant placement after tooth extraction (unclear risk of bias). There was no difference in MBLs in any of the studies, while one study showed superior soft tissue thickness (STT). Four RCTs (129 patients; 133 implants) compared different augmentation techniques before prosthetic treatment. Only one study showed improved STT with CTG compared to XCM (low risk of bias). Finally, three RCTs (124 patients; 160 implants) compared different augmentation techniques after prosthetic treatment (high/unclear risk of bias). FGG was observed to be superior to acellular dermal matrix (ADM) and vestibuloplasty to improve KT. Meta-analyses did not favour CTG to improve MBLs at extraction sites but CTG was superior to XCM to improve STT before prosthetic treatment.Conclusions Notwithstanding the limitations of the systematic review, soft tissue augmentation significantly enhances the amount of soft tissue at the implant site. CTG at the extraction site also improves subsequent bone level of the implants. Moreover, CTG before prosthetic treatment is superior to XCM to improve thickness of peri-implant soft tissues. However, these findings are based on short-term follow-up and future studies with improved methodology are required to establish the long-term benefits of soft tissue augmentation at the dental implant sites.
纳入研究的检索策略包括 PubMed、Cochrane 口腔健康组试验注册库和 Embase。此外,还对以下杂志的问题进行了手工检索:《临床牙周病学杂志》、《牙周病学杂志》、《国际牙周病与修复牙科学杂志》、《欧洲口腔种植学杂志》、《口腔颌面外科学杂志》、《临床种植与相关研究》和《临床口腔植入物研究》。仅纳入涉及牙种植体部位软组织增加的随机对照试验(RCT)。选择仅限于以英语发表的 RCT,每组至少 10 名患者,且最低随访期为 3 个月。采用 PICO 方法组织纳入标准,将软组织增加分为三组;即在修复治疗前、修复治疗后和即刻种植体放置时。两名评审员对标题和摘要进行了筛选,意见分歧由第三名评审员进行了协调。使用全文确定合格性,并使用专门设计的表格提取数据。使用 Cochrane 干预系统评价手册评估偏倚风险。根据干预类型对研究进行分组,并进行定量数据综合。使用随机效应荟萃分析评估连续结局指标,并使用加权均数差值(MD)及其 95%置信区间(CI)表示汇总估计值。
经过初步的电子和手工检索,筛选出 2119 项标题和摘要,对 32 项研究进行了全文筛选。只有 14 项 RCT 符合纳入标准,其余 18 项研究被排除在系统评价之外。纳入的研究描述了在 475 名患者的 538 个种植体上进行的软组织增加。三项研究(68 名患者;78 个种植体)报告说,与种植体部位无增加相比,异种胶原基质(XCM)增加改善了软组织厚度(高/不清楚偏倚风险)。一项研究(28 名患者;41 个种植体)报告说,与种植体部位无增加相比,游离龈移植(FGG)增加改善了角化组织(KT)和边缘骨水平(MBL)(不清楚偏倚风险)。三项 RCT(126 名患者;126 个种植体)专注于结缔组织移植(CTG)和骨移植与拔牙后即刻种植体放置时不移植的比较(不清楚偏倚风险)。在任何一项研究中,MBL 均无差异,而一项研究显示软组织厚度(STT)较好。四项 RCT(129 名患者;133 个种植体)比较了修复治疗前不同的增加技术。只有一项研究显示 CTG 比 XCM 改善 STT(低偏倚风险)。最后,三项 RCT(124 名患者;160 个种植体)比较了修复治疗后不同的增加技术(高/不清楚偏倚风险)。FGG 优于无细胞真皮基质(ADM),而前庭成形术优于 KT 改善。荟萃分析不支持 CTG 改善拔牙部位的 MBL,但 CTG 优于 XCM 改善修复治疗前的 STT。
尽管存在系统评价的局限性,但软组织增加显著增加了种植体部位的软组织量。拔牙部位的 CTG 也改善了随后种植体的骨水平。此外,与 XCM 相比,修复治疗前 CTG 改善了种植体周围软组织的厚度。然而,这些发现基于短期随访,需要进一步进行方法改进的研究来确定牙种植体部位软组织增加的长期益处。