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根尖周病变再治疗的牙髓治疗程序。

Endodontic procedures for retreatment of periapical lesions.

作者信息

Del Fabbro Massimo, Corbella Stefano, Sequeira-Byron Patrick, Tsesis Igor, Rosen Eyal, Lolato Alessandra, Taschieri Silvio

机构信息

Department of Biomedical, Surgical and Dental Sciences, Università degli Studi di Milano, IRCCS Galeazzi Orthopaedic Institute, Via Riccardo Galeazzi 4, Milan, Italy, 20161.

出版信息

Cochrane Database Syst Rev. 2016 Oct 19;10(10):CD005511. doi: 10.1002/14651858.CD005511.pub3.

Abstract

BACKGROUND

When primary root canal therapy fails, periapical lesions can be retreated with or without surgery. Root canal retreatment is a non-surgical procedure that involves removal of root canal filling materials from the tooth, followed by cleaning, shaping and obturating of the canals. Root-end resection is a surgical procedure that involves exposure of the periapical lesion through an osteotomy, surgical removal of the lesion, removal of part of the root-end tip, disinfection and, commonly, retrograde sealing or filling of the apical portion of the remaining root canal. This review updates one published in 2008.

OBJECTIVES

To assess effects of surgical and non-surgical therapy for retreatment of teeth with apical periodontitis.To assess effects of surgical root-end resection under various conditions, for example, when different materials, devices or techniques are used.

SEARCH METHODS

We searched the following electronic databases: the Cochrane Oral Health Trials Register (to 10 February 2016), the Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 1), MEDLINE Ovid (1946 to 10 February 2016) and Embase Ovid (1980 to 10 February 2016). We searched the US National Registry of Clinical Trials (ClinicalTrials.gov) and the World Health Organization (WHO) International Clinical Trials Registry Platform for ongoing trials (to 10 February 2016). We placed no restrictions regarding language and publication date. We handsearched the reference lists of the studies retrieved and key journals in the field of endodontics.

SELECTION CRITERIA

We included randomised controlled trials (RCTs) involving people with periapical pathosis. Studies could compare surgery versus non-surgical treatment or could compare different types of surgery. Outcome measures were healing of the periapical lesion assessed after one-year follow-up or longer; postoperative pain and discomfort; and adverse effects such as tooth loss, mobility, soft tissue recession, abscess, infection, neurological damage or loss of root sealing material evaluated through radiographs.

DATA COLLECTION AND ANALYSIS

Two review authors independently extracted data from included studies and assessed their risk of bias. We contacted study authors to obtain missing information. We combined results of trials assessing comparable outcomes using the fixed-effect model, with risk ratios (RRs) for dichotomous outcomes and mean differences (MDs) for continuous outcomes, and 95% confidence intervals (CIs). We used generic inverse variance for split-mouth studies.

MAIN RESULTS

We included 20 RCTs. Two trials at high risk of bias assessed surgery versus a non-surgical approach: root-end resection with root-end filling versus root canal retreatment. The other 18 trials evaluated different surgical protocols: cone beam computed tomography (CBCT) versus periapical radiography for preoperative assessment (one study at high risk of bias); antibiotic prophylaxis versus placebo (one study at unclear risk); different magnification devices (loupes, surgical microscope, endoscope) (two studies at high risk); types of incision (papilla base incision, sulcular incision) (one study at high risk and one at unclear risk); ultrasonic devices versus handpiece burs (one study at high risk); types of root-end filling material (glass ionomer cement, amalgam, intermediate restorative material (IRM), mineral trioxide aggregate (MTA), gutta-percha (GP), super-ethoxy benzoic acid (EBA)) (five studies at high risk of bias, one at unclear risk and one at low risk); grafting versus no grafting (three studies at high risk and one at unclear risk); and low energy level laser therapy versus placebo (irradiation without laser activation) versus control (no use of the laser device) (one study at high risk).There was no clear evidence of superiority of the surgical or non-surgical approach for healing at one-year follow-up (RR 1.15, 95% CI 0.97 to 1.35; two RCTs, 126 participants) or at four- or 10-year follow-up (one RCT, 82 to 95 participants), although the evidence is very low quality. More participants in the surgically treated group reported pain in the first week after treatment (RR 3.34, 95% CI 2.05 to 5.43; one RCT, 87 participants; low quality evidence).In terms of surgical protocols, there was some inconclusive evidence that ultrasonic devices for root-end preparation may improve healing one year after retreatment, when compared with the traditional bur (RR 1.14, 95% CI 1.00 to 1.30; one RCT, 290 participants; low quality evidence).There was evidence of better healing when root-ends were filled with MTA than when they were treated by smoothing of orthograde GP root filling, after one-year follow-up (RR 1.60, 95% CI 1.14 to 2.24; one RCT, 46 participants; low quality evidence).There was no evidence that using CBCT rather than radiography for preoperative evaluation was advantageous for healing (RR 1.02, 95% CI 0.70 to 1.47; one RCT, 39 participants; very low quality evidence), nor that any magnification device affected healing more than any other (loupes versus endoscope at one year: RR 1.05, 95% CI 0.92 to 1.20; microscope versus endoscope at two years: RR 1.01, 95% CI 0.89 to 1.15; one RCT, 70 participants, low quality evidence).There was no evidence that antibiotic prophylaxis reduced incidence of postoperative infection (RR 0.49, 95% CI 0.09 to 2.64; one RCT, 250 participants; low quality evidence).There was some evidence that using a papilla base incision (PBI) may be beneficial for preservation of the interdental papilla compared with complete papilla mobilisation (one RCT (split-mouth), 12 participants/24 sites; very low quality evidence). There was no evidence of less pain in the PBI group at day 1 post surgery (one RCT, 38 participants; very low quality evidence).There was evidence that adjunctive use of a gel of plasma rich in growth factors reduced postoperative pain compared with no grafting (measured on visual analogue scale: one day postoperative MD -51.60 mm, 95% CI -63.43 to -39.77; one RCT, 36 participants; low quality evidence).There was no evidence that use of low energy level laser therapy (LLLT) prevented postoperative pain (very low quality evidence).

AUTHORS' CONCLUSIONS: Available evidence does not provide clinicians with reliable guidelines for treating periapical lesions. Further research is necessary to understand the effects of surgical versus non-surgical approaches, and to determine which surgical procedures provide the best results for periapical lesion healing and postoperative quality of life. Future studies should use standardised techniques and success criteria, precisely defined outcomes and the participant as the unit of analysis.

摘要

背景

当初次根管治疗失败时,根尖周病变可采用手术或非手术方法进行再治疗。根管再治疗是一种非手术操作,包括从牙齿中取出根管充填材料,随后对根管进行清理、塑形和充填。根尖切除术是一种手术操作,包括通过截骨术暴露根尖周病变、手术切除病变、切除部分根尖、消毒,通常还包括对剩余根管的根尖部分进行逆行封闭或充填。本综述更新了2008年发表的一篇综述。

目的

评估手术和非手术治疗对根尖周炎患牙再治疗的效果。评估在各种条件下,例如使用不同材料、器械或技术时,手术根尖切除术的效果。

检索方法

我们检索了以下电子数据库:Cochrane口腔健康试验注册库(截至2016年2月10日)、Cochrane对照试验中心注册库(CENTRAL;2016年第1期)、MEDLINE Ovid(1946年至2016年2月10日)和Embase Ovid(1980年至2016年2月10日)。我们检索了美国国家临床试验注册库(ClinicalTrials.gov)和世界卫生组织(WHO)国际临床试验注册平台以查找正在进行的试验(截至2016年2月10日)。我们对语言和出版日期没有限制。我们手工检索了检索到的研究的参考文献列表以及牙髓病学领域的关键期刊。

选择标准

我们纳入了涉及根尖周病变患者的随机对照试验(RCT)。研究可以比较手术与非手术治疗,或者可以比较不同类型的手术。结局指标包括在一年或更长时间的随访后评估根尖周病变的愈合情况;术后疼痛和不适;以及通过X线片评估的不良反应,如牙齿脱落、松动、软组织退缩、脓肿、感染、神经损伤或根充材料丧失。

数据收集与分析

两位综述作者独立从纳入的研究中提取数据并评估其偏倚风险。我们联系研究作者以获取缺失信息。我们使用固定效应模型合并评估可比结局的试验结果,二分结局采用风险比(RR),连续结局采用均值差(MD),并给出95%置信区间(CI)。我们对自身对照研究使用通用逆方差法。

主要结果

我们纳入了20项RCT。两项偏倚风险高的试验评估了手术与非手术方法:根尖切除并根尖充填与根管再治疗。其他18项试验评估了不同的手术方案:锥形束计算机断层扫描(CBCT)与根尖X线片用于术前评估(一项偏倚风险高的研究);抗生素预防与安慰剂(一项偏倚风险不明确的研究);不同的放大设备(放大镜、手术显微镜、内窥镜)(两项偏倚风险高的研究);切口类型(乳头基部切口 versus 龈沟切口)(一项偏倚风险高的研究和一项偏倚风险不明确的研究);超声设备与手用钻(一项偏倚风险高的研究);根尖充填材料类型(玻璃离子水门汀、银汞合金、中间修复材料(IRM)、三氧化矿物凝聚体(MTA)、牙胶(GP)、超乙氧基苯甲酸(EBA))(五项偏倚风险高的研究、一项偏倚风险不明确的研究和一项偏倚风险低的研究);植骨与不植骨(三项偏倚风险高的研究和一项偏倚风险不明确的研究);以及低能量激光治疗与安慰剂(无激光激活照射)与对照(不使用激光设备)(一项偏倚风险高的研究)。在一年随访时(RR 1.15,95%CI 0.97至1.35;两项RCT,126名参与者)或四年或十年随访时(一项RCT,82至95名参与者),没有明确证据表明手术或非手术方法在愈合方面更具优势,尽管证据质量非常低。手术治疗组中更多参与者在治疗后的第一周报告疼痛(RR 3.34,95%CI 2.05至5.43;一项RCT,87名参与者;低质量证据)。在手术方案方面,有一些不确定的证据表明,与传统钻相比,超声设备用于根尖预备可能会改善再治疗一年后的愈合情况(RR 1.14,95%CI 1.00至1.30;一项RCT,290名参与者;低质量证据)。在一年随访后,有证据表明根尖用MTA充填比正向GP根充后进行根尖平整处理愈合更好(RR 1.60,95%CI 1.14至2.24;一项RCT,46名参与者;低质量证据)。没有证据表明术前使用CBCT而非X线片对愈合更有利(RR 1.02,95%CI 0.70至1.47;一项RCT,39名参与者;极低质量证据),也没有证据表明任何放大设备对愈合的影响比其他设备更大(一年时放大镜与内窥镜比较:RR 1.05,95%CI 0.92至1.20;两年时显微镜与内窥镜比较:RR 1.01,95%CI 0.89至1.15;一项RCT,70名参与者,低质量证据)。没有证据表明抗生素预防能降低术后感染发生率(RR 0.49,95%CI 0.09至2.64;一项RCT,250名参与者;低质量证据)。有一些证据表明,与完全移动乳头相比,使用乳头基部切口(PBI)可能有利于保留龈乳头(一项RCT(自身对照),12名参与者/24个部位;极低质量证据)。没有证据表明PBI组在术后第1天疼痛更少(一项RCT,38名参与者;极低质量证据)。有证据表明,与不植骨相比,辅助使用富含生长因子的血浆凝胶可减轻术后疼痛(术后第1天视觉模拟评分法测量:MD -51.60 mm,95%CI -63.43至-39.77;一项RCT,36名参与者;低质量证据)。没有证据表明使用低能量激光治疗(LLLT)能预防术后疼痛(极低质量证据)。

作者结论

现有证据未能为临床医生提供治疗根尖周病变的可靠指南。有必要进一步研究以了解手术与非手术方法的效果,并确定哪种手术操作能为根尖周病变愈合和术后生活质量带来最佳结果。未来的研究应采用标准化技术和成功标准,精确界定结局,并以参与者作为分析单位。

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