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下颌智齿拔除的手术技术。

Surgical techniques for the removal of mandibular wisdom teeth.

作者信息

Bailey Edmund, Kashbour Wafa, Shah Neha, Worthington Helen V, Renton Tara F, Coulthard Paul

机构信息

Department of Oral Surgery, Institute of Dentistry, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.

Division of Dentistry, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.

出版信息

Cochrane Database Syst Rev. 2020 Jul 26;7(7):CD004345. doi: 10.1002/14651858.CD004345.pub3.

Abstract

BACKGROUND

Pathology relating to mandibular wisdom teeth is a frequent presentation to oral and maxillofacial surgeons, and surgical removal of mandibular wisdom teeth is a common operation. The indications for surgical removal of these teeth are alleviation of local pain, swelling and trismus, and also the prevention of spread of infection that may occasionally threaten life. Surgery is commonly associated with short-term postoperative pain, swelling and trismus. Less frequently, infection, dry socket (alveolar osteitis) and trigeminal nerve injuries may occur. This review focuses on the optimal methods in order to improve patient experience and minimise postoperative morbidity.

OBJECTIVES

To compare the relative benefits and risks of different techniques for surgical removal of mandibular wisdom teeth.

SEARCH METHODS

Cochrane Oral Health's Information Specialist searched the following databases: Cochrane Oral Health Trials Register (to 8 July 2019), the Cochrane Central Register of Controlled Trials (CENTRAL) (the Cochrane Library; 2019, Issue 6), MEDLINE Ovid (1946 to 8 July 2019), and Embase Ovid (1980 to 8 July 2019). We searched ClinicalTrials.gov and the World Health Organization International Clinical Trials Registry Platform for ongoing trials. We placed no restrictions on the language or date of publication.

SELECTION CRITERIA

Randomised controlled trials comparing different surgical techniques for the removal of mandibular wisdom teeth.

DATA COLLECTION AND ANALYSIS

Three review authors were involved in assessing the relevance of identified studies, evaluated the risk of bias in included studies and extracted data. We used risk ratios (RRs) for dichotomous data in parallel-group trials (or Peto odds ratios if the event rate was low), odds ratios (ORs) for dichotomous data in cross-over or split-mouth studies, and mean differences (MDs) for continuous data. We took into account the pairing of the split-mouth studies in our analyses, and combined parallel-group and split-mouth studies using the generic inverse-variance method. We used the fixed-effect model for three studies or fewer, and random-effects model for more than three studies.

MAIN RESULTS

We included 62 trials with 4643 participants. Several of the trials excluded individuals who were not in excellent health. We assessed 33 of the studies (53%) as being at high risk of bias and 29 as unclear. We report results for our primary outcomes below. Comparisons of different suturing techniques and of drain versus no drain did not report any of our primary outcomes. No studies provided useable data for any of our primary outcomes in relation to coronectomy. There is insufficient evidence to determine whether envelope or triangular flap designs led to more alveolar osteitis (OR 0.33, 95% confidence interval (CI) 0.09 to 1.23; 5 studies; low-certainty evidence), wound infection (OR 0.29, 95% CI 0.04 to 2.06; 2 studies; low-certainty evidence), or permanent altered tongue sensation (Peto OR 4.48, 95% CI 0.07 to 286.49; 1 study; very low-certainty evidence). In terms of other adverse effects, two studies reported wound dehiscence at up to 30 days after surgery, but found no difference in risk between interventions. There is insufficient evidence to determine whether the use of a lingual retractor affected the risk of permanent altered sensation compared to not using one (Peto OR 0.14, 95% CI 0.00 to 6.82; 1 study; very low-certainty evidence). None of our other primary outcomes were reported by studies included in this comparison. There is insufficient evidence to determine whether lingual split with chisel is better than a surgical hand-piece for bone removal in terms of wound infection (OR 1.00, 95% CI 0.31 to 3.21; 1 study; very low-certainty evidence). Alveolar osteitis, permanent altered sensation, and other adverse effects were not reported. There is insufficient evidence to determine whether there is any difference in alveolar osteitis according to irrigation method (mechanical versus manual: RR 0.33, 95% CI 0.01 to 8.09; 1 study) or irrigation volume (high versus low; RR 0.52, 95% CI 0.27 to 1.02; 1 study), or whether there is any difference in postoperative infection according to irrigation method (mechanical versus manual: RR 0.50, 95% CI 0.05 to 5.43; 1 study) or irrigation volume (low versus high; RR 0.17, 95% CI 0.02 to 1.37; 1 study) (all very low-certainty evidence). These studies did not report permanent altered sensation and adverse effects. There is insufficient evidence to determine whether primary or secondary wound closure led to more alveolar osteitis (RR 0.99, 95% CI 0.41 to 2.40; 3 studies; low-certainty evidence), wound infection (RR 4.77, 95% CI 0.24 to 96.34; 1 study; very low-certainty evidence), or adverse effects (bleeding) (RR 0.41, 95% CI 0.11 to 1.47; 1 study; very low-certainty evidence). These studies did not report permanent sensation changes. Placing platelet rich plasma (PRP) or platelet rich fibrin (PRF) in sockets may reduce the incidence of alveolar osteitis (OR 0.39, 95% CI 0.22 to 0.67; 2 studies), but the evidence is of low certainty. Our other primary outcomes were not reported.

AUTHORS' CONCLUSIONS: In this 2020 update, we added 27 new studies to the original 35 in the 2014 review. Unfortunately, even with the addition of these studies, we have been unable to draw many meaningful conclusions. The small number of trials evaluating each comparison and reporting our primary outcomes, along with methodological biases in the included trials, means that the body of evidence for each of the nine comparisons evaluated is of low or very low certainty. Participant populations in the trials may not be representative of the general population, or even the population undergoing third molar surgery. Many trials excluded individuals who were not in good health, and several excluded those with active infection or who had deep impactions of their third molars. Consequently, we are unable to make firm recommendations to surgeons to inform their techniques for removal of mandibular third molars. The evidence is uncertain, though we note that there is some limited evidence that placing PRP or PRF in sockets may reduce the incidence of dry socket. The evidence provided in this review may be used as a guide for surgeons when selecting and refining their surgical techniques. Ongoing studies may allow us to provide more definitive conclusions in the future.

摘要

背景

下颌智齿相关病理情况是口腔颌面外科医生经常面对的问题,下颌智齿拔除术是一项常见手术。拔除这些牙齿的指征包括缓解局部疼痛、肿胀和牙关紧闭,以及预防可能偶尔危及生命的感染扩散。手术通常会伴随术后短期疼痛、肿胀和牙关紧闭。较少见的情况下,可能会发生感染、干槽症(牙槽骨炎)和三叉神经损伤。本综述聚焦于优化方法,以改善患者体验并降低术后发病率。

目的

比较不同技术拔除下颌智齿的相对益处和风险。

检索方法

Cochrane口腔健康信息专家检索了以下数据库:Cochrane口腔健康试验注册库(截至2019年7月8日)、Cochrane对照试验中心注册库(CENTRAL)(Cochrane图书馆;2019年第6期)、MEDLINE Ovid(1946年至2019年7月8日)以及Embase Ovid(1980年至2019年7月8日)。我们检索了ClinicalTrials.gov和世界卫生组织国际临床试验注册平台以查找正在进行的试验。我们对发表语言和日期未设限制。

选择标准

比较不同手术技术拔除下颌智齿的随机对照试验。

数据收集与分析

三位综述作者参与评估所识别研究的相关性,评估纳入研究的偏倚风险并提取数据。对于平行组试验中的二分数据,我们使用风险比(RRs)(如果事件发生率较低则使用Peto比值比),对于交叉或分口研究中的二分数据使用比值比(ORs),对于连续数据使用均值差(MDs)。我们在分析中考虑了分口研究的配对情况,并使用通用逆方差法合并平行组和分口研究。对于三项或更少的研究,我们使用固定效应模型,对于超过三项的研究使用随机效应模型。

主要结果

我们纳入了62项试验,共4643名参与者。其中几项试验排除了健康状况不佳的个体。我们评估33项研究(53%)存在高偏倚风险,29项研究偏倚风险不明确。我们在下文报告主要结局的结果。不同缝合技术以及放置引流管与不放置引流管的比较均未报告任何主要结局。没有研究提供与牙冠切除术相关的任何主要结局的可用数据。没有足够证据确定信封式或三角形瓣设计是否会导致更多牙槽骨炎(OR 0.33,95%置信区间(CI)0.09至1.23;5项研究;低确定性证据)、伤口感染(OR 0.29,95% CI 0.04至2.06;2项研究;低确定性证据)或永久性舌感觉改变(Peto OR 4.48,95% CI 0.07至286.49;1项研究;极低确定性证据)。在其他不良反应方面,两项研究报告了术后30天内伤口裂开情况,但发现不同干预措施之间风险无差异。没有足够证据确定与不使用舌侧牵开器相比,使用舌侧牵开器是否会影响永久性感觉改变的风险(Peto OR 0.14,95% CI 0.00至6.82;1项研究;极低确定性证据)。该比较中纳入的研究均未报告我们的其他主要结局。没有足够证据确定在伤口感染方面,用凿子进行舌侧劈开是否优于手术机头进行骨去除(OR 1.00,95% CI 0.31至3.21;1项研究;极低确定性证据)。未报告牙槽骨炎、永久性感觉改变及其他不良反应。没有足够证据确定根据冲洗方法(机械冲洗与手动冲洗:RR 0.33,95% CI 0.01至8.09;1项研究)或冲洗量(大量与少量;RR 0.52,95% CI 0.27至1.02;1项研究)牙槽骨炎是否存在差异,或者根据冲洗方法(机械冲洗与手动冲洗:RR 0.50,95% CI 0.05至5.43;1项研究)或冲洗量(少量与大量;RR 0.17y,95% CI y0.02至1.37;1项研究)术后感染是否存在差异(所有证据确定性均极低)。这些研究未报告永久性感觉改变和不良反应。没有足够证据确定一期或二期伤口缝合是否会导致更多牙槽骨炎(RR 0.99,95% CI 0.41至2.40;3项研究;低确定性证据)、伤口感染(RR 4.77,95% CI 0.24至96.34;1项研究;极低确定性证据)或不良反应(出血)(RR 0.41,95% CI 0.11至1.47;1项研究;极低确定性证据)。这些研究未报告永久性感觉改变。在牙槽窝内放置富血小板血浆(PRP)或富血小板纤维蛋白(PRF)可能会降低牙槽骨炎的发生率(OR 0.39,95% CI 0.22至0.67;2项研究),但证据确定性较低。我们的其他主要结局未被报告。

作者结论

在本次2020年更新中,我们在2014年综述的35项原始研究基础上新增了27项研究。遗憾的是,即便增加了这些研究,我们仍无法得出许多有意义的结论。评估每项比较并报告我们主要结局的试验数量较少,加之纳入试验存在方法学偏倚,这意味着所评估的九项比较中每项的证据质量均为低或极低确定性。试验中的参与者群体可能不具有一般人群的代表性,甚至也不能代表接受第三磨牙手术的人群。许多试验排除了健康状况不佳的个体,还有几项排除了有活动性感染或第三磨牙深部阻生的个体。因此,我们无法向外科医生提出明确建议以指导其下颌第三磨牙拔除技术。证据并不确定,不过我们注意到有一些有限证据表明在牙槽窝内放置PRP或PRF可能会降低干槽症的发生率。本综述提供的证据可作为外科医生选择和优化手术技术的参考。正在进行的研究可能使我们未来能够得出更明确的结论。

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