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拔牙后出血的治疗干预措施。

Interventions for treating post-extraction bleeding.

作者信息

Sumanth Kumbargere N, Prashanti Eachempati, Aggarwal Himanshi, Kumar Pradeep, Lingappa Ashok, Muthu Murugan S, Kiran Kumar Krishanappa Salian

机构信息

Department of Oral Medicine & Oral Radiology, Faculty of Dentistry, Melaka-Manipal Medical College, Jalan Batu Hampar, Bukit Baru, Melaka, Malaysia, 75150.

出版信息

Cochrane Database Syst Rev. 2016 Jun 10(6):CD011930. doi: 10.1002/14651858.CD011930.pub2.

Abstract

BACKGROUND

Post-extraction bleeding (PEB) is a recognised, frequently encountered complication in dental practice, which is defined as bleeding that continues beyond 8 to 12 hours after dental extraction. The incidence of post-extraction bleeding varies from 0% to 26%. If post-extraction bleeding is not managed, complications can range from soft tissue haematomas to severe blood loss. Local causes of bleeding include soft tissue and bone bleeding. Systemic causes include platelet problems, coagulation disorders or excessive fibrinolysis, and inherited or acquired problems (medication induced). There is a wide array of techniques suggested for the treatment of post-extraction bleeding, which include interventions aimed at both local and systemic causes.

OBJECTIVES

To assess the effects of interventions for treating different types of post-extraction bleeding.

SEARCH METHODS

We searched the following electronic databases: The Cochrane Oral Health Group Trials Register (to 22 March 2016); The Cochrane Central Register of Controlled Trials (CENTRAL; The Cochrane Library 2016, Issue 2); MEDLINE via OVID (1946 to 22 March 2016); CINAHL via EBSCO (1937 to 22 March 2016). Due to the ongoing Cochrane project to search EMBASE and add retrieved clinical trials to CENTRAL, we searched only the last 11 months of EMBASE via OVID (1 May 2015 to 22 March 2016). We placed no further restrictions on the language or date of publication. We searched the US National Institutes of Health Trials Register (http://clinicaltrials.gov), and the WHO Clinical Trials Registry Platform for ongoing trials (http://apps.who.int/trialsearch/default.aspx). We also checked the reference lists of excluded trials.

SELECTION CRITERIA

We considered randomised controlled trials (RCTs) that evaluated any intervention for treating PEB, with male or female participants of any age, regardless of type of teeth (anterior or posterior, mandibular or maxillary). Trials could compare one type of intervention with another, with placebo, or with no treatment.

DATA COLLECTION AND ANALYSIS

Three pairs of review authors independently screened search records. We obtained full papers for potentially relevant trials. If data had been extracted, we would have followed the methods described in the Cochrane Handbook for Systematic Reviews of Interventions for the statistical analysis.

MAIN RESULTS

We did not find any randomised controlled trial suitable for inclusion in this review.

AUTHORS' CONCLUSIONS: We were unable to identify any reports of randomised controlled trials that evaluated the effects of different interventions for the treatment of post-extraction bleeding. In view of the lack of reliable evidence on this topic, clinicians must use their clinical experience to determine the most appropriate means of treating this condition, depending on patient-related factors. There is a need for well designed and appropriately conducted clinical trials on this topic, which conform to the CONSORT statement (www.consort-statement.org/).

摘要

背景

拔牙后出血(PEB)是牙科实践中一种公认的、经常遇到的并发症,定义为拔牙后持续出血超过8至12小时。拔牙后出血的发生率在0%至26%之间。如果拔牙后出血得不到处理,并发症范围可从软组织血肿到严重失血。出血的局部原因包括软组织和骨出血。全身原因包括血小板问题、凝血障碍或纤维蛋白溶解过度,以及遗传性或获得性问题(药物引起)。针对拔牙后出血的治疗,有各种各样的技术被提出,包括针对局部和全身原因的干预措施。

目的

评估治疗不同类型拔牙后出血的干预措施的效果。

检索方法

我们检索了以下电子数据库:Cochrane口腔健康组试验注册库(截至2016年3月22日);Cochrane对照试验中心注册库(CENTRAL;Cochrane图书馆2016年第2期);通过OVID检索的MEDLINE(1946年至2016年3月22日);通过EBSCO检索的CINAHL(1937年至2016年3月22日)。由于Cochrane正在进行检索EMBASE并将检索到的临床试验添加到CENTRAL的项目,我们仅通过OVID检索了EMBASE最近11个月的内容(2015年5月1日至2016年3月22日)。我们对语言或出版日期没有进一步限制。我们检索了美国国立卫生研究院试验注册库(http://clinicaltrials.gov)和世界卫生组织临床试验注册平台以获取正在进行的试验(http://apps.who.int/trialsearch/default.aspx)。我们还检查了排除试验的参考文献列表。

选择标准

我们纳入评估任何治疗拔牙后出血干预措施的随机对照试验(RCT),参与者为任何年龄的男性或女性,无论牙齿类型(前牙或后牙、下颌牙或上颌牙)。试验可将一种干预措施与另一种干预措施、安慰剂或不治疗进行比较。

数据收集与分析

三对综述作者独立筛选检索记录。我们获取了潜在相关试验的全文。如果已经提取了数据,我们将遵循Cochrane系统评价干预措施手册中描述的方法进行统计分析。

主要结果

我们未找到任何适合纳入本综述的随机对照试验。

作者结论

我们未能识别出任何评估不同干预措施治疗拔牙后出血效果的随机对照试验报告。鉴于该主题缺乏可靠证据,临床医生必须根据患者相关因素,利用临床经验来确定治疗这种情况的最合适方法。需要针对该主题设计良好且实施得当的符合CONSORT声明(www.consort-statement.org/)的临床试验。

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