Chang Brent A, Thamboo Andrew, Burton Martin J, Diamond Chris, Nunez Desmond A
Division of Otolaryngology Head & Neck Surgery, University of British Columbia, 2775 Laurel St., 4th Floor Otolaryngology (ENT), Vancouver, BC, Canada, V5Z 1M9.
UK Cochrane Centre, Summertown Pavilion, 18 - 24 Middle Way, Oxford, UK, OX2 7LG.
Cochrane Database Syst Rev. 2016 Dec 23;12(12):CD006287. doi: 10.1002/14651858.CD006287.pub4.
Peritonsillar abscess is a common infection presenting as a collection of pus in the peritonsillar area. The condition is characterised by a severe sore throat, difficulty in swallowing and pain on swallowing, fever and malaise, and trismus. Needle aspiration and incision and drainage are the two main treatment modalities currently used in the treatment of this condition. The effectiveness of one versus the other has not been clearly demonstrated and remains an area of debate.
To assess the effectiveness and risks of needle aspiration versus incision and drainage for the treatment of peritonsillar abscess in older children (eight years of age or older), adolescents and adults.
The Cochrane ENT Information Specialist searched the ENT Trials Register; Central Register of Controlled Trials (CENTRAL 2016, Issue 7); Ovid MEDLINE; Ovid Embase; CINAHL; Web of Science; ClinicalTrials.gov; ICTRP and additional sources for published and unpublished trials. The date of the search was 25 August 2016.
Randomised controlled trials comparing needle aspiration with incision and drainage.
We used the standard methodological procedures expected by Cochrane. Our primary outcomes were recurrence rate (proportion of patients needing repeat intervention) and adverse effects associated with the intervention. Secondary outcomes were time to resumption of normal diet, complications of the disease process and symptom scores. We used GRADE to assess the quality of evidence for each outcome; this is indicated in italics.
We included 11 studies (674 participants). The risk of bias was high or unclear in all of the included studies. All studies compared needle aspiration to incision and drainage.All but one of the 11 studies reported on the primary outcome of recurrence. When we pooled data from the 10 studies the recurrence rate was higher in the needle aspiration group compared with incision and drainage: risk ratio (RR) 3.74 (95% confidence interval (CI) 1.63 to 8.59; 612 participants). We detected moderate heterogeneity in this analysis (I = 48%). In interpreting the pooled result it is important to note that the evidence for this outcome was of very low quality.None of the other outcomes (adverse effects of the intervention, time to resumption of normal diet, complications of the disease process and symptom scores) were consistently measured across all studies.Only three studies reported on adverse effects/events associated with the intervention and only one such event in a single patient was reported (post-procedure bleeding following incision and drainage: 1/28, 3.6%) (very low-quality evidence). Time to resumption of normal diet was compared in two studies; neither found an obvious difference between needle aspiration and incision and drainage (very low-quality evidence).Only three studies stated that they would report complications of the disease process. In these three studies, the only complication reported was admission to hospital for dehydration in two patients who underwent incision and drainage (2/13, 6.7%). Symptom scores were measured in four studies; three evaluated pain using different scales and one other symptoms. The data could not be pooled in a meta-analysis. Two studies evaluating procedural pain reported this to be lower in the needle aspiration groups. One study found comparable rates of pain resolution at five days post-intervention between groups. The quality of the evidence for symptom scores was very low.
AUTHORS' CONCLUSIONS: Although a number of studies have sought to evaluate whether or not needle aspiration or incision and drainage is more effective in patients with peritonsillar abscess, there is no high-quality evidence to allow a firm conclusion to be drawn and the answer remains uncertain. Very low-quality evidence suggests that incision and drainage may be associated with a lower chance of recurrence than needle aspiration. There is some very low-quality evidence to suggest that needle aspiration is less painful.
扁桃体周脓肿是一种常见感染,表现为扁桃体周区域的脓液积聚。该病的特征为严重咽痛、吞咽困难、吞咽时疼痛、发热、不适及牙关紧闭。针吸术和切开引流是目前治疗该病的两种主要方式。但尚无明确证据表明哪种方式更有效,这仍是一个存在争议的领域。
评估针吸术与切开引流术治疗大龄儿童(8岁及以上)、青少年及成人扁桃体周脓肿的有效性和风险。
Cochrane耳鼻喉信息专家检索了耳鼻喉试验注册库、Cochrane对照试验中心注册库(CENTRAL 2016年第7期)、Ovid MEDLINE、Ovid Embase、CINAHL、Web of Science、ClinicalTrials.gov、ICTRP以及其他已发表和未发表试验的来源。检索日期为2016年8月25日。
比较针吸术与切开引流术的随机对照试验。
我们采用了Cochrane期望的标准方法程序。我们的主要结局是复发率(需要重复干预的患者比例)以及与干预相关的不良反应。次要结局包括恢复正常饮食的时间、疾病过程中的并发症及症状评分。我们使用GRADE评估每个结局的证据质量;以斜体表示。
我们纳入了11项研究(674名参与者)。所有纳入研究的偏倚风险均为高或不清楚。所有研究均比较了针吸术与切开引流术。11项研究中除1项外均报告了复发这一主要结局。当我们汇总10项研究的数据时,针吸术组的复发率高于切开引流术组:风险比(RR)为3.74(95%置信区间(CI)为1.63至8.59;612名参与者)。我们在该分析中检测到中度异质性(I² = 48%)。在解释汇总结果时,需注意该结局的证据质量非常低。所有研究均未一致测量其他结局(干预的不良反应、恢复正常饮食的时间、疾病过程中的并发症及症状评分)。仅3项研究报告了与干预相关的不良反应/事件,且仅报告了1例患者的1起此类事件(切开引流术后出血:1/28,3.6%)(证据质量非常低)。两项研究比较了恢复正常饮食的时间;均未发现针吸术与切开引流术之间存在明显差异(证据质量非常低)。仅3项研究表示他们将报告疾病过程中的并发症。在这3项研究中,报告的唯一并发症是两名接受切开引流术的患者因脱水住院(2/13,6.7%)。4项研究测量了症状评分;3项使用不同量表评估疼痛,另一项评估其他症状。数据无法进行Meta分析汇总。两项评估操作疼痛的研究报告称针吸术组的疼痛较低。一项研究发现两组在干预后5天的疼痛缓解率相当。症状评分的证据质量非常低。
尽管多项研究试图评估针吸术或切开引流术对扁桃体周脓肿患者是否更有效,但尚无高质量证据得出确切结论,答案仍不确定。质量非常低的证据表明,切开引流术的复发几率可能低于针吸术。有一些质量非常低的证据表明针吸术的疼痛较轻。