Systemic antibiotics for chronic suppurative otitis media.

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Lee Yee Chong, Karen Head, Katie E Webster, Jessica Daw, Natalie A Strobel, Peter C Richmond, Tom Snelling, Mahmood F Bhutta, Anne Gm Schilder, Christopher G Brennan-Jones
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This is the first update to the review published in 2021, and is one of a suite of seven Cochrane reviews evaluating the effects of non-surgical interventions for CSOM.</p><p><strong>Objectives: </strong>To assess the effects of systemic antibiotics compared to placebo, no treatment, or another systemic antibiotic in people with chronic suppurative otitis media (CSOM).</p><p><strong>Search methods: </strong>We searched the Cochrane Ear, Nose, and Throat Register, CENTRAL, MEDLINE, Embase, four other databases, and two clinical trials registers to 15 June 2022.</p><p><strong>Selection criteria: </strong>We included randomised controlled trials comparing systemic antibiotics (oral, injection) to placebo/no treatment or other systemic antibiotics with at least a one-week follow-up period, involving people with chronic (at least two weeks) ear discharge of unknown cause or due to CSOM. 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This study did not report other outcomes. It is also very uncertain if co-trimoxazole improved resolution of ear discharge after four weeks compared to placebo (RR 1.54, 95% CI 1.09 to 2.16; 1 study, 98 participants; very low-certainty evidence). From the narrative reporting of one study, there was no evidence of a difference between groups for health-related quality of life, hearing, or serious complications (very low-certainty evidence). 4. Systemic antibiotics versus no treatment/placebo (plus topical antiseptics in both study arms) One study (136 participants) used topical antiseptics as background treatment in both arms, and found no difference in the resolution of ear discharge between the amoxicillin and no-treatment groups at three to four months (RR 1.03, 95% CI 0.75 to 1.41; 136 participants; very low-certainty evidence). The narrative report indicated no evidence of differences in hearing or suspected ototoxicity (very low-certainty evidence). 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引用次数: 0

Abstract

Background: Chronic suppurative otitis media (CSOM), sometimes referred to as chronic otitis media (COM), is a chronic inflammation and often polymicrobial infection of the middle ear and mastoid cavity, characterised by ear discharge (otorrhoea) through a perforated tympanic membrane. The predominant symptoms of CSOM are ear discharge and hearing loss. Systemic antibiotics are commonly used to treat people with CSOM. This is the first update to the review published in 2021, and is one of a suite of seven Cochrane reviews evaluating the effects of non-surgical interventions for CSOM.

Objectives: To assess the effects of systemic antibiotics compared to placebo, no treatment, or another systemic antibiotic in people with chronic suppurative otitis media (CSOM).

Search methods: We searched the Cochrane Ear, Nose, and Throat Register, CENTRAL, MEDLINE, Embase, four other databases, and two clinical trials registers to 15 June 2022.

Selection criteria: We included randomised controlled trials comparing systemic antibiotics (oral, injection) to placebo/no treatment or other systemic antibiotics with at least a one-week follow-up period, involving people with chronic (at least two weeks) ear discharge of unknown cause or due to CSOM. Other treatments were allowed if both treatment and control arms received it.

Data collection and analysis: We used standard Cochrane methods. Our primary outcomes were: resolution of ear discharge or 'dry ear' (whether otoscopically confirmed or not, measured at between one week and up to two weeks, two weeks to up to four weeks, and after four weeks); health-related quality of life using a validated instrument; and ear pain (otalgia)/discomfort/local irritation. Secondary outcomes included hearing, serious complications, and ototoxicity measured in several ways. We used GRADE to assess the certainty of the evidence for each outcome.

Main results: This update found three new studies (390 participants). Overall, we included 21 studies (2525 participants). We report four core comparisons below, and describe an additional four in the Results section of the review. 1. Systemic antibiotics versus no treatment/placebo It is very uncertain from a single study if there is a difference between systemic (intravenous) antibiotics and placebo in the resolution of ear discharge between one and two weeks (risk ratio (RR) 8.47, 95% confidence interval (CI) 1.88 to 38.21; 1 study, 33 participants; very low-certainty evidence). The study did not report results for resolution of ear discharge after two weeks, or health-related quality of life. The evidence is very uncertain for hearing and serious (intracranial) complications. The study did not report ear pain and suspected ototoxicity. 2. Systemic antibiotics versus no treatment/placebo (both study arms received topical antibiotics) Seven studies assessed this comparison, with five presenting usable data. There may be little or no difference between oral ciprofloxacin and placebo/no treatment (with all participants receiving ciprofloxacin ear drops) in the resolution of ear discharge between one and two weeks (RR 1.05, 95% CI 0.94 to 1.17; I2 = 0%; 3 studies, 300 participants; low-certainty evidence), with similar results at two to four weeks. One study reported outcomes beyond four weeks, but the results were not usable. No studies reported health-related quality of life. The evidence is very uncertain for ear pain, serious complications, and suspected ototoxicity. 3. Systemic antibiotics versus no treatment/placebo (plus topical antibiotics and topical steroids in both study arms) Two studies used topical antibiotics plus topical steroids as background treatment in both arms. It is very uncertain if there is a difference in resolution of ear discharge between metronidazole and placebo at two to four weeks (RR 0.91, 95% CI 0.51 to 1.65; 1 study, 30 participants). This study did not report other outcomes. It is also very uncertain if co-trimoxazole improved resolution of ear discharge after four weeks compared to placebo (RR 1.54, 95% CI 1.09 to 2.16; 1 study, 98 participants; very low-certainty evidence). From the narrative reporting of one study, there was no evidence of a difference between groups for health-related quality of life, hearing, or serious complications (very low-certainty evidence). 4. Systemic antibiotics versus no treatment/placebo (plus topical antiseptics in both study arms) One study (136 participants) used topical antiseptics as background treatment in both arms, and found no difference in the resolution of ear discharge between the amoxicillin and no-treatment groups at three to four months (RR 1.03, 95% CI 0.75 to 1.41; 136 participants; very low-certainty evidence). The narrative report indicated no evidence of differences in hearing or suspected ototoxicity (very low-certainty evidence). The study reported no other outcomes. Limitations include heterogeneity in the duration and definition of CSOM used by studies included in the review. Although we planned subgroup analyses for different participant characteristics, treatment duration, and spectrum of antibiotic activity, we did not perform these analyses due to lack of available data.

Authors' conclusions: The evidence available to determine whether systemic antibiotics are effective in achieving resolution of ear discharge in people with CSOM is limited. We are very uncertain if systemic antibiotics, when used alone (with or without aural toileting (ear cleaning)), are more effective than placebo or no treatment. When added to an intervention such as topical antibiotics, there may be little or no difference in resolution of ear discharge (very low-certainty evidence). Data were only available for certain classes of antibiotics; it is very uncertain whether one class of systemic antibiotic is more effective than another. Harmful effects of systemic antibiotics were poorly reported in the included studies.

慢性化脓性中耳炎的全身抗生素治疗。
背景:慢性化脓性中耳炎(CSOM),有时也被称为慢性中耳炎(COM),是中耳和乳突腔的一种慢性炎症和多微生物感染,其特征是通过穿孔的鼓膜漏耳(耳漏)。CSOM的主要症状是耳塞和听力丧失。全身抗生素通常用于治疗CSOM患者。这是对2021年发表的综述的第一次更新,也是评估非手术干预对CSOM影响的七篇Cochrane综述之一。目的:评估全身性抗生素与安慰剂、不治疗或其他全身性抗生素对慢性化脓性中耳炎(CSOM)患者的影响。检索方法:我们检索了Cochrane耳鼻喉注册库、CENTRAL、MEDLINE、Embase、其他四个数据库和两个临床试验注册库,截止到2022年6月15日。选择标准:我们纳入了比较全身性抗生素(口服、注射)与安慰剂/无治疗或其他全身性抗生素的随机对照试验,随访期至少一周,涉及原因不明或CSOM引起的慢性(至少两周)耳流患者。如果治疗组和对照组都接受了治疗,则允许进行其他治疗。资料收集与分析:采用标准Cochrane方法。我们的主要结果是:耳部分泌物或“干耳”的消退(无论耳镜检查是否证实,在一周至两周、两周至四周和四周后测量);使用经过验证的仪器检测与健康有关的生活质量;耳痛(耳痛)/不适/局部刺激。次要结果包括听力、严重并发症和耳毒性。我们使用GRADE来评估每个结果证据的确定性。主要结果:本次更新发现了三项新研究(390名参与者)。总的来说,我们纳入了21项研究(2525名受试者)。我们在下面报告四个核心比较,并在综述的结果部分描述另外四个比较。1. 从一项研究来看,非常不确定全身(静脉注射)抗生素和安慰剂在1周至2周内耳液的缓解方面是否存在差异(风险比(RR) 8.47, 95%可信区间(CI) 1.88至38.21;1项研究,33名参与者;非常低确定性证据)。该研究没有报告两周后耳部分泌物消退的结果,也没有报告与健康相关的生活质量。听力和严重(颅内)并发症的证据非常不确定。该研究没有报告耳痛和疑似耳毒性。2. 全身性抗生素与无治疗/安慰剂(两组研究均使用局部抗生素)7项研究评估了这种比较,其中5项提供了可用数据。口服环丙沙星与安慰剂/无治疗(所有受试者均接受环丙沙星滴耳液)在1 - 2周的耳漏缓解方面可能差异不大或没有差异(RR 1.05, 95% CI 0.94 - 1.17;I2 = 0%;3项研究,300名参与者;低确定性证据),两到四周的结果相似。一项研究报告了超过四周的结果,但结果不可用。没有研究报告与健康相关的生活质量。耳部疼痛、严重并发症和疑似耳毒性的证据非常不确定。3. 全身性抗生素与无治疗/安慰剂(两组研究均使用局部抗生素和局部类固醇)两组研究均使用局部抗生素和局部类固醇作为背景治疗。非常不确定甲硝唑和安慰剂在2 - 4周时耳部溢液的消退是否存在差异(RR 0.91, 95% CI 0.51 - 1.65;1项研究,30名参与者)。本研究未报道其他结果。与安慰剂相比,复方新诺明是否在4周后改善了耳部分泌物的消退也非常不确定(RR 1.54, 95% CI 1.09至2.16;1项研究,98名参与者;非常低确定性证据)。从一项研究的叙述性报告来看,没有证据表明两组之间在健康相关的生活质量、听力或严重并发症方面存在差异(非常低确定性的证据)。4. 一项研究(136名受试者)在两组患者中均使用局部杀菌剂作为背景治疗,并发现阿莫西林组和无治疗组在3至4个月时耳部分泌物的消退无差异(RR 1.03, 95% CI 0.75至1.41;136名参与者;非常低确定性证据)。叙述性报告没有显示听力差异或疑似耳毒性的证据(非常低确定性的证据)。该研究没有报告其他结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.60
自引率
2.40%
发文量
173
审稿时长
1-2 weeks
期刊介绍: The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.
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