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口服类固醇治疗 2-8 岁儿童分泌性中耳炎相关听力损失的随机对照试验:OSTRICH RCT。

Oral steroids for hearing loss associated with otitis media with effusion in children aged 2-8 years: the OSTRICH RCT.

机构信息

Division of Population Medicine, School of Medicine, Cardiff University, Cardiff, UK.

Centre for Trials Research, Cardiff University, Cardiff, UK.

出版信息

Health Technol Assess. 2018 Nov;22(61):1-114. doi: 10.3310/hta22610.

DOI:10.3310/hta22610
PMID:30407151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6253325/
Abstract

BACKGROUND

Children with hearing loss associated with otitis media with effusion (OME) are commonly managed through surgical intervention, hearing aids or watchful waiting. A safe, inexpensive, effective medical treatment would enhance treatment options. Small, poorly conducted trials have found a short-term benefit from oral steroids.

OBJECTIVE

To determine the clinical effectiveness and cost-effectiveness of a 7-day course of oral steroids in improving hearing at 5 weeks in children with persistent OME symptoms and current bilateral OME and hearing loss demonstrated by audiometry.

DESIGN

Double-blind, individually randomised, placebo-controlled trial.

SETTING

Ear, nose and throat outpatient or paediatric audiology and audiovestibular medicine clinics in Wales and England.

PARTICIPANTS

Children aged 2-8 years, with symptoms of hearing loss attributable to OME for at least 3 months, a diagnosis of bilateral OME made on the day of recruitment and audiometry-confirmed hearing loss.

INTERVENTIONS

A 7-day course of oral soluble prednisolone, as a single daily dose of 20 mg for children aged 2-5 years or 30 mg for 6- to 8-year-olds, or matched placebo.

MAIN OUTCOME MEASURES

Acceptable hearing at 5 weeks from randomisation. Secondary outcomes comprised acceptable hearing at 6 and 12 months, tympanometry, otoscopic findings, health-care consultations related to OME and other resource use, proportion of children who had ventilation tube (grommet) surgery at 6 and 12 months, adverse effects, symptoms, functional health status, health-related quality of life, short- and longer-term cost-effectiveness.

RESULTS

A total of 389 children were randomised. Satisfactory hearing at 5 weeks was achieved by 39.9% and 32.8% in the oral steroid and placebo groups, respectively (absolute difference of 7.1%, 95% confidence interval -2.8% to 16.8%; number needed to treat = 14). This difference was not statistically significant. The secondary outcomes were consistent with the picture of a small or no benefit, and we found no subgroups that achieved a meaningful benefit from oral steroids. The economic analysis showed that treatment with oral steroids was more expensive and accrued fewer quality-adjusted life-years than treatment as usual. However, the differences were small and not statistically significant, and the sensitivity analyses demonstrated large variation in the results.

CONCLUSIONS

OME in children with documented hearing loss and attributable symptoms for at least 3 months has a high rate of spontaneous resolution. Discussions about watchful waiting and other interventions will be enhanced by this evidence. The findings of this study suggest that any benefit from a short course of oral steroids for OME is likely to be small and of questionable clinical significance, and that the treatment is unlikely to be cost-effective and, therefore, their use cannot be recommended.

FUTURE WORK

Studies exploring optimal approaches to sharing natural history data and enhancing shared decision-making are needed for this condition.

TRIAL REGISTRATION

Current Controlled Trials ISRCTN49798431 and EudraCT 2012-005123-32.

FUNDING

This project was funded by the National Institute for Health Research (NIHR) Health Technology Assessment programme and will be published in full in ; Vol. 22, No. 61. See the NIHR Journals Library website for further project information.

摘要

背景

患有分泌性中耳炎(OME)相关听力损失的儿童通常通过手术干预、助听器或观察等待来治疗。如果有一种安全、廉价且有效的医学治疗方法,将会增加治疗选择。小型、设计不佳的试验发现,口服类固醇在短期内有一定益处。

目的

确定为期 7 天的口服类固醇治疗方案是否能改善持续 OME 症状且双侧 OME 和听力损失的儿童在 5 周时的听力,通过听力测试可确诊 OME 症状和双侧 OME 以及听力损失。

设计

双盲、个体随机、安慰剂对照试验。

地点

威尔士和英格兰的耳鼻喉科门诊或儿科听力和听觉医学诊所。

参与者

年龄 2-8 岁,有听力损失症状归因于 OME 至少 3 个月,在招募当天诊断为双侧 OME,并通过听力测试确诊听力损失。

干预措施

口服可溶性泼尼松龙治疗 7 天,2-5 岁儿童每天单次剂量为 20mg,6-8 岁儿童为 30mg,或匹配的安慰剂。

主要结局测量

随机分组后 5 周时可接受的听力。次要结局包括 6 个月和 12 个月时可接受的听力、鼓室压图、耳镜检查结果、与 OME 相关的医疗保健咨询和其他资源使用情况、6 个月和 12 个月时行鼓膜置管(通气管)手术的儿童比例、不良反应、症状、功能健康状况、健康相关生活质量、短期和长期成本效益。

结果

共有 389 名儿童被随机分配。口服类固醇组和安慰剂组在 5 周时达到可接受听力的比例分别为 39.9%和 32.8%(绝对差异为 7.1%,95%置信区间为-2.8%至 16.8%;需要治疗的人数为 14)。这一差异无统计学意义。次要结局与小或无获益的情况一致,我们没有发现任何亚组从口服类固醇中获得有意义的获益。经济分析表明,与常规治疗相比,口服类固醇治疗更昂贵,且获得的质量调整生命年更少。然而,这些差异很小且无统计学意义,敏感性分析表明结果存在较大差异。

结论

有记录的听力损失和归因于症状至少 3 个月的儿童 OME 有很高的自发缓解率。本研究结果将有助于增强对观察等待和其他干预措施的讨论。本研究的结果表明,口服类固醇治疗 OME 的任何获益都可能很小,且具有临床意义值得怀疑,并且治疗不太可能具有成本效益,因此不能推荐使用。

未来工作

需要研究探索最佳方法来共享自然病史数据并增强共同决策,以解决这种情况。

试验注册

当前对照试验 ISRCTN49798431 和 EudraCT 2012-005123-32。

资金

本项目由英国国家卫生研究院(NIHR)卫生技术评估计划资助,全文将在;第 22 卷,第 61 期。有关该项目的更多信息,请访问 NIHR 期刊库网站。