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诊断不准确和受试者排除使得急性中耳炎的安慰剂研究和观察性研究结果不明确。

Diagnostic inaccuracy and subject exclusions render placebo and observational studies of acute otitis media inconclusive.

作者信息

Pichichero Michael E, Casey Janet R

机构信息

Department of Microbiology and Immunology, University of Rochester Medical Center, Rochester, NY 14642, USA.

出版信息

Pediatr Infect Dis J. 2008 Nov;27(11):958-62. doi: 10.1097/INF.0b013e318179a2ac.

Abstract

BACKGROUND

Diagnostic accuracy and appropriate inclusion/exclusion criteria representative of children at greatest risk is of paramount importance in trials to evaluate placebo or observation as an option for acute otitis media (AOM) management.

METHODS

Twelve observational studies spanning the time frame 1958-2005 and 13 natural history studies spanning the time frame 1968-2006 were evaluated for the diagnostic criteria, inclusion criteria, and exclusion criteria applied within the study design.

RESULTS

Although a bulging or full tympanic membrane (TM) with effusion is the best indication of a diagnosis of bacterial AOM based on tympanocentesis findings, few observational and natural history studies required a bulging TM. Examination of subject inclusion criteria showed that many subjects did not have AOM but rather had no middle ear disease at all or they had otitis media with effusion. Exclusion criteria of subjects were also remarkable. Frequently children <2 years old were excluded; mean age among the studies reflected an older age group, unlike the true epidemiology of AOM. Otitis prone children, those with severe disease, with a bulging TM, with fever, with a definite need for antibiotics, with recent antibiotic treatment, with recent AOM, or with perforation of the TM were often excluded.

CONCLUSIONS

Guidelines and some authorities have overlooked or discounted the importance of the issues of inaccurate diagnosis on study entry, broad inclusion criteria, and the creation of bias in exclusion criteria among placebo/natural history trials in AOM. The current data favoring observation of children with AOM should be reconsidered until better studies are conducted.

摘要

背景

在评估使用安慰剂或观察作为急性中耳炎(AOM)治疗方案的试验中,具有诊断准确性以及能代表最高风险儿童的恰当纳入/排除标准至关重要。

方法

对1958 - 2005年期间的12项观察性研究以及1968 - 2006年期间的13项自然史研究进行评估,分析其研究设计中所应用的诊断标准、纳入标准和排除标准。

结果

尽管根据鼓膜穿刺结果,鼓膜膨出或充满积液是细菌性AOM诊断的最佳指征,但很少有观察性研究和自然史研究要求鼓膜膨出。对受试者纳入标准的审查表明,许多受试者并非患有AOM,而是根本没有中耳疾病,或者患有中耳积液。受试者的排除标准也很显著。经常排除2岁以下儿童;研究中的平均年龄反映出年龄较大的群体,这与AOM的真实流行病学情况不同。易患中耳炎的儿童、患有严重疾病的儿童、鼓膜膨出的儿童、发热的儿童、明确需要使用抗生素的儿童、近期接受过抗生素治疗的儿童、近期患过AOM的儿童或鼓膜穿孔的儿童常常被排除。

结论

指南和一些权威机构忽视或低估了AOM安慰剂/自然史试验中研究入组时诊断不准确、宽泛的纳入标准以及排除标准中产生偏倚等问题的重要性。在开展更好的研究之前,目前支持对AOM儿童进行观察的数据应重新审视。

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