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Effect of antimicrobial treatment of acute otitis media on the daily disappearance of middle ear effusion: A placebo-controlled trial

机译:抗生素治疗急性中耳炎对中耳积液每日消失的影响:一项安慰剂对照试验

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IMPORTANCE: Antimicrobial treatment reduces the symptoms of acute otitis media (AOM). The effect of antimicrobial treatment on the duration of middle ear effusion (MEE) and concomitant hearing impairment is not known. OBJECTIVE: To determine whether the antimicrobial treatment of AOMreduces the duration of MEE. DESIGN, SETTING, AND PARTICIPANTS: This randomized, double-blind, placebo-controlled trial involved a total of 84 children with AOMbetween 6 months and 15 years of age. Participants were recruited from September 14, 1999, to January 4, 2000; October 10, 2005, to December 16, 2005; and September 22, 2009, to June 4, 2012, from among children attending an AOM prevention trial and children visiting local outpatient clinics in Oulu, Finland. INTERVENTIONS: Children were randomly allocated to receive either 40mg/kg of amoxicillin-clavulanate or a placebo mixture per day for 7 days. MAIN OUTCOMES AND MEASURES: The primary outcome measurewas the time to the disappearance of MEE as defined by a normal tympanogram finding (A curve) from both ears on 2 consecutive measurement days. Parents performed daily tympanometry at home. The study physician performed tympanometry and otoscopy at study entry, after 3 and 7 days, and then weekly until both ears were healthy. The main secondary outcome measures were the time to normal otoscopy findings and the proportion of children without persistent MEE at 14 days and 2 months. RESULTS: Middle ear effusion disappeared 2.0 weeks (13.7 days) earlier (P = .02) in the antimicrobial group (mean time, 2.7 weeks; 95%CI, 1.7-3.7) than in the placebo group (4.7 weeks; 95%CI, 3.6-5.7). Normal otoscopy findings were observed 1.4 weeks sooner in the antimicrobial group than in the placebo group (P = .02). On day 14, 69%of children in the antimicrobial group and 38%in the placebo group had normal tympanometry findings (number needed to treat, 3.2; 95%CI, 2.0-10.5). On day 60, 2 children (5%) in the antimicrobial group and 10 children (24%) in the placebo group had persistent MEE (P = .01). CONCLUSIONS AND RELEVANCE: Antimicrobial treatment effectively reduced the duration of MEE and possible concomitant hearing impairment in children with AOM. Antimicrobial treatment also reduced the risk for persistent MEE. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01244581
机译:重要提示:抗菌治疗可减轻急性中耳炎(AOM)的症状。抗菌治疗对中耳积液(MEE)持续时间和伴随的听力障碍的影响尚不清楚。目的:确定抗菌药物对AOM的治疗是否缩短了MEE的持续时间。设计,地点和参加者:这项随机,双盲,安慰剂对照试验涉及84名6个月至15岁的AOM儿童。参与者是从1999年9月14日至2000年1月4日招募的; 2005年10月10日至2005年12月16日; 2009年9月22日至2012年6月4日,参加AOM预防试验的儿童和前往芬兰奥卢的当地门诊就诊的儿童。干预措施:将儿童随机分配为每天接受40mg / kg阿莫西林-克拉维酸盐或安慰剂混合物治疗7天。主要结果和指标:主要结果指标是指在连续2天的测量中,从两只耳朵的正常鼓室图发现(A曲线)所定义的MEE消失的时间。父母每天在家进行鼓室测压。研究医师在入院后的3天和7天,然后每周一次进行鼓室压和耳镜检查,直到两只耳朵都健康为止。主要的次要结局指标是耳镜检查结果恢复正常的时间以及在14天和2个月没有持续MEE的儿童的比例。结果:抗菌药物组(平均时间为2.7周; 95%CI为1.7-3.7)比安慰剂组(4.7周; 95%CI)提前了2.0周(13.7天)(P = .02)消失中耳(P = .02) ,3.6-5.7)。与安慰剂组相比,抗微生物组的耳镜检查结果要早1.4周才能观察到(P = .02)。在第14天,抗菌组的儿童中69%的儿童和安慰剂组的儿童中38%的鼓室检查结果正常(需要治疗的人数为3.2; 95%CI为2.0-10.5)。在第60天,抗菌药物组2名儿童(5%)和安慰剂组10名儿童(24%)持续存在MEE(P = .01)。结论和相关性:抗菌药物治疗有效减少了AOM儿童的MEE持续时间和可能伴随的听力障碍。抗菌治疗还降低了持续性MEE的风险。试验注册:clinicaltrials.gov标识符:NCT01244581

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