Department of Pediatrics, Oulu University Hospital, Oulu, Finland2Institute of Clinical Medicine, University of Oulu, Oulu, Finland.
Department of Otolaryngology, Oulu University Hospital and Institute of Clinical Medicine, University of Oulu, Oulu, Finland.
JAMA Pediatr. 2014 Jul;168(7):635-41. doi: 10.1001/jamapediatrics.2013.5311.
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.
To determine whether the antimicrobial treatment of AOM reduces the duration of MEE.
DESIGN, SETTING, AND PARTICIPANTS: This randomized, double-blind, placebo-controlled trial involved a total of 84 children with AOM between 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.
Children were randomly allocated to receive either 40 mg/kg of amoxicillin-clavulanate or a placebo mixture per day for 7 days.
The primary outcome measure was 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.
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).
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.
clinicaltrials.gov Identifier: NCT01244581.
抗生素治疗可减轻急性中耳炎 (AOM) 的症状。抗生素治疗对中耳积液 (MEE) 持续时间和并发听力障碍的影响尚不清楚。
确定抗生素治疗 AOM 是否会缩短 MEE 的持续时间。
设计、地点和参与者:这是一项随机、双盲、安慰剂对照试验,共纳入 84 名 6 个月至 15 岁患有 AOM 的儿童。参与者于 1999 年 9 月 14 日至 2000 年 1 月 4 日、2005 年 10 月 10 日至 2005 年 12 月 16 日以及 2009 年 9 月 22 日至 2012 年 6 月 4 日期间从参加 AOM 预防试验的儿童和芬兰奥卢当地门诊诊所就诊的儿童中招募。
儿童随机接受 40mg/kg 的阿莫西林-克拉维酸或安慰剂混合物,每天 1 次,持续 7 天。
主要结局指标为双侧连续 2 天测听时均出现正常鼓室图(A 曲线)时的时间。家长在家中每天进行鼓室压测量。研究医生在研究开始时、第 3 天和第 7 天、随后每周进行一次鼓室压和耳镜检查,直至双耳均恢复健康。主要次要结局指标为正常耳镜发现的时间和第 14 天和第 2 个月无持续 MEE 的儿童比例。
与安慰剂组(平均时间 4.7 周;95%CI,3.6-5.7)相比,抗菌组(2.7 周;95%CI,1.7-3.7)中耳积液消失时间提前 2.0 周(P = .02)。抗菌组的正常耳镜检查发现时间比安慰剂组早 1.4 周(P = .02)。第 14 天,抗菌组 69%的儿童和安慰剂组 38%的儿童出现正常鼓室压(治疗需要人数,3.2;95%CI,2.0-10.5)。第 60 天,抗菌组有 2 名(5%)儿童和安慰剂组有 10 名(24%)儿童持续存在 MEE(P = .01)。
抗生素治疗可有效缩短 AOM 儿童 MEE 持续时间和可能并发的听力障碍。抗生素治疗还降低了持续性 MEE 的风险。
clinicaltrials.gov 标识符:NCT01244581。