...
首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Effectiveness of Trimethoprim/Sulfamethoxazole for Children With Chronic Active Otitis Media: A Randomized, Placebo-Controlled Trial
【24h】

Effectiveness of Trimethoprim/Sulfamethoxazole for Children With Chronic Active Otitis Media: A Randomized, Placebo-Controlled Trial

机译:甲氧苄啶/磺胺甲恶唑对儿童患有慢性活动性中耳炎的有效性:随机,安慰剂对照试验。

获取原文
           

摘要

OBJECTIVE. The goal was to determine the clinical effectiveness of prolonged outpatient treatment with trimethoprim/sulfamethoxazole for children with chronic active otitis media.METHODS. We performed a randomized, placebo-controlled trial with 101 children (1–12 years of age) with chronic active otitis media (defined as otorrhea for ≥12 weeks). In addition to a short course of steroid and antibiotic eardrops, children were assigned randomly to receive 6 to 12 weeks of orally administered trimethoprim/sulfamethoxazole (18 mg/kg, 2 times per day) or placebo and were monitored for 1 year.RESULTS. At 6 weeks, 28% of children in the trimethoprim/sulfamethoxazole group and 53% of children in the placebo group had otomicroscopic signs of otorrhea. At 12 weeks, these values were 32% and 47%, respectively. At 1 year, the numbers of children with otorrhea were similar in the 2 groups (25% and 20%, respectively). One child in the trimethoprim/sulfamethoxazole group developed a skin rash. Vomiting or diarrhea was reported for 9% of the trimethoprim/sulfamethoxazole group and 2% of the placebo group. Pure-tone hearing levels and health-related quality of life improved during the study but did not differ between the trimethoprim/sulfamethoxazole group and the placebo group. Pseudomonas aeruginosa was the most frequently isolated bacteria in the otorrhea samples from both groups.CONCLUSIONS. A 6- to 12-week course of high-dose, orally administered trimethoprim/sulfamethoxazole therapy is beneficial for children with chronic active otitis media. The treatment effect is most pronounced with the shorter course and disappears if administration of the medication is discontinued.
机译:目的。目的是确定甲氧苄啶/磺胺甲恶唑延长门诊治疗对慢性活动性中耳炎儿童的临床疗效。我们对101名患有慢性活动性中耳炎(定义为≥12周的耳漏)的儿童(1至12岁)进行了一项随机,安慰剂对照试验。除了短暂的类固醇和抗生素滴耳剂治疗外,还随机分配儿童接受6至12周的口服甲氧苄啶/磺胺甲恶唑(18 mg / kg,每天2次)或安慰剂,并进行1年的监测。在第6周,甲氧苄啶/磺胺甲恶唑组的28%的儿童和安慰剂组的53%的儿童有耳漏的耳镜症状。在第12周时,这些值分别为32%和47%。在1年时,两组的耳漏儿童数量相似(分别为25%和20%)。甲氧苄啶/磺胺甲基异恶唑组中的一名儿童出现皮疹。据报道,甲氧苄啶/磺胺甲基异恶唑组有9%的人呕吐或腹泻,而安慰剂组为2%。在研究期间,纯音听力水平和与健康相关的生活质量得到改善,但甲氧苄啶/磺胺甲恶唑组与安慰剂组之间无差异。铜绿假单胞菌是两组耳漏样本中分离最频繁的细菌。口服高剂量甲氧苄啶/磺胺甲基异恶唑治疗的6至12周疗程对患有慢性活动性中耳炎的儿童有益。疗程越短,治疗效果越明显,如果停止给药,治疗效果会消失。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号