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首页> 外文期刊>BMC Pediatrics >Nebulised hypertonic saline (3?%) among children with mild to moderately severe bronchiolitis - a double blind randomized controlled trial
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Nebulised hypertonic saline (3?%) among children with mild to moderately severe bronchiolitis - a double blind randomized controlled trial

机译:轻度至中度重度细支气管炎患儿雾化高渗盐水(3%)-双盲随机对照试验

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To Assess the efficacy of nebulised hypertonic saline (HS) (3?%) among children with mild to moderately severe bronchiolitis. Infants aged 6?weeks to 24?months, with a first episode of wheezing and Clinical Severity scores (Arch Dis Child 67:289-93, 1992) between 1 and 8, were enrolled over 4?months duration. Those with severe disease, co-morbidities, prior wheezing, recent bronchodilator and steroid use were excluded. Patients were randomized in a double-blind fashion, to receive two doses of nebulized 3?% HS (Group 1) or 0.9?% normal saline (Group 2) with 1.5?mg of L-Epineprine, delivered 30?min apart. Parents were contacted at 24?h and 7?days. The principal outcome measure was the mean change in clinical severity score at the end of 2?h of observation. A total of 100 infants (mean age 9.6?months, range 2–23 months; 61?% males) were enrolled. Patients in both groups had mild to moderately severe disease at presentation. On an intention-to-treat basis, the infants in the HS group had a significant reduction (3.57?±?1.41) in the mean clinical severity score compared to those in the NS group (2.26?±?1.15); [p?
机译:评估轻度至中度严重细支气管炎患儿雾化高渗盐水(HS)(3%)的疗效。年龄在6周至24个月之间的婴儿,其喘息和临床严重程度得分的第一集(1-8岁,Arch Dis Child 67:289-93,1992年)在4个月的时间内入组。那些患有严重疾病,合并症,先前喘息,近期使用支气管扩张剂和类固醇的患者被排除在外。患者以双盲方式随机分组,接受两剂雾化的3%的HS(第1组)或0.9 %%的生理盐水(第2组)以及1.5mg的L-肾上腺素,间隔30分钟。在24小时和7天与父母取得联系。主要结局指标是观察2小时后临床严重程度评分的平均变化。总共入选了100名婴儿(平均年龄9.6?月,范围2-23个月;男性61%)。两组患者在就诊时均患有轻度至中度严重疾病。在意向性治疗的基础上,HS组的婴儿的平均临床严重性评分显着降低(3.57±±1.41),而NS组则为2.26±±1.15。 [p≤0.001; CI:0.78–1.82]。 HS组(n?=?35/50; 70.0%)的儿童在2小时结束时符合ER / OPD排出的条件比NS组(n?=?15/50; 30? %; p 0.001),与NS组相比,在接下来的24小时内需要再次就诊的可能性较小(n == 5/50; 10.0%)。 /50,30.0%;p<<0.001)。治疗耐受良好,无不良反应。雾化的3%HS对门诊轻,中度重度病毒性毛细支气管炎的患者的门诊治疗有效,安全且优于生理盐水,可改善临床严重度评分,促进门诊早期出院并防止住院和再次入院24 ?h的介绍。 Clinicaltrials.gov NCTID012766821。 2011年1月12日注册。

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