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雾化吸入高渗盐水(3%)治疗轻度至中度重度细支气管炎患儿——一项双盲随机对照试验。

Nebulised hypertonic saline (3%) among children with mild to moderately severe bronchiolitis--a double blind randomized controlled trial.

作者信息

Khanal Aayush, Sharma Arun, Basnet Srijana, Sharma Pushpa Raj, Gami Fakir Chandra

机构信息

Department of Pediatrics, Tribhuvan University Teaching Hospital, Institute of Medicine, Maharajgunj-44600, P.O. Box 1524, Kathmandu, Nepal.

Kathmandu Medical College Teaching Hospital, Sinamangal, Kathmandu, Nepal.

出版信息

BMC Pediatr. 2015 Sep 10;15:115. doi: 10.1186/s12887-015-0434-4.

Abstract

BACKGROUND

To Assess the efficacy of nebulised hypertonic saline (HS) (3%) among children with mild to moderately severe bronchiolitis.

METHODS

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.

RESULTS

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 < 0.001; CI: 0.78-1.82]. More children in the HS group (n = 35/50; 70.0%) were eligible for ER/OPD discharge at the end of 2 h than those in the NS group (n = 15/50; 30%; p < 0.001), and less likely to need a hospital re-visit (n = 5/50; 10.0%) in the next 24 h as compared to the NS group (n = 15/50, 30.0%; p < 0.001). The treatment was well tolerated, with no adverse effects.

CONCLUSIONS

Nebulized 3% HS is effective, safe and superior to normal saline for outpatient management of infants with mild to moderately severe viral bronchiolitis in improving Clinical Severity Scores, facilitating early Out-Patient Department discharge and preventing hospital re-visits and admissions in the 24 h of presentation.

TRIAL REGISTRATION

Clinicaltrials.gov NCTID012766821. Registered on January 12, 2011.

摘要

背景

评估雾化吸入高渗盐水(HS)(3%)对轻度至中度重度毛细支气管炎患儿的疗效。

方法

年龄在6周至24个月之间、首次出现喘息且临床严重程度评分(《儿科学杂志》67:289 - 93, 1992)在1至8分之间的婴儿,在4个月的时间内入组。排除患有严重疾病、合并症、既往有喘息史、近期使用过支气管扩张剂和类固醇的患儿。患者以双盲方式随机分组,接受两剂雾化吸入的3% HS(第1组)或0.9%生理盐水(第2组)加1.5毫克L - 肾上腺素,间隔30分钟给药。在24小时和7天时与家长联系。主要观察指标是观察2小时结束时临床严重程度评分的平均变化。

结果

共纳入100名婴儿(平均年龄9.6个月,范围2 - 23个月;61%为男性)。两组患儿就诊时均为轻度至中度重度疾病。在意向性治疗分析中,HS组婴儿的平均临床严重程度评分显著降低(3.57 ± 1.41),而生理盐水组为(2.26 ± 1.15);[p < 0.001;置信区间:0.78 - 1.82]。与生理盐水组(n = 15/50;30%)相比,HS组在2小时结束时有更多患儿(n = 35/50;70.0%)符合急诊/门诊出院标准,且在接下来24小时内需要再次就诊的可能性更低(n = 5/50;10.0%),而生理盐水组为(n = 15/50,30.0%;p < 0.001)。该治疗耐受性良好,无不良反应。

结论

雾化吸入3% HS对轻度至中度重度病毒性毛细支气管炎婴儿的门诊治疗有效、安全,且优于生理盐水,可改善临床严重程度评分,促进早期门诊出院,并防止在就诊后24小时内再次就诊和住院。

试验注册

Clinicaltrials.gov NCTID012766821。于2011年1月12日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5d1/4644020/3ff08486e77f/12887_2015_434_Fig1_HTML.jpg

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