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门诊短疗程大剂量口服阿莫西林治疗儿童重症肺炎:一项随机等效性试验。

Ambulatory short-course high-dose oral amoxicillin for treatment of severe pneumonia in children: a randomised equivalency trial.

作者信息

Hazir Tabish, Fox LeAnne M, Nisar Yasir Bin, Fox Matthew P, Ashraf Yusra Pervaiz, MacLeod William B, Ramzan Afroze, Maqbool Sajid, Masood Tahir, Hussain Waqar, Murtaza Asifa, Khawar Nadeem, Tariq Parveen, Asghar Rai, Simon Jonathon L, Thea Donald M, Qazi Shamim A

机构信息

Children's Hospital, Pakistan Institute of Medical Sciences, Islamabad, Pakistan.

出版信息

Lancet. 2008 Jan 5;371(9606):49-56. doi: 10.1016/S0140-6736(08)60071-9.

Abstract

BACKGROUND

WHO case management guidelines for severe pneumonia involve referral to hospital for treatment with parenteral antibiotics. If equally as effective as parenteral treatment, home-based oral antibiotic treatment could reduce referral, admission, and treatment costs. Our aim was to determine whether home treatment with high-dose oral amoxicillin and inpatient treatment with parenteral ampicillin were equivalent for the treatment of severe pneumonia in children.

METHODS

This randomised, open-label equivalency trial was done at seven study sites in Pakistan. 2037 children aged 3-59 months with severe pneumonia were randomly allocated to either initial hospitalisation and parenteral ampicillin (100 mg/kg per day in four doses) for 48 h, followed by 3 days of oral amoxicillin (80-90 mg/kg per day; n=1012) or to home-based treatment for 5 days with oral amoxicillin (80-90 mg/kg per day in two doses; n=1025). Follow-up assessments were done at 1, 3, 6, and 14 days after enrollment. The primary outcome was treatment failure (clinical deterioration) by day 6. Analyses were done per protocol and by intention to treat. This trial is registered, ISRCTN95821329.

FINDINGS

In the per-protocol population, 36 individuals were excluded from the hospitalised group and 37 from the ambulatory group, mainly because of protocol violations or loss to follow-up. There were 87 (8.6%) treatment failures in the hospitalised group and 77 (7.5%) in the ambulatory group (risk difference 1.1%; 95% CI -1.3 to 3.5) by day 6. Five (0.2%) children died within 14 days of enrollment, one in the ambulatory group and four in the hospitalised group. In each case, treatment failure was declared before death and the antibiotic had been changed. None of the deaths were considered to be associated with treatment allocation; there were no serious adverse events reported in the trial.

INTERPRETATION

Home treatment with high-dose oral amoxicillin is equivalent to currently recommended hospitalisation and parenteral ampicillin for treatment of severe pneumonia without underlying complications, suggesting that WHO recommendations for treatment of severe pneumonia need to be revised.

摘要

背景

世界卫生组织(WHO)针对重症肺炎的病例管理指南涉及转诊至医院接受胃肠外抗生素治疗。如果家庭口服抗生素治疗与胃肠外治疗同样有效,那么可以减少转诊、住院及治疗费用。我们的目的是确定高剂量口服阿莫西林家庭治疗与胃肠外氨苄西林住院治疗对于儿童重症肺炎的治疗是否等效。

方法

这项随机、开放标签的等效性试验在巴基斯坦的7个研究地点开展。2037名3至59个月大的重症肺炎儿童被随机分配至以下两组之一:一是先住院并接受胃肠外氨苄西林治疗(每日100mg/kg,分4次给药)48小时,随后3天口服阿莫西林(每日80 - 90mg/kg;n = 1012);二是接受为期5天的家庭口服阿莫西林治疗(每日80 - 90mg/kg,分2次给药;n = 1025)。在入组后的第1、3、6和14天进行随访评估。主要结局是至第6天的治疗失败(临床病情恶化)。分析按照方案规定及意向性分析进行。本试验已注册,注册号为ISRCTN95821329。

结果

在符合方案人群中,住院组有36人、门诊组有37人被排除,主要原因是违反方案规定或失访。至第6天,住院组有87例(8.6%)治疗失败,门诊组有77例(7.5%)治疗失败(风险差异1.1%;95%置信区间 -1.3至3.5)。5名(0.2%)儿童在入组后14天内死亡,门诊组1名,住院组4名。在每种情况下,均在死亡前宣布治疗失败且已更换抗生素。没有死亡被认为与治疗分配相关;试验中未报告严重不良事件。

解读

对于无潜在并发症的重症肺炎,高剂量口服阿莫西林家庭治疗与目前推荐的住院胃肠外氨苄西林治疗等效,这表明WHO关于重症肺炎治疗的建议需要修订。

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