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首页> 外文期刊>The Lancet >Oral amoxicillin versus injectable penicillin for severe pneumonia in children aged 3 to 59 months: a randomised multicentre equivalency study.
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Oral amoxicillin versus injectable penicillin for severe pneumonia in children aged 3 to 59 months: a randomised multicentre equivalency study.

机译:口服阿莫西林与可注射青霉素治疗3到59个月大的儿童的严重肺炎:一项多中心等效性随机研究。

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BACKGROUND: Injectable penicillin is the recommended treatment for WHO-defined severe pneumonia (lower chest indrawing). If oral amoxicillin proves equally effective, it could reduce referral, admission, and treatment costs. We aimed to determine whether oral amoxicillin and parenteral penicillin were equivalent in the treatment of severe pneumonia in children aged 3-59 months. METHODS: This multicentre, randomised, open-label equivalency study was undertaken at tertiary-care centres in eight developing countries in Africa, Asia, and South America. Children aged 3-59 months with severe pneumonia were admitted for 48 h and, if symptoms improved, were discharged with a 5-day course of oral amoxicillin. 1702 children were randomly allocated to receive either oral amoxicillin (n=857) or parenteral penicillin (n=845) for 48 h. Follow-up assessments were done at 5 and 14 days after enrollment. Primary outcome was treatment failure (persistence of lower chest indrawing or new danger signs) at 48 h. Analyses were by intention-to-treat and per protocol. FINDINGS: Treatment failure was 19% in each group (161 patients, pencillin; 167 amoxillin; risk difference -0.4%; 95% CI -4.2 to 3.3) at 48 h. Infancy (age 3-11 months; odds ratio 2.72, 95% CI 1.95 to 3.79), very fast breathing (1.94, 1.42 to 2.65), and hypoxia (1.95, 1.34 to 2.82) at baseline predicted treatment failure by multivariate analysis. INTERPRETATION: Injectable penicillin and oral amoxicillin are equivalent for severe pneumonia treatment in controlled settings. Potential benefits of oral treatment include decreases in (1) risk of needle-borne infections; (2) need for referral or admission; (3) administration costs; and (4) costs to the family.
机译:背景:可注射的青霉素是推荐用于WHO定义的严重肺炎(下胸部抽搐)的治疗方法。如果口服阿莫西林被证明同样有效,则可以减少转诊,入院和治疗费用。我们旨在确定口服阿莫西林和胃肠外青霉素在治疗3至59个月大的儿童的严重肺炎方面是否等效。方法:这项多中心,随机,开放标签等效性研究是在非洲,亚洲和南美的八个发展中国家的三级医疗中心进行的。年龄在3到59个月之间的严重肺炎患儿入院48 h,如果症状改善,则口服阿莫西林5天疗程出院。 1702名儿童被随机分配接受口服阿莫西林(n = 857)或肠胃外青霉素(n = 845)48小时。入组后5天和14天进行随访评估。主要结局是在48小时治疗失败(下胸部持续抽烟或出现新的危险信号)。通过意向性治疗和每个方案进行分析。结果:在48小时时,每组的治疗失败率为19%(161名患者,pencillin; 167阿莫西林;风险差异为-0.4%; 95%CI为-4.2至3.3)。根据多变量分析,基线时的婴儿期(3-11个月;优势比为2.72,95%CI为1.95至3.79),超快呼吸(1.94、1.42至2.65)和低氧(1.95、1.34至2.82)可预测治疗失败。解释:可注射的青霉素和口服阿莫西林等同于在受控环境中进行的严重肺炎治疗。口服治疗的潜在好处包括:(1)减少针头感染的风险; (二)需要转诊或录取的; (三)管理费用; (4)家庭费用。

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