Clinical Trials Center, University of Washington, Building 29, Suite 250, 6200 NE 74th Street, Seattle, WA, 98115, USA.
Sci Rep. 2022 Mar 3;12(1):3538. doi: 10.1038/s41598-022-07582-w.
Amoxicillin is recommended as first-line antibiotic treatment for community-acquired pneumonia, the leading infectious cause of mortality in children aged less than 5 years. We conducted a double-blind, randomized controlled non-inferiority trial comparing 3- to 5-day amoxicillin treatment for non-severe chest-indrawing pneumonia in HIV-negative children aged 2 to 59 months in Malawi. In a secondary analysis, we assessed the frequency of serious adverse events (SAEs) during the trial to evaluate the safety of treatment with amoxicillin. Enrolled children with non-severe chest-indrawing pneumonia were randomized to either 3- or 5-day amoxicillin and followed for 14 days to track clinical outcomes. In addition to evaluation for treatment failure (primary endpoint, day 6), relapse, and study drug adherence, children were assessed for adverse events, including SAEs, which were managed per local standard clinical practice until resolution or stabilization. Between March 2016 and April 2019, 3000 children were enrolled, with male and younger children (aged less than 24 months) demonstrating more SAEs (10.3% for males vs 8.1% for females, p = 0.04; 10.0% for 2-6 months, 10.8% for 7-11 months, 9.7% for 12-23 months and 5.6% for 24-59 months, p = 0.01). The most common SAEs were progression of or recurrent pneumonia (220 SAEs in 217 children), acute gastroenteritis (14 SAEs in 14 children), and fever (8 SAEs in 8 children); however, there were no significant or substantive differences in the percentage of children with pneumonia-related, acute gastroenteritis, or fever SAEs noted between the 3- versus 5-day amoxicillin treatment groups. In our pediatric community-acquired pneumonia trial evaluating amoxicillin treatment, there were relatively few SAEs overall and very few attributed to amoxicillin. Duration of amoxicillin treatment did not impact the frequency of SAEs. We found male and younger children appear to be more vulnerable to SAEs in our trial; however, our data support previous data demonstrating the safety of amoxicillin use in children with pneumonia.Clinical trial registration: ClinicalTrials.gov (NCT02678195).
阿莫西林被推荐为社区获得性肺炎的一线抗生素治疗药物,这是 5 岁以下儿童死亡的主要感染原因。我们在马拉维开展了一项双盲、随机对照非劣效性试验,比较了 3-5 天阿莫西林治疗 2-59 个月无严重胸部凹陷性肺炎的 HIV 阴性儿童。在一项次要分析中,我们评估了试验期间严重不良事件(SAE)的发生频率,以评估阿莫西林治疗的安全性。患有非严重胸部凹陷性肺炎的入组儿童被随机分为 3 天或 5 天阿莫西林组,并随访 14 天以跟踪临床结局。除了评估治疗失败(主要终点,第 6 天)、复发和研究药物依从性外,还评估了儿童的不良事件,包括 SAE,根据当地标准临床实践进行管理,直至解决或稳定。2016 年 3 月至 2019 年 4 月,共有 3000 名儿童入组,男性和年龄较小的儿童(<24 个月)的 SAE 发生率更高(男性为 10.3%,女性为 8.1%,p=0.04;2-6 个月为 10.0%,7-11 个月为 10.8%,12-23 个月为 9.7%,24-59 个月为 5.6%,p=0.01)。最常见的 SAE 是肺炎进展或复发(217 名儿童中有 220 例 SAE)、急性胃肠炎(14 名儿童中有 14 例 SAE)和发热(8 名儿童中有 8 例 SAE);然而,3 天与 5 天阿莫西林治疗组之间肺炎相关、急性胃肠炎或发热 SAE 的儿童百分比没有显著或实质性差异。在我们评估阿莫西林治疗的儿科社区获得性肺炎试验中,总体而言,SAE 相对较少,很少归因于阿莫西林。阿莫西林治疗时间的长短并未影响 SAE 的发生频率。我们发现男性和年龄较小的儿童在我们的试验中似乎更容易发生 SAE;然而,我们的数据支持先前的数据,表明阿莫西林在肺炎儿童中的使用是安全的。临床试验注册:ClinicalTrials.gov(NCT02678195)。