Primary Care Population Sciences and Medical Education Unit, University of Southampton, Southampton, UK.
Centre for Academic Primary Care, Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
Health Technol Assess. 2023 Jun;27(9):1-90. doi: 10.3310/DGBV3199.
Antimicrobial resistance is a global health threat. Antibiotics are commonly prescribed for children with uncomplicated lower respiratory tract infections, but there is little randomised evidence to support the effectiveness of antibiotics in treating these infections, either overall or relating to key clinical subgroups in which antibiotic prescribing is common (chest signs; fever; physician rating of unwell; sputum/rattly chest; shortness of breath).
To estimate the clinical effectiveness and cost-effectiveness of amoxicillin for uncomplicated lower respiratory tract infections in children both overall and in clinical subgroups.
Placebo-controlled trial with qualitative, observational and cost-effectiveness studies.
UK general practices.
Children aged 1-12 years with acute uncomplicated lower respiratory tract infections.
The primary outcome was the duration in days of symptoms rated moderately bad or worse (measured using a validated diary). Secondary outcomes were symptom severity on days 2-4 (0 = no problem to 6 = as bad as it could be); symptom duration until very little/no problem; reconsultations for new or worsening symptoms; complications; side effects; and resource use.
Children were randomised to receive 50 mg/kg/day of oral amoxicillin in divided doses for 7 days, or placebo using pre-prepared packs, using computer-generated random numbers by an independent statistician. Children who were not randomised could participate in a parallel observational study. Semistructured telephone interviews explored the views of 16 parents and 14 clinicians, and the data were analysed using thematic analysis. Throat swabs were analysed using multiplex polymerase chain reaction.
A total of 432 children were randomised (antibiotics, = 221; placebo, = 211). The primary analysis imputed missing data for 115 children. The duration of moderately bad symptoms was similar in the antibiotic and placebo groups overall (median of 5 and 6 days, respectively; hazard ratio 1.13, 95% confidence interval 0.90 to 1.42), with similar results for subgroups, and when including antibiotic prescription data from the 326 children in the observational study. Reconsultations for new or worsening symptoms (29.7% and 38.2%, respectively; risk ratio 0.80, 95% confidence interval 0.58 to 1.05), illness progression requiring hospital assessment or admission (2.4% vs. 2.0%) and side effects (38% vs. 34%) were similar in the two groups. Complete-case ( = 317) and per-protocol ( = 185) analyses were similar, and the presence of bacteria did not mediate antibiotic effectiveness. NHS costs per child were slightly higher (antibiotics, £29; placebo, £26), with no difference in non-NHS costs (antibiotics, £33; placebo, £33). A model predicting complications (with seven variables: baseline severity, difference in respiratory rate from normal for age, duration of prior illness, oxygen saturation, sputum/rattly chest, passing urine less often, and diarrhoea) had good discrimination (bootstrapped area under the receiver operator curve 0.83) and calibration. Parents found it difficult to interpret symptoms and signs, used the sounds of the child's cough to judge the severity of illness, and commonly consulted to receive a clinical examination and reassurance. Parents acknowledged that antibiotics should be used only when 'necessary', and clinicians noted a reduction in parents' expectations for antibiotics.
The study was underpowered to detect small benefits in key subgroups.
Amoxicillin for uncomplicated lower respiratory tract infections in children is unlikely to be clinically effective or to reduce health or societal costs. Parents need better access to information, as well as clear communication about the self-management of their child's illness and safety-netting.
The data can be incorporated in the Cochrane review and individual patient data meta-analysis.
This trial is registered as ISRCTN79914298.
This project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme and will be published in full in ; Vol. 27, No. 9. See the NIHR Journals Library website for further project information.
抗菌药物耐药性是一个全球性的健康威胁。对于患有单纯性下呼吸道感染的儿童,常开具抗生素进行治疗,但目前仅有少量随机证据支持抗生素在治疗这些感染方面的有效性,无论是总体疗效还是在抗生素应用常见的关键临床亚组(肺部体征;发热;医生判断患儿不适;有痰/喘鸣胸部;呼吸急促)中均无明显疗效。
评估阿莫西林治疗儿童单纯性下呼吸道感染的临床有效性和成本效益,分别从整体和临床亚组进行评估。
安慰剂对照试验,结合定性、观察性和成本效益研究。
英国普通实践。
年龄为 1-12 岁、急性单纯性下呼吸道感染的儿童。
主要结局为症状持续时间(使用经过验证的日记评估中度至重度不良症状)。次要结局为第 2-4 天的症状严重程度(0 = 无问题,6 = 非常严重);症状缓解至轻微/无问题的时间;因新症状或症状恶化而重新就诊;并发症;副作用;以及资源利用。
使用预先准备的包装,通过独立的统计学家使用计算机生成的随机数,将儿童随机分为每天口服 50mg/kg 阿莫西林,分剂量服用 7 天,或安慰剂治疗。未随机分组的儿童可以参加平行观察性研究。半结构化电话访谈对 16 名家长和 14 名临床医生的观点进行了探索,对数据进行了主题分析。对咽喉拭子进行了多重聚合酶链反应分析。
共有 432 名儿童被随机分组(抗生素组,n = 221;安慰剂组,n = 211)。主要分析对 115 名儿童的缺失数据进行了插补。抗生素组和安慰剂组的中度不良症状持续时间相似(中位数分别为 5 天和 6 天,危险比为 1.13,95%置信区间为 0.90 至 1.42),在亚组分析和包括来自 326 名观察性研究儿童的抗生素处方数据时,结果相似。因新症状或症状恶化而重新就诊的比例(分别为 29.7%和 38.2%,风险比为 0.80,95%置信区间为 0.58 至 1.05)、需要住院评估或入院的疾病进展(2.4%与 2.0%)以及副作用(38%与 34%)在两组中相似。完全病例(n = 317)和意向性治疗分析(n = 185)的结果相似,细菌的存在并未影响抗生素的疗效。每名儿童的 NHS 成本略高(抗生素组,£29;安慰剂组,£26),而非 NHS 成本无差异(抗生素组,£33;安慰剂组,£33)。一个预测并发症的模型(有七个变量:基线严重程度、与年龄相关的呼吸频率差异、疾病持续时间、氧饱和度、有痰/喘鸣胸部、排尿次数减少和腹泻)具有良好的区分度(bootstrapped 接收者操作特征曲线下面积 0.83)和校准度。家长发现很难解释症状和体征,使用孩子咳嗽的声音来判断疾病的严重程度,并且经常就诊以获得临床检查和保证。家长承认抗生素只有在“必要”时才应使用,临床医生注意到家长对抗生素的期望降低。
该研究的效力不足以检测关键亚组中的微小益处。
阿莫西林治疗儿童单纯性下呼吸道感染的疗效不太可能具有临床意义,也不太可能降低健康或社会成本。家长需要更好地获取信息,以及关于其孩子疾病管理和安全网的清晰沟通。
可以将这些数据纳入 Cochrane 综述和个体患者数据荟萃分析。
本试验在英国临床试验注册中心注册,注册号为 ISRCTN79914298。
本项目由英国国家卫生与保健优化研究所(NIHR)卫生技术评估计划资助,全文将在《卫生技术评估》杂志上发表;第 27 卷,第 9 期。有关该项目的更多信息,请访问 NIHR 期刊库网站。