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仅口服抗生素治疗儿童骨和关节感染的研究方案:一项全国范围内随机、开放标签、非劣效性试验。

Oral-only antibiotics for bone and joint infections in children: study protocol for a nationwide randomised open-label non-inferiority trial.

机构信息

Department of Paediatrics and Adolescent Medicine, Copenhagen University Hospital, Kobenhavn, Denmark

Department of Paediatrics and Adolescent Medicine, Gødstrup Hospital, Herning, Denmark.

出版信息

BMJ Open. 2023 Jun 1;13(6):e072622. doi: 10.1136/bmjopen-2023-072622.

Abstract

INTRODUCTION

Children with bone and joint infections are traditionally treated with intravenous antibiotics for 3-10 days, followed by oral antibiotics. Oral-only treatment has not been tested in randomised trials.

METHODS AND ANALYSIS

Children (3 months to 18 years) will be randomised 1:1 with the experimental group receiving high-dose oral antibiotics and the control group receiving intravenous antibiotics with a shift in both groups to standard oral antibiotics after clinical and paraclinical improvement. Children in need of acute surgery or systemic features requiring intravenous therapy, including septic shock, are excluded. The primary outcome is defined as a normal blinded standardised clinical assessment 6 months after end of treatment. Secondary outcomes are non-acute treatment failure and recurrent infection. Outcomes will be compared by a non-inferiority assumption with an inferiority margin of 5%.

ETHICS AND DISSEMINATION

The trial has the potential to reduce unnecessary hospitalisation and use of intravenous antibiotics in children with bone or joint infections. Due to the close follow-up, exclusion of severely ill children and predefined criteria for discontinuation of the allocated therapy, we expect the risk of treatment failure to be minimal.

TRIAL REGISTRATION NUMBER

NCT04563325.

摘要

简介

传统上,患有骨和关节感染的儿童需要接受 3-10 天的静脉内抗生素治疗,然后再接受口服抗生素治疗。口服抗生素治疗尚未在随机试验中进行过测试。

方法和分析

将儿童(3 个月至 18 岁)以 1:1 的比例随机分组,实验组接受高剂量口服抗生素治疗,对照组接受静脉内抗生素治疗,两组均在临床和实验室改善后转为标准口服抗生素治疗。需要急性手术或需要静脉内治疗的全身症状(包括感染性休克)的儿童将被排除在外。主要结局定义为治疗结束后 6 个月时正常的盲法标准临床评估。次要结局是非急性治疗失败和复发性感染。将通过非劣效性假设进行比较,劣势界限为 5%。

伦理和传播

该试验有可能减少患有骨或关节感染的儿童不必要的住院治疗和静脉内抗生素的使用。由于密切随访、排除严重患病的儿童以及预先设定的停止分配治疗的标准,我们预计治疗失败的风险极小。

试验注册号

NCT04563325。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bfe/10254855/d67bdbaba5a2/bmjopen-2023-072622f01.jpg

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