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复发性类固醇敏感性肾病综合征儿童上呼吸道感染期间短期每日泼尼松龙治疗(PREDNOS 2):一项随机对照试验方案

Short course daily prednisolone therapy during an upper respiratory tract infection in children with relapsing steroid-sensitive nephrotic syndrome (PREDNOS 2): protocol for a randomised controlled trial.

作者信息

Webb Nicholas J A, Frew Emma, Brettell Elizabeth A, Milford David V, Bockenhauer Detlef, Saleem Moin A, Christian Martin, Hall Angela S, Koziell Ania, Maxwell Heather, Hegde Shivram, Finlay Eric R, Gilbert Rodney D, Booth Jenny, Jones Caroline, McKeever Karl, Cook Wendy, Ives Natalie J

机构信息

Department of Paediatric Nephrology and NIHR/Wellcome Trust Children's Clinical Research Facility, University of Manchester, Manchester Academic Health Science Centre, Royal Manchester Children's Hospital, Manchester, UK.

出版信息

Trials. 2014 Apr 27;15:147. doi: 10.1186/1745-6215-15-147.

Abstract

BACKGROUND

Relapses of childhood steroid-sensitive nephrotic syndrome (SSNS) are treated with a 4- to 8-week course of high-dose oral prednisolone, which may be associated with significant adverse effects. There is a clear association between upper respiratory tract infection (URTI) and relapse development. Previous studies in developing nations have suggested that introducing a 5- to 7-day course of daily prednisolone during an URTI may prevent a relapse developing and the need for a treatment course of high-dose prednisolone. The aim of PREDNOS 2 is to evaluate the effectiveness of a 6-day course of daily prednisolone therapy during an URTI in reducing the development of a subsequent relapse in a developed nation.

METHODS/DESIGN: The subjects will be 300 children with relapsing SSNS (≥2 relapses in preceding year), who will be randomised to receive either a 6-day course of daily prednisolone or no change to their current therapy (with the use of placebo to double blind) each time they develop an URTI over 12 months. A strict definition for URTI will be used. Subjects will be reviewed at 3, 6, 9 and 12 months to capture data regarding relapse history, ongoing therapy and adverse effect profile, including behavioural problems and quality of life. A formal health economic analysis will also be performed. The primary end point of the study will be the incidence of URTI-related relapse (3 days of Albustix +++) following the first infection during the 12-month follow-up period. DNA and RNA samples will be collected to identify a potential genetic cause for the disease. Subjects will be recruited from over 100 UK centres with the assistance of the Medicines for Children Research Network.PREDNOS 2 is funded by the National Institute for Health Research Health Technology Assessment Programme (11/129/261).

DISCUSSION

We propose that PREDNOS 2 will be a pivotal study that will inform the future standard of care for children with SSNS. If it is possible to reduce the disease relapse rate effectively and safely, this will reduce the morbidity and cost associated with drug treatment, notwithstanding hospital admission and parental absence from employment.

TRIAL REGISTRATION

Current Controlled Trials (ISRCTN10900733).

摘要

背景

儿童激素敏感型肾病综合征(SSNS)复发时,需采用4至8周的大剂量口服泼尼松龙进行治疗,这可能会带来显著的不良反应。上呼吸道感染(URTI)与疾病复发之间存在明确关联。此前在发展中国家开展的研究表明,在发生URTI期间采用为期5至7天的每日泼尼松龙疗程,可能预防疾病复发,避免使用大剂量泼尼松龙进行治疗。PREDNOS 2研究的目的是评估在发达国家,于URTI期间采用为期6天的每日泼尼松龙疗法,在减少后续疾病复发方面的有效性。

方法/设计:研究对象为300名复发型SSNS儿童(前一年复发≥2次),每次发生URTI时,他们将被随机分配接受为期6天的每日泼尼松龙疗程,或维持当前治疗不变(使用安慰剂进行双盲),观察期为12个月。将采用严格的URTI定义。在3、6、9和12个月时对研究对象进行评估,以获取有关复发史、当前治疗和不良反应情况的数据,包括行为问题和生活质量。还将进行正式的卫生经济学分析。研究的主要终点是在12个月随访期内首次感染后发生的与URTI相关的复发(尿蛋白试纸检测+++持续3天)的发生率。将收集DNA和RNA样本,以确定该疾病潜在的遗传病因。研究对象将在儿童药物研究网络的协助下,从英国100多个中心招募。PREDNOS 2由英国国家卫生研究院卫生技术评估项目(11/129/261)资助。

讨论

我们认为PREDNOS 2将是一项关键研究,可为SSNS儿童未来的治疗标准提供依据。如果能够有效且安全地降低疾病复发率,这将降低与药物治疗相关的发病率和成本,包括住院治疗以及家长误工。

试验注册

当前受控试验(ISRCTN10900733)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f64c/4030532/ff1ed269fe0e/1745-6215-15-147-1.jpg

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