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Acute severe paediatric asthma: study protocol for the development of a core outcome set, a Pediatric Emergency Reserarch Networks (PERN) study

机译:急性严重儿科哮喘:研究核心成果套装的研究方案,一种儿科紧急重育阵列网络(Pern)研究

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BACKGROUND:Acute severe childhood asthma is an infrequent, but potentially life-threatening emergency condition. There is a wide range of different approaches to this condition, with very little supporting evidence, leading to significant variation in practice. To improve knowledge in this area, there must first be consensus on how to conduct clinical trials, so that valid comparisons can be made between future studies. We have formed an international working group comprising paediatricians and emergency physicians from North America, Europe, Asia, the Middle East, Africa, South America, Central America, Australasia and the United Kingdom.METHODS/DESIGN:A 5-stage approach will be used: (1) a comprehensive list of outcomes relevant to stakeholders will be compiled through systematic reviews and qualitative interviews with patients, families, and clinicians; (2) Delphi methodology will be applied to reduce the comprehensive list to a core outcome set; (3) we will review current clinical practice guidelines, existing clinical trials, and literature on bedside assessment of asthma severity. We will then identify practice differences in tne clinical assessment of asthma severity, and determine whether further prospective work is needed to achieve agreement on inclusion criteria for clinical trials in acute paediatric asthma in the emergency department (ED) setting; (4) a retrospective chart review in Australia and New Zealand will identify the incidence of serious clinical complications such as intubation, ICU admission, and death in children hospitalized with acute severe asthma. Understanding the incidence of such outcomes will allow us to understand how common (and therefore how feasible) particular outcomes are in asthma in the ED setting; and finally (5) a meeting of the Pediatric Emergency Research Networks (PERN) asthma working group will be held, with invitation of other clinicians interested in acute asthma research, and patients/families. The group will be asked to achieve consensus on a core set of outcomes and to make recommendations for the conduct of clinical trials in acute severe asthma. If this is not possible, the group will agree on a series of prioritized steps to achieve this aim.DISCUSSION:The development of an international consensus on core outcomes is an important first step towards the development of consensus guidelines and standardised protocols for randomized controlled trials (RCTs) in this population. This will enable us to better interpret and compare future studies, reduce risks of study heterogeneity and outcome reporting bias, and improve the evidence base for the management of this important condition.
机译:背景:急性严重的童年哮喘是一种不常见的,但潜在的危及生命的紧急情况。这种情况有很多不同的方法,具有很少的支持证据,导致实践中的显着变化。为了提高该领域的知识,必须首先有关于如何进行临床试验的共识,以便在未来的研究之间可以进行有效的比较。我们组建了一个包括北美,欧洲,亚洲,中东,非洲,南美,中美洲,澳大利亚和英国的儿科医生和急诊医生的国际工作组。方法/设计:将使用5阶段方法:(1)将通过系统评价和定性访谈,通过对患者,家庭和临床医生进行综合的与利益攸关方相关的综合成果清单; (2)Delphi方法将应用于将综合列表减少到核心结果集; (3)我们将审查现有的临床实践指南,现有的临床试验和文献对哮喘严重程度的床头算法。然后,我们将识别哮喘严重程度的TNE临床评估的实践差异,并确定需要进一步的预期工作来实现急性小儿哮喘临床试验中的纳入标准的协议(ED)环境; (4)澳大利亚和新西兰的回顾性图表审查将确定严重临床并发症的发病率,如急性严重哮喘住院儿童的插管,ICU入学和死亡。了解此类结果的发生率将使我们了解ED环境中哮喘在哮喘中的常见(以及因此如何可行);最后(5)将举行儿科紧急研究网络(Pern)哮喘工作组的会议,其邀请对急性哮喘研究感兴趣的其他临床医生以及患者/家庭感兴趣。本集团将被要求在核心成果集中达成共识,并为急性严重哮喘的临床试验提出建议。如果这是不可能的,本集团将就一系列优先步骤达成一致,以实现这一目标。关于核心结果的国际共识的制定是发展共识指导方针和随机对照试验标准化议定书的重要第一步(RCT)在这个人口中。这将使我们能够更好地解释和比较未来的研究,减少研究异质性和结果报告偏见的风险,并改善管理这一重要条件的证据基础。

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