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Does a pre-hospital emergency pathway improve early diagnosis and referral in suspected stroke patients? – Study protocol of a cluster randomised trial [ISRCTN41456865]

机译:疑似中风患者的院前急救途径是否可以改善早期诊断和转诊? –一项集群随机试验的研究方案[ISRCTN41456865]

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Background Early interventions proved to be able to improve prognosis in acute stroke patients. Prompt identification of symptoms, organised timely and efficient transportation towards appropriate facilities, become essential part of effective treatment. The implementation of an evidence based pre-hospital stroke care pathway may be a method for achieving the organizational standards required to grant appropriate care. We performed a systematic search for studies evaluating the effect of pre-hospital and emergency interventions for suspected stroke patients and we found that there seems to be only a few studies on the emergency field and none about implementation of clinical pathways. We will test the hypothesis that the adoption of emergency clinical pathway improves early diagnosis and referral in suspected stroke patients. We designed a cluster randomised controlled trial (C-RCT), the most powerful study design to assess the impact of complex interventions. The study was registered in the Current Controlled Trials Register: ISRCTN41456865 – Implementation of pre-hospital emergency pathway for stroke – a cluster randomised trial. Methods/design Two-arm cluster-randomised trial (C-RCT). 16 emergency services and 14 emergency rooms were randomised either to arm 1 (comprising a training module and administration of the guideline), or to arm 2 (no intervention, current practice). Arm 1 participants (152 physicians, 280 nurses, 50 drivers) attended an interactive two sessions course with continuous medical education CME credits on the contents of the clinical pathway. We estimated that around 750 patients will be met by the services in the 6 months of observation. This duration allows recruiting a sample of patients sufficient to observe a 30% improvement in the proportion of appropriate diagnoses. Data collection will be performed using current information systems. Process outcomes will be measured at the cluster level six months after the intervention. We will assess the guideline recommendations for emergency and pre-hospital stroke management relative to: 1) promptness of interventions for hyperacute ischaemic stroke; 2) promptness of interventions for hyperacute haemorrhagic stroke 3) appropriate diagnosis. Outcomes will be expressed as proportions of patients with a positive CT for ischaemic stroke and symptoms onset Discussion The fields in which this trial will play are usually neglected by Randomised Controlled Trial (RCT). We have chosen the Cluster-randomised Controlled Trial (C-RCT) to address the issues of contamination, adherence to real practice, and community dimension of the intervention, with a complex definition of clusters and an extensive use of routine data to collect the outcomes.
机译:背景技术早期干预措施被证明能够改善急性中风患者的预后。及时识别症状,有组织地及时有效地运输至适当的设施,已成为有效治疗的重要组成部分。实施基于证据的院前中风护理途径可能是达到授予适当护理所需组织标准的一种方法。我们进行了系统的搜索,以评估对可疑中风患者进行院前和紧急干预措施的效果,我们发现在紧急领域似乎只有很少的研究,而没有关于临床途径实施的研究。我们将检验以下假设:采用紧急临床途径可以改善可疑中风患者的早期诊断和转诊。我们设计了一项集群随机对照试验(C-RCT),这是评估复杂干预措施影响的最强大的研究设计。该研究已在当前对照试验注册簿中注册:ISRCTN41456865 –院前卒中急救途径的实施–一项整群随机试验。方法/设计两臂聚类随机试验(C-RCT)。将16个急诊室和14个急诊室随机分配给第1组(包括培训模块和指南的管理)或第2组(无干预,目前的做法)。第1臂参加者(152位医师,280位护士,50位驾驶员)参加了为期两节的互动课程,其中包括有关临床途径内容的持续医学教育CME学分。我们估计在6个月的观察期间,大约750名患者将接受该服务。这个持续时间可以招募足以观察到适当诊断比例提高30%的患者样本。数据收集将使用当前的信息系统进行。干预六个月后,将在集群级别上对过程结果进行衡量。我们将评估与以下方面有关的紧急和院前中风管理的指导性建议:1)急性缺血性中风的及时干预措施; 2)对急性出血性中风的干预及时3)适当的诊断。结果将以缺血性中风和症状发作的CT阳性患者的比例表示。讨论该试验的开展领域通常被随机对照试验(RCT)所忽略。我们选择了聚类随机对照试验(C-RCT),以解决污染,坚持实际操作以及干预措施的社区范围等问题,对聚类进行复杂定义,并广泛使用常规数据收集结果。

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