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旨在改善社区获得性肺炎循证管理的IMPROVE-GAP试验:一项阶梯式楔形随机对照试验的研究方案

The IMPROVE-GAP Trial aiming to improve evidence-based management of community-acquired pneumonia: study protocol for a stepped-wedge randomised controlled trial.

作者信息

Skinner Elizabeth H, Lloyd Melanie, Janus Edward, Ong May Lea, Karahalios Amalia, Haines Terry P, Kelly Anne-Maree, Shackell Melina, Karunajeewa Harin

机构信息

Department of Physiotherapy, Western Health, 160 Gordon St, Footscray, Victoria, 3011, Australia.

Department of Physiotherapy, Melbourne School of Health Sciences, University of Melbourne, Parkville, Victoria, 3010, Australia.

出版信息

Trials. 2018 Feb 5;19(1):88. doi: 10.1186/s13063-017-2407-4.

Abstract

BACKGROUND

Community-acquired pneumonia is a leading worldwide cause of hospital admissions and healthcare resource consumption. The largest proportion of hospitalisations now occurs in older patients, with high rates of multimorbidity and complex care needs. In Australia, this population is usually managed by hospital inpatient general internal medicine units. Adherence to consensus best-practice guidelines is poor. Ensuring evidence-based care and reducing length of stay may improve patient outcomes and reduce organisational costs. This study aims to evaluate an alternative model of care designed to improve adherence to four Level 1 or 2 evidence-supported interventions (routine corticosteroids, early switch to oral antibiotics, early mobilisation and routine malnutrition screening).

METHODS/DESIGN: The IMPROVing Evidence-based treatment Gaps and outcomes in community-Acquired Pneumonia (IMPROVE-GAP) trial is a pragmatic, investigator-initiated, stepped-wedge randomised trial. Patients hospitalised under a general internal medicine unit who meet a standard case definition for community-acquired pneumonia will be included. Eight general internal medicine units at two Australian hospitals in a single health service will be randomised using concealed allocation to: (i) usual medical, nursing and allied health care delivered according to existing organisational practice or (ii) care supported by a dedicated "community-acquired pneumonia service": a multidisciplinary team deploying algorithm-based implementation of a bundle of the four evidence-based interventions. The primary outcome measure will be length of hospital stay. Secondary outcome measures include inpatient mortality, 30 and 90 day readmission rates and mortality and health-service utilisation costs. Protocol adherence will be measured and reported, and serious adverse events (rates of hyperglycaemia requiring new insulin; falls during mobilisation) will be collected and reported.

DISCUSSION

IMPROVE-GAP represents an important and unique precedent for testing a new service-delivery model for improving compliance with a number of evidence-based interventions. Its stepped-wedge randomised controlled trial design provides a means to address some significant ethical, organisational and other methodological challenges to evaluating the effectiveness of health-service interventions in complex hospital populations. The new service-delivery model will effectively be fully implemented by trial completion, facilitating rapid, seamless translation into practice should care outcomes be superior. This trial is currently recruiting.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT02835040. Prospectively registered on 22 May 2016.

摘要

背景

社区获得性肺炎是全球范围内导致住院和医疗资源消耗的主要原因。目前,住院患者中比例最大的是老年患者,他们患有多种疾病,护理需求复杂。在澳大利亚,这类患者通常由医院内科住院部进行管理。对共识性最佳实践指南的遵循情况较差。确保循证护理并缩短住院时间可能会改善患者预后并降低机构成本。本研究旨在评估一种替代性护理模式,该模式旨在提高对四项1级或2级循证支持干预措施(常规使用皮质类固醇、早期改用口服抗生素、早期活动和常规营养不良筛查)的遵循率。

方法/设计:改善社区获得性肺炎循证治疗差距与结局(IMPROVE-GAP)试验是一项由研究者发起的实用型阶梯楔形随机试验。纳入在内科住院部住院且符合社区获得性肺炎标准病例定义的患者。一家卫生服务机构中两所澳大利亚医院的8个内科住院部将采用隐藏分配的方式随机分为:(i)按照现有机构实践提供的常规医疗、护理及相关医疗服务,或(ii)由专门的“社区获得性肺炎服务团队”提供的护理:一个多学科团队基于算法实施这四项循证干预措施的组合。主要结局指标为住院时间。次要结局指标包括住院死亡率、30天和90天再入院率以及死亡率和卫生服务利用成本。将对方案遵循情况进行测量和报告,并收集和报告严重不良事件(需要新胰岛素治疗的高血糖发生率;活动期间跌倒)。

讨论

IMPROVE-GAP为测试一种新的服务提供模式以提高对多项循证干预措施的依从性提供了一个重要且独特的范例。其阶梯楔形随机对照试验设计为解决在复杂医院人群中评估卫生服务干预效果时面临的一些重大伦理、机构和其他方法学挑战提供了一种手段。到试验结束时,新的服务提供模式将有效全面实施,如果护理结局更佳,将有助于迅速、无缝地转化为实际应用。本试验目前正在招募患者。

试验注册

ClinicalTrials.gov,NCT02835040。于2016年5月22日前瞻性注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d30/5800278/b6095944d262/13063_2017_2407_Fig1_HTML.jpg

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