Krishnan Jerry A, Martin Molly A, Lohff Cortland, Mosnaim Giselle S, Margellos-Anast Helen, DeLisa Julie A, McMahon Kate, Erwin Kim, Zun Leslie S, Berbaum Michael L, McDermott Michael, Bracken Nina E, Kumar Rajesh, Margaret Paik S, Nyenhuis Sharmilee M, Ignoffo Stacy, Press Valerie G, Pittsenbarger Zachary E, Thompson Trevonne M
Population Health Sciences Program, Office of the Vice Chancellor for Health Affairs, University of Illinois at Chicago, United States; Department of Medicine, University of Illinois at Chicago, United States.
Department of Pediatrics, University of Illinois at Chicago, United States.
Contemp Clin Trials. 2017 Jun;57:10-22. doi: 10.1016/j.cct.2017.03.015. Epub 2017 Mar 31.
Among children with asthma, black children are two to four times as likely to have an emergency department (ED) visit and die from asthma, respectively, compared to white children in the United States. Despite the availability of evidence-based asthma management guidelines, minority children are less likely than white children to receive or use effective options for asthma care. The CHICAGO Plan is a three-arm multi-center randomized pragmatic trial of children 5 to 11years old presenting to the ED with uncontrolled asthma that compares: [1] an ED-focused intervention to improve the quality of care on discharge to home, [2] the same ED-focused intervention together with a home-based community health worker (CHW)-led intervention, and [3] enhanced usual care. All children receive spacers for the metered dose inhaler and teaching about its use. The Patient-Reported Outcomes Measurement Information System (PROMIS) Asthma Impact Scale and Satisfaction with Participation in Social Roles at 6months are the primary outcomes in children and in caregivers, respectively. Other patient-reported outcomes and indicators of healthcare utilization are assessed as secondary outcomes. Innovative features of the CHICAGO Plan include early and continuous engagement of children, caregivers, the Chicago Department of Public Health, and other stakeholders to inform the design and implementation of the study and a shared research infrastructure to coordinate study activities. The objective of this report is to describe the development of the CHICAGO Plan, including the methods and rationale for engaging stakeholders, the shared research infrastructure, and other features of the pragmatic clinical trial design.
在美国,患有哮喘的儿童中,黑人儿童前往急诊科就诊以及死于哮喘的可能性分别是白人儿童的两到四倍。尽管有循证哮喘管理指南,但少数族裔儿童比白人儿童更不可能接受或采用有效的哮喘护理方案。“芝加哥计划”是一项针对5至11岁因哮喘控制不佳而前往急诊科就诊的儿童进行的三臂多中心随机实用试验,该试验比较了:[1] 一项以急诊科为重点的干预措施,以提高出院回家时的护理质量;[2] 同样以急诊科为重点的干预措施加上一项由社区卫生工作者(CHW)主导的家庭干预措施;[3] 强化常规护理。所有儿童均会获得定量吸入器的储物罐并接受使用方法的教导。患者报告结局测量信息系统(PROMIS)哮喘影响量表以及6个月时对参与社会角色的满意度分别是儿童和照顾者的主要结局指标。其他患者报告的结局以及医疗保健利用指标作为次要结局指标进行评估。“芝加哥计划”的创新之处包括让儿童、照顾者、芝加哥公共卫生部及其他利益相关者尽早并持续参与,为研究的设计和实施提供信息,以及一个共享的研究基础设施来协调研究活动。本报告的目的是描述“芝加哥计划”的制定过程,包括让利益相关者参与的方法和基本原理、共享的研究基础设施以及实用临床试验设计的其他特点。