Hess Erik P, Wyatt Kirk D, Kharbanda Anupam B, Louie Jeffrey P, Dayan Peter S, Tzimenatos Leah, Wootton-Gorges Sandra L, Homme James L, Pencille R N Laurie, LeBlanc Annie, Westphal Jessica J, Shepel Kathy, Shah Nilay D, Branda Megan, Herrin Jeph, Montori Victor M, Kuppermann Nathan
Knowledge and Evaluation Research Unit, Mayo Clinic, 200 First Street SW, 55905 Rochester, MN, USA.
Trials. 2014 Jun 25;15:253. doi: 10.1186/1745-6215-15-253.
Blunt head trauma is a common cause of death and disability in children worldwide. Cranial computed tomography (CT), the reference standard for the diagnosis of traumatic brain injury (TBI), exposes children to ionizing radiation which has been linked to the development of brain tumors, leukemia, and other cancers. We describe the methods used to develop and test the effectiveness of a decision aid to facilitate shared decision-making with parents regarding whether to obtain a head CT scan or to further observe their child at home.
METHODS/DESIGN: This is a protocol for a multicenter clinician-level parallel randomized trial to compare an intervention group receiving a decision aid, 'Head CT Choice', to a control group receiving usual care. The trial will be conducted at five diverse emergency departments (EDs) in Minnesota and California. Clinicians will be randomized to decision aid or usual care. Parents visiting the ED with children who are less than 18-years-old, have experienced blunt head trauma within 24 hours, and have one or two risk factors for clinically-important TBI (ciTBI) from the Pediatric Emergency Care Applied Research Network head injury clinical prediction rules will be eligible for enrollment. We will measure the effect of Head CT Choice on: (1) parent knowledge regarding their child's risk of ciTBI, the available diagnostic options, and the risks of radiation exposure associated with a cranial CT scan (primary outcome); (2) parent engagement in the decision-making process; (3) the degree of conflict parents experience related to feeling uninformed; (4) patient and clinician satisfaction with the decision made; (5) the rate of ciTBI at seven days; (6) the proportion of patients in whom a cranial CT scan is obtained; and (7) seven-day healthcare utilization. To capture these outcomes, we will administer parent and clinician surveys immediately after each clinical encounter, obtain video recordings of parent-clinician discussions, administer parent healthcare utilization diaries, analyze hospital billing records, review the electronic medical record, and conduct telephone follow-up.
This multicenter trial will robustly assess the effectiveness of a decision aid on patient-centered outcomes, safety, and healthcare utilization in parents of children with minor head trauma in five diverse EDs.
ClinicalTrials.gov registration number: NCT02063087. Registration date February 13, 2014.
钝性头部外伤是全球儿童死亡和残疾的常见原因。颅脑计算机断层扫描(CT)是诊断创伤性脑损伤(TBI)的参考标准,但会使儿童暴露于电离辐射之下,而这种辐射与脑肿瘤、白血病及其他癌症的发生有关。我们描述了用于开发和测试一种决策辅助工具有效性的方法,该工具旨在促进与家长就是否进行头部CT扫描或在家中进一步观察孩子的情况进行共同决策。
方法/设计:这是一项多中心临床医生层面的平行随机试验方案,旨在比较接受决策辅助工具“头部CT选择”的干预组和接受常规护理的对照组。该试验将在明尼苏达州和加利福尼亚州的五个不同急诊科进行。临床医生将被随机分配接受决策辅助工具或常规护理。因钝性头部外伤在24小时内就诊于急诊科、年龄小于18岁且根据儿科急诊护理应用研究网络头部损伤临床预测规则具有一项或两项临床重要性TBI(ciTBI)风险因素的儿童家长将有资格入选。我们将衡量“头部CT选择”对以下方面的影响:(1)家长对其孩子发生ciTBI的风险、可用诊断选项以及与颅脑CT扫描相关的辐射暴露风险的了解(主要结局);(2)家长在决策过程中的参与度;(3)家长因感觉信息不足而经历的冲突程度;(4)患者和临床医生对所做决策的满意度;(5)七天时ciTBI的发生率;(6)进行颅脑CT扫描的患者比例;(7)七天的医疗保健利用率。为获取这些结局,我们将在每次临床会诊后立即进行家长和临床医生调查,获取家长 - 临床医生讨论的视频记录,发放家长医疗保健利用日记,分析医院账单记录,查阅电子病历,并进行电话随访。
这项多中心试验将有力地评估一种决策辅助工具对五个不同急诊科中轻度头部外伤儿童家长以患者为中心的结局、安全性和医疗保健利用率的有效性。
ClinicalTrials.gov注册号:NCT02063087。注册日期:2014年2月13日。