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Transforming Research and Clinical Knowledge in Traumatic Brain Injury Pilot: Multicenter Implementation of the Common Data Elements for Traumatic Brain Injury

创伤性脑损伤 神经影像学 医学 观察研究 康复 临床试验 毒物控制 磁共振成像 医学物理学 物理疗法 急诊医学 病理 精神科 放射科
作者
John K. Yue,Mary J. Vassar,Hester F. Lingsma,Shelly R. Cooper,David M. Schnyer,Alex B. Valadka,Wayne A. Gordon,Andrew I.R. Maas,Pratik Mukherjee,Esther L. Yuh,Ava M. Puccio,David M. Schnyer,Geoffrey T. Manley and TRACK-TBI Investigators,Scott S. Casey,Maxwell Cheong,Kristen Dams‐O'Connor,Allison J. Hricik,Emily E. Knight,Edwin Kulubya,David Menon,Diane Morabito,Jennifer Pacheco,Tuhin Sinha
出处
期刊:Journal of Neurotrauma [Mary Ann Liebert, Inc.]
卷期号:30 (22): 1831-1844 被引量:309
标识
DOI:10.1089/neu.2013.2970
摘要

Traumatic brain injury (TBI) is among the leading causes of death and disability worldwide, with enormous negative social and economic impacts. The heterogeneity of TBI combined with the lack of precise outcome measures have been central to the discouraging results from clinical trials. Current approaches to the characterization of disease severity and outcome have not changed in more than three decades. This prospective multicenter observational pilot study aimed to validate the feasibility of implementing the TBI Common Data Elements (TBI-CDEs). A total of 650 subjects who underwent computed tomography (CT) scans in the emergency department within 24 h of injury were enrolled at three level I trauma centers and one rehabilitation center. The TBI-CDE components collected included: 1) demographic, social and clinical data; 2) biospecimens from blood drawn for genetic and proteomic biomarker analyses; 3) neuroimaging studies at 2 weeks using 3T magnetic resonance imaging (MRI); and 4) outcome assessments at 3 and 6 months. We describe how the infrastructure was established for building data repositories for clinical data, plasma biomarkers, genetics, neuroimaging, and multidimensional outcome measures to create a high quality and accessible information commons for TBI research. Risk factors for poor follow-up, TBI-CDE limitations, and implementation strategies are described. Having demonstrated the feasibility of implementing the TBI-CDEs through successful recruitment and multidimensional data collection, we aim to expand to additional study sites. Furthermore, interested researchers will be provided early access to the Transforming Research and Clinical Knowledge in TBI (TRACK-TBI) data set for collaborative opportunities to more precisely characterize TBI and improve the design of future clinical treatment trials. (ClinicalTrials.gov Identifier NCT01565551.)
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