Abstract

Objective: Motor vehicle crashes are a leading cause of injury and mortality for children. Mitigation of these injuries requires biofidelic anthropomorphic test devices (ATDs) to design and evaluate automotive safety systems. Effective countermeasures exist for frontal and near-side impacts but are limited for far-side impacts. Consequently, far-side impacts represent increased injury and mortality rates compared to frontal impacts. Thus, the objective of this study was to evaluate the biofidelity of the Hybrid III and Q-series pediatric ATDs in low-speed far-side impacts, with and without shoulder belt pretightening.Methods: Low-speed (2 g) far-side oblique (60°) and lateral (90°) sled tests were conducted using the Hybrid III and Q-series 6- and 10-year-old ATDs. ATDs were restrained by a lap and shoulder belt equipped with a precrash belt pretightener. Photoreflective targets were attached to the head, spine, shoulders, and sternum. ATDs were exposed to 8 low-speed sled tests: 2 oblique nontightened, 2 oblique pretightened, 2 lateral nontightened, 2 lateral pretightened. ATDs were compared with previously collected 9- to 11-year-old (n = 10) volunteer data and newly collected 6- to 8-year-old volunteer data (n = 7) tested with similar methods. Kinematic data were collected from a 3D target tracking system. Metrics of comparison included excursion, seat belt and seat pan reaction loads, belt-to-torso angle, and shoulder belt slip-out.Results: The ATDs exhibited increased lateral excursion of the head top, C4, and T1 as well as increased downward excursion of the head top compared to the volunteers. Volunteers exhibited greater forward excursion than the ATDs in oblique nontightened impacts. These kinematics correspond to increased shoulder belt slip-out for the ATDs in oblique tests (ATDs = 90%; volunteers = 36%). Contrarily, similar shoulder belt slip-out was observed between ATDs and volunteers in lateral impacts (ATDs = 80%; volunteers = 78%). In pretightened impacts, the ATDs exhibited reduced lateral excursion and torso roll-out angle compared to the volunteers.Conclusions: In general, the ATDs overestimated lateral excursion in both impact directions, while underestimating forward excursion of the head and neck in oblique impacts compared to the pediatric volunteers. This was primarily due to pendulum-like lateral bending of the entire ATD torso compared to translation of the thorax relative to the abdomen prior to the lateral bending of the upper torso in the volunteers, likely due to the multisegmented spinal column in the volunteers. Additionally, the effect of belt pretightening on occupant kinematics was greater for the ATDs than the volunteers.

Highlights

  • Traumatic brain injuries are the most common serious injury children sustained in motor vehicle crashes (MVC) [CDC 2011]

  • Due to the lack of specimen supply to be used for pediatric post-mortem human subjects (PMHS) testing, pediatric data has been scaled from the adult PMHS [Irwin and Mertz 1997]

  • The human subject response has been compared to Hybrid III and Q-Series 6 and 10 year-old anthropomorphic test device (ATD); significant differences have been noted in the head and spine kinematics. These results provide a good indication of the biofidelity of pediatric ATDs; frontal collisions are only a subset of MVCs

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Summary

Introduction

Traumatic brain injuries are the most common serious injury children sustained in motor vehicle crashes (MVC) [CDC 2011]. Due to the use of anthropomorphic test device (ATD) motion in developing preventative features in motor vehicles, it is vital that ATDs accurately mimic the kinematics of pediatric occupants in MVCs. 2014 Ohio State University Injury Biomechanics Symposium This paper has not been peer- reviewed. Due to the lack of specimen supply to be used for pediatric PMHS testing, pediatric data has been scaled from the adult PMHS [Irwin and Mertz 1997]. Because of the absence of pediatric PMHS testing, human volunteer testing in low-speed crashes as shown to be a promising route to better evaluate the biofidelity of pediatric ATDs [Begeman et al 1980; Beeman et al 2012]

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