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脑震荡症状消退后,驾驶反应时间减缓。

Slowed driving-reaction time following concussion-symptom resolution.

机构信息

UGA Concussion Research Laboratory, Department of Kinesiology, University of Georgia, Athens, GA 30602, USA.

School of Kinesiology and Recreation, Illinois State University, Normal, IL 61790, USA.

出版信息

J Sport Health Sci. 2021 Mar;10(2):145-153. doi: 10.1016/j.jshs.2020.09.005. Epub 2020 Sep 19.

DOI:10.1016/j.jshs.2020.09.005
PMID:32961301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7987557/
Abstract

BACKGROUND

Concussed patients have impaired reaction time (RT) and cognition following injury that may linger and impair driving performance. Limited research has used direct methods to assess driving-RT post-concussion. Our study compared driving RT during simulated scenarios between concussed and control individuals and examined driving-RT's relationship with traditional computerized neurocognitive testing (CNT) domains.

METHODS

We employed a cross-sectional study among 14 concussed (15.9 ± 9.8 days post-concussion, mean ± SD) individuals and 14 healthy controls matched for age, sex, and driving experience. Participants completed a driving simulator and CNT (CNS Vital Signs) assessment within 48 h of symptom resolution. A driving-RT composite (ms) was derived from 3 simulated driving scenarios: stoplight (green to yellow), evasion (avoiding approaching vehicle), and pedestrian (person running in front of vehicle). The CNT domains included verbal and visual memory; CNT-RT (simple-, complex-, Stroop-RT individually); simple and complex attention; motor, psychomotor, and processing speed; executive function; and cognitive flexibility. Independent t tests and Hedge d effect sizes assessed driving-RT differences between groups, Pearson correlations (r) examined driving RT and CNT domain relationships among cohorts separately, and p values were controlled for false discovery rate via Benjamini-Hochberg procedures (α = 0.05).

RESULTS

Concussed participants demonstrated slower driving-RT composite scores than controls (mean difference = 292.86 ms; 95% confidence interval (95%CI): 70.18-515.54; p = 0.023; d = 0.992). Evasion-RT (p = 0.054; d = 0.806), pedestrian-RT (p = 0.258; d = 0.312), and stoplight-RT (p = 0.292; d = 0.585) outcomes were not statistically significant after false-discovery rate corrections but demonstrated medium to large effect sizes for concussed deficits. Among concussed individuals, driving-RT outcomes did not significantly correlate with CNT domains (r-range: -0.51 to 0.55; p > 0.05). No correlations existed between driving-RT outcomes and CNT domains among control participants either (r-range: -0.52 to 0.72; p > 0.05).

CONCLUSION

Slowed driving-RT composite scores and large effect sizes among concussed individuals when asymptomatic signify lingering impairment and raise driving-safety concerns. Driving-RT and CNT-RT measures correlated moderately but not statistically, which indicates that CNT-RT is not an optimal surrogate for driving RT.

摘要

背景

脑震荡患者在受伤后会出现反应时间(RT)和认知能力受损,这些问题可能会持续存在并影响驾驶表现。有限的研究使用直接方法评估脑震荡后的驾驶 RT。我们的研究比较了脑震荡患者和对照组个体在模拟场景中的驾驶 RT,并研究了驾驶 RT 与传统计算机神经认知测试(CNT)领域的关系。

方法

我们采用了一项横断面研究,共纳入 14 名脑震荡患者(脑震荡后 15.9±9.8 天,平均值±标准差)和 14 名年龄、性别和驾驶经验匹配的健康对照组。参与者在症状缓解后 48 小时内完成驾驶模拟器和 CNT(CNS 生命体征)评估。从 3 个模拟驾驶场景中得出驾驶 RT 综合得分:信号灯(从绿灯变为黄灯)、回避(避开接近的车辆)和行人(车辆前方奔跑的行人)。CNT 领域包括言语和视觉记忆;CNT-RT(简单、复杂、Stroop-RT 分别);简单和复杂注意力;运动、心理运动和处理速度;执行功能;和认知灵活性。独立 t 检验和 Hedge d 效应量评估了两组之间的驾驶 RT 差异,Pearson 相关系数(r)分别评估了队列中驾驶 RT 和 CNT 领域之间的关系,p 值通过 Benjamini-Hochberg 程序(α=0.05)进行了假发现率校正。

结果

与对照组相比,脑震荡组的驾驶 RT 综合得分较慢(平均差异=292.86 毫秒;95%置信区间(95%CI):70.18-515.54;p=0.023;d=0.992)。回避-RT(p=0.054;d=0.806)、行人-RT(p=0.258;d=0.312)和信号灯-RT(p=0.292;d=0.585)结果在进行假发现率校正后无统计学意义,但脑震荡组的缺陷仍具有中到大的效应量。在脑震荡患者中,驾驶 RT 结果与 CNT 领域无显著相关性(r 范围:-0.51 至 0.55;p>0.05)。对照组中也不存在驾驶 RT 结果与 CNT 领域之间的相关性(r 范围:-0.52 至 0.72;p>0.05)。

结论

无症状的脑震荡患者的驾驶 RT 综合得分较慢且具有较大的效应量,这表明存在持续的损伤并引起驾驶安全问题。驾驶 RT 和 CNT-RT 测量中度相关但无统计学意义,这表明 CNT-RT 不是驾驶 RT 的理想替代指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/b5a1d29401cb/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/d30327bbd06c/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/cf1b603128cc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/4e24d52ccd6a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/526b5aa7b209/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/96bc418d58fb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/b5a1d29401cb/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/d30327bbd06c/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/cf1b603128cc/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/4e24d52ccd6a/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/526b5aa7b209/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/96bc418d58fb/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ee/7987557/b5a1d29401cb/gr5.jpg

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