Department of Pediatrics, Division of Child Neurology, Doernbecher Children's Hospital, Oregon Health and Science University, Portland, OR.
Center for Policy and Research in Emergency Medicine, Department of Emergency Medicine, Oregon Health and Science University, Portland, OR.
Pediatr Crit Care Med. 2019 Jan;20(1):38-46. doi: 10.1097/PCC.0000000000001759.
Heart rate variability is controlled by the autonomic nervous system. After brain death, this autonomic control stops, and heart rate variability is significantly decreased. However, it is unknown if early changes in heart rate variability are predictive of progression to brain death. We hypothesized that in brain-injured children, lower heart rate variability is an early indicator of autonomic system failure, and it predicts progression to brain death. We additionally explored the association between heart rate variability and markers of brain dysfunction such as electroencephalogram and neurologic examination between brain-injured children who progressed to brain death and those who survived.
Retrospective case-control study.
PICU, single institution.
Children up to 18 years with a Glasgow Coma Scale score of less than 8 admitted between August of 2016 and December of 2017, who had electrocardiographic data available for heart rate variability analysis, were included.
patients who died of causes other than brain death. Twenty-three patients met inclusion criteria: six progressed to brain death (cases), and 17 survived (controls). Five-minute electrocardiogram segments were used to estimate heart rate variability in the time domain (SD of normal-normal intervals, root mean square successive differences), frequency domain (low frequency, high frequency, low frequency/high frequency ratio), Poincaré plots, and approximate entropy.
None.
Patients who progressed to brain death exhibited significantly lower heart rate variability in the time domain, frequency domain, and Poincaré plots (p < 0.01). The odds of death increased with decreasing low frequency (odds ratio, 4.0; 95% CI, 1.2-13.6) and high frequency (odds ratio, 2.5; 95% CI, 1.2-5.4) heart rate variability power (p < 0.03). Heart rate variability was significantly lower in those with discontinuous or attenuated/featureless electroencephalogram versus those with slow/disorganized background (p < 0.03).
These results support the concept of autonomic system failure as an early indicator of impending brain death in brain-injured children. Furthermore, decreased heart rate variability is associated with markers of CNS dysfunction such as electroencephalogram abnormalities.
心率变异性受自主神经系统控制。脑死亡后,这种自主控制停止,心率变异性显著降低。然而,目前尚不清楚心率变异性的早期变化是否可预测进展为脑死亡。我们假设,在脑损伤儿童中,较低的心率变异性是自主神经系统衰竭的早期指标,并可预测进展为脑死亡。我们还探讨了在进展为脑死亡和存活的脑损伤儿童之间,心率变异性与脑电图和神经检查等脑功能障碍标志物之间的相关性。
回顾性病例对照研究。
儿科重症监护病房(PICU),单机构。
纳入 2016 年 8 月至 2017 年 12 月期间格拉斯哥昏迷评分(Glasgow Coma Scale score)<8 岁并接受心电图(electrocardiogram,ECG)数据以进行心率变异性分析的患儿。
因脑死亡以外的原因死亡的患儿。符合纳入标准的患儿共 23 例:6 例进展为脑死亡(病例),17 例存活(对照)。使用 5 分钟 ECG 片段估计时域(正常-正常间期的标准差,均方根连续差异)、频域(低频、高频、低频/高频比)、庞加莱图和近似熵的心率变异性。
无。
进展为脑死亡的患儿在时域、频域和庞加莱图上的心率变异性明显降低(p<0.01)。低频(优势比,4.0;95%可信区间,1.2-13.6)和高频(优势比,2.5;95%可信区间,1.2-5.4)心率变异性功率降低的患儿死亡风险增加(p<0.03)。与慢/紊乱背景相比,脑电图不连续或衰减/无特征(attenuated/featureless)的患儿的心率变异性明显降低(p<0.03)。
这些结果支持自主神经系统衰竭作为脑损伤儿童即将发生脑死亡的早期指标的概念。此外,心率变异性降低与脑电图异常等中枢神经系统功能障碍标志物相关。