Bose Eliezer, Hravnak Marilyn, Sereika Susan M
Eliezer Bose, PhD, AGACNP-BC, CCRN, was Assistant Professor, School of Nursing, University of Pittsburgh, Pennsylvania, at the time this research was conducted. He is now Assistant Professor, School of Nursing, The University of Texas at Austin. Marilyn Hravnak, PhD, ACNP-BC, FAAN, is Professor; and Susan M. Sereika, PhD, is Professor, School of Nursing, University of Pittsburgh, Pennsylvania.
Nurs Res. 2017 Jan/Feb;66(1):12-19. doi: 10.1097/NNR.0000000000000193.
Patients undergoing continuous vital sign monitoring (heart rate [HR], respiratory rate [RR], pulse oximetry [SpO2]) in real time display interrelated vital sign changes during situations of physiological stress. Patterns in this physiological cross-talk could portend impending cardiorespiratory instability (CRI). Vector autoregressive (VAR) modeling with Granger causality tests is one of the most flexible ways to elucidate underlying causal mechanisms in time series data.
The purpose of this article is to illustrate the development of patient-specific VAR models using vital sign time series data in a sample of acutely ill, monitored, step-down unit patients and determine their Granger causal dynamics prior to onset of an incident CRI.
CRI was defined as vital signs beyond stipulated normality thresholds (HR = 40-140/minute, RR = 8-36/minute, SpO2 < 85%) and persisting for 3 minutes within a 5-minute moving window (60% of the duration of the window). A 6-hour time segment prior to onset of first CRI was chosen for time series modeling in 20 patients using a six-step procedure: (a) the uniform time series for each vital sign was assessed for stationarity, (b) appropriate lag was determined using a lag-length selection criteria, (c) the VAR model was constructed, (d) residual autocorrelation was assessed with the Lagrange Multiplier test, (e) stability of the VAR system was checked, and (f) Granger causality was evaluated in the final stable model.
The primary cause of incident CRI was low SpO2 (60% of cases), followed by out-of-range RR (30%) and HR (10%). Granger causality testing revealed that change in RR caused change in HR (21%; i.e., RR changed before HR changed) more often than change in HR causing change in RR (15%). Similarly, changes in RR caused changes in SpO2 (15%) more often than changes in SpO2 caused changes in RR (9%). For HR and SpO2, changes in HR causing changes in SpO2 and changes in SpO2 causing changes in HR occurred with equal frequency (18%).
Within this sample of acutely ill patients who experienced a CRI event, VAR modeling indicated that RR changes tend to occur before changes in HR and SpO2. These findings suggest that contextual assessment of RR changes as the earliest sign of CRI is warranted. Use of VAR modeling may be helpful in other nursing research applications based on time series data.
接受实时生命体征监测(心率[HR]、呼吸频率[RR]、脉搏血氧饱和度[SpO2])的患者在生理应激情况下会出现相互关联的生命体征变化。这种生理交互作用中的模式可能预示着即将发生的心肺不稳定(CRI)。向量自回归(VAR)建模及格兰杰因果检验是阐明时间序列数据潜在因果机制的最灵活方法之一。
本文旨在说明如何利用危重症监护病房病情较轻的监测患者样本中的生命体征时间序列数据,开发针对特定患者的VAR模型,并在CRI事件发生前确定其格兰杰因果动态关系。
CRI定义为生命体征超出规定的正常阈值(HR = 40 - 140次/分钟,RR = 8 - 36次/分钟,SpO2 < 85%),并在5分钟移动窗口内持续3分钟(占窗口持续时间的60%)。在20名患者中,选择首次CRI发作前6小时的时间段进行时间序列建模,采用六步程序:(a)评估每个生命体征的统一时间序列的平稳性,(b)使用滞后长度选择标准确定合适的滞后,(c)构建VAR模型,(d)用拉格朗日乘数检验评估残差自相关,(e)检查VAR系统的稳定性,(f)在最终稳定模型中评估格兰杰因果关系。
CRI事件的主要原因是SpO2降低(60%的病例),其次是RR超出范围(30%)和HR超出范围(10%)。格兰杰因果检验显示,RR变化导致HR变化(21%;即RR先于HR变化)的情况比HR变化导致RR变化(15%)更常见。同样,RR变化导致SpO2变化(15%)的情况比SpO2变化导致RR变化(9%)更常见。对于HR和SpO2,HR变化导致SpO2变化与SpO2变化导致HR变化的频率相同(18%)。
在这个经历CRI事件的危重症患者样本中,VAR建模表明RR变化往往先于HR和SpO2变化出现。这些发现表明,将RR变化作为CRI最早迹象进行情境评估是有必要的。VAR建模的应用可能有助于基于时间序列数据的其他护理研究。