We hypothesized that acute brain injury results in decreased heart rate (HR) variability and baroreflex sensitivity indicative of uncoupling of the autonomic and cardiovascular systems and that the degree of uncoupling should be proportional to the degree of neurological injury. We used HR and blood pressure (BP) power spectral analysis to measure neuroautonomic regulation of HR and BP and the transfer function magnitude (TF) between BP and HR as a measure of baroreflex modulation of HR. In 24 brain-injured patients [anoxic/ischemic injury ( n = 7), multiple trauma ( n = 6), head trauma ( n = 5), central nervous system infection ( n = 4), and intracranial hemorrhage ( n = 2)], neurological injury and survival was associated with low-frequency (0.01–0.15 Hz) HR and BP power and TF. Brain-dead patients showed decreased low-frequency HR power [0.51 ± 0.36 (SE) vs. 2.54 ± 0.14 beats/min2, P = 0.03] and TF [0.61 ± 0.16 (SE) vs. 1.29 ± 0.07 beats ⋅ min−1 ⋅ mmHg−1, P = 0.05] compared with non-brain-dead patients. We conclude that 1) severity of neurological injury and outcome are inversely associated with HR and BP variability and 2) there is direct evidence for cardiovascular and autonomic uncoupling in acute brain injury with complete uncoupling during brain death.

No abstract

We conclude that power spectral analysis of heart rate variability may be an accurate and clinically useful measure of depth of propofol anesthesia. We speculate that high-frequency heart rate power during propofol anesthesia correlates with depth of anesthesia, whereas low-frequency power allows for assessment of the patient's sympathetic response to pain.

We conclude that uncoupling of the autonomic and cardiovascular systems occurs over both short- and long-range time scales during sepsis, and the degree of uncoupling may help differentiate between sepsis, septic shock, and recovery states.