Autoregulation after traumatic brain injury can be monitored continuously using simple signal processing of intracranial pressure and arterial blood pressure. The pressure reactivity index (PRx) showed several benefits when it was applied to continuous brain monitoring. Among them, a positive and strong correlation with the outcome and possibility of calculation of 'optimal cerebral perfusion pressure' have been listed. For this methodology, prospective clinical trials are missing-few of them are planned in the near future.Keywords Traumatic brain injury . Intracranial pressure . Arterial blood pressure . Optimal cerebral perfusion pressureThe pressure-reactivity index was first described in 1995. Originally, we were inspired by the presentation of Erhard Lang and Randal Chestnut during the ICRAN conference at Gold Coast, Australia (1994). They reported that they could read a state of cerebral autoregulation from relative changes in mean arterial blood pressure (ABP) and intracranial pressure (ICP). They told us that it was enough to ask a research nurse to sit in front of a bedside monitor and instruct her to observe trends of ABP and ICP. The nurse needed to report when the values were changing in the same or opposite directions. When we arrived home, we programmed our computers, running ICM (intensive care monitor) software [7], to calculate a moving correlation coefficient from 30 consecutive 10-s averages of ICP and ABP waveforms. We called this the PRx index (pressure reactivity index) [6].The rationale for averaging ICP and ABP waveforms over 10 s was that only slow waves, of frequencies lower than 0.05 Hz, can carry information about autoregulation [11]. Simple averaging is a sufficient method of filtration of all faster components (mainly respiratory and pulsatile), which do not contain or contain only a little of any autoregulationrelated signatures.The rationale for calculating the correlation coefficient from 5-min-long buffers (30 samples of 10 s produce correlation window of 5 min) is that longer periods (e.g., 30 or 60 min) may include too many reactions to drugs, nursingrelated variations, metabolic reactions, etc. They are all not related to cerebral autoregulation and would produce distortion of the PRx.When a few years later a postgraduate student from S w i t ze r l an d , L uz i u s S t e i n er ( no w P r o f e s s o r o f Anaesthesiology at University of Basel), came to our Laboratory of Brain Physics in Cambridge, asking whether he could be given a PhD project on PRx, we first took it for a joke. However, over the next 3 years we were proven very wrong. Works of Luzius and other clinical neuroscientists who followed in his footsteps brought to light perhaps the most important advantage of PRx, its ability to guide the management of cerebral perfusion pressure. The concept was so simple to understand and so appealing in the clinical setting that many more people than we initially anticipated embraced it enthusiastically and developed it further.After 20 years, summarizing the mile...