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Perioperative anesthetic, surgical and critical careinterventions can affect brain physiology and overall brain health. The clinical utility of electroencephalogram (EEG) monitoring in anesthesia and intensive care settings is multifaceted, offering critical insights into the level of consciousness and depth of anesthesia, facilitating the titration of anesthetic doses, and enabling the detection of ischemic events and epileptic activity. Additionally, EEG monitoring can aid in predicting perioperative neurocognitive disorders, assessing the impact of systemic insults on cerebral function, and informing neuroprognostication. This review provides a comprehensive overview of the fundamental principles of electroencephalography, including the foundations of processed and quantitative electroencephalography. It further explores the characteristic EEG signatures associated wtih anesthetic drugs, the interpretation of the EEG data during anesthesia, and the broader clinical benefits and applications of EEG monitoring in both anesthetic practice and intensive care environments.

Background Spinal cord stimulation is a validated approach for managing chronic pain syndromes. The stimulator placement typically requires sedation, and an awake phase is needed to ensure optimal lead positioning. We describe a novel multimodal sedation approach using target-controlled infusions of propofol, remifentanil, and dexmedetomidine, combined with boluses of ketamine, guided by electroencephalography and nociception-antinociception balance monitoring. Methods This retrospective, single-center cohort study reviewed all spinal cord stimulator procedures, including both trials and permanent implants. A standardized anesthetic protocol, administered by a single anesthesiologist, included target controlled infusions of propofol, remifentanil, and dexmedetomidine, with additional boluses of ketamine. Processed electroencephalogram guided sedation depth, and antinociception was assessed using the Analgesia Nociception Index. Data collected included drug doses, time to intraoperative awakening, hemodynamic stability, and airway management. Results A total of 25 procedures (11 trials, 14 permanent implants) were analyzed in 21 patients, with 4 patients undergoing both procedures. All patients received the same four-drug regimen. The median (interquartile range) minimum and maximum effect-site concentrations of propofol required to achieve an adequate level sedation (level − 4 of the Richmond Agitation-Sedation Scale) were 1 (0.5) µg/mL and 1.5 (0.8) µg/mL, respectively. The median (interquartile range) minimum and maximum effect-site remifentanil concentrations needed to achieve sufficient antinociception (Analgesia Nociception Index between 50 and 70) were 0.5 (0.3) ng/mL and 1.2 (0.4) ng/mL, respectively. The median (interquartile range) minimum and maximum effect-site concentrations of dexmedetomidine required to achieve adequate antinociception were 0.3 (0.1) ng/mL and 0.5 (0.1) ng/mL, respectively. The median (interquartile range) dose of ketamine was 25 (20) mg. The ketamine dose used during the implant was significantly higher than during the trial procedure (30 (30) vs. 20 (10) mg), p  = 0.006. The average time to intraoperative awakening was 114 ± 56 s, and there was no significant difference between the trial and implant groups. Conclusions This study demonstrates the feasibility and safety of a multimodal sedation protocol for the placement of a spinal cord stimulator, combining propofol, remifentanil, dexmedetomidine, and ketamine, guided by electroencephalogram and nociception-antinociception monitoring.

The clinical approach to sedation in critically ill patients has changed dramatically over the last two decades, moving to a regimen of light or non-sedation associated with adequate analgesia to guarantee the patient’s comfort, active interaction with the environment and family, and early mobilization and assessment of delirium. Although deep sedation (DS) may still be necessary for certain clinical scenarios, it should be limited to strict indications, such as mechanically ventilated patients with Acute Respiratory Distress Syndrome (ARDS), status epilepticus, intracranial hypertension, or those requiring target temperature management. DS, if not indicated, is associated with prolonged duration of mechanical ventilation and ICU stay, and increased mortality. Therefore, continuous monitoring of the level of sedation, especially when associated with the raw EEG data, is important to avoid unnecessary oversedation and to convert a DS strategy to light sedation as soon as possible. The approach to the management of critically ill patients is multidimensional, so targeted sedation should be considered in the context of the ABCDEF bundle, a holistic patient approach. Sedation may interfere with early mobilization and family engagement and may have an impact on delirium assessment and risk. If adequately applied, the ABCDEF bundle allows for a patient-centered, multidimensional, and multi-professional ICU care model to be achieved, with a positive impact on appropriate sedation and patient comfort, along with other important determinants of long-term patient outcomes.

Background: Pain assessment is a challenge in critically ill patients, in particular those who are unable to express movements in reaction to noxious stimuli. The purpose of the study was to compare the pupillary response and skin conductance to pain stimulation in critically ill unconscious patients. Methods: This observational study included adult patients admitted to the intensive care unit (ICU) with acute brain injury (Glasgow Coma Scale < 9 with a motor response < 5) and/or requirements for deep level of sedation. Automated pupillometry (Algiscan, ID-MED, Marseille, France) was used to determine pupillary reflex dilation during tetanic stimulation. The maximum intensity of the stimulation value allowed the determination of a pupillary pain index score ranging from 1 (no nociception) to 9 (high nociception): a pupillary pain index (PPI) score of ≤4 was used to reflect adequate pain control. For skin conductance (SC), the number of SC peaks per second (NSCF) was collected concomitantly to tetanic stimulation. An NSCF of ≤0.07 peak/second was used to reflect adequate pain control. Results: Of the 51 included patients, there were 32 with brain injury and 19 receiving deep sedation. Mean PPI score was 5 (Interquartile Range= 2–7); a total of 28 (55%) patients showed inadequate control of the nociceptive stimulation according to the PPI assessment. Only 15 (29%) patients showed a detectable skin conductance, with NSCF values from 0.07 to 0.47/s. No correlation was found between skin conductance algesimeter (SCA)-derived variables and PPI score or pupillary dilation to pain. Conclusions: Detection of inadequate pain control might vary according to the method used to assess nociception in ICU patients. A poor agreement between quantitative pupillometry and skin conductance was observed.

The Brazilian savanna (Cerrado) has been heavily impacted by agricultural activities over the last four to five decades, and reliable estimates of reference evapotranspiration (ETo) are needed for water resource management and irrigation agriculture. The Penman–Monteith (PM) is one of the most accepted models for ETo estimation, but it requires many inputs that are not commonly available. Therefore, assessing the FAO guidelines to compute ETo when meteorological data are missing could lead to a better understanding of which variables are critically important for reliable estimates of ETo and how climatic variables are related to water requirements and atmospheric demands. In this study, ETo was computed for a grass-dominated part of the Cerrado from April 2010 to August 2019. We tested 12 different scenarios considering radiation, relative humidity, and/or wind speed as missing climatic data using guidelines given by the FAO. Our results presented that wind speed and actual vapor pressure do not affect ETo estimates as much as the other climatic variables; therefore, in the Cerrado’s conditions, wind speed and relative humidity measurements are less required than temperature and radiation data. When radiation data were missing, the computed ETo was overestimated compared to the benchmark. FAO procedures to estimate the net radiation presented good results during the wet season; however, during the dry season, their results were overestimated because the method could not estimate negative Rn. Our results indicate that radiation data have the highest impact on ETo for our study area and presumably for regions with similar climatic conditions. In addition, those FAO procedures for estimating radiation are not suitable when radiation data are missing.

Over the past few years, the use of non-invasive neuromonitoring in non-brain injured patients has increased, as a result of the recognition that many of these patients are at risk of brain injury in a wide number of clinical scenarios and therefore may benefit from its application which allows interventions to prevent injury and improve outcome. Among these, are post cardiac arrest syndrome, sepsis, liver failure, acute respiratory failure, and the perioperative settings where in the absence of a primary brain injury, certain groups of patients have high risk of neurological complications. While there are many neuromonitoring modalities utilized in brain injured patients, the majority of those are either invasive such as intracranial pressure monitoring, require special skill such as transcranial Doppler ultrasonography, or intermittent such as pupillometry and therefore unable to provide continuous monitoring. Cerebral oximetry using Near infrared Spectroscopy, is a simple non invasive continuous measure of cerebral oxygenation that has been shown to be useful in preventing cerebral hypoxemia both within the intensive care unit and the perioperative settings. At present, current recommendations for standard monitoring during anesthesia or in the general intensive care concentrate mainly on hemodynamic and respiratory monitoring without specific indications regarding the brain, and in particular, brain oximetry. The aim of this manuscript is to provide an up-to-date overview of the pathophysiology and applications of cerebral oxygenation in non brain injured patients as part of non-invasive multimodal neuromonitoring in the early identification and treatment of neurological complications in this population.

Technologies for monitoring organ function are rapidly advancing, aiding physicians in the care of patients in both operating rooms (ORs) and intensive care units (ICUs). Some of these emerging, minimally or non-invasive technologies focus on monitoring brain function and ensuring the integrity of its physiology. Generally, the central nervous system is the least monitored system compared to others, such as the respiratory, cardiovascular, and renal systems, even though it is a primary target in most therapeutic strategies. Frequently, the effects of sedatives, hypnotics, and analgesics are entirely unpredictable, especially in critically ill patients with multiple organ failure. This unpredictability exposes them to the risks of inadequate or excessive sedation/hypnosis, potentially leading to complications and long-term negative outcomes. The International PRactice On TEChnology neuro-moniToring group (I-PROTECT), comprised of experts from various fields of clinical neuromonitoring, presents this document with the aim of reviewing and standardizing the primary non-invasive tools for brain monitoring in anesthesia and intensive care practices. The focus is particularly on standardizing the nomenclature of different parameters generated by these tools. The document addresses processed electroencephalography, continuous/quantitative electroencephalography, brain oxygenation through near-infrared spectroscopy, transcranial Doppler, and automated pupillometry. The clinical utility of the key parameters available in each of these tools is summarized and explained. This comprehensive review was conducted by a panel of experts who deliberated on the included topics until a consensus was reached. Images and tables are utilized to clarify and enhance the understanding of the clinical significance of non-invasive neuromonitoring devices within these medical settings.