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Biomedical subjects

Markus Weiss

Publications and source records attributed to Markus Weiss.

At least 19 recordsLinked to original sources

Reproducibility of cerebral oxygenation measurement in neonates and infants in the clinical setting using the NIRO 300 oximeter.

OBJECTIVE: To study reproducibility of cerebral tissue oxygenation index (cTOI) values in neonates and infants in a clinical setting using the NIRO 300 oximeter (Hamamatsu Photonics, Hamamatsu City, Japan). DESIGN: Clinical, observational study. SETTING: University hospital, pediatric intensive care unit. PATIENTS: Twenty neonatal and pediatric intensive care patients (age 0-190 days; median 4.5 days). INTERVENTIONS: Reproducibility of cTOI was measured at the lateral forehead of the patients. MEASUREMENTS AND MAIN RESULTS: Sensor exchange experiments were performed by removing the sensor and reapplying another sensor (sensor 1 vs. sensor 2) at the same position. Simultaneous measurements, comparing cTOI values from the right and left forehead, were performed using both sensors. Corresponding sensor exchange experiments were performed within 10 mins. All tests were done under stable, steady-state cardiorespiratory conditions. Data were compared using Bland-Altman bias analysis and paired, two-sided Student's t-test (p < .05). Sensor exchange experiments and simultaneous left-to-right forehead measurements revealed only small mean differences (<5%) and no significant differences between corresponding values (p = .953/.164). However, Bland-Altman bias analysis revealed poor agreement with large 95% limits of agreement in particular for sensor exchange experiments (-17.8% to 17.6%) and less for simultaneous left and right measurements (-14.4% to 10.4%). CONCLUSIONS: The present study shows that cTOI measurements using the NIRO 300 oximeter at the lateral forehead of neonates and infants are not well reproducible under clinical conditions. This raises the question whether generally valid normal values can be defined with the used approach and makes it difficult to determine a normal range of cerebral oxygenation.

Brain↗

Near-infrared spectroscopic cerebral oxygenation reading in neonates and infants is associated with central venous oxygen saturation.

BACKGROUND: The aim of the study was to elucidate easily determinable laboratory and vital parameters in clinical practice to explain variability of near-infrared spectroscopic cerebral oxygenation readings in critically ill newborns and infants using the NIRO 300 spectrometer. METHODS: Near-infrared spectroscopy (NIRS) cerebral tissue oxygenation index (cTOI) was measured on the forehead of critically ill neonates and infants with existing arterial and/or central venous access. We recorded patient characteristics and simultaneously determined sedation state, hemodynamic, respiratory and laboratory data, such as arterial blood gas analysis, electrolytes, hemoglobin and arterial lactate concentration, blood glucose and central venous oxygen saturation. Data were compared using linear, multiple and forward stepwise regression analysis (P < 0.05). RESULTS: A total of 155 neonates and infants aged from 0 to 365 days (median 12 days) were studied. cerebral tissue oxygenation index (cTOI) values ranged from 32.1 to 91.0% (60.5 +/- 11.5%). Simple linear regression analysis revealed significant associations between cTOI and arterial oxygen saturation (r = 0.254, P = 0.001), transcutaneously measured arterial oxygen saturation (r = 0.320, P < or = 0.0001), central venous oxygen saturation (r = 0.489, P < 0.0001), arteriovenous oxygen extraction (r = 0.445, P < 0.0001) and presence of a cardiac shunt (r = 0.250, P = 0.024). Multiple regression analysis and forward stepwise regression revealed two independent, significant predictors for cTOI, namely SvO2 (P < 0.0001) and presence or absence of a cardiac shunt (P = 0.003). SvO2 alone explained 23.9% of the variability of cTOI. The addition of the variable 'cardiac shunt' improved the model to 33%. CONCLUSIONS: Based on our study results cerebral tissue oxygenation readings by the NIRO 300 near-infrared spectrometer is influenced by central venous oxygen saturation, which partially explains intersubject variability of NIRS cerebral oxygenation readings.

Blood Gas Analysis↗

Evaluation of a new combined transcutaneous measurement of PCO2/pulse oximetry oxygen saturation ear sensor in newborn patients.

OBJECTIVE: Arterial oxygen saturation (Sao(2)) and arterial carbon dioxide partial pressure (Paco(2)) are 2 of the most important respiratory parameters in the treatment of critically ill neonates. Noninvasive monitoring of these parameters is desirable for continuous estimating of the respiratory status and reducing blood loss because of repeated blood gas analyses. Transcutaneous measurement of Pco(2) (Ptcco(2)) represents a simple and noninvasive technique for continuous monitoring of ventilation. However, sensor preparation, positioning, taping, and repeated changes of the sensor location make the handling difficult and complicate its use in the neonatal care unit. Recently, a new sensor for combined assessment of pulse oximetry oxygen saturation (Spo(2)) and Ptcco(2) has been introduced (TOSCA Monitor; Linde Medical Sensors, Basel, Switzerland). The monitor combines pulse oximetry and Ptcco(2) measurement in a single ear sensor, which works at 42 degrees C to enhance blood flow in capillaries below the sensor. METHODS: In a prospective, open, nonrandomized study of 60 ill neonates, the new ear sensor for combined assessment of Spo(2) and Ptcco(2) at 42 degrees C was tested. The sensor was adapted to the ear of a neonate with a Varihesive layer (Conva Tec; Princeton, NJ). Data obtained from the ear sensor were compared with Spo(2 Finger/Heel), Sao(2), and Paco(2) obtained from arterial blood gas in 30 patients and with a capillary blood gas in an additional 30 patients using Bland Altman bias analysis. Data are presented as median (range). RESULTS: The postconceptional age of the patients was 38.3 weeks (range: 28 5/7-40 5/7) in the arterial group and 37.9 weeks (range: 29 6/7-41 0/7) in the capillary group. Age of the newborns studied was 3.5 days (range: 1-28) in the arterial blood sample group (n = 30) and 6 days (range: 2-28) in the capillary blood sample group (n = 30). Patient weight was 3.02 kg (range: 1.5-4.5) in the arterial group and 2.76 kg (range: 1.0-3.71) in the other group. Three patients had weights of <1500 g. Twenty-one of 60 patients were conventionally ventilated, 4 patients received high-frequency oscillation, and 35 were not ventilated. Mean difference (bias) and precision (2 SD of the mean difference) between Ptcco(2 TOSCA) and Paco(2) were -0.44 kPa (-3.21 mm Hg) and 0.82 kPa (6.02 mm Hg) and between Ptcco(2 TOSCA) and Pcapco(2) were -0.09 kPa (-0.67 mm Hg) and 1.11 kPa (8.07 mm Hg), respectively. Spo(2) assessment by the TOSCA revealed slightly higher values compared with Sao(2) (bias: -0.48%), whereas Spo(2) (Finger/Heel) values were slightly lower than Sao(2) (bias: 0.52%). CONCLUSION: The TOSCA monitor with the ear sensor adapted to ears of neonates allows reliable estimation of Sao(2) and Paco(2). A potential benefit is the reduction in motion artifacts because of less head movement in newborns and that only a single cable leads form the patient to the monitor. In addition, the sensor is not removed for chest radiograph or for nursing the infant on his or her parent's lap. Long-term studies in a large population with continuous measurements are required to confirm these preliminary findings and to elucidate the benefits in detection of respiratory deterioration and the potential side effects of this sensor.

Blood Gas Monitoring, Transcutaneous↗

The Microcuff tube allows a longer time interval until unsafe cuff pressures are reached in children.

PURPOSE: To compare cuff pressures during nitrous oxide exposure in the new Microcuff pediatric tracheal tube (MPT) with ultrathin high volume - low pressure polyurethane cuff to a tube with a standard polyvinyl chloride (PVC) cuff. METHODS: With approval of the local Ethics Committee, 30 pediatric patients requiring tracheal intubation [tube size internal diameter (ID) 4.0 mm, or ID 7.0 mm) were included. Patients were randomly divided in three groups: A) MPT, baseline cuff pressure 20 cm H(2)O; B) PVC, baseline cuff pressure 20 cm H(2)O; and C) MPT, baseline cuff pressure set to sealing pressure. Anesthesia technique and ventilator settings were standardized. The time required for cuff pressure to increase to 25 cm H(2)O was recorded and pressure reduced to baseline. The number of gas removals required during the first hour was noted. Data are median (range). Groups were compared by the Kruskal-Wallis test (P < 0.05). RESULTS: There were no differences between groups in patient characteristics. PVC and MPT cuffs inflated to a baseline pressure of 20 cm H(2)O were similar regarding the time to first removal of gas [A: nine minutes (4-24), B: eight minutes (4-46)], and number of removals required [A: four (2-6), B: three (1-5)]. In MPT with baseline pressure set to sealing pressure [10 cm H(2)O (8-14)] time to first gas removal and number of removals were significantly less (P < 0.05). CONCLUSION: When baseline inflation pressure was set at 20 cm H(2)O, cuff pressure increased similarly in MPT and PVC tubes. When inflated just to sealing pressure, the MPT allowed a longer time interval until the upper limit of 25 cm H(2)O was reached.

Adolescent↗

Laryngeal damage due to an unexpectedly large and inappropriately designed cuffed pediatric tracheal tube in a 13-month-old child.

PURPOSE: To present a case of laryngeal damage in an infant caused by a too large and inappropriately designed cuffed tracheal tube. CLINICAL FEATURES: A 13-month-old child undergoing cardiac surgery was intubated with an uncuffed endotracheal tube with an internal diameter (ID) of 4.0 mm. Because of an important air leak around the tracheal tube during mechanical ventilation, a cuffed endotracheal tube ID 4.0 mm was inserted. The air leak with the tube cuff not inflated was acceptable at 25 cm H2O airway pressure. After extubation on the third postoperative day, the patient showed increasing stridor and respiratory deterioration. Fibreoptic laryngoscopy of the spontaneously breathing patient showed a large intra-laryngeal web. After surgical removal of the web, the child rapidly recovered and was discharged from the hospital on the 12th postoperative day. Inspection of the 4.0 mm (ID) cuffed tracheal tube revealed a cuff positioned inappropriately high and an increase of 0.7 mm in outer tube diameter compared to the 4.0 mm (ID) uncuffed tracheal tube from the same manufacturer. The tube cuff is likely to be situated within the larynx when placed in accordance to insertion depth formulas or radiological criteria, as used for uncuffed tracheal tubes in children. CONCLUSION: The larger than expected tracheal tube with its intra-laryngeal cuff position in a 13-month-old child likely caused mucosal damage and an inflammatory reaction within the larynx resulting in granulation tissue formation and fibrous healing around the tracheal tube.

Anesthesia, General↗

Evaluation of an improved blood-conserving POCT sampling system.

OBJECTIVE: To evaluate a modified point-of-care (POCT) testing i-STAT analyzing cartridge that connects directly to the sampling port of a blood-conserving sampling line. DESIGN AND METHODS: In an in vitro setup, blood samples were drawn from a blood-conserving sampling line connected to a miniature cardiopulmonary bypass (CPB) system. Blood collection from the sampling port was either performed with a syringe necessitating subsequent sample loading on a standard i-STAT cartridge (conventional procedure) or with a modified i-STAT sampling cartridge allowing blood flow from the sampling port directly into the cartridge (modified procedure). The loaded cartridges were subsequently inserted into the i-STAT Portable Clinical Analyzer for sample analysis. Multiple parameters such as blood gases, electrolytes, hematocrit, and glucose were measured. A series of 30 paired measurements was performed. Corresponding series of values were compared using linear regression analysis and Bland-Altman bias analysis (P < 0.05). RESULTS: Twenty-five complete measurement series consisting of 12 parameters (pH, pCO(2), pO(2), SO(2), base excess, bicarbonate concentration, sodium, potassium, ionized calcium, hemoglobin concentration, hematocrit, glucose) were evaluated. Linear regression analysis between the two sampling methods tested demonstrated an excellent correlation for all parameters (Pearson correlation coefficients: 0.859-0.999). Bias and precision between corresponding series showed clinically acceptable performance levels for all parameters. CONCLUSIONS: The modified i-STAT sampling cartridge allows reliable diagnostic blood sampling directly from a blood-conserving sampling line. The technique presented is also applicable to other POCT systems, thus reducing diagnostic blood loss because of the minimal amount of blood required for analysis.

Blood Chemical Analysis↗

Tracheal sealing characteristics of pediatric cuffed tracheal tubes.

BACKGROUND: The aim of the study was to compare sealing characteristics of the new Microcuff pediatric tracheal tube featuring a high volume-low pressure (HVLP) cuff with ultrathin membrane with three conventional pediatric cuffed tracheal tubes. METHODS: After obtaining approval of the local ethical committee, 80 children aged 2-4 years were tracheally intubated with the following tubes (i.d. 4.0 mm) in random order: Microcuff P-HVLP, Mallinckrodt Hi-Contour P, Rüschelit Super Safety Clear, and Sheridan CF. Cuff pressure to prevent air leakage at standardized ventilator setting (PIP 20 cm H2O/PEEP 5 cm H2O/RR 20 min(-1)) was assessed within 5 min after intubation by auscultation of audible sounds at the mouth. Cuff pressures required with each group were compared with Kruskall-Wallis test (P < 0.05). Values are median and range. RESULTS: No significant differences in patient characteristics were found between the four groups. The Microcuff tube required significantly lower sealing pressures [11 cm H2O (6-26)] compared with the other tracheal tube brands [Mallinckrodt: 36 cm H2O (18-48); Rüschelit: 21 cm H2O (8-46); Sheridan: 26 cm H2O (18-60), (P < 0.0001)]. CONCLUSION: This preliminary investigation suggests that the new Microcuff pediatric tracheal tube with ultrathin high volume-low pressure cuff membrane allows effective tracheal sealing at very low cuff pressures. This represents a benefit for children with regard to their lower mucosal perfusion pressures compared with adult patients.

Auscultation↗

Continuous ventilation technique for laryngeal mask airway (LMA) removal after fiberoptic intubation in children.

BACKGROUND: Fiberoptic tracheal intubation through the laryngeal mask airway (LMA) is a simple technique to establish a safe airway in neonates and infants with a difficult airway. The technique, however, is complicated by the removal of the laryngeal mask from the patient's mouth because of the similarity in length of the LMA and the tracheal tube. METHODS: Several solutions have been presented to stabilize the tracheal tube within the trachea during withdrawal of the LMA. With all these techniques ventilation of the patient is interrupted. RESULTS: We present a modified technique, using a double tube assembly, which allows uninterrupted ventilation of the patient during withdrawal of the LMA from the patient's mouth. CONCLUSIONS: The technique is simple and safe, can be performed without hurry and carries potential advantages for neonates and children with limited cardiorespiratory reserve.

Endoscopes↗

Tissue oxygenation monitoring during major pediatric surgery using transcutaneous liver near infrared spectroscopy.

BACKGROUND: The aim of the study was to compare liver tissue oxygenation determined by near infrared spectroscopy (NIRS) with central venous oxygen saturation (SvO(2)) and intestinal perfusion as measured by gastric intramucosal pH (pHi) in pediatric surgical patients. METHODS: Twenty children undergoing craniofacial surgery with expected major intraoperative blood loss were studied. NIRS tissue oxygenation index (TOI(Liver)) and pHi values were recorded. Arterial blood gas analysis and SvO(2) were assessed from periodically taken blood samples. Data are presented as ranges (median) and were compared using linear regression analysis. Sensitivity and specificity of the intra-individual changes in TOI(Liver) to predict falling SvO(2) or pHi values were calculated. RESULTS: Patients age ranged from 0.79 to 8.27 years (1.92 years). TOI(Liver) ranged from 41.5 to 77.4% (61.5%), gastric pHi from 7.13 to 7.60 (7.37) and SvO(2) from 51 to 86% (74%). Among patients only moderate correlation was found between TOI(Liver) and SvO(2) (r = 0.594, P < 0.0001) and gastric pH(i) (r = 0.502, P < 0.0001). Intra-individual measured TOI(Liver) values, however, demonstrated close correlation with SvO(2) values (r = 0.680 to 0.976) but a varying correlation with gastric pHi values (r = 0.055 to 0.972). Sensitivity/specificity of TOI(Liver) to predict decreasing SvO(2) or gastric pHi values were 76.4/73.4% and 67.4/62.7% respectively. CONCLUSIONS: TOI(Liver) provided a better trend monitor of central venous oxygen saturation than gastric intramucosal pH. Because of its limited sensitivity and specificity to indicate deterioration of SvO(2), liver tissue oxygenation measured by transcutaneous NIRS does not provide additional practical information for clinical management.

Blood Gas Analysis↗

The influence of acupressure on the monitoring of acoustic evoked potentials in unsedated adult volunteers.

Approaches for monitoring depth of anesthesia can be influenced by things other than anesthetics. In this study, we evaluated the influence of acupressure on the A-line autoregressive index (AAI) and on stress levels in unsedated volunteers. Fifteen unsedated adult volunteers received pressure on the acupuncture Extra 1 point (EP) and on a control point for 10 min on different days. AAI was recorded 5 min before, during, and 5 min after the interventions. Before and after the procedures, the volunteers quantified their level of stress by means of a visual analog stress scale (VSS; 0-100). Corresponding data were compared by Wilcoxon's signed rank test (Bonferroni correction, P < 0.05). Data are median (range). AAI decreased from 73 (40-99) to 53 (33-94) after 10 min of pressure on EP (P = 0.0044). Five minutes after release of pressure there was no difference compared with initial values. There was a statistically significant difference between VSS before and after pressure on EP (36 [7-67] to 15 [0-44]; P = 0.0066), but not on control point. In conclusion, there was a wide range of AAI values in awake volunteers. The AAI was influenced by acupressure performed on the EP in unsedated adult volunteers. Acupressure on this point significantly reduced stress levels.

Acupressure↗

Fluid leakage past tracheal tube cuffs: evaluation of the new Microcuff endotracheal tube.

OBJECTIVE: This study compared the recently introduced Microcuff endotracheal tube HVLP ICU featuring an ultrathin (7-microm) polyurethane cuff membrane with endotracheal tubes from different manufacturers regarding fluid leakage past the tube cuff. DESIGN: In vitro setup. MEASUREMENTS AND RESULTS: The following endotracheal tubes (ID 7.5 mm) were compared: Mallinckrodt HiLo, Microcuff HVLP ICU, Portex Profile Soft Seal, Rüsch Super Safety Clear, and Sheridan CF. A vertical PVC trachea model (ID 20 mm) was intubated, and cuffs were inflated to 10, 15, 20, 25, 30, and 60 cmH2O. Colored water (5 ml) was added to the top of the cuff. The amount of leaked fluid past the tube cuff within 5, 10, and 60 min was recorded. Experiments were performed four times using two examples of each tube brand. Fluid leakage past tube cuffs occurred in all conventional endotracheal tubes at cuff pressures from 10 to 60 cmH2O. In the Microcuff tube cuff pressure fluid leakage was observed within 10 min only at 10 cmH2O. Results with the Microcuff tube were significantly better than all other tube brands at cuff pressures of 10-30 cmH2O. CONCLUSIONS: Within the acceptable upper limit for tracheal cuff pressure (25-30 cmH2O) the Microcuff endotracheal tube was the only one of the tested tubes to prevent fluid leakage in our in vitro setup. In vivo studies are required to confirm these findings.

Equipment Design↗

Nitrous oxide does not affect automated air tonometry in children.

PURPOSE: To evaluate the effects of nitrous oxide on automated air tonometry in the clinical setting. MATERIAL AND METHODS: With approval of the Hospital Ethical Committee and after obtaining informed parental consent, an 8-F tonometry catheter was inserted orogastrically in ten children aged one to three years scheduled for elective surgery with combined regional and general anesthesia. A standardized general anesthesia technique with tracheal intubation was used in all patients and consisted of sevoflurane in oxygen/nitrous oxide (30%/70%; n = 5 patients) or in oxygen/air (FIO(2) 0.3; n = 5 patients). After obtaining steady state gastric CO(2) values (PrCO(2)), fresh gas mixtures were rapidly changed from oxygen/nitrous oxide to oxygen/air (A) or vice versa (B). In addition, balloon pressures were recorded using a pressure transducer. Measurements were performed at intervals of ten minutes with recording of balloon pressures, end-tidal CO(2) (PETCO(2)) and PrCO(2) values. Pr-ETCO(2)-gap were calculated to eliminate influences of changes in PaCO(2). RESULTS: Changing the fresh gas mixture from N(2)O/O(2) to O(2)/air resulted in a decrease of balloon pressure of -10.4% (113.4 +/- 14.7 mmHg to 101.6 +/- 25.0 mmHg). Changing the fresh gas mixture from O(2)/air to N(2)O/O(2) resulted in an increase of balloon pressures of 6.4% (107.6 +/- 19.3 mmHg to 114.0 +/- 20.3 mmHg). During both fresh gas exchange experiments no significant changes (> 0.2 kPa) in calculated Pr-ETCO(2)-gaps were observed. CONCLUSIONS: Based on our in vivo data, nitrous oxide during general anesthesia can be used with automated air tonometry and does not affect air tonometric PrCO(2) reading in clinical practice.

Anesthesia, General↗

Arterial fast bolus flush systems used routinely in neonates and infants cause retrograde embolization of flush solution into the central arterial and cerebral circulation.

PURPOSE: To evaluate the risk of retrograde embolization of flush solution in neonates and infants with routinely used electronic syringe pumps and infusion bag pump flush systems. METHODS: With hospital Ethical Committee approval we studied intubated neonates and infants with a 24-GA radial arterial cannula. Fast flush boluses were delivered from the infusion bag pump flush system by opening the flow regulating device for two seconds at bag pump manometre pressures of 100, 200 and 300 mmHg. In the syringe pump flush system, fast flush bolus volumes of 0.5, 1.0, 1.5 and 2.0 mL were programmed on the electronic syringe pump and released by opening the flow regulating device for two seconds. A 12-MHz ultrasonic probe placed in the jugular fossa was used to detect white bubbles indicating retrograde embolization of flush solution into the ipsilateral subclavian and common carotid artery. RESULTS: Sixteen patients, aged from 1-105 days (median 22 days) were studied. In all patients retrograde embolization into the subclavian artery was detected at syringe pump bolus volumes of 0.5-1.5 mL and at 100-200 mmHg bag pump pressure. In nine of the 16 patients a positive signal was detected in the common carotid artery with 1.5-2.0 mL syringe pump bolus volumes and at 200-300 mmHg bag pump pressure. CONCLUSIONS: In neonates and infants, the standard practice of arterial fast bolus flushing using syringe pump and bag pump flush systems causes retrograde embolization of flush solution into the central arterial and even into the cerebral circulation. The mandatory limitation of fast flush bolus volumes and manometre pressures is urgent in order to reduce retrograde embolization of flush solution and the associated risks in these small patients.

Catheters, Indwelling↗

Video-enhanced visualization of the larynx and intubation with the Bullard laryngoscope--equipment report.

PURPOSE: A simple technical solution is presented to provide video transmission from the tip of a Bullard laryngoscope to a bedside video display, while the operator is still able to look through the viewing ocular of the Bullard laryngoscope during tracheal intubation. EQUIPMENT: This is achieved by insertion of an ultrathin fibreoptic video-endoscopic system into the working channel of the Bullard laryngoscope. Thereby the view from the distal blade tip is transmitted to a bedside monitor, without interfering with the use of the Bullards laryngoscope's original eyepiece. The presented technical solution allows video transmission without considerable additional weight normally associated with attaching video endoscopy cameras, light and camera cables to endoscopic devices. Thus, the Bullard laryngoscope remains lightweight and easy to maneuver. A screw-threaded adapter with a side-port is proposed to prevent displacement of the fibreoptic cable while still allowing application of oxygen. CONCLUSION: Experience and skills with tracheal intubation using the presented video-enhanced Bullard laryngoscope can be achieved in the originally intended way, while the supervisor or attending viewers can follow the tracheal intubation procedure on the video display.

Computer Terminals↗

Video-optic cable endoscopy forceps.

We present a video-endoscopic technology for foreign body extractions with forceps. This can easily be followed and is recordable on video monitor in excellent quality. Instead of a rigid rod lens telescope, a fiberoptic video endoscope is inserted into the optical channel of a bronchoscopic forceps. This keeps the endoscopic device lightweight and easily maneuverable in different angles. The principle can be applied to other rigid diagnostic and therapeutic endoscopic equipment and represents a potential alternative technology to the use of cameras attached to rigid telescopes.

Endoscopes↗

Measurement of cerebral oxygenation state in anaesthetized children using the INVOS 5100 cerebral oximeter.

BACKGROUND: Near-infrared spectroscopy is a developing technique for monitoring cerebral oxygenation during anaesthesia. The aim of this study was to evaluate absolute values of cerebral oxygenation during stable anaesthesia conditions in otherwise healthy children using the recently introduced INVOS 5100 cerebral oximeter with a paediatric and adult sensor and to compare them with values obtained from the NIRO 300 oximeter. METHODS: Thirty paediatric surgical patients (aged 0.23-15.97 years) were studied during general anaesthesia with tracheal intubation and controlled ventilation. Comparative measurements of cerebral oxygenation were performed on the forehead with two probes within 10 min under stable cardiorespiratory and anaesthesia conditions. Cerebral oxygenation values (rSO2) obtained from the paediatric and adult INVOS 5100 sensors were compared with the tissue oxygenation index (TOI) obtained from the NIRO 300 cerebral oximeter using 4- and 5-cm emitter-detector separation. RESULTS: Cerebral rSO2 values and the TOI values both showed a large range of cerebral oxygenation in the children studied (rSO2: 59-95%, TOI: 48-85%). Cerebral rSO2 values measured by the INVOS 5100, particularly with the paediatric sensor, were significantly higher than the TOI values obtained from the NIRO 300 (P < 0.0001). Agreement between the INVOS and NIRO oximeter was poor. CONCLUSION: The large range and the poor agreement of cerebral oxygenation values between the two oximeters makes it difficult to define a normal value. Cerebral oxygenation readings by these monitors, based on one single point measurement during anaesthesia, should be viewed with caution. Actually, there may be little indication for routine use of such monitoring during general anaesthesia.

Adolescent↗