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Biomedical subjects

N Gravenstein

Publications and source records attributed to N Gravenstein.

At least 55 records · Page 3Linked to original sources
PubMed1987

Continuous neonatal evaluation in the delivery room by pulse oximetry.

The pulse oximeter, a noninvasive and continuous monitor of arterial oxygenation that is reliable in adults, children, and infants, was evaluated for use in neonates in the delivery suite. One hundred newborn infants, weighing 850 to 5,230 g each, delivered vaginally or by cesarean section with general or epidural anesthesia were studied. After delivery, each infant was placed in a radiant warmer, and a pulse oximetry probe was placed on the right hand. Hemoglobin saturation was then recorded for 15 minutes. Initial pulse oximetry values were obtained in less than one minute after cord clamping in 43% of infants, less than two minutes in 81%, and less than three minutes in 98%. Average arterial oxygen saturation was 59% at 1 minute (43 infants), 68% at 2 minutes (81), 82% at 5 minutes (98), and 90% at 15 minutes (91). Oxygen saturation was less than 30% in 12 neonates and less than 50% in 26 neonates at some time during the 15-minute monitoring period. Oxygen saturation did not differ significantly between neonates delivered vaginally or by cesarean section, regardless of the presence or type of anesthetic used. Arterial oxygen saturation measured by pulse oximetry showed a statistically significant relationship when compared with the traditional Apgar scoring system. Pulse oximetry was found to be very useful in objectively judging the adequacy of resuscitative efforts, as well as in identifying children who had marked arterial desaturation during the early neonatal period.

Humans↗
PubMed1987

Capnography and the Bain circuit II: Validation of a computer model.

Validation of a computer model is described. The behavior of this model is compared both with mechanical ventilation of a test lung in a laboratory setup that uses a washout method and with manual ventilation. A comparison is also made with results obtained from a volunteer breathing spontaneously through a Bain circuit and with results published in the literature. This computer model is a multisegment representation of the Bain circuit and connecting tubing. For each segment, gas pressure, gas volume flow, and partial pressure of carbon dioxide are calculated for any number of breaths wanted. As a result, the time course of these variables can be generated for any location or, conversely, the carbon dioxide distribution in the system can be calculated for any time instant. A test lung, the human lungs, the ventilator bellows, and the reservoir bag are each represented by a single segment. The shapes of pressure and flow curves and of the capnograms taken at different locations in the Bain tubing are in good agreement. The washout study permits measurement of the time delay between the first expiration and the arrival of carbon dioxide at a particular location. The carbon dioxide level in the test lung decreases during inspiration and is stable during expiration. Quantitative agreement between model and experimental transport delays and carbon dioxide levels is such that the differences can be explained by the inaccuracy of the measurement. This is concluded from a sensitivity analysis. The study of the effect of segment size shows an almost optimal agreement between model behavior and experimental results for a 36-segment model. Execution of a thorough validation is imperative before such models can be used for clinical management and decision making or for teaching.

Airway Resistance↗
PubMed1987

Tidal volume changes due to the interaction of anesthesia machine and anesthesia ventilator.

Tidal volume (VT) delivered by mechanical ventilation during anesthesia may be influenced by factors related not only to the patient and the breathing circuit, but also to the interaction between the anesthesia machine and the anesthesia ventilator. To characterize this interaction, we studied in a test lung the effect of fresh-gas-flow (FGF) (0.25, 2.5, 5, and 10 L/min), inspiratory-to-expiratory time ratio (I:E) (1:1, 1:2, and 1:3), and ventilatory frequency (8, 12, and 16 breaths/min) at fixed ventilator bellows excursions of 300, 600, and 900 ml. The influence of these variables was also estimated mathematically for a pediatric situation: a bellows excursion of 50 ml at 20 and 30 breaths/min. Each variable studied was associated with an increase, sometimes dramatic, in the delivered VT compared with that which was set. The VT augmentation was greatest at the highest FGF rate, largest I:E ratio, and slowest respiratory rate. Because the magnitude of the augmentation is independent of the VT setting, the percent increase is much larger for pediatric settings. For example, with VT set at 50 ml, delivered VT ranged from 71 ml (FGF 2.5 L/min, I:E 1:3, and 30 breaths/min) to 300 ml (FGF 10 L/min, I:E 1:1, and 20 breaths/min). Thus it is possible in the pediatric situation to increase the delivered VT by sixfold without changing the ventilator bellows excursion. The magnitude of the changes was slightly larger for the VT settings for adult patients because of the slower respiratory rate. This VT augmentation can be predicted by the product of FGF (ml/s) and inspiratory time (seconds).(ABSTRACT TRUNCATED AT 250 WORDS)

Anesthesia, General↗
PubMed1987

Computer-assisted capnogram analysis.

Characteristic abnormal carbon dioxide waveforms from patients with mechanically ventilated lungs are observed when, for example, valves are incompetent, the airway is obstructed, the breathing circuit becomes disconnected, or a patient overrides mechanical ventilation with spontaneous breaths. Automated observation of the carbon dioxide waveform provides a uniform, concise, and consistent interpretation of the capnogram. This article describes a computer algorithm for analyzing and classifying capnograms as normal or as belonging to one of the categories above. The algorithm also generates a diagnostic message when the capnogram deviates from a learned norm for at least three consecutive waveforms (and thus reduces the influence of artifacts). Clinical experience shows reliable waveform recognition by the algorithm.

Algorithms↗
PubMed1987

Methylene blue and indocyanine green artifactually lower pulse oximetry readings of oxygen saturation. Studies in dogs.

The effects of fluorescein, methylene blue, and indocyanine green on hemodynamic variables and on pulse oximetry and co-oximetry measurements of arterial hemoglobin oxygen saturation (SaO2) and oxyhemoglobin percentage (% HbO2) were evaluated in 16 anesthetized dogs in vitro by co-oximetry (% HbO2) and in vivo by pulse oximetry (SaO2). The light absorbance (optical density) in plasma (range 500 to 800 nm) was measured by a spectrophotometer. Fluorescein did not affect oximetry measurements, plasma light absorbance in the range measured, or hemodynamic variables. Methylene blue caused dose-dependent decreases in measurements made with both forms of oximetry for up to 30 minutes, the decrease being greater and longer lasting with pulse oximetry (P less than 0.05). Hemodynamic measurements in 5 dogs showed that methylene blue (1 to 5 mg/kg) increased arterial pressure transiently, after which cardiac output, stroke index, and left ventricular stroke work index decreased and left ventricular end-diastolic pressure and systemic and pulmonary vascular resistances increased (P less than 0.05 with 5 mg/kg). Methemoglobin concentration measured by co-oximetry increased significantly (to 19.9 +/- 1.4%, P less than 0.05) 1 minute after 5 mg/kg of methylene blue was injected. Methylene blue had a dose- and time-dependent effect on plasma light absorbance, and this effect peaked in the 660- to 670-nm range. The data do not distinguish the relative contributions of physiology (hemodynamic change), chemistry (methemoglobin production), and physics (optical properties) to the decrease in pulse oximetry and co-oximetry measurements that follows injection of methylene blue. Indocyanine green affected neither hemodynamic variables nor co-oximetry readings but decreased pulse oximetry readings for up to 10 minutes dose dependently.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1987

Pulse oximetry fails to accurately detect low levels of arterial hemoglobin oxygen saturation in dogs.

The accuracy of two commercially available pulse oximeters (the Ohmeda Biox 3700, software version "J," and the Nellcor N-100) in detecting low levels of arterial hemoglobin oxygen saturation (SaO2) was evaluated in 10 dogs in which hypoxia was induced by stopping the fresh gas flow into the anesthesia machine circle system. Measurements made in vivo with the pulse oximeters, with detectors placed on the tongue, were compared with measurements made in vitro using an IL 282 CO-Oximeter as SaO2 decreased toward zero. Measurements from the two oximeters correlated poorly over the range from 0 to 100% SaO2 (r = 0.69). In this range, the correlation between Nellcor N-100 measurements and those of the CO-Oximeter had an r of 0.82, a regression line slope of 0.82, and a y intercept of 14.8; the correlation between the Ohmeda Biox 3700 and the CO-Oximeter had an r of 0.83, a regression line slope of 0.66, and a y intercept of 32.7. The correlation with the CO-Oximeter was similar for both the Ohmeda and the Nellcor pulse oximeters at an SaO2 of 80% or more. However, when SaO2 was less than 80%, measurements by pulse oximetry correlated less well with CO-Oximeter measurements (r = 0.62, slope = 0.64, and y intercept = 21.0 for Nellcor; r = 0.71, slope = 0.67, and y intercept = 32.4 for Ohmeda). When SaO2 was less than 60%, both oximeters inaccurately indicated the co-oximetry values (r = 0.36 and y intercept = 26.1 for the Nellcor; r = 0.48 and y intercept = 33.2 for the Ohmeda).(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1987

Thoracic aortic occlusion: somatosensory evoked potential monitoring and neurologic outcome in a canine model.

Somatosensory evoked potentials (SEPs) were monitored in 17 canines during spinal cord ischemia induced by balloon occlusion of the thoracic aorta. Graded distal aortic hypotension to 40 mmHg in seven animals had no significant effect upon the evoked potential. A significant alteration in the SEP did result in 21 +/- 9.8 minutes when distal aortic pressures were reduced in a graded fashion below 30 mmHg. Acute occlusion of the thoracic aorta (10 animals, distal pressure 15-25 mmHg) was associated with a change in the SEP in 8.4 +/- 4.3 minutes. Continuation of aortic occlusion for 30 minutes beyond an evoked potential change resulted in a moderate to severe motor deficit in all cases. Somatosensory evoked potentials obtained 72-96 hours after the ischemic injury were closely correlated with sensory deficits, but were not predictive of motor examination. Histologic examination of the spinal cords demonstrated central gray necrosis of the lumbar region in all animals with a severe deficit, and a variable degree of neuronal loss in the intermediate and dorsal gray matter zones in animals with moderate deficits. This balloon occlusion method is relevant as a model of spinal cord injury during aortic occlusion, such as may occur during aortic surgery.

Acute Disease↗
PubMed1987

Effects of aortic occlusion on regional spinal cord blood flow and somatosensory evoked potentials in sheep.

Somatosensory evoked potentials (SEPs) were recorded continuously during aortic occlusion in sheep, with simultaneous measurement of spinal cord blood flow (SCBF) by radiolabeled microspheres. Aortic occlusion was associated with disappearance of the SEPs in seven of nine sheep in 7.8 +/- 4.1 (SD) minutes. SCBF at the time of initial cross clamping and 30 minutes after the onset of ischemia revealed a severe reduction in white and gray matter flow in the thoracolumbar cord. Release of the aortic clamp was associated with reactive hyperemia in these ischemic regions. In two animals, the SEP persisted during aortic cross clamping. The total SCBF in the thoracic and lumbar regions of these two animals exceeded 20 ml/100 g/min after 30 minutes of ischemia and was significantly greater than the flow recorded in sheep whose evoked response disappeared. The relation between spinal cord ischemia and evoked potential alterations is discussed in detail.

Afferent Pathways↗
PubMed1986

Effects of induced hypotension during experimental vasospasm: a neurological, electrophysiological, and pathological analysis.

Vasospasm of the vertebrobasilar system was induced in seven dogs by the intracisternal injection of autologous blood. Somatosensory and brain stem auditory evoked potentials were recorded before and after the induction of angiographically confirmed vasospasm. Additionally, somatosensory evoked potentials were monitored during graded hypotension to 40 mm Hg. There was no significant alteration in the evoked potentials by vasospasm or hypotension. Detailed clinical examination and postmortem histopathological studies did not demonstrate any focal neurological deficit or infarction attributable to vasospasm. Previous studies have noted close correlations between decreased cerebral blood flow and evoked potential alterations. Induced hypotension to a mean arterial pressure of 40 mm Hg in the presence of documented vasospasm was not sufficient to cause evoked potential changes, focal neurological deficit, or pathological evidence of infarction in the canine model.

Animals↗
PubMed1985

Capnography and the Bain circuit I: A computer model.

The Mapleson D anesthesia breathing system has no valves and allows rebreathing of carbon dioxide. Its coaxial version is known as the Bain system. The interpretation of capnograms obtained during its use requires an understanding of the interrelationships of patient and system variables. Toward that end, a systematic description of mechanical ventilation with the Bain circuit was undertaken based on the physical laws of gas transport. The mathematical formulation of the model contains the relations between pressure, flow, and volume in the tube, alveolar space, and ventilator. The flows, calculated from these relations, are used to determine the CO2 concentrations in the different parts of the model. Two sets of data are used--patient and system. The patient data, used to solve the equations numerically, are lung-thorax compliance, CO2 inflow into alveolar space (CO2 production), functional residual capacity, dead space volume, airway resistance, and respiratory quotient. The ventilation system data comprise the dimensions and volumes of the Bain circuit, ventilator, connectors, and tubes; spill valve pressure; resistances to flow in the individual tube parts; ventilator settings; and fresh-gas flow rates. After incorporation of a volunteer's respiratory variables into the model, capnograms obtained from the model compared well with those obtained from the volunteer. The structure of the model is such that it permits easy introduction or changes of patient and system variables to obtain individual results or model specific circumstances. This flexibility makes it a useful tool for understanding the properties of the Bain circuit under a variety of clinical circumstances. The results may be displayed in a number of different ways.

Anesthesia, General↗
PubMed1985

Factors influencing capnography in the Bain circuit.

The Bain circuit provides continuous fresh gas flow near the airway. The potential mixing of this fresh gas with expired gas may prevent reliable analysis of expired gas. We therefore investigated the interaction of sampling site, fresh gas flow rate, expiratory flow rate, and sampling flow rate on expiratory capnography. Sampling near the fresh gas outlet yielded inaccurate results under several of these conditions. The magnitude of the error was related to the fresh gas and expiratory flow rates. A reliable sampling region near the endotracheal tube was identified.

Anesthesiology↗