Biomedical subjects
Publications and source records attributed to A Saville.
A portable quantitative microstream capnometer (NPB-75) was tested in intubated children. The end-tidal CO(2) values measured by this device showed good agreement with concomitantly measured values of a stationary mainstream capnometer (N-6000). This lightweight device, with a 4-hour battery life, graphic capnogram display, and audiovisual alarms is well suited for the prehospital setting.
OBJECTIVES: Auto-inhalation of nitric oxide (NO) produced in the upper airways may have physiologic effects on lung function. For intubated patients, the upper airway source of NO is eliminated, but the hospital compressed air source from the environment is contaminated with varying levels of NO, creating an "occult" form of NO therapy. We examined the physiologic significance of occult inhaled NO in ventilator-dependent pediatric patients. We hypothesized that very low levels of NO contamination in inspired gas improve PaO2 in ventilator-dependent children. STUDY DESIGN: Inspired NO levels at the mouth were measured by chemiluminescence in 4 pediatric subjects with normal lungs and 3 with parenchymal lung disease. Subjects were sequentially ventilated with first standard hospital gas (H1), switched to pure nitrogen-oxygen at a similar FIO2 but with no NO contamination (A2), hospital gas again (H2), the nitrogen-oxygen (A2) to control for time and sequence, and finally the nitrogen-oxygen mixture with supplemental NO in an amount equal to the NO previously measured in hospital gas (A2 + NO). Inhaled NO levels and PaO2 were recorded 15 minutes into each of the 5 steps. Two patients were studied a second time, remote from their first examination. RESULTS: NO levels in inhaled hospital gas mixtures ranged from 13 to 79 ppb (mean H1 = 53.3 +/- 23.7 ppb, mean H2 = 53.2 +/- 20.7 ppb, mean A2 + NO = 45 +/- 15.3 ppb; P < .0001). Removing NO from ventilator gas decreased PaO2 in all subjects, whereas replacing NO in artificial gas restored PaO2 to baseline values (P < .0001). CONCLUSION: Concentrations of NO in hospital compressed air are variable and have physiologic effects. The long-term implications of these findings remain to be defined.
OBJECTIVE: To evaluate the accuracy of physiologic deadspace (VD/VT) measurement, using a metabolic monitor. DESIGN: Prospective collection of data. SETTING: University-affiliated children's hospital with a 51-bed critical care area. PATIENTS: Infants and children who were sedated and paralyzed and were receiving mechanical ventilation through a cuffed endotracheal tube. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Mixed expired carbon dioxide tension (PECO2) was measured. With the Douglas bag method, mixed expired gas was collected over 15 mins and was analyzed. With the metabolic monitor, FECO2 was measured for 15 mins and the results were averaged. The PECO2 was calculated by multiplying FECO2 by the barometric pressure. The PaCO2 was measured simultaneously. The PECO2 was corrected for the compressible volume in the ventilator circuit. All gas volumes were corrected for body temperature, pressure, and water vapor pressure. The physiologic deadspace/tidal volume ratio (VD/VT) was calculated for both techniques using the Enghoff modification of the Bohr equation. The accuracy of the VD/VT measured, by using the metabolic monitor, was assessed by comparing this measurement against the VD/VT measured by the Douglas bag method. This comparison was done by simple linear regression and correlation and by bias analysis (Bland and Altman method). The magnitude of compressible volume expressed as a fraction of the tidal volume delivered by the ventilator was compared with the error in VD/VT expressed as the difference between the uncorrected and corrected VD/VT. Sixteen paired measurements were made in 12 children. The VD/VT measured by the metabolic monitor correlated well with the VD/VT measured by the Douglas bag method (r2 = .99; p < .0001). There was no correlation between the bias of VD/VT and the average VD/VT. As the magnitude of compressible volume increased, the error in VD/VT increased (r2 =.61; p < .001). CONCLUSIONS: The VD/VT can be measured reliably and accurately in intubated pediatric patients using a metabolic monitor. The metabolic monitor method is a convenient and simple alternative to the standard Douglas bag method.