Biomedical subjects
A Sugden
Publications and source records attributed to A Sugden.
Hemodynamic effects of isoflurane in the newborn piglet: comparison with halothane.
To better understand the mechanism of hypotension and bradycardia that may occur in newborn infants during isoflurane anesthesia, we studied the hemodynamic changes in the major determinants of cardiac output in 15 newborn piglets given 0.5, 1.0, and 1.3 minimal alveolar concentrations (MAC) of isoflurane and in nine sham-instrumented, age-matched control animals. Cardiac output did not differ from the baseline reading or the control group at any isoflurane dose. Mean aortic pressure (MAP) decreased 23-45% in a dose-related manner. Total peripheral resistance index (TPRI) decreased 29% at 0.5 MAC, but did not decline further at higher concentrations. Because the decrease in MAP was offset by a similar reduction in TPRI, cardiac output did not change. Heart rate decreased significantly at 1.3 MAC (-19%). Contractility was depressed at all concentrations: left ventricular dP/dT decreased progressively at 0.5 and 1.0 MAC, and echocardiographic shortening fraction decreased significantly at 1.0 MAC. Left ventricular end-diastolic pressure was not affected. Eight of twelve animals who had bradycardia while breathing isoflurane were atrially paced at their baseline heart rate. Because pacing did not restore MAP, TPRI, and LV dP/dT/DP40 (a contractile index independent of preload and afterload) to control values, bradycardia was not primarily responsible for depression of these variables. At equipotent concentrations, isoflurane reduced MAP and TPRI more than, and cardiac output less than, halothane did in previous studies in this laboratory. Heart rate and dP/dT were decreased to a similar extent by both agents. Blood, heart, and brainstem isoflurane LD:MAC ratios were 2.04, 2.00, and 2.84, respectively, indicating a relatively low margin of safety for isoflurane in young piglets.
Accuracy of expiratory carbon dioxide measurements using the coaxial and circle breathing circuits in small subjects.
Mass spectrometry is widely used to measure the end-tidal concentrations of inhalation anesthetics and other gases during surgery in order to estimate their arterial concentrations. When certain breathing circuits are used in newborns, however, fresh gas or ambient air may contaminate the expired sample, introducing a systematic error in the measurement of any end-tidal gas concentration. We estimated this error in newborn piglets using carbon dioxide as an indicator substance of expired gas. The capnograms and the difference between arterial carbon dioxide tension (PaCO2) and peak-expired carbon dioxide tension (PeCO2) were compared when either a coaxial (Bain) or circle breathing circuit was used. Gas was sampled from the proximal airway and distal trachea. No combination of circuit and sampling site produced a flat alveolar phase until the circle circuit was modified with diversion valves to reduce gas mixing. The mean PaCO2-PeCO2 gradients using the coaxial/proximal sampling, coaxial/distal sampling, and modified circle/proximal sampling circuits were 12.4, 9.2, and 8.8 mm Hg, respectively. The mean PeCO2 in each of these combinations was significantly different from the corresponding mean PaCO2 (p less than 0.05). Using the modified circle circuit with distal sampling, mean PeCO2 was not significantly different from mean PaCO2: the mean PaCO2-PeCO2 gradient was 2.2 +/- 0.2 mm Hg (SEM), range, 0 to 6 mm Hg, with 95% confidence limits less than or equal to 8 mm Hg. When a coaxial breathing circuit is used in small subjects, PaCO2 may be significantly underestimated regardless of sampling site, although the circle breathing circuit with distal tracheal sampling yields accurate results.