Anesthesia and analgesia
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Anesthesia and analgesia · Jan 2001
Randomized Controlled Trial Comparative Study Clinical TrialFast-track office-based anesthesia: a comparison of propofol versus desflurane with antiemetic prophylaxis in spontaneously breathing patients.
Compared to propofol, maintenance of anesthesia with desflurane provided significantly better intraoperative conditions during office-based surgery. In addition, desflurane with routine antiemetic prophylaxis was associated with a faster early recovery and similar incidence of postoperative side effects.
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Anesthesia and analgesia · Jan 2001
Randomized Controlled Trial Clinical TrialThe dose-range effects of sufentanil added to 0.125% bupivacaine on the quality of patient-controlled epidural analgesia during labor.
To determine the minimal sufentanil concentration required to improve the quality of patient-controlled epidural analgesia during labor, we compared the efficacy of a combination of 0.125% bupivacaine with 1:800,000 epinephrine and different concentrations of sufentanil in a double-blinded randomized study. Concentrations were no sufentanil (n = 66), 0.078 microg/mL sufentanil (n = 65), 0.156 microg/mL sufentanil (n = 65), 0.312 microg/mL sufentanil (n = 65), and 0.468 microg/mL sufentanil (n = 67). The patient-controlled epidural analgesia setting was a 12-mL bolus dose and a 25-min lockout interval. Pain was scored at 5-6 cm, 7-8 cm, and full cervical dilation by using a 10-cm visual analog scale. At full cervical dilation, the pain scores were lower in the groups receiving a solution of at least 0.156 microg/mL sufentanil. Few differences were observed when using the larger concentrations, except for increased pruritus intensity. The duration of labor and the mode of delivery were similar in each group. Rescue analgesia, which consisted of 6 mL of 0.25% bupivacaine, was infrequent and comparable between groups. The use of the pump did not differ between groups. Adding a small concentration of sufentanil to 0.125% bupivacaine for patient-controlled epidural analgesia during labor improved the quality of analgesia but did not modify the bupivacaine requirement. Reducing the sufentanil concentrations to 0.156 microg/mL decreased the pruritus intensity without reducing analgesia. ⋯ Adding a small concentration of sufentanil to 0.125% bupivacaine for patient-controlled epidural analgesia during labor improved the quality of analgesia but did not modify the bupivacaine requirement. Reducing the sufentanil concentrations to 0.156 microg/mL decreased the pruritus intensity without reducing analgesia.
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Anesthesia and analgesia · Jan 2001
Randomized Controlled Trial Clinical TrialProfile soft-seal cuff, a new endotracheal tube, effectively inhibits an increase in the cuff pressure through high compliance rather than low diffusion of nitrous oxide.
We assessed the nitrous oxide (N(2)O) gas-barrier properties of a new endotracheal tube cuff, the Profile Soft-Seal Cuff (PSSC) (Sims Portex, Kent, UK). The tracheas of randomly selected patients were intubated with the Trachelon (Terumo, Tokyo, Japan), Profile Cuff (PC) (Sims Portex), or PSSC (n = 15 for each) endotracheal tube. Cuffs were inflated with air, and intracuff pressure was measured during anesthesia with 67% N(2)O. ⋯ The incidence of postoperative sore throat in the Trachelon group was significantly higher than in the other two groups. In summary, the PSSC effectively inhibits an increase in cuff pressure during anesthesia with N(2)O. The underlying mechanism is probably the higher compliance of the thinner cuff, rather than a reduction in N(2)O diffusion into the cuff.
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Anesthesia and analgesia · Jan 2001
Randomized Controlled Trial Comparative Study Clinical TrialDeflationary phenomenon of the nitrous oxide-filled endotracheal tube cuff after cessation of nitrous oxide administration.
After cessation of nitrous oxide (N(2)O) administration, intracuff pressure of the endotracheal tube may decrease through rediffusion of N(2)O. There may then be an increased risk for air leaks, aspiration of gastric contents, or both. In this study, the time required for intracuff pressure to decrease by 50% (T(1/2)) after substituting oxygen for N(2)O inspired was estimated with the least-squares method. Fifty patients were randomly assigned to five groups, and their tracheas were intubated with the Hi-Contour, Sheridan, Rush, Reinforce, or Profile Soft-Seal Cuff endotracheal tubes. Cuffs were inflated with 40% N(2)O, and cuff pressure was measured during anesthesia with 67% N(2)O. After 120 min, N(2)O inspired was replaced with 100% oxygen, and cuff pressure was measured until the cuff pressure decreased by about 30%. In the five groups, stable cuff pressures were achieved during 120 min of anesthesia with N(2)O. The cuff pressures at 120 min were not different among groups (P = 0.098). After cessation of N(2)O administration, the intracuff pressure decreased exponentially. T(1/2) in the Hi-Contour group was 27.8 +/- 8.5 min, which was significantly shorter than in the Profile Soft-Seal Cuff group (49.7 +/- 18.5 min; P < 0.01). Therefore, our results demonstrate that pressure of the N(2)O-filled cuff decreases quickly when N(2)O-inspired concentrations are reduced, and we suggest that intracuff pressure should be checked frequently to avoid air leaks or aspiration of gastric contents during delayed extubation or transportation of patients with tracheal intubations. ⋯ A recently developed method for maintaining stable cuff pressure (N(2)O-filled cuffs) enables us to assess the decrease in cuff pressure after cessation of N(2)O administration. Our results confirm the limitations of N(2)O-filled cuffs when N(2)O-inspired concentrations are reduced.
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Anesthesia and analgesia · Jan 2001
Comparative Study Clinical TrialPeripheral venous pressure as a hemodynamic variable in neurosurgical patients.
Neurosurgical patients undergoing either craniotomy or complex spine surgery are subject to wide variations in blood volume and vascular tone. The ratio of these variables yields a pressure that is traditionally measured at the superior vena cava and referred to as "central venous pressure" (CVP). We have investigated an alternative to CVP by measuring peripheral venous pressure (PVP), which, in parallel animal studies, correlates highly with changes in absolute blood volume (r = 0.997). We tested the hypothesis that PVP trends parallel CVP trends and that their relationship is independent of patient position. We also tested and confirmed the hypothesis, during planned circulatory arrest, that PVP approximates mean systemic pressure (circulatory arrest pressure), which reflects volume status independent of cardiac function. PVP was compared with CVP across 1026 paired measurements in 15 patients undergoing either craniotomy (supine, n = 8) or complex spine surgery (prone, n = 7). Repeated-measures analysis of variance indicated a highly significant relationship between PVP and CVP (P < 0.001), with a Pearson correlation coefficient of 0.82. The correlation was best in cases with significant blood loss (estimated blood loss >1000 mL; r = 0.885) or hemodynamic instability (standard deviation of CVP > 2; r = 0.923). ⋯ In patients undergoing either elective craniotomy or complex spine surgery, peripheral venous pressure (PVP) trends correlated with central venous pressure (CVP) trends with a mean offset of 3 mm Hg (PVP > CVP). PVP trends provided equivalent physiological information to CVP trends in this subset of patients, especially during periods of hemodynamic instability. In addition, measurements made during a planned circulatory arrest support the hypothesis that PVP approximates mean systemic pressure (systemic arrest pressure), which is a direct index of patient volume status independent of cardiac or respiratory activity.