PROPOFOL LINEARLY REDUCES THE VASOCONSTRICTION AND SHIVERING THRESHOLDS

被引:256
作者
MATSUKAWA, T
KURZ, A
SESSLER, DI
BJORKSTEN, AR
MERRIFIELD, B
CHENG, C
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT ANESTHESIA,THERMOREGULAT RES LAB,SAN FRANCISCO,CA 94143
[2] ROYAL MELBOURNE HOSP,DEPT ANAESTHESIA,PARKVILLE,VIC,AUSTRALIA
关键词
ANESTHETICS; INTRAVENOUS; PROPOFOL; TEMPERATURE; REGULATION; THERMOREGULATION; SHIVERING SWEATING VASOCONSTRICTION;
D O I
10.1097/00000542-199505000-00012
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Skin temperature is best kept constant when determining response thresholds because both skin and core temperatures contribute to thermoregulatory control. In practice, however, it is difficult to evaluate both warm and cold thresholds while maintaining constant cutaneous temperature. A recent study shows that vasoconstriction and shivering thresholds are a linear function of skin and core temperatures, with skin contributing 20 +/- 6% and 19 +/- 8%, respectively. (Skin temperature has long been known to contribute approximate to 10% to the control of sweating.) Using these relations, we were able to experimentally manipulate both skin and tore temperatures, subsequently compensate for the changes in skin temperature, and finally report the results in terms of calculated core-temperature thresholds at a single designated skin temperature. Methods: Five volunteers were each studied on 4 days: (1) control; (2) a target blood propofol concentration of 2 mu g/ml; (3) a target concentration of 4 mu g/ml; and (4) a target concentration of 8 mu g/ml. On each day, we increased skin and core temperatures sufficiently to provoke sweating. Skin and core temperatures were subsequently reduced to elicit peripheral vasoconstriction and shivering. We mathematically compensated for changes in skin temperature by using the established linear cutaneous contributions to the control of sweating (10%) and to vasoconstriction and shivering (20%). From these calculated core-temperature thresholds (at a designated skin temperature of 35.7 degrees C), the propofol concentration-response curves for the sweating, vasoconstriction, and shivering thresholds were analyzed using linear regression. We validated this new method by comparing the concentration-dependent effects of propofol with those obtained previously with an established model. Results: The concentration-response slopes for sweating and vasoconstriction were virtually identical to those reported previously. Propofol significantly decreased the core temperature triggering vasoconstriction (slope = -0.6 +/- 0.1 degrees C.mu g(-1).ml(-1); r(2) = 0.98 +/- 0.02) and shivering (slope = -0.7 +/- 0.1 degrees C.mu g(-1).ml(-1); r(2) = 0.95 +/- 0.05). In contrast, increasing the blood propofol concentration increased the sweating threshold only slightly (slope = 0.1 +/- 0.1 degrees C.mu g(-1).ml(-1); r(2) = 0.46 +/- 0.39). Conclusions: Advantages of this new model include its being nearly noninvasive and requiring relatively Little core-temperature manipulation. Propofol only slightly alters the sweating threshold, but markedly reduces the vasoconstriction and shivering thresholds. Reductions in the shivering and vasoconstriction thresholds are similar; that is, the vasoconstriction-to-shivering range increases only slightly during anesthesia.
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页码:1169 / 1180
页数:12
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