Effects of desflurane on systemic, preportal and renal circulatory responses to infra-renal aortic cross-clamping in the pig

被引:4
作者
Sundeman, H
Biber, B
Henriksson, BA
Raner, C
SeemanLodding, H
Winso, O
机构
[1] GOTHENBURG UNIV,SAHLGRENSKA HOSP,DEPT ANESTHESIOL,S-41685 GOTHENBURG,SWEDEN
[2] UMEA UNIV HOSP,DEPT ANESTHESIOL,S-90185 UMEA,SWEDEN
关键词
aortic cross clamping; chloralose; desflurane; pigs; portal blood flow vascular resistance; renal blood flow vascular resistance; mean arterial pressure;
D O I
10.1111/j.1399-6576.1996.tb04553.x
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Different pharmacological approaches have been used in the control of cardiovascular responses to surgical infra-renal aortic occlusion (AXC). The aim of the present study was to explore the modulatory effects of desflurane (DES) on these responses. Methods: The study was performed in normoventilated chloralose-anesthetized pigs (n=14). Measurements included cardiac output (CO), pulmonary vascular pressures, heart rate (HR) and mean arterial pressure proximal to the AXC site (MAP(PROX)). Renal arterial (Q(REN)) and portal venous (Q(PORT)) blood flows were measured ultrasonically. Systemic (SVR), preportal (R(PORT)) and renal (R(REN)) vascular resistances were derived. Sets of measurements were done a) prior to, b) during and c) 5 min after AXC. This was repeated, in a randomized fashion, at control (no DES) and with 4.9% and 9.8% DES, respectively. Results: DES decreased MAP(PROX), CO, HR, SVR, R(REN) and R(PORT). At control, AXC increased MAP(PROX) (+27%), SVR (+27%), Q(PORT) (+14%), R(PORT) (+12%) and R(REN) (+43%). DES 4.9% did not change this response pattern. With 9.8% DES, the AXC-induced increases in MAP(PROX) (+17%) and SVR (+21%) were attenuated. At this stage, AXC caused no demonstrable changes in R(REN) or R(PORT), while both Q(REN) (+16%) and Q(PORT) increased (+9%). Conclusions: DES effectively controlled increases in proximal blood pressure during AXC. The increases in R(REN) and R(PORT) that were seen during AXC at control were inhibited by 9.8% DES. Consequently, at this DES dose, both Q(REN) and Q(PORT) increased during AXC.
引用
收藏
页码:876 / 882
页数:7
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