Ouzounian J G, Masaki D I, Abboud T K, Greenspoon J S
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Southern California Medical Center, Los Angeles 90033, USA.
Am J Obstet Gynecol. 1996 Mar;174(3):1019-25. doi: 10.1016/s0002-9378(96)70343-5.
Our purpose was to evaluate the predictive value of the baseline systemic vascular resistance index for the development of maternal hypotension during regional anesthesia for cesarean delivery.
Patients receiving a standardized spinal or epidural anesthetic for nonemergency cesarean delivery were studied prospectively. Hemodynamic data were obtained noninvasively with an NCCOM-3 cardiac output monitor (Bomed Medical Manufacturing, Irvine, Calif.), which uses thoracic electrical bioimpedance to estimate stroke volume and cardiac output. Measurements obtained were indexed to body surface area. The systemic vascular resistance index was calculated from mean arterial pressure and thoracic electrical bioimpedance-derived cardiac index. Hemodynamic data obtained were analyzed to identify statistically significant predictors of maternal hypotension.
Maternal hypotension occurred in 24 of 42 (57%) patients studied. The incidence of hypotension did not differ between the types of anesthesia: spinal 17 of 274 (62%) versus epidural 7 of 15 (47%, p=0.48). The mean interval to the onset of hypotension was 12.2 minutes (SD 2.2 minutes, range 2 to 24 minutes). Mean (SD) baseline maternal systolic blood pressure was higher in patients who had hypotension (145 torr [4]) than those who did not (129 torr [4], p=0.01). The mean (SD) baseline systemic vascular resistance index was higher in patients who had hypotension (633 [SD 36] dyne . cm . sec-5/m2) than those who did not (454 [SD 29] dyne . cm . sec-5/m2; p =0.001). With receiver-operator characteristic curves, a baseline systemic vascular resistance index of 500 had a sensitivity of 83%, a specificity of 78%, a positive predictive value of 83%, and a negative predictive value of 78% for maternal hypotension (odds ratio 17.5, 95% confidence interval 3.1 to 109.4). A baseline systolic blood pressure of 140 torr had a sensitivity and specificity of 42% and 72%, respectively (odds ratio 1.9, 95% confidence interval 0.4 to 8.8).
Baseline systemic vascular resistance index obtained by noninvasive cardiac output monitoring with thoracic electrical bioimpedance and systolic blood pressure are useful to predict the risk for maternal hypotension with regional anesthesia. Patients with increased baseline systemic vascular resistance index or systolic blood pressure are at increased risk for hypotension.
我们的目的是评估剖宫产区域麻醉期间基线全身血管阻力指数对产妇低血压发生的预测价值。
对接受标准化脊髓或硬膜外麻醉进行非急诊剖宫产的患者进行前瞻性研究。使用NCCOM - 3心输出量监测仪(Bomed Medical Manufacturing,加利福尼亚州欧文市)无创获取血流动力学数据,该监测仪利用胸部电阻抗来估计每搏输出量和心输出量。所测数据按体表面积进行校正。全身血管阻力指数由平均动脉压和胸部电阻抗衍生的心指数计算得出。对获取的血流动力学数据进行分析,以确定产妇低血压的统计学显著预测因素。
42例研究患者中有24例(57%)发生产妇低血压。低血压发生率在不同麻醉类型之间无差异:脊髓麻醉274例中有17例(62%),硬膜外麻醉15例中有7例(47%,p = 0.48)。低血压发作的平均间隔时间为12.2分钟(标准差2.2分钟,范围2至24分钟)。发生低血压的患者基线产妇收缩压平均值(标准差)(145托[4])高于未发生低血压的患者(129托[4],p = 0.01)。发生低血压的患者基线全身血管阻力指数平均值(标准差)(633[标准差36]达因·厘米·秒⁻⁵/平方米)高于未发生低血压的患者(454[标准差29]达因·厘米·秒⁻⁵/平方米;p = 0.001)。通过受试者工作特征曲线分析,基线全身血管阻力指数为500时,对产妇低血压的敏感性为83%,特异性为78%,阳性预测值为83%,阴性预测值为78%(优势比17.5,95%置信区间3.1至109.4)。基线收缩压为140托时,敏感性和特异性分别为42%和72%(优势比1.9,95%置信区间0.4至8.8)。
通过胸部电阻抗无创心输出量监测获得的基线全身血管阻力指数和收缩压有助于预测区域麻醉时产妇低血压的风险。基线全身血管阻力指数或收缩压升高的患者发生低血压的风险增加。