Fuda Giuseppe, Denault André, Deschamps Alain, Bouchard Denis, Fortier Annik, Lambert Jean, Couture Pierre
From the Departments of Anesthesiology and Cardiac Surgery, Montreal Heart Institute, Université de Montréal, Montreal, Quebec, Canada; Coordinating Center, Montreal Heart Institute, Montreal, Quebec, Canada; and Department of Preventive and Social Medicine, Université de Montréal, Montreal, Quebec, Canada.
Anesth Analg. 2016 Mar;122(3):624-632. doi: 10.1213/ANE.0000000000001096.
A central-to-radial arterial pressure gradient may occur after cardiopulmonary bypass (CPB), which, in some patients, may last for a prolonged time after CPB. Whenever there is a pressure gradient, the radial artery pressure measure may underestimate a more centrally measured systemic pressure, which may result in a misguided therapeutic strategy. It is clinically important to identify the risk factors that may predict the appearance of a central-to-radial pressure gradient, because more central sites of measurements might then be considered to monitor systemic arterial pressure in high-risk patients. The objective of this study was to assess preoperative and intraoperative risk factors for central-to-radial pressure gradient.
Seventy-three patients undergoing cardiac surgery using CPB were included in this prospective observational study. A significant central-to-radial arterial pressure gradient was defined as a difference of 25 mm Hg in systolic pressure or 10 mm Hg in mean arterial pressure for a minimum of 5 minutes. Preoperative data included demographics, presence of comorbidities, and medications. Intraoperative data included type of surgery, CPB and aortic clamping time, use of inotropic drugs, and vasodilators or vasopressors agents. The diameter of the radial and femoral artery was measured before the induction of anesthesia using B-mode ultrasonography.
Thirty-three patients developed a central-to-radial arterial pressure gradient (45%). Patients with a significant pressure gradient had a smaller weight (71.0 ± 16.9 vs 79.3 ± 17.3 kg, P = 0.041), a smaller height (162.0 ± 9.6 vs 166.3 ± 8.6 cm, P = 0.047), a smaller radial artery diameter (0.24 ± 0.03 vs 0.29 ± 0.05 cm, P < 0.001), and were at a higher risk as determined by the Parsonnet score (30.3 ± 24.9 vs 17.0 ± 10.9, P = 0.007). In addition, a longer aortic clamping time (85.8 ± 51.0 vs 64.2 ± 29.3 minutes, P = 0.036), mitral and complex surgery (P = 0.007 and P = 0.017, respectively), and administration of vasopressin (P = 0.039) were identified as potential independent predictors of a central-to-radial pressure gradient. By using multivariate logistic regression analysis, the following independent risk factors were identified: Parsonnet score (odds ratio [OR], 1.076; 95% confidence interval [CI], 1.027-1.127, P = 0.002), aortic clamping time >90 minutes (OR, 8.521; 95% CI, 1.917-37.870, P = 0.005), and patient height (OR, 0.933, 95% CI, 0.876-0.993, P = 0.029). The relative risk (RR) estimates remained statistically significant for the Parsonnet score and the aortic clamping time ≥90 minutes (RR, 1.010; 95% CI, 1.003-1.018, P = 0.009 and RR, 2.253; 95% CI, 1.475-3.443, P < 0.001 respectively) while showing a trend for patient height (RR, 0.974; 95% CI, 0.948-1.001, P = 0.058).
Central-to-radial gradients are common in cardiac surgery. The threshold for using a central site for blood pressure monitoring should be low in small, high-risk patients undergoing longer surgical interventions to avoid inappropriate administration of vasopressors and/or inotropic agents.
体外循环(CPB)后可能会出现中心动脉至桡动脉的压力梯度,在某些患者中,这种压力梯度在CPB后可能会持续较长时间。只要存在压力梯度,桡动脉压力测量值可能会低估更中心部位测量的体循环压力,这可能导致治疗策略出现偏差。识别可能预测中心至桡动脉压力梯度出现的危险因素在临床上很重要,因为这样在高危患者中可能会考虑采用更中心的测量部位来监测体循环动脉压力。本研究的目的是评估中心至桡动脉压力梯度的术前和术中危险因素。
本前瞻性观察性研究纳入了73例行CPB心脏手术的患者。显著的中心至桡动脉压力梯度定义为收缩压相差25 mmHg或平均动脉压相差10 mmHg,且持续至少5分钟。术前数据包括人口统计学资料、合并症情况和用药情况。术中数据包括手术类型、CPB和主动脉阻断时间、使用的正性肌力药物以及血管扩张剂或血管升压药。在麻醉诱导前使用B型超声测量桡动脉和股动脉的直径。
33例患者出现了中心至桡动脉压力梯度(45%)。有显著压力梯度的患者体重较轻(71.0±16.9 vs 79.3±17.3 kg,P = 0.041),身高较矮(162.0±9.6 vs 166.3±8.6 cm,P = 0.047),桡动脉直径较小(0.24±0.03 vs 0.29±0.05 cm,P < 0.001),且根据Parsonnet评分确定的风险较高(30.3±24.9 vs 17.0±10.9,P = 0.007)。此外,较长的主动脉阻断时间(85.8±51.0 vs 64.2±29.3分钟,P = 0.036)、二尖瓣和复杂手术(分别为P = 0.007和P = 0.017)以及血管升压素的使用(P = 0.039)被确定为中心至桡动脉压力梯度的潜在独立预测因素。通过多因素逻辑回归分析,确定了以下独立危险因素:Parsonnet评分(比值比[OR],1.076;95%置信区间[CI],1.027 - 1.127,P = 0.002)、主动脉阻断时间>90分钟(OR,8.521;95% CI,1.917 - 37.870,P = 0.005)以及患者身高(OR,0.933,95% CI,0.876 - 0.993,P = 0.029)。Parsonnet评分和主动脉阻断时间≥90分钟的相对风险(RR)估计值仍具有统计学意义(RR,1.010;95% CI,1.003 - 1.018,P = 0.009和RR,2.253;95% CI,1.475 - 3.443,P < 0.001),而患者身高呈现出一种趋势(RR,0.974;95% CI,0.94