Conzen Peter F, Kharasch Evan D, Czerner Stephan F A, Artru Alan A, Reichle Florian M, Michalowski Piotr, Rooke G Alec, Weiss Branko M, Ebert Thomas J
Department of Anesthesiology, Ludwig-Maximilians-University, Munich, Germany.
Anesthesiology. 2002 Sep;97(3):578-84. doi: 10.1097/00000542-200209000-00010.
Sevoflurane is degraded to compound A (CpA) by carbon dioxide absorbents containing strong base. CpA is nephrotoxic in rats. Patient exposure to CpA is increased with low fresh gas flow rates, use of Baralyme, and high sevoflurane concentrations. CpA formation during low-flow and closed circuit sevoflurane anesthesia had no significant renal effects in surgical patients with normal renal function. Preexisting renal insufficiency is a risk factor for postoperative renal dysfunction. Although preexisting renal insufficiency is not affected by high-flow sevoflurane, the effect of low-flow sevoflurane in patients with renal insufficiency is unknown.
After obtaining institutional review board approval, 116 patients with a stable preoperative serum creatinine concentration 1.5 mg/dl or greater were assessable. Patients were randomized to receive either sevoflurane (n = 59, 0.8-2.5 vol%) or isoflurane (n = 57, 0.5-1.4 vol%) at a fresh gas flow rate of 1 l/min or less. Use of opioids was restricted to a minimum, and Baralyme was used to increase CpA exposure. Inspiratory and expiratory CpA concentrations were measured during anesthesia. Renal function (serum creatinine and blood urea nitrogen, urine protein and glucose, creatinine clearance) was measured preoperatively and 24 and 72 h after induction.
Demographic patient data did not differ between groups. Patients received 3.1 +/- 2.4 minimum alveolar concentration-hours sevoflurane or 3.8 +/- 2.6 minimum alveolar concentration-hours isoflurane (mean +/- SD). Durations of low flow were 201.3 +/- 98.0 and 213.6 +/- 83.4 min, respectively. Maximum inspiratory CpA with sevoflurane was 18.9 +/- 7.6 ppm (mean +/- SD), resulting in an average total CpA exposure of 44.0 +/- 30.6 ppm/h. There were no statistically significant changes from baseline to 24- and 72-h values for serum creatinine or blood urea nitrogen, creatinine clearance, urine protein, and glucose, nor were there significant differences between both anesthetics.
There were no statistically significant differences in measured parameters of renal function after low-flow sevoflurane anesthesia compared with isoflurane. These results suggest that low-flow sevoflurane anesthesia is as safe as low-flow isoflurane and does not alter kidney function in patients with preexisting renal disease.
七氟醚会被含强碱的二氧化碳吸收剂降解为化合物A(CpA)。CpA对大鼠具有肾毒性。在低新鲜气流量、使用钡石灰以及高七氟醚浓度的情况下,患者接触CpA的量会增加。在肾功能正常的外科手术患者中,低流量和闭合回路七氟醚麻醉期间CpA的形成对肾脏没有显著影响。术前存在肾功能不全是术后肾功能障碍的一个危险因素。虽然术前存在肾功能不全不受高流量七氟醚的影响,但低流量七氟醚对肾功能不全患者的影响尚不清楚。
在获得机构审查委员会批准后,对116例术前血清肌酐浓度稳定在1.5mg/dl或更高的患者进行评估。患者被随机分为两组,分别接受七氟醚(n = 59,0.8 - 2.5体积%)或异氟醚(n = 57,0.5 - 1.4体积%),新鲜气流量为1L/分钟或更低。阿片类药物的使用被限制在最低限度,并且使用钡石灰以增加CpA暴露。在麻醉期间测量吸气和呼气时的CpA浓度。在术前以及诱导后24小时和72小时测量肾功能(血清肌酐、血尿素氮、尿蛋白和葡萄糖、肌酐清除率)。
两组患者的人口统计学数据没有差异。患者接受了3.1±2.4最低肺泡浓度 - 小时的七氟醚或3.8±2.6最低肺泡浓度 - 小时的异氟醚(平均值±标准差)。低流量持续时间分别为201.3±98.0分钟和213.6±83.4分钟。七氟醚的最大吸气CpA为18.9±7.6ppm(平均值±标准差),导致平均总CpA暴露为44.0±30.6ppm/小时。从基线到24小时和72小时,血清肌酐、血尿素氮、肌酐清除率、尿蛋白和葡萄糖的值没有统计学上的显著变化,两种麻醉剂之间也没有显著差异。
与异氟醚相比,低流量七氟醚麻醉后肾功能测量参数没有统计学上的显著差异。这些结果表明,低流量七氟醚麻醉与低流量异氟醚麻醉一样安全,并且不会改变术前存在肾脏疾病患者的肾功能。