Department of Anesthesiology, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, PR China.
Department of Anesthesiology, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, PR China.
J Clin Anesth. 2024 Oct;97:111562. doi: 10.1016/j.jclinane.2024.111562. Epub 2024 Jul 23.
Previous studies have shown that a 0.05 μg/kg/min of norepinephrine infusion in combination with an initial bolus reduces the incidence of spinal hypotension during cesarean delivery. The initial norepinephrine bolus influences the incidence of spinal hypotension during continuous norepinephrine infusion; however, the ideal initial bolus dose for 0.05 μg/kg/min of continuous infusion remains unknown.
This randomized, controlled, dose-finding study randomly allocated 120 parturients scheduled for elective cesarean delivery to receive initial bolus doses of 0, 0.05, 0.10, and 0.15 μg/kg of norepinephrine, followed by continuous infusion at a rate of 0.05 μg/kg/min. The primary outcome was the dose-response relationship of the initial norepinephrine bolus in preventing the incidence of spinal hypotension. Spinal hypotension was defined as systolic blood pressure (SBP) decreased to <80% of the baseline value or to an absolute value of <90 mmHg from intrathecal injection to delivery, and severe spinal hypotension was defined as SBP decreased to <60% of the baseline value. The secondary outcomes included the incidence of nausea and/or vomiting, hypertension, and bradycardia, as well as the Apgar scores and results of the umbilical arterial blood gas analysis. The effective dose (ED) 90 and ED95 were estimated using probit regression.
The per-protocol analysis included 117 patients. The incidence of spinal hypotension varied significantly among the groups: Group 0 (51.7%), Group 0.05 (44.8%), Group 0.10 (23.3%), and Group 0.15 (6.9%). The ED90 and ED95 values were 0.150 μg/kg (95% confidence interval [CI], 0.114-0.241 μg/kg) and 0.187 μg/kg (95% CI, 0.141-0.313 μg/kg), respectively. However, the ED95 value fell outside the dose range examined in this study. The incidence of severe spinal hypotension differed significantly (P = 0.02) among Groups 0 (17.2%), 0.05 (10.3%), 0.10 (3.3%), and 0.15 (0.0%); however, the incidence of hypertension and bradycardia did not. The incidence of nausea and/or vomiting decreased with an increase in the initial bolus dose (P = 0.03). The fetal outcomes were comparable among the groups.
An initial bolus of 0.150 μg/kg of norepinephrine may be the optimal dose for preventing spinal hypotension during cesarean delivery with a continuous infusion rate of 0.05 μg/kg/min, and does not significantly increase the incidence of hypertension but substantially reduces the risk of nausea and/or vomiting.
先前的研究表明,在剖宫产术中,以 0.05μg/kg/min 的速度输注去甲肾上腺素,并联合使用初始推注,可降低脊髓低血压的发生率。初始去甲肾上腺素推注会影响持续输注去甲肾上腺素期间脊髓低血压的发生率;然而,对于 0.05μg/kg/min 的持续输注,理想的初始推注剂量仍不清楚。
这是一项随机、对照、剂量探索研究,将 120 例择期剖宫产的产妇随机分为 0、0.05、0.10 和 0.15μg/kg 的去甲肾上腺素初始推注剂量组,随后以 0.05μg/kg/min 的速度进行持续输注。主要结局是预防脊髓低血压的初始去甲肾上腺素推注的剂量-反应关系。脊髓低血压定义为收缩压(SBP)从蛛网膜下腔注射到分娩时降至基线值的<80%或绝对<90mmHg,严重脊髓低血压定义为 SBP 降至基线值的<60%。次要结局包括恶心和/或呕吐、高血压和心动过缓的发生率,以及新生儿的 Apgar 评分和脐动脉血气分析结果。使用概率回归估计有效剂量(ED)90 和 ED95。
意向治疗分析纳入了 117 例患者。各组脊髓低血压的发生率差异有统计学意义:0 组(51.7%)、0.05 组(44.8%)、0.10 组(23.3%)和 0.15 组(6.9%)。ED90 和 ED95 值分别为 0.150μg/kg(95%置信区间 [CI],0.114-0.241μg/kg)和 0.187μg/kg(95% CI,0.141-0.313μg/kg)。然而,ED95 值落在本研究检查的剂量范围之外。0 组(17.2%)、0.05 组(10.3%)、0.10 组(3.3%)和 0.15 组(0.0%)之间严重脊髓低血压的发生率差异有统计学意义(P=0.02);然而,高血压和心动过缓的发生率没有差异。随着初始推注剂量的增加,恶心和/或呕吐的发生率呈下降趋势(P=0.03)。各组的胎儿结局无差异。
在 0.05μg/kg/min 的持续输注速率下,0.150μg/kg 的去甲肾上腺素初始推注可能是预防剖宫产术中脊髓低血压的最佳剂量,不会显著增加高血压的发生率,但可显著降低恶心和/或呕吐的风险。