Cardiovascular Disease Program, Biomedicine Discovery Institute and Department of Physiology, Monash University, Melbourne, Australia.
Pre-Clinical Critical Care Unit, Florey Institute of Neuroscience and Mental Health, Melbourne, Australia.
Anaesthesia. 2023 Dec;78(12):1481-1492. doi: 10.1111/anae.16152. Epub 2023 Oct 25.
Cardiac surgery requiring cardiopulmonary bypass is associated with postoperative acute kidney injury and neurocognitive disorders, including delirium. Intra-operative inflammation and/or impaired tissue perfusion/oxygenation are thought to be contributors to these outcomes. It has been hypothesised that these problems may be ameliorated by the highly selective α -agonist, dexmedetomidine. We tested the effects of dexmedetomidine on renal and cerebral microcirculatory tissue perfusion, oxygenation and histology in a clinically relevant ovine model. Sixteen sheep were studied while conscious, after induction of anaesthesia and during 2 h of cardiopulmonary bypass. Eight sheep were allocated randomly to receive an intravenous infusion of dexmedetomidine (0.4-0.8 μg.kg .h ) from induction of anaesthesia to the end of cardiopulmonary bypass, and eight to receive an equivalent volume of matched placebo (0.9% sodium chloride). Commencement of cardiopulmonary bypass decreased renal medullary tissue oxygenation in the placebo group (mean (95%CI) 5.96 (4.24-7.23) to 1.56 (0.84-2.09) kPa, p = 0.001), with similar hypoxic levels observed in the dexmedetomidine group (6.33 (5.33-7.07) to 1.51 (0.33-2.39) kPa, p = 0.002). While no differences in kidney function (i.e. reduced creatinine clearance) were evident, a greater incidence of histological renal tubular injury was observed in sheep receiving dexmedetomidine (7/8 sheep) compared with placebo (2/8 sheep), p = 0.041. Graded on a semi-quantitative scale (0-3), median (IQR [range]) severity of histological renal tubular injury was higher in the dexmedetomidine group compared with placebo (1.5 (1-2 [0-3]) vs. 0 (0-0.3 [0-1]) respectively, p = 0.013). There was no difference in cerebral tissue microglial activation (neuroinflammation) between the groups. Dexmedetomidine did not reduce renal medullary hypoxia or cerebral neuroinflammation in sheep undergoing cardiopulmonary bypass.
体外循环心脏手术后会发生急性肾损伤和神经认知障碍,包括谵妄。术中炎症和/或组织灌注/氧合受损被认为是这些结果的原因。有人假设,这些问题可以通过高度选择性的α-激动剂右美托咪定来改善。我们在一个临床相关的绵羊模型中测试了右美托咪定对肾脏和脑微循环组织灌注、氧合和组织学的影响。16 只绵羊在清醒、麻醉诱导和体外循环 2 小时期间进行了研究。8 只绵羊随机分配接受麻醉诱导至体外循环结束时静脉输注右美托咪定(0.4-0.8μg.kg.h ),8 只接受等量匹配的安慰剂(0.9%氯化钠)。体外循环开始时,安慰剂组的肾脏髓质组织氧合降低(平均值(95%CI)为 5.96(4.24-7.23)至 1.56(0.84-2.09)kPa,p=0.001),在右美托咪定组也观察到类似的低氧水平(6.33(5.33-7.07)至 1.51(0.33-2.39)kPa,p=0.002)。尽管肾功能(即肌酐清除率降低)没有差异,但接受右美托咪定的绵羊中肾小管损伤的发生率更高(7/8 只绵羊)与安慰剂(2/8 只绵羊)相比,p=0.041。在半定量评分(0-3)上,右美托咪定组的组织学肾小管损伤严重程度中位数(IQR[范围])高于安慰剂组(1.5(1-2[0-3])与 0(0-0.3[0-1]),p=0.013)。两组间脑组织小胶质细胞活化(神经炎症)无差异。在接受体外循环的绵羊中,右美托咪定并未降低肾脏髓质缺氧或脑神经炎症。