Department of Intensive Care, Fundación Valle del Lili, Cali, Colombia.
Translational Research Laboratory in Critical Care Medicine (TransLab-CCM), Universidad Icesi, Cali, Colombia.
Crit Care Med. 2023 Aug 1;51(8):e157-e168. doi: 10.1097/CCM.0000000000005885. Epub 2023 May 30.
To investigate the effects of immediate start of norepinephrine versus initial fluid loading followed by norepinephrine on macro hemodynamics, regional splanchnic and intestinal microcirculatory flows in endotoxic shock.
Animal experimental study.
University translational research laboratory.
Fifteen Landrace pigs.
Shock was induced by escalating dose of lipopolysaccharide. Animals were allocated to immediate start of norepinephrine (i-NE) ( n = 6) versus mandatory 1-hour fluid loading (30 mL/kg) followed by norepinephrine (i-FL) ( n = 6). Once mean arterial pressure greater than or equal to 75 mm Hg was, respectively, achieved, successive mini-fluid boluses of 4 mL/kg of Ringer Lactate were given whenever: a) arterial lactate greater than 2.0 mmol/L or decrease less than 10% per 30 min and b) fluid responsiveness was judged to be positive. Three additional animals were used as controls (Sham) ( n = 3). Time × group interactions were evaluated by repeated-measures analysis of variance.
Hypotension was significantly shorter in i-NE group (7.5 min [5.5-22.0 min] vs 49.3 min [29.5-60.0 min]; p < 0.001). Regional mesenteric and microcirculatory flows at jejunal mucosa and serosa were significantly higher in i-NE group at 4 and 6 hours after initiation of therapy ( p = 0.011, p = 0.032, and p = 0.017, respectively). Misdistribution of intestinal microcirculatory blood flow at the onset of shock was significantly reversed in i-NE group ( p < 0.001), which agreed with dynamic changes in mesenteric-lactate levels ( p = 0.01) and venous-to-arterial carbon dioxide differences ( p = 0.001). Animals allocated to i-NE showed significantly higher global end-diastolic volumes ( p = 0.015) and required significantly less resuscitation fluids ( p < 0.001) and lower doses of norepinephrine ( p = 0.001) at the end of the experiment. Pulmonary vascular permeability and extravascular lung water indexes were significantly lower in i-NE group ( p = 0.021 and p = 0.004, respectively).
In endotoxemic shock, immediate start of norepinephrine significantly improved regional splanchnic and intestinal microcirculatory flows when compared with mandatory fixed-dose fluid loading preceding norepinephrine. Immediate norepinephrine strategy was related with less resuscitation fluids and lower vasopressor doses at the end of the experiment.
研究在脓毒性休克中,与先进行 1 小时液体负荷再给予去甲肾上腺素(i-FL)相比,立即开始给予去甲肾上腺素(i-NE)对宏观血流动力学、内脏局部和肠道微循环的影响。
动物实验研究。
大学转化研究实验室。
15 头长白猪。
通过递增剂量的脂多糖诱导休克。动物被分为立即开始给予去甲肾上腺素(i-NE)组(n=6)和强制性 1 小时液体负荷(30ml/kg)后给予去甲肾上腺素(i-FL)组(n=6)。一旦平均动脉压大于或等于 75mmHg,分别在以下情况下给予连续的 4ml/kg 林格乳酸盐小容量输液:a)动脉血乳酸大于 2.0mmol/L 或每 30min 减少小于 10%,b)判断液体反应性为阳性。另外 3 只动物作为对照组(Sham)(n=3)。通过重复测量方差分析评估时间×组间的相互作用。
i-NE 组的低血压持续时间明显更短(7.5min[5.5-22.0min]与 49.3min[29.5-60.0min];p<0.001)。在治疗开始后 4 和 6 小时,i-NE 组肠系膜和肠道黏膜和浆膜的局部微循环流量明显更高(p=0.011,p=0.032,p=0.017)。休克发作时肠道微循环血流的分布不均在 i-NE 组得到明显逆转(p<0.001),这与肠系膜乳酸水平的动态变化(p=0.01)和静脉-动脉二氧化碳差(p=0.001)一致。与 i-FL 组相比,i-NE 组的整体舒张末期容积明显更高(p=0.015),需要的复苏液明显更少(p<0.001),去甲肾上腺素的剂量也明显更低(p=0.001)。i-NE 组肺血管通透性和肺血管外水指数明显较低(p=0.021 和 p=0.004)。
在脓毒性休克中,与先进行固定剂量的液体负荷再给予去甲肾上腺素相比,立即开始给予去甲肾上腺素可显著改善内脏局部和肠道微循环的血流。立即给予去甲肾上腺素的策略与实验结束时复苏液用量减少和血管加压药剂量降低有关。