Vincendeau Maud, Klein Thomas, Groubatch Frederique, Tran N'Guyen, Kimmoun Antoine, Levy Bruno
Service de Médecine Intensive et Réanimation Brabois, Université de Lorraine, CHRU de Nancy, Nancy, France.
Université de Lorraine, INSERM U1116, Nancy, France.
Intensive Care Med Exp. 2024 Aug 27;12(1):74. doi: 10.1186/s40635-024-00655-2.
Acute respiratory distress syndrome (ARDS) remains a significant challenge in critical care, with high mortality rates despite advancements in treatment. Venovenous extracorporeal membrane oxygenation (VV-ECMO) is employed as salvage therapy for refractory cases. However, some patients may continue to experience persistent severe hypoxemia despite being treated with VV-ECMO. To achieve this, moderate hypothermia and short-acting selective β1-blockers have been proposed.
Using a swine model of severe ARDS treated with VV-ECMO, this study investigated the efficacy of moderate hypothermia or β-blockade in improving arterial oxygen saturation (SaO) three hours after VV-ECMO initiation. Primary endpoints included the ratio of VV-ECMO flow to cardiac output and arterial oxygen saturation before VV-ECMO start (H0) and three hours after ECMO start (H3). Secondary safety criteria encompassed hemodynamics and oxygenation parameters.
Twenty-two male pigs were randomized into three groups: control (n = 6), hypothermia (n = 9) and β-blockade (n = 7). At H0, all groups demonstrated similar hemodynamic and respiratory parameters. Both moderate hypothermia and β-blockade groups exhibited a significant increase in the ratio of VV-ECMO flow to cardiac output at H3, resulting in improved SaO. At H3, despite a decrease in oxygen delivery and consumption in the intervention groups compared to the control group, oxygen extraction ratios across groups remained unchanged and lactate levels were normal.
In a swine model of severe ARDS treated with VV-ECMO, both moderate hypothermia and β-blockade led to an increase in the ratio of VV-ECMO flow to cardiac output resulting in improved arterial oxygen saturation without any impact on tissue perfusion.
急性呼吸窘迫综合征(ARDS)仍是重症监护中的一项重大挑战,尽管治疗取得了进展,但死亡率仍然很高。静脉-静脉体外膜肺氧合(VV-ECMO)被用作难治性病例的挽救治疗。然而,一些患者尽管接受了VV-ECMO治疗,仍可能持续出现严重低氧血症。为此,有人提出了中度低温和短效选择性β1受体阻滞剂的治疗方法。
本研究使用接受VV-ECMO治疗的重症ARDS猪模型,调查中度低温或β受体阻滞剂在VV-ECMO启动后三小时改善动脉血氧饱和度(SaO)的疗效。主要终点包括VV-ECMO流量与心输出量的比值以及VV-ECMO开始前(H0)和ECMO开始后三小时(H3)的动脉血氧饱和度。次要安全标准包括血流动力学和氧合参数。
22只雄性猪被随机分为三组:对照组(n = 6)、低温组(n = 9)和β受体阻滞剂组(n = 7)。在H0时,所有组的血流动力学和呼吸参数相似。中度低温组和β受体阻滞剂组在H3时VV-ECMO流量与心输出量的比值均显著增加,从而改善了SaO。在H3时,尽管与对照组相比,干预组的氧输送和消耗有所下降,但各组的氧摄取率保持不变,乳酸水平正常。
在接受VV-ECMO治疗的重症ARDS猪模型中,中度低温和β受体阻滞剂均导致VV-ECMO流量与心输出量的比值增加,从而改善动脉血氧饱和度,且对组织灌注无任何影响。