VanZalen Jensyn J, Harvey Stephen, Hála Pavel, Phillips Annie, Nakashima Takahiro, Gok Emre, Tiba Mohamad Hakam, McCracken Brendan M, Hill Joseph E, Liao Jinhui, Jung Joshua, Mergos Joshua, Stacey William C, Bartlett Robert H, Hsu Cindy H, Rojas-Peña Alvaro, Neumar Robert W
Department of Surgery and Extracorporeal Life Support Laboratory, University of Michigan Medical School, Ann Arbor, MI.
Department of Emergency Medicine and The Max Harry Weil Institute for Critical Care Research and Innovation, University of Michigan Medical School, Ann Arbor, MI.
Crit Care Explor. 2023 May 10;5(5):e0902. doi: 10.1097/CCE.0000000000000902. eCollection 2023 May.
Prolonged cardiac arrest (CA) causes microvascular thrombosis which is a potential barrier to organ reperfusion during extracorporeal cardiopulmonary resuscitation (ECPR). The aim of this study was to test the hypothesis that early intra-arrest anticoagulation during cardiopulmonary resuscitation (CPR) and thrombolytic therapy during ECPR improve recovery of brain and heart function in a porcine model of prolonged out-of-hospital CA.
Randomized interventional trial.
University laboratory.
Swine.
In a blinded study, 48 swine were subjected to 8 minutes of ventricular fibrillation CA followed by 30 minutes of goal-directed CPR and 8 hours of ECPR. Animals were randomized into four groups ( = 12) and given either placebo (P) or argatroban (ARG; 350 mg/kg) at minute 12 of CA and either placebo (P) or streptokinase (STK, 1.5 MU) at the onset of ECPR.
Primary outcomes included recovery of cardiac function measured by cardiac resuscitability score (CRS: range 0-6) and recovery of brain function measured by the recovery of somatosensory-evoked potential (SSEP) cortical response amplitude. There were no significant differences in recovery of cardiac function as measured by CRS between groups ( = 0.16): P + P 2.3 (1.0); ARG + P = 3.4 (2.1); P + STK = 1.6 (2.0); ARG + STK = 2.9 (2.1). There were no significant differences in the maximum recovery of SSEP cortical response relative to baseline between groups ( = 0.73): P + P = 23% (13%); ARG + P = 20% (13%); P + STK = 25% (14%); ARG + STK = 26% (13%). Histologic analysis demonstrated reduced myocardial necrosis and neurodegeneration in the ARG + STK group relative to the P + P group.
In this swine model of prolonged CA treated with ECPR, early intra-arrest anticoagulation during goal-directed CPR and thrombolytic therapy during ECPR did not improve initial recovery of heart and brain function but did reduce histologic evidence of ischemic injury. The impact of this therapeutic strategy on the long-term recovery of cardiovascular and neurological function requires further investigation.
长时间心脏骤停(CA)会导致微血管血栓形成,这是体外心肺复苏(ECPR)期间器官再灌注的潜在障碍。本研究的目的是检验以下假设:在心肺复苏(CPR)期间进行早期心脏骤停期抗凝以及在ECPR期间进行溶栓治疗可改善长时间院外心脏骤停猪模型的脑和心脏功能恢复。
随机干预试验。
大学实验室。
猪。
在一项盲法研究中,48头猪经历8分钟室颤性心脏骤停,随后进行30分钟目标导向的心肺复苏和8小时的体外心肺复苏。动物被随机分为四组(每组n = 12),在心脏骤停12分钟时给予安慰剂(P)或阿加曲班(ARG;350mg/kg),在体外心肺复苏开始时给予安慰剂(P)或链激酶(STK,1.5MU)。
主要结局包括通过心脏复苏能力评分(CRS:范围0 - 6)测量的心脏功能恢复以及通过体感诱发电位(SSEP)皮层反应幅度恢复测量的脑功能恢复。各组间通过CRS测量的心脏功能恢复无显著差异(P = 0.16):P + P组为2.3(1.0);ARG + P组为3.4(2.1);P + STK组为1.6(2.0);ARG + STK组为2.9(2.1)。各组间相对于基线的SSEP皮层反应最大恢复无显著差异(P = 0.73):P + P组为23%(13%);ARG + P组为20%(13%);P + STK组为25%(14%);ARG + STK组为26%(13%)。组织学分析表明,与P + P组相比,ARG + STK组心肌坏死和神经变性减少。
在这个接受体外心肺复苏治疗的长时间心脏骤停猪模型中,目标导向的心肺复苏期间早期心脏骤停期抗凝以及体外心肺复苏期间的溶栓治疗并未改善心脏和脑功能的初始恢复,但确实减少了缺血性损伤的组织学证据。这种治疗策略对心血管和神经功能长期恢复的影响需要进一步研究。