Doubling survival and improving clinical outcomes using a left ventricular assist device instead of chest compressions for resuscitation after prolonged cardiac arrest: A large animal study

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Abstract

Introduction: Despite improvements in pre-hospital and post-arrest critical care, sudden cardiac arrest (CA) remains one of the leading causes of death. Improving circulation during cardiopulmonary resuscitation (CPR) may improve survival rates and long-term clinical outcomes after CA. Methods: In a porcine model, we compared standard CPR (sCPR; n =10) with CPR using an intravascular cardiac assist device without additional chest compressions (iCPR; n =10) following 10 minutes of electrically induced ventricular fibrillation (VF). In a separate crossover experiment, 10 additional pigs were subjected to 10 minutes of VF and 6 minutes of sCPR; the iCPR device was then implanted if a return of spontaneous circulation (ROSC) was not achieved using sCPR. Animals were evaluated in respect to intra- and post-arrest hemodynamics, survival, functional outcome and cerebral and myocardial lesions following CPR. We hypothesized that iCPR would result in more frequent ROSC and better functional recovery than sCPR. Results: iCPR produced a mean flow of 1.36 ± 0.02 L/min, leading to significantly higher coronary perfusion pressure (CPP) values during the early period of CPR (22 ± 10 mmHg vs. 9 ± 5 mmHg, P ≤0.01, 1 minute after start of CPR; 20 ± 11 mmHg vs. 10 ± 7 mmHg, P =0.03, 2 minutes after start of CPR), resulting in high ROSC rates (100% in iCPR vs. 50% in sCPR animals; P =0.03). iCPR animals showed significantly lower serum S100 levels at 10 and 30 minutes following ROSC (3.5 ± 0.6 ng/ml vs. 7.4 ± 3.0 ng/ml 30 minutes after ROSC; P ≤0.01), as well as superior clinical outcomes based on overall performance categories (2.9 ± 1.0 vs. 4.6 ± 0.8 on day 1; P ≤0.01). In crossover experiments, 80% of animals required treatment with iCPR after failed sCPR. Notably, ROSC was still achieved in six of the remaining eight animals (75%) after a total of 22.8 ± 5.1 minutes of ischemia. Conclusions: In a model of prolonged cardiac arrest, the use of iCPR instead of sCPR improved CPP and doubled ROSC rates, translating into improved clinical outcomes.

Figures

  • Figure 1 Photograph of the Impella 2.5 intravascular cardiopulmonar placement. (A) Photograph of the unmodified percutaneous left ventricul used in this investigation. The lower portion of the picture is a magnificatio with the tip in the left ventricle. Note that the inlet area of the pump is po ascending aorta, serving both the coronary and carotid arteries. Both pictu cardiopulmonary resuscitation.
  • Figure 2 Intravascular cardiopulmonary resuscitation device placeme cardiopulmonary resuscitation (iCPR) device (modified Impella 2.5; Abiomed depicted by fluoroscopy (Ziehm Vision; Ziehm Imaging GmbH, Nuremberg (thoracic) aorta. SG, Swan-Ganz catheter; PT, Pigtail catheter. (B) The guidew (C) Final position of the guidewire (GW) following removal of the pigtail ca the guidewire. (E) The iCPR device passes through the aortic arch. (F) Final following the removal of the guidewire. I, Inlet; O, Outlet; AO, Approximate depicted above, a 13-French sheath introducer (Impella 2.5 introducer kit 13 (Impella Controller; Abiomed) are required for placement and operation of t
  • Table 1 Hemodynamics and blood gas dataa
  • Figure 3 End-tidal carbon dioxide pressure in animals treated with intravascular cardiopulmonary resuscitation vs. standard cardiopulmonary resuscitation. End-tidal carbon dioxide pressure (etCO2) in animals treated with standard chest compression (sCPR) (n =10) or the intravascular cardiopulmonary resuscitation (iCPR) device (n =10). Data are presented as the mean ± standard error of the mean. BL, Baseline (that is, 5 minutes prior to cardiac arrest).
  • Figure 4 Standard cardiopulmonary resuscitation vs. intravascular cardiopulmonary resuscitation. Comparison of standard cardiopulmonary resuscitation (sCPR) (n =10) or intravascular cardiopulmonary resuscitation (iCPR) (n =10). Data are presented as the mean ± standard error of the mean. *P ≤0.05, comparing sCPR vs. iCPR. BL, Baseline (that is, 5 minutes prior to cardiac arrest). (A) Calculated coronary perfusion pressure (CPP). (B) Mean pulmonary artery pressure (MPAP). (C) Survival data. Animals with severe neurocognitive outcomes were killed 48 hours post-CPR (n =5) or when they were not able to stand or walk (n =1). ROSC, Return of spontaneous circulation. (D) Overall Performance Categories (OPC). OPC 1, Normal; no obvious neurologic damage; OPC 2, Moderate disability; animals being conscious and aware, standing but unable to walk; OPC 3, Severe disability; animals being neither fully aware nor unconscious, but with reaction to pain and auditory stimuli, not able to stand or walk; OPC 4, Coma; OPC 5, Death or brain death.
  • Table 2 Hemodynamics and blood gas data in crossover expe
  • Figure 5 Biomarkers. Serum values of animals treated with standard cardiopulmonary resuscitation (sCPR) (n =10) or intravascular cardiopulmonary resuscitation (iCPR) (n =10) before CPR at baseline (BL) or at 10 (PR10), 30 (PR30), 60 (PR60), or 120 (PR120) minutes following return of spontaneous circulation. Data are presented as the mean ± standard error of the mean. *Significant difference between iCPR and sCPR. (A) Myoglobin serum levels were used as a correlate of myocardial ischemia. (B) Serum S100 levels were employed as an indicator of the degree of cerebral ischemia–reperfusion injury.
  • Figure 6 Crossover experiments. Crossover experiments in ten pigs usin following failed standard CPR (sCPR). Data are presented as the mean ± sta perfusion pressure (CPP) in eight pigs that either developed no return of sp circulation (ROSC, n =6) following treatment with iCPR. Values estimated 30 following at least 2 minutes of iCPR treatment, 30 seconds prior to defibrill

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Derwall, M., Brücken, A., Bleilevens, C., Ebeling, A., Föhr, P., Rossaint, R., … Fries, M. (2015). Doubling survival and improving clinical outcomes using a left ventricular assist device instead of chest compressions for resuscitation after prolonged cardiac arrest: A large animal study. Critical Care, 19(1). https://doi.org/10.1186/s13054-015-0864-2

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