A randomized comparison of manual, mechanical and high-impulse chest compression in a porcine model of prolonged ventricular fibrillation

Resuscitation. 2006 Jun;69(3):495-501. doi: 10.1016/j.resuscitation.2005.09.026. Epub 2006 Mar 24.

Abstract

Background: Elevated coronary perfusion pressure (CPP) during CPR is associated with return of spontaneous circulation (ROSC). We compared CPP achieved with three methods of chest compression: manual (MAN), mechanical (MECH) and high-impulse mechanical (HI) in a porcine model of prolonged ventricular fibrillation (VF). We hypothesized that HI (very rapid acceleration of the down-stroke) would produce greater CPPs than MAN or MECH, and that HI would also produce a higher rate of ROSC.

Methods: Twenty-eight domestic swine (mean 27.8 kg) were randomly assigned to three methods of chest compression. Animals were instrumented under anesthesia, and VF was induced and untreated for 8 min. After 2 min of CPR, epinephrine (adrenaline) (0. 1 mg/kg), vasopressin (40 U) and propranolol (1.0 mg) were administered. CPR continued for three more minutes, after which up to three rescue shocks were delivered. CPP was determined in an automated fashion by measuring the difference between aortic and right atrial pressures 0.1s prior to the down-stroke of each compression (i.e. end-relaxation). ROSC was defined as a systolic pressure greater than 80 mmHg sustained for at least 1 min. We analyzed CPP and ROSC using repeated measures ANOVA and Fisher's exact test.

Results: Over the 5 min of CPR, CPP increased more with HI compression than with MAN compression (p=0.017). ROSC was attained in 4/9 MAN, 6/9 MECH and 10/10 HI (HI versus MAN p=0.01).

Conclusions: Over the course of CPR, HI compression increased CPP more than MAN compression. HI compression produced a significantly higher rate of ROSC than MAN, but not MECH compression.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Agonists / administration & dosage
  • Adrenergic alpha-Agonists / pharmacology
  • Adrenergic beta-Antagonists / administration & dosage
  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Cardiopulmonary Resuscitation / methods*
  • Cerebrovascular Circulation / physiology
  • Coronary Circulation / physiology*
  • Disease Models, Animal
  • Epinephrine / pharmacology
  • Perfusion
  • Pressure / adverse effects
  • Propranolol / administration & dosage
  • Propranolol / pharmacology
  • Random Allocation
  • Reference Values
  • Regional Blood Flow
  • Sus scrofa
  • Thoracic Wall / physiopathology
  • Time Factors
  • Vasoconstrictor Agents / administration & dosage
  • Vasoconstrictor Agents / pharmacology
  • Vasopressins / administration & dosage
  • Vasopressins / pharmacology
  • Ventricular Fibrillation / physiopathology*

Substances

  • Adrenergic alpha-Agonists
  • Adrenergic beta-Antagonists
  • Vasoconstrictor Agents
  • Vasopressins
  • Propranolol
  • Epinephrine