Physiologic effect of repeated adrenaline (epinephrine) doses during cardiopulmonary resuscitation in the cath lab setting: A randomised porcine study

• Published in: Resuscitation Vol. 101; no. C; pp. 77 - 83
• Main Authors: Hardig, Bjarne Madsen, Götberg, Michael, Rundgren, Malin, Götberg, Matthias, Zughaft, David, Kopotic, Robert, Wagner, Henrik
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 01.04.2016; Elsevier
• Subjects: Adrenaline; Anestesi och intensivvård; Anesthesiology and Intensive Care; Animals; Arterial Pressure - drug effects; Carbon Dioxide - blood; Cardiac arrest; Cardiopulmonary Resuscitation - methods; Clinical Medicine; CPR; Emergency; Epinephrine - administration & dosage; Heart Arrest - physiopathology; Heart Arrest - therapy; Klinisk medicin; Medical and Health Sciences; Medicin och hälsovetenskap; Oxygen - blood; Random Allocation; Swine; CPR; Adrenaline; Cardiac arrest
• DOI: 10.1016/j.resuscitation.2016.01.032
• ISSN: 0300-9572; 1873-1570

This porcine study was designed to explore the effects of repetitive intravenous adrenaline doses on physiologic parameters during CPR. Thirty-six adult pigs were randomised to four injections of: adrenaline 0.02mg(kgdose)−1, adrenaline 0.03mg(kgdose)−1 or saline control. The effect on systolic, diastolic and mean arterial blood pressure, cerebral perfusion pressure (CePP), end tidal carbon dioxide (ETCO2), arterial oxygen saturation via pulse oximetry (SpO2), cerebral tissue oximetry (SctO2), were analysed immediately prior to each injection and at peak arterial systolic pressure and arterial blood gases were analysed at baseline and after 15min. In the group given 0.02mg(kgdose)−1, there were increases in all arterial blood pressures at all 4 pressure peaks but CePP only increased significantly after peak 1. A decrease in ETCO2 following peak 1 and 2 was observed. SctO2 and SpO2 were lowered following injection 2 and beyond. In the group given a 0.03mg(kgdose)−1, all ABP's increased at the first 4 pressure peaks but CePP only following 3 pressure peaks. Lower ETCO2, SctO2 and SpO2 were seen at peak 1 and beyond. In the two adrenaline groups, pH and Base Excess were lower and lactate levels higher compared to baseline as well as compared to the control. Repetitive intravenous adrenaline doses increased ABP's and to some extent also CePP, but significantly decreased organ and brain perfusion. The institutional protocol number: Malmö/Lund Committee for Animal Experiment Ethics, approval reference number: M 192-10.