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Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or Placebo
BACKGROUND: The effect of vasoconstrictors in prolonged cardiopulmonary resuscitation (CPR) has not been fully clarified. OBJECTIVES: To evaluate adrenaline and vasopressin pressure effect, and observe the return of spontaneous circulation (ROSC). METHODS: A prospective, randomized, blinded, and pla...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cardiologia
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4106812/ https://www.ncbi.nlm.nih.gov/pubmed/24173134 http://dx.doi.org/10.5935/abc.20130213 |
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author | Palácio, Manoel Ângelo Gomes de Paiva, Edison Ferreira de Azevedo, Luciano Cesar Pontes Timerman, Ari |
author_facet | Palácio, Manoel Ângelo Gomes de Paiva, Edison Ferreira de Azevedo, Luciano Cesar Pontes Timerman, Ari |
author_sort | Palácio, Manoel Ângelo Gomes |
collection | PubMed |
description | BACKGROUND: The effect of vasoconstrictors in prolonged cardiopulmonary resuscitation (CPR) has not been fully clarified. OBJECTIVES: To evaluate adrenaline and vasopressin pressure effect, and observe the return of spontaneous circulation (ROSC). METHODS: A prospective, randomized, blinded, and placebo-controlled study. After seven minutes of untreated ventricular fibrillation, pigs received two minutes cycles of CPR. Defibrillation was attempted (4 J/kg) once at 9 minutes, and after every cycle if a shockable rhythm was present, after what CPR was immediately resumed. At 9 minutes and every five minutes intervals, 0.02 mg/kg (n = 12 pigs) adrenaline, or 0.4 U/kg (n = 12) vasopressin, or 0.2 mL/kg (n = 8) 0.9% saline solution was administered. CPR continued for 30 minutes or until the ROSC. RESULTS: Coronary perfusion pressure increased to about 20 mmHg in the three groups. Following vasoconstrictors doses, pressure level reached 35 mmHg versus 15 mmHg with placebo (p < 0.001). Vasopressin effect remained at 15-20 mmHg after three doses versus zero with adrenaline or placebo. ROSC rate differed (p = 0.031) among adrenaline (10/12), vasopressin (6/12), and placebo (2/8). Time-to-ROSC did not differ (16 minutes), nor the number of doses previously received (one or two). There was no difference between vasoconstrictors, but against placebo, only adrenaline significantly increased the ROSC rate (p = 0.019). CONCLUSION: The vasoconstrictors initial pressure effect was equivalent and vasopressin maintained a late effect at prolonged resuscitation. Nevertheless, when compared with placebo, only adrenaline significantly increased the ROSC rate. |
format | Online Article Text |
id | pubmed-4106812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Sociedade Brasileira de Cardiologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-41068122014-07-24 Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or Placebo Palácio, Manoel Ângelo Gomes de Paiva, Edison Ferreira de Azevedo, Luciano Cesar Pontes Timerman, Ari Arq Bras Cardiol Original Articles BACKGROUND: The effect of vasoconstrictors in prolonged cardiopulmonary resuscitation (CPR) has not been fully clarified. OBJECTIVES: To evaluate adrenaline and vasopressin pressure effect, and observe the return of spontaneous circulation (ROSC). METHODS: A prospective, randomized, blinded, and placebo-controlled study. After seven minutes of untreated ventricular fibrillation, pigs received two minutes cycles of CPR. Defibrillation was attempted (4 J/kg) once at 9 minutes, and after every cycle if a shockable rhythm was present, after what CPR was immediately resumed. At 9 minutes and every five minutes intervals, 0.02 mg/kg (n = 12 pigs) adrenaline, or 0.4 U/kg (n = 12) vasopressin, or 0.2 mL/kg (n = 8) 0.9% saline solution was administered. CPR continued for 30 minutes or until the ROSC. RESULTS: Coronary perfusion pressure increased to about 20 mmHg in the three groups. Following vasoconstrictors doses, pressure level reached 35 mmHg versus 15 mmHg with placebo (p < 0.001). Vasopressin effect remained at 15-20 mmHg after three doses versus zero with adrenaline or placebo. ROSC rate differed (p = 0.031) among adrenaline (10/12), vasopressin (6/12), and placebo (2/8). Time-to-ROSC did not differ (16 minutes), nor the number of doses previously received (one or two). There was no difference between vasoconstrictors, but against placebo, only adrenaline significantly increased the ROSC rate (p = 0.019). CONCLUSION: The vasoconstrictors initial pressure effect was equivalent and vasopressin maintained a late effect at prolonged resuscitation. Nevertheless, when compared with placebo, only adrenaline significantly increased the ROSC rate. Sociedade Brasileira de Cardiologia 2013-12 /pmc/articles/PMC4106812/ /pubmed/24173134 http://dx.doi.org/10.5935/abc.20130213 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Palácio, Manoel Ângelo Gomes de Paiva, Edison Ferreira de Azevedo, Luciano Cesar Pontes Timerman, Ari Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or Placebo |
title | Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or
Placebo |
title_full | Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or
Placebo |
title_fullStr | Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or
Placebo |
title_full_unstemmed | Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or
Placebo |
title_short | Experimental Cardiac Arrest Treatment with Adrenaline, Vasopressin, or
Placebo |
title_sort | experimental cardiac arrest treatment with adrenaline, vasopressin, or
placebo |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4106812/ https://www.ncbi.nlm.nih.gov/pubmed/24173134 http://dx.doi.org/10.5935/abc.20130213 |
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