Literature DB >> 21458138

Correlations between hemodynamic, oxygenation and tissue perfusion parameters during asphyxial cardiac arrest and resuscitation in a pediatric animal model.

Jesús López-Herce1, Bárbara Fernández, Javier Urbano, Santiago Mencía, Maria José Solana, Jimena Del Castillo, Antonio Rodríguez-Núñez, Jose María Bellón, Angel Carrillo.   

Abstract

AIM: To analyze the correlations between hemodynamic, oxygenation and tissue perfusion values in an infant animal model of asphyctic cardiac arrest (ACA).
METHODS: A prospective observational animal study was performed in seventy one, two month-old piglets. CA was induced by removal of mechanical ventilation and was followed by advanced life support after at least 10 min. Correlations between hemodynamic [heart rate (HR), mean arterial pressure (MAP), cardiac index (CI), stroke volume index (SVI) and intrathoracic blood index (ITBI) measured by PiCCO method], blood gas values (arterial and central venous saturation), and tissue perfusion values [intramucosal gastric pH (pHi), and tissue oxygenation (cerebral and renal saturation)] were analyzed during asphyxia, resuscitation and after return of spontaneous circulation (ROSC).
RESULTS: Among global hemodynamic parameters, the only moderate significant correlation observed was between CI and ITBI (r = .551). Among tissue oxygenation/perfusion values, a moderate to good significant correlation (r = .460-.763) between arterial oxygen saturation, central venous, renal and cerebral oxygen saturation was observed. Lactic acid, potassium (K) and pHi were correlated (r = .561-.639), but no correlation was found between them and tissue oxygenation parameters. Global hemodynamic parameters (CI, HR, MAP) did not correlate with renal and cerebral saturations and tissue perfusion parameters.
CONCLUSIONS: During ACA and after ROSC global hemodynamic parameters do not correlate with oxygenation and tissue perfusion values. Additional studies which assess the potential usefulness of tissue oxygenation/perfusion parameters during cardiac arrest and ROSC are needed.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21458138     DOI: 10.1016/j.resuscitation.2011.02.013

Source DB:  PubMed          Journal:  Resuscitation        ISSN: 0300-9572            Impact factor:   5.262


  5 in total

1.  Combined Cerebral and Renal Near-Infrared Spectroscopy After Congenital Heart Surgery.

Authors:  Javier Gil-Anton; Silvia Redondo; Diego Garcia Urabayen; Manuel Nieto Faza; Irene Sanz; Javier Pilar
Journal:  Pediatr Cardiol       Date:  2015-03-13       Impact factor: 1.655

2.  Enhanced external counterpulsation improves cardiac function in Beagles after cardiopulmonary resuscitation.

Authors:  Jing Xiong; Wei Zhang; Hongyan Wei; Xin Li; Gang Dai; Chunlin Hu
Journal:  Braz J Med Biol Res       Date:  2020-01-13       Impact factor: 2.590

3.  Determinants of venous return in steady-state physiology and asphyxia-induced circulatory shock and arrest: an experimental study.

Authors:  Athanasios Chalkias; Eleni Laou; Nikolaos Papagiannakis; Giolanda Varvarousi; Dimitrios Ragias; Anastasios Koutsovasilis; Demosthenes Makris; Dimitrios Varvarousis; Nicoletta Iacovidou; Ioannis Pantazopoulos; Theodoros Xanthos
Journal:  Intensive Care Med Exp       Date:  2022-04-12

4.  Cerebral hemodynamic response during the resuscitation period after hypoxic-ischemic insult predicts brain injury on day 5 after insult in newborn piglets.

Authors:  Yasuhiro Nakao; Shinji Nakamura; Yinmon Htun; Tsutomu Mitsuie; Kosuke Koyano; Kenichi Ohta; Yukihiko Konishi; Takanori Miki; Masaki Ueno; Takashi Kusaka
Journal:  Sci Rep       Date:  2022-08-01       Impact factor: 4.996

5.  Different Respiratory Rates during Resuscitation in a Pediatric Animal Model of Asphyxial Cardiac Arrest.

Authors:  Jorge López; Sarah N Fernández; Rafael González; María J Solana; Javier Urbano; Jesús López-Herce
Journal:  PLoS One       Date:  2016-09-12       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.