TY - JOUR
T1 - Brain oxygen and metabolism during circulatory arrest with intermittent brief periods of low-flow cardiopulmonary bypass in newborn piglets
AU - Schultz, Steven
AU - Antoni, Diego
AU - Shears, Gregory
AU - Markowitz, Scott
AU - Pastuszko, Peter
AU - Greeley, William
AU - Wilson, David F.
AU - Pastuszko, Anna
N1 - Funding Information:
Supported by United States National Institutes of Health grants NS-31465 and HD041484.
PY - 2006/10
Y1 - 2006/10
N2 - Objective: We performed this study to determine whether brief intermittent periods of low-flow cardiopulmonary bypass during deep hypothermic circulatory arrest would improve cortical metabolic status and prolong the "safe" time of deep hypothermic circulatory arrest. Methods: After a 2-hour baseline, newborn piglets were placed on cardiopulmonary bypass and cooled to 18°C. The animals were then subjected to 80 minutes of deep hypothermic circulatory arrest interrupted by 5-minute periods of low-flow cardiopulmonary bypass at either 20 mL · kg-1 · min-1 (LF-20) or 80 mL · kg-1 · min-1 (LF-80) during 20, 40, 60, and 80 minutes of deep hypothermic circulatory arrest. All animals were rewarmed, separated from cardiopulmonary bypass, and maintained for 2 hours (recovery). The oxygen pressure in the cerebral cortex was measured by the quenching of phosphorescence. The extracellular dopamine level in the striatum was determined by microdialysis. Results are means ± SD. Results: Prebypass oxygen pressure in the cerebral cortex was 65 ± 7 mm Hg. During the first 20 minutes of deep hypothermic circulatory arrest, cortical oxygen pressure decreased to 1.3 ± 0.4 mm Hg. Four successive intermittent periods of LF-20 increased cortical oxygen pressure to 6.9 ± 1.2 mm Hg, 6.6 ± 1.9 mm Hg, 5.3 ± 1.6 mm Hg, and 3.1 ± 1.2 mm Hg. During the intermittent periods of LF-80, cortical oxygen pressure increased to 21.1 ± 5.3 mm Hg, 20.6 ± 3.7 mm Hg, 19.5 ± 3.95 mm Hg, and 20.8 ± 5.5 mm Hg. A significant increase in extracellular dopamine occurred after 45 minutes of deep hypothermic circulatory arrest alone, whereas in the groups of LF-20 and LF-80, the increase in dopamine did not occur until 52.5 and 60 minutes of deep hypothermic circulatory arrest, respectively. Conclusions: The protective effect of intermittent periods of low-flow cardiopulmonary bypass during deep hypothermic circulatory arrest is dependent on the flow rate. We observed that a flow rate of 80 mL · kg-1 · min-1 improved brain oxygenation and prevented an increase in extracellular dopamine release.
AB - Objective: We performed this study to determine whether brief intermittent periods of low-flow cardiopulmonary bypass during deep hypothermic circulatory arrest would improve cortical metabolic status and prolong the "safe" time of deep hypothermic circulatory arrest. Methods: After a 2-hour baseline, newborn piglets were placed on cardiopulmonary bypass and cooled to 18°C. The animals were then subjected to 80 minutes of deep hypothermic circulatory arrest interrupted by 5-minute periods of low-flow cardiopulmonary bypass at either 20 mL · kg-1 · min-1 (LF-20) or 80 mL · kg-1 · min-1 (LF-80) during 20, 40, 60, and 80 minutes of deep hypothermic circulatory arrest. All animals were rewarmed, separated from cardiopulmonary bypass, and maintained for 2 hours (recovery). The oxygen pressure in the cerebral cortex was measured by the quenching of phosphorescence. The extracellular dopamine level in the striatum was determined by microdialysis. Results are means ± SD. Results: Prebypass oxygen pressure in the cerebral cortex was 65 ± 7 mm Hg. During the first 20 minutes of deep hypothermic circulatory arrest, cortical oxygen pressure decreased to 1.3 ± 0.4 mm Hg. Four successive intermittent periods of LF-20 increased cortical oxygen pressure to 6.9 ± 1.2 mm Hg, 6.6 ± 1.9 mm Hg, 5.3 ± 1.6 mm Hg, and 3.1 ± 1.2 mm Hg. During the intermittent periods of LF-80, cortical oxygen pressure increased to 21.1 ± 5.3 mm Hg, 20.6 ± 3.7 mm Hg, 19.5 ± 3.95 mm Hg, and 20.8 ± 5.5 mm Hg. A significant increase in extracellular dopamine occurred after 45 minutes of deep hypothermic circulatory arrest alone, whereas in the groups of LF-20 and LF-80, the increase in dopamine did not occur until 52.5 and 60 minutes of deep hypothermic circulatory arrest, respectively. Conclusions: The protective effect of intermittent periods of low-flow cardiopulmonary bypass during deep hypothermic circulatory arrest is dependent on the flow rate. We observed that a flow rate of 80 mL · kg-1 · min-1 improved brain oxygenation and prevented an increase in extracellular dopamine release.
UR - http://www.scopus.com/inward/record.url?scp=33748758739&partnerID=8YFLogxK
U2 - 10.1016/j.jtcvs.2006.06.025
DO - 10.1016/j.jtcvs.2006.06.025
M3 - Article
C2 - 17000295
AN - SCOPUS:33748758739
SN - 0022-5223
VL - 132
SP - 839
EP - 844
JO - Journal of Thoracic and Cardiovascular Surgery
JF - Journal of Thoracic and Cardiovascular Surgery
IS - 4
ER -