TY - JOUR
T1 - Acute hemodynamic changes during lung recruitment in lavage and endotoxin-induced ALI
AU - Odenstedt, Helena
AU - Åneman, Anders
AU - Kárason, Sigurbergur
AU - Stenqvist, Ola
AU - Lundin, Stefan
PY - 2005/1
Y1 - 2005/1
N2 - Objective: To assess acute cardiorespiratory effects of recruitment manoeuvres in experimental acute lung injury. Design: Experimental study in animal models of acute lung injury. Setting: Experimental laboratory at a University Medical Centre. Animals: Ten pigs with bronchoalveolar lavage and eight pigs with endotoxin-induced ALI. Interventions: Two kinds of recruitment manoeuvres during 1 min; a) vital capacity manoeuvres (ViCM) consisting in a sustained inflation at 30 cmH2O and 40 cmH2O; b) manoeuvres obtained during ongoing pressure-controlled ventilation (PCRM) with peak airway pressure 30 cmH2O, positive end-expiratory pressure (PEEP) 15 and peak airway pressure 40, PEEP 20. Recruitment manoeuvres were repeated after volume expansion (dextran 8 ml/kg). Oxygenation, mean arterial, and pulmonary artery pressures, aortic, mesenteric, and renal blood flow were monitored. Measurements and results: Lower pressure recruitment manoeuvres (ViCM30 and PCRM30/15) did not significantly improve oxygenation. With ViCM and PCRM at peak airway pressure 40 cmH2O, PaO2 increased to similar levels in both lavage and endotoxin groups. Aortic blood flow was reduced from baseline during PCRM40/20 and ViCM40 by 57±3% and 61±6% in the lavage group and by 57±8% and 82±7% (P<0.05 vs PCRM40/20) in endotoxin group. The decrease in blood pressure was less pronounced. Prior volume expansion attenuated circulatory impairment. After cessation of recruitment hemodynamic parameters were restored within 3 min. Conclusion: Effective recruitment resulted in systemic hypotension, pulmonary hypertension, and decrease in aortic blood flow especially in endotoxinemic animals. Circulatory depression may be attenuated using recruitment manoeuvres during ongoing pressure-controlled ventilation and by prior volume expansion.
AB - Objective: To assess acute cardiorespiratory effects of recruitment manoeuvres in experimental acute lung injury. Design: Experimental study in animal models of acute lung injury. Setting: Experimental laboratory at a University Medical Centre. Animals: Ten pigs with bronchoalveolar lavage and eight pigs with endotoxin-induced ALI. Interventions: Two kinds of recruitment manoeuvres during 1 min; a) vital capacity manoeuvres (ViCM) consisting in a sustained inflation at 30 cmH2O and 40 cmH2O; b) manoeuvres obtained during ongoing pressure-controlled ventilation (PCRM) with peak airway pressure 30 cmH2O, positive end-expiratory pressure (PEEP) 15 and peak airway pressure 40, PEEP 20. Recruitment manoeuvres were repeated after volume expansion (dextran 8 ml/kg). Oxygenation, mean arterial, and pulmonary artery pressures, aortic, mesenteric, and renal blood flow were monitored. Measurements and results: Lower pressure recruitment manoeuvres (ViCM30 and PCRM30/15) did not significantly improve oxygenation. With ViCM and PCRM at peak airway pressure 40 cmH2O, PaO2 increased to similar levels in both lavage and endotoxin groups. Aortic blood flow was reduced from baseline during PCRM40/20 and ViCM40 by 57±3% and 61±6% in the lavage group and by 57±8% and 82±7% (P<0.05 vs PCRM40/20) in endotoxin group. The decrease in blood pressure was less pronounced. Prior volume expansion attenuated circulatory impairment. After cessation of recruitment hemodynamic parameters were restored within 3 min. Conclusion: Effective recruitment resulted in systemic hypotension, pulmonary hypertension, and decrease in aortic blood flow especially in endotoxinemic animals. Circulatory depression may be attenuated using recruitment manoeuvres during ongoing pressure-controlled ventilation and by prior volume expansion.
KW - Acute lung injury
KW - Bronchoalveolar lavage
KW - Endotoxin
KW - Hemodynamics
KW - Lung recruitment
KW - Oxygen delivery
UR - http://www.scopus.com/inward/record.url?scp=12944298288&partnerID=8YFLogxK
U2 - 10.1007/s00134-004-2496-x
DO - 10.1007/s00134-004-2496-x
M3 - Article
C2 - 15605230
AN - SCOPUS:12944298288
SN - 0342-4642
VL - 31
SP - 112
EP - 120
JO - Intensive Care Medicine
JF - Intensive Care Medicine
IS - 1
ER -