Objective
Pulmonary dysfunction is a common complication in patients undergoing heart surgery. Current clinical practice does not include any specific strategy for lung protection. To compare the anti‐inflammatory effects of low‐frequency ventilation (LFV), as measured by nuclear factor κ‐light‐chain‐enhancer of activated B cells (NF‐κB) p65 pathway activation, for the entire cardiopulmonary bypass (CPB) vs both lungs left collapsed in patients undergoing coronary artery bypass grafting (CABG).
Methods
Two groups parallel randomized controlled trial. The primary outcome was inflammation measured by NF‐κB p65 activation in pre‐ and post‐CPB lung biopsies. Secondary outcomes were additional inflammatory markers in both biopsy tissue and blood.
Results
Thirty‐seven patients were randomly allocated to LFV (18) and to both lungs left collapsed (19). The mean concentration of NF‐κB p65 in the biopsies before chest closure (adjusted for pre‐CPB concentration) was higher in the LFV group compared to both lungs left collapsed group but this was not significant (0.102, 95% confidence interval, −0.022 to 0.226, P = 0.104). There were no significant differences between groups in the other inflammatory markers measured in tissue and blood.