Key result
Randomly altering cardiopulmonary bypass flow rates caused no significant changes in mean jejunal mucosal perfusion, demonstrating that autoregulation is maintained during nonpulsatile CPB.
Why the study?
Does altering cardiopulmonary bypass flow rate or administering prostacyclin affect jejunal mucosal perfusion in patients undergoing elective cardiac surgery?
RCT (n=10)
Randomly assigned
Does altering cardiopulmonary bypass flow rate or administering prostacyclin affect jejunal mucosal perfusion in patients undergoing elective cardiac surgery?
Autoregulation of intestinal mucosal perfusion is maintained during nonpulsatile cardiopulmonary bypass in humans, contrary to previous animal studies, but is lost with prostacyclin-induced vasodilation.
Intestinal autoregulation appears preserved during nonpulsatile CPB; challenges prior animal data but leaves open clinical translation.
In Brief Animal studies have suggested that autoregulation of intestinal blood flow is severely impaired during cardiopulmonary bypass (CPB). We investigated the jejunal mucosal capacity to autoregulate perfusion during nonpulsatile CPB (34°C) in 10 patients undergoing elective cardiac surgery. Changes in mean arterial blood pressure (MAP) were induced by altering the CPB flow rate randomly for periods of 3 min from 2.4 L/min/m2 to either 1.8 or 3.0 L/min/m2. Jejunal mucosal perfusion (JMP) was continuously recorded by laser Doppler flowmetry. A typical pattern of flow motion (vasomotion) was recorded in all patients during CPB. Variations in CPB flow rates caused no significant changes in mean JMP, jejunal mucosal hematocrit, or red blood cell velocity within a range of MAP from 50 ± 15 to 74 ± 16 mm Hg. The vasomotion frequency and amplitude was positively correlated with CPB flow rate. IV injections of prostacyclin (10 μg, Flolan®) blunted vasomotion and increased JMP from 192 ± 53 to 277 ± 70 (P < 0.05) perfusion units despite a reduction in MAP from 59 ± 12 to 45 ± 10 mm Hg (P < 0.05). Prostacyclin-induced vasodilation resulted in loss of mucosal autoregulation (pressure-dependent perfusion). We conclude that autoregulation of intestinal mucosal perfusion is maintained during CPB in humans. IMPLICATIONS: Hypoperfusion of the intestinal mucosa has been suggested to be an important pathogenic mechanism for development of postoperative complications after cardiac surgery. In this study, the autoregulatory response of the intestinal mucosal perfusion to variations in perfusion pressure was found to be well maintained in humans undergoing nonpulsatile cardiopulmonary bypass.
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Nygren et al. (2006) conducted an RCT in Patients undergoing elective cardiac surgery (n=10). Altered cardiopulmonary bypass (CPB) flow rate vs. 2.4 L/min/m2 was evaluated on Mean jejunal mucosal perfusion (JMP). Randomly altering cardiopulmonary bypass flow rates caused no significant changes in mean jejunal mucosal perfusion, demonstrating that autoregulation is maintained during nonpulsatile CPB.
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