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Published on: March 23, 2018
Inadequate Oxygen Delivery During Cardiopulmonary Bypass Drives Inflammatory Reaction after Cardiac Surgery
Enrico Squiccimarro1,2, Roberto Lorusso2,3, Giuseppe Boccaforno4
1Division of Cardiac Surgery, Department of Medical and Surgical Sciences, University of Foggia, Foggia, 71122, Italy.
Objectives:
Systemic inflammatory response syndrome (SIRS) is a common complication following cardiopulmonary bypass (CPB), associated with increased mortality. We assessed the relationship between indexed oxygen delivery (DO2i) during CPB and SIRS.
Methods:
We conducted a prospective observational study at 2 institutions. The primary end-point was clinically-defined SIRS 12 hours after surgery. The secondary end-point was a composite outcome comprising death, TIA/stroke, renal replacement therapy, bleeding, mechanical circulatory support, or intensive care unit (ICU) stay >96 hours. The primary analysis modelled DO2i in multivariable logistic regression. Linearity was assessed with restricted cubic splines, knot-sensitivity, quintiles, and piecewise fits. The optimal ROC-derived threshold was explored. Patients above and below the threshold were matched 1:1 by propensity score. Structural equation modelling (SEM) assessed mediation between DO2i, SIRS, and outcomes.
Results:
Of 1154 patients screened, 908 were analysed; 221 (24.3%) developed SIRS. Median DO2i was lower in the SIRS group (274 vs 302 mL/min/m2, P < .001). DO2i was inversely associated with SIRS (aOR 0.798; 95% CI 0.750-0.850, P < .001, per +10 mL/min/m2). In the secondary analysis, DO2i ≤293 mL/min/m2 was identified as threshold (sensitivity 62%, specificity 74%). Propensity score matched 390 patient pairs, with higher SIRS incidence in the low-DO2i group (33.3% vs 14.4%; P < .001). The composite outcome occurred more frequently in the low-DO2i cohort (17.7% vs 8.2%; P < .001). SEM showed mediation by SIRS, accounting for 46.2% of the DO2i effect on outcomes (OR 1.052; 95% CI 1.036-1.067; P < .001).
Conclusions:
Low DO2i during CPB predicts SIRS and adverse outcomes. Goal-directed perfusion to reduce inflammation warrants evaluation in randomized trials.
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