Abstract

Background: In septic shock, both oxygen delivery (DO2) and oxygen consumption (VO2) are dysfunctional. The current therapeutic regimens are geared to normalize global oxygen delivery (DO2) to tissues via goal directed therapies but mortality remains high at 10–20%.Methods: We studied cardiac index (CI), systemic vascular resistance index (SVRI), central venous oxygen saturation (ScvO2), central venous pressure (CVP), peripheral oxygen saturation (SpO2), mean blood pressure (MBP), body temperature, blood lactate, base excess and hemoglobin concentration (Hb) in a cohort of children admitted in “fluid-refractory” severe septic shock to pediatric intensive care, over 4.5-years. We calculated their 6 h global oxygen delivery (DO2) and global oxygen consumption (VO2) over the first 42 h and looked at factors associated with VO2/DO2 ratio (i.e., global oxygen extraction, gO2ER) and 28-day mortality.Results: Sixty-two children mean age (SD) 7.19 (5.44) years were studied. Fifty-seven (93%) children were sedated and mechanically ventilated and all received adrenaline or noradrenaline or both and added milrinone in 6 (9.6%). At 28 days, 9 (14.5%) were dead. The global oxygen extraction ratio (gO2ER) was consistently lower amongst the survivors and independently predicted mortality (ROC AUC = 0.75). A lactate level of 4 mmol/l or above, when associated with a concurrent metabolic acidosis predicted mortality with a sensitivity of 100% (95% CI 90.5–100) and a specificity of 67.7% (95% CI 62.2–72.9). A gO2ER of 0.48 or above on admission to the PICU was associated with death with a 66.7% sensitivity (95%CI 29.9–92.5) and 90.5% specificity (95%CI 79.3–96.8). A global O2ER of >0.48 combined with a concurrent blood lactate >4.0 mmol/l at any time within the first 42 h of therapy predicted death with a sensitivity of 63.9% (95% CI, 46.2–79.1) and specificity of 97.8% (95% CI, 95.7–99.0). A radar plot identified MBP-CVP difference, and CI as additional goals of therapy that may offer a survival benefit.Conclusions: Global O2ER of >0.48 with a concurrent blood lactate >4.0 mmol/l in children with metabolic acidosis was an independent factor associated with death in fluid resistant septic shock. Trends of gO2ER seem useful to recognize survivors and non-survivors early in the illness.

Highlights

  • In septic shock, both oxygen delivery (DO2) and oxygen consumption (VO2) are dysfunctional

  • We retrospectively studied hemodynamic variables during initial stabilization for 42 h and 28-day outcome in all children admitted from June 2009–Feb 2014 in fluid refractory septic shock to a regional 16-bed Pediatric Intensive Care Unit (PICU)

  • Vasoactive agents were used to optimize hemodynamics as per the ACCM-CPP protocol [12]. Their cardiac index (CI) and systemic vascular resistance index (SVRI) were measured approximately 6-h by an Ultrasonic Cardiac Output Monitor (USCOM model 1-A, USCOM Limited Australia http://www.uscom.com.au/) using a trans-cutaneous Doppler probe placed at the supra sternal notch [13, 14]

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Summary

Introduction

Both oxygen delivery (DO2) and oxygen consumption (VO2) are dysfunctional. The current therapeutic regimens are geared to normalize global oxygen delivery (DO2) to tissues via goal directed therapies but mortality remains high at 10–20%. Clinicians target global oxygen delivery (DO2) as the therapeutic goal with the hope of matching the supplydemand gap of oxygen during the treatment of shock. In septic shock, both oxygen delivery and oxygen consumption are dysfunctional. Higher ScvO2 can indicate improved oxygen delivery but it does not rule out continuing hypoxia [7] This is because high ScvO2 can reflect poor tissue oxygen consumption resulting from sepsis induced dysfunctional capillary perfusion and altered mitochondrial function.

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