PRECISION AUTOMATED CRITICAL CARE MANAGEMENT (PACC-MAN): CLOSED-LOOP CRITICAL CARE FOR THE TREATMENT OF DISTRIBUTIVE SHOCK IN A SWINE MODEL OF ISCHEMIA-REPERFUSION

• Published in: The journal of trauma and acute care surgery
• Main Authors: Ganapathy, Aravindh S, Patel, Nathan T P, Wiley, Aidan P, Lane, Magan R, Jordan, James E, Johnson, M Austin, Adams, Jason Y, Neff, Lucas P, Williams, Timothy K
• Format: Journal Article
• Language: English
• Published: United States 01.10.2023
• ISSN: 2163-0763
• DOI: 10.1097/TA.0000000000004054

Goal-directed blood pressure management in the intensive care unit can improve trauma outcomes but is labor-intensive. Automated critical care systems can deliver scaled interventions to avoid excessive fluid or vasopressor administration. We compared a first generation automated drug and fluid delivery platform, Precision Automated Critical Care Management (PACC-MAN), to a more refined algorithm, incorporating additional physiologic inputs and therapeutics. We hypothesized that the enhanced algorithm would achieve equivalent resuscitation endpoints with less crystalloid utilization in the setting of distributive shock. Twelve swine underwent 30% hemorrhage and 30 min of aortic occlusion to induce an ischemia-reperfusion injury and distributive shock state. Next, animals were transfused to euvolemia and randomized into a standardized critical care (SCC) of PACC-MAN or an enhanced version (SCC+) for 4.25 hrs. SCC+ incorporated lactate and urine output to assess global response to resuscitation and added vasopressin as an adjunct to norepinephrine at certain thresholds. Primary and secondary outcomes were decreased crystalloid administration and time at goal blood pressure, respectively. Weight-based fluid bolus volume was lower in SCC+ compared to SCC (26.9 ml/kg vs. 67.5 ml/kg, p = 0.02). Cumulative norepinephrine dose required was not significantly different (SCC+: 26.9 mcg/kg vs. SCC: 13.76 mcg/kg, p = 0.24). Three of 6 animals (50%) in SCC+ triggered vasopressin as an adjunct. Percent time spent between 60-70 mmHg, terminal creatinine and lactate, and weight-adjusted cumulative urine output were equivalent. Refinement of the PACC-MAN algorithm decreased crystalloid administration without sacrificing time in normotension, reducing urine output, increasing vasopressor support, or elevating biomarkers of organ damage. Iterative improvements in automated critical care systems to achieve target hemodynamics in a distributive-shock model are feasible. Level IIIJTACS Study Type: Therapeutic/care management.