Fluid Resuscitation Optimization in Surgical Trauma Patients (FROST) (FROST)
Critical Illness, Trauma
About this trial
This is an interventional treatment trial for Critical Illness focused on measuring Trauma, Minimally Invasive Hemodynamic Monitoring, Perioperative, Complications, Hemodynamics, Operative procedures
Eligibility Criteria
Inclusion Criteria:
- 18 years of age or older
- Injury Severity Score > 15 (indicator of anticipated trauma mortality)
- Admission to Surgical-Trauma ICU (STICU)
- Anticipated surgery within 72 hours of admission
- American Society of Anesthesiology patient classification status (ASA) 2-5
- Lactic acid > 2.5 within 24 hours of surgical procedure or Base deficit ≥ - 5 mmol/L, or persistent requirement for vasopressor support within 24 hours of surgical procedure
- Patient requires mechanical ventilation prior to consenting surgery
- Vascular devices that include a minimum of an arterial line
- Minimally invasive hemodynamic monitoring initiated prior to first surgical procedure unless patient is taken emergently, e.g. OR from trauma bay
- Patients requiring emergent initial operative procedures will be eligible for consenting if above criteria are met prior to their second surgical procedure
Anticipated operative procedure precipitating evaluation and/or consenting for study must be > 30 minutes in duration
- Procedures < 30 minutes would not result in significant metabolic stress necessitating a continuation of MIHM
Exclusion Criteria:
- Pregnancy
Exclusions due to limitations with respect to accuracy of MIHM:
- Patients not intubated prior to surgical procedure
- Patients requiring an open thoracotomy
- Patients with known history of surgical intervention for peripheral vascular disease
- Patients with pre-existing atrial arrhythmias
- Patients who are on cardiopulmonary bypass
Isolated acute cerebral injury and/or traumatic cerebral injury
- Hemodynamic management in this patient population does not always follow typical/standard endpoints due to nuances of managing intracranial pressures
- Cardiac arrest prior to enrollment
Patients with pre-existing, dialysis dependent, renal failure upon admission
- Hemodynamic management in this patient population does not always follow typical/standard endpoints due to nuances of managing renal failure
Patients with pre-existing cirrhosis
- Hepatic failure results in abnormal clearance of lactic acid
- Patients with no survival injuries, e.g. gunshot wound to the head
Sites / Locations
- Charleston Area Medical Center, General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
FloTrac™ and EV1000™ pre and post-operatively
FloTrac™ and EV1000™ peri-operatively
Cardiovascular management guided by minimally invasive hemodynamic monitoring via FloTrac™ and EV1000™ will be utilized in the pre and post-operative period in the control arm.
Cardiovascular management guided by minimally invasive hemodynamic monitoring via FloTrac™ and EV1000™ will be utilized in the perioperative period for the intervention arm