An Upgrading of the Resuscitative Patterns by Utilization of the Balanced Crystalloids and Synthetic Colloids and the Non-Invasive Hemodynamic Monitoring During Burn Shock (FACT in BURNS)
Burns, Shock
About this trial
This is an interventional treatment trial for Burns focused on measuring Burned shock, Volume resuscitative patterns, Non-invasive hemodynamic monitoring
Eligibility Criteria
Inclusion Criteria:
- extensively burnt patients (age range 18-75 years) with second and third degree burns
- with TBSA above 15%
- with or without inhalation injury
Exclusion Criteria:
- patients meeting inclusion criteria but with an adverse critical prognosis from the beginning of hospitalization
- with surgically insoluble extent of burns
- dialyzed patients will be excluded
Sites / Locations
- Faculty Hospital Kralovske Vinohrady
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
LIDCO
Standard care
The extensively burnt patients (age range 18-75 years) with second and the third degree burns, with TBSA above 15%, with or without inhalation injury will be included to the study. We will compare the standard monitored and volume resuscitated group of patients with the LIDCO monitored group. We will use in the LIDCO group the continuous real-time hemodynamic monitoring through transpulmonal lithium dilution additionally. The monitor Lithium Dilution Cardiac Output (LIDCO) Plus permits, through analysis of the arterial blood pressure trace, to acquire items about CO, SVR and DO2. In fluid resuscitation, we will use a combination of the balanced crystalloids and synthetic colloids (of the middle molecular weight) in the ratio 2 ml/kg/% TBSA: 1 ml/kg/% TBSA.
We will compare the standard monitored and volume resuscitated group of patients with the LIDCO monitored group. The control group will be composed of the patients supervised in a standard way, volume resuscitated according to the Brooke or Parkland formulas.