The purpose of this study is to evaluate PPI as a surrogate for clinical signs of peripheral perfusion in patients in septic shock and after cardiac surgery.
The aim of this study is to validate PPI as a continuous, objective measurement of peripheral perfusion indicated by clinical sings of tissue perfusion in patients with septic shock. Furthermore, PPI shall be compared to the perfusion of solid organs evaluated by ultrasound of liver, kidney and gut. In a group of healthy volunteers the investigators will determine normal values in ambient temperature and after cooling of an extremity. Another group of patients after cardiac surgery, where usually a poor tissue perfusion without metabolic failure is present will serve as another "control" population in their post-surgery stabilization period. The values from healthy volunteers and cardiac surgery patients will be compared to those of patients in septic shock.
Study Type
OBSERVATIONAL
Enrollment
100
Peripheral Perfusion index measured with pulse-oximetry by Carescape Patientenmonitor
Bern University Hospital
Bern, Switzerland
peripheral perfusion index
PPI in healthy controls, septic shock patients and patients rewarming after cardiac surgery
Time frame: measurement at ICU admission and hourly till extubation or normalization of lactate, during the hospitalization without follow-up (maximal up to 72h)
capillary refill time
CRT in healthy controls, septic shock patients and patients rewarming after cardiac surgery
Time frame: measurement at ICU admission and hourly till extubation or normalization of lactate, during the hospitalization without follow-up (maximal up to 72h)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.