The purpose of the research (pilot study) is to determine the impact of the use of the autotransfusion device on hemodynamic parameters during resuscitation. 24 people will be included in the pilot study (12 people will be included in the intervention group - with the usage of "autotransfusion socks" during resuscitation and 12 people in the control group - without "autotransfusion socks"). Investigators will compare the hemodynamic parameters and also neurological outcome between both groups.
The purpose of the research (pilot study) is to determine the impact of the use of the autotransfusion device on hemodynamic parameters during resuscitation. Out-of-hospital cardiac arrest (OHCA) is one of the leading causes of death in Europe. In order to improve the hemodynamic parameters during resuscitation, device for autotransfusion was developed. Devices are basically a very strong elastic stockings that also block arterial circulation. While "putting on" stockings, blood is being squeezed from the lower extremities (approximately 500 ml of blood for each lower limb). With blood being squeezed from the lower limb into the central circulation the filling of the heart is being improved; thus the device will improve the preload and also cardiac output. A study done on an animal model showed that during resuscitation using "autotransfusion socks" increases both systolic and diastolic blood pressure during resuscitation, the perfusion of the coronary arteries improves and also the values of the partial pressure of carbon dioxide increases.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
24
The HemaShock is a tight silicone ring attached to a pressure stocking. It comes wrapped into a doughnut and has a set of handles. The operator simply puts the doughnut over the foot or hand, and pulls on the handles to unravel the HemaShock while applying pressure throughout the appendage. The device displace blood from limbs to central blood system, thus improving preload and cardiac output.
Maribor University Medical Centre
Maribor, Maribor City Municipality, Slovenia
Community health center Maribor, Prehospital unit
Maribor, Slovenia
Blood pressure
Non-invasive blood pressure (both systolic and diastolic blood pressure) will be measured.
Time frame: Immediately after arrival to the victim
End tidal CO2 (Carbon dioxide) after intubation
capnography
Time frame: Immediately after an intubation
End tidal CO2 (Carbon dioxide) after application of Hemashock Socks
capnography
Time frame: Immediately after an application of Hemashock Socks
End tidal CO2 (Carbon dioxide) every 5 minutes after first application of Hemashock Socks
capnography
Time frame: 5 minutes after the first application of HemaShock socks
End tidal CO2 (Carbon dioxide) every 5 minutes after first application of Hemashock Socks
capnography
Time frame: 10 minutes after the first application of HemaShock socks
End tidal CO2 (Carbon dioxide) every 5 minutes after first application of Hemashock Socks
capnography
Time frame: 15 minutes after the first application of HemaShock socks
End tidal CO2 (Carbon dioxide) every 5 minutes after first application of Hemashock Socks
capnography
Time frame: 20 minutes after the first application of HemaShock socks
End tidal CO2 (Carbon dioxide) every 5 minutes after first application of Hemashock Socks
capnography
Time frame: 25 minutes after the first application of HemaShock socks
End tidal CO2 (Carbon dioxide) every 5 minutes after first application of Hemashock Socks
capnography
Time frame: 30 minutes after the first application of HemaShock socks
End tidal CO2 (Carbon dioxide) after removal of HemaShock Socks
capnography
Time frame: Immediately after the removal of HemaShock socks
Blood pressure
Noninvasive blood pressure ((both systolic and diastolic blood pressure)) after removal of HemaShock Socks
Time frame: Immediately after ROSC
Cerebral Performance Category Scale
Neurological outcome assessed with Cerebral Performance Category Scale (CPC). CPC 1-2 means good outcome, CPC 3-5 means poor outcome.
Time frame: Through study completion, an average of 1 year
Tissue/skin malfunction under HemaShock Socks
Irrigation, oedema, tissue malperfusion
Time frame: From removal of the HemaShock socks up to 15 weeks
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