Detection of liver dysfunction and coagulation failure in severely burned patients using non-invasive monitoring (LiMON®, FA Getinge)
- Conditions
- K72.0Acute and subacute hepatic failureT29-T32Burns and corrosions of multiple and unspecified body regions
- Registration Number
- DRKS00027883
- Lead Sponsor
- Klinik für Anästhesiologie, Intensiv- und Schmerzmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 40
– mindestens eine operative Versorgung im stationären Verlauf
– Alter > 18 Jahre
– Erstversorgung in Allgemeinanästhesie unter kontrollierter Beatmung
202 / 5 000
Fordítási találatok
– Burn > 30% body surface, grade II-IV
– at least one surgical treatment during the inpatient course
– Age > 18 years
– First aid in general anesthesia with controlled ventilation
– pregnancy
– Age < 18 years
– Refusal to participate in the study by patients or carers or survivors
– TEN/Lyell syndrome
– Primary palliative therapy concept
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The aim of the study is to investigate the correlation of ICG-PDR, classic laboratory diagnostic markers of liver synthesis and parameters of hemostasis<br>The data collected during the course of treatment with the LiMON should be compared with the classic markers of liver function or<br>damage (transaminases, cholestasis parameters, cholinesterase, total protein, etc.) that occur in the routine course of treatment. In addition, it is planned to change the previous diagnostic routine processes<br>to systematically supplement a more intensive recording of haemostaseological changes and to correlate them with<br>the ICG-PDR and with the classical laboratory chemistry. The hemostasis characterization should at least include: aPTT, INR, D-dimer, fibrinogen, antithrombin, factor XIII, protein C, protein S, factors II, V, VII, VIII, IX,<br>X and thromboelastometry (ROTEM®)<br>Based on the above investigations, a relation to the clinical course of the burn injury is to be analysed.
- Secondary Outcome Measures
Name Time Method