R57.9 R96.0 I95
Conditions
Interventions
Group 1: Interventional group: Intra arterial blood pressure
Group 2: Control group: Non invasive blood pressure
Sponsors
Universitätsklinikum des Saarlandes
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Study group: Indication for usage of intra arterial blood pressure is out-of-hospital intubation or refractive hypotension (estimated one time catecholamine administration without effect or intial volume administration estimated higher than 1000 ml) Control group: Indication for usage of intra arterial blood pressure is out-of-hospital intubation or refractive hypotension (estimated one time catecholamine administration without effect or intial volume administration estimated higher than 1000 ml). Patients brought to the hospital with an emergency physician and administration in context of an anaesthesiology protocol including interventional areas such as e.g. OR, ICU. Also patients with indication according to study group without intervention.
Exclusion criteria
Exclusion criteria: < 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in shock index measured from out-of-hospital until administration as well as 72h mortality | — |
Secondary
| Measure | Time frame |
|---|---|
| Out-of-hospital catecholamine administered, out-of-hospital volume administered, detection of hypotension out-of-hospital, BGA, pH, Lac, BE, hemodialysis, CPC, brain edema, stroke, cardiac events in 72h after administration (TropT, NT-proBNP, TropI, arrhythmia, acute heart failure), renal parameters in 72h after administration (serum creatinine, serum urea, BGA, pH, potassium, BE, Cystatine C, eGFR using CDK-EPI), urine volume in 72h after administration | — |
Countries
Germany
Contacts
Public ContactThomas Volk
Universitätsklinikum des Saarlandes Institut für Anästhesiologie, Intensiv- und Schmerzmedizin
Outcome results
None listed