I95.8
Conditions
Interventions
Group 1: Group 1 (Anesthesia protocols on paper): invasively measured blood pressure values were documented every 5 minutes.
Group 2: Group 2 (Anesthesia protocols digital ICCA-AR): The transmission o
Sponsors
Universität Marburg Fachbereich Medizin
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who have undergone an elective minimally invasive bypass surgery using the TCRAT method at the Fulda Hospital are included in the study. Inclusion is independent of age and gender.
Exclusion criteria
Exclusion criteria: • Patients who were supposed to undergo a planned minimally invasive operation but had to switch to open surgery with sternotomy for technical or medical reasons will be excluded. • Patients for whom an emergency indication for the performance of aortocoronary bypass surgery was established will be excluded. • Patients will be excluded if they experienced unexpected complications (massive bleeding, arrhythmias) with predictable effects on circulatory stability resulting in consecutive drops in blood pressure. • Patients who showed no documented hypotensive episode requiring pharmacological intervention during TCRAT surgery will be excluded. • Inadequately legible documentation on paper or visibly inconsistent documentation will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Timing of the administration of a vasopressor for the treatment of intraoperative hypotension after its occurrence in minutes. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Number of documented hypotensive events • Duration in minutes of the hypotensive events • Duration in minutes until the start of antihypertensive therapy • Number of active ingredients used for therapy and their cumulative dosage in milligrams. | — |
Countries
Germany
Contacts
Public ContactBenedikt Schäfer
Klinikum Fulda
Outcome results
None listed