Perioperative Personalized Blood Pressure Management
Blood Pressure, Intraoperative Hypotension, Postoperative Complications
About this trial
This is an interventional treatment trial for Blood Pressure focused on measuring Blood Pressure, Intraoperative Hypotension, Cardiovascular Dynamics
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 45
- American Society of Anesthesiologists physical status class (ASA) II-IV
- scheduled for elective major surgery under general anesthesia
- surgery expected to last ≥ 120 minutes
Exclusion Criteria:
- emergency surgery
- patients having liver or kidney transplantation
- laparoscopic surgery
- pregnancy
- status of post transplantation of kidney, liver, heart, or lung
- sepsis (according to current Sepsis-3 definition)
- impossibility of preoperative automated blood pressure monitoring
- MAP differences between the right and the left arm of more than 20 mmHg surgery that requires controlled hypotension
Sites / Locations
- University Hospital RWTH Aachen
- Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine, University Medical Center Hamburg-Eppendorf
Arms of the Study
Arm 1
Arm 2
Other
No Intervention
Personalized management group
Control group
Intraoperative MAP will be maintained at least at the mean nighttime MAP (assessed using preoperative automated blood pressure monitoring). If the mean nighttime MAP is below 65 mmHg, intraoperative MAP will be maintained at least at 65 mmHg.
Routine intraoperative blood pressure management with a lower intervention threshold of 65 mmHg. In contrast to the patients in the personalized management group, the individual mean nighttime MAP assessed using preoperative automated blood pressure monitoring is not taken into account and the treating anesthesiologists are blinded to the data of preoperative automated blood pressure monitoring.