About this trial
Pulse pressure variation is a monitoring index that indicates the response to fluid therapy in patients receiving mechanical ventilation, and is used as a reference for patients with unstable hemodynamic conditions. However, it is invasive because it requires arterial puncture to collect it. In a previous study by the investigators, the investigators developed and verified an artificial intelligence model that predicts stroke volume variation, in real time using only the central venous pressure waveform. However, since a large vein such as the jugular vein must be punctured to collect the central venous pressure waveform, it is still invasive, and its clinical utility is low. Therefore, in this study, the investigators collected waveforms from peripheral veins that are less invasive and can be a wide range of applications because all surgical patients have them. The investigators aimed to develop and verify an artificial intelligence model that predicts pulse pressure variation obtained from peripheral venous waveforms .
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients who voluntarily agreed and signed the written informed consent form before participating in this study
Adult aged 19 years or older
American Society of Anesthesiologists physical class (ASA) 1-3
Patients scheduled for elective hepatectomy under general anesthesia
Disqualifiers
Patients with abnormal findings on electrocardiogram before surgery
Patients who cannot undergo peripheral venous puncture
Trial population
Patients scheduled for elective hepatectomy under general anesthesia
Trial design
Cohort
Prospective
Treatments tested in this trial
peripheral waveform collection
Other interventionThe peripheral venous pressure waveform is collected by connecting a pressure transducer that is currently in use to the placed central venous line. In addition, the pulse pressure variation or stroke volume variation value that can be obtained from the arterial catheter. This extracts the medical records and bio-signal information of the subjects registered through the previously approved 'Establishment of a Bio-signal and Clinical Information Registry for the Development of Patient Monitoring Algorithm' study (B-2202-738-401).
Treatment groups
Trial outcomes
Primary outcomes
Pulse pressure variation
from arterial waveform
Sponsors and contacts
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