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Algorithm Predicting Intraoperative Changes in Cardiac Output Using Capnography

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Samsung Medical Center

Status

Enrolling

Conditions

General Anesthesia Using Endotracheal Intubation

Treatments

Other: No Intervention: Observational Cohort

Study type

Observational

Funder types

Other

Identifiers

NCT07061548
SMC2025-06-120-001

Details and patient eligibility

About

Conventional monitoring of cardiac output requires an invasive procedure and an additional device, which can lead to increased risk and cost. Investigators developed an artificial intelligence algorithm to predict intraoperative changes in cardiac output using capnography in patients undergoing surgery under general anesthesia.

Full description

Anesthesiologists strive to maintain adequate cardiac output during surgery. However, conventional monitoring of cardiac output requires an invasive procedure (risk) and an additional device (cost).

Because most surgeries are performed without any invasive monitors, anesthesiologists must manage the patients without cardiac output information.

However, modern anesthesia machines usually provide capnography, and continuous capnography monitoring can help estimate changes in cardiac output. Therefore, investigators aim to develop an artificial intelligence algorithm to predict intraoperative changes in cardiac output using capnography in patients undergoing surgery under general anesthesia.

Investigators train a model using capnography data (5-minute duration) related to a 20% or greater decrease in cardiac output during the same period. The developed model can provide an alarm for a decrease in cardiac output based on the change in capnography.

Enrollment

2,005 estimated patients

Sex

All

Ages

19 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective surgery under general anesthesia
  • Adult patients (18 < age < 76)
  • Patients who were monitored invasive arterial blood pressure (waveform) and capnography (numeric)

Exclusion criteria

  • Emergency surgery
  • Cardiovascular and thoracic surgery
  • Known Asthma and Chronic obstructive pulmonary disease (COPD)
  • Preoperative pulmonary function test (PFT) abnormality over moderate grade
  • Intraoperative monitoring duration less than 30 minutes

Trial design

2,005 participants in 1 patient group

capnography-cardiac output cohort
Description:
Adult patients who underwent surgery under general anesthesia with capnography and invasive arterial blood pressure monitor
Treatment:
Other: No Intervention: Observational Cohort

Trial contacts and locations

1

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Central trial contact

Heejoon Jeong, MD

Data sourced from clinicaltrials.gov

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