Does Capnography Prevent Hypoxemia During Endoscopic Retrograde Cholangiopancreatography and Endoscopic Ultrasound?
Hypoxemia
About this trial
This is an interventional prevention trial for Hypoxemia focused on measuring Hypoxemia, Capnography, Apnea, Sedation, ERCP, EUS
Eligibility Criteria
Inclusion Criteria:
- Adults age 18 or greater
- Subjects undergoing elective ERCP and EUS
- ASA class 1-3
- Inpatient and outpatient
- Able to give informed consent
Exclusion Criteria:
- ASA Class 4 and 5
- Emergent procedures
- Procedures requiring MAC sedation
- Subjects unable to give informed consent
- Subjects on oxygen before procedure
- Subjects on CPAP/BiPAP
- Allergies to fentanyl/demerol/midazolam
Sites / Locations
- Cleveland Clinic Foundation
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Capnography
Standard Monitoring
Capnography: Subjects randomized to capnography-titration arm: The endoscopy team would be made aware of the capnographic abnormalities as they arise. In this arm, the endoscopy team will have the graphic representation of respiratory activity (capnography) as well as end-epxiratory levels of carbon dioxide in addition to the normal physiologic monitoring portfolio of pulse oximetry, blood pressure and electrocradiography. This observation phase would take place for a baseline prior to sedation, during the administration of sedation as well as throughout the procedure. Monitoring for the study would stop upon completion of the endoscopic procedure.
Subjects randomized to capnography-blinded arm: In this arm, the endoscopy team will not have the graphic representation of respiratory activity (capnography) as well as end-expiratory levels of carbon dioxide available. Only a standard of care physiologic monitoring portfolio of pulse oximetry, blood pressure and electrocradiography at the disposal of the endoscopy team to titrate the sedative medications.