None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients undergoing sedative gastroscopy; 2. Age 18-65 years old. 3. ASA classification I-III; 4. BMI 30kg/m^2-40 kg/m^2; 5. Interincisal distance >6.5cm, no micrognathia, limited mouth opening and limited cervical spine movement; 6. Compliance with ethics, patient willing to participate in the trial, signed informed consent form;
Exclusion criteria
Exclusion criteria: 1. Contraindications for endoscopic procedures or patients refusing sedation/anesthesia. 2. Patients with allergies to propofol, eggs, soybeans, or milk. 3. Patients with gastrointestinal obstruction and gastric emptying disorders. 4. Patients with acute pharyngitis, tonsillitis, and upper respiratory tract infections. 5. Patients with acute exacerbations of respiratory diseases such as asthma, bronchitis, and COPD. 6. Patients with acute arrhythmias and severe heart disease (congenital, valvular disease). 7. Patients requiring replacement therapy for severe liver or kidney dysfunction. 8. Patients with severe mental illnesses requiring medication to control symptoms. 9. Patients with moderate to severe anemia, coagulation disorders, and hematological diseases. 10. Patients with severe nasal congestion caused by nasal cavity lesions. 11. Pregnant and lactating patients.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of hypoxia in obese patients undergoing sedative gastroscopy using HFNC 30L/min, 50L/m; | — |
Secondary
| Measure | Time frame |
|---|---|
| Airway interventions (jaw lift , increasing oxygen flow, mask ventilation, intubation);Occurrence of adverse reactions other than hypoxia (body movements, vomiting, reflux, bronchospasm,;occurrence of respiratory depression and severe hypoxia; | — |
Countries
China
Contacts
NanJing First Hospital