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Determining the possibility of difficult intubation in adult patients to be applied to general anesthesia with obstructive sleep apnea screening tests

Comparison of the effectiveness of obstructive sleep apnea screening tests in determining the possibility of difficult intubation in adult patients to be applied to general anesthesia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12625000276459
Enrollment
230
Registered
2025-04-10
Start date
2021-02-15
Completion date
2021-05-03
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Our aim in this study is to use OSA non-invasive screening tests (STOP-Bang Test, No-Apnea Test, NoSAS Test, OSA-50 Test, DES-OSA Score, P-SAP Score, GOAL Questionnaire, SPOSA Score, Epworth Sleepiness Questionnaire) to determine their use values and compare their effectiveness.This prospective observational study was conducted on a total of 230 ASA I-III patients aged 18 years and older who underwent non-cardiac elective surgery under general anesthesia at Health Sciences University Ankara Training and Research Hospital. Age, gender, body weight, height, BMI (body mass index) and ASA value were recorded in the preoperative evaluation of all patients. For anthropometric measurements, thyromental distance, neck circumference, waist circumference were measured and recorded. OSA non-invasive screening tests were applied to the patients.

Interventions

This prospective observational study was conducted in the Operating Room of the Health Sciences University Ankara Training and Research Hospital, after the approval of the Clinical Research Ethics Committee of the University of Health Sciences Ankara Training and Research Hospital, dated 11.02.2021 and numbered E-93471371-514.10. All patients participating in the study were informed and their written consent was obtained. Patients who would undergo non-cardiac surgery and who would undergo gener

This prospective observational study was conducted in the Operating Room of the Health Sciences University Ankara Training and Research Hospital, after the approval of the Clinical Research Ethics Committee of the University of Health Sciences Ankara Training and Research Hospital, dated 11.02.2021 and numbered E-93471371-514.10. All patients participating in the study were informed and their written consent was obtained. Patients who would undergo non-cardiac surgery and who would undergo general anesthesia were included in the study. Patients were observed throughout the preoperative period and the intraoperative period starting with induction. Age, gender, body weight, height, body mass index and ASA value were recorded in the preoperative evaluation of all patients. The oropharyngeal structures of all patients included in the study were examined and recorded according to the Modified Mallampati Score (opening the mouth completely in the sitting position, sticking out the tongue without making any sound). While screening tests and anthropometric measurements (thyromental distance, neck circumference, waist circumference) were completed at the preoperative anesthesia evaluation 1 week before the surgical procedure, the Cormack-Lehane score was recorded during post-induction laryngoscopy. Thyromental distance was measured from the thyroid cartilage level with the tip of the chin while the head was in extension, without contacting the skin with a ruler. A thyromental distance of 6 cm or less was determined as a difficult airway criterion Neck circumference was measured at the level of the thyroid cartilage with the head in a neutral position. Difficult airway criterion was recorded as 40 cm and above . Waist circumference was measured from the mid-axillary line between the lowest point of the rib cage and the highest point of the iliac crest, with the patient in an upright position. Over 102 cm for men and 88 cm for women were considered associated with high risk. Screening tests of the patients were completed during the preoperative anesthesia evaluation.Screening tests were completed 1 day before the preoperative period.

Sponsors

Health Sciences University Ankara Training and Research Hospital
Lead SponsorUniversity

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Inclusion criteria: Patients who will receive general anesthesia Adults aged between 18 and 65 years Patients with American Society of Anesthesiology (ASA) Score I-II-III No history of previous obstructive sleep apnea (OSA)

Exclusion criteria

Exclusion criteria: Patients with facial abnormalies Patients undergoing cardiothoracic surgery, head and neck surgery, neurosurgery and emergency surgery

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026