A prospective observational study was conducted after obtaining approval from the Institutional Ethics Committee (IEC KMC MLR 06/2022/255) and Clinical trial registry of India (CTRI/2023/02/049398). Patients were selected by convenience sampling. The inclusion criteria were all individuals aged 18 and above with a history of type 2 diabetes mellitus of more than two years undergoing general anesthesia of ASA physical status II, III, IV, and were willing to give informed consent. Patients not willing to provide consent, pediatric patients, uncooperative patients, patients with a Glasgow Coma scale (GCS) less than 15, obstetric patients, patients with tumor masses in the oral cavity, immobile atlanto-occipital joint, maxillofacial trauma, large anterior neck mass, patients on long-term anti-inflammatory drugs, and patients undergoing regional anesthesia were excluded from the study. The sample size was calculated using MedCalc (ver. 20.110). Considering an alpha error of 5%, power of 80%, assuming the area under the curve to be 0.82 (supine) and 0.65 (sitting) for variables of interest in the present study, and keeping a ratio of easy vs. difficult tracheal intubation as 2, we needed a minimum sample size of 34 difficult tracheal intubation patients and 68 easy tracheal intubation patients for the present study. Therefore, a total of 102 diabetic patients would be required in the present study. The study protocol was explained to the patients, and written informed consent was obtained. Pre-operative airway assessment was done in sitting and supine positions using the modified Mallampati classification (MMC). The study was single-blinded, meaning the observer who assessed the Cormack Lehane score in the operating theatre was blinded to preoperative airway assessment. The study was conducted in teaching hospitals affiliated with Kasturba Medical College, Mangalore, Karnataka, from February 2023 to February 2024. Assessment in the sitting position was done with the head in a neutral position, mouth opened to the maximum, and tongue protruded maximally with the observer seated opposite the patient's eye level. While conducting the assessment in the supine position, the participant’s head was placed on a 10 cm high pillow, and the observer assessed the airway by looking vertically downward with the table height fixed at the observer’s hip level. It was categorized as (1) class I – visualization of the soft palate, fauces, uvula, and pillars; (2) class II – visualization of the soft palate, fauces, and uvula; (3) class III – visualization of the soft palate and base of the uvula; (4) class IV – soft palate not visible. In the operating room, the participants were pre-oxygenated, premedicated with Midazolam (0.02 mg/kg) and Fentanyl (2 – 3 mcg/kg), induced with Propofol (2 mg/kg). Neuromuscular blockade was administered with Atracurium (0.5 mg/kg)/ Vecuronium (0.1 mg/kg) after confirming the depth of anesthesia, and participants were ventilated with a bag and mask until adequate muscle relaxation was achieved.
Laryngoscopy was attempted by an anesthesiologist with more than 2 years of experience blinded to the MMC. All laryngoscopies were done using a metallic Macintosh blade, and the blade size was chosen according to the patient. During intubation, glottic exposure was graded using the Cormack – Lehane grading: (1) Grade I – Full view of the glottis; (2) Grade IIA – Partial view of the glottis, anterior commissure not visible; (3) Grade IIB – Only arytenoids seen; (4) Grade III – Only epiglottis seen; (5) Grade IV – Neither epiglottis nor glottis seen. Difficult Tracheal Intubation in the present study followed the definition: 'insertion of the endotracheal tube with conventional laryngoscopy requiring more than 2 attempts or lasting > 10 minutes, or requiring an alternate technique (bougie, video laryngoscope, fiberoptic)', and accordingly, tracheal intubation was classified as easy, difficult, and impossible. modified Mallampati classification in the sitting and supine positions was then compared to Cormack Lehane grading, and diagnostic accuracy (sensitivity, specificity, positive and negative predictive values, and positive and negative likelihood ratios) were calculated.
3.1. Statistical Analysis
The data were analyzed using SPSS for Windows (SPSS ver. 22.0, IBM Corp., Armonk, NY). Quantitative data were reported as mean and standard deviation, whereas qualitative data were reported in percentages. The chi-square test was used to associate categorical data with demographic factors like age, gender, and Body Mass Index. Data were presented as graphs and tables. Sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy were calculated for MMC in the sitting and supine positions with CL grading, respectively. The level of significance was set at P ≤ 0.05.