This is a secondary analysis of a previously-published prospective cohort study [14], which was approved by the Quanzhou Women’s and Children’s Hospital Institutional Review Board (dated 11 November 2013) and registered at Clinicaltrials.gov registry (NCT02026882). The study was conducted at Quanzhou Women’s and Children’s Hospital, Fujian Province, China, and patient recruitment occurred between December 2013 and November 2014. Largely due to patient preference, approximately 35% of parturients undergo cesarean section at the study center, with the majority performed under general anesthesia using the Supreme™ LMA (SLMA). Hence, the SLMA has been established as part of the routine airway management at the study center.
Parturients who were healthy or with well-controlled medical conditions (American Society of Anesthesiologists (ASA) physical status classification II) undergoing elective cesarean section under general anesthesia were recruited. We excluded patients with BMI > 35 kg/m2, upper respiratory tract or neck pathology, or self-reported reflux disease. After fasting for a minimum of 4 h, the modified Mallampati score was determined by an independent assessor and the patients divided into two groups: Mallampati III/IV (High MP) and Mallampati I/II (Low MP).
The induction of anesthesia and SLMA insertion reflects the clinical practice at the study center, as well as the cohort study that forms the basis for this secondary analysis [14]. As per institutional standard, all parturients were premedicated with intravenous ranitidine, and monitored with electrocardiogram, pulse oximetry, capnography and non-invasive blood pressure monitor. The chosen SLMA size was based on the manufacturer’s guidelines and the discretion of the attending anesthesiologist. All SLMA were inserted by three investigators (Yao, Li, and Yuan), each with at least five years of experience in its use for cesarean delivery. Anesthesia was commenced via rapid sequence induction with the application of cricoid pressure by a trained anesthetic assistant, and administration of propofol and succinylcholine, followed by SLMA insertion using the recommended rotational technique. After cuff inflation to 60 cmH2O via a manometer, assessment of successful SLMA placement was made by auscultation of breath sounds and the capnographic evidence of end-tidal carbon dioxide, and cricoid pressure was released. The use of additional maneuvers such as chin lift, jaw thrust, or head tilt were permitted. Rocuronium was used to maintain intraoperative muscle relaxation, and fentanyl was administered for analgesia after delivery of the fetus.
We recorded (1) the number of insertion attempts required, with each attempt defined as insertion and complete removal of the SLMA; and (2) the time to effective airway placement, from when the SLMA was picked up until the first end-tidal carbon dioxide capnogram appeared. Subsequently, a pre-mounted #14 orogastric tube was inserted through the gastric drainage port, and placement confirmed by aspiration of gastric contents and auscultation of a “swoosh” over the epigastrium with air injection, followed by suctioning of the orogastric tube before surgery commenced. Finally, oropharyngeal leak pressure was measured by shutting the adjustable pressure-limiting valve and maintaining 3 L/min fresh gas flow into the closed circuit. Cesarean section was allowed to commence if the following were met: presence of square-wave capnogram, cuff pressure of 60 cmH2O, positioning of the SLMA bite block between the incisors, successful orogastric tube insertion, and leak pressure > 20cmH2O. If successful SLMA insertion was not accomplished (1) after two attempts, (2) within one minute, or (3) before desaturation ensued, endotracheal intubation would be performed.
Perioperative anesthesia management during the original cohort study [14] reflects the clinical practice at the study center. With all parturients positioned left lateral tilt using a wedge, anesthesia was maintained with 1.5 to 2% sevoflurane and 50:50 mix of nitrous oxide in oxygen. We recorded the incidence of airway complications including airway obstruction, inadequate oxygenation or ventilation, and the presence of signs of clinical aspiration such as hypoxemia, auscultation of wheezing or crepitations, and postoperative dyspnea. Parturients were ventilated with tidal volume of 6 to 10 ml/kg, and respiratory rate of 10 to 16 breaths/min. The obstetricians were advised to avoid excessive fundal pressure during fetal delivery. Upon completion of surgery, suctioning and removal of the orogastric tube was performed, and the SLMA was withdrawn and inspected for blood. An independent assessor determined the incidence of sore throat and voice hoarseness prior to discharge from the post anesthesia care unit.
Our primary outcome was time to effective ventilation, as defined above. Secondary outcomes included the rate of successful first-attempt SLMA insertion, oropharyngeal leak pressure, ventilation parameters such as tidal volume and respiratory rate, hemodynamic parameters including heart rate and blood pressure at 2 and 5 min after induction, amount and pH of gastric aspirate, the pH of the SLMA laryngeal surface, and the presence of clinical aspiration. Obstetric and fetal outcomes included neonatal weight, Apgar scores, and umbilical venous pH.
Statistical analysis
All demographic, anesthetic, and clinical categorical data were summarized as frequency with corresponding proportion, and continuous variables were expressed as mean (standard deviation (SD)) or median [interquartile range (IQR)], whichever appropriate. The difference between categorical data was tested using the Chi-Square test, while Student’s t-test and Mann-Whitney U test were used for parametric and non-parametric continuous data, respectively. Simple linear and multivariable linear regression methods were utilized to determine associated risk factors for our primary outcome of time to effective ventilation. Associations identified from linear regression were expressed as estimate (β) with 95% confidence interval (95%CI). Significance level was set at p < 0.05 and all tests were two-sided. Data analysis was generated using SAS 9.3 software (SAS Institute Inc., Cary, NC, USA).
We performed a sample size calculation based on the following assumptions: a meaningful clinical difference of at least 10 s in time to effective ventilation between “High MP” and “Low MP” groups, pooled SD of 4.5, allocation ratio of 1:8, use of two-sample independent t-test, level of significance of 5% and > 95% power. The study was adequately powered (> 95%) with 584 parturients.