The laryngeal mask (LM) is widely used in ambulatory anaesthesia. Current anaesthetic practice requires rapid recovery and overall time-optimization, particularly in the ambulatory setting . The aim of the present study was to compare sevoflurane consumption in LM vs. tracheal intubation (TI) anaesthesia guided by BIS (bispectral index monitoring), during outpatient gynaecological surgery, and also to determine the difference in the recovery profile between the two anaesthetic techniques.
After institutional approval and informed consent, 50 female patients, ASA physical status I or II, scheduled for hysteroscopy on an ambulatory basis were recruited for the study. Patients were randomly assigned to one of the following two groups: the LM group (n = 25) and the TI group (n = 25). Exclusion criteria were a history of significant cardiorespiratory, renal or hepatic dysfunction, gross obesity (body mass index >30 kg m−2), alcohol intake, concurrent treatment with medication known to affect anaesthetic requirements, as well as a history of gastro-oesophageal reflux. Patients received no premedication.
On arrival in the operating room, patients were asked to perform the ‘picking up matches' test . Apart from standard monitoring, end-tidal carbon dioxide (etCO2) and inspired and end-tidal sevoflurane concentrations were recorded (Datex-Ohmeda S/5TM Anaesthesia Monitor, Helsinki, Finland). The sevoflurane vaporizer (Sevorane® Abbott Vapor19.3, Lubeck, Germany) was filled to the top and weighed in a scale with a precision of 0.1 g in the range up to 15 000 g (NJW-HGS Series, Scale Direct (Scotland) Ltd, Glasgow, UK). We tailored the anaesthetic concentrations using the BISTM Monitor, Model 1A-2000TM, System Rev. 3.12 Main Program 0289242B. The BIS signal and its trend line were obtained from ZipprepTM electrodes (Aspect Medical Systems Inc., Newton, MA, USA).
Before anaesthetic induction, metoclopramide 10 mg and ranitidine 50 mg were administered intravenously (i.v.). After preoxygenation, anaesthesia was induced with propofol 2–2.5 mg kg−1 followed by i.v. succinylcholine 0.8 mg kg−1 to facilitate direct laryngoscopy or LM insertion. Before attempting direct laryngoscopy or LM insertion, anaesthesia was supplemented with sevoflurane in oxygen under manual ventilation to ensure a BIS value between 35 and 45. When the airway was secured, ventilation was assisted with 60% nitrous oxide in oxygen plus sevoflurane using a circle breathing system with a CO2 absorber at a fresh gas flow of 2 L min−1 and setting the vaporizer to maintain intraoperatively a BIS value of 35–45 in both the groups. When succinylcholine had worn off and spontaneous ventilation resumed, patients in both groups were allowed to breathe spontaneously. All patients received analgesics upon completion of the surgical procedure, thus 1200 mg of paracetamol i.v. and 75 mg of diclofenac i.m.
Measurements were recorded: (1) just before anaesthetic induction (baseline); (2) prior to LM or tracheal tube insertion; and (3) immediately after airway instrumentation. End-tidal sevoflurane concentrations and etCO2 were recorded in patients of both groups at 5-min time intervals. Those values were averaged and the mean end-tidal sevoflurane concentration and mean etCO2 were calculated for each patient. After completion of the hysteroscopy, nitrous oxide and sevoflurane administration were discontinued and the times from sevoflurane discontinuation to: (a) spontaneous eye opening and (b) to the removal of the LM or of the tracheal tube were recorded. The quantity of sevoflurane consumed in g during the operation was measured after completion of surgery by disconnecting and reweighing the vaporizer as described previously. The inhaled anaesthetic consumption per minute (g min−1) was then calculated for each patient. Patients were assessed for orientation, sedation and sitting ability at 0, 15, and 30 min after extubation or LM removal by an anaesthesiologist blinded to the study design. To assess orientation, the following questions were asked: (a) where are you? (b) what is the day today? (c) what is the date? (d) what is your date of birth? The patient was accredited 1 point for each correct answer. Sedation was assessed as sleepy (1 point), sleepy but arousable (2 points) and spontaneously awake (3 points). Sitting ability with (scored as no) and without (scored as yes) help was also assessed. The ‘picking up matches' test was performed at the same time points. The time from arrival to discharge from the PACU and the occurrence of postoperative nausea and vomiting were recorded. Patients were discharged from PACU using the maximum score of the criteria for fast-tracking after outpatient anaesthesia proposed by White and Song .
The primary outcome measure of the study was sevoflurane consumption. Prior to the study, the estimated sample size was calculated to be 23 patients in each group in order to detect a 30% difference in sevoflurane consumption rate between the two groups with a power of 80% and an α level of 0.05. Sevoflurane consumption rate in patients anaesthetized with an LM had been estimated from initial pilot observations at approximately 0.50 ± 0.18 g min−1 at a fresh gas flow rate of 2 L min−1. Patient characteristics data were analysed with the unpaired t-test. Orientation and sedation scores, sitting ability and nausea and vomiting were analysed with the χ2 test or Fisher's exact test where appropriate. Intergroup comparisons of time required to complete the ‘picking up matches' test was performed with repeated measures Analysis of variance. P values of less than 0.05 were accepted as statistically significant.
The two groups were comparable with respect to patient characteristics. Sevoflurane requirements and consumption to obtain the same BIS values were significantly smaller in the LM group than in the TI group. The time interval between sevoflurane discontinuation and eye-opening and the time to airway removal was shorter in the LM group as compared with the TI group.
No difference was detected between the two groups in orientation score, sedation score or sitting ability at the specified time points after emergence.
The incidence of nausea and vomiting during patient stay in the recovery area was similar in the two groups. Time required to perform the ‘picking up matches' test was different between the two groups only immediately after awakening (16.3 ± 4.8 s in the LM group vs. 21.0 ± 7.8 s in the TI group, P = 0.013). No difference was detected in the scores of this test between the two groups 15 and 30 min after emergence. Finally, time to discharge from PACU did not differ between the two groups (Table 1).
Previous studies have shown that LM insertion in children can be performed at a lower sevoflurane concentration than that required for tracheal intubation [4,5]. However, those studies were confined to anaesthetic requirements during airway instrumentation and not to maintenance of anaesthesia. Cork and colleagues  compared the LM vs. TI in ambulatory surgery regarding haemodynamics and laryngeal reflexes protection. They did not quantify hypnosis as we did using the BIS monitor neither did they calculate the amount of the anaesthetic consumed with each technique.
In our study, we used an objective monitor to quantify hypnosis, thus ensuring comparable levels of anaesthesia in both groups intraoperatively. We maintained BIS values between 35 and 45, which are lower than those required to prevent awareness, because in studies specifically relating BIS to sevoflurane, values lower than 50 reliably indicated an adequate depth of anaesthesia . Another reason is that our patients were breathing spontaneously and lower BIS values might minimize movement or EMG interference.
Increased sevoflurane requirements to maintain predetermined BIS values might account for the longer awakening time in the TI group. Immediate co-ordination ability and subtle manual dexterity assessed by the ‘picking up matches test' were affected by exposure to higher concentrations of sevoflurane in the TI group as shown by the difference in the test results immediately after arousal. No significant difference in performing the test was observed thereafter. In fact, in short-duration procedures such as half an hour or so, inhalational anaesthetic uptake is mostly limited to the vessel-rich group and recovery times for different inhalational anaesthetics or for different amounts of the same anaesthetic will be similar. Nonetheless, less amount of anaesthetic for the same procedure costs less money. This may explain the fact that the different sevoflurane consumption did not affect nausea and vomiting or duration of stay in PACU between the two groups. The lack of blinding, not feasible for technical reasons, may be considered a limitation of our study. However, the amount of anaesthetic consumed, the ‘picking up matches' test and BIS values consist objective recordings, minimizing the bias in interpretation of our results.
Today, improved recovery times leading to safe reduction of turnaround times and optimization of resource utilization are becoming the target of the so-called ‘fast track' anaesthesia . Under the present study design, use of the LM was associated with lower sevoflurane requirements and consumption, shorter awakening time and shorter time to remove the airway device but similar duration of stay in the PACU when compared with the TI group.
This work was supported by a grant by the National and Kapodistrian University of Athens, code number: 70/4/8207.
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