A randomised comparison between Cobra PLA and classic laryngeal mask airway and laryngeal tube during mechanical ventilation for general anaesthesia

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ORIGINAL AND CLINICAL PAPERS Anaesthesiology Intensive Therapy 2013, vol. 45, no 1, 20 24 ISSN 1642 5758 DOI: 10.5603/AIT.2013.0004 www.ait.viamedica.pl A randomised comparison between Cobra PLA and classic laryngeal mask airway and laryngeal tube during mechanical ventilation for general anaesthesia Paweł Ratajczyk 1, Beata Małachowska 1, Ewelina Gaszyńska 2, Tomasz Gaszyński 1 1 Department of Emergency Medicine and Disaster Medicine, Medical University of Lodz, Poland 2 Department of Hygiene and Health Promotion, Medical University of Lodz, Poland Abstract Background. The aim of this study was to compare ventilation parameters during mechanical ventilation using Laryngeal Mask Airway (LMA), Laryngeal Tube (LT), and Peri-Laryngeal Airway Cobra (PLA). Methods. In a prospective, randomised controlled trial, 90 patients undergoing general anaesthesia for elective surgery were divided into three subgroups. The settings of controlled ventilation were: oxygen 50%, air 50%, sevoflurane 1.5 2.0%, TV 7 ml kg 1, RR 10 breath min 1, inspiratory/expiratory ratio 1:2 and FGF 3 L min 1. The number of attempts, time taken to insert the device, airway pressure (peak airway pressure, plateau airway pressure), air leak (inspiratory and expiratory volume difference), and dynamic compliance were measured. The timepoints for collecting data were after successful insertion of the device, and after ten, 20, 30 and 50 mins of ventilation. The presence of visible blood traces, patients assessment of their throat soreness, dysphonia and dysphagia were noted postoperatively. Results. The success rates at first insertion were 90% and 80% and 90%, while time for insertion was 5 sec and 21.94 sec and 5.24 sec in the Cobra PLA, LMA and LT groups respectively. Ventilation pressures during procedure were highest in the LT group, where compliance was lowest compared to the Cobra PLA and LMA groups. The air leak was similar in all the groups. 30% vs. 40% vs. 10% of devices had positive blood traces; 20% vs. 40% vs. 30% of patients suffered from a sore throat; and 30% vs. 30% and 30% of patients suffered from dysphagia in the Cobra PLA, LMA and LT groups respectively. Conclusion. The differences were small, but Cobra PLA seemed to be slightly superior in terms of the measured parameters. Key words: airways, artificial, extraglottic devices, ventilation, mechanical Anaesthesiology Intensive Therapy 2013, vol. 45, no 1, 20 24 Establishing the airway is the primary aim during general anaesthesia as well as in emergency situations. While tracheal intubation is considered the gold standard, it requires adequate skill to secure the airway. The laryngeal mask airway (LMA, Laryngeal Mask Company, Henley-on-Thames, UK) and the laryngeal tube (LT ; VBM Medizintechnik, Sulz, Germany) are two of the most popular, safe methods of tracheal intubation for airway maintenance during general anaesthesia in selected patients and surgical procedures. The perilaryngeal airway Cobra PLA (PLA ; Engineered Medical Systems, Indianapolis, IN, USA) is a relatively new extraglottic airway device. The aim of this study was to assess the efficacy of the Cobra PLA, LMA and LT during controlled mechanical ventilation in paralysed patients during surgical procedures. Methods After Ethics Committee approval and informed written consent had been obtained, 90 ASA I II patients, with Mallampati 1 and 2, BMI under 30, at minimal risk of pulmonary aspiration, and scheduled for surgical procedures lasting about 60 minutes, were included in the study and randomly assigned to one of the three subgroups: LMA, LT, or Cobra PLA. Standard monitoring was used throughout the study: 20

Paweł Ratajczyk et al., Cobra, LMA and LT for mechanical ventilation Table 1. Demographic characteristics of patients (x ± SD) Parameter Cobra PLA LMA LT Age (yrs) 45.7 ± 19.51 46.04 ± 18.75 46.16 ± 14.21 BMI (kg m -2 ) 24.04 ± 2.9 23.97 ± 2.81 24.64 ± 2.74 Gender (M/F) 13/17 15/15 14/16 Table 2. Mean ventilation parameters during procedures (x ± SD) Group Peak pressure (cm H 2 O) Plateau pressure (cm H 2 O) Compliance (ml cm H 2 O -1 ) Cobra PLA 16.2 ± 3.8* 14.4 ± 3.5 61.7 ± 19.4 # LMA 14 ± 1.1 13.5 ± 0.9 62.1 ± 8.7 LT 18.8 ± 3.3 16 ± 3.4 50.5 ± 4.5 * P < 0.05 compared to LMA; # P < 0.05 compared to LT ECG, HR, SpO 2, non-invasive MAP, Et CO 2, airway pressures, tidal volumes and compliance. The patients lungs were ventilated with volume-controlled mechanical ventilation using an AS/3 anaesthesia delivery unit (Datex-Ohmeda, Helsinki, Finland). Mechanical ventilation was performed with tidal volume of 7 ml kg -1, respiratory rate of 10 breath min -1, inspiratory/expiratory ratio of 1:2 and a fresh gas flow of 3 L min -1. The number of attempts, the time taken to insert the device, airway pressures (peak and plateau), air leak (inspiratory and expiratory tidal volume difference) and any unwanted effects were recorded. Also recorded (in patients in whom it was possible to ventilate the lung) was the time taken to insert the airway measured from the time that the airway was blinded, attaching it to the breathing system after inflating the cuffs. Breath to breath spirometry data was obtained using a sidestream spirometry device (D-lite flow sensor, Datex- -Ohmeda) attached between the proximal end of devices and the Y-piece of the anaesthetic breathing system. Data measured was recorded immediately after insertion of the device (T0) and again after ten min (T10), 20 min (T20), 30 min (T30) and 50 min (T50) of ventilation. The following intraoperative complications were documented: aspiration/regurgitation, hypoxia (SpO 2 < 90%), bronchospasm, airway obstruction, gastric insufflations, oropharyngeal leak, coughing/gagging/hiccup. At the end of surgery, the devices were removed and examined for the presence of visible blood traces. Patients were asked to rate their throat soreness, dysphonia (difficulty/pain on speaking), and dysphagia (difficulty/pain on swallowing) one, six and 24 h postoperatively using a visual analogue score (VAS). Statistical analysis was performed between groups using ANOVA test and post-hoc analysis. P < 0.05 was considered as significant. RESULTS There was no difference in terms of demographic data between the groups (Tab. 1). The success rates at first insertion were 90% and 80% and 90%, and the time taken to insert was 5, 21.94 and 5.24 sec in the Cobra PLA, LMA and LT groups respectively. Ventilation pressures during the whole procedure were highest in the LT group, where compliance was lowest compared to the Cobra PLA and LMA groups (Tab. 2). When comparing ventilatory parameters at measurement points, there were no significant differences between the Cobra PLA group and the LMA group. However, between the Cobra PLA group and the LT group, and between the LMA group and the LT group, there were differences in every measurement point in terms of dynamic lung compliance (Fig. 1). Inspiratory peak pressure was significantly higher in the Cobra PLA group compared to the LMA group at T0, T10 and T20. When comparing the Cobra PLA and LT groups, the inspiratory peak pressure increased significantly in LT only at T30 (Fig. 2). In the LT group, plateau pressure increased at T20, T30 and T50 compared to the Cobra PLA group. There were also significant differences in this parameter between the LT group and the LMA and PLA groups (Fig. 3). The air leak was significantly higher in the Cobra PLA group compared to the LMA group at all measurement points (Tab. 3), and post-hoc analysis revealed significant differences between the LMA and LT groups, as well as the Cobra PLA and LT groups (Tab. 4). Dynamic lung compliance decreased when all evaluated devices were in use. Peak inspiratory pressure increased over time, but for LT this tendency was more expressed than for other devices. The same observation was made for plateau pressure. Air leak was highest at the beginning in the LT group, but decreased and was comparable to other devices. For all evaluated parameters at measurement points, the LMA 21

Anaesthesiol Intensive Ther 2013, vol. 45, no 1, 20 24 Figure 1. Plateau inspiratory pressure (cm H 2 O). Means and 95% CI of means Figure 2. Peak inspiratory pressure (cm H 2 O). Means and 95% CI of means Table 3. Air leak at measurement points (x ± SD) Time-points Cobra PLA (%) LMA (%) LT (%) T0 7.16 ± 1.61 5.23 ± 1.73 9.11 ± 3.32 T10 7.02 ± 1.72 4.37 ± 2.09 7.72 ± 1.81 T20 7.53 ± 2.07 4.76 ± 2.83 7.19 ± 2.22 T30 7.82 ± 0.12 4.54 ± 2.05 6.99 ± 2.47 T50 7.14 ± 2.36 4.74 ± 1.7 6.6 ± 1.69 22

Paweł Ratajczyk et al., Cobra, LMA and LT for mechanical ventilation Figure 3. Dynamic lungs compliance (ml cm H 2 O -1 ) means Table 4. Air leak: post-hoc analysis (MS = 385.66, df = 362.00) Device Cobra PLA 7.2750 LMA 4.7755 LT 139.56 PLA 0.765170 0.000022 LMA 0.765170 0.000022 LT 0.000022 0.000022 group had the best results: lowest peak inspiratory and plateau pressures, smallest air leak, and highest dynamic lung compliance. After completion of surgery in the Cobra PLA, LMA and LT groups respectively, 30% vs. 40% vs. 10% of devices had positive blood traces, 20% vs. 40% vs. 30% of patients suffered from a sore throat, and 30% vs. 30% and 30% of patients suffered from dysphagia. DISCUSSION In this study, the success rates for first insertion attempts were higher for Cobra PLA and LT than for LMA. The mean insertion times of the Cobra PLA and LT were comparable to and lower than the LMA. Lower insertion success rates and longer insertion times in the LMA group were observed, confirming previous findings [1]. Air leaks to the mouth and to the stomach were not recorded, probably because the peak airway pressures in our study in all groups were lower than airway sealing pressures, as described by others [1, 2, 3]. The Cobra PLA device generates a sealing pressure of above 20 cm H 2 O [4, 5]. In the case of LT, this pressure is higher: about 36 ± 3 cm H 2 O [7]. It has also been shown that the airway sealing pressure is about 5 cm H 2 O greater with Cobra PLA than LMA [4, 8]. In our study, during the whole procedure, the ventilation pressures were highest and compliance lowest in the LT group compared to the Cobra PLA and LMA groups, and similar to those found by other investigators [6, 7, 8]. At any measurement points, there were no significant differences either between the PLA and the LMA group or between the PLA and the LT group according to dynamic lung compliance. Our findings did not demonstrate any differences in air leak between the Cobra PLA and LT groups. However, the differences between Cobra PLA and LMA were significant, except at T0. A higher leak pressure for Cobra PLA compared to LMA has also been observed by other investigators [9]. During our study, the incidences of sore throat using Cobra PLA were lower than using LT and LMA, and were lower than previously reported [1]. The incidence of sore throat after using LMA was higher than with Cobra PLA and similar to that registered by Brimacombe [10] and lower than reported by others [1, 11, 12]. The occurrence of sore throat following LT use was consistent with the results of similar reports [2, 13, 14, 15]. The blood traces were detec- 23

Anaesthesiol Intensive Ther 2013, vol. 45, no 1, 20 24 ted on LT devices upon removal similarly to those reported by other authors [2, 13, 14, 15, 16] and were less common than when using Cobra PLA and LMA. The mucosal trauma determined by incidence of sore throat and blood traces was more frequent in the case of LMA. According to some published data, this complication is more common following Cobra PLA use, which results from the construction of this device and its rigid head. However, the LT construction is more rigid than LMA and the mucosal trauma determined by this device is less frequent than LMA [1]. In our study, we have not observed such complications as aspiration/regurgitation, hypoxia, bronchospasm or airway obstruction. The incidences of dysphagia were similar in all groups of patients; when LMA and LT were used, it was higher than has been reported by others [17, 18]. CONCLUSIONS 1. Cobra PLA, LMA and LT all provide adequate airway maintenance during general anaesthesia for surgical procedures. 2. A comparison between the ventilator parameters during procedures in all time-points was generally similar between the PLA, LT and LMA groups. There were slight advantages in favour of the PLA. The LT group performed the most poorly. References: 1. Turan A, Kaya G, Koyuncu O, Karamanlioglu B, Pamukçu Z.: Comparison of the laryngeal mask (LMA ) and laryngeal tube (LT ) with the new perilaryngeal airway (Cobra PLA ) in short surgical procedures. Eur J Anaesthesiol 2006; 23: 234 238. 2. Cook TM, McCormic B, Asai T: Randomized comparison of laryngeal tube with classic laryngeal mask airway for anesthesia with controlled ventilation. Br J Anaesth 2003; 91 373 378. 3. Asai T, Kawashima A, Hidaka I, Kawachi S: The laryngeal tube compared with the laryngeal mask: insertion, gas leak pressure and gastric insufflation. Br J Anaesth 2002; 89: 729 732. 4. Szmuk P, Ezri T, Akça O, Alfery DD: Use of a new supraglottic airway device the Cobra PLA in a difficult to intubate/difficult to ventilate scenario. Acta Anaesthesiol Scand 2005; 49: 421 423. 5. Gaitini LA, Somri MJ, Kersh K, et al.: A comparison of Laryngeal Mask Airway Unique Pharyngeal Airway Xpress and Perilaryngeal Airway Cobra in paralyzed anesthetized adults patients. Anesthesiology 2003; 99: A 1495. 6. Gaitini LA, Vaida SJ, Somri M, et al.: An evaluation of the laryngeal tube during general anesthesia using mechanical ventilation. Anesth Analg 2003; 96: 1750 1755. 7. Ocker H, Wenzel V, Schmucker P, et al.: A comparison of the laryngeal tube with the laryngeal mask airway during routine surgical procedures. Anesth Analg 2002; 95: 1094 1097. 8. Akca O, Wadhawa A, Sengupta P, et al.: The new perilaryngeal airway (CobraPLA) is as efficient as the laryngeal mask airway (LMA) but provides better airway sealing pressure. Anesth Analg 2004; 99: 272 278. 9. Wronska-Sewruk A, Nestorowicz A, Kowalczyk M: Classic laryngeal mask airway vs. COBRA-PLA device for airway maintenance during minor urological procedures. Anaesthesiol Intensive Ther 2009; 41: 61 64. 10. Brimacombe J, Holyoake L, Keller C, et al.: Pharyngolaryngeal, neck, and jaw discomfort after anesthesia with the face mask and laryngeal mask airway at high and low cuff volumes in males. Anesthesiology 2000; 93: 26 31. 11. Wakeling HG, Butler PJ, Baxter PJC: The laryngeal mask airway: a comparison between two insertion techniques. Anesth Analg 1997; 85: 687 690. 12. Dingley J, Whitehead MJ, Wareham K: A comparative study of the incidence of sore throat with the laryngeal mask airway. Anesthesiology 1994; 49: 251 254. 13. Asai T, Kawashima A, Hidaka I: Laryngeal tube: its use for controlled ventilation. Masui 2001; 50: 1340 1341. 14. Asai T, Shingu K, Cook T: Use of the laryngeal tube in 100 patients. Acta Anaesthesiol Scand 2003; 47: 828 832. 15. Brimacombe J, Keller C, Puhringer F: Pharyngeal mucosal pressure and perfusion: a fiberoptic evaluation of the posterior pharynx in anesthetized adult patients with a modified cuffed oropharyngeal airway. Anesthesiology 1999; 91: 1661 1665. 16. Figuerdo E, Martinez M, Pintanel T: A comparison of the ProSeal laryngeal mask and the laryngeal tube in spontaneously breathing anesthetized patients. Anesth Analg 2003; 96: 600 605. 17. Asai T, Shingu K: The laryngeal tube. Br J Anaesth 2005; 95: 729 736. 18. van Zundert T, Brimacombe J: Comparison of cuff-pressure changes in silicone and PVC laryngeal masks during nitrous oxide anaesthesia in spontaneously breathing children. Anaesthesiol Intensive Ther 2012; 44: 63 70. Corresponding author: Prof. Tomasz Gaszyński, MD, PhD Department of Anesthesiology and Intensive Therapy, Medical University of Lodz ul. Kopcińskiego 22, 90 158 Lodz, Poland tel./fax. +48 42 678 37 48 e-mail: tomgaszyn@poczta.onet.pl Received: 20.07.2012 Accepted: 20.11.2012 24