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* From the Department of Anaesthesia Intensive Care, The Chinese University of Hong Kong Prince, of Wales Hospital, Shatin, and
Department of Anaesthesia and Intensive Care, Tuen Mun Hospital, Tuen Mun, New Territories, Hong Kong, Peoples Republic of China.
Address correspondence to: Dr. Lester A.H. Critchley, Department of Anaesthesia and Intensive Care, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong, SAR, Peoples Republic of China. Phone: 852-2632-2735; Fax: 852-2637-2422; E-mail: hcritchley{at}cuhk.edu.hk
| Abstract |
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Methods: One hundred forty ASA I or II patients, age 1881 yr, requiring minor surgery were recruited. They were randomized to receive either alfentanil (10 µgkg-1; n = 73) or fentanyl (1 µgkg-1; n = 67) with propofol (2.5 mgkg-1) 90 sec prior to LMA (size 3 or 4) insertion. A six variable (mouth opening, ease of insertion, swallowing, coughing, movement and laryngospasm) three-point (nil / partial / total) score was used to assess insertion conditions. Duration of postinsertion apnea was recorded. Insertion conditions were compared using Chi-square for trends.
Results: The two groups were demographically similar. Mouth opening and ease of insertion were not improved with alfentanil co-administration. Alfentanil-propofol reduced the incidence of swallowing, gagging, movement and laryngospasm (P < 0.05), with 29% (alfentanil) compared to 45% (fentanyl) of patients responding (P = 0.05) to LMA insertion. Apnea [mean (SD)] following alfentanil lasted 154 (139) sec compared to 82 (61) sec following fentanyl (P = 0.001).
Conclusion: Co-administration of alfentanil-propofol provided better insertion conditions than fentanyl-propofol, though apnea was prolonged by 72 sec.
| Introduction |
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Yet, insertion of a LMA is not always straightforward and requires sufficient depth of anesthesia for the jaw muscles to relax and the inserted LMA to be tolerated within the hypopharynx, without undue coughing, gagging, breath holding and patient movement.1,2 Such conditions are normally provided by a generous dose of an iv anesthetic induction agent and recent studies have shown propofol (2.5 mgkg-1) to be superior to thiopentone (5 mgkg-1) in this respect.3,4 To further improve LMA insertion conditions, a number of adjuncts to induction, such as lidocaine, midazolam, low doses of muscle relaxant and opioids,58 have been advocated. Of these, the opiates are most commonly used. In general, adjuncts increase successful insertion rates to over 90%.59
Recent data from our department has shown that the short acting opiate fentanyl (1 µgkg-1) with propofol (2.5 mgkg-1) given 90 sec prior to LMA insertion provided excellent conditions (i.e., easy insertion with minimal patient response) in 77% (23/30) of patients.A However, recently published data by Sivalingham et al.10 and Ang et al.11 suggest that this success rate can be further improved to 8896% by using the short-acting opiate alfentanil, instead of fentanyl. The objective of our study was to compare the LMA insertion conditions provided by propofol (2.5 mgkg-1) co-administered with alfentanil (10 µgkg-1) vs fentanyl (1 µgkg-1).
| Methods |
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All patients were fasted for over six hours and no premedication was prescribed. One of two identical 10 mL syringes containing either alfentanil 10 µgkg-1 or fentanyl 1 µgkg-1, made up to 10 mL with normal saline, was randomly selected as the study drug. The content of the syringe was decoded after the study. Standard anesthetic monitoring was applied and the patient pre-oxygenated for three minutes. The study drug, followed by propofol 2.5 mgkg-1, without additives, was injected intravenously over ten seconds and flushed with normal saline. The patient was not ventilated and 90 sec later a lubricated LMA, size 3 for females or size 4 for males, was inserted by one of the authors using the technique described by Brain.1,9
The study investigator assessed insertion conditions using a six-variable, three-point score which graded mouth opening, ease of LMA insertion and patient response: i.e., swallowing, gagging-coughing, head/limb movement and laryngospasm. The percentage of patients exhibiting each response was calculated. The position of the LMA was checked by observing respiratory movements and chest expansion. Any malpositioned or non-functioning LMA was removed, the patient given a further dose of propofol 1 mgkg-1 and, 60 sec later, reinsertion attempted. The number of attempts for successful insertion was noted.
Once the LMA had been successfully inserted, the patient was intermittently ventilated via the LMA to maintain the arterial oxygen saturation above 95% and the end-tidal carbon dioxide concentration between 5.36.6 kPa until resumption of spontaneous respiration. Following successful LMA insertion, the duration of apnea until regular spontaneous respiration resumed was recorded. Anesthesia was then maintained with 1.5% isoflurane and 70% nitrous oxide in oxygen. Surgery was allowed to start before spontaneous respiration resumed.
The patient's blood pressure and heart rate were recorded before induction of anesthesia, one minute after induction and one minute after successful LMA insertion.
Statistical analysis was performed using Statview 4.02 (Abacus Concepts, Inc., USA). Previous studies had shown a success rate for fentanyl of 77%A compared with 8896% for alfentanil.10,11 Based on these data, a sample size of n = 140 was required to show an improvement in success rate of 15% with
= 0.05 and a power of 80%. The number and percentage of patients with each score for all six variables were calculated. Insertion scores were then compared using Chi-square for trends.13 This adaptation of the Chi-squared test takes into account the ranking of categories, such as easy to difficult to impossible. Blood pressure and heart rate changes during insertion were compared using analysis of variance for repeated measures, with Bonferroni-Dunn for post-hoc comparisons. Data are presented as mean (SD or range) and a P < 0.05 was considered significant.
| Results |
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LMA insertion was unsuccessful on the first attempt in four patients receiving alfentanil compared with six patients receiving fentanyl (P = 0.7). It was totally unsuccessful and an alternative method of airway management was required in three alfentanil and two fentanyl patients (P = 0.8).
Apnea following LMA insertion lasted 154 (139) sec in patients receiving alfentanil compared with 82 (61) sec in patients receiving fentanyl (P = 0.0002).
Systolic and diastolic blood pressures decreased following induction in both groups (P < 0.0001). The decreases in blood pressure were greater in those patients receiving alfentanil (P < 0.05; Figure
). Heart rate decreased only in those patients that received alfentanil (P = 0.0016; Figure
).
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| Discussion |
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We used a methodology similar to that developed by previous LMA researchers to assess insertion conditions.8,10 Early investigators confined their assessment to mouth opening, gagging and coughing3,4 but, recently, a six-variable/three-grade score was developed (Table II
).8,10 With some modification to include swallowing, we were able to use this score to assess both the ease of placement and the patient's response.
Few authors have studied the effects of alfentanil co-administration on LMA insertion. In 1996 Driver et al. studied the effects of alfentanil (10 µgkg-1) on LMA insertion, which they compared to those of midazolam (0.04 mgkg-1).7 They concluded that a combination of alfentanil with midazolam reduced propofol requirements and improved insertion conditions.7 The same authors, a year later, used alfentanil when comparing propofol with thiopentone for LMA insertion.14 In 1999 Ang et al. showed that alfentanil in doses of 5 and 10 µgkg-1 with propofol improved mouth opening and reduced patient responses.11 In the same year, Sivalingam et al. used alfentanil co-administration in doses of 5 µgkg-1 to compare propofol with sevoflurane inhalation for LMA insertion and showed that alfentanil improved insertion conditions with both induction techniques.10
In the present study mouth opening was recorded as non-ideal in nearly half (4749%) of our patients. Insertion of the LMA was not easily performed in 32% of patients receiving alfentanil compared to 42% of patients receiving fentanyl, though this difference was not statistically significant. Our incidence of difficult LMA insertion is higher than that reported previously. Ang et al. reported a 20% incidence of difficult insertion when co-administering alfentanil 10 µgkg-1 11 and Sivalingham et al. reported a 28% incidence of difficult jaw opening when using alfentanil 5 µgkg-1 and a 4% incidence of difficult insertion.10 However, the latter author did wait until the jaw was fully relaxed by giving additional boluses of propofol before inserting the LMA. Our higher incidence of reported difficulty with mouth opening and insertion may reflect stricter study criteria. In addition, we frequently encountered difficulty in passing the LMA cuff between the patients front incisors, which we attribute to our patients being mainly ethnic Chinese who, in our experience, have smaller jaws than the Caucasian population for whom the LMA was originally designed. However, a number of authors have reported recently much lower incidences of difficulty when using doses of propofol of 2.5 to 3.5 mgkg-1, suggesting that our 2.5 mgkg-1 dose was at the lower end of the acceptable range and that a larger dose may be beneficial.15,16
The main positive finding of our study was the reduced number of patients that responded adversely to LMA insertion, 45% with fentanyl compared to 29% with alfentanil. We graded four fundamental patient responses to LMA insertion: swallowing, coughing-gagging, movement and laryngospasm. Swallowing was the response that we encountered most frequently (Table II
). This was not surprising as swallowing is the natural response to a food bolus entering the hypopharynx and the cuff of the LMA acts similarly, triggering this response if the patient is insufficiently anesthetized.2 Some anesthesiologists take advantage of this reflex and use swallowing as an indication of emergence from anesthesia when using the LMA.2 Coughing and gagging are more potent reflexes, triggered by irritation of the larynx or epiglottis and prevents foreign material entering the trachea and lungs. The LMA is designed to avoid triggering coughing and gagging because its cuff sits posterior to the larynx in the hypopharynx, as evidenced by the observed low incidence of coughing and gagging. Patient movement was more commonly encountered when using fentanyl (30% vs 11%) and laryngospasm was the least frequent response. It is not uncommon for LMA insertion to cause some transient cord closure or partial laryngospasm, which was more frequent with fentanyl.2 However, total laryngospasm only occurred in three patients receiving fentanyl.
Our study supports the hypothesis that alfentanil-propofol co-administration is more effective than fentanyl-propofol at suppressing reflex responses to LMA insertion. The dosages of alfentanil (10 µgkg-1) and fentanyl (1 µgkg-1) used in the study were chosen because they had been used successfully in previous LMA studies3,4,7,11,A and were convenient to calculate in a clinical setting. However, these two doses are not equipotent. According to Stanski et al., alfentanil is five to six times less potent than fentanyl.17 Also, due to differences in pKa, the speed of onset following iv administration of alfentanil is two to three times more rapid than fentanyl, resulting in times of onset of one to two minutes, compared to five to six minutes for fentanyl.18 In our study, we required an onset of effect by two minutes. Furthermore, the more rapid onset time of alfentanil allows a relatively smaller drug mass to be administered to achieve a similar clinical end point.19 Thus, in theory, a greater depth of anesthesia and reflex suppression is to be expected at the moment of LMA insertion when using alfentanil according to our study protocol. Possibly smaller doses of alfentanil (< 10 µgkg-1) are equally efficacious in facilitating LMA insertion and with less prolongation of the apnea time. This is a hypothesis that merits further investigation.
Blood pressure and heart rate are usually reported to increase by 020% following LMA insertion and by 2550% following tracheal intubation.2 Following alfentanil co-administration decreases in blood pressure and heart rate were observed (Figure
). Interestingly, Ang et al. found that 14% of patients receiving 10 µgkg-1 of alfentanil with propofol developed bradycardias requiring atropine.11 However, these authors only waited 60 sec before inserting the LMA, which may have been insufficient. We waited 90 sec and no bradycardias were observed using a similar alfentanil dose.
The main problem when using alfentanil, other than increased cost, was the prolongation of apnea from 82 sec to 154 sec. However, we did not find this delay to be a major clinical inconvenience.
Despite the advantages of using opiate co-administration,7,10,14 in five patients (3.5%) LMA insertion remained unsuccessful. We believe that this represents a small percentage of patients, common to all studies, in whom upper airway anatomy is unfavourable and successful LMA insertion is not possible.
In conclusion, co-administration of alfentanil-propofol provides better LMA insertion conditions than fentanyl-propofol.
| Footnotes |
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Revision received February 1, 2002. Accepted for publication December 20, 2001.
| References |
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2 Brimacombe J, Berry A. The laryngeal mask airway anatomical and physiological implications. Acta Anaesthesiol Scand 1996; 40: 2019.[Medline]
3 Brown GW, Patel N, Ellis FR. Comparison of propofol and thiopentone for laryngeal mask insertion. Anaesthesia 1991; 46: 7712.[Medline]
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Scanlon P, Carey M, Power M, Kirby F. Patient response to laryngeal mask insertion after induction of anaesthesia with propofol or thiopentone. Can J Anaesth 1993; 40: 8168.
5 Stoneham MD, Bree SE, Sneyd JR. Facilitation of laryngeal mask insertion. Effects of lignocaine given intravenously before induction with propofol. Anaesthesia 1995; 50: 4646.[Medline]
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12 Mallampati SR, Gatt SP, Gugino LD, et al. A clinical sign to predict difficult tracheal intubation: a prospective study. Can Anaesth Soc J 1985; 32: 42934.[Medline]
13 Altman DG. Comparing groups categorical data. In: Altman DG (Ed). Practical Statistics for Medical Research, 1st ed. London: Chapman & Hall, 1991: 2615.
14 Driver I, Wilson C, Wiltshire S, Mills P, Howard-Griffin R. Co-induction and laryngeal mask insertion. A comparison of thiopentone versus propofol. Anaesthesia 1997; 52: 698700.[Medline]
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Keller C, Sparr HJ, Luger TJ, Brimacombe J. Patient outcomes with positive pressure versus spontaneous ventilation in non-paralysed adults with the laryngeal mask. Can J Anaesth 1998; 45: 5647.
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Ti LK, Chow MYH, Lee TL. Comparison of sevoflurane with propofol for laryngeal mask airway insertion in adults. Anesth Analg 1999; 88: 90812.
17 Stanski DR. The clinical pharmacology of alfentanil. Eur J Anaesthesiol 1987; 1(Suppl 1): 311.
18 Stanski DR, Hug CC. Alfentanil a kinetically predictable narcotic analgesic (Editorial). Anesthesiology 1982; 57: 4358.[Medline]
19 Shafer SL, Varvel JR. Pharmacokinetics, pharmacodynamics, and rational opioid selection. Anesthesiology 1991; 74: 5363.[Medline]
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