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Original Article

Comparative Evaluation of Sevoflurane, Propofol, and


Combination of Sevoflurane and Propofol on Insertion
Characteristics of Reusable Classic Laryngeal Mask Airway
Yamini Gupta, Tek Chand Kriplani1, Vansh Priya2
Department of Cardiac Anaesthesia, L. P. S. Institute of Cardiology, GSVM Medical College, Kanpur, 2Department of Anaesthesia, T. S. Misra Medical College,
Lucknow, Uttar Pradesh, 1Department of Anaesthesia and Critical Care, NSCB Medical College, Jabalpur, Madhya Pradesh, India

Abstract
Background and Aim: Adequate depth of anaesthesia is needed for successful placement LMA.under lighter plane of anaesthesia inadequate
mouth opening,coughing,body movements can lead to rejection of LMA and may be associated with breath holding and bronchospasm.
Use of propofol in doses which allow adequqate jaw relaxation and prevent patient reaction to LMA commonly results in hypotension and
prolonged apnoea.Apart from minimal respiratory irritant properties sevoflurane as compared to propofol has the advantage of providing better
hemodynamic stability and a smoother transition to the maintainance phase without a period of apnea.However sevoflurane is associated with
delayed jaw relaxation and a longer time for the insertion of the LMA.Our hypothesis is that induction of anaesthesia with the combination
of sevoflurane and small dose of propofol may optimize the insertion conditions of LMA and decrease the side effects of individual drugs.
Methods: 90 patients aged 18-65 yrs ASA physical status I and II undergoing elective procedures were randomly allocated into 3 groups of
30 patients each. No patient had been given any premedication.Patients in group P were induced with iv inj propofol 3 mg/kg. Patients in
group S an SP were induced with tidal volume breathing induction technique using sevoflurane 8% along withN20: 02: 67:33 @ 6L/MIN
In addition, in group SP after loss of eye lash reflex patients were given IV propofol 1.5 mg/kg.An independent observer assessed insertion
characteristics. Results: our results showed that induction of anesthesia using the combination of sevoflurane and propofol resulted in the
most frequent successful LMA insertion at first attempt as compared with induction of anesthesia with either sevoflurane or propofol alone.

Keywords: Classic laryngeal mask airway, propofol, sevoflurane

Introduction of the LMA while preserving spontaneous ventilation. [5]


Sevoflurane as compared to propofol has the advantage
Propofol is a preferred induction agent for laryngeal mask
of providing better hemodynamic stability and a smoother
airway (LMA) insertion due to its propensity of suppressing
transition to the maintenance phase without a period of
oropharyngeal and cough reflexes.[1] Adequate jaw relaxation
apnea.[6] However, sevoflurane is associated with delayed jaw
is an absolute prerequisite for successful LMA placement.
relaxation and a longer time for the insertion of the LMA.[7,8]
However, use of propofol in dosages  (usually  >2.5  mg/kg)
This study was based on our hypothesis that induction of
required for adequate jaw relaxation and adequate depth
anesthesia with the combination of sevoflurane and small
of anesthesia for LMA insertion may result in arterial
hypotension, apnea, and collapse of upper airways.[1‑4]
Sevoflurane is a nonpungent inhalation anesthetic agent Address for correspondence: Dr. Vansh Priya,
which can be used as an induction agent. Its nonpungent 3/279, Vishwas Khand, Gomti Nagar, Lucknow ‑ 226 010,
odor with minimal respiratory irritant properties makes it Uttar Pradesh, India.
E‑mail: vanshkhr@gmail.com
suitable for inhalation induction of anesthesia and insertion

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How to cite this article: Gupta Y, Kriplani TC, Priya V. Comparative


DOI: evaluation of sevoflurane, propofol, and combination of sevoflurane and
10.4103/aer.AER_30_18 propofol on insertion characteristics of reusable classic laryngeal mask
airway. Anesth Essays Res 2018;12:386-91.

386 © 2018 Anesthesia: Essays and Researches | Published by Wolters Kluwer ‑ Medknow


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Gupta, et al.: Effect of sevoflurane with propofol on insertion charactersitics of classic reusable LMA.

dose of propofol may optimize the insertion conditions of of the induction was taken as the time at which patient starts
LMA while reducing the incidence of associated side effects breathing from the circuit (time zero). Patients were further
of individual drugs. instructed to open their eyes every 10 s. Failure to do so was
In this prospective randomized study, a comparative evaluation taken as loss of consciousness, further confirmed by testing
of anesthesia induction with combination of sevoflurane and for loss of eyelash reflex. In Group  S, 90 s into inhalation
propofol, sevoflurane alone, or propofol alone on insertion induction, the ease of mouth opening was assessed as adequate
characteristics of reusable silicone classic LMA (CLMA) or inadequate. If mouth opening was inadequate, attempts were
(LMA North America, Inc.) in adult patients undergoing made every 30 s up to a maximum of 4. In between attempts,
elective surgery. We also compared the incidence of side depth of anesthesia was maintained with sevoflurane at 8% in
effects such as gagging, coughing, and laryngospasm and the 67%:33% ratio of N2O‑O2 at 8 L/min.
incidence of duration of apnea. Patients in Group  SP were induced with TVB technique
similar to that used in Group S. Time to loss of consciousness
Patients and Methods was determined as it has been for Group S. In addition, at the
After institutional ethics committee approval and written loss of eyelash reflex, the patients were given IV propofol
informed consent from patients, ninety adult American (1.5  mg/kg) over  15 s. Thirty seconds after completion of
Society of Anesthesiologists Physical Status I–II patients aged propofol induction, ease of mouth opening was assessed. If
18–65 years undergoing elective general surgery, orthopedics, inadequate, attempt every 30 s up to a maximum of four were
and plastic or gynecologic procedures were studied over a made, each time preceded by IV propofol bolus of 0.5 mg/kg.
period of 1 year. In between attempts, depth of anesthesia was maintained with
sevoflurane at 8% in 67%:33% ratio of N2O‑O2 at 8 L/min.
Exclusion criteria
1. Patients with a history of difficult intubation or anticipated Patients in Group P were induced with IV propofol 3 mg/kg
difficult intubation given over 30 s. Midway through induction at 15 s, the patients
2. Allergy or sensitivity to volatile anesthetics or to propofol were asked if they were feeling any pain from the injection. Loss
3. Body mass index >1.5 times normal of consciousness was assessed as for Group S and Group SP.
4. Heavy smokers (>20 cigarettes/day) Time to loss of consciousness was calculated from the time of
5. Patients with diabetes, hypertension, cardiovascular start of injection of propofol until loss of eyelash reflex and
disease, ischemic heart disease, liver disease, and renal inability to open eyes upon verbal command. Thirty seconds
impairment. after the completion of propofol induction, i.e., 60 s after the
start of propofol injection, ease of mouth opening was assessed.
Routine preoperative preparation was followed. In the morning
If inadequate, attempts every 30 s up to a maximum of four
of the surgery, patients were examined and blood pressure,
were made, each time preceded by IV propofol bolus of 0.5 mg/
pulse rate, and respiratory rate were recorded for further
comparison. kg. In case of apnea during induction, ventilation was assisted
manually between LMA insertion attempts. Additional propofol
The patients were then randomly allocated to the following was given if there was any adverse response such as movement,
three groups by computer‑generated slips. gagging, coughing, or laryngospasm. Noninvasive arterial
• Group S – Patients were induced with circuit primed with blood pressure, oxygen saturation, and heart rate were recorded
sevoflurane 8%, nitrous oxide and oxygen  (67%:33%) every minute for 5 min. An independent observer recorded:
at fresh gas flow  (FGF) rate 8  L/min by tidal volume 1. Time taken to loss of eyelash reflex
breathing (TVB) technique 2. Time taken to jaw relaxation
• Group SP – Patients were induced with circuit primed 3. Time taken to completion of successful insertion of LMA
with sevoflurane 8%, nitrous oxide and oxygen (67%:33%) 4. Successful insertion of LMA at first attempt
at FGF 8  L/min by TVB technique and injection 5. Apnea duration
intravenous (IV) propofol (1.5 mg/kg) 6. Incidence of apnea.
• Group  P  –  Patients were induced with IV injection
propofol only (3 mg/kg). The presence of complications related to anesthetic induction
was noted namely:
Technique 1. Excitatory movements during induction
All the CLMA insertion were performed by the same 2. Cough
anesthesia consultant well versed with LMA placement 3. Laryngospasm
(LMA classic >1000 procedures). All the patients in Group S
4. Hiccup and insertion of the LMA were noted.
and Group SP were induced with inhalation anesthetic mixture
comprising sevoflurane 8% and N2O:O2 67%:33% and FGF The presence of complications during LMA insertion was
at 8 L/min employing TVB technique through Bain’s circuit. noted namely:
The patients were instructed to continue breathing normally 1. Cough
through face mask during induction of anesthesia. The start 2. Gagging.

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Gupta, et al.: Effect of sevoflurane with propofol on insertion charactersitics of classic reusable LMA.

Subsequent to CLMA placement, IV vecuronium was was shortest in Group P (93.50 ± 31.92 s) which was statistically
administered and anesthesia was maintained on sevoflurane significant when compared to Group SP (115.73 ± 10.863 s)
and intermittent IV bolus of fentanyl. and Group S (202.7 ± 20.405 s) [Table 6].
Once fully awake, the patients were asked by a blinded First pass success rate of CLMA insertion was found to be
investigator for induction experience, sore throat, nausea, highest in Group SP (90%), which was statistically significant
and vomiting. when compared to Group  P  (56.7%) and Group  S  (13%)
Postoperative assessment instead of post operative interview: [Table 7].

1. Presence of sore throat (yes or no) There was no significant difference between incidence of
2. Pleasant induction (yes or no) laryngospasm and cough during induction between the three
3. Repeat same technique (yes or no) groups. Group P was found to have the highest incidence of
4. Postoperative nausea and vomiting (PONV) (yes or no). apnea during induction (73.3%) followed by Group SP (16.7%)
and least in Group S (6.71%). Duration of apnea was found
The sample size was calculated after a pilot study of 20 patients to be longest in Group  P  (178.23  ±  42.29 s), followed by
and was based on a difference of 20% between the groups for Group SP (40.16 ± 7.05 s) and least in Group S (41.33 ± 10.07
insertion characteristics for a type 1 error of 0.05 and a power s). No statistically significant difference was found between
of 0.8. Data analysis was done with the help of SPSS Software the three groups with respect to patient acceptance to induction
Version 15 (IBM, Chicago, USA) and Sigma Plot Version 12 technique.
12 (windows 8,Richmond,Washington,USA). Quantitative data
were presented with the help of mean and standard deviation. 83.3% in Group SP, 76.7% in Group P, and 83.3% in Group S
Comparison among the study groups was done with the help remarked their respective induction technique as pleasant
of unpaired t‑test and Mann–Whitney test as per the results of [Table 8].
normality test. Qualitative data were presented with the help of 93.3% patients in Group SP, 76.67% in Group P, and 73.3%
frequency and percentage table. Association among the study patients in Group S preferred repeating the same induction
groups was assessed with the help of Chi‑square test. P < 0.05 technique [Table 9].
was considered statistically significant.
73.43% in Group SP, 80% patients in Group P, and Group S
had postoperative sore throat.
Results
All the three groups were comparable with respect to Incidence of PONV was highest in Group S (33.3%), followed
age, sex, and weight  [Table  1]. The induction endpoint by Group SP (30%) and least in Group P (10%).
(loss of eyelash reflex) was 47.63  ±  6 s, 35.67  ±  5.85 s,
and 44.93  ±  8.737 s in Group  SP, Group  P, and Group  S, Discussion
respectively. The difference between time taken for loss of Majority of studies evaluating LMA insertion characteristics
eyelash reflex between the three groups was found to be using sevoflurane or propofol have employed the use of
statistically insignificant (P > 0.05) [Table 2]. In all the groups, CLMA and in the pediatric population. Limited evidence in
hemodynamic parameters were comparable at baseline and the form of literature is available regarding CLMA insertion
thereafter every 60 s during induction and insertion of CLMA characteristics using sevoflurane or propofol in adults, thereby
[Tables 3 and 4]. making this study unique. Chavan et  al. in their study on
Time taken for jaw relaxation was observed to be shortest in sixty patients compared CLMA insertion characteristics
Group P (68.67 ± 17.2 s) which was statistically significant using sevoflurane or propofol. Insertion time in this study in
when compared to Group  SP  (96.73  ±  7.10) and Group  S sevoflurane group was significantly shorter when compared
(145.93 ± 53.075 s) [Table 5]. Similarly, time to CLMA insertion to our study, albeit the method of induction was similar.

Table 1: The age‑ and sex‑wise distribution of the cases in studied groups


Age (years) S P SP
Male (%) Female (%) Total (%) Male (%) Female (%) Total (%) Male (%) Female (%) Total (%)
20‑29 0 2 (11.8) 2 (6.7) 2 (12.5) 0 2 (6.7) 0 1 (6.25) 1 (3.3)
30‑39 6 (46.2) 10 (58.8) 16 (53.3) 7 (43.8) 8 (57.1) 15 (50) 8 (57.1) 7 (43.8) 15 (50)
40‑49 4 (30.8) 4 (23.5) 8 (26.7) 5 (31.3) 3 (21.4) 8 (26.7) 5 (35.7) 8 (50.0) 13 (43.3)
50‑59 1 (7.7) 1 (5.9) 2 (6.7) 1 (6.3) 3 (21.4) 4 (13.3) 1 (7.1) 0 1 (3.3)
60‑65 2 (15.4) 0 2 (6.7) 1 (6.3) 0 1 (3.3) 0 0 0
Total 13 17 30 16 14 30 14 16 30
Mean±2SD 43.46±10.26 37.76±7.02 40.23±8.89 38.19±8.03 40.64±9.17 39.33±8.52 38.71±6.73 37.81±6.03 38.23±6.27
No significant differences in mean age of males of all the three groups and as well as females of these groups were found (P>0.05). SD=Standard deviation

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Gupta, et al.: Effect of sevoflurane with propofol on insertion charactersitics of classic reusable LMA.

Reduced insertion time in sevoflurane group in this study Siddik‑Sayyid et al. on comparing combination of sevoflurane
could be attributed to the use of vital capacity breath (VCB) (8% by VCB induction technique) and IV propofol (1.5 mg/kg)
during inhalation induction as compared to TVB method of with sevoflurane or propofol (2.5 mg/kg) in terms of insertion
inhalation induction in our study. The study also concluded characteristics of CLMA, observed results similar to our
that the first pass success rate of CLMA insertion was high study.[11]
and comparable in both sevoflurane and propofol group which Insertion characteristics may be influenced by both induction
is in marked contrast to our study.[9] agent, method of induction, and type of LMA. Therefore,
“ease of insertion” is a highly subjective, operator‑dependent
Shao and Zhang in their study on 90 elderly patients evaluated
assessment and thus subject to bias. Consequently, the first
CLMA insertion characteristics by comparing IV induction
insertion success rate and time taken to insert the LMA are
by propofol with inhalation induction using 8% sevoflurane
considered as surrogate markers of “ease of insertion.”
VCB technique or using 8% sevoflurane TVB technique. Their
observation that inhalation induction using 8% sevoflurane Molloy et  al. observed that anesthetic induction with
TVB technique provides a stable hemodynamic profile, a sevoflurane requires longer time to jaw relaxation and
prolonged CLMA insertion time concurs well with our study. even causes jaw tightness.[12] Dwivedi et  al. also reported
Further incidence of apnea was more in propofol group when jaw tightness after sevoflurane anesthetic induction, which
resulted in failure to insert the LMA in several patients.[13]
compared to sevoflurane groups which further cement our
However, in our study, LMA was successfully inserted in
observation.[10]
all patients.
In a meta‑analysis comparing anesthetic induction between
Table 2: Time taken for loss of eyelash reflex (s) sevoflurane and propofol, Joo and Perks found that
Group Mean±2SD n sevoflurane induction was associated with more patient
SP 47.63±7.645 30 dissatisfaction and increased PONV which is akin to our
P 35.67±5.857 30 observation.[14]
S 44.93±8.737 30
Group SP and S showed longer time taken for loss of eyelash reflex, as
Smith and Thwaites compared target‑controlled infusion of
compared with Group P which was found to be statistically very highly propofol with large initial concentration of sevoflurane for
significant (P<0.001). SD=Standard deviation LMA insertion.[15] Inhalation induction was associated with

Table 3: Mean heart rate in various groups after start of induction including laryngeal mask airway insertion (/min)
Group Baseline 1st 2nd 3rd 4th 5th
SP
Mean±SD 83.37±8.307 86.10±8.434 87.97±8.600 88.23±8.365 83.57±16.338 84.43±8.161
n 30 30 30 30 30 30
P
Mean±SD 83.23±8.169 86.47±7.995 88.00±8.120 88.60±7.762 86.90±7.783 84.83±7.639
n 30 30 30 30 30 30
S
Mean±SD 80.60±12.244 84.07±11.582 85.53±11.551 86.10±11.152 84.20±11.096 82.30±11.189
n 30 30 30 30 30 30
No statistically significant difference in heart rate. SD=Standard deviation

Table 4: Mean blood pressure (mmHg) in various groups after start of induction including laryngeal mask airway
insertion (/min)
Group Baseline 1st 2nd 3rd 4th 5th
SP
Mean±SD 93.10±9.561 89.10±9.248 87.40±8.985 86.63±6.790 84.63±5.684 84.60±5.587
n 30 30 30 30 30 30
P
Mean±SD 92.33±5.785 84.03±5.308 82.83±5.754 82.00±5.754 81.50±4.607 83.90±4.483
n 30 30 30 30 30 30
S
Mean±SD 90.27±5.471 88.70±8.371 87.23±9.269 84.97±6.672 82.37±5.720 83.73±5.681
n 30 30 30 30 30 30
No statistically significant difference in mean arterial pressure. SD=Standard deviation

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Gupta, et al.: Effect of sevoflurane with propofol on insertion charactersitics of classic reusable LMA.

Table 5: Time taken for jaw relaxation (s) Conclusion


Group Mean±2SD n In accordance with other similar studies, propofol owing to its
SP 96.73±7.100 30
quick onset is an excellent agent for LMA insertion. Rapidity
P 68.67±17.121 30 and ease of insertion it affords are better than sevoflurane or
S 145.93±53.075 30 its combination with propofol. Propofol was also associated
Time taken for jaw relaxation was found to be longest in Group S and with reduced incidence of nausea and vomiting. However,
statistically significant when compared to Group SP with t=5.033; the incidence and duration of apnea appear to be much more
P<0.0001 or Group P with t=7.589; P<0.0001. SD=Standard deviation longer with propofol induction.
Induction with sevoflurane was observed to be more
Table 6: Time taken for laryngeal mask airway time‑consuming as compared to propofol and was associated
insertion (s) with an increased number of attempts. Its use was also
Group Mean±2SD n associated with increased incidence of nausea and vomiting.
SP 115.73±10.863 30 The combination of sevoflurane and propofol appears to
P 93.50±31.921 30
be a better choice as it confers advantages of either agent.
S 202.70±20.405 30
Although time required for induction is considerably more
Time taken for LMA insertion at first attempt was found to be longest
in Group S and was statistically significant when compared to Group P with combination, the first attempt success rate is significantly
(t=15.787; P<0.0001) and Group SP (t=0.606; P<0.0001). LMA=Laryngeal more when compared to either agent alone. The combination
mask airway, SD=Standard deviation is associated with reduced incidence of apnea although it is
associated with nausea and vomiting. Our study did not observe
any statistically significant variation in hemodynamic variables
Table 7: Incidence of insertion of laryngeal mask airway
among the three groups.
at first attempt
Attempts SP (%) P (%) S (%) We did not measure the depth of anesthesia and this stands
1 27 (90.0) 17 (56.7) 13 (43.3) out as a limitation of our study as we employed two different
2 3 (10.0) 13 (43.3) 12 (40.0) methods of induction. Other limitation of this study is that we
3 0 0 5 (16.7) did not evaluate the three groups in terms of cost incurred.
Total 30 30 30
Financial support and sponsorship
Significant statistical difference was found in incidence of LMA insertion
at first attempt, between Groups SP and S (P<0.001) and Group P (P<0.01). Nil.
LMA=Laryngeal mask airway
Conflicts of interest
There are no conflicts of interest.
Table 8: Postoperative interview for pleasant induction
(yes/no) References
PI SP (%) P (%) S (%) 1. Taguchi M, Watanabe S, Asakura N, Inomata S. End‑tidal sevoflurane
Yes 25 (83.3) 23 (76.7) 25 (83.3) concentrations for laryngeal mask airway insertion and for tracheal
intubation in children. Anesthesiology 1994;81:628‑31.
No 5 (16.7) 7 (23.3) 5 (16.7)
2. Scanlon P, Carey M, Power M, Kirby F. Patient response to laryngeal
PI=Pleasant induction mask insertion after induction of anaesthesia with propofol or
thiopentone. Can J Anaesth 1993;40:816‑8.
3. Bilotta  F, Spinelli  F, Centola  G, Caramia  R, Rosa  G. A  comparison
Table 9: Postoperative interview for repeating same of propofol and sevoflurane anaesthesia for percutaneous trigeminal
technique ganglion compression. Eur J Anaesthesiol 2005;22:233‑5.
4. Hillman  DR, Walsh  JH, Maddison  KJ, Platt  PR, Kirkness  JP,
RST SP (%) P (%) S (%) Noffsinger WJ, et al. Evolution of changes in upper airway collapsibility
Yes 28 (93.3) 23 (76.67) 22 (73.3) during slow induction of anesthesia with propofol. Anesthesiology
No 2 (66.7) 7 (23.3) 8 (26.67) 2009;111:63‑71.
RST=Repeating same technique 5. Baker CE, Smith I. Sevoflurane: A comparison between vital capacity
and tidal breathing techniques for the induction of anaesthesia and
laryngeal mask airway placement. Anaesthesia 1999;54:841‑4.
more PONV (30% versus 3%) with delayed discharge; in our 6. Suzuki  KS, Oohata  M, Mori  N. Multiple‑deep‑breath inhalation
study, patients in Group S and Group SP had more frequent induction with 5% sevoflurane and 67% nitrous oxide: Comparison with
PONV than patients in Group P. This could be attributed to intravenous injection of propofol. J Anesth 2002;16:97‑101.
7. Ganatra SB, D’Mello J, Butani M, Jhamnani P. Conditions for insertion
antiemetic property of propofol, initial large concentration of of the laryngeal mask airway: Comparisons between sevoflurane and
sevoflurane, or swallowing of air and gases during inhalation propofol using fentanyl as a co‑induction agent. A  pilot study. Eur J
induction.[8] Anaesthesiol 2002;19:371‑5.

390 Anesthesia: Essays and Researches  ¦  Volume 12  ¦  Issue 2  ¦  April-June 2018
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Gupta, et al.: Effect of sevoflurane with propofol on insertion charactersitics of classic reusable LMA.

8. Yogendran S, Prabhu A, Hendy A, McGuire G, Imarengiaye C, Wong J, Massouh  FM, et  al. A  comparison of sevoflurane‑propofol versus
et al. Vital capacity and patient controlled sevoflurane inhalation result sevoflurane or propofol for laryngeal mask airway insertion in adults.
in similar induction characteristics. Can J Anaesth 2005;52:45‑9. Anesth Analg 2005;100:1204‑9.
9. Chavan  SG, Mandhyan  S, Gujar  SH, Shinde  GP. Comparison of 12. Molloy ME, Buggy DJ, Scanlon P. Propofol or sevoflurane for laryngeal
sevoflurane and propofol for laryngeal mask airway insertion and mask airway insertion. Can J Anaesth 1999;46:322‑6.
13. Dwivedi  R, Dwivedi  S, Chourasia  HK. A  comparative study of
pressor response in patients undergoing gynecological procedures.
sevoflurane and propofol for laryngeal mask airway insertion in adults.
J Anaesthesiol Clin Pharmacol 2017;33:97‑101. Int J Sci Study 2015;3:67‑71.
10. Shao  G, Zhang  G. Comparison of propofol and sevoflurane for 14. Joo HS, Perks WJ. Sevoflurane versus propofol for anesthetic induction:
laryngeal mask airway insertion in elderly patients. South Med J A meta‑analysis. Anesth Analg 2000;91:213‑9.
2007;100:360‑5. 15. Thwaites A, Edmends S, Smith I. Inhalation induction with sevoflurane:
11. Siddik‑Sayyid  SM, Aouad  MT, Taha  SK, Daaboul  DG, Deeb  PG, A double‑blind comparison with propofol. Br J Anaesth 1997;78:356‑61.

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