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Lee, Lee, Oh, Shin, Kim, Choe, Cheong, Lee, Lee, Lim, Kim, and Cho: The effect of propofol on emergence agitation in children receiving sevoflurane for adenotonsillectomy

Abstract

Background

The administration of a single dose of propofol is reported to be effective in decreasing the incidence and severity of emergence agitation (EA) in children following sevoflurane anesthesia. The aim of this study was to investigate the clinical usefulness of a single dose of propofol 1 mg/kg at the end of adenotonsillectomy for reducing the incidence of EA after sevoflurane anesthesia.

Methods

Ninety children, aged 3-8 years, undergoing adenotonsillectomy were randomized into two groups: the propofol group (n = 45) and the saline group (n = 45), of which 88 children completed the study. Anesthesia was maintained with sevoflurane 2-2.5 vol% and nitrous oxide/oxygen (50%/50%). At the completion of adenotonsillectomy, the propofol group patients were given 1 mg/kg of propofol and the saline group patients were given saline 0.1 ml/kg in the same volume. The incidence of EA was assessed with Aono's four point scale and the severity of EA was assessed with pediatric anesthesia emergence delirium (PAED) scale at 5 min (T5), 15 min (T15) and 30 min (T30) after emergence.

Results

Of the 88 patients, the incidence of EA at T5, T15 and T30 was 61.4%, 27.3%, and 4.5% in the propofol group while in the saline group was 68.2%, 29.5%, and 9.1%, respectively. The incidence and severity of EA were not found to be significantly different between the two groups, but the scales in each group decreased significantly over time.

Conclusions

The administration of propofol 1 mg/kg at the end of surgery did not have any significant effect in reducing the incidence and severity of EA in children undergoing adenotonsillectomy under sevoflurane anesthesia.

Introduction

Sevoflurane is widely used as an anesthetic agent for children because of its less pungent nature and also as it has a lower solubility and greater hemodynamic stability than the other potent inhaled anesthetics [1]. However, sevoflurane may have a greater incidence of emergence agitation (EA) in preschool aged children [2].
EA is characterized by non-purposeful restlessness and agitation, thrashing, crying or moaning, disorientation, and incoherence. Although generally self-limiting, EA can be dangerous and may occasionally result in physical harm to children. Sometimes sedative or analgesic drugs are used in post-anesthesia care units to treat EA. Therefore, recovery time can be prolonged and adverse events may result in these children [3].
Propofol is a short-acting sedative and hypnotic agent. Generally, propofol is used in children for its sedative action as well as for induction and maintenance of general anesthesia [4]. A recent study showed that continuous intravenous infusion of propofol decreased the incidence of EA in the children undergoing tonsillectomy [5] and the administration of 1 mg/kg propofol at the end of procedure decreased the incidence of EA in children undergoing magnetic resonance imaging (MRI) [6].
The administration of a single dose of propofol (1 mg/kg) at the end of surgery was also effective in decreasing the incidence of EA in children undergoing strabismus surgery under sevoflurane [7]. However, adenotonsillectomy is more distressing to children than strabismus surgery. The effect of administration of 1 mg/kg propofol in children following adenotonsillectomy may work differently from those undergoing MRI as reported by previous studies [6,7]. Therefore, the aim of this study was to investigate the clinical usefulness of a single dose of propofol at the end of adenotonsillectomy in reducing the incidence and severity of EA after sevoflurane anesthesia.

Materials and Methods

Children, between the ages of 3 and 8 years, with American Society of Anesthesiologists physical status I, who were scheduled to undergo adenotonsillectomy without myringotomy at the department of otolaryngology, were prospectively enrolled in this study. Prior to their enrollment, institutional review board approval and informed written parental consent were obtained. Children with mental, neurologic disease, or those using sedative medication were excluded.
Ninety children joined the study at our hospital between June 2007 and April 2009. A computer generated randomization was placed in sealed envelopes, which were opened on the day of the scheduled operation. Forty five children were randomly assigned to the propofol group and another forty five to the saline group. One child from the propofol group was excluded from the study because of intra-operative ST depression on EKG and one other child from the saline group was also excluded due to bleeding at the surgical region after extubation. Thus, the data for this study were collected from eighty-eight patients. Demographic profile, duration of surgery, duration of sevoflurane administration, and recovery characteristics are shown in Table 1, which shows no significant difference between the two groups.
Children were in fasting state for 8 hours and received 1 mg/kg of intravenous thiopental sodium before entering the operating room. An electrocardiogram, pulse oximeter and noninvasive arterial blood pressure monitor were attached. Anesthesia was induced with 5 mg/kg of intravenous thiopental sodium and 0.5 mg/kg of intravenous atracurium. Orotracheal intubation was performed. Anesthesia was maintained with O2 2 L/min, N2O 2 L/min and sevoflurane 2-2.5 vol%. Mechanical ventilation was performed to maintain an end-tidal CO2 between 30 and 35 mmHg. About 20 minutes prior to the end of surgery, ketorolac 1 mg/kg was administered intravenously to each patient for postoperative pain control.
At the completion of the operation, following the discontinuation of sevoflurane and nitrous oxide, children in the propofol group were given 1 mg/kg of propofol and children in the saline group were given the same volume of normal saline, 0.1 ml/kg. The orotracheal tube was removed when patients demonstrated spontaneous regular respiratory pattern and the rate of train of four (TOF) was higher than 0.8 by a nerve stimulator (TOF-Watch®, Organon, Ireland). Anticholinesterase agents that reverse the effect of neuromuscular blockade were not administered. Children were transferred to the post-anesthesia care unit (PACU) and one of their parents accompanied them at the PACU until discharge.
An anesthesiologist, who was blinded to the treatment allocation, evaluated the incidence of EA using Aono's four point scale (Appendix 1) and severity of EA using pediatric anesthesia emergence delirium (PAED, Appendix 2) scale, at 5 (T5), 15 (T15) and 30 (T30) minutes (min) after emergence. Emergence time was defined as the time of first response to command or eye opening on command after extubation. Aono's four point scale of 1 and 2 were considered as the absence of EA, and scales of 3 and 4 were considered as the presence of EA. PAED scale was used to assess the severity of EA. Pain was evaluated using children and infants postoperative pain (CHIPP, Appendix 3) scale and consciousness was evaluated using Ramsay sedation scale (Appendix 4) in the PACU by the same anesthesiologist at 5, 15 and 30 minutes after emergence. The incidence of postoperative nausea and vomiting (PONV) was also noted.
The following time intervals were recorded: the duration of surgery (from the time of opening mouth to the completion of the procedure), duration of sevoflurane administration (from the start of induction until discontinuation of sevoflurane), duration of extubation (from the time of discontinuation of sevoflurane to the removal of endotracheal tube) and duration of PACU stay (from arrival to the PACU until discharge). Children were discharged from the PACU to a ward when the modified Aldrete score was more than 9 without agitation and vomiting.
Statistical analysis was performed using MedCalc for Windows version 11.0 (MedCalc Software, Mariakerke, Belgium). A sample size of 40 in each group was calculated to achieve 80% power to detect a decrease in the incidence of agitation from 60% to 30% with a significance P value 0.05. Ninety patients were included. Continuous variables such as age, weight, duration of surgery, duration of sevoflurane administration, duration of extubation and duration of PACU stay were reported as mean ± SD and analyzed using independent samples t-test. Categorical variables were compared using chi-square test for gender and the incidence of EA and using Fisher's exact test for the incidence of PONV. Serial measurements such as Aono's four point scale, PAED scale, CHIPP scale, and Ramsay sedation scale were analyzed by repeated measures analysis of variance. A P value less than 0.05 was considered statistically significant.

Results

The mean scores of the Aono's four point scale at T5, T15 and T30 were 2.6 ± 1.1, 2.0 ± 0.8, and 1.5 ± 0.6 respectively in the propofol group while 2.9 ± 1.0, 2.0 ± 0.8, and 1.5 ± 0.7 in the saline group. The mean scores of the PAED scale at T5, T15 and T30 were 12.6 ± 4.6, 8.2 ± 3.8, and 5.0 ± 3.1 respectively in the propofol group while 13.8 ± 4.7, 8.0 ± 3.9, and 4.5 ± 3.1 in the saline group. The incidence and severity of EA at T5, T15, and T30 shows no significant difference between the two groups (Table 2, Fig. 1 and 2). CHIPP scale and Ramsay sedation scale were similar in the two groups at T5, T15, and T30 (Fig. 3 and 4). Therefore, there were no difference of the intensity of pain and the level of consciousness between the two groups at 5, 15, and 30 min after emergence. Aono's four point scale, PAED scale and CHIPP scale in each group decreased significantly over time. All agitation episodes were self-limited.
9.1% of the propofol group and 13.6% of the saline group had episodes of PONV, but there was no significant statistical difference between the two groups. No adverse events such as laryngospasm and oxygen desaturation episodes were recorded in any of the children. Time to discharge from the PACU was not significantly different between the two groups.

Discussion

Several previous studies have reported that sevoflurane anesthesia caused children to have a higher incidence of EA. Children anaesthetized with sevoflurane had a 67% incidence of postoperative agitation while halothane group had a 29.2% incidence [8]. Although the possible etiological factors of EA are post-anesthesia, surgery, rapid emergence, postoperative pain, age, preoperative anxiety, child temperament, and adjuvant medication, the causes for higher incidence of EA after sevoflurane are not fully understood. Because inhalational anesthetics with low blood solubility such as sevoflurane generally tend to cause a higher incidence of EA, rapid awakening in an unfamiliar environment has also been posited as a cause for this phenomenon.
Propofol allows for rapid emergence from general anesthesia and is not associated with a high incidence of EA in young children [9]. Recovery from propofol anesthesia is smooth and delayed, so propofol anesthesia is associated with a lower incidence of EA compared to sevoflurane [5]. The decreased incidence of EA could be accounted for the residual sedative effect and euphoric effect of propofol in the early recovery period [10]. Based on previous studies, propofol seems to be effective in preventing EA and is dependent on the timing of administration [11]. Despite this fact, sevoflurane is considered the agent of choice for induction and maintenance of anesthesia for children and is widely used among pediatric anesthesiologists. A single dose of propofol at the end of surgery could delay or modify emergence and decrease the incidence of EA after sevoflurane anesthesia.
Abu-Shahwan's study [6] showed that the administration of sub-hypnotic doses of propofol at the end of sevoflurane general anesthesia was effective in decreasing the incidence and severity of EA in children undergoing MRI. Aouad et al. [7] reported that the administration of a single dose of propofol 1 mg/kg after discontinuation of sevoflurane at the end of surgery in children undergoing strabismus surgery significantly decreased the incidence of EA and improved patient satisfaction, and they concluded that the delayed emergence from anesthesia reduced PAED scales without delaying discharge from the PACU. However, Abu-Shahwan's case did not include painful procedures and the characteristics of strabismus surgery in Aouad's research were different from those of adenotonsillectomy in our study.
We supposed that the effect of propofol on EA in patients undergoing adenotonsillectomy may be different from that in strabismus patients, and then tried to investigate the effect of 1 mg/kg propofol administration on the incidence and severity of EA at the end of adenotonsillectomy after discontinuation of sevoflurane. The single dose of propofol administration didn't have significant effect on the decrease of the incidence and severity of EA in the present study.
The percentage of EA at T5 was 61.4% in the propofol group and 68.2% in the saline group using Aono's four point scale in our study. The definition of EA in the study included children who were inconsolably crying as well as restless and therefore the incidence of EA might increase from 10 to 30% compared to other studies [12]. The PAED scale is a reliable and valid measurement that may minimize measurement errors in the clinical evaluation of EA [13]. However, the calculation of the incidence of EA with this scale is difficult, so, we assess the presence of EA using Aono's four point scale and the severity of EA using the PAED scale.
What causes the propofol to have no effect on preventing EA in our study? First, sevoflurane-related EA is affected by a combination of surgical procedures rather than the impact of propofol alone. The administration of propofol 1 mg/kg after sevoflurane anesthesia is effective on EA in Aouad's with strabismus surgery but this method is not effective in our study with adenotonsillectomy. Although the surgery type itself that involves the tonsil, middle ear, and eye are a major factor for inducing EA, adenotonsillectomy is the more important independent risk factor for EA than strabismus surgery [14]. Strabismus surgery may be related to visual disturbance. On the other hand, adenotonsillectomy may be associated with throat pain and bleeding irritation. Eckenhoff et al. [15] speculated that "sense of suffocation" during emergence from anesthesia may contribute to EA in patients undergoing head and neck surgery. Second, inadequate pain relief may be the stronger cause of EA than sevoflurane. Cohen et al. [16] reported a 2.5 µg/kg dose of fentanyl minimized the incidence of EA to 18% after general anesthesia with sevoflurane. Bakhamees et al. [17] reported that the combination of low dose fentanyl before surgery and propofol at the end of surgery decreased the incidence and level of emergence agitation in children after adenotonsillectomy procedure under sevoflurane anesthesia. Kim et al. [18] reported that propofol 1 mg/kg at the strabismus surgery under sevoflurane anesthesia did not reduce EA in children, and they emphasized the importance of pain control. Ketorolac 1 mg/kg was administered to all children in both groups but it was not effective against EA, although it decreased the incidence EA in children undergoing myringotomy after sevoflurane anesthesia (38% vs. 14%) [19]. Compared with other studies, a smaller amount of analgesic agents were used in our study and additional analgesic drugs were not administered to children in the PACU. Nevertheless, CHIPP scales in this study were increasingly reduced than previous values as patient's recovery progressed. CHIPP scales were not influenced by propofol because propofol is not an analgesic agent. Third, there is a question about a larger dose than 1 mg/kg propofol can be effective in preventing EA in children undergoing adenotonsillectomy. The duration of extubation was 13.7 ± 3.8 min in the propofol group while the duration of extubation was 12.2 ± 4.1 min in the saline group. The administration of propofol 1 mg/kg at end of surgery did not prolong the duration of extubation significantly compared with the saline group in our study. Although several studies reported that rapid awakening is an independent risk factor of EA [14,20], delayed awakening with a large dose of propofol could increase adverse effects such as hypotension, bradycardia, apnea and close observation should be necessary. In addition, the effect of propofol in children undergoing painful procedures is still controversial and a study on the amount of propofol about incidence of EA has not been reported yet. Further investigations are necessary to assess the relation between the dose of propofol and the incidence of EA.
Many studies have shown that EA is self-limited and is resolved without pharmacologic intervention over time [12,14,20]. Our data also demonstrated that the incidence and severity of EA and pain intensity are improved over time without analgesic or sedative drugs. Our study allowed children to stay with one of parents in the PACU and this seemed to help them to acclimate themselves to a strange and naïve environment.
In our study, there was no significant decrease in the incidence and severity of emergence agitation after the administration of a single dose of 1 mg/kg propofol at the end of surgery in children undergoing adenotonsillectomy under sevoflurane anesthesia. However, the incidence and severity of emergence agitation significantly decreased over time and there was a statistically significant time effect. It is not recommended to administer 1 mg/kg of propofol at the end of surgery to children who follow sevoflurane anesthesia for adenotonsillectomy in order to reduce emergence agitation. One of the limitations of this study was the difficulty in differentiating between pain and delirium. Considering the type of surgery, adequate analgesic modalities should be chosen to minimize postoperative pain. There is a need to further investigate the effects or benefits on different doses, different methods of administration, or additional analgesic treatments to examine the effects of propofol on emergence agitation in children receiving sevoflurane for adenotonsillectomy.

Acknowledgements

I sincerely thank my family and colleagues for their encouragement and support.

Notes

This is a theisis for a master's degree.

References

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Appendix

Appendix 1

Aono's Four Point Scale

kjae-59-75-a001.jpg

Appendix 2

Pediatric Anesthesia Emergence Delirium Scale

kjae-59-75-a002.jpg
The scores of each item were summed to obtain a Pediatric Anesthesia Emergence Delirium (PAED) scale. The highest value of PAED scale is 20.

Appendix 3

Children and Infants Postoperative Pain Scale

kjae-59-75-a003.jpg
The scores of each item were summed to obtain a children and infants postoperative pain (CHIPP) scale. The highest value of CHIPP scale is 10.

Appendix 4

Ramsay Sedation Scale

kjae-59-75-a004.jpg
Fig. 1
Aono's four point scale at 5 (T5), 15 (T15) and 30 (T30) minutes after emergence. Aono's four point scales significantly decreased over time (P < 0.001) and there was a statistically significant time effect in each group (*P < 0.001 in the propofol group and P < 0.001 in the saline group). Group effect averaged across time did not show significant difference (P = 0.465) and the interaction effect of group and time was also not statistically significant (P = 0.196). Values are presented as mean ± SEM.
kjae-59-75-g001.jpg
Fig. 2
Pediatric anesthesia emergence delirium (PAED) scale at 5 (T5), 15 (T15), and 30 (T30) minutes after emergence. PAED scales significantly decreased over time (P < 0.001) and there was a statistically significant time effect in each group (*P < 0.001 in the propofol group, P < 0.001 in the saline group). Group effect averaged across time did not show significant difference (P = 0.709) and the interaction effect of group and time was not statistically significant (P = 0.093). Values are presented as mean ± SEM.
kjae-59-75-g002.jpg
Fig. 3
Children and infants postoperative pain (CHIPP) scale at 5 (T5), 15 (T15), and 30 (T30) minutes after emergence. CHIPP scales significantly decreased by time (P < 0.001) and there was a statistically significant time effect in each group (*P < 0.001 in propofol group, P < 0.001 in saline group). Group effect averaged across time did not show significant difference (P = 0.428) and the interaction effect of group and time was not statistically significant (P = 0.312). Values are presented as mean ± SEM.
kjae-59-75-g003.jpg
Fig. 4
Ramsay sedation scale at 5 (T5), 15 (T15), and 30 (T30) minutes after emergence. Ramsay sedation scales did not show significant difference over time (P = 0.436). Group effect and interaction effect of group and time were not statistically significant (P = 0.116 and 0.679). Values are presented as mean ± SEM.
kjae-59-75-g004.jpg
Table 1
Demographic and Recovery Characteristics
kjae-59-75-i001.jpg

Values are presented as mean ± SD or number. Children in the propofol group were given 1 mg/kg of propofol and children in the saline group were given the same volume of normal saline, 0.1 ml/kg. PACU: post-anesthesia care unit, PONV: postoperative nausea and vomiting.

Table 2
Incidence of Emergence Agitation
kjae-59-75-i002.jpg

Values are presented as number (%). T5, T15, and T30 represent the time after emergence (min). Children in the propofol group were given 1 mg/kg of propofol and children in the saline group were given the same volume of normal saline, 0.1 ml/kg.



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