Year : 2009 | Volume
| Issue : 2 | Page : 61-66
Sevoflurane-emergence agitation: Effect of supplementary low-dose oral ketamine premedication in preschool children undergoing dental surgery
Ahmed Metwally Khattab, Zeinab Ahmed El-Seify
Ain Shams University, Cairo, Egypt, Doha Clinic Hospital, Department of Anesthesia, Doha, Qatar
Ahmed Metwally Khattab
Ain Shams University, Cairo, Egypt, Doha Clinic Hospital, Department of Anesthesia, Doha, Qatar
Source of Support: None, Conflict of Interest: None
|Date of Web Publication||27-Nov-2009|
Background and Objectives: The use of sevoflurane in pediatric anesthesia, which could enable a more rapid emergence and recovery, is complicated by the frequent occurrence of post-anesthesia agitation. This study aims to test the efficacy of adding a low dose of ketamine orally, as a supplement to the midazolam-based oral premedication for reducing sevoflurane-related emergence agitation. Materials and Methods: Ninety-two preschool children, aged between two and six years, with an American Society of Anesthesiologists physical status I or II, scheduled for elective dental filling and extractions under general anesthesia were included. The patients were allocated into two groups: Group M (46 patients) received oral midazolam 0.5 mg/kg, mixed with ibuprofen 10 mg/kg, while group KM (46 patients) received a similar premedication mixture, in addition to ketamine 2 mg/kg. The acceptance of the drug mixture, the onset of action, and the occurrence of vomiting were monitored over the next 30 minutes. Induction of anesthesia was carried out using sevoflurane 8 Vol% in 100% oxygen via face mask. Anesthesia was maintained with sevoflurane 1.5-2 Vol% in an oxygen-nitrous oxide mixture. After extubation, the standard scoring scale was used for assessing the quality of emergence. Agitation parameters were measured using a five-point scale. Agitated children were managed by giving intravenous increments of fentanyl 1 μg/ kg. The time of hospital discharge allowance was recorded. Results: Drug palatability, vomiting, and onset of action of premedication; showed no significant differences between both groups. Time of eye opening after discontinuation of sevoflurane showed no significant differences between both groups. Postoperative agitation score and rescue fentanyl consumption were higher in group M than in group KM on admission to the PACU ( P < 0.01). The time of hospital discharge allowance in group M was longer than in group KM ( P< 0.05). Conclusion: Adding a low dose of oral ketamine to midazolam-based oral premedication in preschool children undergoing dental surgery reduced sevoflurane-related emergence agitation without delaying discharge.
Keywords: Agitation, ketamine, midazolam, pediatric anesthesia, premedication, sevoflurane
|How to cite this article:|
Khattab AM, El-Seify ZA. Sevoflurane-emergence agitation: Effect of supplementary low-dose oral ketamine premedication in preschool children undergoing dental surgery. Saudi J Anaesth 2009;3:61-6
|How to cite this URL:|
Khattab AM, El-Seify ZA. Sevoflurane-emergence agitation: Effect of supplementary low-dose oral ketamine premedication in preschool children undergoing dental surgery. Saudi J Anaesth [serial online] 2009 [cited 2021 Jul 31];3:61-6. Available from: https://www.saudija.org/text.asp?2009/3/2/61/57878
| Introduction|| |
Sevoflurane is widely used in pediatric anesthesia because of fast and well-tolerated inhalational induction, low hepatotoxicity, hemodynamic stability, and rapid emergence from anesthesia.  However, the occurrence of emergence agitation in children is the major disadvantage of this volatile anesthetic, with the reported incidence up to 80%. 
Emergence agitation (also called emergence delirium) can be defined as a 'disturbance in a child's awareness of his/her environment with disorientation and perceptual alteration including hypersensitivity to stimuli and hyperactive motor behavior in the immediate post anesthesia period'.  It may not only cause injury to the child or to the surgical site, but also lead to the accidental removal of the surgical dressings, IV catheters, and drains. Extra nursing care may often be necessary as well as supplemental sedative and/or analgesic medications. Parents who witness emergence agitation in their child may worry about permanent sequelae. 
Rapid emergence and increased pain sensation have been proposed as possible causes of emergence agitation seen with sevoflurane.  However anxiolytic premedication and effective analgesia does not necessarily prevent emergence agitation and may even cause delayed recovery and hospital discharge or affect the quality of life of the child after discharge. ,
Various pre-, intra-, and immediate postoperative pharmacological (analgesics, opioids, benzodiazepines, clonidine, and dexmedetomidine) and non-pharmacological techniques were used with the aim of reducing the occurrence of emergence agitation after sevoflurane-based anesthesia, with variable results. , Oral premedication with midazolam and/or ketamine is widely used in pediatric anesthesia, to reduce emotional trauma, ensure smooth induction, and minimize emergence agitation. However, various dosing regimens were used alone or in combination, with variable efficacies and side effect profiles. , Only few studies tested the role of intravenous ketamine in reducing emergence agitation after sevoflurane, with no available data regarding its use in small oral doses alone or in combination with oral midazolam.
The aim of the this study was to investigate the effects of adding a low oral dose of ketamine to midazolam-based oral premedication in preschool children undergoing dental surgical procedures, focusing on its effect on sevoflurane-related emergence agitation in comparison to midazolam alone.
| Materials and Methods|| |
This was a prospective, randomized, double blind, single center study that was carried out in the Doha Clinic Hospital (75 beds). The child was given a toy by the anesthetist who was going to anesthetize him, and what was going to occur on the morning of surgery was explained to him, but he was blind to the used drug.
The anesthetist who saw the patient preoperatively and anesthetized him was blind to the premedication. Parents were not aware of the premedication components.
After receiving approval from the Hospital Ethics Committee and with written consents from the parents, 92 preschool children, aged between two and six years, were scheduled for elective dental filling and extractions under general anesthesia, with the expected duration of surgery being one to two hours. The sample size was determined assuming that the probability of sevoflurane agitation was 40%. We calculated that a sample size of 42 children per treatment group would have at least a 90% power (B error = 0.1) to detect a difference of 30% in the incidence of emergence agitation. Because we expected some exclusions and failures to follow up during the course of the study (which almost did not happen), we increased the number of the sample size to 48 children. Flow chart of patients through the trial [Figure 1].
The children were randomly allowed to participate in this study. Any child who was either ASA I or II was a candidate. Exclusion criteria included, 'children with developmental problems, cerebral palsy, Down syndrome, inborn errors of metabolism, a history of epileptic fits, body weight less than 10 kg, or greater than 26 kg (Children below age of six years with body weight more than 26 kg were definitely obese with a risk of airway obstruction, along with the abnormal volume of distribution of drugs if given according to their actual body weight). Patients with known allergy to any of the medications used for procedures that lasted less than 30 minutes or longer than two hours, were excluded'. The patients were randomly assigned to receive either midazolam (Group M) or ketamine-midazolam (Group KM) as oral premedication, via computer-generated random numbers.
During the preoperative visit, each enrolled child was asked to choose a sealed envelope with his code number inside. The name, file number, and body weight were recorded on the sealed envelope after been chosen.
On the morning of operation, the study drugs were prepared by a trained nurse (who was not involved in any other part of the study) into identical 5 ml-syringes being sequentially numbered. Labeled syringes were mixed with ibuprofen just before giving to the child. Premedication was given by one of the parents, under the supervision of another nurse.
Group M patients received oral midazolam (Dormicum 5 mg/1 ml-F. Hoffmann-La Roche Ltd, Switzerland) in a dose of 0.5 mg/kg mixed with ibuprofen suspension 10 mg/kg, and Group KM patients received a similar premedication mixture in addition to ketamine (Ketalar™, Pfizer, 50 mg/ml) in a dose of 2 mg/kg. Acceptance of the drug (palatability) [Table 1],  onset of action, and the occurrence of vomiting were monitored by the attending nurse over the next 30 minutes. The patient was then transferred to the operating room accompanied by his parent(s). Presence of the parents in the induction room is not routinely permitted in our hospital. Induction of anesthesia was carried out using sevoflurane (Abbott) 8 Vol% in 100% oxygen (6 Ls/min) through a face mask. Intravenous cannulation was allowed for 60 seconds from initiation of mask induction. Atropine 0.02 mg/kg, fentanyl 1mg/kg, and cisatracurium 0.15 mg/kg were given.
Manual ventilation was started for three minutes, and then intubation with a suitable size, lubricated, and cuffed nasal endotracheal tube was carried out. Anesthesia was maintained using sevoflurane 1.5-2 Vol% in (35:65%) oxygen and nitrous oxide. Ventilation was adjusted to keep end-tidal CO 2 between 32-40 mmHg. Intravenous paracetamol (Perfalgan® 100 ml vial UPSA France) 15 mg/ kg was infused shortly after induction. All patients were monitored using electrocardiography, pulse oximetry, non-invasive blood pressure/5 min., inspiratory and expiratory N 2 O, O 2 and sevoflurane, end-tidal CO 2 ; and the peak and plateau airway pressures.
At the end of surgery, the anesthetic agents were discontinued (T zero) and replaced with O 2 100% (6 Ls/ min). Residual neuromuscular blockade was reversed by neostigmine and atropine. The endotracheal tube (ETT) was removed when the patients were awake. The time from the discontinuation of anesthesia (T zero) till the time of eye opening (defined as the time until the eye opened on verbal command) was recorded.
Agitation parameters were assessed with a five-point emergence agitation scale [Table 2],  and measured on admission to the post anesthesia care unit (PACU) and one hour after extubation. Delirium was defined as the agitation score of ≥4 for more than five minutes, despite all calming efforts done by the parents. 
In the PACU, parents were allowed to be with their child. Agitated children were managed by giving intravenous increments of fentanyl 1 μg/kg with at least a 10-minute time interval between each dose, during which time the children were monitored for any signs of respiratory depression. All scores and observations were recorded by the anesthesia technician who was unaware of the type of premedication. The time of hospital discharge allowance was recorded (starting from the time of eye opening). Patients were not allowed to go home unless they fulfilled the discharge criteria. 
The sample size was determined assuming that the probability of sevoflurane agitation was 40%. We calculated that a sample size of 42 children per treatment group would have at least a 90% power (B error = 0.1) to detect a difference of 30% in the incidence of emergence agitation. Because we expected some exclusions and failure to follow up during the course of the study (which almost did not happen), we increased the number of the sample size to 48 children. Analysis of data was done by IBM computer using SPSS (Statistical program for social science) as follows:-
Unpaired t-test was used to compare quantitative variables between two independent groups in the parametric data.
- Description of quantitative variables in the forms of mean, standard deviation (SD), and range.
- Description of qualitative variables in the forms of numbers and percentage (%).
Chi-square test was used to compare qualitative variables.
| Results|| |
Ninety-two patients (46 of them were premedicated using midazolam only ͻGroup M and 46 with midazolam and ketamine ͻGroup KM), were included in this study from October 2007 to November 2008. Demographic data, duration of anesthesia, and the number of extracted teeth are presented in [Table 3] and they showed no evidence of differences between groups. Children of both groups accepted the premedication mixture according to the *Acceptance Score* as shown in [Table 4], with no evidence of difference between groups, P > 0.05. Vomiting was recorded in one patient in group KM, in whom half of the initial premedication dose was repeated. Although there was no evidence of difference between groups with regard to the onset of action of premedication, clinically the onset was shorter in group KM., as shown in [Table 4].
Time to eye opening, agitation scoring, postoperative fentanyl consumption, and time of hospital discharge allowance are shown in [Table 5]. Time to eye opening was similar in both groups. On admission to the PACU, 37% (17 out of 46, with 10 of them matching score 5) of the children in group M, developed signs and symptoms of agitation that necessitated giving a rescue dose(s) of fentanyl, in comparison to the agitated children within group KM of 11% (Five out of 46 with three of them matching score 5) P < 0.01 [Figure 2]. Fentanyl was given once to all agitated children within group KM, while three of the agitated children in group M needed a second rescue fentanyl dose. Total fentanyl consumption within group M was significantly higher in comparison to group KM (5.08 ± 9.6 vs. 2.021 ± 5.97) P < 0.01.
The time for hospital discharge of group M (211.± 6 21.8) was longer than group KM (191.7 ± 30.6) P < 0.05.
| Discussion|| |
Sevoflurane-related emergence agitation (EA) with a reported incidence of up to 80%, remains a significant post-anesthetic problem that interferes with children's recovery, and challenges the PACU staff in terms of assessment and treatment. 
It is, however, usually self-limited (15-30 min.).  The exact etiology of sevoflurane-related EA remains unclear. Inadequate pain relief may be the cause of agitation,  particularly after short surgical procedures for which peak effects of analgesics may be delayed until the child is completely awake.  Intraoperative administration of I.V. ketorolac 1 mg/kg for minor otorhinolaryngological procedures decreases the incidence of EA three to four times, after both halothane and sevoflurane anesthesia.  Fentanyl given either I.V. 2.5 μg/kg  or intranasal 2 μg/ kg  also decreases EA. Similarly; caudal block using clonidine  has been seen to be effective.
In our study, we used preemptive ibuprofen (10 mg/ kg), induction I.V. fentanyl 1 μg/kg, and intravenous paracetamol 15 mg/kg to optimize pain management.
On the other hand, post anesthesia agitation has been observed when pain is efficiently treated , or even when absent. 
It has been postulated that rapid awakening after the use of the insoluble anesthetics, such as sevoflurane, may initiate EA. 
However, recovery from propofol anesthesia, which is also rapid, is smooth and pleasant in comparison to sevoflurane. 
It is becoming increasingly clear that sevoflurane-related EA is probably an intrinsic characteristic of the anesthetic itself, having central nervous effects different from other volatile anesthetics, particularly in younger children.  Epileptiform activity has been reported during the use of sevoflurane anesthesia in non-epileptic patients.  This could be caused by rapid changes in sevoflurane concentration at the target sites in the brain where the g-aminobutric acid-ergic properties of sevoflurane would induce changes in the balance between neuronal synaptic inhibition and excitation. 
Data on the possible role of premedication in reducing EA were conflicting. Preoperative administration of 0.5 mg/ kg midazolam orally, for 15 minutes before induction, in children undergoing bilateral ear tube insertion reduced the incidence of EA with sevoflurane (from 66.7 to 39.3%),  This was almost identical to the 37% incidence of EA recorded within the midazolam-premedicated patients in the current study. Similar studies using oral midazolam premedication in comparison to other drugs failed to show an improved incidence of EA following sevoflurane anesthesia. ,
Ketamine is commercially available as a racemic mixture of R (-) and S (+) enantiomeres. It is a non-competitive N-methyl D-aspartate (NMDA) receptor antagonist that can inhibit the 'wind up phenomenon' (central sensitization) in spinal cord neurons. It is this antagonistic effect that accounts for most of the analgesic, amnesic, psychotomimetic, and neuroprotective effects.  Two previous studies have been investigated for the efficacy of using intravenous ketamine in small doses, in reducing the incidence of EA following sevoflurane. There are no available studies using oral ketamine to test this point. The results of the current study support the conclusion reached by Kawarguchi et al. who used ketamine 1 mg/kg intravenously after induction of sevoflurane anesthesia in children undergoing strabismus surgery.  Similarly, small doses of ketamine (0.25 mg/kg) given just before sevoflurane discontinuation in the study carried out by Dalens et al. (2006), on children undergoing cerebral magnetic resonance imaging were shown to be effective in ameliorating EA.  The discharge time was not prolonged in both studies. Orally administered ketamine has a very high hepatic first pass effect, with only 16% of the dose being bioavailable. Most of the drug is metabolized into norketamine, which may contribute to the analgesic effect. 
Oral ketamine premedication avoids the very high peak concentrations produced by I.V. injection, which may be associated with the undesirable side effects. 
In animal studies, ketamine was shown to potentiate the release of melatonin, while halothane did the opposite.  Melatonin demonstrated beneficial results in children, in attenuating emergence agitation following sevoflurane anesthesia. 
One of the limitations of the current study is the absence of a placebo-controlled group. It was initially suggested, but rejected by the Hospital Ethics Committee. There is much debate about the reliability and validity of the tool used to measure emergence agitation in young children. Although the Pediatric Anesthesia Emergence Delirium (PAED) scale, which was developed in 2004,  appears to be the most reliable tool for the measurement of EA; yet it was difficult for us to train the observers to apply it in a short time. Therefore we used the simpler and rapidly applicable 'Five-point scale'. Although the focus of our study was to evaluate EA, one cannot neglect the effects of the used drugs on the induction criteria and the reaction to parents' separation.
| Conclusion|| |
Adding a low dose of oral ketamine to midazolam-based oral premedication in preschool children undergoing dental surgery reduces sevoflurane-related emergence agitation, without delaying discharge. The results of this study should open a new concept of 'multi-modal premedication'.
| References|| |
|1.||Isik B, Arslan M, Tunga AD, Kurtipek O. Dexmedetomidine decreases emergence agitation in pediatric patients after sevoflurane anaesthesia without surgery. Pediatr Anesth 2006;16:748-53. |
|2.||Kuka PJ, Bressem M, Tryba M. Clonidine prevents sevoflurane-induced agitation in children. Anesth Analg 2001;93:335-8. |
|3.||Sikich N, Lerman J. Development and psychometric evaluation of pediatric anesthesia-emergence delirium scale. Anesthesiology 2004;100:1138-45. [PUBMED] [FULLTEXT] |
|4.||Veyckemans F. Excitation phenomena during sevoflurane anaesthesia in children. Curr Opin Anaesthesiol 2001;14:339-43. [PUBMED] [FULLTEXT] |
|5.||Aono J, Ueda W, Mamiya K, Takimoto E, Manabe M. Greater incidence of delirium during recovery from sevoflurane anesthesia in preschool boys. Anesthesiology 1997;87:1298-300. [PUBMED] [FULLTEXT] |
|6.||Viitanen H, Annila P, Viitanen M, Tarkkila P. Premedication with midazolam delays recovery after ambulatory sevoflurane anesthesia in children. Anesth Analg 1999;9:75-9. |
|7.||Weldon BC, Bell M, Graddock T. The effect of caudal analgesia on emergence agitation in children after sevoflurane versus halothane anesthesia. Anesth Analg 2004;98:321-6. |
|8.||Kulka PJ, Bressem M, Wiebalck A, Tryba M. Prevention of post-sevoflurane delirium with midazolam. Anaesthesist 2001;50:401-5. [PUBMED] [FULLTEXT] |
|9.||Funk W, Jakob W, Riedl T, Taeger K. Oral pre-anaethetic medication for children: Double-blind randomized study of a combination of midazolam and ketamine vs midazolam or ketamine alone. Br J Anaesth 2000;48:335-40. |
|10.||Pandit UA, Collier PJ, Malviya S, Voepel-Lewis T, Wagner D, Siewert MJ. Oral transmucosal midazolam premedication for preschool children. Can J Anaesth 2001;48:191-5. [PUBMED] [FULLTEXT] |
|11.||Brennan LJ. Day-stay surgery. In: Sumner E, Hatch DJ, editors. Textbook of Paediatric Anaesthetic Practice. 2 nd ed. London: Edward Arnold; 1999. |
|12.||Davis PJ, Greenberg JA, Gendelman M, Fertal K. Recovery characteristics of sevoflurane and halothane in preschool-aged children undergoing bilateral myringotomy and pressure equalization tube insertion. Anesth Analg 1999;88:34-8. [PUBMED] [FULLTEXT] |
|13.||Cohen IJ, Finkel JC, Hannalla RS, Hummer KA, Patel KM. The effect of fentanyl on the emergence characteristics after desflurane or sevoflurane anesthesia in children. Anesth Analg 2002;94:1178-81. |
|14.||Galinkin JL, Fazi LM, Cuy RM, Chiavacci RM, Kurth CD, Shah UK, et al. Use of intranasal fentanyl in children undergoing myringotomy and tube placement during halothane and sevoflurane anesthesia. Anesthesiology 2000;93:1378-83. [PUBMED] [FULLTEXT] |
|15.||Bock M, Kunz P, Schreckenberger R, Graf BM, Martin E, Motsch J. Comparison of caudal and intravenous clonidine in the prevention of agitation after sevoflurane in children. Br J Anaesth 2002;88:790-6. [PUBMED] [FULLTEXT] |
|16.||Uezono S, Goto T, Terui K, Ichinose F, Ishguro Y, Nakata Y, et al. Emergence agitation after sevoflurane versus propofol in pediatric patients. Anesth Analg 2000;91:563-6. [PUBMED] [FULLTEXT] |
|17.||Welborn LG, Hannallah RS, Norden JM, Ruttimann UE, Callan CM. Comparison of emergence and recovery characteristics of sevoflurane and halothane in pediatric ambulatory patients. Anesth Analg 1996;83:917-20. [PUBMED] [FULLTEXT] |
|18.||Yli-Hankala A, Vakkuri A, Sδrkelδ M, Lindgren L, Korttila K, Jδntti V. Epileptiform electroencephalogram during mask induction of anesthesia with sevoflurane. Anesthesiology 1999;91:1596-603. |
|19.||Lapin SL, Auden SM, Goldsmith LJ,Reynolds AM. Effect of sevoflurane anesthesia on recovery in children: A comparison with halothane. Pediatr Anesth 1999;9:299-304. |
|20.||Woolf CJ, Thompson SW. The induction and maintenance of central sensitization is dependent on N-methyl-D-aspartic acid receptor activation: Implications for the treatment of post injury pain hypersensitivity states. Pain 1991;44:293-9. [PUBMED] [FULLTEXT] |
|21.||Kawaraguchi Y, Miyamoto Y, Fukumitsu K, Taniguchi A, Hirao O, Kitamura S, et al. The effect of ketamine on reducing postoperative agitation of sevoflurane in pediatric strabismus surgery. Masui 2002;51:1343-8. [PUBMED] [FULLTEXT] |
|22.||Dalens BJ, Pinard AM, Lιtourneau DR, Albert NT, Truchon RJ. Prevention of emergence agitation after sevoflurane anesthesia for pediatric magnetic resonance imaging by small doses of ketamine or nalbuphine administered just before discontinuing anesthesia. Anesth Analg 2006;102:1056-61. |
|23.||Grant IS, Nimmo WS, Clements JA. Pharmacokinetics and analgesic effects of IM and oral ketamine. Br J Anaesth 1981;53:805-9. [PUBMED] [FULLTEXT] |
|24.||Yvonne Humphries RN, Michelle Melson RN, Gore D. Superiority of oral ketamine as an analgesic and sedative for wound care procedures in the pediatric patient with burns. J Burn Care Rehabil 1997;18:34-6. |
|25.||Pang CS, Mulnier C, Pang S, Yang JCS. Effects of halothane, pentobarbital, and ketamine on serum melatonin levels in the early scotophase in NewZeland white rabbits. Biological Signals and Receptors 2001;10:310-6. |
|26.||Samarkandi A, Naguib M, Riad W, Thalaj A, Alotibi W, Aldammas F, et al. Melatonin vs. midazolam premedication in children: A double-blind, placebo-controlled study. Eur J Anaesth 2005;22:189-96. |
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]
|This article has been cited by|
||Melatonin, ketamine and their combination in half doses for management of sevoflurane agitation in children undergoing adenotonsillectomy
| ||Omyma Shehata Mohamed Khalifa,Abeer Ahmed Mohamed Hassanin |
| ||Egyptian Journal of Anaesthesia. 2013; 29(4): 337 |
|[Pubmed] | [DOI]|
||Paradoxical and Bidirectional Drug Effects
| ||Silas W. Smith,Manfred Hauben,Jeffrey K. Aronson |
| ||Drug Safety. 2012; : 1 |
|[Pubmed] | [DOI]|
||Effect of oral dextromethorphan versus oral ketamine on sevoflurane related emergence agitation in children undergoing adenotonsillectomy
| ||Ashraf Abdelmawgoud,Ahmed Mohy |
| ||Egyptian Journal of Anaesthesia. 2012; 28(4): 243 |
|[Pubmed] | [DOI]|
||Sevoflurane-emergence agitation: effect of supplementary low-dose oral ketamine premedication in preschool children undergoing dental surgery: Retraction
| ||Ahmed &NA; |
| ||European Journal of Anaesthesiology. 2011; 28(4): 310 |
|[Pubmed] | [DOI]|