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Ondansetron does not modify emergence agitation in children.

Emergence agitation (EA) is defined as "a disturbance in a child's awareness and attention to the environment with disorientation and perceptual alterations including hypersensitivity to stimuli and hyperactive motor behavior in the immediate postanesthesia period" (1).

Many factors such as age, stressful induction, rapid awakening in an unfamiliar environment, presence of pain, duration of the anaesthesia, anaesthetic technique and medication (scopolamine scopolamine (skōpŏl`əmēn, –mĭn) or hyoscine (hī`əsēn', –sĭn), alkaloid drug obtained from plants of the nightshade family (Solanaceae), chiefly from henbane, , droperidol, barbiturates, ketamine ketamine /keta·mine/ (ke´tah-men) a rapid-acting general anesthetic, used as the hydrochloride salt.

, opioids, benzodiazepines, metoclopramide and atropine atropine (ăt`rəpēn, –pĭn), alkaloid drug derived from belladonna and other plants of the family Solanaceae (nightshade family). ) and type of surgery may contribute to EA (2-5). On the other hand, primary metabolic disturbances, hypoxaemia or bladder distension dis·ten·tion also dis·ten·sion  
The act of distending or the state of being distended.

[Middle English distensioun, from Old French, from Latin
 may be the cause of agitation which should be distinguished from EA (6).

It has been suggested that alterations in plasma serotonin (5-hydroxytryptamine, 5-HT) levels might promote EA. It has been concluded that serotonin metabolism is significantly suppressed in EA which may be attributed to an uncertain mechanism in sevoflurane anaesthesia (7). Bayindir et al (8) achieved successful results in postcardiotomy delirium with ondansetron, which is a 5H[T.sub.3] receptor antagonist. Similarly, Lankinen et al (9) found that the usage of tropisetron, another 5H[T.sub.3] receptor antagonist, was of use in preventing EA in children. On the contrary, in some other studies, serotonin levels were found to be decreased in patients with postoperative delirium (10,11).

Medications which have been used to prevent and treat EA in children include midazolam, clonidine clonidine /clo·ni·dine/ (klo´ni-den) a centrally acting antihypertensive agent, used as the hydrochloride salt; also used in the prophylaxis of migraine and the treatment of dysmenorrhea, menopausal symptoms, opioid withdrawal, and , dexmedetomidine, fentanyl fentanyl /fen·ta·nyl/ (fen´tah-nil) an opioid analgesic; the citrate salt is used as an adjunct to anesthesia, in the induction and maintenance of anesthesia, in combination with droperidol (or similar agent) as a neuroleptanalgesic, and , ketorolac and physostigmine physostigmine /phy·so·stig·mine/ (-stig´men) a cholinergic alkaloid usually obtained from dried ripe seed of Physostigma venenosum  (12). Ondansetron is a drug commonly used in anaesthesia-related nausea and vomiting Nausea and Vomiting Definition

Nausea is the sensation of being about to vomit. Vomiting, or emesis, is the expelling of undigested food through the mouth.
. It is also used in other central nervous system related disorders (13,14). The aim of this randomised Adj. 1. randomised - set up or distributed in a deliberately random way

irregular - contrary to rule or accepted order or general practice; "irregular hiring practices"
, placebo-controlled study was to assess the efficacy of prophylactic ondansetron therapy in children who experienced EA following sevoflurane anaesthesia.


After institutional ethics committee approval and informed parental consent, 70 paediatric Adj. 1. paediatric - of or relating to the medical care of children; "pediatric dentist"
 patients (American Society of Anesthesiologists physical status I) aged one to six years scheduled for minor surgery below the umbilicus umbilicus /um·bil·i·cus/ (um-bil´i-kus) [L.] the navel; the scar marking the site of attachment of the umbilical cord in the fetus.

n. pl um·bil·i·ci
See navel.
 (inguinal hernia repair, undescended testis, hypospadias, circumcision) were included the study. The children were randomly assigned to receive either ondansetron or placebo in combination with caudal anaesthesia. Randomisation was performed immediately before anaesthetic induction by drawing prepared numbers from closed envelopes. Children with neurological or psychiatric diseases or attention deficit disorder attention deficit (hyperactivity) disorder (ADD or ADHD)
 formerly hyperactivity

Behavioral syndrome in children, whose major symptoms are inattention and distractibility, restlessness, inability to sit still, and difficulty concentrating on one thing for any
, emergency procedures, medical contraindication contraindication /con·tra·in·di·ca·tion/ (-in?di-ka´shun) any condition which renders a particular line of treatment improper or undesirable.

 to performance of the caudal block or a previous anaesthesia experience were not included in the study.

The modified Yale Preoperative Anxiety Scale (mYPAS) score was used for preoperative anxiety assessment (23 to 100) (15). This was performed by the preoperative anaesthesia technician who noted the child's vital signs before rectal midazolam premedication premedication /pre·med·i·ca·tion/ (pre?med-i-ka´shun)
1. preliminary administration of a drug preceding a diagnostic, therapeutic, or surgical procedure, as an antibiotic or antianxiety agent.

 (0.5 mg/kg). Thirty minutes after premedication, the patients were separated from their parents and transported to the operating room. Heart rate, non-invasive mean arterial pressure The mean arterial pressure (MAP) is a term used in medicine to describe a notional average blood pressure in an individual. It is defined as the average arterial pressure during a single cardiac cycle. Calculation  and peripheral haemoglobin oxygen saturation (SpO2) were monitored. After pre-oxygenation, general anaesthesia was induced by facemask face·mask  
A protective or disguising cover for the face, often enveloping the entire head: wore a facemask while diving; a skier's facemask; armed robbers who wore facemasks. 
 with 8% sevoflurane and 50% nitrous oxide in oxygen. After insertion of an intravenous line and laryngeal mask airway Invention and development
The first laryngeal mask airway, the LMATM airway, was invented in the 1980s by the British anaesthetist, Dr. Archie Brain. Since their introduction twenty plus years ago as a safe, effective alternative to the endotracheal tube doctors and
 without the use of a neuromuscular blocking agent neuromuscular blocking agent
Any of various compounds, such as curare, that compete with neurotransmitters for nerve cell receptor sites, thus preventing the contraction of skeletal muscles.
, patients were assigned to two groups. Group O (n=35) received ondansetron (Zofer 4 mg/2 ml amp, ADEKA, Turkey) (0.1 mg/kg for children weighing <40 kg, 4 mg for children weighing >40 kg) and Group P (n=35) received 0.9% NaCl 2 ml. Ondansetron was diluted in 2 ml saline as needed. Then a single-dose caudal caudal /cau·dal/ (kaw´d'l)
1. pertaining to a cauda.

2. situated more toward the cauda, or tail, than some specified reference point; toward the inferior (in humans) or posterior (in animals) end of the body.
 blockwas performed in all patients with 0.8 ml/kg 0.25% levobupivacaine by the same anaesthetist (TH). Anaesthesia was maintained with 1.0 to 2.0% sevoflurane (corrected for stable intraoperative haemodynamic measurements). All patients were ventilated mechanically with a 60 to 40% nitrous oxide-oxygen mixture with a laryngeal mask airway in situ. Fifteen minutes after the caudal block, surgery commenced. The caudal block was judged as inadequate if the child's heart rate and/or blood pressure increased by more than 10% of pre-incision values at the beginning of the skin incision. The insufficient analgesia was treated with a rescue opioid analgesic (fentanyl 1 [micro]g/kg) and the patient was excluded from the study. After skin closure, anaesthetic gases were discontinued and replaced with 100% oxygen 5 l/minute. The laryngeal mask airway was removed when patients were fully conscious and they were then transferred to the recovery room. No other antiemetic drugs were given during anaesthesia. Intraoperatively, heart rate, mean arterial pressure and Etsevoflurane concentration were recorded every 10 minutes. Intraoperative fluid therapy was standardised and all children received lactated Ringer solution according to body weight (16). Assessments of the EA and pain levels were performed every 10 minutes for the first 30 minutes after admission to the recovery room. Assessment of EA was performed by a 10-point scale (TPS), ranging from 1 (calm or asleep) to 10 (worst possible and inconsolable agitation) and EA was defined as TPS >5 (17). The patients' pain scores were evaluated using a modified Children's Hospital of Eastern Ontario The Children's Hospital of Eastern Ontario (CHEO) is a major university teaching children's hospital located at 401 Smyth Road, Ottawa, Canada (Tel (613) 737-7600). It is affiliated with The Ottawa Hospital and the University of Ottawa.  pain scale (mCHEOPS) (18) (Table 1). A postoperative pain score of >4 was regarded as inadequate analgesia and the patient was given 40 mg/kg rectal paracetamol paracetamol

see acetaminophen.

acetaminophen, paracetamol

an analgesic and antipyretic drug in dogs. It is contraindicated for cats because of serious side-effects which include intravascular hemolysis, methemoglobinemia and hepatic necrosis.
 and excluded from the study. The incidence of EA was defined as at least one event during any given assessment observation period when compared to the agitated and non-agitated groups. If the scores in the TPS continued between 8 to 10 points for longer than five minutes, intravenous propofol (0.5 mg/kg) was given as rescue therapy and the child was excluded from the study. The patients were considered as 'ready for discharge' from the recovery room when they had no pain, a calm status and a modified Aldrete score of >10. Intraoperative and postoperative data were collected by an independent observer (MO) blinded to the group assignment. Major complications such as oxygen desaturation desaturation /de·sat·u·ra·tion/ (de-sach?ah-ra´shun) the process of converting a saturated compound to one that is unsaturated, such as the introduction of a double bond between carbon atoms of a fatty acid.  (Sp[O.sub.2] <95), laryngospasm, arrhythmia and allergic reaction were recorded.

Statistical analysis

The sample size required to reduce EA incidence, which was 37% with placebo according to the results of a previous study, to 10% with ondansetron was calculated as 34 for each group taking alpha 0.05 and beta 0.80 (19). We included 35 patients in each group to increase the power of the study and also to secure patient dropouts for any reason. The SPSS A statistical package from SPSS, Inc., Chicago ( that runs on PCs, most mainframes and minis and is used extensively in marketing research. It provides over 50 statistical processes, including regression analysis, correlation and analysis of variance.  13.0 statistical software system (SPSS Inc., Chicago, IL, USA) was used for statistical analyses. Results are presented as mean [+ or -] standard deviation or frequences (n) and percentages (%). Statistical comparison of the groups was performed with independent t-test for parametric analyses and Mann-Whitney U test for non-parametric analyses. Levene's Test was run for the parametric values to assess whether the parameters' variances were equal. The changes occurring within groups were analysed by Bonferroni and Wilcoxon signed-rank test The Wilcoxon signed-rank test is a non-parametric alternative to the paired Student's t-test for the case of two related samples or repeated measurements on a single sample. .


Seventy children were initially randomised for the study. Three children were excluded from further evaluation; one in each group received fentanyl following skin incision and one patient had a mCHEOPS score >4 in Group P. Finally, 33 children met the criteria for the placebo group and 34 children for the ondansetron group. EA incidence at 10 minutes was 31.3% which differed significantly from the 30 minute results (19.4%, P=0.03) (Table 2). The patients neither required rescue propofol in the postoperative period nor had high mYPAS scores. There were no significant differences between the placebo and ondansetron groups with respect to demographic, anaesthetic and surgical details. Preoperative mYPAS scores were similar. Ten children (30.3%) in the placebo group and seven children (20.6%) in the ondansetron group vomited. Times to 'ready for discharge' were similar in both groups (Table 3). Intraoperative heart rate and mean arterial pressure decreases were comparable in both groups (Figures 1 and 2).

The incidences of EA in ondansetron and placebo groups were 32.4% and 30.3% at 10 minutes; 23.5% and 18.2% at 20 minutes; and 20.6% and 18.2% at 30 minutes. EA incidence decreased after 10 minutes in both groups with comparable values. Mean mCHEOPS scores and mean TPS scores also decreased after 10 minutes in both groups. All changes were similar between groups (Table 4).


Comparison of agitated and non-agitated patients showed that distributions of age, gender, mYPAS scores, anaesthetic and surgical features, fluid therapy, Etsevoflurane concentrations at the end of the surgery, mCHEOPS scores and vomiting ratios were similar in agitated and non-agitated groups. Agitated patients had significantly increased 'ready time for discharge' compared to non-agitated patients (P=0.001) (Table 5).



The clinical findings in acute delirium and EA are similar in many aspects, with a dissociative state and altered cognitive perception (20). Greater incidence of agitation after sevoflurane anaesthesia is observed in preschool-age children compared with school-age children (1,2). Previous investigators found the incidence of EA with preschool-age range between 6.3% and 74.1% (21).

Although there are many studies regarding the role of the serotonergic se·ro·to·ner·gic or se·ro·to·ni·ner·gic
Activated by or capable of liberating serotonin, especially in transmitting nerve impulses.


containing or activated by serotonin.
 system and 5-H[T.sub.3] receptors in acute delirium, there is no consensus on their effects (7-9). Ogasawara et al (7) observed significant increases in plasma serotonin levels during sevoflurane anaesthesia. Bayindir et al8 had successful results with ondansetron in treatment of post-cardiotomy delirium, which was assumed to be because of increased serotonin levels due to cardiopulmonary bypass. A 5H[T.sub.3] receptor antagonist tropisetron was used successfully after sevoflurane anaesthesia to prevent EA in small children (9). Despite the probable anxiolytic anxiolytic /anx·io·lyt·ic/ (ang?ze-o-lit´ik)
1. antianxiety.

2. an antianxiety agent.

A drug that relieves anxiety.
 effect of ondansetron (22), the exact mechanism of tropisetron in preventing EA could not be clarified (9). On the other hand, in other studies serum serotonin levels were found to be decreased in patients with delirium (10,11). In addition, it was reported that anaesthetic agents may cause consumption of serotonin at a steady rate, while they increase the plasma level of melatonin melatonin: see pineal gland.

Hormone secreted by the pineal gland of most vertebrates. It appears to be important in regulating sleeping cycles; more is produced at night, and test subjects injected with it become sleepy.
 in rats (23). Thus, the medical literature lacks a consensus about the serotonin levels and both increased and decreased serotonergic activity have been found to be associated with delirium (24).

The only study using 5H[T.sub.3] antagonists in EA was that by Lankinen et al which compared the effects of prophylactic tropisetron with placebo in children undergoing adenoidectomy (9). The EA incidence in the placebo group was found to be 62%, which is twice that of our placebo group results. The difference may be due to the type of surgery, as otorhinolaryngological procedures may contribute to increased incidence of EA (25). On the other hand, the difference may be also because of the lack of premedication in their study (9). It is obvious that the use of midazolam in our study reduced the preoperative anxiety in our patients (25,26). The differences may also be attributable to individualised conditions.

Otorhinolaryngological procedures have high incidences of postoperative nausea and vomiting Postoperative nausea and vomiting (PONV) is an unpleasant complication affecting about a third of the 10% of the population undergoing general anaesthesia each year. This equates to about two million people in the United Kingdom annually. , and 5-H[T.sub.3] receptor antagonists have well-established roles in the prophylaxis and treatment of postoperative nausea and vomiting (27). Thus, it is possible that the reduction in the EA incidence observed by Lankinen et al (9) was due to the antiemetic property of tropisetron. However, this hypothesis could not be verified and the exact mechanism remains unclear. We were not able to find a reduction in the incidence of EA in the ondansetron group. We believe that the difference between that study (9) and ours is probably due to the difference of the study population. Although recent studies and current antiemetic guidelines showed that tropisetron, ondansetron and granisetron are equivalent in efficacy (28), there are some differences in metabolism and receptor specificities. For example, cytochrome p450 enzyme systems are slow metabolisers in some individuals secondary to a mutation, the frequency of which is reported as 6% in caucasians (29).

Primary metabolic disturbances and pain should be excluded in agitated children in order to make a differential diagnosis with EA. In our study, mCHEOPS scores in the recovery room were similar in agitated and non-agitated groups. We did not observe any episode of oxygen desaturation and fluid therapy was similar. Therefore, we excluded metabolic change as a cause of agitation.

Although the occurrence of EA in children after sevoflurane anaesthesia due to high blood sevoflurane concentrations was commonly reported (30), in our study Etsevoflurane concentration at the end of the surgery was similar between agitated and non-agitated groups.

In conclusion, our study demonstrated that prophylactic administration of intravenous ondansetron did not reduce EA compared to placebo after sevoflurane anaesthesia in preschool children who underwent minor surgery below the umbilicus.

Accepted for publication on March 17, 2011.


(1.) Sikich N, Lerman J. Development and psychometric psy·cho·met·rics  
n. (used with a sing. verb)
The branch of psychology that deals with the design, administration, and interpretation of quantitative tests for the measurement of psychological variables such as intelligence, aptitude, and
 evaluation of the pediatric pediatric /pe·di·at·ric/ (pe?de-at´rik) pertaining to the health of children.

Of or relating to pediatrics.
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(3.) Veyckemans F. Excitation phenomena during sevoflurane anaesthesia in children. Curr Opin Anaesthesiol 2001; 14:339-343.

(4.) Galford RE: Problems in Anesthesiology: Approach to Diagnosis. Little, Brown and Company, Boston, MA 1992; p. 341-343.

(5.) Mecca RS. Postoperative recovery. In: Barash PG, Cullen BF, Stoelting RK, eds. Clinical Anesthesia, 4th ed. Philadelphia, PA: Lippincott Williams & Wilkins 2001. p. 1398-1399.

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(7.) Ogasawara H, Takahashi S, Kudo ku·do  
n. pl. ku·dos
Usage Problem A praising remark; an accolade or compliment: "Children's book author Virginia Hamilton added another kudo to her prize-laden career" 
 T, Kudo M, Ishihara H, Matsuki A. Effects of sevoflurane anesthesia on serotonin metabolism in rat brain. Masui 1993; 42:1412-1417.

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(11.) Uchida K, Aoki T, Ishizuka B. Postoperative delirium and plasma melatonin. Med Hypotheses 1999; 53:103-106.

(12.) Dorre N. The Post Operative Care Unit. In: Miller RD, ed. Miller's Anesthesia, 7th ed. Pennsylvania: Churchill Livingstone 2010. p. 2707-2726.

(13.) Akhondzadeh S, Mohammadi N, Noroozian M, Karamghadiri N, Ghoreishi A, Jamshidi AH et al. Added ondansetron for stable schizophrenia: a double blind, placebo controlled trial. Schizophr Res 2009; 107:206-212.

(14.) Ye JH, Ponnudurai R, Schaefer R. Ondansetron: a selective 5-ht(3) receptor antagonist and its applications in cns-related disorders. CNS See Continuous net settlement.


See continuous net settlement (CNS).
 Drug Rev 2001; 7:199-213.

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(16.) Cote CJ. Pediatric anesthesia. In: Miller Ronald D, ed. Miller's Anesthesia, 7th ed. Pennsylvania: Churchill Livingstone 2010. p. 2559-2594.

(17.) Meyer RR, Munster P, Werner C, Brambrink AM. Isoflurane is associated with a similar incidence of emergence agitation/ delirium as sevoflurane in young children - a randomized controlled study. Paediatr Anaesth 2007; 17:56-60.

(18.) Splinter WM, Semelhago LC, Chou S. The reliability and validity of a modified CHEOPS pain score. Anesth Analg 1994; 78:413.

(19.) Ibacache ME, Munoz HR, Brandes V, Morales AL. Single-dose dexmedetomidine reduces agitation after sevoflurane anesthesia in children. Anesth Analg 2004; 98:60-63.

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(22.) Freeman AM 3rd, Westphal JR, Norris GT, Roggero BA, Webb PB, Freeman KL et al. Efficacy of ondansetron in the treatment of generalized anxiety disorder Generalized Anxiety Disorder Definition

Generalized anxiety disorder is a condition characterized by "free floating" anxiety or apprehension not linked to a specific cause or situation.
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(27.) Furst SR, Rodarte A. Prophylactic antiemetic treatment with ondansetron in children undergoing tonsillectomy tonsillectomy /ton·sil·lec·to·my/ (ton?si-lek´tah-me) excision of a tonsil.

Surgical removal of tonsils or a tonsil.
. Anesthesiology 1994; 81:799-803.

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Pharmacogenetics is the study of how the actions of and reactions to drugs vary with the patient's genes.
, and clinical efficacy of 5-hydroxytryptamine type 3 receptor antagonists for postoperative nausea and vomiting. Curr Opin Anaesthesiol 2006; 19:606-611.

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T. Hosten *, M. Solak ([dagger]), L. Element, M. Ozgun [section], K. TOKER Toker may refer to:
  • One who smokes cannabis (slang)
  • Toker Dam, located in Eritrea
  • Cem Toker, The president of Liberal Democratic Party
 ([dagger]) Department of Anesthesiology and Reanimation Re`an`i`ma´tion   

n. 1. The act or operation of reanimating, or the state of being reanimated; reinvigoration; revival.
, Kocaeli University Medical School, Kocaeli, Turkey

* M.D., Assistant Professor.

([dagger]) M.D., Professor and Consultant.

([double dagger]) M.D., Assistant Professor and Consultant, Department of Pediatric Surgery, Kocaeli University Medical School.

([section]) M.D., Resident.

Address for correspondence: Dr T. Hosten, email:
Table 1

Modified CHEOPS scoring

Item structure       Parameter                            Points

Crying               None                                 0
                     Crying, moaning                      1
                     Screaming                            2

Facial expression    Smiling                              0
                     Neutral                              1
                     Grimacing                            2

Verbal expression    Positive                             0
                     None or another complaint            1
                     Complaining of pain                  2

Torso                Neutral                              0
                     Squirming, tense, upright            1
                     Restrained                           2

Legs                 Neutral                              0
                     Kicking, restless foetal position    1
                     Restrained                           2

CHEOPS=Children's Hospital of Eastern Ontario pain scale.

Table 2

Statistical analyses of emergence agitation incidences

             Time after emergence    n (%)        P

Agitation    10 min                  21 (31.3)
incidence    20 min                  14 (20.9)    0.05
             30 min                  13 (19.4)    0.03 *

* Comparison of emergence agitation incidence according to
10 minute values with Wilcoxon signed-rank test.

Table 3

Statistical analyses of demographic, anaesthetic and surgical details
in the placebo and ondansetron groups (mean  [+ or -]  SD or numbers)

                                 Group P,

Age, y                             3.1 [+ or -] 1.4
Weight, kg                        14.5 [+ or -] 5.1
Gender, female/male               25/8
mYPAS score                       29.3 [+ or -] 6.4
Anaesthesia duration, min         49.3 [+ or -] 0.7
Surgery duration, min             63.5 [+ or -] 10.1
Fluid therapy, ml                156.7 [+ or -] 44.4
Time to eye-opening, min           8.6 [+ or -] 4.4
[Et.sub.Sevo] concentration end    1.26 [+ or -] 0.07
of the surgery, %
Ready time for discharge, min     29.1 [+ or -] 6.0

Vomiting, yes/no                 10/23

                                 Group O,

Age, y                             3.1 [+ or -] 1.6
Weight, kg                        15.3 [+ or -] 4.8
Gender, female/male               25/9
mYPAS score                       28.8 [+ or -] 5.0
Anaesthesia duration, min         49.3 [+ or -] 8.2
Surgery duration, min             63.6 [+ or -] 7.2
Fluid therapy, ml                154.6 [+ or -] 62.3
Time to eye-opening, min           9.9 [+ or -] 4.0
[Et.sub.Sevo] concentration end    1.25 [+ or -] 0.07
of the surgery, %
Ready time for discharge, min     27.6 [+ or -] 4.9

Vomiting, yes/no                 7/27


Age, y                           0.80
Weight, kg                       0.53
Gender, female/male              0.83
mYPAS score                      0.71
Anaesthesia duration, min        0.98
Surgery duration, min            0.97
Fluid therapy, ml                0.87
Time to eye-opening, min         0.23
[Et.sub.Sevo] concentration end  0.32
of the surgery, %
Ready time for discharge, min    0.26

Vomiting, yes/no                 0.36

mYPAS=modified Yale Preoperative Anxiety Scale.

Table 4

Statistical analyses of agitation scores, pain scores and agitation
incidences between the placebo and ondansetron groups,
(mean [+ or -] SD or numbers (%))

                                  Group P, n=33          P *

Emergence agitation    10 min     10 (30.3)
                       20 min     6 (18.2)               0.10
                       30 min     6 (18.2)               0.10

TPS score              10 min     3.18 [+ or -] 2.99
                       20 min     2.58 [+ or -] 2.63     0.40
                       30 min     2.42 [+ or -] 2.33     0.10

mCHEOPS score          10 min     2.76 [+ or -] 0.44
                       20 min     2.64 [+ or -] 0.49     0.76
                       30 min     2.58 [+ or -] 0.50     0.24

                                  Group O, n=34          P *

Emergence agitation    10 min     11 (32.4)
                       20 min     8 (23.5)               0.25
                       30 min     7 (20.6)               0.15

TPS score              10 min     3.50 [+ or -] 3.03
                       20 min     2.62 [+ or -] 2.69     0.07
                       30 min     2.44 [+ or -] 2.23     0.13

mCHEOPS score          10 min     2.68 [+ or -] 0.47
                       20 min     2.56 [+ or -] 0.50     0.31
                       30 min     2.50 [+ or -] 0.51     0.09

                                  Group O, n=34          P **

Emergence agitation    10 min     11 (32.4)              0.85
                       20 min     8 (23.5)               0.59
                       30 min     7 (20.6)               0.80

TPS score              10 min     3.50 [+ or -] 3.03     0.66
                       20 min     2.62 [+ or -] 2.69     0.94
                       30 min     2.44 [+ or -] 2.23     0.97

mCHEOPS score          10 min     2.68 [+ or -] 0.47     0.46
                       20 min     2.56 [+ or -] 0.50     0.52
                       30 min     2.50 [+ or -] 0.51     0.54

TPS=10-point scale, mCHEOPS=modified Children's Hospital of Eastern
Ontario pain scale.

* In-group comparison of 10-minute values with Wilcoxon signed-rank
and Bonferroni tests.

** Inter-group comparison at the same measurement time values with
Mann-Whitney U test and t-tests.

Table 5

Statistical analyses of demographic, anaesthetic and surgical details
between the agitated and non-agitated patients (mean [+ or -] SD
or numbers)

                                              Agitated, n=21

Age, y                                          3.01 [+ or -] 1.3
Weight, kg                                     15.3 [+ or -] 8.1
Gender, female/male                           18/3
mYPAS score                                    29.95 [+ or -] 5.7
Anaesthesia duration, min                      52.6 [+ or -] 11.7
Surgery duration, min                          66.2 [+ or -] 9.9
Fluid therapy, ml                             141.43 [+ or -] 60.3
Time to eyes opening, min                      10.0 [+ or -] 4.4
EtSevo concentration end of the surgery, %      1.24 [+ or -] 0.08
mCHEOPS score                                   2.57 [+ or -] 0.5
Vomiting, yes/no                              8/13
Ready time for discharge, min                  31.5 [+ or -] 4.7

                                              Non-agitated, n=46

Age, y                                          3.1 [+ or -] 1.5
Weight, kg                                     14.7 [+ or -] 5.1
Gender, female/male                           32/14
mYPAS score                                    28.6 [+ or -] 5.8
Anaesthesia duration, min                      47.8 [+ or -] 7.9
Surgery duration, min                          62.4 [+ or -] 8.0
Fluid therapy, ml                             162.1 [+ or -] 50.0
Time to eyes opening, min                       8.9 [+ or -] 4.1
EtSevo concentration end of the surgery, %      1.26 [+ or -] 0.07
mCHEOPS score                                   2.8 [+ or -] 0.4
Vomiting, yes/no                              9/37
Ready time for discharge, min                  26.9 [+ or -] 5.3


Age, y                                        0.77
Weight, kg                                    0.57
Gender, female/male                           0.16
mYPAS score                                   0.36
Anaesthesia duration, min                     0.10
Surgery duration, min                         0.13
Fluid therapy, ml                             0.14
Time to eyes opening, min                     0.32
EtSevo concentration end of the surgery, %    0.37
mCHEOPS score                                 0.10
Vomiting, yes/no                              0.10
Ready time for discharge, min                 0.001 *

mYPAS=modified Yale Preoperative Anxiety Scale, mCHEOPS=modified
Children's Hospital of Eastern Ontario pain scale. * t-test.
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Author:Hosten, T.; Solak, M.; Elemen, L.; Ozgun, M.; Toker, K.
Publication:Anaesthesia and Intensive Care
Article Type:Clinical report
Geographic Code:1USA
Date:Jul 1, 2011
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