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Departments of
*Anesthesiology and
Ophthalmology, Academic Hospital Vrije Universiteit, Amsterdam, The Netherlands
Address correspondence and reprint requests to Celia E. Allison, MD, Department of Anesthesiology, Academic Hospital Vrije Universiteit, de Boelelaan 117, 1018 HV Amsterdam, the Netherlands. Address e-mail to c.e.allison{at}cable.A2000.nl
| Abstract |
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Implications: Some children experience a sudden slowing of the heart and impaired breathing when the surgeon pulls on the eye muscles during squint operations under anesthesia. Sevoflurane, a recently developed anesthetic vapor, may reduce this problem when compared with the established vapor halothane.
| Introduction |
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During strabismus surgery, traction on the ocular muscles causes abrupt changes in the cardiovascular and respiratory systems. The oculocardiac response (OCR) is defined as a decrease in heart rate (HR) of more than 20% of the baseline value, dysrhythmias, or sinoatrial arrest (3). The oculorespiratory reflex (ORR) is the development of a reduction in tidal volume (VT) and respiratory rate (RR) (4). Because sevoflurane and halothane cause similar levels of respiratory depression in children at 1 minimum alveolar concentration (MAC) (5), and because halothane is associated with a lower HR (6) and a higher incidence of dysrhythmia (7), we hypothesized that sevoflurane might cause less a severe OCR and ORR than halothane during strabismus surgery with spontaneous respiration.
The purpose of our study was to determine the degree of change in HR, RR, VT, PETCO2, and SpO2 during strabismus surgery in children anesthetized with equipotent concentrations of sevoflurane or halothane breathing spontaneously via a LMA.
| Methods |
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Children were allowed food and milk products on the evening before surgery until midnight. On the day of surgery, the children were advised to drink sweet drinks until 2 h before daycare admission. Surgery took place within 1 h of admission. Children were not premedicated. Parents accompanied their children into the operating room and were present during the induction of anesthesia. Before the induction a Clip-Tip SpO2 probe was attached to a finger or toe (Oh- meda, Louisville, CO). Anesthesia was induced through an unscented face mask with oxygen in 66% nitrous oxide (N2O) via the Bain system with fresh gas flows sufficient to eliminate rebreathing. Inspiratory and expiratory gas concentrations and volumes were measured with a pediatric Datex Capnomac Ultima by using the Datex D-lite sensor (Datex, Helsinki, Finland). Children were randomly allocated to the study groups at the time of the induction of anesthesia by having a nurse pick a colored marble out of an opaque bag with equal numbers of red and blue marbles signifying sevoflurane (Group S) and halothane (Group H), respectively. The overpressure technique was used for induction. After four breaths of oxygen and N2O, the vaporizers were set at the maximal concentration deliverable, 8% for sevoflurane or 4% for halothane.
After loss of consciousness, a three-lead electrocardiogram and noninvasive blood pressure monitoring were applied. Clinical readiness for LMA insertion was jaw relaxation. The presence of an IV line was not a prerequisite for this procedure. An appropriately sized LMA was placed and checked for absence of obstruction. The polyethylene gas-sampling catheter (Lectocath, Vygon, France, internal diameter 1.0 mm) was advanced via a latex membrane on the Luer lock port at the elbow connector to within the distal end of the LMA. Gas sampling speed was 250 mL/min. If hypoventilation was present at this time, ventilation was briefly assisted manually. Vaporizers were then adjusted to an approximate MAC multiple of 1.3 for either anesthetic, 2.5% in the sevoflurane group and 0.5% in the halothane group. In calculating equipotent concentrations the following data were used. The MAC reducing effect of 60% N2O on 1 MAC sevoflurane is 24% (8), and on that of 1 MAC halothane is 60% (9).
Sevoflurane 2.5% is 1 MAC [MAC is 2.5% in this age group (8)]; 66% N2O adds approximately 0.24 MAC when combined with sevoflurane; sevoflurane contributes 1 MAC and N2O 0.24 MAC = 1.24 total MAC. 0.5% halothane is 0.55 MAC, [1 MAC is 0.91% in this age group (10)]; 66% N2O adds 0.66 MAC; halothane contributes 0.55 MAC and N2O contributes 0.66 = 1.21 total MAC.
Ringers lactate was administered via an IV cannula. Paracetamol 40 mg/kg was given, but no opiates or prophylactic anticholinergics.
After the operative field was prepared, HR (average of 3 s) was noted, and this was taken as baseline. The OCR was considered present if the HR decreased by 20% from this value or if dysrhythmias or sinoatrial arrest occurred during traction of the ocular muscles. If the HR did not increase after release of muscle tension, atropine 0.02 mg/kg was administered. If SpO2 decreased to values <95% fraction of inspired oxygen (FIO2) was increased to 50%. If there was no improvement in the SpO2, ventilation was assisted manually. Similarly, ventilation was assisted in children whose PETCO2 increased above 60 mm Hg. Children with persistent dysrhythmias were to be changed to isoflurane as the maintenance anesthetic, and those with persistent airway irritability were to be changed to IV propofol.
After surgery was completed, the child was given 100% oxygen, and the LMA was removed under deep anesthesia with the vaporizer on maintenance concentrations. The child was then turned on his or her side and transported to the recovery room.
Binary data were presented as frequencies, and continuous variables were presented as mean and standard deviations. Comparisons between Groups S and H were made by using Fishers exact test, unpaired t-tests, or Mann-Whitney U-tests for nonnormally distributed variables as appropriate.
| Results |
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| Discussion |
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We also observed considerably fewer dysrhythmias in children receiving sevoflurane than in those receiving halothane. This has also been observed in other studies in children (7) and may be attributed to the lack of effect of sevoflurane on myocardial conduction as compared with halothane (11).
We found that at 1.3 MAC sevoflurane or halothane the RR was higher with sevoflurane. We also observed higher minute volumes with sevoflurane, but the PETCO2 was similar to that of halothane. One possible explanation for this apparent discrepancy is a lower cardiac output with halothane when compared with an equivalent MAC of sevoflurane (12). Data from the literature on sevoflurane are inconclusive regarding whether the RR increases or decreases with increasing MAC. Doi et al. (13) and Komatsu et al. (14) showed a dose-dependent tachypnea. In contrast, Yamakage et al. (15) found a progressive decrease in RR, although in that study, halothane interestingly produced no change in RR. Johannesson et al. (16) found that the RR and PETCO2 were similar with both anesthetics during surgery. These findings may be explained by their definition of equipotency, which was based on clinical signs, and the fact that the authors used larger halothane concentrations than in our study. Brown et al. (5), in a group of younger children aged 624 months, also found no difference in VT or PETCO2 between sevoflurane and halothane in 60% N2O, but observed a higher RR with halothane. As higher halothane MAC values were used (S 1.4 MAC, H 1.8 MAC), and halothane is known to cause a dose-related tachypnea (17), this might explain the difference in RR observed by the authors.
Three children in our study, all anesthetized with halothane, had irritable airways and required assisted ventilation. Attempts to settle the children by deepening the level of anesthesia only resulted in apnea, suggesting that these respiratory problems were not caused by inadequate levels of anesthesia.
In our study, during positive OCRs, a decrease in VT and PETCO2 occurred, and this was similar in both groups. The observed decrease in minute ventilation during the OCR was not accompanied by an increase in PETCO2 but by a transient decrease. This may have been caused by the decrease in cardiac output during the OCR bradycardia.
A proportion of children had evidence of hypoventilation with spontaneous respiration through a LMA. Three had problems after LMA insertion, presumably because of high vapor concentrations, and this may be considered acceptable as a temporary consequence of this technique. However, 22% of the total number of children, of whom most had received halothane, required an increase in FIO2 and/or assisted ventilation to maintain the criteria of adequate ventilation during maintenance.
The crucial issue in this study is whether the compared alveolar vapor concentrations were equipotent. Various authors have commented on this problem (5).
The principle of overpressure induction consists of the creation of the steepest possible gradient between inspired and alveolar vapor concentrations to hasten the achievement of a specified endpoint. The endpoint chosen determines the MAC reached and will be similar to the accepted MAC for that endpoint. The inspired vapor must then be immediately reduced to prevent overdosing. If this is not done, this technique may create potentially dangerous large tissue vapor concentrations, similar to the circumstances seen with intubation under deep volatile anesthesia.
The endpoint in this study was readiness for LMA insertion which was between two and three minutes after beginning the induction for both anesthetics. Therefore, both were equipotent at the time that the vaporizer was switched off and the mask removed for LMA insertion.
We chose to use the overpressure technique with sevoflurane and halothane as it had been shown to be associated with minor complications (18). Interestingly, in that study, the authors were of the opinion that the lack of respiratory problems was the result of the use of preoperative oral atropine. We found that there were more respiratory complications with halothane than with sevoflurane, and this has also been observed in two other studies in childrenone with incremental vapor induction (19) and one on ease of LMA insertion (20).
As halothane has a slower uptake and washout than sevoflurane, the time to the achievement of maintenance alveolar concentrations may have differed and have led to discrepancies. An average of 10 minutes passed from the time that the vaporizer concentration was reduced to the time surgery began. During this time, the remaining monitors were applied and the operative field was prepared. End tidal and inspired vapor concentrations had then reached equilibrium. The OCR and ORR were determined only after surgery started.
In determining equipotent maintenance concentrations, the term "MAC multiple" has been used, although it is not known what distortions arise from this concept. Moreover, the use of N2O creates further difficulties in calculating equipotency. When N2O and halothane are used together in children, it has been stated that MAC multiples of halothane and N2O can be simply added when the total MAC is 1 (9). From the only two existing studies in children on this subject (8,21), the evidence suggests that MAC multiples of sevoflurane and N2O are less than purely additive, and the hypothesis is that they act at a common site of action or mechanism. Furthermore, the amount of the MAC-reducing effect of N2O on sevoflurane is different for MAC skin incision, as it is for MAC tracheal intubation. The MAC multiples we used were 1.21 for the sevoflurane group and 1.24 for the halothane group. Considering the many points where inaccuracies can enter in the concept of MAC multiples, we feel that the comparison of the two anesthetics in our study was acceptable.
In conclusion, children undergoing outpatient strabismus surgery with spontaneous breathing must be intensively monitored for bradycardia and hypoventilation. We found that sevoflurane was associated with a lower incidence of the OCR, airway irritability, and fewer ventilatory interventions compared with halothane. Sevoflurane may be the better choice of inhaled anesthetic for this procedure.
| Footnotes |
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| References |
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