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October 1999

Sevoflurane vs Halothane - Is the Change in Practice Away From Halothane Justified?

  • Effects of sevoflurane anaesthesia on recovery in children: a comparison with halothane.
    Lapin SL; Auden SM; Goldsmith LJ; Reynolds AM. Paediatr Anaesth. 1999;9(4):299-304.

  • Changing aspects of sevoflurane in paediatric anaesthesia: 1975-99.
    Holzki J; Kretz FJ. Paediatr Anaesth. 1999;9(4):283-6.
Commentary by Charles Coté,

Return to the Current Literature Review Front Page

[ see abstract below ]

Effects of sevoflurane anaesthesia Holzki and Kretz are to be congratulated for reviewing the literature and comparing the gold standard halothane with the newer agent sevoflurane [1]. The authors raise several interesting questions: Are anesthesiologists who care for children changing to sevoflurane because it is a new drug, because of excellent marketing, or because it is superior to halothane? The authors review the shortfalls of the many studies which compare the two drugs�in particular, the differences in MAC multiples used for induction and the fact that many studies have ignored the nearly 60% reduction in MAC seen in nitrous oxide-halothane-anesthetized children compared with the 25% reduction seen in MAC in nitrous oxide-sevoflurane-anesthetized children. They question the reported differences in myocardial function as a possible artifact caused by the supplemental use of nitrous oxide and postulate that differences in induction and emergence time reflect the use of different MAC multiples during induction. Of primary concern is the apparent incidence of seizures during anesthetic induction, particularly when inspired concentrations greater than 6% are utilized [2-5]. I have not personally observed seizure, despite the reported incidence of up to 6%. Perhaps I have not been paying attention to this aspect of the induction process and have been concentrating more on the loss of consciousness. Of greater concern is the apparent high incidence of emergence phenomena, which is attenuated in part by the use of midazolam premedication [6]. The authors also report a number of anecdotal cases of children who were described by their parents as "this is not my child" for several days following a sevoflurane anesthetic. I have had several similar experiences. However, before blaming sevoflurane, I believe we need more carefully conducted studies because these anecdotal responses may reflect observer bias.

In the same issue of Paediatric Anaesthesia, Lapin et al compared 80 children anesthetized with either halothane or sevoflurane, with or without midazolam premedication, all having myringotomy tube insertion [7]. They used a unique method of evaluating emergence excitement. Nurses were asked a simple yes/no question: "Did this patient become uncontrollable to the point that you had to restrain him or her and could not perform other functions?" They also recorded accumulated crying times. The sevoflurane unpremedicated patients were discharged from PACU nearly twice as quickly, but 67% were described as agitated and 71% had prolonged crying compared with 29%and 33%, respectively, for halothane unpremedicated children. Premedication with midazolam reduced the incidence of emergence excitement, but it was still higher than halothane. These observations are consistent with studies currently being conducted in my institution.

The bottom line is that we still do not know if sevoflurane offers significant safety and efficacy advantages compared with halothane. We do not know if the markedly increased cost of the former agent justifies substantial changes in practice. We do not know if maintenance of anesthesia with sevoflurane is any safer than halothane from the patient�s standpoint, especially since there have been cases reports of acute hepatic dysfunction reported with sevoflurane [8-12]. Finally, it is still unclear if the purported safety of sevoflurane during induction is simply a "systems issue" since we are able to administer nearly twice the MAC multiples of halothane compared with sevoflurane. It may be that the cardiac depression observed simply reflects hitting the heart with a higher concentration of drug. My inclination is to accept sevoflurane as a wonderful induction agent that without doubt results in a more rapid induction and perhaps a smoother induction compared with halothane. However after induction, I change to halothane because I do not see any benefits beyond that time. Since most cardiac arrests occur during induction, the limited MAC multiples one can deliver with a sevoflurane vaporizer may be protective to the patient! I am concerned with the emergence phenomena that occur with all anesthetized children but we don�t need to double the rate of this complication for the as yet unproven benefits of the new drugs over the old. I am also concerned about the apparent prolonged changes in behavior occasionally observed. If good science bears this out, then again there is even less an indication to change to the new drug. I suspect some of my comments will be met with an outcry of "foul play" and the comments of an older generation but those of you that know me understand that I am very open minded but also very skeptical. I need to be convinced with good science which I can then confirm myself. Then this old dinosaur will change.

1. Changing aspects of sevoflurane in paediatric anaesthesia: 1975-99. AUTHORS: Holzki J; Kretz FJ.
SOURCE: Paediatr Anaesth. 1999;9(4):283-6.
ABSTRACT: Not available.

2. [Anesthetic induction of children with high concentrations of sevoflurane]. Haga S, Shima T, Momose K, et al. [Japanese]. Masui. 1992;41:1951-1955.

3. Effects of sevoflurane on central nervous system electrical activity in cats. Osawa M, Shingu K, Murakawa M, et al. Anesth Analg.1994;79: 52-57.

4. Convulsive movements with sevoflurane in children. Zacharias M. Anaesth Intensive Care. 1997;25: 727.

5. Electrical seizures during sevoflurane anesthesia in two pediatric patients with epilepsy. Komatsu H, Taie S, Endo S, et al. Anesthesiology 1994;81: 1535-1537.

6. Postoperative behavioral outcomes in children: effects of sedative premedication. Kain ZN, Mayes LC, Wang SM, et al. Anesthesiology 1999;90: 758-765.

7. Effects of sevoflurane anaesthesia on recovery in children: a comparison with halothane.

AUTHORS: Lapin SL; Auden SM; Goldsmith LJ; Reynolds AM.
SOURCE: Paediatr Anaesth. 1999;9(4):299-304.



Return to the Current Literature Review Front Page




ABSTRACT

We prospectively studied one hundred ASA physical status I-II children, ages six months to six years, undergoing myringotomy surgery. Children were randomly assigned to one of four anaesthetic groups receiving either halothane or sevoflurane for anaesthesia and oral midazolam premedication or no premedication. We found that children anaesthetized with sevoflurane had significantly faster recovery times and discharge home times than those who received halothane. Patients given oral midazolam premedication had significantly longer recovery times, but no delay in discharge home compared with those not premedicated. However, children anaesthetized with sevoflurane and no premedication had an unacceptably high incidence (67%) of postoperative agitation. The use of oral midazolam preoperatively did decrease the amount of postoperative agitation seen with sevoflurane. We conclude that although sevoflurane does shorten recovery times, the degree of associated postoperative agitation makes it unacceptable as a sole anaesthetic for myringotomy surgery. 8. Drug induced hepatitis following sevoflurane anesthesia in a child. Ogawa M, Doi K, Mitsufuji T, et al. Masui. 1991;40: 1542-1545.

9. [Drug induced hepatitis following sevoflurane anesthesia in a child]. [Japanese]. Ogawa M, Doi K, Mitsufuji T, et al. Masui. 1991;40: 1542-1545.

10. A case of postoperative hepatic injury after sevoflurane anesthesia. Schichinohe Y, Masuda Y, Takahashi H, et al. Masui. 1992;41: 1802-1805.

11. [A case of postoperative hepatic injury after sevoflurane anesthesia]. [Japanese]. Shichinohe Y, Masuda Y, Takahashi H, et al. Masui. 1992;41: 1802-1805.

12. A case of suspected liver dysfunction induced by sevoflurane anesthesia. Watanabe K, Hatakenaka S, Ikemune K, et al. Masui. 1993;42: 902-905.

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