THE JOURNAL OF JAPAN SOCIETY FOR CLINICAL ANESTHESIA
Online ISSN : 1349-9149
Print ISSN : 0285-4945
ISSN-L : 0285-4945
Volume 21, Issue 2
Displaying 1-14 of 14 articles from this issue
  • [in Japanese], [in Japanese], [in Japanese]
    2001 Volume 21 Issue 2 Pages 61-65
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese]
    2001 Volume 21 Issue 2 Pages 66-69
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    2001 Volume 21 Issue 2 Pages 70-74
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese]
    2001 Volume 21 Issue 2 Pages 75-78
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese]
    2001 Volume 21 Issue 2 Pages 79-82
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese]
    2001 Volume 21 Issue 2 Pages 83-85
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese]
    2001 Volume 21 Issue 2 Pages 86-89
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese]
    2001 Volume 21 Issue 2 Pages 90-93
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    2001 Volume 21 Issue 2 Pages 94-98
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
    2001 Volume 21 Issue 2 Pages 99-101
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • [in Japanese]
    2001 Volume 21 Issue 2 Pages 102-104
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
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  • Motoko MIKAMI, Takeshi SHIMA, Shinobu HAGA, Shu MATSUKAWA, Masato KATO
    2001 Volume 21 Issue 2 Pages 105-108
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
    We have studied the antiemetic effects of propofol after Laparoscopic cholecystectomy. One-hundred and fifty patients were allocated into three groups at random. Anesthesia was induced with thiopental 6mg•kg-1 (Group T, n=50), propofol 3mg•kg-1 (Group P1, n=50), and propofol 2mg•kg-1 and 5mg•kg-1•h-1 was infused until the end of operation (Group P2, n=50). In all patients anesthesia was maintained with nitrous oxide in oxygen and epidural anesthesia. The rates of post operative nausea of Group T, P1 and P2 were 50, 32, and 40%, respectively. There were no significant differences among the three groups in the rate of vomiting and the frequency in the use of metoclopramide. Therefore, propofol did not reduce the incidence of post operative nausea and vomiting in patients undergoing Laparoscopic cholecystectomy.
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  • Yuko MATSUOKA, Kumi NAKAMURA, Yukimasa OGINO, Makoto KUGE
    2001 Volume 21 Issue 2 Pages 109-113
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
    JOURNAL FREE ACCESS
    Volatile anesthetics, but not propofol, potentiate in general vecuronium-induced neuromuscular block. This study elucidated whether the amplitude of the first electromyographic response (T1) to a sequence of four stimulations should be kept at a lower level in anesthesia using propofol than that using sevoflurane. With the approval of the Kyoto City Hospital Ethics Committee, 119 patients undergoing elective operations were assigned randomly to the sevoflurane group or the propofol group. Anesthesia was induced with thiamylal and maintained with sevoflurane and nitrous oxide in two sevoflurane groups (S-30% and S-20%). Anesthesia was induced with propofol and maintained with propofol and nitrous oxide in two propofol groups (P-30% and P-20%). Vecuronium (0.1mg•kg-1) was given intravenously in all cases and an increment of 0.02mg•kg-1 was given when T1 had recovered to 30% of its control value in S-30% and P-30%, and 20% in S-20% and P-20%. Cases where additional vecuronium was required clinically were counted as "failures". The failure rate did not vary significantly among three of the four groups, but was significantly higher in P-30%. We conclude that T1 should be kept at 20% or lower in anesthesia with propofol, but can be at a higher percentage with sevoflurane.
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  • [in Japanese], [in Japanese]
    2001 Volume 21 Issue 2 Pages 114
    Published: March 15, 2001
    Released on J-STAGE: December 11, 2008
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