A Preliminary Study on the Estimation of Liquid Gastric Emptying Based on Two Serial Plasma Concentrations of Acetaminophen Given Orally.

  • SANAKA Masaki
    Department of Preventive Medicine, Division of Social Medicine, Medical Research Institute, Tokyo Medical and Dental University The First Department of Internal Medicine, Teikyo University School of Medicine
  • KOIKE Yuichi
    Department of Preventive Medicine, Division of Social Medicine, Medical Research Institute, Tokyo Medical and Dental University
  • YAMAMOTO Takatsugu
    Department of Preventive Medicine, Division of Social Medicine, Medical Research Institute, Tokyo Medical and Dental University
  • MINESHITA Satoru
    Department of Preventive Medicine, Division of Social Medicine, Medical Research Institute, Tokyo Medical and Dental University
  • YAMAKAWA Yasutoshi
    The First Department of Internal Medicine, Teikyo University School of Medicine
  • KATSUTA Eisuke
    The First Department of Internal Medicine, Teikyo University School of Medicine
  • TSUCHIYA Akihiko
    The First Department of Internal Medicine, Teikyo University School of Medicine
  • KUYAMA Yasushi
    The First Department of Internal Medicine, Teikyo University School of Medicine
  • YAMANAKA Masami
    The First Department of Internal Medicine, Teikyo University School of Medicine

この論文をさがす

抄録

Because acetaminophen (ACAP) is entirely absorbed from the small bowel while little is absorbed from the stomach, its pharmacokinetic parameters after oral doses have frequently been used to assess the gastric emptying rate (GER), including the plasma ACAP concentration at a fixed t time (Ct), the maximum plasma concentration (Cmax), the time to reach Cmax (tmax), and the area under the plasma concentration-time curve from zero to t time (AUCt). However, none of these are ideal because they depend not only on the rate but also on the extent of absorption, and because multiple blood samples are necessary for calculating them. Under these circumstances, we have found a simple and reasonable index, the C2t/Ct ratio, for the assessment of GER. This index is independent of the extent of absorption, and is easy to compute, requiring only two serial blood samples once t is fixed. However, in this study, a direct comparison has not been made between the new index and the emptying half time measured by the scintigraphic method, which is now the “gold standard” of the GER measurement. Further studies are needed on the relationship between the two to validate the new index.

収録刊行物

  • 臨床薬理

    臨床薬理 27 (3), 617-625, 1996

    一般社団法人 日本臨床薬理学会

参考文献 (21)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ