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Pharmacokinetics of midazolam and its main metabolite 1-hydroxymidazolam in intensive care patients

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Summary

The pharmacokinetics of midazolam and of its main metabolite, 1-hydroxymidazolam, were investigated in intensive care patients after intravenous bolus of 0.2mg/kg followed by a 0.1mg/kg/h intravenous infusion of midazolam over 2 hours. A wide interpatient variability of the main pharmacokinetic parameters of midazolam was found. The mean values of elimination half life and volume of distribution, 4.5±5.4 h and 1.7±0.7l/kg respectively, were higher than those reported in healthy subjects. Total plasma clearance was significantly increased in patients taking drugs that induce hepatic metabolism. Significant concentrations of the unconjugated form of 1-hydroxymidazolam were recovered in plasma. The volume of distribution and the elimination half life of the metabolite were higher than those of the parent drug. These results show that 1-hydroxymidazolam might contribute to the pharmacodynamic effect of midazolam and consequently must be taken into account during pharmacokinetic and pharmacodynamic studies.

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References

  1. Dundee J.W., Halliday N.J., Harper K.W., Brogden R.N. (1984): Midazolam, a review of its pharmacological properties and therapeutic use. Drugs 28, 519–543.

    Article  CAS  PubMed  Google Scholar 

  2. Heizmann P., Eckert M., Zeigler W.H. (1983): Pharmacokinetics and bioavailability of midazolam in man. Br. J. Clin. Pharmacol. 16, 435–495.

    Google Scholar 

  3. Ziegler W.H., Schalch E., Leishman B., Eckert M. (1983): Comparison of the effects of intravenously administered midazolam, triazolam and their hydroxy metabolites. Br. J. Clin. Pharmacol. 16, 63S-69S.

    PubMed  Google Scholar 

  4. Oldenhof H., De Jong M., Steenhoek A., Janknegt R. (1988): Clinical pharmacokinetics of midazolam in intensive care patients, a wide interpatient variability? Clin. Pharmacol. Ther. 43, 263–269.

    CAS  PubMed  Google Scholar 

  5. Lehmann B., Boulieu R. (1995): Determination of midazolam and its unconjugated 1-hydroxy metabolite in human plasma by high performance liquid chromatography. J. Chromatogr., 674, 138–142.

    Article  CAS  Google Scholar 

  6. Gomeni C., Gomeni R., Siphar. (1987): An integrated computer system for statistical and pharmacokinetic data analysis. Proceedings of seventh International congress of Medical Informatics. Serrio A., OÆWoore R., Tardini A., Roger F. eds. European Federation of Medical Informatics, Rome.

    Google Scholar 

  7. Akaike H. (1974): A new look at the statistical identification model. IEEE Auto Control 19, 716–723.

    Article  Google Scholar 

  8. Brown C.R., Sarnquist F.H., Canup C.A., Pedley T.A. (1979): Clinical electroencephalographic and pharmacokinetic studies of a water-soluble benzodiazepine, midazolam maleate. Anesthesiology 50, 467–470.

    Article  CAS  PubMed  Google Scholar 

  9. Allonen H., Ziegler G., Klotz U. (1981): Midazolam kinetics. Clin. Pharmacol. Ther., 30, 5, 653–660.

    CAS  PubMed  Google Scholar 

  10. Michalk S., Moncorge C., Fichelle A. et al. (1988): Midazolam infusion for basal sedation in intensive care: absence of accumulation. Int. Care Med. 15, 37–41.

    Article  CAS  Google Scholar 

  11. Malacrida R., Fritz M.E., Suter P.M., Crevoisier C. (1991): Pharmacokinetics of midazolam administered by continuous intravenous infusion to intensive care patients. Crit. Care Med. 20, 1123–1126.

    Article  Google Scholar 

  12. Vree T.N., Shimoda M., Driessen J.J. et al. (1989): Decreased plasma albumin concentration results in increased volume of distribution and decreased elimination of midazolam in intensive care patients. Clin. Pharmacol. Ther. 46, 537–544.

    CAS  PubMed  Google Scholar 

  13. Crevoisier C., Ziegler W.H., Cano J.P. et al. (1986): Relation between the pharmacokinetics and pharmacodynamics of intravenously administered midazolam, triazolam and their hydroxy metabolites. In: Second Congress of the Inter American Society for Clinical Pharmacology and Therapeutics, pp. 47.

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Boulieu, R., Lehmann, B., Salord, F. et al. Pharmacokinetics of midazolam and its main metabolite 1-hydroxymidazolam in intensive care patients. European Journal of Drug Metabolism and Pharmacokinetics 23, 255–258 (1998). https://doi.org/10.1007/BF03189348

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