Skip to main content

Advertisement

Log in

Efficacy and pharmacokinetics of teicoplanin in hemodialysis patients

Klinische Wirksamkeit und Pharmakokinetik von Teicoplanin bei Hämodialysepatienten

  • Addendum
  • Published:
Infection Aims and scope Submit manuscript

Summary

In order to establish guidelines for the dosage of teicoplanin, a new glycopeptide antibiotic, in patients with end stage renal failure, 40 cases of suspected or proven gram-positive infections were treated with teicoplanin. Three different dosage regimens were used and peak/trough serum levels measured. Thirty-one patients were cured and six patients died. Teicoplanin was well tolerated. For severe cases of septicemia with staphylococci in patients undergoing hemodialysis a teicoplanin therapy consisting of 800 mg on day 1 followed by administrations of 400 mg on days 2, 3, 5, 12, and 19 is recommended. Minor infections are treated initially with 800 mg followed by administration of 400 mg at weekly intervals.

Zusammenfassung

Mit dem Ziel, Richtlinien für die Dosierung von Teicoplanin, einem neuen Glykopeptidantibiotikum, bei chronischer Niereninsuffizienz aufzustellen, wurden 40 Fälle von vermuteter oder nachgewiesener Infektion mit grampositiven Erregern mit Teicoplanin behandelt. Drei verschiedene Dosierungen wurden untersucht und die Spitzen- und Talserumspiegel gemessen. 31 Patienten wurden geheilt und sechs Patienten verstarben. Die Substanz wurde gut vertragen. In schweren Fällen von Sepsis verursacht durch Staphylokokken wird eine initiale Behandlung mit 800 mg gefolgt von 400 mg am 2., 3., 5., 12. und 19. Tag empfohlen. Mildere Verläufe werden initial mit 800 mg gefolgt von 400 mg in wöchentlichen Abständen behandelt.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Faßbinder, W. Langzeitergebnisse bei Dialysepatienten. In:Franz, H. E. (ed.): Blutreinigungsverfahren. Technik und Klinik. Georg Thieme Verlag, Stuttgart, New York 1990, pp. 494–499.

    Google Scholar 

  2. Brodersen, H. P., Beckers, B., Hoyme, H., Larbig, D. Bakteriämien bei Patienten mit verschiedenen Formen des Nierenversagens. Nieren-und Hochdruckkrankh. 17 (1988) 315–320.

    Google Scholar 

  3. Keane, W. F., Raij, L. R. Host defenses and infectious complications in maintenance hemodialysis patients. In:Drukker, W., Parsons, F. M., Maher, J. F. (eds.): Replacement of renal function by dialysis. Martinus Nijhoff, Boston 1983, pp. 646–658.

    Google Scholar 

  4. Brumfitt, W., Hamilton, J. M., Miller, T. The world wide problem of methicillin-resistance. Drugs Exp. Clin. Res. 15 (1990) 205–214.

    Google Scholar 

  5. Brodersen, H. P., Beckers, B., Stolpmann, R. M., Willkomm, F. J., Jansen, G., Larbig, D. Grampositive Septikämie bei Patienten mit terminaler Niereninsuffizienz und ihre Behandlung mit Teicoplanin. Intensivmed. 28 (1991) 356–359.

    Google Scholar 

  6. Brodersen, H. P., Beckers, B., Stolpmann, R. M., Larbig, D., Jansen, G. Calculated teicoplanin therapy in hemodialysis patients and dosage recommendations for repeated doses. Zeitschr. Antimikrob. Antineopl. Chemother. 8 (1990) 39–42.

    Google Scholar 

  7. Höffler, D. Dialyse und Medikamente. In:Franz, H. E. (ed.): Blutreinigungsverfahren. Technik und Klinik. Georg Thieme-Verlag Stuttgart, New York 1990, pp. 331–346.

    Google Scholar 

  8. Höffler, D., Koeppe, P., Naumann, E., Lang, E., Sörgel, F. Pharmacokinetics of teicoplanin in hemodialysis patients. Infection 19 (1991) 324–327.

    Google Scholar 

  9. Bowley, J., Pickering, S. J., Scantlebury, A. J., Ackrill, P., Jones, D. M. Intraperitoneal teicoplanin in the treatment of peritonitis associated with continuous ambulatory peritoneal dialysis. J. Antimicrob. Chemother. 21 (Suppl. A) (1988) 133–139.

    Google Scholar 

  10. Lewis, P., Garand, J. J., Parenti, F. A multicentre open clinical trial of teicoplanin in infections caused by gram-positive bacteria. J. Antimicrob. Chemother. 21 (Suppl. A) (1988) 61–79.

    Google Scholar 

  11. Simon, C., Stille, W. Antibiotikatherapie in Klinik und Praxis. Schattauer Verlag, Stuttgart, New York 1989, p. 202.

    Google Scholar 

  12. Stille, W., Sietzen, W., Dietrich, H. A., Tell, J. J. Clinical efficacy and safety of teicoplanin. J. Antimicrob. Chemother. 21 (Suppl. A) (1988) 69–79.

    Google Scholar 

  13. Kureishi, A., Jewesson, P. J., Cole, C. D., Reece, D. E., Phillips, G. L.: The nephrotoxic potential of teicoplanin vs. vancomycin in the empiric treatment of febrile neutropenic patients. 29th Intersc. Conf. Antimicrob. Agents Chemother., Houston, Texas, USA, 1989. Abstract no. 0597.

  14. Sahai, J., Healy, D. P., Shelton, M. J., Miller, J. S., Ruberg, S. J., Polk, R. Comparison of vancomycin- and teicoplanin-induced histamine release and “Red Man Syndrome.” Antimicrob. Agents. Chemother. 34 (1990) 765–769.

    Google Scholar 

  15. Buniva, G., Del Favero, A., Bernareggi, A., Patoia, L., Palumbo, R. Pharmacokinetics of14C-teicoplanin in healthy volunteers. J. Antimicrob. Chemother. 21 (Suppl. A) (1988) 23–28.

    Google Scholar 

  16. Domart, Y., Pierre, C., Claire, B., Garand, J. J., Regnier, B. Pharmacokinetics of teicoplanin in critically ill patients with various degrees of renal impairment. Antimicrob. Agents Chemother. 31 (1987) 1600–1604.

    Google Scholar 

  17. Traina, G. L., Bonati, M. Pharmacokinetics of teicoplanin in man after intravenous administration. J. Pharmacokinet. and Biopharm. 12 (1984) 119–128.

    Google Scholar 

  18. Verbist, L., Tjandramaga, B., Hendrickx, B., van Hecken, A. N., van Meile, P. In vitro activity and human pharmacokinetics of teicoplanin. Antimicrob. Agents Chemother. 26 (1984) 881–886.

    Google Scholar 

  19. Traina, G. L., Gentile, M. G., Fellin, G., Rosina, R., Cavenaghi, L. Pharmacokinetics of teicoplanin in patients on continuous ambulatory peritoneal dialysis. Eur. J. Clin. Pharmacol. 31 (1986) 501–504.

    Google Scholar 

  20. Bonati, M., Traina, G. L., Rosina, R., Buniva, G. Pharmacokinetics of a single intravenous dose of teicoplanin in subjects with various degrees of renal impairment. J. Antimicrob. Chemother. 21 (Suppl. A) (1988) 29–37.

    Google Scholar 

  21. Falcoz, C., Ferry, N., Pozet, N., Cuisinand, G., Zech, P. Y. Pharmacokinetics of teicoplanin in renal failure. Antimicrob. Agents Chemother. 31 (1987) 1255–1262.

    Google Scholar 

  22. Wopperer, J., Pilgrim, R., Stolpmann, R., Muth, P., Sörgel, F.: Pharmacokinetics of teicoplanin in renal failure patients. Dosing by experience: Inter. Congr. Chemother., Berlin, June 24–27, 1991. Abstract no. 451.

  23. Jehl, F., Monteil, B., Tarral, A. HPLC quantitation of the six main components of teicoplanin in biological fluids. J. Antimicrob. Chemother. 21 (Suppl. A) (1988) 53–59.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Beckers, B., Jansen, G., Brodersen, H.P. et al. Efficacy and pharmacokinetics of teicoplanin in hemodialysis patients. Infection 21, 71–74 (1993). https://doi.org/10.1007/BF01739321

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01739321

Keywords

Navigation