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Primary and secondary detoxification in severe flecainide intoxication

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Abstract

Since experience with primary and secondary detoxification in severe flecainide intoxications is limited, 2 different cases of flecainide intotoxications are reported. In the first case, with plasma concentrations of 6500 ng/ml (therapeutic range: 200–980 ng/ml), the patient survived with a pacemaker and catecholamine support. In the second case, hemoperfusion terminated the need for emergency resuscitation during the initial phase, but was unsuccessful 3 h later. Even with a lower plasma concentration the patient died. Both patients had rapid onset of symptoms due to the very good bioavailability of the drug. Although it may be a rare in toxication, it is dangerous because of its quick onset and its efficiency in altering the cardiac stability. We recommend the prophylactic use of a pacemaker and gastric suction. The usefulness of hemoperfusion has not yet been proven.

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References

  1. Anderson JL, Steward JR, Perry BA, Van Hamersveld DD, Johnson TA, Conard GJ, Chang SF, Kvam DC, Pitt B (1981) Oral flecainide acetate for the treatment of ventricular arrhythmias. N Engl J Med 305:473–477

    Google Scholar 

  2. Borgeat A, Biollaz J, Freymond B, Bayer-Berger M, Chiolero R (1988) Hemofiltration clearance of flecainide in a patient with acute renal failure. Intensive Care Med 14:236–237

    Google Scholar 

  3. Braun J, Kollert JR, Becker JU (1987) Pharmacokinetics of flecainide in patients with mild and moderate renal failure compared with patients with normal renal function. Eur J Clin Pharmacol 31:711–714

    Google Scholar 

  4. Braun J, Kollert JR, Gessler U, Becker JU (1987) Failure of haemoperfusion to reduce flecainide intoxication. A case study. Med Toxicol 2:463–467

    Google Scholar 

  5. Fach WA, Mai BV, Preusler W, Becker H-J (1984), Flecainid-Intoxikation. Innere Med 11:27–31

    Google Scholar 

  6. Johnston A, Muhiddin KA, Hamer J (1982) Serum protein binding of flecainide. Br J Clin Pharmacol 13:606

    Google Scholar 

  7. Johnston A, Carrington S, Turner P (1985) Flecainide pharmacocinetics in healthy volunteers: the influence of urinary pH. Br J Clin Pharmacol 20:333–338

    Google Scholar 

  8. Köppel C, Tenczer J (1983) Identification and quantitation of drugs on an emergency basis with El, Cl and negative Cl gas chromatography/mass spectrometry in a toxicological laboratory—an evaluation of experience in 2000 intoxocations. Int J Mass Spectrom Jon Phys 48:221–226

    Google Scholar 

  9. Köppel C, Oberdisse U, Heimeyer G (in press) Clinical course and outcome in class IC-antiarrhythmic overdose. J. Toxicol Clin Toxicol

  10. Muhiddin KA, Johnston A, Turner P (1984) The influence of urinary pH on flecainide excretion and its serum pharmacokinetics. Br J Clin Pharmacol 17:447–451

    Google Scholar 

  11. Nitsch J, Köhler U, Lüderitz B (1987) Hemmung der Flecainidresorption durch Aktivkohle. Z Kardiol 76:289–291

    Google Scholar 

  12. Wurzberger R, Witter E, Avenhaus H, Hennemann H, Becker JU (1986) Hämoperfusion bei Flecainidintoxikation. Klin Wochenschr 64:442–444

    Google Scholar 

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Götz, D., Pohle, S. & Barckow, D. Primary and secondary detoxification in severe flecainide intoxication. Intensive Care Med 17, 181–184 (1991). https://doi.org/10.1007/BF01704725

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  • DOI: https://doi.org/10.1007/BF01704725

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