Literature DB >> 2594003

[Extracorporeal adriamycin-removal following hepatic artery infusion: use of direct hemoperfusion combined with veno-venous bypass].

Y Ku1, M Saitoh, H Nishiyama, S Fujiwara, T Iwasaki, H Ohyanagi, Y Saitoh.   

Abstract

Systemic toxicity of adriamycin (ADR) has limited its high dosage application in hepatic artery infusion. We developed a new extracorporeal device combining direct hemoperfusion (DHP) and veno-venous bypass to eliminate ADR following hepatic artery infusion. Mongrel dogs were divided into three group, I: controls without DHP (n = 3), II: DHP under single venous bypass from IVC to left external jugular vein (n = 3) and III: DHP under hepatic venous isolation using veno-venous bypass (n = 5). Blood specimens were obtained to determine plasma drug levels until 60 min after ADR injection (3 mg/kg body weight, 1 min). Blood flow through DHP, which was averaged 200 ml/min in both groups II and III, was monitored with ultrasonic flowmeter. In groups I and II, peripheral ADR levels rapidly increased, reaching the peak values of 5.61 +/- 2.42 and 1.17 +/- 0.31 micrograms/ml respectively at 1 min after injection. The peak level in group III was markedly reduced, the value being 0.42 +/- 0.17 microgram/ml, which was 7.5% of the peak value of group I. The removal rates in groups II and III were 10.9 and 27.5% respectively. In conclusion, DHP under hepatic venous isolation can be an useful method to reduce systemic distribution of ADR during hepatic artery infusion.

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Year:  1989        PMID: 2594003

Source DB:  PubMed          Journal:  Nihon Geka Gakkai Zasshi        ISSN: 0301-4894


  2 in total

1.  Isolated hepatic perfusion as a treatment for liver metastases of uveal melanoma.

Authors:  Ilan Ben-Shabat; Christoffer Hansson; Malin Sternby Eilard; Christian Cahlin; Magnus Rizell; Per Lindnér; Jan Mattsson; Roger Olofsson Bagge
Journal:  J Vis Exp       Date:  2015-01-25       Impact factor: 1.355

2.  Isolated hepatic perfusion as a treatment for uveal melanoma liver metastases (the SCANDIUM trial): study protocol for a randomized controlled trial.

Authors:  Roger Olofsson; Lars Ny; Malin Sternby Eilard; Magnus Rizell; Christian Cahlin; Ulrika Stierner; Ulf Lönn; Johan Hansson; Ingrid Ljuslinder; Lotta Lundgren; Gustav Ullenhag; Jens Folke Kiilgaard; Jonas Nilsson; Per Lindnér
Journal:  Trials       Date:  2014-08-09       Impact factor: 2.279

  2 in total

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