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Effect of cardiopulmonary bypass on the pharmacokinetics of propranolol and atenolol
Carmona, M. J. C; Pereira, V. A; Malbouisson, L. M. S; Auler Jr, J. O. C; Santos, S. R. C. J.
  • Carmona, M. J. C; Universidade de São Paulo. Faculdade de Medicina. Instituto do Coração. Serviço de Anestesiologia e Terapia Intensiva Cirúrgica. São Paulo. BR
  • Pereira, V. A; Universidade de São Paulo. Faculdade de Ciências Farmacêuticas. Departamento de Farmácia. São Paulo. BR
  • Malbouisson, L. M. S; Universidade de São Paulo. Faculdade de Medicina. Instituto do Coração. Serviço de Anestesiologia e Terapia Intensiva Cirúrgica. São Paulo. BR
  • Auler Jr, J. O. C; Universidade de São Paulo. Faculdade de Medicina. Instituto do Coração. Serviço de Anestesiologia e Terapia Intensiva Cirúrgica. São Paulo. BR
  • Santos, S. R. C. J; Universidade de São Paulo. Faculdade de Ciências Farmacêuticas. Departamento de Farmácia. São Paulo. BR
Braz. j. med. biol. res ; 42(6): 574-581, June 2009. graf, tab
Article in English | LILACS | ID: lil-512757
ABSTRACT
The pharmacokinetics of some β-blockers are altered by cardiopulmonary bypass (CPB). The objective of this study was to compare the effect of coronary artery bypass graft (CABG) surgery employing CPB on the pharmacokinetics of propranolol and atenolol. We studied patients receiving oral propranolol with doses ranging from 80 to 240 mg (N = 11) or atenolol with doses ranging from 25 to 100 mg (N = 8) in the pre- and postoperative period of CABG with moderately hypothermic CPB (32°C). On the day before and on the first day after surgery, blood samples were collected before β-blocker administration and every 2 h thereafter. Plasma levels were determined using high-performance liquid chromatography and data were treated by pharmacokinetics-modelling. Statistical analysis was performed using ANOVA or the Friedman test, as appropriate, and P < 0.05 was considered to be significant. A prolongation of propranolol biological half-life from 5.41 ± 0.75 to 11.46 ± 1.66 h (P = 0.0028) and an increase in propranolol volume of distribution from 8.70 ± 2.83 to 19.33 ± 6.52 L/kg (P = 0.0032) were observed after CABG with CPB. No significant changes were observed in either atenolol biological half-life (from 11.20 ± 1.60 to 11.44 ± 2.89 h) or atenolol volume of distribution (from 2.90 ± 0.36 to 3.83 ± 0.72 L/kg). Total clearance was not changed by surgery. These CPB-induced alterations in propranolol pharmacokinetics may promote unexpected long-lasting effects in the postoperative period while the effects of atenolol were not modified by CPB surgery.
Subject(s)

Full text: Available Index: LILACS (Americas) Main subject: Propranolol / Atenolol / Cardiopulmonary Bypass / Coronary Artery Bypass / Adrenergic beta-Antagonists / Coronary Disease Limits: Female / Humans / Male Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2009 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Propranolol / Atenolol / Cardiopulmonary Bypass / Coronary Artery Bypass / Adrenergic beta-Antagonists / Coronary Disease Limits: Female / Humans / Male Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2009 Type: Article / Project document Affiliation country: Brazil Institution/Affiliation country: Universidade de São Paulo/BR