Pharmacokinetics of Bisoprolol and Its Effect on Dialysis Refractory Hypertension

Author:

Kanegae K.1,Hiroshige K.2,Suda T.1,Iwamoto M.1,Ohta T.1,Nakashima Y.1,Ohtani A.2

Affiliation:

1. Second Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Fukuoka

2. Renal Division, Social Insurance Chikuho Hospital, Fukuoka - Japan

Abstract

The efficacy, safety, and pharmacokinetics of bisoprolol were investigated following oral administration once daily for 12 weeks in hyperreninemic patients with dialysis-refractory hypertension. Mean blood pressure rapidly fell from 132 to 112 mmHg in the 5.0-mg/day (n = 6) and from 142 to 128 mmHg in the 2.5-mg/day patients (n = 5), which were accompanied by a fall in plasma renin activity. On nondialysis days, Cmax and T1/2 were significantly higher in patients than in healthy control subjects. However, Cmax in the 2.5-mg/day patients was almost equal to that in healthy control subjects receiving 5.0 mg/day of bisoprolol. Plasma bisoprolol was dialyzable. During the course of the study, dialysis hypotension and bradycardia occurred in two patients receiving 5.0 mg/day of bisoprolol. In conclusion, a daily dose of 2.5 mg bisoprolol seems to be an adequate and relatively effective dose in our patients with dialysis-refractory hypertension.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,General Medicine,Medicine (miscellaneous),Bioengineering

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