Elimination and clearance of pamidronate by haemodialysis

被引:21
作者
Buttazzoni, Mirena [1 ]
Diez, Guillermo J. Rosa [1 ]
Jager, Victor [1 ]
Crucelegui, Maria S. [1 ]
Algranati, Salomon L. [1 ]
Plantalech, Luisa [1 ]
机构
[1] Hosp Italiano Buenos Aires, Serv Nefrol, RA-1181 Buenos Aires, DF, Argentina
关键词
bisphosphonate; clearance; haemodialysis; hypercalcaemia; pamidronate; renal failure;
D O I
10.1111/j.1440-1797.2006.00569.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Pamidronate (APD), a third-generation bisphosphonate, has proven to be useful in haemodialysis (HD) patients with ectopic calcifications and hypercalcaemia. Little is known about bisphosphonates clearance in patients undergoing HD. The authors' main objective was to study HD removal and clearance of APD. In total, 23 HD-requiring anuric end-stage renal disease (ESRD) adult individuals (12 men) aged 61.7 +/- 13 (mean +/- SD) years were admitted into the study. APD clearance and elimination were evaluated by (99m)Technetium APD (half-life 6 h). In total, 1 mg of labelled APD was injected via the arteriovenous graft prior to the start of HD. Blood samples were then drawn from the arterial (predialyser) and venous (postdialyser) lines of the extracorporeal circuit 2 h after the HD onset. In a subgroup of patients (n: 15) the dialysate was collected and quantified during the three initial HD hours. Venous APD concentrations (postdialyser) were 72 + 7% of arterial (predialyser) concentrations. Mean APD clearance was 69.3 + 16.6 mL/min, and mean APD extraction during dialysis session was 31.6 + 10.1%. In the present study involving HD-requiring anuric ESRD patients APD was successfully eliminated by HD. At the dose administered here none of the participants reported adverse events. APD is a potentially useful drug to be administered to HD-requiring ESRD patients, the understanding of its removal during HD as well as its dialytic clearance allows for a safer management of a drug that is usually eliminated by renal excretion.
引用
收藏
页码:197 / 200
页数:4
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