Lin J H, Chremos A N, Yeh K C, Antonello J, Hessey G A
Merck Sharp & Dohme Research Laboratories, West Point, PA.
Eur J Clin Pharmacol. 1988;34(1):41-6. doi: 10.1007/BF01061415.
The plasma and urine concentrations of famotidine, a new, potent H2-receptor antagonist, have been measured in 16 healthy young adults, 8 healthy elderly people and 18 patients with varying degrees of renal dysfunction after intravenous administration. Both the plasma elimination and renal excretion of famotidine were decreased in the elderly volunteers and renal patients. The renal clearance of famotidine averaged 4.43 ml/min/kg (310 ml/min) in normal young volunteers, which exceeded the mean creatinine clearance 1.55 ml/min/kg (109 ml/min), suggesting net secretion is a significant mechanism for elimination of famotidine. The ratio of famotidine renal clearance to creatinine clearance decreased as creatinine clearance decreased; these results suggest that the deterioration in the secretion process was much faster than that in glomerular filtration and are incompatible with the "intact nephron hypothesis". Nevertheless, both total body clearance and renal clearance were significantly correlated with creatinine clearance. The apparent half-life was also significantly correlated with creatinine clearance. Since famotidine is essentially free of dose-related adverse effects, dose adjustment in patients with mild renal insufficiency and in elderly people is not required; however, either a prolonged dosing interval or a decrease in daily dose during long-term therapy may be adapted for the patients with severe renal insufficiency to avoid accumulation and the potential undesirable effects.
对16名健康年轻成年人、8名健康老年人和18名不同程度肾功能不全患者静脉注射新型强效H2受体拮抗剂法莫替丁后,测定了其血浆和尿液浓度。老年志愿者和肾病患者中法莫替丁的血浆清除率和肾排泄率均降低。正常年轻志愿者中法莫替丁的肾清除率平均为4.43 ml/min/kg(310 ml/min),超过了平均肌酐清除率1.55 ml/min/kg(109 ml/min),这表明净分泌是法莫替丁消除的重要机制。随着肌酐清除率降低,法莫替丁肾清除率与肌酐清除率的比值下降;这些结果表明,分泌过程的恶化比肾小球滤过过程快得多,与“完整肾单位假说”不一致。然而,总体清除率和肾清除率均与肌酐清除率显著相关。表观半衰期也与肌酐清除率显著相关。由于法莫替丁基本无剂量相关不良反应,轻度肾功能不全患者和老年人无需调整剂量;然而,对于严重肾功能不全患者,长期治疗期间可延长给药间隔或减少每日剂量,以避免蓄积和潜在的不良影响。