Horadam V W, Sharp J G, Smilack J D, McAnalley B H, Garriott J C, Stephens M K, Prati R C, Brater D C
Ann Intern Med. 1981 Apr;94(4 pt 1):454-8. doi: 10.7326/0003-4819-94-4-454.
Amantadine is useful for the prevention and treatment of influenza A and for the treatment of Parkinson's disease and drug-induced extrapyramidal disorders. We have compared the pharmacokinetics of amantadine in patients with impaired or negligible renal function to that in normal subjects. The half-life of elimination in subjects with normal renal function was 11.8 +/- 2.1 hours (range, 9.7 to 14.5 h). Eight patients with various degrees of renal insufficiency (creatinine clearance from 43.1 to 5.9 mL/min . 1.73 m2) had half-lives of elimination from 18.5 h to 33.8 days. We also studied 10 patients on thrice-weekly hemodialysis. Assuming complete bioavailability of the drug, less than 5% of the dose was removed by each 4-hour hemodialysis. The mean half-life of elimination during chronic hemodialysis was 8.3 days (range, 7.0 to 10.3). We present guidelines for use of amantadine in patients with impaired renal function, including those on maintenance hemodialysis.
金刚烷胺可用于预防和治疗甲型流感,以及治疗帕金森病和药物性锥体外系疾病。我们比较了肾功能受损或可忽略不计的患者与正常受试者体内金刚烷胺的药代动力学。肾功能正常受试者的消除半衰期为11.8±2.1小时(范围为9.7至14.5小时)。8例不同程度肾功能不全(肌酐清除率为43.1至5.9 mL/min·1.73 m²)的患者消除半衰期为18.5小时至33.8天。我们还研究了10例每周接受三次血液透析的患者。假设药物生物利用度完全,每次4小时的血液透析清除的剂量不到5%。慢性血液透析期间的平均消除半衰期为8.3天(范围为7.0至10.3天)。我们提出了肾功能受损患者(包括维持性血液透析患者)使用金刚烷胺的指南。