Thomas B H, Hynie I, Zeitz W
Int J Clin Pharmacol Ther Toxicol. 1980 Jan;18(1):26-30.
Nephropathy due to excessive consumption of phenacetin-containing analgesic mixtures has been a problem in Canada. Following the withdrawal of phenacetin it seems probable that acetaminophen consumption will increase and this study investigated the metabolism of 14C-Acetaminophen in patients with nephropathy and in healthy women. The respective alpha T1/2s of excretion of Acetaminophen and its metabolites were 2.58 h in the controls, 4.28 h in patients with analgesic nephropathy and 6.53 h in patients with nephropathy due to causes other than analgesic abuse. Both groups of patients had T1/2s that were significantly longer than the controls. The total 12 h recovery of 14C was highly positively correlated with creatinine clearance. (R = 0.92, P less than 0.001). No significant shifts in metabolism were discernable. It is concluded that patients with either analgesic nephropathy or nephropathy due to other causes metabolise Acetaminophen normally but excretion is delayed in proportion to the degree of renal impairment.
在加拿大,因过量服用含非那西丁的止痛合剂而导致肾病一直是个问题。非那西丁停用后,对乙酰氨基酚的消费量似乎可能会增加,本研究调查了肾病患者和健康女性体内14C-对乙酰氨基酚的代谢情况。对照组中对乙酰氨基酚及其代谢产物排泄的各自α半衰期为2.58小时,止痛性肾病患者为4.28小时,非止痛药物滥用导致的肾病患者为6.53小时。两组患者的半衰期均明显长于对照组。14C的12小时总回收率与肌酐清除率高度正相关(R = 0.92,P < 0.001)。未发现代谢有明显变化。结论是,无论是止痛性肾病患者还是其他原因导致的肾病患者,对乙酰氨基酚的代谢正常,但排泄会因肾功能损害程度而延迟。