Hernandez Stephanie H, Howland Maryann, Schiano Thomas D, Hoffman Robert S
a Division of Medical Toxicology, Department of Emergency Medicine , Icahn School of Medicine at Mount Sinai , New York , NY , USA.
b St. John's University College of Pharmacy and Health Sciences , Queens , NY , USA.
Clin Toxicol (Phila). 2015;53(10):941-9. doi: 10.3109/15563650.2015.1100305. Epub 2015 Oct 20.
Acetaminophen-induced fulminant hepatic failure is associated with acute kidney injury, metabolic acidosis, and fluid and electrolyte imbalances, requiring treatment with renal replacement therapies. Although antidote, acetylcysteine, is potentially extracted by renal replacement therapies, pharmacokinetic data are lacking to guide potential dosing alterations. We aimed to determine the extracorporeal removal of acetylcysteine by various renal replacement therapies.
Simultaneous urine, plasma and effluent specimens were serially collected to measure acetylcysteine concentrations in up to three stages: before, during and upon termination of renal replacement therapy. Alterations in pharmacokinetics were determined by applying standard pharmacokinetic equations.
Over 2 years, 10 critically ill patients in fulminant hepatic failure requiring renal replacement therapy coincident with acetylcysteine were consecutively enrolled. All 10 patients required continuous venovenous hemofiltration (n = 10) and 2 of the 10 also required hemodialysis (n = 2). There was a significant alteration in the pharmacokinetics of acetylcysteine during hemodialysis; the area under the curve (AUC) decreased 41%, the mean extraction ratio was 51%, the mean hemodialytic clearance was 114.01 ml/kg/h, and a mean 166.75 mg/h was recovered in the effluent or 41% of the hourly dose. Alteration in the pharmacokinetics of acetylcysteine during continuous venovenous hemofiltration did not appear to be significant: the AUC decreased 13%, the mean clearance was 31.77 ml/kg/h and a mean 62.12 mg/h was recovered in the effluent or 14% of the hourly dose.
There was no significant extraction of acetylcysteine from continuous venovenous hemofiltration. In contrast, there was significant extracorporeal removal of acetylcysteine during hemodialysis. A reasonable dose adjustment may be to double the IV infusion rate or possibly supplement with oral acetylcysteine during hemodialysis.
对乙酰氨基酚所致暴发性肝衰竭与急性肾损伤、代谢性酸中毒以及液体和电解质失衡相关,需要进行肾脏替代治疗。尽管解毒剂乙酰半胱氨酸可能会被肾脏替代治疗清除,但缺乏药代动力学数据来指导潜在的剂量调整。我们旨在确定各种肾脏替代治疗对乙酰半胱氨酸的体外清除情况。
连续收集尿液、血浆和流出液标本,分三个阶段测量乙酰半胱氨酸浓度:肾脏替代治疗前、治疗期间和治疗结束时。通过应用标准药代动力学方程确定药代动力学的变化。
在2年多的时间里,连续纳入了10例暴发性肝衰竭的危重症患者,这些患者需要进行肾脏替代治疗且同时使用乙酰半胱氨酸。所有10例患者均需要持续静静脉血液滤过(n = 10),其中2例还需要血液透析(n = 2)。血液透析期间乙酰半胱氨酸的药代动力学有显著变化;曲线下面积(AUC)下降41%,平均清除率为51%,平均血液透析清除率为114.01 ml/kg/h,流出液中平均回收166.75 mg/h,占每小时剂量的41%。连续静静脉血液滤过期间乙酰半胱氨酸的药代动力学变化似乎不显著:AUC下降13%,平均清除率为31.77 ml/kg/h,流出液中平均回收62.12 mg/h,占每小时剂量的14%。
连续静静脉血液滤过对乙酰半胱氨酸的清除不显著。相比之下,血液透析期间乙酰半胱氨酸有显著的体外清除。合理的剂量调整可能是在血液透析期间将静脉输注速率加倍或可能补充口服乙酰半胱氨酸。