Efficacy of charcoal hemoperfusion in massive carbamazepine poisoning

被引:24
作者
Cameron, RJ
Hungerford, P
Dawson, AH
机构
[1] Univ Newcastle, Newcastle Mater Hosp, Dept Clin Toxicol, Newcastle, NSW 2310, Australia
[2] Gosford Hosp, Gosford, NSW, Australia
[3] Tamworth Base Hosp, Tamworth, NSW, Australia
来源
JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY | 2002年 / 40卷 / 04期
关键词
carbamazepine; toxicity; hemoperfusion;
D O I
10.1081/CLT-120006754
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Back-ground: Carbamazepinc poisoning can be life threatening. The role and efficacy of extracorporeal drug clearance is not clearly defined. Case Report: A 16-year-old male ingested 34 g of slow-release carbamazepine. His course was complicated by seizures, recurrent cardiac arrests, and renal failure. Intestinal ileus at the time of presentation prevented effective gastrointestinal decontamination. His carbamazepine concentration peaked at 93.8 mg/L (397 mumol/L) 106 hours after ingestion. There was evidence suggesting ongoing absorption for 120 hours. He underwent seven episodes of charcoal hemoperfusion for a total of 109.25 hours. He subsequently made a full recovery Methods: The efficacy of charcoal hemoperfusion was evaluated by measuring the carbamazepine concentrations in the afferent and efferent loops of the hemoperfusion cartridge using 17 paired convenience samples. Extraction ratios were calculated and plotted against time for each individual episode of charcoal hemoperfusion. Conclusion: The extraction ratio was linearly related to time, and ranged 0.46-0.02. The peak clearance was 69 mL/min. Cartridge saturation was defined as a clearance that was equal to an estimate of the patient's intrinsic clearance. In our patient, this was equivalent to an extraction ratio of 0.2 at a flow rate of 150 mL/min. By this definition, cartridge saturation appeared to occur at 7 hours. Charcoal hemoperfusion was associated with a significant reduction in the apparent half-life, which is most easily explained by clearance from the central vascular compartment, during a prolonged absorptive phase. The patient made full recovery without evidence of neurological deficit.
引用
收藏
页码:507 / 512
页数:6
相关论文
共 20 条
[11]   Treatment of acute carbamazepine poisoning by hemoperfusion [J].
Low, CL ;
Haqqie, SS ;
Desai, R ;
Bailie, GR .
AMERICAN JOURNAL OF EMERGENCY MEDICINE, 1996, 14 (05) :540-541
[12]  
Mordel A., 1998, Journal of Toxicology Clinical Toxicology, V36, P472
[13]  
NILSSON C, 1984, ACTA MED SCAND, V216, P137
[14]  
PATRSALOS PN, 1987, HUM TOXICOL, V6, P241
[15]  
Spiller H. A., 1998, Journal of Toxicology Clinical Toxicology, V36, P472
[16]   ACUTE CARBAMAZEPINE TOXICITY RESULTING FROM OVERDOSE [J].
SULLIVAN, JB ;
RUMACK, BH ;
PETERSON, RG .
NEUROLOGY, 1981, 31 (05) :621-624
[17]   ACUTE TOXIC REACTION TO CARBAMAZEPINE - CLINICAL EFFECTS AND SERUM CONCENTRATIONS [J].
TIBBALLS, J .
JOURNAL OF PEDIATRICS, 1992, 121 (02) :295-299
[18]   MASSIVE CARBAMAZEPINE OVERDOSE - CLINICAL AND PHARMACOLOGIC OBSERVATIONS IN 5 EPISODES [J].
WEAVER, DF ;
CAMFIELD, P ;
FRASER, A .
NEUROLOGY, 1988, 38 (05) :755-759
[19]   Recurrent respiratory distress associated with carbamazepine overdose [J].
Wilschut, FA ;
Cobben, NAM ;
Thunnissen, FBJM ;
Lamers, RJS ;
Wouters, EFM ;
Drent, M .
EUROPEAN RESPIRATORY JOURNAL, 1997, 10 (09) :2163-2165
[20]  
2001, GOODMAN GILMANS PHAR