Intralipid outperforms sodium bicarbonate in a rabbit model of clomipramine toxicity

被引:134
作者
Harvey, Martyn
Cave, Grant
机构
[1] Waikato Hosp, Dept Emergency Med, Hamilton, New Zealand
[2] Monash Med Ctr, Dept Intens Care Med, Melbourne, Vic, Australia
关键词
D O I
10.1016/j.annemergmed.2006.07.016
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Study objective: Previous investigators have demonstrated amelioration of lipid-soluble drug toxidromes with infusion of lipid emulsions. Clomipramine is a lipid-soluble tricyclic antidepressant with significant cardiovascular depressant activity in human overdose. We compare resuscitation with Intralipid versus sodium bicarbonate in a rabbit model of clomipramine toxicity. Methods: Thirty sedated and mechanically ventilated New Zealand White rabbits were infused with clomipramine at 320 mg/kg per hour. At target mean arterial pressure of 50% initial mean arterial pressure, animals were rescued with 0.9% NaCl 12 mL/kg, 8.4% sodium bicarbonate 3 mL/kg, or 20% Intralipid 12 mL/kg. Pulse rate, mean arterial pressure, and QRS duration were sampled at 2.5-minute intervals to 15 minutes. In the second phase of the experiment, 8 sedated and mechanically ventilated rabbits were infused with clomipramine at 240 mg/kg per hour to a mean arterial pressure of 25 mm Hg. Animals received either 2 mL/kg 8.4% sodium bicarbonate or 8 mL/kg 20% Intralipid as rescue therapy. External cardiac compression and intravenous adrenaline were administered in the event of cardiovascular collapse. Results: Mean difference in mean arterial pressure between Intralipid- and saline solution-treated groups was 21.1 mm Hg (95% confidence interval [CI] 13.5 to 28.7 mm Hg) and 19.5 mm Hg (95% CI 10.5 to 28.9 mm Hg) at 5 and 15 minutes, respectively. Mean difference in mean arterial pressure between Intralipid- and bicarbonate-treated groups was 19.4 mm Hg (95% CI 18.8 to 27.0 mm Hg) and 11.5 mm Hg (95% CI 2.5 to 20.5 mm Hg) at 5 and 15 minutes. The rate of change in mean arterial pressure was greatest in the Intralipid-treated group at 3 minutes (6.2 mm Hg/min [95% CI 3.8 to 8.6 mm Hg/min] Intralipid versus -0.25 mm Hg/min [95% CI -1.9 to 1.4 mm Hg/min] saline solution) and 5 minutes (4.4 mm Hg/min [95% CI 3.0 to 5.9 mm Hg/min] Intralipid versus 0.06 mm Hg/min [95% CI -0.9 to 1.1 mm Hg/min] saline solution). In the second phase of the experiment spontaneous circulation was maintained in all Intralipid-treated rabbits (n = 4). All animals in the bicarbonate-treated group developed pulseless electrical activity and proved refractory to resuscitation at 10 minutes (n = 4, P = .023). Conclusion: In this rabbit model, Intralipid infusion resulted in more rapid and complete reversal of clomipramine-induced hypotension compared with sodium bicarbonate. Additionally, Intralipid infusion prevented cardiovascular collapse in a model of severe clomipramine toxicity.
引用
收藏
页码:178 / 185
页数:8
相关论文
共 29 条
[1]   HEMODYNAMIC-EFFECTS OF INTRAVENOUS 20-PERCENT SOY OIL EMULSION FOLLOWING CORONARY-BYPASS SURGERY [J].
ABEL, RM ;
FISCH, D ;
GROSSMAN, ML .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 1983, 7 (06) :534-540
[2]   The role of fat emulsion therapy in a rodent model of propranolol toxicity: a preliminary study. [J].
Cave G. ;
Harvey M.G. ;
Castle C.D. .
Journal of Medical Toxicology, 2006, 2 (1) :4-7
[3]  
Cave Grant, 2005, Emerg Med Australas, V17, P180, DOI 10.1111/j.1742-6723.2005.00714.x
[4]   Antidepressant-related deaths and antidepressant prescriptions in England and Wales, 1998-2000 [J].
Cheeta, S ;
Schifano, F ;
Oyefeso, A ;
Webb, L ;
Ghodse, AH .
BRITISH JOURNAL OF PSYCHIATRY, 2004, 184 :41-47
[5]  
Chelly JE, 1996, ANESTHESIOLOGY, V85, pA555
[6]  
Citak A, 2002, Eur J Emerg Med, V9, P63
[7]   Lipid emulsion to treat bupivacaine toxicity [J].
Dalgleish, D ;
Kathawaroo, S .
ANAESTHESIA, 2005, 60 (08) :822-822
[8]   TIANEPTINE, A NEW TRICYCLIC ANTIDEPRESSANT METABOLIZED BY BETA-OXIDATION OF ITS HEPTANOIC SIDE-CHAIN, INHIBITS THE MITOCHONDRIAL OXIDATION OF MEDIUM AND SHORT CHAIN FATTY-ACIDS IN MICE [J].
FROMENTY, B ;
FRENEAUX, E ;
LABBE, G ;
DESCHAMPS, D ;
LARREY, D ;
LETTERON, P ;
PESSAYRE, D .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (21) :3743-3751
[9]   Tricyclic antidepressants directly depress human myocardial mechanical function independent of effects on the conduction system [J].
Heard, K ;
Cain, BS ;
Dart, RC ;
Cairns, CB .
ACADEMIC EMERGENCY MEDICINE, 2001, 8 (12) :1122-1127
[10]   Tricyclic antidepressant overdose: a review [J].
Kerr, GW ;
McGuffie, AC ;
Wilkie, S .
EMERGENCY MEDICINE JOURNAL, 2001, 18 (04) :236-241