Faculty of Medicine, Department of Pharmacology, Nursing and Health Sciences, Monash University, Clayton, Victoria, Australia.
Clin Toxicol (Phila). 2013 May;51(4):208-15. doi: 10.3109/15563650.2013.778994. Epub 2013 Mar 26.
Overdose with lipophilic drugs, such as amitriptyline, may cause cardiotoxicity in overdose. Severe poisoning can be resistant to traditional treatments. Intravenous lipid emulsion (ILE) has been recommended as a novel therapy for the treatment of such overdoses; however, a little is known about the effects of ILE-infusion on drug concentration and haemodynamics in the early/absorptive phase after oral poisoning.
Thirty minutes after oro-gastric administration of amitriptyline (70 mg/kg), either 20% intravenous lipid emulsion (ILE), 8.4% sodium bicarbonate or Hartmann's solution was infused to anaesthetized and ventilated rodents (n = 10 per group). Heart rate, blood pressure, cutaneous ECG - QRS interval duration (QRS-d), and survival were serially recorded over 120 min. Blood drug concentrations were also collected during this period. Continuous variables were compared using one-way ANOVA.
ILE infusion significantly decreased the survival compared to other treatments (10% ILE vs 70% bicarbonate vs 70% Hartmann's solution, p = 0.005). There was a gradual prolongation of QRS-d and fall in blood pressure over time compared to baseline (T0) measurement for both ILE and Hartmann's solution treatments. This was associated with significantly increased blood AMI concentration with ILE treatment at T60, T90 and T120 min to the other treatments (p < 0.02).
Administration of ILE early after oral amitriptyline overdose resulted in worse survival and no improvement in haemodynamics. In addition, blood amitriptyline concentrations were higher in the ILE-treated group. This suggests that either drug absorption from the gastrointestinal-tract was facilitated or drug redistribution was retarded when ILE was given early after oral poisoning.
脂溶性药物(如阿米替林)过量可能导致中毒性心肌毒性。严重中毒可能对传统治疗方法产生耐药性。静脉内脂肪乳剂(ILE)已被推荐为治疗此类中毒的新疗法;然而,对于 ILE 输注对口服中毒后早期/吸收期药物浓度和血液动力学的影响知之甚少。
在口服给予阿米替林(70mg/kg)后 30 分钟,将 20%静脉内脂肪乳剂(ILE)、8.4%碳酸氢钠或哈特曼溶液输注到麻醉和通气的啮齿动物(每组 10 只)。在 120 分钟内连续记录心率、血压、皮肤心电图 - QRS 间期持续时间(QRS-d)和存活率。在此期间还收集了血液药物浓度。使用单向方差分析比较连续变量。
ILE 输注与其他治疗方法相比显著降低了存活率(10%ILE 与 70%碳酸氢钠与 70%哈特曼溶液,p=0.005)。ILE 和哈特曼溶液治疗组的 QRS-d 逐渐延长,血压随时间逐渐下降,与基线(T0)测量值相比。这与 ILE 治疗组在 T60、T90 和 T120 分钟时的血液 AMI 浓度显著增加有关,与其他治疗方法相比(p<0.02)。
在口服阿米替林中毒后早期给予 ILE 导致存活率下降,血液动力学无改善。此外,ILE 治疗组的血液阿米替林浓度更高。这表明 ILE 在口服中毒后早期给予时,可能促进了胃肠道药物吸收或延缓了药物重新分布。