Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Clin Toxicol (Phila) ; 51(4): 208-15, 2013 May.
Article in English | MEDLINE | ID: mdl-23530458

ABSTRACT

BACKGROUND: 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. METHOD: 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. RESULTS: 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). CONCLUSION: 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.


Subject(s)
Amitriptyline/poisoning , Antidepressive Agents, Tricyclic/poisoning , Cardiovascular System/drug effects , Disease Models, Animal , Drug Overdose/therapy , Fat Emulsions, Intravenous/adverse effects , Hemodynamics/drug effects , Administration, Oral , Amitriptyline/administration & dosage , Amitriptyline/blood , Amitriptyline/pharmacokinetics , Animals , Antidepressive Agents, Tricyclic/administration & dosage , Antidepressive Agents, Tricyclic/blood , Antidepressive Agents, Tricyclic/pharmacokinetics , Blood Pressure/drug effects , Cardiovascular System/physiopathology , Drug Overdose/blood , Drug Overdose/physiopathology , Emulsions/adverse effects , Emulsions/therapeutic use , Fat Emulsions, Intravenous/therapeutic use , Heart/drug effects , Heart/physiopathology , Heart Rate/drug effects , Intestinal Absorption , Male , Phospholipids/adverse effects , Phospholipids/therapeutic use , Pilot Projects , Random Allocation , Rats , Rats, Wistar , Soybean Oil/adverse effects , Soybean Oil/therapeutic use , Survival Analysis
SELECTION OF CITATIONS
SEARCH DETAIL
...