Key result
Vasopressin alone was the most effective treatment for desipramine overdose in a swine model, with both vasopressin and lipid emulsion independently increasing survival.
RCT
Randomly assigned to 1 of 8 groups
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May support vasopressin in desipramine overdose; hypothesis-generating from swine model, requiring human trials.
A toxic dose of desipramine (tricyclic antidepressant) causes cardiac arrhythmias and ultimately asystole. Resuscitation is difficult and almost always unsuccessful. Anecdotal evidence suggests that an infusion of lipid emulsion may be an effective treatment. The purpose of this study was to determine the optimal combination of lipid rescue and traditional Advanced Cardiac Life Support therapy for the treatment of desipramine overdose. We use a prospective, experimental, between subjects design with a swine model investigating the effectiveness of the drugs and drug combinations administered with cardiopulmonary resuscitation. Subjects were randomly assigned to 1 of 8 cardiopulmonary resuscitation/drug combination interventions, and the results from each group were compared using an analysis of variance and post hoc Tukey where appropriate. The groups that received vasopressin were more likely to survive than those that did not receive vasopressin, and the groups that received lipid emulsion were more likely to survive than those that did not receive lipid emulsion. Vasopressin alone was shown to be the most effective treatment in the management of desipramine overdose. The results of this study may warrant changes in treatment protocols for desipramine overdose.
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O'Sullivan et al. (2014) conducted an RCT in Desipramine overdose. Vasopressin and/or lipid emulsion vs. Other CPR/drug combinations was evaluated on Survival. Vasopressin alone was the most effective treatment for desipramine overdose in a swine model, with both vasopressin and lipid emulsion independently increasing survival.
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