The Australiasian clinical toxicology investigators collaboration randomized trial of different loading infusion rates of N-Acetylcysteine
Study objective: We determine whether the incidence of adverse events caused by intravenous N-acetylcysteine is significantly less when the initial dose is infused over a 60-minute period compared with the standard infusion period of 15 minutes. A secondary objective is to assess the efficacy of the 2 treatment arms. Methods: This was a multicenter, randomized, prospective trial of patients who presented with acetaminophen poisoning and who were treated with N-acetylcysteine and had no history...[Show more]
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|Source:||Annals of Emergency Medicine|
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