Peer-reviewed veterinary case report
Maropitant stops vomiting from chemo drug cisplatin in dogs
By de la Puente-Redondo, Victor A et al.·Published in American journal of veterinary research·2007·Veterinary Medicine Research & Development, United Kingdom·View original on PubMed →
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Original publication title: Efficacy of maropitant for treatment and prevention of emesis caused by intravenous infusion of cisplatin in dogs.
- Species:
- dog
Plain-English summary
A group of healthy 6-month-old Beagles was given a chemotherapy drug called cisplatin, which often causes vomiting. To help prevent or treat this vomiting, some dogs received a medication called maropitant, while others received a placebo. The dogs that received maropitant vomited significantly less and stopped vomiting faster compared to those that didn’t get the medication. This study shows that maropitant is both safe and effective for managing vomiting caused by cisplatin in dogs.
People also search for: dog vomiting after chemotherapy · maropitant for dog nausea · cisplatin side effects in dogs
Abstract
OBJECTIVE: To evaluate the efficacy of maropitant, a novel neurokinin-1 receptor antagonist, to treat and prevent emesis caused by IV infusion of a chemotherapeutic dose of cisplatin (70 mg/m(2)) in dogs. ANIMALS: 64 healthy 6-month-old Beagles (32 males and 32 females). PROCEDURES: To evaluate the effect of maropitant on ongoing emesis, 24 dogs were randomized to 2 treatment groups (12 dogs each). Saline (0.9% NaCl) solution or maropitant (1 mg/kg) was administered once by SC injection immediately following the first emetic event after cisplatin infusion. Dogs were assessed for emesis for 6 hours after initiation of cisplatin infusion. To evaluate the use of maropitant for the prevention of emesis, 40 dogs were randomized to 4 treatment groups (10 dogs each). Placebo or maropitant (1, 2, or 3 mg/kg) was administered PO as a tablet. Cisplatin infusion was initiated at 19 hours after treatment, and dogs were assessed for emesis for 6 hours. RESULTS: No treatment-related adverse events were observed in either study. For the treatment of ongoing emesis, significantly fewer emetic events were observed for maropitant-treated dogs, compared with placebo-treated dogs (mean, 5.2 vs 15.8), and the mean time to cessation of emesis was significantly shorter (0.65 vs 1.65 hours). In the prevention of emesis, maropitant-treated dogs had significantly fewer emetic events (means, 2.7, 1.1, and 0.5 for maropitant at 1, 2, and 3 mg/kg, respectively), compared with placebo-treated dogs (mean, 20.3). CONCLUSIONS AND CLINICAL RELEVANCE: Results suggest that maropitant is safe and effective in the treatment and prevention of cisplatin-induced emesis in dogs.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/17199418/