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Palliative medicine · Jan 2005
Clinical TrialLow-dose levomepromazine in refractory emesis in advanced cancer patients: an open-label study.
- Jorge H Eisenchlas, Nicolás Garrigue, Marta Junin, and Gustavo G De Simone.
- Pallium Latinoamerica and Hospital Bonorino Udaondo, Buenos Aires, Argentina. jeisen@fibertel.com.ar
- Palliat Med. 2005 Jan 1; 19 (1): 71-5.
AbstractSeventy patients with advanced cancer and refractory emesis were treated with subcutaneous boluses of levomepromazine (median daily dose: 6.25 mg; range: 3.12-25) in an open-label prospective study. Treatment was associated with a decrease in nausea from a median of 8/10 at baseline (IQR 7-8) to a median of 1 (IQR 0-2) after two days of treatment (P<0.0001); vomiting ceased in 92% of cases. It was possible to remove the nasogastric tube from all 11 patients who had one. The most frequently reported side effect was sedation, with a median of 2/10 (25-75% percentile 1-3), which was not correlated with the dose of levomepromazine. This study suggests that treatment with low-dose levomepromazine is an effective and safe option for advanced cancer patients who fail to respond to first-line antiemetic treatment.
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