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Pharmacology ; 83(4): 205-10, 2009.
Article in English | MEDLINE | ID: mdl-19174617

ABSTRACT

INTRODUCTION: In this prospective, randomized, and double-blinded study we investigated the efficacy of haloperidol (10 microg/kg) and the combination of haloperidol (10 microg/kg) with ondansetron (0.1 mg/kg) for the prophylaxis of postoperative nausea and vomiting (PONV) after ophthalmologic surgery. METHODS: 60 patients (ASA status 1-3) with risk factors for PONV (female, non-smoker, motion sickness or PONV in history, opioids for postoperative analgesia) undergoing retinal or strabismus surgery were included into the study and randomised to the haloperidol group (H-Group) or the haloperidol-ondansetron group (H/O-Group). 20 min before the end of anaesthesia the study medication was given. Nausea, vomiting, pain scores, and adverse events were assessed postoperatively over 24 h. RESULTS: The incidence of PONV was lower for the H/O-Group (23 vs. 57% for the H-Group). Especially the incidence of vomiting was reduced for the H/O-Group (7 vs. 27% in the H-Group). No significant differences could be detected regarding adverse events. CONCLUSION: The single use of haloperidol for the prophylaxis of PONV is doubtful. Better results were obtained with the combination therapy of haloperidol with ondansetron, especially for vomiting.


Subject(s)
Haloperidol/administration & dosage , Haloperidol/therapeutic use , Ondansetron/administration & dosage , Ondansetron/therapeutic use , Ophthalmologic Surgical Procedures/adverse effects , Postoperative Nausea and Vomiting/prevention & control , Double-Blind Method , Drug Therapy, Combination , Female , Haloperidol/adverse effects , Humans , Middle Aged , Ondansetron/adverse effects , Pain Measurement , Pain, Postoperative/drug therapy , Risk Factors , Time Factors
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