Objective: To compare ondansetron and domperidone for the treatment of delayed nausea/vomiting (DN/V) following highly emetogenic chemotherapy, after attaining total suppression of emesis on the day of chemotherapy by means of ondansetron (combined with dexamethasone in the case of cisplatin-treated patients). Methods: Domperidone (3 x 20 mg daily) was compared with ondansetron (3 x 8 mg daily) in a randomized double-blind placebo-controlled study. Out of 65 consecutive patients who received a first course of either cyclophosphamide and cisplatin for advanced stage ovarian cancer or cyclophosphamide, doxorubicin and 5-fluorouracil for metastatic breast carcinoma, 60 patients were eligible for entering the study. According to data from the literature these chemotherapeutic regimens will induce DN/V to a comparable degree. The patients were questioned daily from day 2 through day 5 by the same investigator and the severity of nausea or vomiting was scored on a numerical scale. Results: Emesis was totally suppressed in all patients on the day of chemotherapy. As to DN/V, 16 out of 20 patients receiving placebo required ''rescue'' medication versus none in the other two groups (p < 0.001). Only 2 (10%) patients were symptomatic with domperidone versus 9 (45%) symptomatic patients in the ondansetron-treated group (p < 0.05). Conclusions: Both drugs are effective, but domperidone (3 x 20 mg) is more effective than ondansetron (3 x 8 mg) for the prevention of the delayed nausea and/or vomiting which occur after highly emetogenic chemotherapy (p < 0.05).
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Washington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Waqar, Saiama N.
Mann, Janelle
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St Louis Coll Pharm, Dept Pharm Practice, St Louis, MO USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Mann, Janelle
Baggstrom, Maria Q.
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Washington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Baggstrom, Maria Q.
Waqar, Muhammad Atif
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Univ Nevada, Sch Med, Dept Internal Med, Reno, NV 89557 USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Waqar, Muhammad Atif
Chitneni, Pooja
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New York Presbyterian Hosp, Dept Hospitalist Med, New York, NY USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Chitneni, Pooja
Williams, Kristina
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Washington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Williams, Kristina
Gao, Feng
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Washington Univ, Sch Med, Dept Surg, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Gao, Feng
Morgensztern, Daniel
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Washington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA
Morgensztern, Daniel
Govindan, Ramaswamy
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Washington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USAWashington Univ, Sch Med, Dept Internal Med, Div Oncol, St Louis, MO 63110 USA