PROPHYLAXIS OF DELAYED NAUSEA AND VOMITING AFTER CANCER-CHEMOTHERAPY

被引:9
|
作者
ESSEBOOM, EU
ROJER, RA
BORM, JJJ
VANEPS, LWS
机构
[1] ST ELIZABETH HOSP, DEPT INTERNAL MED, CURACAO, NETH ANTILLES
[2] SLOTERVAART HOSP, DEPT INTERNAL MED, AMSTERDAM, NETHERLANDS
[3] FREE UNIV AMSTERDAM, FAC MED, DEPT GEOG PATHOL, AMSTERDAM, NETHERLANDS
来源
NETHERLANDS JOURNAL OF MEDICINE | 1995年 / 47卷 / 01期
关键词
ONDANSETRON; DOMPERIDONE; DELAYED NAUSEA; EMETOGENIC CHEMOTHERAPY;
D O I
10.1016/0300-2977(95)00027-K
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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).
引用
收藏
页码:12 / 17
页数:6
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