Ondansetron was the first of several selective 5-hydroxytryptamine (5-
HT3) antagonists to be available as an antiemetic. Its uses in the set
ting of highly and moderately emetogenic chemotherapy and radiotherapy
are well established. Ondansetron has also been used to manage nausea
and vomiting in other patients. We report a retrospective analysis of
its use in all 16 patients who were commenced on ondansetron after ad
mission to our institution for nausea and/or vomiting over a 4-year pe
riod. Nine patients had advanced human immunodeficiency virus/acquired
immunodeficiency syndrome (HIV/AIDS), and seven had malignancy. These
patients were not undergoing disease-modifying treatment and had inad
equate responses to therapeutic doses of standard antiemetics, used ei
ther singly or in combination. Responses were independently reviewed a
nd graded by two investigators. Response was judged at 48 hr after com
mencing therapy. Potential causes of nausea were also reviewed. Overal
l, 13 of 16 [81%, 95% confidence interval (CI) 54%-96%] derived benefi
t. Twelve of 15 patients (80%) with nausea had a demonstrable improvem
ent, and ten of 14 patients (71%) with vomiting also improved. Eight o
f ten patients (80%) admitted with nausea and/or vomiting as one of th
eir presenting problems had the symptom controlled within 48 hr of ond
ansetron therapy. Treatment with ondansetron was well tolerated, onset
of action was rapid, and response rates were high and sustained over
time. Seven of the 16 patients continued ondansetron therapy for more
than 10 days. With minimal reductions in inpatient bed stays, the tota
l costs of ondansetron could be met while at the same time better supp
orting patients remaining in the community. (C) U.S. Cancer Pain Relie
f Committee, 1997.