TY - JOUR
T1 - The clinical use of ondansetron
AU - New South Wales Therapeutic Assessment Group
AU - Currow, D. C.
AU - Noble, P. D.
AU - Stuart-Harris, R. C.
PY - 1995/2
Y1 - 1995/2
N2 - Objective: To establish guidelines for use of ondansetron. Data sources: MEDLINE computer search (to July 1993) and information from the manufacturer. Data extraction: We circulated a position paper based on our literature review for comment by clinicians and directors of pharmacy in major teaching hospitals in New South Wales who had an interest in ondansetron. Data synthesis: Ondansetron is effective in the control of nausea and vomiting occurring 24-48 hours after highly emetogenic chemotherapy and after radiotherapy. There are no data to support its use in delayed emesis. Combination with dexamethasone may improve emetic control. The most commonly reported adverse effects are headache and constipation. Optimal dose, frequency of dosing and route of administration have not been established. The cost for each inpatient treated successfully is about 3% more than conventional antiemetic therapy. Conclusions: Ondansetron shows clinical benefit in the management of acute nausea and vomiting in patients receiving highly emetogenic chemotherapy, those who have responded poorly to other antiemetics after moderately emetogenic chemotherapy, those who have intolerable side effects with conventional antiemetic agents and those receiving radiotherapy to the upper abdomen. It is also marketed for the prevention and treatment of postoperative nausea and vomiting.
AB - Objective: To establish guidelines for use of ondansetron. Data sources: MEDLINE computer search (to July 1993) and information from the manufacturer. Data extraction: We circulated a position paper based on our literature review for comment by clinicians and directors of pharmacy in major teaching hospitals in New South Wales who had an interest in ondansetron. Data synthesis: Ondansetron is effective in the control of nausea and vomiting occurring 24-48 hours after highly emetogenic chemotherapy and after radiotherapy. There are no data to support its use in delayed emesis. Combination with dexamethasone may improve emetic control. The most commonly reported adverse effects are headache and constipation. Optimal dose, frequency of dosing and route of administration have not been established. The cost for each inpatient treated successfully is about 3% more than conventional antiemetic therapy. Conclusions: Ondansetron shows clinical benefit in the management of acute nausea and vomiting in patients receiving highly emetogenic chemotherapy, those who have responded poorly to other antiemetics after moderately emetogenic chemotherapy, those who have intolerable side effects with conventional antiemetic agents and those receiving radiotherapy to the upper abdomen. It is also marketed for the prevention and treatment of postoperative nausea and vomiting.
UR - http://www.scopus.com/inward/record.url?scp=0028925565&partnerID=8YFLogxK
U2 - 10.5694/j.1326-5377.1995.tb138480.x
DO - 10.5694/j.1326-5377.1995.tb138480.x
M3 - Article
C2 - 7854228
AN - SCOPUS:0028925565
SN - 0025-729X
VL - 162
SP - 145
EP - 149
JO - Medical Journal of Australia
JF - Medical Journal of Australia
IS - 3
ER -