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Article: Single-dose aprepitant vs ondansetron for the prevention of postoperative nausea and vomiting: A randomized, double-blind Phase III trial in patients undergoing open abdominal surgery
Title | Single-dose aprepitant vs ondansetron for the prevention of postoperative nausea and vomiting: A randomized, double-blind Phase III trial in patients undergoing open abdominal surgery |
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Authors | |
Keywords | Antagonism Aprepitant Clinical trials Ondansetron PONV Serotonin (5-hydroxy-tryptamine) |
Issue Date | 2007 |
Publisher | Oxford University Press. The Journal's web site is located at http://bja.oxfordjournals.org/ |
Citation | British Journal Of Anaesthesia, 2007, v. 99 n. 2, p. 202-211 How to Cite? |
Abstract | Background: The neurokinin1 antagonist aprepitant is effective for prevention of chemotherapy-induced nausea and vomiting. We compared aprepitant with ondansetron for prevention of postoperative nausea and vomiting. Methods: Nine hundred and twenty-two patients receiving general anaesthesia for major abdominal surgery were assigned to receive a single preoperative dose of oral aprepitant 40 mg, oral aprepitant 125 mg, or i.v. ondansetron 4 mg in a randomized, double-blind trial. Vomiting episodes, use of rescue therapy, and nausea severity (verbal rating scale) were documented for 48 h after surgery. Primary efficacy endpoints were complete response (no vomiting and no use of rescue therapy) 0-24 h after surgery and no vomiting 0-24 h after surgery. The secondary endpoint was no vomiting 0-48 h after surgery. Results: Aprepitant at both doses was non-inferior to ondansetron for complete response 0-24 h after surgery (64% for aprepitant 40 mg, 63% for aprepitant 125 mg, and 55% for ondansetron, lower bound of 1-sided 95% CI > 0.65), superior to ondansetron for no vomiting 0-24 h after surgery (84% for aprepitant 40 mg, 86% for aprepitant 125 mg, and 71% for ondansetron; P < 0.001), and superior for no vomiting 0-48 h after surgery (82% for aprepitant, 40 mg, 85% for aprepitant, 125 mg, and 66% for ondansetron; P < 0.001). The distribution of peak nausea scores was lower in both aprepitant groups vs ondansetron (P < 0.05). Conclusions: Aprepitant was non-inferior to ondansetron in achieving complete response for 24 h after surgery. Aprepitant was significantly more effective than ondansetron for preventing vomiting at 24 and 48 h after surgery, and in reducing nausea severity in the first 48 h after surgery. Aprepitant was generally well tolerated. © The Board of Management and Trustees of the British Journal of Anaesthesia 2007. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/145546 |
ISSN | 2023 Impact Factor: 9.1 2023 SCImago Journal Rankings: 2.397 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Diemunsch, P | en_HK |
dc.contributor.author | Gan, TJ | en_HK |
dc.contributor.author | Philip, BK | en_HK |
dc.contributor.author | Girao, MJ | en_HK |
dc.contributor.author | Eberhart, L | en_HK |
dc.contributor.author | Irwin, MG | en_HK |
dc.contributor.author | Pueyo, J | en_HK |
dc.contributor.author | Chelly, JE | en_HK |
dc.contributor.author | Carides, AD | en_HK |
dc.contributor.author | Reiss, T | en_HK |
dc.contributor.author | Evans, JK | en_HK |
dc.contributor.author | Lawson, FC | en_HK |
dc.contributor.author | Aprepitant-PONV Protocol 091 International Study Group | - |
dc.date.accessioned | 2012-02-28T01:53:19Z | - |
dc.date.available | 2012-02-28T01:53:19Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | British Journal Of Anaesthesia, 2007, v. 99 n. 2, p. 202-211 | en_HK |
dc.identifier.issn | 0007-0912 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/145546 | - |
dc.description.abstract | Background: The neurokinin1 antagonist aprepitant is effective for prevention of chemotherapy-induced nausea and vomiting. We compared aprepitant with ondansetron for prevention of postoperative nausea and vomiting. Methods: Nine hundred and twenty-two patients receiving general anaesthesia for major abdominal surgery were assigned to receive a single preoperative dose of oral aprepitant 40 mg, oral aprepitant 125 mg, or i.v. ondansetron 4 mg in a randomized, double-blind trial. Vomiting episodes, use of rescue therapy, and nausea severity (verbal rating scale) were documented for 48 h after surgery. Primary efficacy endpoints were complete response (no vomiting and no use of rescue therapy) 0-24 h after surgery and no vomiting 0-24 h after surgery. The secondary endpoint was no vomiting 0-48 h after surgery. Results: Aprepitant at both doses was non-inferior to ondansetron for complete response 0-24 h after surgery (64% for aprepitant 40 mg, 63% for aprepitant 125 mg, and 55% for ondansetron, lower bound of 1-sided 95% CI > 0.65), superior to ondansetron for no vomiting 0-24 h after surgery (84% for aprepitant 40 mg, 86% for aprepitant 125 mg, and 71% for ondansetron; P < 0.001), and superior for no vomiting 0-48 h after surgery (82% for aprepitant, 40 mg, 85% for aprepitant, 125 mg, and 66% for ondansetron; P < 0.001). The distribution of peak nausea scores was lower in both aprepitant groups vs ondansetron (P < 0.05). Conclusions: Aprepitant was non-inferior to ondansetron in achieving complete response for 24 h after surgery. Aprepitant was significantly more effective than ondansetron for preventing vomiting at 24 and 48 h after surgery, and in reducing nausea severity in the first 48 h after surgery. Aprepitant was generally well tolerated. © The Board of Management and Trustees of the British Journal of Anaesthesia 2007. All rights reserved. | en_HK |
dc.language | eng | en_US |
dc.publisher | Oxford University Press. The Journal's web site is located at http://bja.oxfordjournals.org/ | en_HK |
dc.relation.ispartof | British Journal of Anaesthesia | en_HK |
dc.subject | Antagonism | en_HK |
dc.subject | Aprepitant | en_HK |
dc.subject | Clinical trials | en_HK |
dc.subject | Ondansetron | en_HK |
dc.subject | PONV | en_HK |
dc.subject | Serotonin (5-hydroxy-tryptamine) | en_HK |
dc.subject.mesh | Abdomen - surgery | - |
dc.subject.mesh | Antiemetics - administration and dosage - therapeutic use | - |
dc.subject.mesh | Morpholines - administration and dosage - therapeutic use | - |
dc.subject.mesh | Ondansetron - therapeutic use | - |
dc.subject.mesh | Postoperative Nausea and Vomiting - prevention and control | - |
dc.title | Single-dose aprepitant vs ondansetron for the prevention of postoperative nausea and vomiting: A randomized, double-blind Phase III trial in patients undergoing open abdominal surgery | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Irwin, MG:mgirwin@hku.hk | en_HK |
dc.identifier.authority | Irwin, MG=rp00390 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1093/bja/aem133 | en_HK |
dc.identifier.pmid | 17540667 | - |
dc.identifier.scopus | eid_2-s2.0-34547866543 | en_HK |
dc.identifier.hkuros | 134903 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34547866543&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 99 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 202 | en_HK |
dc.identifier.epage | 211 | en_HK |
dc.identifier.isi | WOS:000248683000009 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.issnl | 0007-0912 | - |