Murakami, Chiaki Tokushima University
Kakuta, Nami Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Sakai, Yoko Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Kasai, Asuka Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Oyama, Takuro Tokushima University Tokushima University Educator and Researcher Directory
Tanaka, Katsuya Tokushima University Tokushima University Educator and Researcher Directory KAKEN Search Researchers
Postoperative nausea and vomiting (PONV) occur in 30–50% of patients undergoing general anesthesia and in 70–80% of high PONV risk patients. In this study, we investigated the efficacy of fosaprepitant, a neurokinin-1 (NK1) receptor antagonist, compared to ondansetron, a selective 5-hydroxytryptamine type 3 (5-HT3) receptor antagonist, in moderate to high PONV risk patients from our previous randomized controlled trials. Patients (171 patients from 4 pooled studies) with the Apfel simplified score ≥ 2 and undergoing general anesthesia were randomly allocated to receive intravenous fosaprepitant 150 mg (NK1 group, 𝑛 = 82) and intravenous ondansetron 4 mg (ONS group, 𝑛 = 89) before induction of anesthesia. Incidence of vomiting was significantly lower in the NK1 group compared to the ONS group 0–2, 0–24, and 0–48 hours after surgery (2 versus 17%, 2 versus 28%, and 2 versus 29%, resp.). However, no significant differences in PONV, complete response, rescue antiemetic use, and nausea score were observed between groups 0–48 hours after surgery. In moderate to high PONV risk patients, fosaprepitant decreased the incidence of vomiting and was superior to ondansetron in preventing postoperative vomiting 0–48 hours after surgery.
BioMed Research International
Copyright © 2017 Chiaki Murakami et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
|DOI (Published Version)|
|URL ( Publisher's Version )|
bmri_2017_5703528.pdf 1.3 MB