A Randomized, Double-Blind Comparison of the NK1 Antagonist, Aprepitant, Versus Ondansetron for the Prevention of Postoperative Nausea and Vomiting

消炎药 昂丹司琼 医学 恶心 呕吐 麻醉 止吐药 耐受性 药理学 不利影响
作者
Tong J. Gan,Christian C. Apfel,Anthony L. Kovac,Beverly K. Philip,Neil Singla,Harold S. Minkowitz,Ashraf S. Habib,Jennifer Knighton,Alexandra D. Carides,Hong Zhang,Kevin J. Horgan,Judith K. Evans,F. Lawson,Farshad Ahadian,David Aguinaga,Jane Blood,Keith Candiotti,Jacques E. Chelly,Paul Cook,Robert DʼAngelo
出处
期刊:Anesthesia & Analgesia [Lippincott Williams & Wilkins]
卷期号:104 (5): 1082-1089 被引量:194
标识
DOI:10.1213/01.ane.0000263277.35140.a3
摘要

In Brief BACKGROUND: Antiemetics currently in use are not totally effective. Neurokinin-1 receptor antagonists are a new class of antiemetic that have shown promise for chemotherapy-induced nausea and vomiting. This is the first study evaluating the efficacy and tolerability of the neurokinin-1 receptor antagonist, aprepitant, for the prevention of postoperative nausea and vomiting. METHODS: In this multicenter, double-blind trial, we randomly assigned 805 patients receiving general anesthesia for open abdominal surgery to a preoperative dose of aprepitant 40 mg orally, aprepitant 125 mg orally, or ondansetron 4 mg IV. Vomiting, nausea, and use of rescue therapy were assessed over 48 h after surgery. Treatments were compared using logistic regression. RESULTS: Incidence rates for the primary end point (complete response [no vomiting and no use of rescue] over 0–24 h after surgery, tested for superiority of aprepitant) were not different across groups (45% with aprepitant 40 mg, 43% with aprepitant 125 mg, and 42% with ondansetron). The incidence of no vomiting (0–24 h) was higher with aprepitant 40 mg (90%) and aprepitant 125 mg (95%) versus ondansetron (74%) (P < 0.001 for both comparisons), although between-treatment use of rescue and nausea control was not different. Both aprepitant doses also had higher incidences of no vomiting over 0–48 h (P < 0.001). No statistically significant differences were seen among the side effect profiles of the treatments. CONCLUSIONS: Aprepitant was superior to ondansetron for prevention of vomiting in the first 24 and 48 h, but no significant differences were observed between aprepitant and ondansetron for nausea control, use of rescue, or complete response. IMPLICATIONS: Aprepitant and the active comparator ondansetron did not differ for the composite end point of no vomiting and no rescue 0-24 h after major surgery; aprepitant provided better protection against vomiting 0-24 h and 0-48 h.
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