Department of Anesthesia, All India Institute of Medical Sciences, New Delhi 110029, India.
New York University, New York, NY 110003.
J Clin Anesth. 2016 Nov;34:459-82. doi: 10.1016/j.jclinane.2016.05.018. Epub 2016 Jun 28.
Palonosetron is a second-generation 5-HT3 receptor antagonist with proposed higher efficacy and sustained action for prophylaxis of postoperative nausea and vomiting (PONV).
Randomized controlled trials involving adult population undergoing elective surgery under general anesthesia comparing palonosetron to placebo, ramosetron, granisetron, and ondansetron were included. Data were extracted for vomiting incidence (VI), complete response (no nausea/vomiting; Complete Response [CR]), and rescue antiemetic need. This was categorized as early phase (24 hours postoperative for ramosetron and 6 hours for rest) and delayed phase (48 hours for ramosetron and 24 hours for rest). VI and CR were used as markers of drug efficacy. Any adverse effects were evaluated.
Twenty-two trials (4 with 3 groups) were included (comparing palonosetron to placebo in 5, ramosetron in 5, granisetron in 4, and ondansetron in 12 subgroups). Palonosetron demonstrated statistical superiority over placebo for VI and CR, both early/delayed PONV prevention. For delayed phase, palonosetron surpassed ramosetron in all 3 variables; however, none of the variables attained statistical significance during early phase. In early phase, palonosetron had better VI and CR than did granisetron; however, variables other than CR (better for palonosetron) failed to achieve statistical significance for delayed phase. All 3 outcomes were significantly better for palonosetron compared with ondansetron in delayed phase, but statistical superiority could only be demonstrated for VI in early phase. Being inconsistently documented across trials, nausea scores could not be evaluated.
Palonosetron is as safe as and more effective than placebo, ramosetron, granisetron, and ondansetron in preventing delayed PONV. For early PONV, it has higher efficacy over placebo, granisetron, and ondansetron.
帕洛诺司琼是一种第二代 5-HT3 受体拮抗剂,据推测其预防术后恶心呕吐(PONV)的疗效更高且作用持续时间更长。
纳入了涉及接受全身麻醉下择期手术的成年人群的随机对照试验,比较了帕洛诺司琼与安慰剂、雷莫司琼、格拉司琼和昂丹司琼。提取了呕吐发生率(VI)、完全缓解(无恶心/呕吐;完全缓解[CR])和需要解救性止吐药的数据。这被分为早期阶段(雷莫司琼术后 24 小时,其余为 6 小时)和延迟阶段(雷莫司琼术后 48 小时,其余为 24 小时)。VI 和 CR 用作药物疗效的标志物。评估了任何不良反应。
纳入了 22 项试验(4 项为 3 组)(比较帕洛诺司琼与安慰剂在 5 项、雷莫司琼在 5 项、格拉司琼在 4 项和昂丹司琼在 12 项亚组中的疗效)。帕洛诺司琼在预防早期/延迟性 PONV 方面,在 VI 和 CR 方面均优于安慰剂。在延迟阶段,帕洛诺司琼在所有 3 个变量方面均优于雷莫司琼;然而,在早期阶段,没有一个变量达到统计学意义。在早期阶段,帕洛诺司琼的 VI 和 CR 优于格拉司琼;然而,除 CR 以外的其他变量(帕洛诺司琼更好)在延迟阶段未能达到统计学意义。在延迟阶段,帕洛诺司琼在所有 3 项结果方面均明显优于昂丹司琼,但在早期阶段仅能证明 VI 有统计学优势。由于在各试验中记录不一致,无法评估恶心评分。
帕洛诺司琼在预防延迟性 PONV 方面与安慰剂、雷莫司琼、格拉司琼和昂丹司琼一样安全且更有效。对于早期 PONV,它比安慰剂、格拉司琼和昂丹司琼的疗效更高。