Department of Anaesthesiology and Intensive Care, University Hospital of Muenster, Muenster, Germany.
Eur J Anaesthesiol. 2010 Dec;27(12):1044-51. doi: 10.1097/EJA.0b013e32833b7969.
despite the introduction of newer antiemetics in the prevention of postoperative nausea and vomiting (PONV), perphenazine is recommended in current guidelines, as the concept of multimodal management of PONV in high-risk patients requires more than two drugs to be combined. The aim of this quantitative systematic review was to assess the efficacy and safety of perphenazine in the prophylaxis of PONV in adults and children.
randomised controlled trials investigating the efficacy of perphenazine in the prevention of PONV in comparison with any other drug or placebo were systematically searched in MEDLINE, EMBASE, CINAHL and the Cochrane Library. Dichotomous data on the efficacy and adverse effects were combined and relative risks (RRs) as well as corresponding 95% confidence intervals (CIs) were calculated.
eleven trials published between 1965 and 1999 including a total of 2081 participants fulfilled the inclusion criteria and were further analysed. In children, perphenazine 0.07 mg kg was effective in preventing vomiting (RR, 0.31; 95% CI, 0.18-0.54), whereas in adults, a dose of about 5 mg was effective for the prevention of PONV (RR, 0.50; 95% CI, 0.37-0.67). When compared with established newer drugs, for example, ondansetron, dexamethasone or droperidol, no significant differences were observed in the pooled analysis with limited data. Reporting of adverse events was poor. Transient sedation was reported in three eligible trials (RR, 0.9; 95% CI, 0.40-2.05).
there is evidence that perphenazine is effective in the prevention of PONV in children and adults without serious adverse effects compared with placebo.
尽管在预防术后恶心和呕吐 (PONV) 方面引入了更新的止吐药,但培高利特仍被当前指南推荐,因为高危患者的 PONV 多模式管理概念需要联合使用两种以上药物。本定量系统评价的目的是评估培高利特预防成人和儿童 PONV 的疗效和安全性。
系统检索 MEDLINE、EMBASE、CINAHL 和 Cochrane 图书馆中关于培高利特预防 PONV 疗效的随机对照试验。对疗效和不良反应的二项数据进行合并,并计算相对风险 (RR) 及其相应的 95%置信区间 (CI)。
1965 年至 1999 年期间发表的 11 项试验符合纳入标准,共纳入 2081 名参与者,并进一步进行了分析。在儿童中,培高利特 0.07 mg/kg 有效预防呕吐 (RR,0.31;95%CI,0.18-0.54),而在成人中,约 5mg 的剂量可有效预防 PONV (RR,0.50;95%CI,0.37-0.67)。在汇总分析中,与已建立的更新型药物(例如昂丹司琼、地塞米松或氟哌利多)相比,尽管数据有限,但未观察到差异有统计学意义。不良反应报告情况较差。在 3 项合格试验中报告了短暂镇静 (RR,0.9;95%CI,0.40-2.05)。
与安慰剂相比,培高利特在预防儿童和成人 PONV 方面有效,且无严重不良反应。