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经皮尼古丁不能预防术后恶心呕吐:一项随机对照试验。

Transcutaneous nicotine does not prevent postoperative nausea and vomiting: a randomized controlled trial.

机构信息

Division of Anaesthesiology Clinical Trial Unit, University Hospitals of Geneva, Geneva, Switzerland Department of Neurosciences Medical Faculty, University of Geneva, Geneva, Switzerland.

出版信息

Br J Clin Pharmacol. 2011 Mar;71(3):383-90. doi: 10.1111/j.1365-2125.2010.03844.x.

Abstract

AIMS

There is empirical evidence that smokers are less likely to suffer from postoperative nausea and vomiting (PONV). We sought to investigate whether transcutaneus nicotine prevents PONV.

METHODS

Non-smokers receiving general anaesthesia for surgery were randomly allocated to Nicotinell Patch 10cm(2) (TTS 10), containing 17.5mg of nicotine (average delivery rate, 7mg 24h(-1) ) or matching placebo patch. Patches were applied 1h before surgery and were left in situ until 24h after surgery (or until the first PONV symptoms occurred).

RESULTS

We randomized 90 patients (45 nicotine, 45 placebo). In the post-anaesthetic care unit, the incidence of nausea was 22.2% with nicotine and 24.4% with placebo (P= 0.80), and the incidence of vomiting was 20.0% with nicotine and 17.8% with placebo (P= 0.78). Cumulative 24h incidence of nausea was 42.2% with nicotine and 40.0% with placebo (P= 0.83), and of vomiting was 31.1% with nicotine and 28.9% with placebo (P= 0.81). PONV episodes tended to occur earlier in the nicotine group. Postoperative headache occurred in 17.8% of patients treated with nicotine and in 15.6% with placebo (P= 0.49). More patients receiving nicotine reported a low quality of sleep during the first postoperative night (26.7% vs. 6.8% with placebo; P= 0.01).

CONCLUSIONS

Non-smokers receiving a prophylactic nicotine patch had a similar incidence of PONV during the first 24h and tended to develop PONV symptoms earlier compared with controls. They had a significantly increased risk of insomnia during the first postoperative night.

摘要

目的

有经验证据表明,吸烟者术后恶心和呕吐(PONV)的发生率较低。我们旨在研究经皮尼古丁贴片是否可以预防 PONV。

方法

择期全麻手术的非吸烟者被随机分配到尼古丁贴片 10cm²(TTS 10)组(含 17.5mg 尼古丁,平均透皮给药率为 7mg/24h)或匹配的安慰剂贴片组。贴片在手术前 1 小时贴敷,并在手术后 24 小时(或直至首次 PONV 症状出现)时去除。

结果

我们随机分配了 90 例患者(尼古丁 45 例,安慰剂 45 例)。在麻醉后护理病房中,尼古丁组恶心的发生率为 22.2%,安慰剂组为 24.4%(P=0.80),呕吐的发生率分别为 20.0%和 17.8%(P=0.78)。24 小时内累积恶心发生率分别为 42.2%和 40.0%(P=0.83),呕吐发生率分别为 31.1%和 28.9%(P=0.81)。PONV 发作在尼古丁组中倾向于更早发生。尼古丁组有 17.8%的患者出现术后头痛,安慰剂组为 15.6%(P=0.49)。接受尼古丁治疗的患者中有更多的人报告在第一个术后夜晚睡眠质量较差(26.7% vs. 6.8%,安慰剂;P=0.01)。

结论

接受预防性尼古丁贴片的非吸烟者在术后 24 小时内 PONV 的发生率相似,但与对照组相比,PONV 症状出现更早。他们在第一个术后夜晚失眠的风险显著增加。

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