甲状腺和甲状旁腺手术中不含阿片类药物和含阿片类药物异丙酚麻醉的比较:答复

IF 7.5 1区 医学 Q1 ANESTHESIOLOGY Anaesthesia Pub Date : 2024-09-17 DOI:10.1111/anae.16438
Dan Wang, Fu-hai Ji, Ke Peng
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引用次数: 0

摘要

我们感谢Chen等人[1]对我们的研究[2]的关注,我们在研究中发现,无阿片类药物麻醉与含阿片类药物的异丙酚麻醉相比,可降低术后48小时内恶心和呕吐(PONV)的发生率(5% vs. 24%;几率比0.17,95%CI 0.08-0.35;需要治疗的人数5.3;P < 0.001)。Chen等人建议,恶心、反胃和呕吐发作应分别记录和分析。根据文献[3],我们将 PONV 定义为包括任何恶心、反胃或呕吐发作的综合结果。我们最近对胸腔镜肺部手术患者进行的研究也采用了这一定义[4]。很少有研究将单次恶心、反胃或呕吐作为主要结果。我们没有报告患者PONV的单次发生率;但是,在次要结果中,PONV严重程度的降低和对止吐药的需求减少表明,无阿片麻醉减轻了甲状腺和甲状旁腺手术患者的PONV。无阿片麻醉与含阿片麻醉相比,轻度、中度和重度PONV发作的发生率分别为5%对16%(p < 0.001)、1%对4%(p = 0.037)和0%对3%(p = 0.030)。在多重比较校正之前,组间差异均具有统计学意义。在合并中度和重度 PONV 类别的事后分析中,我们发现无阿片类药物组的中度至重度 PONV 发生率降低(1% 对 7%,p <0.001),即使经过多重比较校正,这一结果仍具有显著性。基于这些数据,我们不同意无阿片类药物丙泊酚麻醉仅减少了患者轻度 PONV 的说法。此外,我们还发现无阿片组患者的满意度更高。在不良反应方面,无阿片组噩梦或幻觉发生率为4%,而含阿片组为2%(几率比1.78,95%CI 0.56-5.50,p = 0.617),组间差异不显著。我们不能假设不含阿片类药物组中会有更多患者出现噩梦或幻觉。无阿片类药物组的气管拔管时间稍长(中位数为 5 分钟),而麻醉后护理病房的住院时间在两组之间不相上下。无阿片类药物组和含阿片类药物组的术中丙泊酚剂量中位数分别为740毫克和690毫克。这一差异在临床上并不明显。因此,这些结果表明,不含阿片类药物的异丙酚麻醉不会延长患者的恢复时间或增加资源利用率。根据我们的临床实践,阿片类药物全包组使用的舒芬太尼中位剂量为 40 微克(约 0.6 微克.kg-1)。这提供了足够的镇痛效果,与文献报道的剂量一致[5, 6]。
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Comparison of opioid-free and opioid-inclusive propofol anaesthesia for thyroid and parathyroid surgery: a reply

We thank Chen et al. [1] for their interest in our study [2], in which we found that opioid-free versus opioid-inclusive propofol anaesthesia reduced the incidence of postoperative nausea and vomiting (PONV) during the first 48-h postoperatively (5% vs. 24%; odds ratio 0.17, 95%CI 0.08–0.35; number needed to treat 5.3; p < 0.001). Opioid-free anaesthesia was also associated with a reduced need for rescue anti-emetics, lower incidences of hypotension and oxygen desaturation after tracheal extubation, and improved patient satisfaction.

Chen et al. suggest that nausea, retching and vomiting episodes should be documented and analysed separately. We defined PONV as a composite outcome including any episodes of nausea, retching or vomiting based on the literature [3]. This definition was also used in our recent study conducted in patients undergoing thoracoscopic lung surgery [4]. Few studies specified an individual occurrence of nausea, retching or vomiting as the primary outcome. We did not report the individual occurrences of PONV in our patients; however, among the secondary outcomes, the reduced PONV severity and need for rescue anti-emetics suggests that opioid-free anaesthesia alleviated PONV in patients undergoing thyroid and parathyroid surgery.

To assess the severity of PONV, we applied the PONV impact scale [3]. For opioid-free versus opioid-inclusive anaesthesia, the incidences of mild, moderate and severe PONV episodes were 5% versus 16% (p < 0.001), 1% versus 4% (p = 0.037) and 0% versus 3% (p = 0.030), respectively. The between-group differences were all statistically significant before multiple comparison corrections. In a post hoc analysis of combining moderate and severe PONV categories, we found a reduced incidence of moderate-to-severe PONV (1% vs. 7%, p < 0.001) in the opioid-free group, which remains significant even after correction for multiple comparison. Based on these data, we respectfully disagree that opioid-free propofol anaesthesia reduced only mild PONV in our patients. Moreover, we showed that patient satisfaction was higher in the opioid-free group. It is clinically meaningful that opioid-free anaesthesia improved patient comfort after thyroid and parathyroid surgery.

In terms of adverse effects, the incidence of nightmares or hallucination was 4% in the opioid-free group versus 2% in the opioid-inclusive group (odds ratio 1.78, 95%CI 0.56–5.50, p = 0.617), without a significant between-group difference. We cannot assume that more patients in the opioid-free group would experience nightmares or hallucinations. The tracheal extubation time was slightly longer (median 5 min) in the opioid-free group, while the duration of post-anaesthesia care unit stay was comparable between groups. The median dose of intra-operative propofol was 740 mg and 690 mg in the opioid-free group and opioid-inclusive group, respectively. This is a clinically insignificant difference. Hence, these results suggested that opioid-free propofol anaesthesia did not prolong recovery or increase resource utilisation in our patients. The median dose of sufentanil used in the opioid-inclusive group was 40 μg (approximately 0.6 μg.kg-1) as per our clinical practice. This provides sufficient analgesia and is in line with doses reported in the literature [5, 6].

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来源期刊
Anaesthesia
Anaesthesia 医学-麻醉学
CiteScore
21.20
自引率
9.30%
发文量
300
审稿时长
6 months
期刊介绍: The official journal of the Association of Anaesthetists is Anaesthesia. It is a comprehensive international publication that covers a wide range of topics. The journal focuses on general and regional anaesthesia, as well as intensive care and pain therapy. It includes original articles that have undergone peer review, covering all aspects of these fields, including research on equipment.
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