氯胺酮和褪黑素预防结直肠癌术后谵妄的可行性研究。

IF 2.1 3区 医学 Q2 ANESTHESIOLOGY
Kousha Farhadi, Mojgan Rahimi, Hesam Varpaei, Erta Rajabi, Seyyed Mohammad Mahdi Tayebi Tafreshi, Parsa Mohammadi, Mostafa Mohammadi
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引用次数: 0

摘要

目的:探讨术前5 mg褪黑素和术中50 mg氯胺酮预防结直肠癌手术候选者术后谵妄(POD)的可行性及效果。方法:在这项随机对照试验中,研究对象为选择结肠直肠癌手术的成人(bb0 - 18岁)。患者被随机分为四组:安慰剂/生理盐水(PS)、褪黑素/生理盐水(MS)、安慰剂/氯胺酮(PK)和褪黑素/氯胺酮(MK)。各组在手术前一晚口服褪黑素5mg或安慰剂,麻醉诱导后服用氯胺酮50mg或生理盐水。分别采用重症监护病房(CAM-ICU)混淆评定法和视觉模拟评分法(VAS)评估POD的发生、严重程度和疼痛程度(每日2次),直至术后第4天。结果:共入组104例,男性占51%,平均年龄56.29±12.65岁,平均每周4.7例,损耗率13.3%。PS组、MS组、MK组、PK组POD患病率分别为17.3%、22.23%、16.67%、16.67%。与对照组相比,所有干预措施均未显著降低POD发生的可能性。结论:这项随机对照试验证明了招募和保留手术患者进行多臂围手术期干预研究的可行性。虽然这些干预措施并没有显著降低POD的发病率,但研究设计和程序是可行的,招募率和损耗率都是可以接受的。与安慰剂相比,没有一种干预措施显著降低POD的发病率;然而,时间是一个重要因素,POD的发病率、严重程度和疼痛呈纵向下降趋势。试验注册号:IR.TUMS.IKHC.REC.1401.374,注册日期:2023年2月14日;IRCT代码:IRCT20120527009886N2,注册日期:07/03/2023。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ketamine and melatonin for the prevention of postoperative delirium in patients with colorectal cancer: a feasibility study.

Ketamine and melatonin for the prevention of postoperative delirium in patients with colorectal cancer: a feasibility study.

Ketamine and melatonin for the prevention of postoperative delirium in patients with colorectal cancer: a feasibility study.

Purpose: This study aimed to examine the feasibility and effects of preoperative 5 mg of melatonin and intraoperative 50 mg of ketamine on postoperative delirium (POD) prevention in candidates for colorectal cancer surgery.

Methods: In this randomized controlled trial, adults (> 18 years) who were candidates for elective colorectal cancer surgery were included in the study. Patients were randomized into four groups: placebo/saline (PS), melatonin/saline (MS), placebo/ketamine (PK), and melatonin/ketamine (MK). The groups received either 5 mg of oral melatonin or a placebo the night before surgery and 50 mg of ketamine or normal saline after anesthesia induction. The occurrence and severity of POD and pain severity were assessed via the confusion assessment method for the intensive care unit (CAM-ICU) and visual analogue scale (VAS), respectively (twice daily), until postoperative day 4.

Results: One-hundred and four patients (51% male, mean age: 56.29 ± 12.65) with a rate of 4.7 patients per week were recruited, with an attrition rate of 13.3%. The prevalence of POD was 17.3%, 22.23%, 16.67%, and 16.67% in the PS group, the MS group, the MK group, and the PK group, respectively. Compared with the control, none of the interventions significantly reduced the likelihood of POD occurrence.

Conclusion: This randomized controlled trial demonstrated the feasibility of recruiting and retaining surgical patients for a multi-arm perioperative intervention study. Although the interventions did not significantly reduce the incidence of POD, the study design and procedures were feasible, with acceptable recruitment and attrition rates. Compared to placebo, none of the interventions significantly reduced the incidence of POD; however, time was a significant factor, with POD incidence, severity, and pain decreasing longitudinally.

Trial regsitration: IR.TUMS.IKHC.REC.1401.374, registration date: 14 February 2023 and IRCT code: IRCT20120527009886N2, registration date: 07/03/2023.

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