静脉注射对乙酰氨基酚/布洛芬固定剂量组合对视频辅助胸腔手术后阿片类药物消耗量和疼痛的影响:双盲随机对照试验

Ho-Jin Lee, Seungeun Choi, Soohyuk Yoon, Susie Yoon, Jae-Hyon Bahk
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引用次数: 0

摘要

背景视频辅助胸腔镜手术(VATS)通常会引起明显的术后疼痛,可能导致慢性疼痛和生活质量下降。本研究旨在评估对乙酰氨基酚/布洛芬联合用药在减少 VATS 患者镇痛需求和疼痛强度方面的效果。研究设计这是一项双盲随机对照试验。方法对计划接受择期 VATS 肺切除术的成人患者进行随机分组,分别接受静脉注射对乙酰氨基酚和布洛芬(干预组)或 100 mL 生理盐水(对照组)。治疗在麻醉诱导后进行,每 6 小时一次,共三个周期。主要结果是术后 24 小时的镇痛药总用量。次要结果是 2 小时和 48 小时的累计镇痛剂消耗量;2、24 和 48 小时的镇痛剂相关副作用;术后 24 小时和 48 小时的恢复质量;休息时和咳嗽时的疼痛强度;以及抢救性镇痛剂的使用。术后 3 个月通过电话访谈对慢性术后疼痛(CPSP)进行评估。干预组在术后 24 小时和 48 小时的镇痛剂用量明显降低(24 小时:中位数差异为 100 µg 当量静脉注射芬太尼,48 小时:中位数差异为 100 µg 当量静脉注射芬太尼):- 100 μg 当量静脉注射芬太尼[95% 置信区间 (CI) - 200 至 - 5 μg],P = 0.037;48 h:中位数差异:140 μg [95% CI],P = 0.037:- 140 μg [95% CI - 320 至 - 20 μg],P = 0.035)。与对照组相比,干预组在术后 24 小时的恢复质量明显较低,而在术后 48 小时则无明显差异。干预组在术后 48 小时除咳嗽外的所有疼痛评分均明显低于对照组。结论术前服用对乙酰氨基酚/布洛芬可明显减少 VATS 患者的镇痛需求,提供了一种有效的术后疼痛管理策略,并有可能最大限度地减少对强效镇痛药的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of an intravenous acetaminophen/ibuprofen fixed-dose combination on postoperative opioid consumption and pain after video-assisted thoracic surgery: a double-blind randomized controlled trial

Effect of an intravenous acetaminophen/ibuprofen fixed-dose combination on postoperative opioid consumption and pain after video-assisted thoracic surgery: a double-blind randomized controlled trial

Background

Video-assisted thoracoscopic surgery (VATS) often induces significant postoperative pain, potentially leading to chronic pain and decreased quality of life. This study aimed to evaluate the acetaminophen/ibuprofen combination effectiveness in reducing analgesic requirements and pain intensity in patients undergoing VATS.

Study design

This is a double-blinded randomized controlled trial.

Methods

Adult patients scheduled for elective VATS for lung resection were randomized to receive either intravenous acetaminophen and ibuprofen (intervention group) or 100 mL normal saline (control group). Treatments were administered post-anesthesia induction and every 6 h for three cycles. The primary outcome was total analgesic consumption at 24 h postoperatively. Secondary outcomes were cumulative analgesic consumption at 2 and 48 h; analgesic-related side effects at 2, 24, and 48 h; quality of recovery at 24 h and 48 h postoperatively; pain intensity at rest and during coughing; and rescue analgesics use. Chronic postsurgical pain (CPSP) was assessed through telephone interviews 3 months postoperatively.

Results

The study included 96 participants. The intervention group showed significantly lower analgesic consumption at 24 h and 48 h postoperatively (24 h: median difference: − 100 µg equivalent intravenous fentanyl [95% confidence interval (CI) − 200 to − 5 μg], P = 0.037; 48 h: median difference: − 140 μg [95% CI − 320 to − 20 μg], P = 0.035). Compared to the controls, the intervention group exhibited a significantly lower quality of recovery 24 h post-surgery, with no significant difference at 48 h. All pain scores except for coughing at 48 h post-surgery were significantly lower in the intervention group compared to the controls. No significant differences were observed between the groups in postoperative nausea and vomiting occurrence, hospital stay length, and CPSP.

Conclusion

Perioperative administration of acetaminophen/ibuprofen significantly decreased analgesic needs in patients undergoing VATS, providing an effective postoperative pain management strategy, and potentially minimizing the need for stronger analgesics.

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