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随机对照试验:甲状腺切除术后阿片类药物与非阿片类药物镇痛的比较。

Randomized control trial of opioid- versus nonopioid-based analgesia after thyroidectomy.

机构信息

Department of Surgery, MedStar Georgetown University/Washington Hospital Center, Washington, DC.

Department of Anesthesiology, MedStar Washington Hospital Center, Washington, DC.

出版信息

Surgery. 2020 Jun;167(6):957-961. doi: 10.1016/j.surg.2020.01.011. Epub 2020 Feb 29.

Abstract

BACKGROUND

Opioid-based analgesia is the most common method for pain control in the postoperative period. Limited data exist to compare the adequacy of pain control in the post thyroidectomy period with nonopioid-based analgesia. We aimed to evaluate the efficacy of nonopioid-based, postoperative analgesia.

METHODS

After institutional review board approval, patients were randomized to 1 of 2 pain control regimens. Sample size was calculated to assess for a pain score difference of 1 based on a visual analog scale. The control group received opioid-based, postoperative analgesia, whereas the study group received nonopioid-based analgesia of acetaminophen and ibuprofen. Pain scores (measured on visual analog scale) and opioid use (converted to morphine equivalent dose) were measured after completion of the operation.

RESULTS

The sample sizes for the study and control groups were 49 and 46 patients, respectively. The pain score for the study and control groups 1 hour after the operation (3.3 vs 3.9, P = .35), 6 hours after the operation (2.8 vs 3.0, P = .08), on postoperative day 1 (1.6 vs 2.4, P = .08) and on the first office visit (0.2 vs 0.1, P = .82) did not have a statistically significant difference. Morphine equivalent opioid requirement for pain control in the postoperative period was 0.8 vs 6.9 mg (P < .01), respectively.

CONCLUSION

In a randomized control trial, we showed that patients treated with nonopioid analgesia had similar pain scores to those treated with opioids, with the benefit of having lower opioid exposure in the perioperative period.

摘要

背景

阿片类药物镇痛是术后控制疼痛最常用的方法。目前仅有有限的数据可用于比较术后甲状腺切除术期间非阿片类药物镇痛的疼痛控制效果。我们旨在评估非阿片类药物术后镇痛的效果。

方法

在获得机构审查委员会批准后,患者被随机分为 2 种疼痛控制方案组之一。根据视觉模拟量表评估疼痛评分差异 1 分的需要,计算了样本量。对照组接受阿片类药物术后镇痛,而研究组接受对乙酰氨基酚和布洛芬的非阿片类药物镇痛。术后测量疼痛评分(用视觉模拟量表测量)和阿片类药物使用量(换算为吗啡等效剂量)。

结果

研究组和对照组的样本量分别为 49 例和 46 例。术后 1 小时,研究组和对照组的疼痛评分分别为 3.3 分和 3.9 分(P =.35);术后 6 小时,分别为 2.8 分和 3.0 分(P =.08);术后第 1 天,分别为 1.6 分和 2.4 分(P =.08);首次就诊时,分别为 0.2 分和 0.1 分(P =.82),差异均无统计学意义。术后疼痛控制所需吗啡等效阿片类药物用量分别为 0.8 mg 和 6.9 mg(P <.01)。

结论

在一项随机对照试验中,我们发现接受非阿片类药物镇痛治疗的患者疼痛评分与接受阿片类药物治疗的患者相似,而在围手术期的阿片类药物暴露量较低。

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