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经皮芬太尼贴剂用于全膝关节置换术后镇痛:一项随机双盲对照试验。

Transdermal fentanyl patch for postoperative analgesia in total knee arthroplasty: a randomized double-blind controlled trial.

机构信息

Department of Anesthesiology, Faculty of Medicine, Khon Kaen University, Khon Kaen.

Chulabhorn Hospital, Bangkok, Thailand.

出版信息

J Pain Res. 2014 Aug 1;7:449-54. doi: 10.2147/JPR.S66741. eCollection 2014.

Abstract

PURPOSE

To assess the efficacy of a transdermal fentanyl patch (TFP) (50 μg/hour) applied 10-12 hours before surgery versus placebo for postoperative pain control of total knee arthroplasty (TKA).

MATERIALS AND METHODS

We enrolled 40 patients undergoing elective TKA under spinal anesthesia using isobaric or hyperbaric bupivacaine. Subjects were randomized to receive a TFP (Duragesic(®) 50 μg/hour) or placebo patch applied with a self-adhesive to the anterior chest wall 10-12 hours before spinal anesthesia. Every patient was given patient-controlled morphine for postoperative pain control. Patients were evaluated every 4 hours until 48 hours.

RESULTS

Morphine consumption at 24 and 48 hours in the TFP group versus the placebo group was 15.40±12.65 and 24.90±20.11 mg versus 33.60±19.06 and 57.80±12.65 mg (P≤0.001). Numeric rating scale scores at rest and during movement over 48 hours were lower in the TFP group. Ambulation and nausea/vomiting scores were statistically greater, but not clinically significant in the TFP group. Sedation scores were low and not statistically significantly different between groups. There was no severe respiratory depression.

CONCLUSION

TFP (50 μg/hour) applied 10-12 hours before surgery can effectively and safely decrease morphine consumption and pain scores during the first 48 hours after TKA surgery.

摘要

目的

评估术前 10-12 小时应用透皮芬太尼贴剂(TFP)(50μg/小时)与安慰剂相比,用于全膝关节置换术(TKA)术后疼痛控制的疗效。

材料和方法

我们纳入了 40 例在等比重或重比重布比卡因脊麻下择期行 TKA 的患者。受试者随机接受 TFP(Duragesic®50μg/小时)或安慰剂贴剂,在脊麻前 10-12 小时用自粘剂贴在前胸壁上。每位患者均给予患者自控吗啡用于术后疼痛控制。患者在 48 小时内每 4 小时评估一次。

结果

TFP 组与安慰剂组在 24 小时和 48 小时时的吗啡消耗量分别为 15.40±12.65 和 24.90±20.11mg 与 33.60±19.06 和 57.80±12.65mg(P≤0.001)。TFP 组在 48 小时内静息和运动时的数字评分量表评分均较低。TFP 组的活动和恶心/呕吐评分更高,但无统计学意义。镇静评分较低,两组间无统计学差异。无严重呼吸抑制。

结论

术前 10-12 小时应用 TFP(50μg/小时)可有效、安全地减少 TKA 术后前 48 小时内吗啡消耗量和疼痛评分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a56/4128837/2fe5dd62403d/jpr-7-449Fig1.jpg

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