Comparison of the Preemptive/Preventive Effect of Dexmedetomidine and Ketorolac on Post-operative Pain of Appendectomy Patients: A Randomized Clinical Trial.

Q2 Medicine
Anesthesiology and Pain Medicine Pub Date : 2024-12-16 eCollection Date: 2024-12-01 DOI:10.5812/aapm-146868
Sepideh Pakniyat, Ghasem Mousavi, Hashem Jarineshin, Fereydoon Fekrat, Narjes Sabet, Alireza Abdullahzadeh-Baghaei
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Abstract

Objectives: The primary objective was to test the hypothesis that the preemptive/preventive effect of Dexmedetomidine would attenuate the post-operative pain more effectively compared to ketorolac and control groups.

Methods: This study was conducted in Shahid Mohamadi Hospital. Sixty patients undergoing appendectomy operations were randomized in 3 groups. Group A received intravenous Dexmedetomidine bolus (1 μg/kg) and infusion (0.5 μg/kg/h). Group B received slow intravenous bolus ketorolac 30 mg. Group C was the control group. Post-operatively fentanyl (5µg/mL) as patient control analgesia (PCA) was provided only on demand. The primary outcome was the Visual Analogue Scale (VAS) pain scores recorded at 1, 3, 6, 12 and 24 hours postoperatively. The secondary outcome was the 24-hour cumulative fentanyl PCA dose. Tertiary outcomes; changes in blood pressure, heart rate, body temperature, SpO2 perioperatively. Quaternary outcomes were PONV, shivering.

Results: In the Dexmedetomidine group the mean ± SD pain VAS scores 1.15 ± 1.98 and 0.95 ± 1.76 were significantly lower at 12 and 24 hours after operation (P = 0.004 and P = 0.003) compared to the other two (ketorolac and control) groups. The cumulative volume dose of fentanyl PCA 21.35 ± 11.77 mL was less in the Dexmedetomidine group compared to ketorolac (28.35 ± 9.82 mL, P = 0.629) and control (40.35 ± 12.90 mL, P = 0.003) groups.

Conclusions: Preemptive/preventive effects of Dexmedetomidine were greatest after operation compared to the ketorolac and control groups in the terms of pain scores and amount of analgesia needed postoperatively.

右美托咪定与酮咯酸对阑尾切除术患者术后疼痛的先发制人/预防效果比较:一项随机临床试验。
目的:主要目的是验证右美托咪定的先发制人/预防作用比酮罗拉酸和对照组更有效地减轻术后疼痛的假设。方法:本研究在Shahid Mohamadi医院进行。60例阑尾切除术患者随机分为3组。A组患者给予右美托咪定静脉滴注(1 μg/kg)和输液(0.5 μg/kg/h)。B组患者慢速静脉滴注酮咯酸30 mg。C组为对照组。术后芬太尼(5µg/mL)作为患者对照镇痛(PCA)仅在需要时提供。主要观察指标为术后1、3、6、12、24小时的视觉模拟评分(VAS)疼痛评分。次要终点是24小时累积芬太尼PCA剂量。三级结果;血压、心率、体温、血氧饱和度的变化。第四纪结果为PONV,发抖。结果:右美托咪定组术后12、24 h疼痛VAS平均±SD评分(1.15±1.98)和(0.95±1.76)显著低于酮洛酸组和对照组(P = 0.004和P = 0.003)。右美托咪定组芬太尼PCA累积体积剂量21.35±11.77 mL低于酮洛拉酸组(28.35±9.82 mL, P = 0.629)和对照组(40.35±12.90 mL, P = 0.003)。结论:与酮罗拉酸组和对照组相比,右美托咪定在术后疼痛评分和术后需要的镇痛量方面的先发制人/预防作用最大。
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来源期刊
Anesthesiology and Pain Medicine
Anesthesiology and Pain Medicine Medicine-Anesthesiology and Pain Medicine
CiteScore
4.60
自引率
0.00%
发文量
49
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