Comparing the effect of local injection of combined morphine, triamcinolone and lidocaine and lidocaine injection on pain intensity after mastoidectomy-tympanoplasty; a triple-blind clinical trial

IF 1.1 Q4 IMMUNOLOGY Immunopathologia Persa Pub Date : 2023-08-11 DOI:10.34172/ipp.2023.39525
R. Talakoub, Gholamreza Khalili, Hoda Sadat Rohani
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Abstract

Introduction: Postoperative pain control is one of the patient’s rights and the challenges of surgeons and anesthesiologists since about 20% of patients experience severe pain in the first 24 hours after surgery. Mastoidectomy and tympanoplasty are common surgeries in the head and neck area, in which profound and long-term analgesia is essential. Objectives: The present study investigated the effect of the combination of topical morphine, triamcinolone, and lidocaine compared to the control group. Patients and Methods: In the current clinical trial, 68 patients’ candidates for mastoidectomy-tympanoplasty surgery were included and randomly divided into intervention and control groups. The variables of demographic, pain, hemodynamics, extubation time, and received opioids were measured. Results: The results of the current study indicated a significant reduction in the patient’s pain scores in both groups (P=0.001), while the patients of group 1 had significantly lower pain scores than group 2 after 8, 12, and 24 hours in the ward (P<0.05). Moreover, a significant reduction was observed in systolic blood pressure (SBP), diastolic blood pressure (DBP), and mean arterial pressure (MAP) in all patients during surgery (P<0.001). However, in patients who received morphine, triamcinolone, and lidocaine (group 1), SBP and MAP were significantly lower than group 2 after 40, 80, 100, 120, 140, and 160 minutes during surgery (P<0.05). Conclusion: The present study indicated that the combination of morphine, triamcinolone, and lidocaine compared to the control group could lead to better pain control, further reduction of SBP and MAP, reduction of post-operative opioid use, and delay during the first opioid administration. Trial Registration: The trial protocol was approved by the Iranian Registry of Clinical Trials (identifier: IRCT20200825048515N39; https://irct.ir/trial/57931, ethical code; IR.MUI.MED.REC.1400.064).
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比较局部注射吗啡、曲安奈德、利多卡因与利多卡因注射对乳突切除-鼓室成形术后疼痛强度的影响;一项三盲临床试验
引言:术后疼痛控制是患者的权利之一,也是外科医生和麻醉师的挑战,因为大约20%的患者在术后的前24小时内会出现剧烈疼痛。乳突切除术和鼓室成形术是头颈部常见的手术,其中深度和长期的镇痛至关重要。目的:与对照组相比,本研究调查了局部吗啡、曲安奈德和利多卡因联合使用的效果。患者和方法:在目前的临床试验中,68名乳突切除术鼓室成形术患者被纳入,并随机分为干预组和对照组。测量人口统计学、疼痛、血液动力学、拔管时间和接受阿片类药物的变量。结果:目前的研究结果表明,两组患者的疼痛评分均显著降低(P=0.001),而第1组患者在病房8、12和24小时后的疼痛评分显著低于第2组(P<0.05)。此外,观察到收缩压(SBP)、舒张压(DBP),和平均动脉压(MAP)(P<0.001)。然而,在接受吗啡、曲安奈德和利多卡因治疗的患者(1组)中,术中40、80、100、120、140和160分钟后,SBP和MAP显著低于2组(P<0.05),与对照组相比,利多卡因可以更好地控制疼痛,进一步降低SBP和MAP,减少术后阿片类药物的使用,并延迟首次阿片类药给药。试验注册:试验方案由伊朗临床试验注册处批准(标识符:IRCT20200825048515N39;https://irct.ir/trial/57931,道德规范;IR.MUI.MED.REC.1400.064)。
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来源期刊
CiteScore
1.70
自引率
0.00%
发文量
65
审稿时长
3 weeks
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