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腹腔镜疝修补术患者的预防性疼痛控制:酮咯酸与布洛芬的比较

Preemptive pain control in patients having laparoscopic hernia repair: a comparison of ketorolac and ibuprofen.

作者信息

Mixter C G, Meeker L D, Gavin T J

机构信息

Department of Surgery, Exeter Hospital, NH, USA.

出版信息

Arch Surg. 1998 Apr;133(4):432-7. doi: 10.1001/archsurg.133.4.432.

Abstract

OBJECTIVES

To determine if nonsteroidal anti-inflammatory drugs provide adequate pain control for patients having laparoscopic hernia repair and to compare the effectiveness of ketorolac tromethamine with ibuprofen in reducing postoperative laparoscopic hernia pain.

DESIGN AND SETTING

Prospective double-blind randomized study at a 100-bed community hospital.

PATIENTS

Seventy patients ranging in age from 16 to 83 years scheduled for elective laparoscopic inguinal hernia repair.

INTERVENTIONS

Patients undergoing laparoscopic hernia repair were enrolled in a double-blind randomized study to compare the 2 treatments. Group 1 received a placebo capsule 1 hour before surgery and ketorolac tromethamine, 60 mg intravenously, at the time of trocar insertion. Group 2 received ibuprofen, 800 mg an hour before surgery, and isotonic sodium chloride solution, 2 mL intravenously, at the time of trocar insertion. In addition, all patients received local infiltration of 30 mL of bupivacaine hydrochloride into their trocar sites. All patients were discharged within 5 hours of the operation and were instructed to take 400 mg of ibuprofen orally every 4 hours for 24 hours whether or not they were experiencing pain. A 24-hour supply of ibuprofen was provided to all study patients. Pain was assessed using the Visual Analog Pain Scale with a maximum pain rating of 100. Assessments were done at the time of and 18 hours after discharge.

MAIN OUTCOME MEASURE

Postoperative pain 18 and 24 hours after discharge was assessed using a standardized questionnaire in a telephone interview by a registered nurse from the Outpatient Surgical Unit.

RESULTS

There was no significant difference in the level of pain experienced by 35 patients who received ketorolac intravenously and 35 who received ibuprofen orally. There was no significant difference between the 2 treatment groups in the amount of pain experienced at discharge and 18 hours after discharge.

CONCLUSIONS

Pain relief from ibuprofen, 800 mg, administered orally an hour before laparoscopic hernia repair was not statistically different from that obtained with intravenous ketorolac, 60 mg, administered intraoperatively when comparing the hospital discharge pain score and the mean and highest pain scores 18 hours after discharge. Ibuprofen offers equivalent pain control at a lower cost and reduced potential for adverse drug events compared with intravenous ketorolac in patients having laparoscopic hernia repair. No patient required narcotic supplementation, and pain control was judged satisfactory by all the patients.

摘要

目的

确定非甾体抗炎药是否能为接受腹腔镜疝修补术的患者提供充分的疼痛控制,并比较酮咯酸氨丁三醇与布洛芬在减轻腹腔镜疝修补术后疼痛方面的效果。

设计与地点

在一家拥有100张床位的社区医院进行的前瞻性双盲随机研究。

患者

70例年龄在16至83岁之间计划接受择期腹腔镜腹股沟疝修补术的患者。

干预措施

接受腹腔镜疝修补术的患者参与一项双盲随机研究以比较两种治疗方法。第1组在手术前1小时服用一粒安慰剂胶囊,并在插入套管针时静脉注射60毫克酮咯酸氨丁三醇。第2组在手术前1小时服用800毫克布洛芬,并在插入套管针时静脉注射2毫升等渗氯化钠溶液。此外,所有患者在其套管针穿刺部位接受30毫升盐酸布比卡因的局部浸润。所有患者在手术后5小时内出院,并被指示无论是否疼痛,均每4小时口服400毫克布洛芬,共服用24小时。为所有研究患者提供了24小时剂量的布洛芬。使用视觉模拟疼痛量表评估疼痛,最高疼痛评分为100分。在出院时和出院后18小时进行评估。

主要观察指标

门诊手术科室的注册护士通过电话访谈,使用标准化问卷评估出院后18小时和24小时的术后疼痛情况。

结果

35例静脉注射酮咯酸的患者和35例口服布洛芬的患者所经历的疼痛程度没有显著差异。两个治疗组在出院时和出院后18小时所经历的疼痛量没有显著差异。

结论

在比较出院时的疼痛评分以及出院后18小时的平均疼痛评分和最高疼痛评分时,腹腔镜疝修补术前1小时口服800毫克布洛芬的止痛效果与术中静脉注射60毫克酮咯酸氨丁三醇的效果在统计学上没有差异。与静脉注射酮咯酸氨丁三醇相比,布洛芬在接受腹腔镜疝修补术的患者中能提供同等的疼痛控制,且成本更低,药物不良事件的可能性更小。没有患者需要补充麻醉剂,所有患者对疼痛控制的评价均为满意。

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