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Efficacy of dexamethasone on postoperative analgesiain children undergoing hypospadias repair

机译:地塞米松对尿道下裂修复患儿术后镇痛的疗效

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Background and Objective: Management of post operative pain in children undergoing hypospadiasis repair, accounts for optimized surgery outcomes and improved patients’ satisfaction. Thus, various studies have widely investigated the best approaches for the pain management. In this study our aim was to determine the effect of dexamethasone in combination with penile nerve block on the postoperative pain and complications in the children undergoing hypospadias surgery.Methods: In this randomized double-blind placebo controlled trial, after obtaining informed consent from parents or legal guardians, 42 children undergoing surgical treatment of hypospadias were randomized in two groups to receive either IV dexamethasone 0.5 mg/kg (n=23) or placebo (normal saline) (n=19) during the operation. Penile block was performed in both groups using Bupivacaine 0.5% (1mg/kg) at the end of the procedure. By the end of the operation, FLACC (Face, Leg, Activity, Cry, Consolability) pain score was assessed as the primary outcome of the study. Secondary outcomes includes timing and episodes of rescue medication consumption, post operative nausea omiting and bleeding. All the outcomes were assessed in the recovery room and after 2, 6, 12, and 24 hours.Results: The median of FLACC pain scores at the recovery room and 2, 6, 12, and 24 hours post operation was 2, 1, 1, 1, and 2 for the dexamethasone group and 8, 8, 7, 7, and 8 for the placebo group respectively.This were significantly different (P<0.000). The median time of first rescue medication consumption was 8 hours post operation for the dexamethasone group and three hours for the placebo group which was significantly different (z= 4.57, p<0.000). The maximum episode of post operative rescue medication consumption in dexamethasone group was 4 episodes in only one patient and the minimum was one episode in 11 patients. In comparison numbers in placebo group were five episodes in seven patients and three episodes in four patients. The result indicated that there was statistically significant difference between two groups in terms of episodes of rescue medication consumption (Chi2= 31.4, p<0.000).Conclusion: Single dose of intravenous dexamethasone (0.5 mg/kg) in combination with penile block decreased the post operative pain measures, and total post operative analgesic requirement. It also increased the onset of the first analgesic requirement compared to penile block alone.doi: http://dx.doi.org/10.12669/pjms.321.9089How to cite this:Shirazi M, Mahmoudi H, Nasihatkon B, Ghaffaripour S, Eslahi A. Efficacy of dexamethasone on postoperative analgesia in children undergoing hypospadias repair. Pak J Med Sci. 2016;32(1):125-129. doi: http://dx.doi.org/10.12669/pjms.321.9089This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
机译:背景与目的:对尿道下裂修复术患儿的术后疼痛进行管理,可以优化手术效果并提高患者满意度。因此,各种研究已广泛研究了疼痛治疗的最佳方法。在这项研究中,我们的目的是确定地塞米松联合阴茎神经阻滞对尿道下裂手术患儿术后疼痛和并发症的影响。方法:在这项随机双盲安慰剂对照试验中,在获得父母或患者的知情同意后法定监护人将接受尿道下裂手术治疗的42例儿童随机分为两组,分别在手术期间接受0.5 mg / kg的地塞米松静脉注射(n = 23)或安慰剂(生理盐水)(n = 19)。在手术结束时,两组均使用0.5%布比卡因(1mg / kg)进行阴茎阻滞。手术结束时,FLACC(面部,腿部,活动,哭泣,可安慰性)疼痛评分被评估为研究的主要结果。次要结果包括抢救性药物消耗的时间和发作,术后恶心,呕吐和出血。所有结果均在恢复室以及2、6、12和24小时后进行评估。结果:恢复室以及术后2、6、12和24小时的FLACC疼痛评分中位数为2、1,地塞米松组分别为1、1、2和8、8、7、7和8为安慰剂组,差异有统计学意义(P <0.000)。地塞米松组首次服用急救药物的中位时间为术后8小时,安慰剂组为3小时,这有显着差异(z = 4.57,p <0.000)。地塞米松组术后抢救性用药的最大发作只有4例,最小发作为11例。相比之下,安慰剂组中有7名患者发生5次发作,而4名患者发生3次发作。结果表明,两组的抢救用药次数差异有统计学意义(Chi2 = 31.4,p <0.000)。结论:静脉地塞米松单剂量(0.5 mg / kg)与阴茎阻滞剂合用可降低两组之间的差异。术后疼痛措施以及术后总镇痛要求。与单独使用阴茎阻滞相比,它也增加了首次镇痛的需要。doi:http://dx.doi.org/10.12669/pjms.321.9089如何引用此信息:Shirazi M,Mahmoudi H,Nasihatkon B,Ghaffaripour S, Eslahi A.地塞米松对尿道下裂修复患儿术后镇痛的疗效。朴J医学。 2016; 32(1):125-129。 doi:http://dx.doi.org/10.12669/pjms.321.9089,这是根据知识共享署名许可(http://creativecommons.org/licenses/by/3.0)条款发布的开放获取文章,只要适当引用了原始作品,便可以在任何介质中不受限制地使用,分发和复制。

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