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首页> 外文期刊>British journal of anaesthesia >Effect of dexamethasone in combination with caudal analgesia on postoperative pain control in day-case paediatric orchiopexy.
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Effect of dexamethasone in combination with caudal analgesia on postoperative pain control in day-case paediatric orchiopexy.

机译:地塞米松联合尾巴镇痛对日间儿科睾丸手术患者术后疼痛控制的作用。

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BACKGROUND: Dexamethasone has a powerful anti-inflammatory action and has demonstrated reduced morbidity after surgery. The aim of this study was to examine the effects of a single i.v. dose of dexamethasone in combination with caudal block on postoperative analgesia in children. METHODS: Seventy-seven children (aged 1-5 yr) undergoing day-case orchiopexy were included in this prospective, randomized, double-blinded study at a single university hospital. After inhalation induction of general anaesthesia, children received either dexamethasone 0.5 mg kg(-1) (maximum 10 mg) (n=39) or the same volume of saline (n=38) i.v. A caudal anaesthetic block was then performed using 1.5 ml kg(-1) of ropivacaine 0.15% in all patients. After surgery, rescue analgesic consumption, pain scores, and adverse effects were evaluated for 24 h. RESULTS: Significantly, fewer patients in the dexamethasone group required fentanyl for rescue analgesia (7.9% vs 38.5%) in the post-anaesthetic care unit or acetaminophen (23.7% vs 64.1%) after discharge compared with the control group. The time to first administration of oral acetaminophen was significantly longer in the dexamethasone group (646 vs 430 min). Postoperative pain scores were lower in the dexamethasone group and the incidence of adverse effects was similar in both groups. CONCLUSIONS: Intravenous dexamethasone 0.5 mg kg(-1) in combination with a caudal block augmented the intensity and duration of postoperative analgesia without adverse effects in children undergoing day-case paediatric orchiopexy. Trial registration: ClinicalTrials.gov. The number of registration: NCT01041378.
机译:背景:地塞米松具有强大的抗炎作用,并已显示出术后降低的发病率。这项研究的目的是检查单个i.v.剂量地塞米松联合尾巴阻滞对儿童术后镇痛的作用。方法:在一家大学医院的这项前瞻性,随机,双盲研究中纳入了接受日间矫正手术的77名儿童(1-5岁)。吸入全麻后,儿童接受静脉注射地塞米松0.5 mg kg(-1)(最大10 mg)(n = 39)或等量生理盐水(n = 38)。然后在所有患者中使用1.5 ml kg(-1)罗哌卡因0.15%进行尾巴麻醉阻滞。手术后,评估24小时的急救镇痛剂消耗量,疼痛评分和不良反应。结果:与对照组相比,在麻醉后护理单位或对乙酰氨基酚出院后,地塞米松组需要芬太尼进行抢救镇痛的患者较少(7.9%vs 38.5%)(23.7%vs 64.1%)。地塞米松组首次口服对乙酰氨基酚的时间明显更长(646比430分钟)。地塞米松组术后疼痛评分较低,两组的不良反应发生率相似。结论:静脉地塞米松0.5 mg kg(-1)与尾巴阻滞相结合可增加术后镇痛的强度和持续时间,而对患日间儿科睾丸手术的儿童无不良影响。试用注册:ClinicalTrials.gov。注册号:NCT01041378。

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