国际麻醉学与复苏杂志   2011, Issue (4): 10-10
    
帕瑞昔布钠对脊柱融合术后镇痛效果及肾功能的影响:一项前瞻、单盲、随机、安慰剂对照临床研究
徐惠杰, 邱晓东, 景亮1()
1.东南大学附属中大医院麻醉科
Effects of parecoxib sodium on postoperative analgesia and renal function after Spinal Fusion Surgery: a randomized controlled single-blind clinical trial
 全文:
摘要:

目的 观察帕瑞昔布钠对脊柱融合术病人术后镇痛效果及肾功能的影响。 方法 择期行脊柱融合手术患者60例,ASA Ⅰ~Ⅱ级,年龄20-60岁,随机分为三组,每组20例。A组(帕瑞昔布Ⅰ组)麻醉诱导时静脉注射帕瑞昔布钠40mg;B组(帕瑞昔布Ⅱ组)手术结束前10min静脉注射帕瑞昔布钠40mg;C组(对照组)诱导和手术结束前10min给予等容量生理盐水静脉注射。所有病人术后接受自控吗啡静脉镇痛。记录术后2h,4h,6h,12h,24h,48h的VAS评分及阿片类相关副反应。观察术中出血量及监测术后次日肾功能。 结果 1)拔管后5min及术后2h静息及咳嗽状态下的VAS评分,A组明显低于B、C两组(P<0.05),但B组与C组之间没有统计学意义差异。术后4h至48h时点内,三组病人之间的VSA评分均无明显差异。2)术后2h至12h内A、B两组的吗啡累计消耗量较之C组明显降低(P < 0.05)。3)术后24h、48h时点A组吗啡累计消耗量较之B、C组明显减少(P < 0.05),但B、C组之间没有统计学意义差异。4)术后首次给予镇痛药物的时间A组较B、C组明显延长(P < 0.05),但B、C组组间比较没有统计学意义差异。术后镇痛满意度A、B两组明显优于C组。5)三组病人术中出血量及术后肾功能检测也无明显改变。 6)术后48h内,A、B两组与C组相比,阿片类相关副作用显著降低(P < 0.05)。 结论 麻醉诱导前和手术结束时给予帕瑞昔布钠40mg明显减少了术后吗啡的用量和相关副反应,对肾功能无影响。麻醉诱导前使用帕瑞昔布较之手术结束时使用似乎有更好的治疗效果。

关键词: 帕瑞昔布钠 ;脊柱融合术;术后镇痛;超前镇痛;肾功能安全性
Abstract:

【Abstract】 Objective To observe the effects of parecoxib sodium on the post-operative pain relief elective decompressive lumbar laminectomy with posterior spinal fusion were randomly divided into three groups following intravenous administration of dosing schedule: Group A ( parecoxib I ) parecoxib 40 mg was injected during anesthesia induction; Group B (parecoxib II) parecoxib 40 mg was injected 10 min before the completion of sugrey; Group C ( placebo) the isochoric 0.9% physiological saline were injected either at anesthesia induction or 10 min before the completion of sugrey. All patients received the patient -controlled intravenous analgesia with morphine after surgery. The scores of visual analog scale (VAS), the total morphine consumption, and the opioid-related symptom distress were recorded at 2hr ,4hr ,6hr ,12hr ,24hr and 48hr after surgery. The red cell loss rate and the renal function in perioperative were measured, respectively. Results 1) The VAS scores of resting and coughing in group A significantly less than the group B and C at 5 minutes post-extubation and 2 hr after surgery (p<0.05), but it dose not show differences among the group B and C. The VAS scores were no statistically significance among three groups from 24hr to 48hr after surgery. 2)The total morphine consumption at 2hr,4hr,6hr,12hr were significantly reduced in the A and B groups compared with the control group (P < 0.05) .3)The total morphine consumption at 24hr and 48hr in the group A was significantly less than those in the B and C groups ( P < 0.05), but no statistically differences among the B and C groups . 4)The delay for first analgesic demand was increased obviously in the group A compared to the B and C groups (P < 0.05),but no statistically significance between the B and C groups. Satisfaction with postoperative analgesia A and B groups were significantly better than the C group. 5)The red cell loss rate and the renal function in perioperative were no significant differences among the three groups. 6) The opioid-related symptom distress associated with opioid therapy were less in group A and B more than those in group C within 48hr after surgery. Conclusions Intravenous administration of the parecoxib sodium 40mg either at anesthesia induction or 10 min before the completion of surgery significantly decreased morphine consumption and side effects associated with opioid therapy, and did not affect the renal function compared with the control group. Administration of the parecoxib sodium at anesthesia induction rather than the completion of surgery showed more beneficial therapeutic effects on the patients with spinal fusion surgery.

Key words: parecoxib sodium;Spinal Fusion;postoperative analgesia ;