国际麻醉学与复苏杂志   2017, Issue (9): 0-0
    
右美托咪啶复合羟考酮用于脊椎手术后静脉镇痛的临床效果
汪涛, 王茹, 王勤, 周巧林, 季小青, 石教辉1()
1.江苏省沭阳县人民医院麻醉科
Efficacy of dexmedetomidine combined with oxycodone for patient-controlled intravenous analgesia for post spine surgery
 全文:
摘要:

目的 评价右美托咪定复合羟考酮用于脊柱手术后病人自控静脉镇痛的临床效果。方法 择期全麻下行脊柱外科手术患者100例,年龄29~63岁,ASA分级Ⅰ或Ⅱ级,体重49~77kg,性别不限,采用随机数字表法分为四组(n=20):羟考酮组(O组)、羟考酮1.0mg•kg+右美托咪定2.5μg•kg组(OD1组)、羟考酮0.8mg•kg+右美托咪定2.5μg•kg组(OD2组)和羟考酮0.6mg•kg+右美托咪定2.5μg•kg组(OD3组),各组均用生理盐水稀释至200ml。手术结束前15 min,静脉注射羟考酮0.1 mg•kg,同时连接自控静脉镇痛泵,背景输注速率3.5~4.5ml/h,PCA剂量2ml,锁定时间20min。采用静脉注射羟考酮0.05mg•kg进行补救镇痛,维持VAS评分≤4分。记录术后48 h内补救镇痛情况,PCA有效按压次数、心动过缓、低血压、恶心、呕吐、镇静过度、嗜睡、皮肤瘙痒、呼吸抑制等不良反应的发生情况;记录术后72 h时病人镇痛满意度。结果 四组均未行补救镇痛,均未见镇静过度、呕吐、呼吸抑制和低血压发生。与O组比较,OD1组嗜睡发生率升高,OD2组和OD3组恶心、嗜睡、心动过缓和皮肤瘙痒发生率降低,三组病人术后镇痛满意度升高(P<0.05);与OD1组比较,OD2组和OD3组恶心、嗜睡、心动过缓和皮肤瘙痒发生率降低,OD2组病人术后镇痛满意度显著升高(P<0.05),D3组病人术后镇痛满意度降低(P<0.05);与OD2组比较,OD3组不良反应发生率无统计学意义(P>0.05),OD3组病人术后镇痛满意度降低(P<0.05);与O组、OD1组和OD2组比较,OD3组PCA有效按压次数显著增加(P<0.01)。结论 右美托咪定2.5μg•kg复合合羟考酮0.8 mg•kg用于脊柱术后静脉镇痛效果确切,可减少羟考酮的用量和降低其不良反应的发生率,且患者对术后镇痛的总体满意度高。

关键词: 羟考酮;右美托咪啶;镇痛;病人控制;手术后
Abstract:

Objective To evaluate the efficacy of dexmedetomidine combined with oxycodone for patient-controlled intravenous analgesia (PCIA) for post spine surgery. Methods One hundred ASA I or II patients of both sexes,aged 29-63 yr,weighing 49-77 kg,undergoing elective spine surgery,were randomly divided into 4 groups(n= 25 each) using a random number table:1.0mg•kg oxycodone group (group O), 1.0mg•kg oxycodone combined with 2.5μg•kg dexmedetomidine group (group OD1), 0.8mg•kg oxycodone combined with 2.5μg•kg dexmedetomidine group (group OD2)and 0.6mg•kg oxycodone combined with 2.5μg•kg dexmedetomidine group (group OD3),In each group, the PCIA solution contained oxycodone or oxycodone and dexmedetomidine in 200 ml of normal saline. At 15 min before the end of surgery,oxycodone 0.1 mg•kg was injected intravenously, and PCIA pump was connected simuhaneously. The PCIA pump was set up to deliver a 2 ml bolus dose with a 20-min lockout interval and background infusion at 3.5~4.5 ml•h. Oxycodone 0.05 mg•kg was injected intravenously as a rescue analgesic,and VAS was maintained≤4. The requirement for the rescue analgesic was re- corded within 48h after surgery.The number of successfully delivered doses,and the occur- rence of adverse reactions such as bradycardia, hypotension, nausea,vomiting, over-seda- tion,somnolence, pruritus, and respiratory depression were recorded. Patient’s satisfaction with analgesia was recorded at 72 h after surgery. Results No patients required the rescue analgesic or developed over-sedation, vomiting, respiratory depression and hypotension in the four groups. Compared with group O,the incidence of somnolence was significantly increased in group OD1, the incidence of nausea, somnolence, bradycardia and pruritus was decreased in OD2 and OD3 groups,and the degree of patient’s satisfaction with analgesia was increased in OD1-3 groups(P<0.05). Compared with group OD1, the incidence of nausea,somnolence,bradycardia and pruritus was significantly decreased in OD2 and OD3 groups,the degree of patient’s satisfaction with analgesia was significantly increased in group OD2 (P<0.01), and the degree of patient’s satisfaction with analgesia was decreased in group OD3(P<0.05). Compared with group OD2, no significant was found in the incidence of adverse reactions (P>0.05), and the degree of patient’s satisfaction with analgesia was decreased in group OD3 (P<0.05). The number of successfully delivered doses was larger in group OD3 than in O, OD1 and OD2 groups (P<0.05). Conclusion Dexmedetomidine 2.5μg•kg added to oxycodone 0.8mg•kg for PCIA is an effective approach for post spine surgery. It Can significantly reduce the consumption of oxycodone, decrease the incidence of adverse reactions and improve the overall satisfaction of analgesia from patients.

Key words: Oxycodone;dexmedetomidine;Analgesia;patient-controlled; postoperative