曲马多复合芬太尼在小儿术后持续静脉镇痛中的应用  被引量:3

Postoperative intravenous analgesia with a combination of tramadol and fentanyl continuously infused in children

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作  者:周碧云[1] 罗爱林[1] 喻红辉[1] 田玉科[1] 

机构地区:[1]华中科技大学同济医学院附属同济医院麻醉学教研室,湖北武汉430030

出  处:《中国妇幼保健》2007年第32期4618-4621,共4页Maternal and Child Health Care of China

摘  要:目的:比较曲马多与不同剂量芬太尼复合用于小儿术后持续静脉自控镇痛(PCIA)效果和副作用。方法:选择行全麻择期手术患儿120例(ASAⅠ~Ⅱ级)进行术后PCIA,随机分成四组:T组:1%曲马多;TF1组:1%曲马多+芬太尼2μg·ml^-1;FT2组:1%曲马多+芬太尼4μg·ml^-1;TF3组:1%曲马多+芬太尼6μg·ml^-1。手术缝皮时开启镇痛泵,负荷量0.1ml·kg^-1 +持续量0.5^-1ml·h^-1,+PCA量0.5^-1 ml^-1次。(由患儿双亲或护士控制,NPCIA/PPCIA),锁定时间10min。均静脉注射格拉司琼40μg·k^-1。记录术后24h内的血压、心率、脉氧饱和度(SPO2)、呼吸频率(RR)、CHEOPS(Children's Hospital of Estem Ontario Pain Score)镇痛评分〈4分:无痛,〉6分:中度疼痛,〉13分:重度疼痛)、表情疼痛评分(FRS)、TSS镇静评分、24h用药量以及不良反应。结果:四组术后24h的BP、HR、呼吸频率(RR)无明显变化,均可达到满意的镇痛效果,FRS各组间的差异无显著性(P〉0.05),T组和TF1组HEOPS在术后30min时明显降低(P〈0.05);24h曲马多用量T组〉TF1组〉TF2组(P〈0.05),TR组〉TF3组,但差异无统计学意义(P〉0.05);按压次数(PCAe)、术后恶心呕吐(PONV)发生率四组间的差异无显著性,TF3组术后苏醒时间较另三组明显延长,各组内均有一例患儿出现眩晕。结论:小剂量芬太尼与曲马多复合用于小儿PCIA镇痛效果良好,可明显减少曲马多的用量,最佳方案是镇痛用药为1%曲马多+芬太尼4μg·ml^-1,负荷量0.1ml·kg^-1 +持续量0.5^-1ml·h^-1 +PCA0.5~1ml;格拉司琼在小儿中的应用尚需进一步的研究。Objective: To compare the efficacy of patient - controlled intravenous analgesia (PICA) with a eo - application of different dosage of tramadol and fentanyl in postoperative analgesia in children. Methods: By an observer -blinded design, 120 ASA Ⅰ-Ⅱ pediatrle patients (1 ~ 12 years old) underwent general anesthesia were randomly given a postoperative intravenous infusion of 1% tramadol ( Group T), 1% tramadol plus fentanyl 2 μg/ml ( Group TF1 ) , 1% tramadol plus fentanyl 4 μg/ml ( Group TF2 ) , or 1% tramadol plus fentanyl 6μg/ml ( Group TF3 ) . Exclusion erlteria included children with mental disorders, hypothyroidism pilepsy, and long - term analgesic users. All the patients received Granisentran Hydrochloride 40 μg/kg via intravenous injection at the end of surgery. PCIA was commenced and continued for 24 h. The analgesic effect was assessed by Wong- Baker Faces Pain Rating Scale (FRS) and the Children's Hospital of Ontario Pain Scale (CHEOPS), less than 4 (no pain), more than 6 (moderate pain), more than 13 (severe pain), eousumption of analgosies and the ineideneos of side - effects were recorded. Results: ( 1 ) There were no significant differences in the demographic data ineluding sex, age, body weight, types of surgery and duration of operation among the four groups ( P 〉 0. 05 ) ; ( 2 ) No significant differenees were found in BP, HR, RR (respiratory rate) and SpO2 among the four groups (P 〉0. 05) ; (3) The FRS did not significantly change among the four groups, and the CHEOPS at the point of 30 min were significantly decreased in both group T and group TF1 ; (4) With the dosages of fentanyl increased, the 24 h consumptions of tramadol were significantly reduced in Group T , Group TF1 and Group TF2 (P 〈0. 05), but the tendency was disturbed in Group TF3; (5) The incidences of vertigo, nausea and vomiting had no significant differenees among the four groups, while the recovery time of Group TF3 was sig

关 键 词:小儿 静脉镇痛 CHEOPS评分 曲马多 

分 类 号:R971[医药卫生—药品]

 

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