临床麻醉学杂志
臨床痳醉學雜誌
림상마취학잡지
THE JOURNAL OF CLINICAL ANESTHESIOLOGY
2014年
12期
1152-1155
,共4页
王瑜%蒋蓉%邓佳%苏文杰%徐广民
王瑜%蔣蓉%鄧佳%囌文傑%徐廣民
왕유%장용%산가%소문걸%서엄민
右美托咪定%瑞芬太尼%痛觉过敏%全身麻醉
右美託咪定%瑞芬太尼%痛覺過敏%全身痳醉
우미탁미정%서분태니%통각과민%전신마취
Dexmedetomidine%Remifentanil%Hyperalgesia%General anesthesia
目的:观察右美托咪定联合帕瑞昔布钠用于预防瑞芬太尼麻醉后痛觉过敏的效果及安全性。方法择期行腹腔镜胆囊切除手术的女性患者100例。按照数字表将患者分为四组:对照组(C 组)、帕瑞昔布钠组(P 组)、右美托咪定组(D 组)、右美托咪定联合帕瑞昔布钠组(DP 组)。患者入室后行常规监测,所有患者均行静脉麻醉,静脉泵注丙泊酚4~12 mg·kg-1·h-1和瑞芬太尼0.2μg· kg-1· min-1,P 组手术结束前30 min 静脉注射帕瑞昔布钠40 mg;D 组诱导后以0.6μg·kg-1·min-1的剂量静脉恒速泵注右美托咪定至手术结束前30 min;DP 组诱导后以0.6μg·kg-1·min-1的剂量静脉恒速泵注右美托咪定至手术结束前30 min 并注射帕瑞昔布钠40 mg。记录术后1、2、6、12、24 h 的 VAS 评分;以及术后发生躁动、寒颤、恶心呕吐和24 h 内追加镇痛药物的例数。结果与C 组比较,P 组、D 组、DP 组术后各时点 VAS 评分明显降低(P<0.05),DP 组患者在术后各时点 VAS 评分明显低于 P 组和 D 组(P<0.05)。D 组和 DP 组术后躁动和寒颤发生率明显低于 C 组(P<0.05)。DP 组术后24 h 镇痛药物的追加明显低于 C 组、P 组和 D 组(P<0.05)。结论麻醉诱导后以0.6μg·kg-1·min-1静脉恒速泵注右美托咪定至手术结束前30 min 并注射帕瑞昔布钠40 mg 能够减少瑞芬太尼停药后导致的痛觉过敏,并减少术后躁动和寒颤的发生率。
目的:觀察右美託咪定聯閤帕瑞昔佈鈉用于預防瑞芬太尼痳醉後痛覺過敏的效果及安全性。方法擇期行腹腔鏡膽囊切除手術的女性患者100例。按照數字錶將患者分為四組:對照組(C 組)、帕瑞昔佈鈉組(P 組)、右美託咪定組(D 組)、右美託咪定聯閤帕瑞昔佈鈉組(DP 組)。患者入室後行常規鑑測,所有患者均行靜脈痳醉,靜脈泵註丙泊酚4~12 mg·kg-1·h-1和瑞芬太尼0.2μg· kg-1· min-1,P 組手術結束前30 min 靜脈註射帕瑞昔佈鈉40 mg;D 組誘導後以0.6μg·kg-1·min-1的劑量靜脈恆速泵註右美託咪定至手術結束前30 min;DP 組誘導後以0.6μg·kg-1·min-1的劑量靜脈恆速泵註右美託咪定至手術結束前30 min 併註射帕瑞昔佈鈉40 mg。記錄術後1、2、6、12、24 h 的 VAS 評分;以及術後髮生躁動、寒顫、噁心嘔吐和24 h 內追加鎮痛藥物的例數。結果與C 組比較,P 組、D 組、DP 組術後各時點 VAS 評分明顯降低(P<0.05),DP 組患者在術後各時點 VAS 評分明顯低于 P 組和 D 組(P<0.05)。D 組和 DP 組術後躁動和寒顫髮生率明顯低于 C 組(P<0.05)。DP 組術後24 h 鎮痛藥物的追加明顯低于 C 組、P 組和 D 組(P<0.05)。結論痳醉誘導後以0.6μg·kg-1·min-1靜脈恆速泵註右美託咪定至手術結束前30 min 併註射帕瑞昔佈鈉40 mg 能夠減少瑞芬太尼停藥後導緻的痛覺過敏,併減少術後躁動和寒顫的髮生率。
목적:관찰우미탁미정연합파서석포납용우예방서분태니마취후통각과민적효과급안전성。방법택기행복강경담낭절제수술적녀성환자100례。안조수자표장환자분위사조:대조조(C 조)、파서석포납조(P 조)、우미탁미정조(D 조)、우미탁미정연합파서석포납조(DP 조)。환자입실후행상규감측,소유환자균행정맥마취,정맥빙주병박분4~12 mg·kg-1·h-1화서분태니0.2μg· kg-1· min-1,P 조수술결속전30 min 정맥주사파서석포납40 mg;D 조유도후이0.6μg·kg-1·min-1적제량정맥항속빙주우미탁미정지수술결속전30 min;DP 조유도후이0.6μg·kg-1·min-1적제량정맥항속빙주우미탁미정지수술결속전30 min 병주사파서석포납40 mg。기록술후1、2、6、12、24 h 적 VAS 평분;이급술후발생조동、한전、악심구토화24 h 내추가진통약물적례수。결과여C 조비교,P 조、D 조、DP 조술후각시점 VAS 평분명현강저(P<0.05),DP 조환자재술후각시점 VAS 평분명현저우 P 조화 D 조(P<0.05)。D 조화 DP 조술후조동화한전발생솔명현저우 C 조(P<0.05)。DP 조술후24 h 진통약물적추가명현저우 C 조、P 조화 D 조(P<0.05)。결론마취유도후이0.6μg·kg-1·min-1정맥항속빙주우미탁미정지수술결속전30 min 병주사파서석포납40 mg 능구감소서분태니정약후도치적통각과민,병감소술후조동화한전적발생솔。
Objective To observe the preventive efficacy and safety of dexmedetomidine with parecoxib sodium on the patients with postoperative hyperalgesia induced by remifentanil. Methods A total of 100 female patients undergoing elective surgery under general anesthesia were as-signed into four groups according to the table of random number:the control group (group C),the parecoxib sodium group (group P),the dexmedetomidine group (group D)and the parecoxib sodium combined with the dexmedetomidine group (group DP).The vital signs were monitored and the total intravenous anesthesia was performed.All the patients were give intravenous injection of 0.2μg·kg-1 ·min-1 remifentanil and 4-12 mg·kg-1 ·h-1 propofol to maintain the anesthesia.Patients in group P were given 40 mg parecoxib sodium 30 minutes before the end of the operation.Patients in group D were give intravenous injection of 0.6μg·kg-1 ·min-1 dexmedetomidine consistently till 30 min before the end of the operation.Patients in group DP were given 0.6 μg·kg-1 ·min-1 till 30 min before the end of the operation and were given 40 mg parecoxib sodium.The VAS scores were re-corded at 1,2,6,12,24 hours.The cases of agitation,rigors,nausea and vomiting and increasing of analgesics were recorded.Results The postoperative VAS scores in group P,group D and group DP were significantly lower than group C(P <0.05).The postoperative VAS scores in group DP were significantly lower in group P and group D (P<0.05).Cases of agitation and rigors in group D and group DP were less than group C(P <0.05).The increasing of analgesics in group DP was much higher than other groups(P<0.05).Conclusion After induced,patients were given intravenous in-jection of 0.6 μg·kg-1 ·min-1 dexmedetoniding consistently till 30 min before the end of the opera-tion were given 40 mg parecoxib sodium can effectively prevent hyperalgesia after remifentanil anes-thesia without significant increase in revival time and obtain a better sedation.