Singh Ranju, Kumar Nishant, Jain Aruna, Joy Sudipta
Department of Anaesthesiology and Critical Care, Lady Hardinge Medical College and Associated Shrimati Sucheta Kriplani Hospital, New Delhi, India.
J Anaesthesiol Clin Pharmacol. 2016 Oct-Dec;32(4):501-504. doi: 10.4103/0970-9185.173358.
The aim was to compare duration of postoperative analgesia with addition of clonidine to bupivacaine in bilateral transversus abdominis plane (TAP) block after lower segment cesarean section (LSCS).
One hundred American Society of Anesthesiologists (ASA) grade I and II pregnant patients undergoing LSCS under spinal anesthesia were randomly divided to receive either 20 ml bupivacaine 0.25% (Group B; = 50) or 20 ml bupivacaine+1ug/kg clonidine bilaterally (Group BC; = 50) in TAP block in a double-blind fashion. The total duration of analgesia, patient satisfaction score, total requirement of analgesics in the first 24 h, and the side effects of clonidine such as sedation, dryness of mouth, hypotension, and bradycardia were observed. < 0.05 was taken as significant.
In 99 patients analyzed, TAP block failed in five patients. Duration of analgesia was significantly longer in Group BC (17.8 ± 3.7 h) compared to Group B (7.3 ± 1.2 h; < 0.01). Mean consumption of diclofenac was 150 mg and 65.4 mg in Groups B and BC ( < 0.01), respectively. All patients in Group BC were extremely satisfied ( < 0.01) while those in Group B were satisfied. Thirteen patients (28%) in Group BC were sedated but arousable ( = 0.01) compared to none in Group B. In Group BC, 19 patients complained of dry mouth compared to 13 in Group B ( = 0.121). None of the patients experienced hypotension or bradycardia.
Addition of clonidine 1 μg/kg to 20 ml bupivacaine 0.25% in TAP block bilaterally for cesarean section significantly increases the duration of postoperative analgesia, decreases postoperative analgesic requirement, and increases maternal comfort compared to 20 ml of bupivacaine 0.25% alone.
目的是比较剖宫产术后双侧腹横肌平面(TAP)阻滞中布比卡因添加可乐定后的术后镇痛时长。
100例美国麻醉医师协会(ASA)分级为I级和II级、接受腰麻下行剖宫产术的孕妇,被随机分为两组,双盲法接受双侧TAP阻滞,其中一组接受20ml 0.25%布比卡因(B组;n = 50),另一组接受20ml布比卡因+1μg/kg可乐定(BC组;n = 50)。观察镇痛总时长、患者满意度评分、术后24小时内镇痛药总需求量以及可乐定的副作用,如镇静、口干、低血压和心动过缓。P < 0.05为有统计学意义。
在分析的99例患者中,5例TAP阻滞失败。与B组(7.3 ± 1.2小时)相比,BC组的镇痛时长显著更长(17.8 ± 3.7小时;P < 0.01)。B组和BC组双氯芬酸的平均消耗量分别为150mg和65.4mg(P < 0.01)。BC组所有患者均非常满意(P < 0.01),而B组患者为满意。BC组有13例患者(28%)出现镇静但可唤醒(P = 0.01),而B组无此情况。BC组有19例患者主诉口干,B组有13例(P = 0.121)。所有患者均未出现低血压或心动过缓。
剖宫产术中双侧TAP阻滞时,在20ml 0.25%布比卡因中添加1μg/kg可乐定,与单独使用20ml 0.25%布比卡因相比,可显著延长术后镇痛时长,减少术后镇痛药需求量,并提高产妇舒适度。