Siddiqui Ali Sarfraz, Raees Umme Summayya, Siddiqui Safia Zafar, Raza Syed Amir
Department of Anaesthesia, The Aga Khan University Hospital, Karachi, Pakistan.
J Coll Physicians Surg Pak. 2013 Aug;23(8):533-7.
To assess the efficacy of pre-incisional peritonsillar infiltration of two doses of ketamine on postoperative analgesia compared with peritonsillar normal saline in children undergoing tonsillectomy.
Double blind, randomized controlled trial.
Department of Anaesthesiology, Surgical Intensive Care and Pain Management, Civil Hospital, Karachi, Dow University of Health Sciences, from August 2008 to January 2009.
Seventy-five ASA physical status one patients, aged 5 - 12 years scheduled for tonsillectomy were enrolled in this study. Patients were divided into three groups of 25 each. Group-A received normal saline, Group-B, ketamine 0.5 mg/kg while group-C ketamine 1 mg/kg respectively. All medications were 2 ml and were applied 1 ml per tonsil; 3 minutes before tonsillectomy incision. Anaesthesia was induced and maintained with standard technique. All patients were monitored throughout surgery. The Children's Hospital of Eastern Ontario Pain Scale (CHEOPS) and Wilson sedation scale were used to evaluate pain levels and sedation respectively after operation.
Mean duration of analgesia was significantly higher in group-C (17.28 ± 5.33 hours) as compared to group-B (11.36 ± 4.15 hours) and A (3.2 ± 0.71 hours) as well as group-B was also significantly higher than group-A (p < 0.05). Group-A had significantly higher pain scores than group-B and group-C. Both B and C groups had comparable pain scores, which were statistically significant at 6 and 8 hours.
Single 0.5 or 1 mg/kg injection of ketamine given before surgical incision by peritonsillar infiltration provides efficient pain relief during postoperative period without significant side-effects in children undergoing tonsillectomy.
评估在扁桃体切除术中,与扁桃体周围注射生理盐水相比,两种剂量的氯胺酮术前扁桃体周围浸润对术后镇痛的效果。
双盲随机对照试验。
2008年8月至2009年1月,卡拉奇市民医院麻醉科、外科重症监护及疼痛管理科,道健康科学大学。
本研究纳入75例年龄在5至12岁、美国麻醉医师协会(ASA)身体状况为1级、计划行扁桃体切除术的患者。患者被分为三组,每组25例。A组接受生理盐水,B组接受0.5mg/kg氯胺酮,C组接受1mg/kg氯胺酮。所有药物均为2ml,每侧扁桃体注射1ml;在扁桃体切除术前3分钟注射。采用标准技术诱导和维持麻醉。整个手术过程中对所有患者进行监测。术后分别使用安大略东部儿童医院疼痛量表(CHEOPS)和威尔逊镇静量表评估疼痛程度和镇静情况。
与B组(11.36±4.15小时)和A组(3.2±0.71小时)相比,C组的平均镇痛持续时间显著更长(17.28±5.33小时),且B组也显著高于A组(p<0.05)。A组的疼痛评分显著高于B组和C组。B组和C组的疼痛评分相当,在6小时和8小时时具有统计学意义。
在扁桃体切除术患儿中,术前扁桃体周围浸润注射单次0.5或1mg/kg氯胺酮可在术后提供有效的疼痛缓解,且无明显副作用。