Bano Fauzia, Sabbar Saleem, Zafar Safia, Rafeeq Nabeela, Iqbal Mirza Nasir, Haider Saeeda, Aftab Sadqa, Sultan S Tipu
Department of Anesthesiology, Surgical I.C.U and Pain Management, Dow University of Health Sciences and Civil Hospital, Karachi.
J Coll Physicians Surg Pak. 2006 Feb;16(2):87-90.
To compare the effect of adding fentanyl to intrathecal bupivacaine on the onset, duration and quality of spinal anesthesia and its effect of mother and neonate.
Single blind randomized controlled clinical trial.
Department of Anesthesiology, Surgical Intensive Care Unit and Pain Management, Dow University of Health Sciences and Civil Hospital, Karachi, from January 2003 to June 2004.
Sixty young adult females, ASA physical status I and II, with singleton pregnancy undergoing elective or emergency cesarean section under spinal anesthesia were randomly allocated to receive spinal anesthesia either by using 0.75% hyperbaric bupivacaine 1.5 ml with 0.25 ml normal saline or 0.75% hyperbaric bupivacaine 1.5 ml with 0.25 ml fentanyl (12.5 microg). Blood pressure, heart rate, respiratory rate, oxygen saturation, sensory level, motor block, pain score and side effects were observed every 2 minutes for first 20 minutes, then at-5 minute interval throughout the surgery, thereafter at 30 minutes interval until the patient complained of pain.
Comparing the bupivacaine group, time to achieve highest sensory level was significantly shorter in fentanyl group (*p < 0.05), while the duration of complete analgesia (time from injection to first report of pain) lasted significantly more longer in fentanyl group (184+/-20 minutes) than bupivacaine group (126+/-10 minutes). Duration of effective analgesia was also significantly more prolonged in fentanyl group (p < 0.05). There was no significant difference in the incidence of side effects between the two groups.
Addition of fentanyl to intrathecal bupivacaine results in faster onset with improved peri-operative anesthesia without increasing the side effects.
比较鞘内注射布比卡因时添加芬太尼对脊麻起效时间、持续时间、麻醉质量及其对母婴的影响。
单盲随机对照临床试验。
2003年1月至2004年6月,卡拉奇道健康科学大学和市民医院麻醉科、外科重症监护室及疼痛管理科。
60例ASA身体状况为I级和II级的单胎妊娠成年女性,在脊麻下行择期或急诊剖宫产术,随机分配接受脊麻,一组使用1.5 ml 0.75% 高压布比卡因加0.25 ml生理盐水,另一组使用1.5 ml 0.75% 高压布比卡因加0.25 ml芬太尼(12.5微克)。前20分钟每2分钟观察一次血压、心率、呼吸频率、血氧饱和度、感觉平面、运动阻滞、疼痛评分及副作用,然后在手术全程每隔5分钟观察一次,此后每隔30分钟观察一次,直至患者主诉疼痛。
与布比卡因组相比,芬太尼组达到最高感觉平面的时间显著缩短(*p < 0.05),而芬太尼组完全镇痛持续时间(从注射至首次疼痛报告时间)显著长于布比卡因组(184±20分钟)(布比卡因组为126±10分钟)。芬太尼组有效镇痛持续时间也显著延长(p < 0.05)。两组副作用发生率无显著差异。
鞘内注射布比卡因时添加芬太尼可加快起效,改善围手术期麻醉效果,且不增加副作用。